abdominal 1 dorsal campaniform sensillum dc1 [FBbt_00002800]
Any abdominal dorsal campaniform sensillum dc1 (FBbt:00002799) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal dorsal campaniform sensillum dc1 (FBbt:00002799) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal dorsal campaniform sensillum dc2 (FBbt:00002807) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal dorsal trichoid sensillum dh1 (FBbt:00002783) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal dorsal trichoid sensillum dh2 (FBbt:00100033) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal lateral campaniform sensillum lc1 (FBbt:00002855) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal lateral monoscolopidial chordotonal organ lch1 (FBbt:00002823) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal lateral pentascolopidial chordotonal organ lch5 (FBbt:00002831) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal lateral trichoid sensillum lh1 (FBbt:00002839) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal lateral trichoid sensillum lh2 (FBbt:00002847) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal ventral campaniform sensillum vc1 (FBbt:00002863) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal ventral campaniform sensillum vc2 (FBbt:00002871) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal ventral campaniform sensillum vc3 (FBbt:00002879) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal ventral campaniform sensillum vc4a (FBbt:00002887) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal ventral campaniform sensillum vc4b (FBbt:00002895) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal ventral campaniform sensillum vc5 (FBbt:00002903) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal ventral monoscolopidial chordotonal organ vch1 (FBbt:00002904) that is part of some larval abdominal segment 1 (FBbt:00001748).
Any abdominal ventral monoscolopidial chordotonal organ vch2 (FBbt:00007255) that is part of some larval abdominal segment 1 (FBbt:00001748).
Basiconic sensillum of the ventral region of the larval abdominal segment 10. It is innervated by three bipolar neurons whose dendrites are apposed. This sensillum is also innervated by several multidendritic neurons from which two neurites emerge.
Campaniform sensillum of the ventral region of the larval abdominal segment 10, in the ventral midline, anteriorly adjacent to the anal pads. It is innervated by 2 neurons.
Small group of densely packed denticles located at the most ventral point of larval abdominal segment 11, and flanked by the anal sense organs (caudal sense organs).
Any abdominal dorsal campaniform sensillum dc1 (FBbt:00002799) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal dorsal campaniform sensillum dc2 (FBbt:00002807) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal dorsal trichoid sensillum dh1 (FBbt:00002783) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal dorsal trichoid sensillum dh2 (FBbt:00100033) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal lateral campaniform sensillum lc1 (FBbt:00002855) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal lateral monoscolopidial chordotonal organ lch1 (FBbt:00002823) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal lateral pentascolopidial chordotonal organ lch5 (FBbt:00002831) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal lateral trichoid sensillum lh1 (FBbt:00002839) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal lateral trichoid sensillum lh2 (FBbt:00002847) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal ventral campaniform sensillum vc1 (FBbt:00002863) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal ventral campaniform sensillum vc2 (FBbt:00002871) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal ventral campaniform sensillum vc3 (FBbt:00002879) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal ventral campaniform sensillum vc4a (FBbt:00002887) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal ventral campaniform sensillum vc4b (FBbt:00002895) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal ventral campaniform sensillum vc5 (FBbt:00002903) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal ventral monoscolopidial chordotonal organ vch1 (FBbt:00002904) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal ventral monoscolopidial chordotonal organ vch2 (FBbt:00007255) that is part of some larval abdominal segment 2 (FBbt:00001749).
Any abdominal dorsal campaniform sensillum dc1 (FBbt:00002799) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal dorsal campaniform sensillum dc2 (FBbt:00002807) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal dorsal trichoid sensillum dh1 (FBbt:00002783) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal dorsal trichoid sensillum dh2 (FBbt:00100033) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal lateral campaniform sensillum lc1 (FBbt:00002855) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal lateral monoscolopidial chordotonal organ lch1 (FBbt:00002823) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal lateral pentascolopidial chordotonal organ lch5 (FBbt:00002831) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal lateral trichoid sensillum lh1 (FBbt:00002839) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal lateral trichoid sensillum lh2 (FBbt:00002847) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal ventral campaniform sensillum vc1 (FBbt:00002863) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal ventral campaniform sensillum vc2 (FBbt:00002871) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal ventral campaniform sensillum vc3 (FBbt:00002879) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal ventral campaniform sensillum vc4a (FBbt:00002887) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal ventral campaniform sensillum vc4b (FBbt:00002895) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal ventral campaniform sensillum vc5 (FBbt:00002903) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal ventral monoscolopidial chordotonal organ vch1 (FBbt:00002904) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal ventral monoscolopidial chordotonal organ vch2 (FBbt:00007255) that is part of some larval abdominal segment 3 (FBbt:00001750).
Any abdominal dorsal campaniform sensillum dc1 (FBbt:00002799) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal dorsal campaniform sensillum dc2 (FBbt:00002807) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal dorsal trichoid sensillum dh1 (FBbt:00002783) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal dorsal trichoid sensillum dh2 (FBbt:00100033) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal lateral campaniform sensillum lc1 (FBbt:00002855) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal lateral monoscolopidial chordotonal organ lch1 (FBbt:00002823) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal lateral pentascolopidial chordotonal organ lch5 (FBbt:00002831) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal lateral trichoid sensillum lh1 (FBbt:00002839) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal lateral trichoid sensillum lh2 (FBbt:00002847) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal ventral campaniform sensillum vc1 (FBbt:00002863) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal ventral campaniform sensillum vc2 (FBbt:00002871) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal ventral campaniform sensillum vc3 (FBbt:00002879) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal ventral campaniform sensillum vc4a (FBbt:00002887) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal ventral campaniform sensillum vc4b (FBbt:00002895) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal ventral campaniform sensillum vc5 (FBbt:00002903) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal ventral monoscolopidial chordotonal organ vch1 (FBbt:00002904) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal ventral monoscolopidial chordotonal organ vch2 (FBbt:00007255) that is part of some larval abdominal segment 4 (FBbt:00001751).
Any abdominal dorsal campaniform sensillum dc1 (FBbt:00002799) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal dorsal campaniform sensillum dc2 (FBbt:00002807) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal dorsal trichoid sensillum dh1 (FBbt:00002783) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal dorsal trichoid sensillum dh2 (FBbt:00100033) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal lateral campaniform sensillum lc1 (FBbt:00002855) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal lateral monoscolopidial chordotonal organ lch1 (FBbt:00002823) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal lateral pentascolopidial chordotonal organ lch5 (FBbt:00002831) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal lateral trichoid sensillum lh1 (FBbt:00002839) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal lateral trichoid sensillum lh2 (FBbt:00002847) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal ventral campaniform sensillum vc1 (FBbt:00002863) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal ventral campaniform sensillum vc2 (FBbt:00002871) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal ventral campaniform sensillum vc3 (FBbt:00002879) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal ventral campaniform sensillum vc4a (FBbt:00002887) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal ventral campaniform sensillum vc4b (FBbt:00002895) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal ventral campaniform sensillum vc5 (FBbt:00002903) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal ventral monoscolopidial chordotonal organ vch1 (FBbt:00002904) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal ventral monoscolopidial chordotonal organ vch2 (FBbt:00007255) that is part of some larval abdominal segment 5 (FBbt:00001752).
Any abdominal dorsal campaniform sensillum dc1 (FBbt:00002799) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal dorsal campaniform sensillum dc2 (FBbt:00002807) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal dorsal trichoid sensillum dh1 (FBbt:00002783) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal dorsal trichoid sensillum dh2 (FBbt:00100033) that is part of some larval abdominal segment 6 (FBbt:00001753).
[abdominal lateral campaniform sensillum lc1; larval abdominal segment 6; abdominal 6 lateral campaniform sensillum lc1; is part of; abdominal 6 lateral sensillum campaniformium lc1]
Any abdominal lateral monoscolopidial chordotonal organ lch1 (FBbt:00002823) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal lateral pentascolopidial chordotonal organ lch5 (FBbt:00002831) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal lateral trichoid sensillum lh1 (FBbt:00002839) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal lateral trichoid sensillum lh2 (FBbt:00002847) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal ventral campaniform sensillum vc1 (FBbt:00002863) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal ventral campaniform sensillum vc2 (FBbt:00002871) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal ventral campaniform sensillum vc3 (FBbt:00002879) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal ventral campaniform sensillum vc4a (FBbt:00002887) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal ventral campaniform sensillum vc4b (FBbt:00002895) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal ventral campaniform sensillum vc5 (FBbt:00002903) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal ventral monoscolopidial chordotonal organ vch1 (FBbt:00002904) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal ventral monoscolopidial chordotonal organ vch2 (FBbt:00007255) that is part of some larval abdominal segment 6 (FBbt:00001753).
Any abdominal dorsal campaniform sensillum dc1 (FBbt:00002799) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal dorsal campaniform sensillum dc2 (FBbt:00002807) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal dorsal trichoid sensillum dh1 (FBbt:00002783) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal dorsal trichoid sensillum dh2 (FBbt:00100033) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal lateral campaniform sensillum lc1 (FBbt:00002855) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal lateral monoscolopidial chordotonal organ lch1 (FBbt:00002823) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal lateral pentascolopidial chordotonal organ lch5 (FBbt:00002831) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal lateral trichoid sensillum lh1 (FBbt:00002839) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal lateral trichoid sensillum lh2 (FBbt:00002847) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal ventral campaniform sensillum vc1 (FBbt:00002863) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal ventral campaniform sensillum vc2 (FBbt:00002871) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal ventral campaniform sensillum vc3 (FBbt:00002879) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal ventral campaniform sensillum vc4a (FBbt:00002887) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal ventral campaniform sensillum vc4b (FBbt:00002895) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal ventral campaniform sensillum vc5 (FBbt:00002903) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal ventral monoscolopidial chordotonal organ vch1 (FBbt:00002904) that is part of some larval abdominal segment 7 (FBbt:00001754).
Any abdominal ventral monoscolopidial chordotonal organ vch2 (FBbt:00007255) that is part of some larval abdominal segment 7 (FBbt:00001754).
Basiconic sensillum of the dorsal cluster of the larval abdominal segment 8, located at the base of the posterior spiracle.
Trichoid sensillum of the dorsal cluster of the larval abdominal segment 8, located at the base of the posterior spiracle.
Basiconic sensillum of the lateral cluster of the larval abdominal segment 8, located in the niche between the lateral transverse muscle LT1 and the epidermis. It could correspond to t5.
Trichoid sensillum of the dorsal cluster of the larval abdominal segment 8, located in the niche between the lateral transverse muscle LT1 and the epidermis. It could correspond to t6.
Triscolopidial chordotonal organ of larval abdominal segment 8, located laterally in the niche between the lateral transverse muscle LT1 and the epidermis.
Unpaired campaniform sensillum of the ventral region of the larval abdominal segment 8, in the ventral midline, anteriorly adjacent to the anal pads. It is innervated by 2 neurons.
Trichoid sensillum of the posterior cluster of the larval abdominal segment 9.
Basiconic sensillum of the posterior cluster of the larval abdominal segment 9.
Lateral chordotonal organ group located in larval abdominal segment 9 close to the dorsocaudal sensory cone (Campos-Ortega and Hartenstein, 1997). It is composed of a triscolopidial and a monoscolopidial chordotonal organ.
A dorsal, mono-innervated campaniform sensillum of larval abdominal segments 1-7.
A dorsal, mono-innervated campaniform sensillum of larval abdominal segments 1-7.
Small, mono-innervated hair of the dorsal sensory complex of larval abdominal segments 1-7. Note that this organ (identified as the anterior organ in the dh1-dh2 organ pair) is reported to be tri-innervated in Campos-Ortega and Hartenstein, 1997. The formerly separate term ‘h3’ (FBbt:00002791) has been merged with dh1: It is clear from comparing the diagrams in Dambly-Chaudiere and Ghysen (1986) with Campos-Ortega and Hartenstein (1997), that the authors are referring to the same sensillum; FlyPNS also states that these are synonyms.
Dorsal, bi-innervated hair of larval abdominal segments 1-7. Note that this organ is reported to be mono-innervated by Campos-Ortega and Hartenstein (1997).
Lateral mono-innervated campaniform sensilla of larval abdominal segments 1-7.
Monoscolopidial chordotonal organ of the lateral sensory cluster of larval segments A1-7. There is one of these organs per cluster. It is innervated by the abdominal v’ch1 neuron.
Pentascolopidial chordotonal organ located in the lateral sensory cluster of the embryonic/larval abdominal segment. Each of the five scolopidia that constitute the LCh5 organ contains a sensory unit composed of a neuron and a scolopale cell, and two accessory cells between which the sensory unit is stretched: a cap cell at the dendritic side and a ligament cell at the axonal side of the neuron (Halachmi et al., 2016). The cap and the ligament cells of all five organs are anchored to the cuticle by two cap attachment cells and one ligament attachment cell (Halachmi et al., 2016). The neuron, scolopale, cap, ligament and cap attachment cells of each scolopidium are derived from a single ato-expressing precursor through four asymmetric cell divisions (Halachmi et al., 2016).
Lateral mono-innervated hair of larval abdominal segments 1-7. Campos-Ortega and Hartenstein, 1997, state in table 9.1 that lh1 is innervated by lesA and innervates ‘h1’. This appears to be a misrepresentation of Ghysen et al., (1986) as this paper does not appear to make that claim. sr080210.
Lateral mono-innervated hair of larval abdominal segments 1-7.
Microchaeta of a sternite of the abdominal segments.
Microchaeta found on the posterior margin of a tergite of the abdominal segments.
A campaniform sensillum of larval abdominal segments 1-7. It is the ventral-most sensillum of these segments, and is innervated by the dendrite of a single neuron - vesA.
A ventrally located campaniform sensillum of larval abdominal segments 1-7, innervated by the dendrite of a single neuron - vesB. Fasciculates in branch c of the segmental nerve, SNc (Campos-Ortega and Hartenstein, 1997).
A ventrally located campaniform sensillum of larval abdominal segments 1-7, innervated by the dendrite of a single neuron - vesC. The tormogen (socket) cell of this sensillum is unusual in having numerous short cytoplasmic extensions (Barolo et al., 2000). It fasciculates in branch c of the segmental nerve, SNc (Campos-Ortega and Hartenstein, 1997).
A ventrally located campaniform sensillum of larval abdominal segments 1-7 buried in a narrow slit of the cuticle among the denticles, innervated by the dendrite of a single neuron - v’esB.
A ventrally located campaniform sensillum of larval abdominal segments 1-7, innervated by the dendrite of a single neuron - v’esA.
A ventrally located campaniform sensillum of larval abdominal segments 1-7 whose external sensory structure is surrounded by a ruffled annulus and which is innervated by the 2 dendrites of the v’es2 neurons.
Ventral monoscolopidial chordotonal organ of larval abdominal segments 1-7, innervated by a single neuron - vch1 (vchA).
Ventral monoscolopidial chordotonal organ of larval abdominal segments 1-7, innervated by a single neuron - vch2 (vchB).
Microchaeta of the scutum of the adult dorsal mesothorax in the acrostichal region. They are located on either side of the midline and medially to the dorsocentral region. These bristles are arranged roughly in anterior/posterior rows, with a few rows present.
Mechanosensory chaeta found on the surface of the adult abdomen. They are found on the dorsal surface and close to the ventral midline (Tsubouchi et al., 2017). Any mechanosensory chaeta of the terminalia are also covered by this term [FBC:CP].
Sensillum of the adult abdomen.
Bristle of the antenna. There are approximately 20 of these on each side, found on the first and second antennal segments (Eichler et al., 2023).
Any sense organ (FBbt:00005155) that is part of some antenna (FBbt:00004511).
Any chordotonal organ (FBbt:00005215) that is part of some adult (FBbt:00003004).
Any chordotonal organ (FBbt:00005215) that is part of some adult prothoracic segment (FBbt:00003020).
Any sensillum (FBbt:00007152) that is part of some adult head (FBbt:00003007).
Sense organ that extends along the adult hypopharynx. It comprises a heterogeneous group of nine sensilla, numbered from proximal to distal, containing a total of 8 mechanosensory and 10 gustatory receptor neurons. Three of these sensilla are gustatory, one with 3 neurons and the others with one each. The remaining 6 sensilla are mechanosensory (Nayak and Singh, 1985). It develops from the epiphysis (larval labral sense organ).
Any sensillum (FBbt:00007152) that is part of some adult mesothoracic segment (FBbt:00003021).
Any sensillum (FBbt:00007152) that is part of some adult metathoracic segment (FBbt:00003022).
Any sensillum (FBbt:00007152) that is part of some adult prothoracic segment (FBbt:00003020).
Any sense organ (FBbt:00005155) that is part of some adult (FBbt:00003004).
Any sensillum (FBbt:00007152) that is part of some adult (FBbt:00003004).
Mechanosensory chaeta found on the surface of the adult thorax (excluding legs, wings and halteres) (Tsubouchi et al., 2017).
Any sensillum (FBbt:00007152) that is part of some adult thorax (FBbt:00003018).
A large olfactory basiconic sensillum of the antenna, innervated by 4 ORNs. There are more of these sensilla in females than males (Grabe et al, 2016).
Small antennal basiconic sensillum innervated by the dendrites of two ORNs. It is distinguishable from other small bidendritic ab sensilla by its odor response profile (de Bruyne and Baker, 2008) and the identity of the ORNs that innervate it (49a/85f and 67a). There are more of these sensilla in females than males (Grabe et al., 2016).
An olfactory basiconic sensillum of the lateral surface of the antenna, innervated by 3 ORNs.
An olfactory basiconic sensillum of the lateral surface of the antenna, innervated by 3 ORNs.
A large olfactory basiconic sensillum of the antenna, innervated by 2 ORNs. It is distinguishable from ab3 by its odor response profile (De Bruyne et al., 2001) and the identity of the ORNs that innervate it (59b and 85a/33b; Couto et al., 2005). There are more of these sensilla in females than males (Grabe et al, 2016). Based on its size and the number of innervating ORNS, this is likely to correspond to LB-I (FBbt:00007355) or LB-II2 (FBbt:00007356) of Shanbhag et al., 1999, but it is not clear which.
A large olfactory basiconic sensillum of the antenna, innervated by 2 ORNs. It is distinguishable from ab2 by its odor response profile (De Bruyne et al., 2001) and the identity of the ORNs that innervate it (22 and 85b; Couto et al., 2005; de Bruyne and Baker, 2008). Based on its size and the number of innervating ORNS, this is likely to correspond to LB-I (FBbt:00007355) or LB-II2 (FBbt:00007356) of Shanbhag et al., 1999, but it is not clear which.
Thin antennal basiconic sensillum innervated by the dendrites of two ORNs. It is distinguishable from ab5 - ab10 by its odor response profile (De Bruyne et al., 2001) and the identity of the ORNs that innervate it 7a and 56/33a; Couto et al., 2005).
Thin antennal basiconic sensillum innervated by the dendrites of two ORNs. It is distinguishable from ab5 - ab10 by its odor response profile (De Bruyne et al., 2001) and the identity of the ORNs that innervate it (82a and 47a; Couto et al., 2005; de Bruyne and Baker, 2008).
Thin antennal basiconic sensillum innervated by the dendrites of two ORNs. It is distinguishable from ab5 - ab10 by its odor response profile (De Bruyne et al., 2001) and the identity of the ORNs that innervate it (49b; Couto et al., 2005; de Bruyne and Baker, 2008). There are more of these sensilla in females than males (Grabe et al, 2016).
Small antennal basiconic sensillum innervated by the dendrites of two ORNs. It is distinguishable from ab5 - ab10 by its odor response profile (De Bruyne et al., 2001) and the identity of the ORNs that innervate it (49b and 98a; Couto et al., 2005; de Bruyne and Baker, 2008).
Small antennal basiconic sensillum innervated by the dendrites of two ORNs. It is distinguishable from other small bidendritic ab sensilla by its odor response profile (de Bruyne and Baker, 2008) and the identity of the ORNs that innervate it (43b and 9a).
Small antennal basiconic sensillum innervated by the dendrites of two ORNs. It is distinguishable from other small bidendritic ab sensilla the identity of the ORNs that innervate it (69a and 67b).
Olfactory basiconic sensillum of antennal segment 3 with about the same length as the large ab sensilla, but thinner and with longitudinal rows of pores like those found in the small ab sensilla. Believed to be a class of olfactory sensillum based on morphology (Shanbhag et al., 1999).
Thin ab basiconic sensillum innervated by 2 olfactory receptor neurons (ORNs). In some subtypes the innervating dendrites are highly branched, while in others are innervated by unbranched, hollow dendrites.
Thin ab basiconic sensillum innervated by the branched dendrites of 4 olfactory receptor neurons (ORNs).
Coeloconic olfactory sensillum of the antenna that is innervated by three olfactory receptor neurons (ORN). It is distinguishable from ac2, ac3 and ac4 by its odor response profile (Yao et al., 2005) and the identity of the ORNs that innervate it. The sensilla are present in the anterior antennal surface just ventral to the arista (Benton et al., 2009).
Coeloconic olfactory sensillum of the antenna that is innervated by three olfactory receptor neurons (ORN). It is distinguishable from ac1, ac3 and ac4 by its odor response profile (Yao et al., 2005) and the identity of the ORNs that innervate it (Benton et al., 2009).
Coeloconic olfactory sensillum of the antenna that is innervated by two olfactory receptor neurons (ORN). It is distinguishable from ac1, ac2 and ac4 by its odor response profile (Yao et al., 2005) and the identity of the ORNs that innervate it (Benton et al., 2009). The sensilla are present in the posterior antennal surface (Benton et al., 2009).
Coeloconic olfactory sensillum of the antenna that is innervated by three olfactory receptor neurons (ORN). It is distinguishable from a1, ac2 and ac3 by its odor response profile (Yao et al., 2005) and the identity of the ORNs that innervate it (Benton et al., 2009). There are more of these sensilla in females than males (Grabe et al, 2016).
Coeloconic sensillum of antennal segment 3 that is innervated by two olfactory receptor neuron dendrites.
Coeloconic sensillum of antennal segment 3 that is innervated by three olfactory receptor neuron dendrites.
Antennal intermediate sensillum thought to contain olfactory receptor neuron Or13a (Couto et al., 2005). It is not currently known which other ORN(s) are found in this sensillum or whether it belongs to the I2 or I3 class (FBC:CP).
Olfactory intermediate sensillum of antennal segment 3 that is innervated by olfactory receptor neuron Or83c and olfactory receptor neuron Or23a. There are more of these sensilla in males than females (Grabe et al, 2016). Reclassified from trichoid to intermediate by fluorescence-guided single sensillum recording (FG-SSR) (Lin and Potter, 2015; FBC:CP).
Olfactory intermediate sensillum of antennal segment 3 that is innervated by 3 ORNs (2a, 19a/b and 43a). Reclassified from trichoid to intermediate by fluorescence-guided single sensillum recording (FG-SSR) (Lin and Potter, 2015; FBC:CP).
Intermediate sized sensilla of antennal segment 3 that contains two receptor cells.
Intermediate sized sensillum of the third antennal segment that contains three receptor cells.
Bristles of antennal segment 1.
Bristles of antennal segment 2. There are around 25 of these.
Any sense organ (FBbt:00005155) that is part of some second segment of antenna (FBbt:00004514).
Any sense organ (FBbt:00005155) that is part of some third segment of antenna (FBbt:00004515).
Thermosensory organ of antennal segment 3. Sayeed and Benzer, 1996, inferred the presence of thermosensory organ(s) on antennal segment 3 from the results of antennal segment ablation experiments. However, they did not identify which sensilla are responsible. These same experiments showed no effect on thermosensation when the arista alone was removed.
Any sense organ (FBbt:00005155) that is part of some antennal segment (FBbt:00000009).
Mono-innervated olfactory trichoid sensillum of antennal segment 3. May be identical to antennal trichoid sensillum T1 (FBbt:00007348) of Shanbhag et al., 1999.
Olfactory trichoid sensillum of antennal segment 3 that is innervated by 3 ORNs (47b, 65a/b/c, 88a). There are more of these sensilla in males than females (Grabe et al, 2016).
Antennal segment 3 trichoid sensillum innervated by a single ORN dendrite.
Antennal segment 3 trichoid sensillum innervated by the dendrites of two olfactory receptor neurons.
Antennal segment 3 trichoid sensillum innervated by the dendrites of three olfactory receptor neurons.
Anterior-most of the two dorsocentral bristles.
One of a group of 3 campaniform sensilla found on the wing hinge (Dinges et al., 2020).
Anterior-most of the two notopleural bristles.
Anterior-most orbital bristle that points anteriorly.
Sensillum of the lateral part of the embryonic/larval dorsal pouch (Campos-Ortega and Hartenstein, 1997). It contains a single neuron (first seen at embryonic stage 15) that is located dorsal to Bolwig’s nerve (at stages 16-17) and fasciculates with the lateropharyngeal nerve (SN-V). Schmidt-Ott et al., (1994) tentatively assign this to the mandibular segment on the basis of its fasciculation pattern. This evidence is much weaker than the genetic evidence they use to determine the segmental identity of other head sensilla.
Anterior-most of the two postalar bristles.
V-shaped chordotonal organ with one arm attached to the anterior wall of the thorax at the articulation of the head, immediately below the prosternal sense organ and the other arm fixed to the hypotremal apodeme (Power, 1948). The joint between the two arms is directed posteromedially and pressed against the anterolateral corner of the prothoracic neuromere (Power, 1948). A thick, short group of fibers, the prothoracic chordotonal nerve, connects this organ to the ventral nerve cord (Power et al., 1948).
Anterior-most macrochaeta of the scutellum. There is one pair of these.
Most anterior of the two dorsal cibarial sensilla of the adult pharynx (Montell, 2009). It is innervated by three gustatory receptors (Gendre et al., 2004).
The most anterior of the sternopleural bristles of the adult mesothoracic preepisternum, located at the same dorso/ventral level as the middle and posterior bristles.
Anterior-most of the two supraalar bristles.
The anterior-most of each pair of vertical bristles that curves inwards.
One of a group of three sensilla in the anterior of the pharynx.
Multiply innervated sensillum of the anteroventral group of the larval pharynx. It has a single pore, plugged with amorphous material and is innervated by 9 dendrites in three groups, each group within a cuticular sheath.
Unidendritic sensillum of the anteroventral group of the larval pharynx located in a pit lateral to V1. It has a tuft of hair at its distal tip and its dendrite has a tubular body.
Unidendritic sensillum of the anteroventral group of the larval pharynx located in a pit lateral to V2. It has a tuft of hair at its distal tip and its dendrite has a tubular body.
Sensillum of the arista. There are three of these per arista, each consisting of a pair of sensory neurons surrounded by 2 sheath cells. They project into the lymph space of the arista core, where they float freely - unattached to the epidermis. These projections consist of specialized dendrites surrounded throughout their length by sheath cells and distally by an electron dense dendritic sheath. The three projections terminate at different points along the shaft. Foelix et al., 1989, suggest that the morphology of the highly lamellated neurons found in these sensilla is consistent with a thermosensory function based on the similarity of this morphology to that of thermosensory neurons in the antennae of other insects. However, Sayeed and Benzer, 1996, show that surgical removal of the arista has no effect on the temperature preference of flies, but it does eliminate the preference of flies for dry vs moist air, suggesting a hygrosensory function.
A cluster of 4-6 sensory neurons attached to the basal aspect of neurons belonging to the terminal organ. These neurons have no associated cuticular structure and do not have the typical morphology of bipolar sensory neurons.
Any sense organ (FBbt:00005155) that capable of some detection of mechanical stimulus involved in sensory perception of sound (GO:0050910).
A eo-type sensillum in which the external part has the form of a minute projecting cone or peg.
Large olfactory basiconic sensillum of antennal segment 3, with a pore size of about 50nm and a pore density of about 19 pores per square micrometer, innervated by 2 highly branched ORN dendrites. Likely to correspond to ab2 or ab3, but not clear which.
Large olfactory basiconic sensillum of antennal segment 3, with a pore size of about 100nm and a pore density of about 30 pores per square micrometer, innervated by 2 highly branched ORN dendrites. Likely to correspond to ab2 or ab3, but not clear which.
Large olfactory basiconic sensillum of antennal segment 3, with a pore size of about 100nm and a pore density of about 30 pores per square micrometer, innervated by 4 highly branched ORN dendrites.
Any basiconic sensillum (FBbt:00005185) that is part of some third segment of antenna (FBbt:00004515).
Sensillum of chamber I of the sacculus of the antenna. The sensilla are devoid of pores, have no socket at the base and gradually taper at the distal end. The sensilla have an irregularly sculpted external surface at their distal end. They are innervated by two or three sensory cells. There are 5-7 of these sensilla; two of these contain both water- and thermo-sensitive neurons, the remaining are water-sensitive (Shanbhag et al., 1995).
Labellar taste bristle that is innervated by a neuron that expresses bitter receptors and responds to bitter stimuli (Weiss et al., 2011).
Sensillum of the coeloconic type that does not have a pore. It is 2 micrometers long and 1.7 micrometers wide at the base, tapering towards the tip. A pore-like structure at the distal end is plugged by electron-dense material. At the very tip, the sensillum is covered by a similar electron-dense structure. The outer cuticular surface is smooth. Internally, the cuticle has a spongy appearance. There is a single central lumen that terminates below the electron-dense layer.
Coeloconic sensillum of chamber II of the sacculus of the antenna. The sensilla are blunt-tipped with a smooth cuticular surface and have a pore-like structure at their distal end. They are innervated by three sensory cells, which include water- and thermo-sensitive neurons. There are 6 sensilla of this type (Shanbhag et al., 1995).
Visual organ of the larva. It consists of a dense cluster of 12 ciliated photoreceptor neurons located on either side of the midline in a dorsomedial position in the anterior region of the larva. Location in ocular segment on basis of FBrf0075072.
Any chaeta (FBbt:00005177) that is part of some mesothoracic tergum (FBbt:00004580).
Bitter-sensitive labellar taste bristle that detects a wide range of bitter stimuli, with a smaller response to most stimuli than the S-b group (Weiss et al., 2011).
Bitter-sensitive labellar taste bristle that detects a wide range of bitter stimuli, with a greater response to most stimuli than the S-a group (Weiss et al., 2011).
Innervated cuticular specialization just inside the larval mouth. This could correspond to epipharyngeal sense organ.
An eo-type sensillum in which the cuticular part typically has the form of a papilla, bell or hollow cone receiving the distal process of a sensory neuron.
Most proximal of the three dorsal campaniform sensilla of wing vein L3. It is a large circular sensillum, with a high profile and a distinct discontinuity between the dome and socket.
Medial of the three dorsal campaniform sensilla of wing vein L3. It is a large circular sensillum, with a high profile and a distinct discontinuity between the dome and socket.
Distal most of the three dorsal campaniform sensilla of wing vein L3. It is a large circular sensillum, with a high profile and a distinct discontinuity between the dome and socket.
Campaniform sensillum associated with the anterior cross vein and wing vein L3. It is a large circular sensillum, with a high profile and a distinct discontinuity between the dome and socket.
Campaniform sensillum located in the distal region of the terminal organ, on the head of the embryo/larva. There are three of these sensilla and each contains the dendrite of a mechanosensory neuron, which terminates more proximally and ends with a tubular body, as well as dendrites from gustatory receptor neurons (Rist and Thum, 2017).
Humeral crossvein campaniform sensillum located on the dorsal side of the wing. It is situated close to the ventral humeral crossvein campaniform sensillum separated by the intermediate portion of the costal nerve (Murray et al., 1984). It is circular with a high profile and with a socket which is prominent on one side but becomes indistinct on the other. The sensillum is around 8 micrometers in diameter.
Campaniform sensillum found on the dorsal side of the radial vein of the adult wing.
Sensillum belonging to the more proximal, posterior subgroup of Sc25 sensilla. There are seven of these elliptical sensilla, which have a low profile and a socket (type 6). Each sensillum is approximately 2.5-3.0 micrometers in length.
Sensillum belonging to the more distal, anterior subgroup of Sc25 sensilla. There are around 17 of these circular sensilla, which have a low profile and no socket (type 4). Each sensillum is approximately 2.5-3.5 micrometers in diameter.
Sensillum belonging to the anterior group of campaniform sensilla of the dorsal surface of the medial radius. There are four of these circular sensilla, which have a high profile and a socket (type 1). Each sensillum is approximately 4.5 micrometers in diameter.
Sensillum belonging to the posterior group of campaniform sensilla of the dorsal surface of the medial radius. There are eight of these circular sensilla, which have a low profile and a socket (type 3). Each sensillum is approximately 5.0-5.5 micrometers in diameter.
Campaniform sensillum of the dorsal side of the medial radius of the adult wing. These cells are arranged in two distinct fields. The first has four circular sensilla with high profile and with a socket (type 1), distributed on the anterior face of the medial radius, with each sensillum around 4.5 micrometers in diameter (d.Rad.D). The second has eight circular sensilla, with low profile and with socket (type 3), with each sensillum between 5.0-5.5 micrometers in diameter (d.Rad.E).
Campaniform sensillum belonging to a more dispersed group of cells, distal to the Sc4d cells, on the dorsal side of the proximal radius of the adult wing. These cells belong to two distinct fields. The first has seven elliptical sensilla with low profile and with a socket (type 6), distributed in a round patch, with each sensillum between 2.5-3.0 micrometers in length (d.Rad.B). The second has around 17 circular sensilla, with low profile and without socket (type 4), with each sensillum between 2.5-3.5 micrometers in diameter (d.Rad.C).
Campaniform sensillum of the most proximal cluster of the dorsal side of the proximal radius of the adult wing. There are four of these circular sensilla with a high profile and without a socket (type 2), they are arranged in a row and increase in diameter distally, from 3.5 to 4.5 micrometers.
Any campaniform sensillum (FBbt:00005183) that is part of some larval intercalary segment (FBbt:00001736). Dinges et al. (2020) confirmed that there is no campaniform sensilla on the adult head, so this term can only refer to a larval campaniform sensillum. [FlyBase: FBrf0247616]
Campaniform sensillum that is found on a leg.
Campaniform sensillum of the proximal dorsal radius of the adult wing.
Campaniform sensillum of the tegula in the adult wing. There are two distinct fields of elliptical sensilla with high profile and with a socket (type 5): a main one with 18 sensilla and two peripheral sensilla located more anteriorly.
Campaniform sensillum located in the trochanter.
Humeral crossvein campaniform sensillum located on the ventral side of the wing. It is situated close to the dorsal humeral crossvein campaniform sensillum separated by the intermediate portion of the costal nerve (Murray et al., 1984). It is a large circular sensillum which bears a socket that is tightly fused to the dome and diminishes on one side. The sensillum is around 6.5 micrometers in diameter.
Campaniform sensillum of the ventral side of the radial vein of the adult wing.
A single campaniform sensillum of the medial radius on the ventral surface of the adult wing, located about 15 micrometers distally to the most distal campaniform sensillum of the v.Rad.C group (Dinges et al., 2020). This sensillum was previously described as being part of the v.Rad.C group, but Dinges et al. (2020) define it as a distinct single campaniform sensillum, due to its distance to that group and its clear morphological differences.
Campaniform sensillum on the border of the proximal and medial radius, on the ventral surface of the adult wing. There are three circular sensilla with a high profile and with a socket (type 1), with the cuticle of the domes often peaked. Each sensillum is between 2.5-3.5 micrometers in diameter.
Campaniform sensillum that is part of group of 4 sensilla on the ventral surface of the adult wing, arranged linearly along the medial radius. Each sensillum has a low profile and a socket (type 3), and is around 4.5 micrometers in diameter (Bryant, 1975; Cole and Palka, 1982; Dinges et al., 2020). The term v.Rad.C initially referred to all 5 sensilla of the ventral medial radius, but Dinges et al. (2020) suggest that it should only refers to this group of 4, excluding the one they call v.Rad.C.1.
Campaniform sensillum of the proximal radius on the ventral surface of the adult wing. There are four or five elliptical sensilla with low profile and with a socket (type 6), often arranged in a diamond pattern. Each sensillum is between 2.5-3.5 micrometers in length.
Campaniform sensillum of the medial radius on the ventral surface of the adult wing. There are five circular sensilla with low profile and with a socket (type 3), arranged linearly along the medial radius. Each sensillum is around 4.5 micrometers in diameter. Dinges et al. (2020) suggest that v.Rad.C be used to refer only to the 4 most proximal campaniform sensilla (campaniform sensillum of ventral radius Sc4) instead of all 5 sensilla of the ventral radius.
The most ventral of the three campaniform sensilla located in the distal region of the terminal organ, on the head of the embryo/larva. It is innervated by gustatory receptor neurons C2 and C8, as well as a mechanosensory neuron (Rist and Thum, 2017).
The most dorsal of the three sensilla campaniform located in the distal region of the terminal organ, on the head of the embryo/larva. It is innervated by gustatory receptor neurons C1 and C9, two other putative taste neurons, and a mechanosensory neuron (Rist and Thum, 2017).
The most distal of the three sensilla campaniform located in the distal region of the terminal organ, on the head of the embryo/larva. It is innervated by gustatory receptor neurons C3 and C16, as well as a mechanosensory neuron (Rist and Thum, 2017).
A trichoid sensillum of the capitellum. There are around 15-19 of these, all unpigmented. Close to 6 of these cluster into a group, the others are more dispersed.
Dome shaped cuticular process of the larval dorsal organ, innervated by seven circularly arranged triplets of olfactory receptor neuron (ORN) dendrites. The wall of the dome has numerous pore channels, consistent with a role as an olfactory sense organ.
Any bristle that is part of the cercus. There are nearly 40 of these.
Any bristle that is part of the cercal dorsal lobe. They are longer and less rigid than the cercal ventral lobe bristle.
Any bristle that is part of the cercal ventral lobe. They are shorter and more rigid than the cercal dorsal lobe bristle.
A sensillum with a long, unicellular, setiform outgrowth that is strongly chitinized. This term is sometimes used to refer to the ‘bristle-like’ outgrowth only, but is here used to refer to the entire sensillum of which it is a part.
Ventral-most chamber of the sacculus of the antenna, where the opening is located (Shanbhag et al., 1995).
Middle chamber of the sacculus of the antenna. It has several compartments, each containing a single sensillum (Shanbhag et al., 1995).
Dorsal-most and largest chamber of the sacculus of the antenna. It has a ventral and a dorsal compartment, which differ in the type of sensilla they contain. The compartments are separated by a thick cuticular flap that extends lateromedially (Shanbhag et al., 1995).
Multiply innervated, recurved bristle of the dorsal double row involved in chemosensation. This bristle also shows a conspicuous terminal pore. Palka et al., (1979) show that of the five dendrites innervating the wing margin chemosensory bristles, one contains a microtubular body, suggesting it to be a mechanosensory neuron. That this bristle is chemosensory in nature is based on the presence of the terminal pore and multiple innervation with dendrites extending to the pore (Palka et al., 1979).
Third most distal sensillum of the adult labral sense organ in the adult pharynx. It is innervated by 8 gustatory receptor neurons, arranged as two triplets and a pair. It is the largest of the three chemosensory sensilla of the labral sense organ.
Short, blunt-tipped thorn bristle or spine bristle located on the adult vaginal plate. There are around 10 bilateral pairs of thorn bristles and around 3 bilateral pairs of spine bristles. Note: currently there is no direct evidence that these neurons are definitely chemosensory. That they are likely to be chemosensory in nature is based on their morphology (Taylor, 1989), that they are multiply innervated (Taylor, 1989), and behavioral observations of the animals during egg laying (Yang et al., 2008).
Any sense organ (FBbt:00005155) that capable of some detection of chemical stimulus involved in sensory perception (GO:0050907).
Multiply innervated, recurved chemosensory bristle of the ventral double row with a conspicuous terminal pore. Palka et al., (1979) show that of the five dendrites innervating the wing margin chemosensory bristles, one contains a microtubular body, suggesting it to be a mechanosensory neuron. That this bristle is chemosensory in nature is based on the presence of the terminal pore and multiple innervation with dendrites extending to the pore (Palka et al., 1979).
Multiply innervated, recurved taste bristle of the ventral triple row and the ventral row. This bristle also shows a conspicuous terminal pore. Palka et al., (1979) show that of the five dendrites innervating the wing margin chemosensory bristles, one contains a microtubular body, suggesting it to be a mechanosensory neuron. That this bristle is chemosensory in nature is based on the presence of the terminal pore and multiple innervation with dendrites extending to the pore (Palka et al., 1979).
Mechanosensory organ, generally attached to the body wall, spanning different parts of the exoskeleton. It consists of one or more scolopidia and detects tension or vibration.
Chordotonal organ that is part of a leg.
Any chordotonal organ (FBbt:00005215) that is part of some prothoracic segment (FBbt:00000017).
Any chordotonal organ (FBbt:00005215) that is part of some scabellum (FBbt:00004786). Original reference for these (FlyBase:FBrf0239028) is based on other flies. Chordotonal organs were not identified in Drosophila halteres by Tsubouchi et al. (2017) (FlyBase:FBrf0237124) [FBC:CP].
Chordotonal organ found in the tegula.
Any chordotonal organ (FBbt:00005215) that is part of some wing (FBbt:00004729).
Sensory bristle on the anterior plate of the cibarium of the adult pharynx, near the ventral cibarial sense organ (VCSO). These bristles project upwardly and are arranged in two rows, dorsal and ventral to the VCSO. There are 18 to 23 bristles, each innervated by a mechanosensory neuron.
Compound sense organ located in the cibarium of the adult pharynx, near the upper end of the posterior cibarial plate. It comprises two sense organs, dorsal and ventral, that are innervated by gustatory receptor neurons. This term, as used by Miller in Demerec (1994) refers only to the dorsal cibarial sense organ (Stocker and Schorderet, 1981).
A general name for various olfactory or gustatory sense organs of conical shape in which the external process is sunken in a cavity of the body wall. Usually found in the extra-oral cavity or other mouthparts.
Olfactory coeloconic sensillum that is part of antennal segment 3. A short conical peg arising from a broad basal platform, basally smooth but distally having deep longitudinal grooves. The peg has a double cuticular wall. The inner wall encloses a central lumen innervated by olfactory receptor neuron dendrites. Distally, the central lumen is connected to the outer, sensillum lymph-filled chamber by radial spoke channels. Morphology is consistent with these sensilla being olfactory (Shanbhag et al., 1999). This function has been directly confirmed by electrophysiology (Clyne et al., 1997).
Any compound cell cluster organ (FBbt:00007230) that capable of some detection of stimulus involved in sensory perception (GO:0050906).
One of a group of 11 sensilla arranged in a circle in the distal region of the larval terminal organ.
Trichoid sensillum located at the distal end of the rostral membrane of the adult head, near to the insertion of the palpus. There are two to four of these.
Distal-most sensillum of the ventral cibarial sense organ of the adult pharynx. It is innervated by four gustatory receptor neurons (Gendre et al., 2003).
Dorsal-most cibarial sense organ near the upper end of the posterior cibarial plate of the adult pharynx, and innervated by the pharyngeal nerve. It comprises two sensilla (anterior and posterior), each containing three gustatory receptor neurons. This term corresponds to the cibarial sense organ as used by Miller in Demerec (1994) and to the fulcral organ as used by Hertweck (1931).
Dorsal compartment of chamber III of the sacculus. It contains sensillum of the type grooved sensillum 2 (Shanbhag et al., 1995).
Bristle that is part of the dorsal double row.
Sensillum of the lateral group, located on the internal dorsal fold of the larval pharynx. There is one of these, found on either side of the vertical midplane.
Sensillum of the medial group, located on the internal dorsal fold of the larval pharynx. There are three of these, found on either sides of the vertical midplane.
One of the three sensilla of the dorsal medial fold, located on the internal dorsal fold of the larval pharynx.
One of the three sensilla of the dorsal medial fold, located on the internal dorsal fold of the larval pharynx.
One of the three sensilla of the dorsal medial fold, located on the internal dorsal fold of the larval pharynx.
One of a group of 6 sensilla in the pharynx between the antero-ventral group and posterio-lateral sensillum V4.
Most medial sensillum of the dorsal group of the larval pharynx, innervated by 2 dendrites (Singh and Singh, 1984).
Second most medial sensillum of the dorsal group of the larval pharynx, innervated by a single dendrite (Singh and Singh, 1984).
Third most medial sensillum of the dorsal group of the larval pharynx, innervated by 2 dendrites (Singh and Singh, 1984).
Fourth most medial sensillum of the dorsal group of the larval pharynx, innervated by 3 dendrites (Singh and Singh, 1984).
Fifth most medial sensillum of the dorsal group of the larval pharynx, innervated by a single dendrite (Singh and Singh, 1984).
Sixth most medial (most lateral) sensillum of the dorsal group of the larval pharynx, innervated by a single dendrite (Singh and Singh, 1984).
Bristle on the dorsal lateral side of antennal segment 1. There is only one of these.
An ommatidial subtype located in a single row at the dorsal margin of the eye. This ommatidial subtype is specialized to detect the e-vector of polarized sunlight. The dorsal margin ommatidium expresses the opsin Rh3 (FBgn0003249) that detects polarized light in both photoreceptor R7 and R8 cells (Fortini and Rubin, 1990).
Bristle on the dorsal medial side of antennal segment 1. There are four of these.
An external compound sense organ of the antenno-maxillary complex of the larval head consisting of a dome shaped cuticular process, innervated by seven circularly arranged triplets of olfactory receptor neuron dendrites. Six small papillae surround the base of the central dome.
A campaniform sensillum that is one of around 40 sensilla arranged in 10 transverse rows on the dorsal side of the pedicel. It is elliptical with a low profile and socket (type 5). The central cuticular specialization has a raised profile, and the sockets are fused to the sockets of adjacent sensilla in the same row. It is around 3-4 micrometers in length.
A single campaniform sensillum at the anterior-most end of the field of campaniform sensilla on the dorsal surface of the pedicel. It is morphologically different from the other sensilla in the d.Ped field (Dinges et al., 2020).
One of 14 innervated pits located in two groups of 7 on either side of the dorsal midline in the dorsal-most part of the larval head. There is no associated external cuticular sensory structure.
Postorbital bristle with a relatively dorsal position that is innervated by a mechanosensory neuron that fasciculates with the occipital nerve (Eichler et al., 2023). There are approximately 7 of these on each side (Eichler et al., 2023).
One of 6-8 singly innervated bristles of dorsal row of the cibarial fish-trap bristle, dorsal to the ventral cibarial sense organ. They are innervated by mechanosensory neurons. Disambiguation: these bristles are sometimes referred to as the ‘dorsal row’ (Stocker and Schorderet, 1981; Nayak and Singh, 1983), which may be confused with the ‘dorsal row’ sensilla of the anterior wing margin (Bate and Martinez Arias, 1991). They are also referred to as the upper (or proximal) fishtrap bristles (Gendre et al., 2004).
One of around 42 circular socket-less campaniform sensilla with a high profile (type 2), arranged in 6 longitudinal rows on the dorsal surface of the scabellum. Their diameters increase distally in each row, to be around 2.5-4.0 micrometers.
A single campaniform sensillum at the anterior-most end of the field of campaniform sensilla on the dorsal surface of the scabellum. It is morphologically different from the other sensilla in the d.Scab field (Dinges et al., 2020).
Multiply innervated, recurved bristle of the dorsal triple row involved in chemosensation. This bristle has a conspicuous terminal pore. Palka et al., (1979) show that of the five dendrites innervating the wing margin chemosensory bristles, one contains a microtubular body, suggesting it to be a mechanosensory neuron. That this bristle is chemosensory in nature is based on the presence of the terminal pore and multiple innervation with dendrites extending to the pore (Palka et al., 1979).
One of 3 dorso-laterally located sensilla of the larval terminal organ. Jurgens et al. (1986), explain that the DLP and DMP are considered to be of different origins to the other 7 papillae of the terminal organ/MxSO because their axons do not join the maxillary nerve and they are found in different locations in certain homeotic mutants.
A large, dorso-centrally located macrochaeta of the scutum. There are two pairs of these, anterior and posterior.
Papilla of the dorsolateral group of the terminal organ, on the head of the embryo/larva. It is located more laterally than the dorsomedial papilla, next to the spot sensillum of the dorsolateral group. This sensillum is innervated by one dendrite, which ends with a tubular body, indicative of mechanosensation, below the bud-shaped cuticle shaft (Rist and Thum, 2017).
Papilla of the dorsolateral group of the terminal organ, on the head of the embryo/larva. It is located more medially than the dorsolateral papilla and the spot sensillum of the dorsolateral group. This sensillum is innervated by three dendrites, from gustatory receptor neuron B1, B2 and B3 (Rist and Thum, 2017).
Sensillum of the larval head that is located posterior to the epiphysis (labral sensory organ). It is innervated by 3 neurons.
Sense organ of the embryonic antennal segment that gives rise to the dorsal organ of the larval head. It is posterior to the embryonic brain by stage 13 and migrates ventrally and anteriorly to establish its final position, dorsal to the terminal organ, by stage 17.
Any internal compound sense organ (FBbt:00007236) that is part of some embryonic foregut (FBbt:00005606).
Sense organ of the embryonic maxillary segment that gives rise to the terminal organ of the larval head. It is posterior and ventral to the embryonic brain by stage 13 and migrates ventrally and anteriorly to establish its final position, ventral to the dorsal organ, by stage 17.
Any sensillum (FBbt:00007152) that is part of some larval abdominal segment 10 (FBbt:00001757).
Any sensillum (FBbt:00007152) that is part of some larval abdominal segment 11 (FBbt:00001758).
Any sensillum (FBbt:00007152) that is part of some larval abdominal segment 8 (FBbt:00001755).
Any sensillum (FBbt:00007152) that is part of some larval abdominal segment 9 (FBbt:00001756).
Any sense organ (FBbt:00005155) that is part of some larval antennal segment (FBbt:00001735).
Any sensillum (FBbt:00007152) that is part of some embryonic/larval foregut (FBbt:00001862).
Any sense organ (FBbt:00005155) that is part of some larval head (FBbt:00001730).
Any sensillum (FBbt:00007152) that is part of some larval head (FBbt:00001730).
Any sense organ (FBbt:00005155) that is part of some larval intercalary segment (FBbt:00001736).
A compound external sense organ of the late embryo or larva. It is located in the lower lip of the external opening of the atrium. It consists of 3 sensilla, one with 3 neurons and the others with one each. Neurons of the labial organ and hypophysis (labial sensory organ) form a large cluster flanking the salivary duct.
Any sensillum (FBbt:00007152) that is part of some larval labial segment (FBbt:00001740).
Any sense organ (FBbt:00005155) that is part of some larval labral segment (FBbt:00001734).
Chordotonal organ of the larval maxillary segment that possesses two scolopidia.
Any embryonic/larval sense organ (FBbt:00002639) that is part of some larval ocular segment (FBbt:00001731).
Any sensillum (FBbt:00007152) that is part of some larval prothoracic segment (FBbt:00001743).
Any sense organ (FBbt:00005155) that is part of some larva (FBbt:00001727).
Any sensillum (FBbt:00007152) that is part of some larva (FBbt:00001727).
Any sensillum (FBbt:00007152) that is part of some larval thorax (FBbt:00001741).
Sensillum with innervated external cuticular sensory structure consisting of one or more bipolar sensory neurons, and 3 support cells: a trichogen cell which makes the external cuticular sensory structure, a thecogen cell which makes the socket that holds the base of the external sensory structure and a tormogen cell which makes the cuticular matrix (cap) at the tip of the innervating dendrite(s).
Any bristle that is part of the epandrium. There are 30 of these.
Any bristle that is part of the epandrial dorsal lobe. There are 8 of these.
Any bristle that is part of the epandrial ventral lobe. There are 22 of these on each lobe.
Paired compound sense organ of the labral complex in the larval head. It consists of 6 sensilla in the larval pharynx: one tri-dendritic, 2 bi-dendritic and 3 mono-dendritic. Projections from the epiphysis generally, though not exclusively, target the contralateral subesophageal ganglion area 1 (Colomb et al., 2007). Colomb et al., (2007) report that labral nerve projections pass through area 2 and into area 1 of the subesophageal ganglion. In the majority of cases they then target the contralateral area 2. An exception to this is one epiphysis fiber (which labels with Gr2a-GAL4) which targets inside area 4.
Compound sense organ that is located within the epidermis.
Sensillum which is embedded in the body wall and has a specific cuticular structure involved in the transduction of some sensory signal as a part. This is a parent term for the mechanosensory bristles referred to as external sensilla (es) in some references e.g. Tsubouchi et al., 2017 (FBrf0237124).
Sensory organ that has external structures that detect mechanical or chemical stimuli.
A bilaterally paired compound sense organ of the adult head that functions in visual perception.
A cluster of 4 extra-retinal photoreceptors located beneath the basement membrane, at the posterior margin of the compound eye, near to the equator. Derived from the larval Bolwig’s organ.
Darkly pigmented and straight hair found dorsally on the base of the stigmatophore. There are around 7 rows of hairs, that densely cover this area.
Small unpigmented bristle of the female abdominal tergite 8. There are 4 to 5 of these.
Any sensillum (FBbt:00007152) that is part of some female terminalia (FBbt:00004830).
Campaniform sensillum located in the femur.
Large chordotonal organ found in the proximal femur.
Scolopidium of a femoral chordotonal organ. At least in the prothoracic leg, there are around 76 of these and each is innervated the sensory dendrites of two chordotonal neurons (Kuan et al., 2020).
Small bristle of the anterior head, located above the antennae on the medial postfrons in two arcs of 6 bristles each, arranged so that the ventral-most bristle occupies a more medial position than the dorsal-most.
Small bristle of the anterior head, located on the postfrons immediately medial to the eye and arranged in a dorsal to ventral line. There are around 6 of these.
Large, singly-innervated campaniform sensillum on the posterior face of the distal radius of the adult wing. It is a large circular sensillum, with a high profile and a distinct discontinuity between the dome and socket. It is around 9 micrometers in diameter. Note that several references use the term ‘giant sensillum of the radius’ (e.g. Palka et al., 1979), and others use the term ‘giant sensillum of the dorsal radius’ (e.g. Huang et al., 1991). For consistency, we adopt this latter usage.
Single long bristle of the female gonopod. Note: currently there is no direct evidence that these neurons are definitely chemosensory. That they are likely to be chemosensory in nature is based on their morphology (Taylor, 1989), that they are multiply innervated (Taylor, 1989), and behavioral observations of the animals during egg laying (Yang et al., 2008).
Thorn bristle of the female gonopod. There are 11-16 of these. Note: currently there is no direct evidence that these neurons are definitely chemosensory. That they are likely to be chemosensory in nature is based on their morphology (Taylor, 1989), that they are multiply innervated (Taylor, 1989), and behavioral observations of the animals during egg laying (Yang et al., 2008).
Trichoid sensillum of the female gonopod. There are three of these.
Sensillum that is double-walled, containing an open slit channel system. For three-fourths of its length from the tip, the cuticular surface bears alternating longitudinal grooves and ridges. In cross-section, the cuticle is hollow and looks like a ring of spheres, each with a small solid cuticular ridge on its external surface. In the groove, between two ridges, there is a small slit, exposing the interior of the sensillum to the outside. Proximally, the lateral walls of adjacent cuticular ridges fuse. The inner wall surrounds the lumen of the hair, which contains a thin, loosely scattered, electron-lucent homogeneous material. It is innervated by two sensory neurons. There are 2 types of grooved sensillum, both found in chamber III of the sacculus.
Sensillum of the ventral compartment of chamber III of the sacculus of the antenna. The sensilla are thick, blunt-tipped and bear 9-12 grooves with slit channels. They are innervated by 2 sensory cells, one olfactory and one thermo-sensitive neuron. There are 11-13 sensilla of this type (Shanbhag et al., 1995).
Sensillum of the dorsal compartment of chamber III of the sacculus of the antenna. The sensilla are slender than the grooved sensillum 1 and bear 6-8 grooves with slit channels. They are innervated by 2 sensory cells, one olfactory and one thermo-sensitive neuron. There are 11 sensilla of this type (Shanbhag et al., 1995).
Sensillum of chamber III of the sacculus of the antenna. The sensilla are double-walled and bear alternating longitudinal grooves and ridges for three-quarters of their length from the tip. They are innervated by two sensory neurons (Shanbhag et al., 1995).
[confocal microscopy; gustatory system; McKellar_Gr66a; gustatory sensory organ; capable of; McKellar_Gr64f; chemosensory sensory organ; is part of; JRC2018Unisex; detection of chemical stimulus involved in sensory perception of taste]
Any campaniform sensillum that is part of the haltere. There are four groups of these, found on the dorsal and ventral sides of the proximal and middle parts.
Any sensillum (FBbt:00007152) that is part of some haltere (FBbt:00004783).
Bristle found on the posterior haustellum. There are usually five of these on each side (Eichler et al., 2023).
Any chaeta (FBbt:00005177) that is part of some head capsule (FBbt:00004482).
Any sensillum (FBbt:00007152) that is part of some head (FBbt:00000004).
Macrochaeta of the humerus, on the adult prothorax. There are two of these.
Any sense organ (FBbt:00005155) that capable of some detection of humidity stimulus involved in sensory perception (GO:0098512).
Long bristle located on the median gonocoxite. There are two of these on the hypandrium.
A multiply innervated sensillum of the larval head, located next to the labial organ whose axons project into the maxillary nerve.
Multiply innervated sensillum, composed of an anterior and a posterior sensillum, located on the floor of the larval pharynx. It is innervated by 3 or 4 neurons whose axons join an anteriorly directed bundle that joins the labral nerve.
Paired compound sense organ of the labial segment in the larval head, located on the floor of the atrium, anterior to the opening of the salivary duct. It is composed of 4 sensilla. Sensory neurons travel via the labial nerve and innervate area 2 of the embryonic/larval subesophageal ganglion. Neurons of the hypophysis and labial organ form a large cluster flanking the salivary duct.
Most anterior I-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I0 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Tenth most anterior I-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I9 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Second most anterior I-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). There is no correspondence to the sensillum in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Third most anterior I-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I1 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Fourth most anterior I-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I2 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Fifth most anterior I-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I3 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Sixth most anterior I-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I4 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Seventh most anterior I-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I5 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Eight most anterior I-type chemosensillum of the labellum. It can respond to bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I7 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present. Weiss et al., (2011) found that it had a variable identity and could not assign it to a specific group.
Ninth most anterior I-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I8 in Weiss et al., (2011). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Any sense organ (FBbt:00005155) that is part of some intercalary segment (FBbt:00000010).
Intermediate sized taste bristle of the outside of the labellum: each bristle is around 25 micrometers long. These bristles are located dorsally, on the labellar lobe periphery. These taste bristles house the sensory dendrites of 2 gustatory receptor neurons (Shanbhag et al., 2001): one sensitive to sugars and low concentrations of salt and the other to bitter and high salt concentrations (Hiroi et al., 2004). These taste bristles also contains the sensory dendrite of one mechanosensory neuron (Shanbhag et al., 2001).
Sensillum with external sensory structure whose morphology is in between that of a trichoid sensillum and a basiconic sensillum.
Olfactory sensillum of antennal segment 3. It resembles antennal segment 3 trichoid sensillum in cuticular morphology, pore structure and dimensions, but, like antennal segment 3 basiconic sensilla, it lacks a basal drum and is innervated by branched dendrites from 2-3 ORNs. Morphology is consistent with olfactory function, as is the expression and localization of odorant binding proteins (Shanbhag et al., 2001; Shanbhag et al., 2005).
Compound sense organ that is located in the inside of the body, including chordotonal organ.
Sense organ that is internal to the animal - i.e. having no part that is part of the cuticle.
Sensillum that is internal to the animal - i.e. having no part that is part of the cuticle.
Small bristle of the dorsal head, located between the ocelli, arranged in two anterior-posterior rows.
Mechanosensory microchaete that projects from alternate facet vertices of the ommatidia, over most of the adult eye, usually at the anterior end of the horizontal face. The placement is less regular towards the anterior region of the eye.
Compound chordotonal organ of antennal segment 2 involved in hearing (Gopfert and Robert, 2002), direction-sensitive wind detection (Yorozu et al., 2009) and gravitaxis (Kamikouchi et al., 2009). The actin-filament rich basal tips of the Johnston’s organ scolopidia connect to the inner surface of antennal segment 2, and the apical tips connect to the hook of antennal segment 3 (Gopfert and Robert, 2002). Its sensory neurons (Johnston’s organ neurons or JONs) are connected to the Johnston’s organ nerve (Kamikouchi et al., 2006), and predominantly innervate the antennal mechanosensory and motor center (AMMC). There are 477 +/- 24 cell bodies, arranged in a bowl shape lying vertically with the ’top’ facing the lateral side, and forming a ring around the antennal nerve (Kamikouchi et al., 2006). JONs connecting to opposing sides of the hook are alternatively stimulated by stretching or compression according to the hook’s oscillatory movement (Gopfert and Robert, 2002). Yorozu et al., 2009, identify tonically activated Johnston’s organ neurons that respond to forward or reverse deflection of the antenna. Genetic ablation of these neurons inhibits wind-induced behavioral responses without impairing hearing. Further, by expression of tetanus toxin, Kamikouchi et al., 2009, identify the same neuronal population as essential for gravitaxis behavior.
Bristle of the mesothoracic episternum or katepisternum. On the dorsal aspect there are 5 to 8 bristles, with 1 to 3 of them being very large (Bb-). In the ventral aspect there is an isolated bristle (I) and in the anterior region there are 2 to 4 yellow bristles (YB).
Anterior lateral hair of a Keilin organ. It is innervated by a single dendrite, belonging to a thoracic vesA neuron (Ghysen et al., 1986).
Anterior medial hair of a Keilin organ. It is innervated by two dendrites, belonging to thoracic vesB and vesC neurons (Ghysen et al., 1986).
Posterior hair of a Keilin organ. It is innervated by two dendrites, belonging to thoracic vesD and vesE neurons (Ghysen et al., 1986).
A sensillum of the embryonic/larval thorax whose external sensory structure consists of a cluster of three hairs. It is innervated by 5 dendrites.
Paired external sensillum situated dorso-laterally on the larval head and consisting of a knob shaped cuticular structure located in a pit and innervated by 3 dendrites - one terminating at its base and the other two extending into the knob. Putative combined mechanoreceptor (Singh and Singh, 1984) and taste sensillum (Singh, 1997).
Sensillum that resembles a knob. Two of these sensilla are found in the terminal organ of the embryo/larva.
The most dorsal of the two knob sensilla located in the distal region of the terminal organ, on the head of the embryo/larva. It houses the dendrite of gustatory receptor sensillum C15 (Rist and Thum, 2017).
The most ventral of the two knob sensilla located in the distal region of the terminal organ, on the head of the embryo/larva. Its dendrite, that of the osmolarity-sensitive C6 neuron, appears lamellated in the enlarged tip of the sensillum (Rist and Thum, 2017).
Knob sensillum located in the distal region of the terminal organ, on the head of the embryo/larva. There are two of these sensilla on each side of the head, they each house one dendrite that continues to the sensillum tip, becoming fragmented (Rist and Thum, 2017).
Club-like sensory structure found in the thoracic segments of the embryo/larva. Dambly-Chaudiere and Ghysen (1986) argue that since the Kolbchen is not black (except when viewed with phase contrast) and is more than a pit, the original name of Kolbchen (meaning ‘small club’) is preferable to ‘pit’ or ‘black dot’.
Most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
Second most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
Third most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum L7 in Weiss et al., (2011). Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
Fourth most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum L3 in Weiss et al., (2011). Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
Fifth most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum L8 in Weiss et al., (2011). Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
Sixth most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum L4 in Weiss et al., (2011). Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
Seventh most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum L9 in Weiss et al., (2011). Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
If present, eighth most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum L5 in Weiss et al., (2011). Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
If present, ninth most anterior L-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum L6 in Weiss et al., (2011). Note that Shanbhag et al., (2001) report that there are between 7 and 9 L-type sensilla, whilst Hiroi et al., (2002) claim no variation from 9 sensilla.
Gustatory bristle on the outer surface of the labellum. Three different types are present: short, intermediate and large bristles. They are innervated by 2 or 4 chemosensory neurons and one mechanosensory neuron.
Gustatory peg between the cuticular folds of pseudotrachea of the adult labellum. They measure around 4um in length with a distal shaft of about 2.5um arising from a base that is 1-1.5um high. They are innervated by one chemosensory neuron and one mechanosensory neuron.
Any sensillum (FBbt:00007152) that is part of some labellum (FBbt:00004531).
Any external sensillum (FBbt:00007231) that is part of some embryonic/larval labial organ (FBbt:00002720).
Any sensillum (FBbt:00007152) that is part of some labial segment (FBbt:00000014).
One of the three labial sensilla located in the labial organ, on the head of the embryo/larva. It is innervated by one dendrite, similarly to labial sensillum 2.
One of the three labial sensilla located in the labial organ, on the head of the embryo/larva. It is innervated by one dendrite, similarly to labial sensillum 1.
One of the three labial sensilla located in the labial organ, on the head of the embryo/larva. It is innervated by three dendrites.
Large bristle on the anterior side of antennal segment 2. There are 5 of these.
Large vibrissal bristle with a relatively anterior position within the vibrissae, directly below the antenna. There are usually 2-4 of these on each side. Especially in other species, these are sometimes specifically referred to as vibrissae, though melanogaster papers tend to refer to the full line of gena bristles as vibrissae.
The largest subtype of basiconic sensilla. It measures 12 micrometers and 2.5 micrometers wide with blunt tips. Directly above the base of the sensillum, the shaft diameter is often somewhat reduced resulting in a club-shaped appearance. The pores are arranged in lines, positioned wider apart than in the small basiconic sensillum. It is innervated by two or 4 sensory neurons. Two subtypes can be identified, base on the internal morphology of the peg (LB-I and LB-II). Large basiconic sensilla are found in the antennal segment 3.
Large, blunt tipped, olfactory basiconic sensillum of antennal segment 3. The external sensory structure is perforated by pores, arranged along a complicated pattern of branched lines, that connect to a lymph-filled lumen containing the highly branched dendrites of 2-4 ORNs. Morphology is consistent with these sensilla being olfactory (Shanbhag et al., 1999). This function has been directly confirmed by electrophysiology (Clyne et al., 1997).
Large chordotonal organ of the base of the haltere, that is inserted axially in this region. Original reference for these (FlyBase:FBrf0239028) is based on other flies. Chordotonal organs were not identified in Drosophila halteres by Tsubouchi et al. (2017) (FlyBase:FBrf0237124) [FBC:CP].
Largest taste bristle subtype of the outside labellum: each bristle is around 35 micrometres long. These bristles are located in the region between the intermediate bristles on the lobe periphery and the medial-ventrally located short taste bristles. These taste bristles contain 4 gustatory receptor neurons (Shanbhag et al., 2001) sensitive to: sugars, low concentrations of salt, bitter or high salt concentrations and water or low osmolarity (Meunier et al., 2003; Fujishiro et al., 1984) and one mechanosensory neuron (Shanbhag et al., 2001). Large taste bristles do not respond to bitter stimuli and their gustatory receptor neurons do not express the bitter receptor Gr66a (Weiss et al., 2011).
Any sensillum (FBbt:00007152) that is part of some larval abdomen (FBbt:00001746).
Any embryonic/larval sense organ (FBbt:00002639) that is part of some larval mandibular segment (FBbt:00001738).
Any sense organ (FBbt:00005155) that is part of some larval maxillary segment (FBbt:00001739).
Any sensillum (FBbt:00007152) that is part of some larval mesothoracic segment (FBbt:00001744).
Any sensillum (FBbt:00007152) that is part of some larval metathoracic segment (FBbt:00001745).
Laterally located club-like sensory structure found in the mesothoracic and metathoracic segments of the larva.
Lateral ocellus located on the ocellar triangle of the dorsal postfrons of the adult head, medial to the interocellar bristles. There are two of these, each one with around 75 photoreceptors.
Sensory organ associated with the larval pharynx and connected to the hypopharyngeal nerve. Part relation to ocular segment from Schmidt-Ott et al., 1994, based on relating gene expression during early segmentation to loss of function phenotypes of segmentally expressed genes.
Sensillum of the lateral fold of the dorsal pouch in the larval head. It contains 2 or 3 sensory neurons.
Any chaeta that is a part of the leg and is involved in the detection of mechanical stimuli.
Any sensillum (FBbt:00007152) that is part of some leg (FBbt:00004640).
Any chaeta that is a part of the leg and is involved in chemical detection for the purpose of taste.
The most ventral of the humeral bristles.
A long, unicellular, setiform outgrowth that is strongly chitinized and may be in connection with a sensory nerve.
Campaniform sensillum found on the medial surface of the tegula of the adult wing. There are 18 elliptical sensilla with high profile and with a socket (type 5). Fourteen of these form a compact central population oriented with their major axis perpendicular to the proximodistal axis of the wing. Two larger sensilla of the same type flank this population, oriented parallel to the wing axis.
Any sensillum (FBbt:00007152) that is part of some male terminalia (FBbt:00004835).
Olfactory basiconic sensillum of the maxillary palp. The surface of the sensillum is perforated by numerous pores, arranged along a complicated pattern of branched lines, connecting to a lymph space innervated by branched dendrites from two ORNs. These sensilla are located predominantly on the distal half of the dorsal surface and the lateral edge of each maxillary palp.
Basiconic olfactory sensillum of maxillary palp that is innervated by the dendrites of two ORNs. It is distinguishable from pb2 and pb3 by its odor response profile (Goldman et al., 2005) and the identity of the ORNs that innervate it (42a and 71a; Couto et al., 2005; Goldman et al., 2005).
Basiconic olfactory sensillum of maxillary palp that is innervated by the dendrites of two ORNs. It is distinguishable from pb1 and pb3 by its odor response profile (Goldman et al., 2005) and the identity of the ORNs that innervate it (85e/33c and 46a; Couto et al., 2005; Goldman et al., 2005).
Basiconic olfactory sensillum of maxillary palp that is innervated by the dendrites of two ORNs. It is distinguishable from pb1 and pb2 by its odor response profile (Goldman et al., 2005) and the identity of the ORNs that innervate it (59c and 85d; Couto et al., 2005; Goldman et al., 2005).
Trichoid sensillum of the maxillary palp with an external sensory structure that is anchored in a socket and consists of a small bundle of closely apposed fibers, each of which has grooves running longitudinally. No obvious pores are present. Structure is consistent with these sensilla being mechanosensory rather than chemosensory (Riesgo-Escovar et al., 1997).
Any sense organ (FBbt:00005155) that is part of some maxillary palpus (FBbt:00004546).
effector genotype: ‘20XUAS-IVS-mCD8::GFP in su(Hw)attP5 (pJFRC2)’ [confocal microscopy; adult brain; gustatory sensory organ; adult neuron; male organism; McKellar_Gr64f; expression pattern fragment; is part of; JRC2018Unisex; P{Gr64f-GAL4.9.7} expression pattern; sugar-sensing neuron; adult sense organ]
effector genotype: ‘20XUAS-IVS-mCD8::GFP in su(Hw)attP5 (pJFRC2)’ [confocal microscopy; McKellar_Gr66a; gustatory sensory organ; adult neuron; male organism; expression pattern fragment; is part of; JRC2018Unisex; bitter-sensing neuron; adult brain; adult sense organ; P{Gr66a-GAL4.D} expression pattern]
Sensillum of the adult labral sense organ in the adult pharynx that is innervated both by a mechanosensory and gustatory receptor neuron. There are 2 of these sensilla.
Second most distal sensillum of the adult labral sense organ in the adult pharynx. It is innervated both by a gustatory and mechanosensory receptor neurons. One of two medium sized, hairless sensilla of the labral sense organ.
Most distal sensillum of the adult labral sense organ in the adult pharynx. It is innervated both by a gustatory and mechanosensory receptor neurons. One of two medium sized, hairless sensilla of the labral sense organ.
Bristle that is innervated by a mechanosensory neuron that detects its movement due to wind, contact or other stimuli.
Slender, singly-innervated mechanosensory bristle of the dorsal double row. That this bristle is mechanosensory is primarily based on the presence of a characteristic microtubular body present in the single innervating neuron (Palka et al., 1979).
Sensillum of the adult labral sense organ in the adult pharynx that is innervated only by a mechanosensory receptor neuron. There are 6 of these sensilla, numbered from proximal to distal.
Most proximal sensillum of the adult labral sense organ in the adult pharynx. The external sensory structure is a hair of 5 micrometers long by 0.5-1 micrometers thick. It is innervated by a mechanosensory receptor neuron.
Second most proximal sensillum of the adult labral sense organ in the adult pharynx. The external sensory structure is a hair of 5 micrometers long by 0.5-1 micrometers thick. It is innervated by a mechanosensory receptor neuron.
Third most proximal sensillum of the adult labral sense organ in the adult pharynx. The external sensory structure is a hair of 5 micrometers long by 0.5-1 micrometers thick. It is innervated by a mechanosensory receptor neuron.
Fourth most sensillum of the adult labral sense organ in the adult pharynx. The external sensory structure is a hair of 5 micrometers long by 0.5-1 micrometers thick. It is innervated by a mechanosensory receptor neuron.
Fifth most sensillum of the adult labral sense organ in the adult pharynx. The external sensory structure is a hair of 5 micrometers long by 0.5-1 micrometers thick. It is innervated by a mechanosensory receptor neuron.
Sixth most sensillum of the adult labral sense organ in the adult pharynx. The external sensory structure is a hair of 5 micrometers long by 0.5-1 micrometers thick. It is innervated by a mechanosensory receptor neuron.
Any sense organ (FBbt:00005155) that capable of some detection of mechanical stimulus involved in sensory perception (GO:0050974).
Mechanosensory bristle of the ventral double row. That this bristle is mechanosensory is primarily based on the presence of a characteristic microtubular body present in the single innervating neuron (Palka et al., 1979).
Slender, singly innervated mechanosensory bristle of the ventral triple row. That this bristle is mechanosensory is primarily based on the presence of a characteristic microtubular body present in the single innervating neuron (Palka et al., 1979).
Medial ocellus located on the ocellar triangle of the dorsal postfrons of the adult head, just anterior to, and in between the two medial ocelli. It has around 100 photoreceptors.
Stout, singly innervated bristle of the medial triple row. This bristle is mechanosensory. This bristle type is believed to be mechanosensory based on the presence of a characteristic microtubular body present in the single innervating neuron (Palka et al., 1979).
Any chaeta found in the mesothoracic segment of the adult.
A relatively long bristle located on a small island of hairs (trichomes) in an otherwise bare region of cuticle on the ventral side of the mesothoracic coxa, adjacent to its joint with the trochanter.
Any trichoid sensillum (FBbt:00005184) that is part of some mesothoracic coxa (FBbt:00004686).
Any one of the row of 4 trichoid sensillum, on the hindside of the mesothoracic coxa.
Any one of a group of 8 trichoid sensilla located proximally and medially in two rows near the joint between the mesothoracic coxa and the thorax.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval mesothoracic segment.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval mesothoracic segment.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval mesothoracic segment.
The most ventral of the two trichoid sensilla of the dorsal sensory cluster of the embryonic/larval mesothoracic segment.
The most dorsal of the two trichoid sensilla of the dorsal sensory cluster of the embryonic/larval mesothoracic segment.
Triscolopidial chordotonal organ located in the dorsal sensory cluster of the embryonic/larval mesothoracic segment.
Any campaniform sensillum (FBbt:00005183) that is part of some mesothoracic femur (FBbt:00004689).
An isolated campaniform sensillum located proximally on the anterior edge of the mesothoracic femur, close to the joint between the femur and the trochanter.
Any one of a group of 11 campaniform sensilla located in a cluster in the posterior proximal region of the mesothoracic femur, close to the joint between the femur and the trochanter. They are arranged in 3 rows with 4, 4 and 3 sensilla each.
Chordotonal organ of the adult mesothoracic femur. There are three chordotonal organs, located in the ventral chamber near the longitudinal septum. There is one large group, on the ventrolateral side, and two smaller ones in the center of the femur.
Large chordotonal organ of the adult mesothoracic femur. It is located on the ventrolateral side and has around 32 well-aligned scolopidia. Its distal tip terminates at the distal epicuticular surface of the tip of the femur.
One of the small chordotonal organ of the adult mesothoracic femur. It is located in the center of the femur and has around 14 scolopidia. Distally, the scolopidia are more scattered than the mesothoracic femoral chordotonal organ 1, with a majority of them connected to the femoral muscle membrane.
One of the small chordotonal organ of the adult mesothoracic femur. It is located in the center of the femur and has between 25-28 scolopidia. Distally, the scolopidia are more scattered than the mesothoracic femoral chordotonal organ 1, with a majority of them connected to the femoral muscle membrane.
Any Keilin organ anterior lateral hair (FBbt:00052160) that is part of some larval mesothoracic segment (FBbt:00001744).
Any Keilin organ anterior medial hair (FBbt:00052161) that is part of some larval mesothoracic segment (FBbt:00001744).
Any Keilin organ posterior hair (FBbt:00052162) that is part of some larval mesothoracic segment (FBbt:00001744).
Any Keilin’s organ (FBbt:00005198) that is part of some larval mesothoracic segment (FBbt:00001744).
The most ventral of the two campaniform sensilla of the lateral sensory cluster of the embryonic/larval mesothoracic segment.
The most dorsal of the two campaniform sensilla of the lateral sensory cluster of the embryonic/larval mesothoracic segment.
Any Kolbchen (FBbt:00005199) that is part of some embryonic/larval mesothoracic lateral sensory cluster (FBbt:00007303).
Trichoid sensillum of the lateral sensory cluster of the embryonic/larval mesothoracic segment.
Any chaeta that is a part of the mesothoracic leg and is involved in the detection of mechanical stimuli.
Any sensillum (FBbt:00007152) that is part of some mesothoracic leg (FBbt:00004685).
Gustatory bristle found on the tarsal segments of the mesothoracic (2nd) leg of the adult. It has a straight tip. In the female, most sensilla are organized in symmetric pairs (with two exceptions), with lateral sensilla having a counterpart on the medial side of the leg. The male sensilla appear similar to the female ones. The organization of taste sensilla is similar in all three legs with a few exceptions.
Taste bristle of the metatarsus of the mesothoracic leg. It is located most proximally on the dorsal tarsal segment 1. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of the metatarsus of the mesothoracic leg. It is located second most proximally on the dorsal tarsal segment 1. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of the metatarsus of the mesothoracic leg. It is located most distally on the dorsal tarsal segment 1. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 2 of the mesothoracic leg. It is located proximally on the dorsal tarsal segment 2. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 2 of the mesothoracic leg. It is located distally on the ventral tarsal segment 2. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 3 of the mesothoracic leg. It is located proximally on the dorsal tarsal segment 3. One is found on the lateral side of the leg.
Taste bristle of tarsal segment 4 of the mesothoracic leg. It is located distally on the dorsal tarsal segment 4. One is found on the medial side of the leg and one on the lateral side.
Short taste bristle of tarsal segment 4 of the mesothoracic leg. It is located distally on the ventral tarsal segment 4. One is found on the medial side of the leg and one on the lateral side. It responds to some sugars, and some bitter compounds.
Taste bristle of tarsal segment 5 of the mesothoracic leg. It is located most proximally on the dorsal tarsal segment 5. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 5 of the mesothoracic leg. It is located most distally on the dorsal tarsal segment 5. One is found on the medial side of the leg and one on the lateral side. It responds to some sugars, and some bitter compounds.
Short taste bristle of tarsal segment 5 of the mesothoracic leg. It is located distally on the ventral tarsal segment 5. One is found on the medial side of the leg and one on the lateral side. It responds to sugars, and a narrow set of bitter compounds.
Spine shaped gustatory bristle, between 12-45 micrometres long, found on the mesothoracic (2nd) leg of the adult. There are approximately 30 of these bristles per mesothoracic leg.
A campaniform sensillum located on the metatarsal segment of the mesothoracic leg.
A single campaniform sensillum located ventrally on the metatarsus of the mesothoracic leg (Dinges et al., 2020).
One of two campaniform sensilla located dorsally on the metatarsus of the mesothoracic leg, near the distal end of the segment (Dinges et al., 2020).
One of two campaniform sensilla located on the third tarsal segment of the mesothoracic leg, dorsally near the distal end of the segment (Dinges et al., 2020).
One of four campaniform sensilla located on the fifth tarsal segment of the mesothoracic leg, ventrally near the distal end of the segment (Dinges et al., 2020).
Any microchaeta (FBbt:00005182) that is part of some mesothoracic tarsal segment (FBbt:00004690).
Any bristle in one of the 8 longitudinal bracted or 4 bractless bristle rows in a mesothoracic tarsal segment. Row 1 is at the ventro-posterioventral position, with numbering continuing through the posterior, dorsal, and anterior surfaces.
Longitudinal bracted bristle row of the adult tarsi of the mesothoracic leg. It is at a ventro-posterioventral position.
Longitudinal bracted bristle row of the adult tarsi of the mesothoracic leg. It is posterior to row 1, in a posterioventral position.
Longitudinal bractless bristle row of the adult tarsi of the mesothoracic leg. It is posterior to row 2, in a posterior position.
Longitudinal bracted bristle row of the adult tarsi of the mesothoracic leg. It is anterior to row 2.5, in a postero-posteriodorsal position.
Longitudinal bractless bristle row of the adult tarsi of the mesothoracic leg. It is anterior to row 3, in a posteriodorsal position.
Longitudinal bracted bristle row of the adult tarsi of the mesothoracic leg. It is anterior to row 3.5, in a posteriodorsal-dorso position.
Longitudinal bracted bristle row of the adult tarsi of the mesothoracic leg. It is anterior to row 4, in a dorsal position.
Longitudinal bractless bristle row of the adult tarsi of the mesothoracic leg. It is anterior to row 5, in an anterodorsal position.
Longitudinal bracted bristle row of the adult tarsi of the mesothoracic leg. It is anterior to row 5.5, in an anterior position.
Longitudinal bractless bristle row of the adult tarsi of the mesothoracic leg. It is anterior to row 6, in an antero-anterioventral position.
Longitudinal bracted bristle row of the adult tarsi of the mesothoracic leg. It is posterior to row 6.5, in an anterioventral position.
Longitudinal bracted bristle row of the adult tarsi of the mesothoracic leg. It is posterior to row 1, in a ventral position.
Longer and thicker bristle without bracts in the anterior compartment, on the ventral distal region of the mesothoracic tibia, near the joint with the first tarsal segment. It is part of the longitudinal bristle row 8 and it is surrounded by 4 or 5 spur bristles.
A campaniform sensillum located on the tibia of the mesothoracic leg.
One of two campaniform sensilla located dorsally on the tibia of the mesothoracic leg, toward the posterior end of the segment (Dinges et al., 2020).
One of three campaniform sensilla located ventrally on the tibia of the mesothoracic leg, toward the posterior end of the segment (Dinges et al., 2020).
Longer and thicker bristle without bracts in the anterior compartment, on the dorsal distal region of the mesothoracic tibia, near the joint with the first tarsal segment. It is part of the longitudinal bristle row 5.
An oval sense organ in the dorsal, proximal mesothoracic tibia. It is composed of 4 sensilla campaniform.
Short, thick and peg-shaped bracted bristle that surrounds the mesothoracic tibial apical bristle. There are 4 or 5 of these.
Any trichoid sensillum (FBbt:00005184) that is part of some mesothoracic tibia (FBbt:00004687).
Any campaniform sensillum (FBbt:00005183) that is part of some mesothoracic trochanter (FBbt:00004688).
Any one of 8 laterally located mesothoracic trochanter campaniform sensillum Sc13. These are located in naked cuticle.
Any one of 5 medially located mesothoracic trochanter campaniform sensillum Sc13. These are located in hairy cuticle.
Any one of a cluster of ~11-13 campaniform sensilla located posteriorly and distally on the mesothoracic trochanter - near to its joint with the femur. This cluster is divided into two subfields by a cuticular ridge (Dinges et al., 2020).
Any one of a row of 3 campaniform sensilla located laterally distally on the mesothoracic trochanter.
A distinctive, posterior pointing bristle located on the posterior edge of the medial side of the mesothoracic trochanter.
Any trichoid sensillum (FBbt:00005184) that is part of some mesothoracic trochanter (FBbt:00004688).
Any one of ~10-14 trichoid sensilla located medially in two adjacent clusters of ~5-7 each (GSt1 and GSt2) on the condyle of the joint between the mesothoracic coxa and the trochanter.
A single, isolated trichoid sensillum located medially and distally on the mesothoracic trochanter.
Any one of a row of 5-6 trichoid sensilla located proximally and laterally on the mesothoracic coxa.
The most ventral of the two campaniform sensilla of the ventral sensory cluster of the embryonic/larval mesothoracic segment.
The most dorsal of the two campaniform sensilla of the ventral sensory cluster of the embryonic/larval mesothoracic segment.
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Monoscolopidial chordotonal organ of the ventral sensory cluster of the embryonic/larval mesothoracic segment.
A campaniform sensillum located on the metatarsal segment of the leg.
Any chaeta found in the metathoracic segment of the adult.
Any trichoid sensillum (FBbt:00005184) that is part of some metathoracic coxa (FBbt:00004708).
Any one of a row of 4 trichoid sensilla located proximally and laterally, near the joint between the metathoracic coxa and the thorax.
Any one of a group of 8 trichoid sensilla located proximally and medially in two rows near the joint between the metathoracic coxa and the thorax.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval metathoracic segment.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval metathoracic segment.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval metathoracic segment.
The most ventral of the two trichoid sensilla of the dorsal sensory cluster of the embryonic/larval metathoracic segment.
The most dorsal of the two trichoid sensilla of the dorsal sensory cluster of the embryonic/larval metathoracic segment.
Triscolopidial chordotonal organ located in the dorsal sensory cluster of the embryonic/larval metathoracic segment.
Any campaniform sensillum (FBbt:00005183) that is part of some metathoracic femur (FBbt:00004711).
An isolated campaniform sensillum located proximally on the anterior edge of the metathoracic femur, close to the joint between the femur and the trochanter.
Any one of a group of 11 campaniform sensilla located in a cluster in the posterior proximal region of the metathoracic femur, close to the joint between the femur and the trochanter. They are arranged in 3 rows with 4, 4 and 3 sensilla each.
Chordotonal organ of the adult metathoracic femur. There are three chordotonal organs, located in the ventral chamber near the longitudinal septum. There is on large group, on the ventrolateral side, and two smaller ones in the center of the femur.
Large chordotonal organ of the adult metathoracic femur. It is located on the ventrolateral side and has around 32 well-aligned scolopidia. Its distal tip terminates at the distal epicuticular surface of the tip of the femur.
One of the small chordotonal organ of the adult metathoracic femur. It is located in the center of the femur and has around 14 scolopidia. Distally, the scolopidia are more scattered than the metathoracic femoral chordotonal organ 1, with a majority of them connected to the femoral muscle membrane.
One of the small chordotonal organ of the adult metathoracic femur. It is located in the center of the femur and has between 25-28 scolopidia. Distally, the scolopidia are more scattered than the metathoracic femoral chordotonal organ 1, with a majority of them connected to the femoral muscle membrane.
A short yellow bristle that borders a region of naked cuticle (ZNB) in the metathoracic femur. There are two incomplete rows running proximo-distally.
Any Keilin organ anterior lateral hair (FBbt:00052160) that is part of some larval metathoracic segment (FBbt:00001745).
Any Keilin organ anterior medial hair (FBbt:00052161) that is part of some larval metathoracic segment (FBbt:00001745).
Any Keilin organ posterior hair (FBbt:00052162) that is part of some larval metathoracic segment (FBbt:00001745).
Any Keilin’s organ (FBbt:00005198) that is part of some larval metathoracic segment (FBbt:00001745).
The most ventral of the two campaniform sensilla of the lateral sensory cluster of the embryonic/larval metathoracic segment.
The most dorsal of the two campaniform sensilla of the lateral sensory cluster of the embryonic/larval metathoracic segment.
Any lateral Kolbchen lbd (FBbt:00100361) that is part of some larval metathoracic segment (FBbt:00001745).
Trichoid sensillum of the lateral sensory cluster of the embryonic/larval metathoracic segment.
Any chaeta that is a part of the metathoracic leg and is involved in the detection of mechanical stimuli.
Any sensillum (FBbt:00007152) that is part of some metathoracic leg (FBbt:00004707).
Gustatory bristle found on the tarsal segments of the metathoracic (3rd) leg of the adult. It has a straight tip. In the female, most sensilla are organized in symmetric pairs (with two exceptions), with lateral sensilla having a counterpart on the medial side of the leg. The male sensilla appear similar to the female ones. The organization of taste sensilla is similar in all three legs with a few exceptions.
Taste bristle of the metatarsus of the metathoracic leg. It is located most proximally on the dorsal tarsal segment 1. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of the metatarsus of the metathoracic leg. It is located second most proximally on the dorsal tarsal segment 1. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of the metatarsus of the metathoracic leg. It is located most distally on the dorsal tarsal segment 1. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 2 of the metathoracic leg. It is located proximally on the dorsal tarsal segment 2. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 2 of the metathoracic leg. It is located distally on the ventral tarsal segment 2. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 3 of the metathoracic leg. It is located proximally on the dorsal tarsal segment 3. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 4 of the metathoracic leg. It is located distally on the dorsal tarsal segment 4. One is found on the medial side of the leg and one on the lateral side.
Short taste bristle of tarsal segment 4 of the metathoracic leg. It is located distally on the ventral tarsal segment 4. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 5 of the metathoracic leg. It is located most proximally on the dorsal tarsal segment 5. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 5 of the metathoracic leg. It is located most distally on the dorsal tarsal segment 5. One is found on the medial side of the leg and one on the lateral side.
Short taste bristle of tarsal segment 5 of the metathoracic leg. It is located distally on the ventral tarsal segment 5. One is found on the medial side of the leg and one on the lateral side.
Spine shaped gustatory bristle, between 12-45 micrometres long, found on the metathoracic (3rd) leg of the adult. There are approximately 31-32 of these bristles per metathoracic leg.
A campaniform sensillum located on the metatarsal segment of the metathoracic leg.
A single campaniform sensillum located ventrally on the metatarsus of the metathoracic leg (Dinges et al., 2020).
One of two campaniform sensilla located dorsally on the metatarsus of the metathoracic leg, near the distal end of the segment (Dinges et al., 2020).
One of a pair of campaniform sensilla of the haltere sclerite. It is an elliptical sensillum with a high profile and socket (type 5). The two sensilla are fused to each other by the cuticle of their sockets. It is around 5 micrometers in diameter.
One of two campaniform sensilla located on the third tarsal segment of the metathoracic leg, dorsally near the distal end of the segment (Dinges et al., 2020).
One of four campaniform sensilla located on the fifth tarsal segment of the metathoracic leg, ventrally near the distal end of the segment (Dinges et al., 2020).
A bristle of the tarsal segment of the adult metathoracic leg.
Any bristle in one of the 8 longitudinal bracted or bractless bristle rows in a metathoracic tarsal segment. Row 1 is at the ventro-posterioventral position, with numbering continuing through the posterior, dorsal, and anterior surfaces. Row 2 has been replaced by the transverse bristle rows.
Longitudinal bracted bristle row of the adult tarsi of the metathoracic leg. It is at a ventro-posterioventral position.
Longitudinal bracted bristle row of the adult tarsi of the metathoracic leg. It is dorsoposterior anterior to row 1, in a postero-posteriodorsal position.
Longitudinal bracted bristle row of the adult tarsi of the metathoracic leg. It is anterior to row 3, in a posteriodorsal-dorso position.
Longitudinal bracted bristle row of the adult tarsi of the metathoracic leg. It is anterior to row 4, in a dorsal position.
Longitudinal bractless bristle row of the adult tarsi of the metathoracic leg. It is anterior to row 5, in an anterodorsal position.
Longitudinal bracted bristle row of the adult tarsi of the metathoracic leg. It is anterior to row 5.5, in an anterior position.
Longitudinal bracted bristle row of the adult tarsi of the metathoracic leg. It is posterior to row 6, in a anterioventral position.
Longitudinal bracted bristle row of the adult tarsi of the metathoracic leg. It is posterior to row 1, in a ventral position.
Any bracted bristle in one of the transverse bristle rows (TR) of the metathoracic tarsal segments. There are 11 TRs in the posterior region of the metatarsus, and 6 TRs in tarsal segment 3. These transverse rows replace the tarsal bristle longitudinal row 2.
A campaniform sensillum located on the tibia of the metathoracic leg.
One of two campaniform sensilla located dorsally on the tibia of the metathoracic leg, toward the posterior end of the segment (Dinges et al., 2020).
One of three campaniform sensilla located ventrally on the tibia of the metathoracic leg, toward the posterior end of the segment (Dinges et al., 2020).
Longer and thicker bristle in the anterior compartment, on the dorsal distal region of the metathoracic tibia, near the joint with the first tarsal segment.
An oval sense organ in the dorsal, proximal metathoracic tibia. It is composed of 4 sensilla campaniform.
Any bristle located in the only transversely oriented row (TR) on the posterior side of the metathoracic tibia.
Any trichoid sensillum (FBbt:00005184) that is part of some metathoracic tibia (FBbt:00004709).
Any campaniform sensillum (FBbt:00005183) that is part of some metathoracic trochanter (FBbt:00004710).
Any one of 8 laterally located metathoracic trochanter campaniform sensillum Sc13. These are located in naked cuticle.
Any one of 5 medially located metathoracic trochanter campaniform sensillum Sc13. These are located in hairy cuticle.
Any one of a cluster of ~11-13 campaniform sensilla located posteriorly and distally on the metathoracic trochanter - near to its joint with the femur. This cluster is divided into two subfields by a cuticular ridge (Dinges et al., 2020).
Any one of a row of 3 campaniform sensilla located laterally distally on the metathoracic trochanter.
Any trichoid sensillum (FBbt:00005184) that is part of some metathoracic trochanter (FBbt:00004710).
Any one of ~10-14 trichoid sensilla located medially in two adjacent clusters of ~5-7 each on the condyle of the joint between the metathoracic coxa and the trochanter.
A single, isolated trichoid sensillum located medially and distally on the metathoracic trochanter.
Any one of a row of 5-6 trichoid sensilla located proximally and laterally on the metathoracic coxa.
The most ventral of the two campaniform sensilla of the ventral sensory cluster of the embryonic/larval metathoracic segment.
The most dorsal of the two campaniform sensilla of the ventral sensory cluster of the embryonic/larval metathoracic segment.
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Monoscolopidial chordotonal organ of the ventral sensory cluster of the embryonic/larval metathoracic segment.
A sensillum of the adult whose external sensory structure is a hair or short thin bristle. Note that entomologists working in other species may call such sensilla trichoid, but Drosophila biologists typically reserve this for only the very smallest hairs. The reference for the term microchaeta among Drosophilist dates back to at least Lees and Waddington (1942).
Medial orbital bristle that points posteriorly.
Middle-most sensillum of the ventral cibarial sense organ of the adult pharynx. It is innervated by 2 gustatory receptor neurons (Gendre et al., 2003).
The middle of the sternopleural bristles of the adult mesothoracic preepisternum, located at the same dorso/ventral level as the anterior and posterior bristles.
Chordotonal organ with a single scolopidium.
Bitter-sensitive labellar taste bristle that detects a narrow range of bitter stimuli, with greater responses to denatonium benzoate, berberine chloride, lobeline hydrochloride, sparteine sulfate salt and escin (Weiss et al., 2011).
Bitter-sensitive labellar taste bristle that detects a narrow range of bitter stimuli, with greater responses to caffeine, umbelliferone and theophylline (Weiss et al., 2011).
A short sensory bristle of the notum (mesothoracic tergum ; FBbt:00004580). There are around 200 of these, all with a bristle pointing posterior to their socket. They are arranged into approximately parallel rows running anterior to posterior.
A laterally located macrochaeta of the prescutum. There are two pairs of these per prescutum, anterior and posterior.
Small bristle of the posterior head, located just above the neck (occipital foramen) arranged in a dense cluster. There are around 17 bristles in each cluster.
Large bristle of the adult dorsal head, located immediately ventral to the lateral ocelli. There are two of these.
A simple visual organ on the top of the adult head. There are three of these, arranged in a triangle.
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Any sense organ (FBbt:00005155) that capable of some detection of chemical stimulus involved in sensory perception of smell (GO:0050911).
One of the facets of the compound eye. It is composed of eight light-sensing photoreceptor cells (photoreceptor cell R1-R8) and accessory cells. There are around 800 ommatidia in each compound eye.
Large bristle at the medial edge of the eye. There are three of these.
Ommatidial subtype with stochastic distribution throughout the retina, making up about 30% of all ommatidia. This ommatidial subtype is specialized to detect shorter wavelengths (near UV + blue) than yellow ommatidia. The pale ommatidium expresses the near ultraviolet-specific opsin Rh3 (FBgn0003249) in photoreceptor R7 cells and the blue-sensitive Rh5 (FBgn0014019) in photoreceptor R8 cells (Wernet and Desplan, 2004).
Small papilla at the base of the central dome sensillum of the larval dorsal organ. There are 6 of these, all bi-innervated except for one which is mono-innervated.
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Multiply innervated sensillum of the lateral atrial wall of the larval foregut.
[peg sensillum; eo-type sensillum]
A chordotonal organ containing 5 scolopidia.
Campaniform sensillum found on the anterior medial surface of the tegula of the adult wing. There are two large elliptical sensilla with high profile and with a socket (type 5), arranged orthogonally to the main tegula campaniform sensillum, with their long axis parallel to the proximo-distal axis of the wing. Each sensillum is around 5 micrometers in diameter. These sensilla were not found in a recent comprehensive study of campaniform sensilla, which only mention the 18 sensilla of what is called here the main field of the tegula (Dinges et al., 2020). [FlyBase:FBrf0247616]
Monoscolopidial chordotonal organ located immediately posterior to the dorsal pharyngeal organ. Its neuron fasciculates with the labral nerve.
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A light sensitive sense organ.
Sensillum that resembles a pit, with a terminal pore which is plugged by an electron-dense material. It can be innervated by one or several dendrites.
Pit sensillum located in the distal region of the terminal organ, on the head of the embryo/larva. There are five of these sensilla.
The most ventral of the five pit sensilla located in the distal region of the terminal organ, on the head of the embryo/larva. It is innervated by three dendrites, one of which terminates more proximally and ends with a tubular body, indicative of mechanosensation, the other two are the chemosensitive gustatory receptor C10 and C11 neurons (Rist and Thum, 2017).
One of the five pit sensilla located in the distal region of the terminal organ, on the head of the embryo/larva, distal to pit sensillum T3. It is innervated by four dendrites that do not contain mechanosensory tubular bodies, including gustatory receptor neurons C5, C7 and C12 (Rist and Thum, 2017).
One of the five pit sensilla located in the distal region of the terminal organ, on the head of the embryo/larva, proximal to pit sensillum T2. It is innervated by two dendrites, neither of which contain mechanosensory tubular bodies and one of which is gustatory receptor neuron C13 (Rist and Thum, 2017).
One of the five pit sensilla located in the distal region of the terminal organ, on the head of the embryo/larva. It is proximal to pit sensillum T5. It is innervated by two dendrites, neither of which contain mechanosensory tubular bodies and one of which is gustatory receptor neuron C14 (Rist and Thum, 2017).
One of the five pit sensilla located in the distal region of the terminal organ, on the head of the embryo/larva. It is distal to pit sensillum T4. It is innervated by three dendrites, one of which terminates more proximally and ends with a tubular body, indicative of mechanosensation and one of which is gustatory receptor neuron C4 (Rist and Thum, 2017).
The most posterior macrochaeta of the scutum, located laterally in two pairs, anterior and posterior.
A sensillum of the larval pharynx that lies posterior to dorsal group of pharyngeal sensilla. It is innervated by 6 dendrites. Candidate for merge with hypopharyngeal sense organ / X-organ.
Posterior-most of the two dorsocentral bristles.
Posterior-most of the two notopleural bristles.
Posterior-most orbital bristle that points posteriorly.
Posterior-most of the two postalar bristles.
Posterior-most macrochaeta of the scutellum. There is one pair of these.
Most posterior of the two dorsal cibarial sensilla of the adult pharynx (Montell, 2009). It is innervated by three gustatory receptors (Gendre et al., 2004).
The most posterior of the sternopleural bristles of the adult mesothoracic preepisternum, located at the same dorso/ventral level as the anterior and middle bristles.
Posterior-most of the two supraalar bristles.
Thorn-like bristle on the posterior side of the antennal segment 2. There are 7 of these that form a transverse row.
The posterior-most of each pair of vertical bristles that curves outwards.
Bristle at the ventral margin of the postgena of the adult head, ventral to the postorbital bristles. There is a group of these.
Trichoid sensillum of the postgena of the adult head, located in the medial region, ventral to the premandibular bristles. There is a group of these.
Trichoid sensillum that is located on the dorsal region of a narrow band that borders the occipital foramen of the adult head dorsally. There are two of these.
Small bristle of the adult postgena, located immediately adjacent to the posterior of the eye. There is a row of these from dorsal to ventral.
Large bristle of the adult dorsal head, located immediately posterior to the ocelli. There are two of these.
Any bristle that is part of the pregonite. There are 3 of these.
Small bristle on the dorsal postgena of the adult head. There is a group of these.
A macrochaeta of the prescutum, located medial to the notopleural bristles.
A sense organ located in a pit in the anterior wall of the thorax - immediately under the neck. It consists of a plate of sensory hairs whose innervating neurons have their cell bodies in a small ganglion behind the organ and project through the prosternal nerve to the prothoracic neuromere. See figure 24 of FBrf0007196 == Power, 1948.
Basiconic sensillum of the dorsal sensory cluster of the embryonic/larval prothoracic segment.
Any chaeta found in the prothoracic segment of the adult.
Any chaeta (FBbt:00005177) that is part of some prothoracic coxa (FBbt:00004664).
A relatively long bristle located on a small island of hairs (trichomes) in an otherwise bare region of cuticle on the lateral side of the costa at the distal end, adjacent to its joint with the trochanter.
Any trichoid sensillum (FBbt:00005184) that is part of some prothoracic coxa (FBbt:00004664).
Any one of a row of 3 trichoid sensilla located laterally, in the joint between the prothoracic coxa and the thorax.
Any one of a row of 4 trichoid sensilla located proximally and laterally, near the joint between the prothoracic coxa and the thorax.
Any one of a group of 8 trichoid sensilla located proximally and medially in two rows near the joint between the prothoracic coxa and the thorax.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval prothoracic segment.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval prothoracic segment.
One of the three campaniform sensilla of the dorsal sensory cluster of the embryonic/larval prothoracic segment.
Dorsal Kolbchen of the embryonic/larval prothoracic (T1) segment. It is innervated by two neurons (Dambly-Chaudiere and Ghysen, 1986) and is located more dorsally in the segment than the dorsal-most Kolbchen of the meso- and metathoracic (T2-T3) segments.
The most ventral of the two trichoid sensilla of the dorsal sensory cluster of the embryonic/larval prothoracic segment.
The most dorsal of the two trichoid sensilla of the dorsal sensory cluster of the embryonic/larval prothoracic segment.
Triscolopidial chordotonal organ located in the dorsal sensory cluster of the embryonic/larval prothoracic segment.
Any chaeta (FBbt:00005177) that is part of some prothoracic femur (FBbt:00004667).
Any campaniform sensillum (FBbt:00005183) that is part of some prothoracic femur (FBbt:00004667).
An isolated campaniform sensillum located proximally on the anterior edge of the prothoracic femur, close to the joint between the femur and the trochanter.
Any one of a group of 11 campaniform sensilla located in a cluster in the posterior proximal region of the femur, close to the joint between the femur and the trochanter. They are arranged in 3 rows with 4, 4 and 3 sensilla each.
Chordotonal organ of the adult prothoracic femur. There are three chordotonal organs, located in the ventral chamber near the longitudinal septum. There is one large group, on the ventro-medial side, and two smaller ones in the center of the femur. The three groups contain in total 76 scolopidia (Kuan et al., 2020).
Large chordotonal organ of the adult prothoracic femur. It is located on the ventro-medial side and has around 32 well-aligned scolopidia. Its distal tip terminates at the distal epicuticular surface of the tip of the femur.
One of the small chordotonal organ of the adult prothoracic femur. It is located in the center of the femur and has around 14 scolopidia. Distally, the scolopidia are more scattered than the prothoracic femoral chordotonal organ 1, with a majority of them connected to the femoral muscle membrane.
One of the small chordotonal organ of the adult prothoracic femur. It is located in the center of the femur and has between 25-28 scolopidia. Distally, the scolopidia are more scattered than the prothoracic femoral chordotonal organ 1, with a majority of them connected to the femoral muscle membrane.
Any Keilin organ anterior lateral hair (FBbt:00052160) that is part of some larval prothoracic segment (FBbt:00001743).
Any Keilin organ anterior medial hair (FBbt:00052161) that is part of some larval prothoracic segment (FBbt:00001743).
Any Keilin organ posterior hair (FBbt:00052162) that is part of some larval prothoracic segment (FBbt:00001743).
Any Keilin’s organ (FBbt:00005198) that is part of some larval prothoracic segment (FBbt:00001743).
The most ventral of the two campaniform sensilla of the lateral sensory cluster of the embryonic/larval prothoracic segment.
The most dorsal of the two campaniform sensilla of the lateral sensory cluster of the embryonic/larval prothoracic segment.
Trichoid sensillum of the lateral sensory cluster of the embryonic/larval prothoracic segment.
Triscolopidial chordotonal organ of the lateral sensory cluster of the embryonic/larval prothoracic segment.
Any chaeta that is a part of the prothoracic leg and is involved in the detection of mechanical stimuli.
Any sensillum (FBbt:00007152) that is part of some prothoracic leg (FBbt:00004663).
Gustatory bristle found on the tarsal segments of the prothoracic (1st) leg of the adult. It has a straight tip. In the female, most sensilla are organized in symmetric pairs (with two exceptions), with lateral sensilla having a counterpart on the medial side of the leg. The male contains more sensilla and more of them are asymmetric. The organization of taste sensilla is similar in all three legs with a few exceptions.
Taste bristle of the metatarsus of the prothoracic leg. It is located most proximally on the dorsal metatarsus. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of the metatarsus of the prothoracic leg. It is located proximally on the ventral metatarsus. One is found on the lateral side of the leg.
Taste bristle of the metatarsus of the prothoracic leg. It is located second most proximally on the dorsal metatarsus. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of the metatarsus of the prothoracic leg. It is located most distally on the dorsal metatarsus. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 2 of the prothoracic leg. It is located proximally on the dorsal tarsal segment 2. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 2 of the prothoracic leg. It is located distally on the ventral tarsal segment 2. One is found on the medial side of the leg and one on the lateral side. It can respond to a limited extent to some sugars.
Taste bristle of tarsal segment 2 of the prothoracic leg. This is a male-specific sensillum, found distal to taste bristle 2a.
Taste bristle of tarsal segment 2 of the prothoracic leg. This is a male-specific sensillum, found distal to taste bristle 2c.
Taste bristle of tarsal segment 2 of the prothoracic leg. This is a male-specific sensillum, found distal to taste bristle 2d.
Taste bristle of tarsal segment 3 of the prothoracic leg. It is located proximally on the dorsal tarsal segment 3. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 3 of the prothoracic leg. It is located distally on the ventral tarsal segment 3. One is found on the medial side of the leg and one on the lateral side. It can respond to a limited extent to some sugars.
Taste bristle of tarsal segment 3 of the prothoracic leg. This is a male-specific sensillum, found distal to taste bristle 3a on the dorsal tarsal segment 3. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 4 of the prothoracic leg. This is a male-specific sensillum located proximally on the dorsal tarsal segment 4. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 4 of the prothoracic leg. It is located distally on the dorsal tarsal segment 4. One is found on the medial side of the leg and one on the lateral side. It can respond to a limited extent to some sugars.
Short taste bristle of tarsal segment 4 of the prothoracic leg. It is located distally on the ventral tarsal segment 4. One is found on the lateral side of the leg. It can respond to some bitter compounds, but not sugars.
Taste bristle of tarsal segment 4 of the prothoracic leg. This is a male-specific sensillum located distal to bristle 4b on the dorsal tarsal segment 4. One is found on the medial side of the leg and one on the lateral side.
Short taste bristle of tarsal segment 4 of the prothoracic leg. It is located distal to bristle 4c on the ventral tarsal segment 4. One is found on the medial side of the leg and one on the lateral side. It can respond to a range of sugars and some bitter compounds.
Taste bristle of tarsal segment 5 of the prothoracic leg. It is located most proximally on the dorsal tarsal segment 5. One is found on the medial side of the leg and one on the lateral side.
Taste bristle of tarsal segment 5 of the prothoracic leg. It is located most distally on the dorsal tarsal segment 5. One is found on the medial side of the leg and one on the lateral side. It can respond to a range of sugars and some bitter compounds.
Short taste bristle of tarsal segment 5 of the prothoracic leg. It is located proximal to bristle 5v on the ventral tarsal segment 5. One is found on the medial side of the leg and one on the lateral side. It responds to the widest array of tastants of any prothoracic leg taste bristle present in the female, including sugars, bitter compounds and amino acids.
Short taste bristle of tarsal segment 5 of the prothoracic leg. It is located distal to bristle 5s on the ventral tarsal segment 5. One is found on the medial side of the leg and one on the lateral side. It responds to sugars, but not bitter compounds.
Spine shaped gustatory bristle, between 12-45 micrometres long, found on the prothoracic (1st) leg of the adult. There are approximately 37 of these bristles per female prothoracic leg, and 50 per male prothoracic leg (Stocker 1994).
A campaniform sensillum located on the metatarsal segment of the prothoracic leg.
A single campaniform sensillum located ventrally on the metatarsus of the prothoracic leg (Dinges et al., 2020).
One of two campaniform sensilla located dorsally on the metatarsus of the prothoracic leg, near the distal end of the segment (Dinges et al., 2020).
Any bristle in one of the 8 longitudinal bristle rows in the metatarsal segment. Row 1 is at the most ventral position.
A distinctive, large, straight microchaeta located on the medial prothoracic metatarsus (tarsal segment 1) of males, posterior to the sex comb.
Any bracted bristle in one of the transverse bristle rows (TR) of the prothoracic metatarsus (tarsal segment 1). The TRs are located in the anterior compartment. There is sexual dimorphism, with females having 7 to 8 TRs, whereas in males, 2 of the TRs have been replaced by the male specific sex comb and central bristle.
The most ventral of the two slit papillar sensilla of the lateral sensory cluster of the embryonic/larval prothoracic segment, located close to the anterior boundary.
The most dorsal of the two slit papillar sensilla of the lateral sensory cluster of the embryonic/larval prothoracic segment, located close to the anterior boundary.
One of two campaniform sensilla located on the third tarsal segment of the prothoracic leg, dorsally near the distal end of the segment (Dinges et al., 2020).
One of three or four campaniform sensilla located on the fifth tarsal segment of the prothoracic leg, dorsally near the distal end of the segment (Dinges et al., 2020).
Any microchaeta (FBbt:00005182) that is part of some prothoracic tarsal segment (FBbt:00004668).
Any bristle in one of the 8 longitudinal bristle rows in a prothoracic tarsal segment. Row 1 is at the most ventral position.
Any bristle of the ventral-most longitudinal row of the prothoracic tarsal segments.
Any bristle of the second longitudinal row of the prothoracic tarsal segments, dorsal to row 1.
Any bristle of the third longitudinal row of the prothoracic tarsal segments, dorsal to row 2. see Bryant, 1978 figure 15.
Any bristle of the fourth longitudinal row of the prothoracic tarsal segments, the most dorsoposterior.
Any bristle of the fifth longitudinal row of the prothoracic tarsal segments, anterior to row 4.
Any bristle of the sixth longitudinal row of the prothoracic tarsal segments, anterior to row 5.
Any bristle of the seventh longitudinal row of the prothoracic tarsal segments, ventral to row 6.
Any bristle of the eight longitudinal row of the prothoracic tarsal segments, anterior to row 1.
Longer and thicker bristle in the anterior compartment, on the ventral distal region of the tibia, near the joint with the first tarsal segment.
Any chaeta (FBbt:00005177) that is part of some prothoracic tibia (FBbt:00004665).
A campaniform sensillum located on the tibia of the prothoracic leg.
One of two campaniform sensilla located dorsally on the tibia of the prothoracic leg, toward the posterior end of the segment (Dinges et al., 2020).
One of three campaniform sensilla located ventrally on the tibia of the prothoracic leg, toward the posterior end of the segment (Dinges et al., 2020).
Campaniform sensillum of the prothoracic ventral tibia (Sc3 group) found between the two TiCSv2 sensilla (Merritt and Murphey, 1992). It is smaller and less eccentric than TiCSv2 (Dinges et al., 2020).
Campaniform sensillum of the prothoracic ventral tibia (Sc3 group), there are two of these per prothoracic tibia, with one found either side of TiCSv1 (Merritt and Murphey, 1992). It is larger and more eccentric than TiCSv1 (Dinges et al., 2020).
Longer and thicker bristle in the anterior compartment, on the dorsal distal region of the tibia, near the joint with the first tarsal segment.
An oval sense organ in the dorsal, proximal prothoracic tibia. It is composed of 4 sensilla campaniform.
Any bristle located in one of 5-7 transversely oriented rows (TR) in the anterior distal side of the tibia. These bristles are thin, straight, more yellow and without bracts.
Any trichoid sensillum (FBbt:00005184) that is part of some prothoracic tibia (FBbt:00004665).
Any campaniform sensillum (FBbt:00005183) that is part of some prothoracic trochanter (FBbt:00004666).
Any one of 7 or 8 laterally located prothoracic trochanter campaniform sensillum Sc13. These are located in naked cuticle.
Any one of 5 medially located prothoracic trochanter campaniform sensillum Sc13. These are located in hairy cuticle.
Any one of a cluster of ~11-13 campaniform sensilla located posteriorly and distally on the prothoracic trochanter - near to its joint with the femur. The cluster is divided into two subfields by a cuticular ridge (Dinges et al., 2020).
Any one of a row of 3 campaniform sensilla located laterally distally on the prothoracic trochanter.
A distinctive, posterior pointing bristle located on the posterior edge of the medial side of the trochanter.
Any trichoid sensillum (FBbt:00005184) that is part of some prothoracic trochanter (FBbt:00004666).
Any one of ~10-14 trichoid sensilla located medially in two adjacent clusters of ~5-7 each (GSt1 and GSt2) on the condyle of the joint between the prothoracic coxa and the trochanter.
A single, isolated trichoid sensillum located medially and distally on the prothoracic trochanter.
Any one of a row of 5-6 trichoid sensilla located proximally and laterally on the prothoracic coxa.
Any chaeta (FBbt:00005177) that is part of some prothoracic trochanter (FBbt:00004666).
The most ventral of the two campaniform sensilla of the ventral sensory cluster of the embryonic/larval prothoracic segment.
The most dorsal of the two campaniform sensilla of the ventral sensory cluster of the embryonic/larval prothoracic segment.
Kolbchen ventrally located in the embryonic/larval prothorax. It is part of the prothoracic ventral sensory cluster.
Monoscolopidial chordotonal organ of the ventral sensory cluster of the embryonic/larval prothoracic segment.
Trichoid sensillum located medial to the anterior tentorial pit in the rostral membrane of the adult head. There are four of these.
Most proximal sensillum of the ventral cibarial sense organ of the adult pharynx. It is innervated by two gustatory receptor neurons (Gendre et al., 2003).
Taste peg located in rows between and on the lateral sides of the 6 pseudotracheal rows of the adult labellum. Each peg sensillum contains one putative chemosensory and one mechanosensory neuron. The lateral rows contain 1-5 taste pegs per row, whereas the remaining rows contain 7-9 pegs. There is significant sexual dimorphism in the number of pseudotracheal taste pegs, with females having 20% more taste pegs than males (Shanbag et al., 2001).
Taste peg at the distal end of the pseudotrachea in the adult labellum.
Trichoid sensillum of the rostral membrane of the adult head.
Most anterior S-type chemosensillum of the labellum. Naming of this sensillum is based on figure 1A of Weiss et al., (2011). There is no correspondence in Hiroi et al., (2002). Note that both Shanbhag et al., (2001) and Hiroi et al., (2002) claim there are between 9 and 10 I-type sensilla present.
Second most anterior S-type chemosensillum of the labellum. It can respond to a broad range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
Tenth most anterior S-type chemosensillum of the labellum. It can respond to a broad range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum S9 in Weiss et al., (2011). Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
If present, eleventh most anterior S-type chemosensillum of the labellum. It can respond to a broad range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum S10 in Weiss et al., (2011). Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
If present, twelfth most anterior S-type chemosensillum of the labellum. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. It corresponds to sensillum I10 in Weiss et al., (2011). Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
S-type chemosensillum of the labellum, located posterodorsal to S-type sensillum S1, and more dorsally than S-type sensillum S3. It can respond to a narrow range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum I6 in Weiss et al., (2011). Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
Anterior S-type chemosensillum of the labellum. Less dorsally located than S-type sensillum S2. It can respond to a broad range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum S2 in Weiss et al., (2011). Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
Fourth most anterior S-type chemosensillum of the labellum. It can respond to a broad range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., (2002). It corresponds to sensillum S3 in Weiss et al., (2011). Sensillum S4 in Weiss et al., (2011) does not correspond to any sensilla of Hiroi et al., (2002). Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
Fifth most anterior S-type chemosensillum of the labellum. It can respond to a broad range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
Sixth most anterior S-type chemosensillum of the labellum, located slightly more dorsally than S-type sensillum S5. It can respond to a broad range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
Seventh most anterior S-type chemosensillum of the labellum. It can respond to a broad range of bitter stimuli (Weiss et al., 2011). Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
Eighth most anterior S-type chemosensillum of the labellum. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
Ninth most anterior S-type chemosensillum of the labellum, located slightly more dorsally than S-type sensillum S8. Naming of sensilla is based on figure 2(b) of Hiroi et al., 2002. There is no corresponding sensillum described in Weiss et al., (2011). Note that Shanbhag et al., (2001) claim 10-13 bristles are present, whilst Hiroi et al., (2002) claim between 12-13.
A three-chambered pit organ on antennal segment 3 that contains many sensilla. It extends ventrodorsally, with an opening to the posterior side of the antennal segment (Shanbhag et al., 1995).
Sensillum unit of a chordotonal organ, consisting of a cap cell, a ligament cell, a scolopale cell (sheath cell) and the dendrites of one or more sensory neurons. The basal end of the scolopidium is held in place by a ligament cell, usually attached to the integument. The dendrite of each sensory neuron has a cilium projecting from its tip through the scolopale, a rod like structure secreted by the scolopale cell. The cilium terminates in a dendritic cap, embedded in the cap cell. The cap cell is attached to the integument.
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103027 (T1LEG:604480); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [scolopidium 103036 (T1LEG:604522); prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); scolopidium 103041 (T1LEG:604551); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; scolopidium 103046 (T1LEG:604579); CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103051 (T1LEG:604608); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103056 (T1LEG:604634); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [scolopidium 103061 (T1LEG:604675); prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103066 (T1LEG:604715); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103071 (T1LEG:604770); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; scolopidium 103076 (T1LEG:604811); CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103081 (T1LEG:604851); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [scolopidium 103087 (T1LEG:604891); prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103094 (T1LEG:604904); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [scolopidium 103099 (T1LEG:604933); prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103104 (T1LEG:604961); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103111 (T1LEG:604990); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; scolopidium 103150 (T1LEG:605214); CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; scolopidium 103155 (T1LEG:605227); CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103160 (T1LEG:605267); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103204 (T1LEG:605467); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103209 (T1LEG:605480); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103229 (T1LEG:605599); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103234 (T1LEG:605652); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); scolopidium 103239 (T1LEG:605680); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103244 (T1LEG:605733); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); scolopidium 103250 (T1LEG:605787); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103264 (T1LEG:605856); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; Adult T1 Leg (Kuan2020); female organism; scolopidium 103270 (T1LEG:605909); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103276 (T1LEG:605962); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103281 (T1LEG:606035); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103286 (T1LEG:606100); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; scolopidium 103291 (T1LEG:606113); CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); scolopidium 103296 (T1LEG:606190); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; scolopidium 103301 (T1LEG:606244); CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to distal branch of FeCO medial tendon [scolopidium 103306 (T1LEG:606284); prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); scolopidium 103311 (T1LEG:606348); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103317 (T1LEG:606401); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); scolopidium 103322 (T1LEG:606438); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103327 (T1LEG:606452); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103332 (T1LEG:606519); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to proximal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103337 (T1LEG:606589); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103343 (T1LEG:606614); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103349 (T1LEG:606670); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103355 (T1LEG:606708); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [scolopidium 103361 (T1LEG:606763); prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103367 (T1LEG:606800); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103372 (T1LEG:606837); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103377 (T1LEG:606874); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103382 (T1LEG:606911); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103388 (T1LEG:606924); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); scolopidium 103394 (T1LEG:606974); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; scolopidium 103399 (T1LEG:607027); CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; scolopidium 103404 (T1LEG:607077); Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103415 (T1LEG:607126); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103420 (T1LEG:607190); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [scolopidium 103425 (T1LEG:607203); prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103430 (T1LEG:607240); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103435 (T1LEG:607277); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; scolopidium 103440 (T1LEG:607329); CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; scolopidium 103445 (T1LEG:607354); X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); scolopidium 103450 (T1LEG:607407); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103455 (T1LEG:607438); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); scolopidium 103461 (T1LEG:607489); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); scolopidium 103466 (T1LEG:607526); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103471 (T1LEG:607567); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103476 (T1LEG:607608); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103481 (T1LEG:607648); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103486 (T1LEG:607673); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103491 (T1LEG:607726); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103496 (T1LEG:607751); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103501 (T1LEG:607792); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; scolopidium 103506 (T1LEG:607830); female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; scolopidium 103511 (T1LEG:607883); VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
dually-innervated scolopidium, femoral scolopidium, attaches to FeCO lateral tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 103516 (T1LEG:607911); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
neuron 103223, femoral scolopidium, dually-innervated scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; Adult T1 Leg (Kuan2020); female organism; scolopidium 120598 (T1LEG:610048); femoral chordotonal organ scolopidium]
neuron 103218, femoral scolopidium, dually-innervated scolopidium, attaches to distal branch of FeCO medial tendon [prothoracic leg sensillum; CC-BY_4.0; X-ray computed tomography; Millimeter-scale imaging of a Drosophila leg at single-neuron resolution; VFB CATMAID Adult T1 Leg (T1Leg); is part of; female organism; scolopidium 120611 (T1LEG:610112); Adult T1 Leg (Kuan2020); femoral chordotonal organ scolopidium]
A macrochaeta of the scutellum. Each scutellum bears two pairs of these, located close to the lateroposterior margin of the scutellum, with one pair being anterior to the other.
A sense organ embedded in the integument and consisting of one or a cluster of sensory neurons and associated sensory structures, support cells and glial cells forming a single organized unit with a largely bona fide boundary.
Any sensillum (FBbt:00007152) that is part of some sacculus (FBbt:00004179).
A stout, darkly pigmented, slightly curved chaeta that is a single element of the sex comb. Each tooth has a small bract at the base.
Shortest subclass of taste bristle of the labellum: each bristle is around 15 micrometres long and is curved in the medial direction. These bristles are located in the most medial and ventral regions of the outside labellum. These taste bristles contain the sensory dendrites of 4 gustatory receptor neurons (Shanbhag et al., 2001) sensitive to: sugars; low concentrations of salt; bitter or high salt concentrations; water or low osmolarity (Meunier et al., 2003; Fujishiro et al., 1984).These taste bristles also contains the sensory dendrite of one mechanosensory neuron (Shanbhag et al., 2001).
[campaniform sensillum; slit papilla sensillum]
Small bristle on the anterior side of antennal segment 2. There are around 13 of these forming a row.
The smallest subtype of basiconic sensilla. It measures around 9 micrometers in length and around 1.7 micrometers in width at the base. It shows slight tapering towards the tip. The cuticular wall is 100-200nm thick and contains pores or around 40nm wide. Except for the base, the pores are arranged in longitudinal rows, with 80nm between pores and 200nm between parallel rows. It is innervated by two sensory neurons. Small basiconic sensillum are found in the antennal segment 3.
Small olfactory basiconic sensillum on antennal segment 3. The surface of the sensillum is perforated by longitudinal rows of pores, connecting to a lymph space innervated by 2 branched olfactory receptor neuron dendrites. Morphology is consistent with these sensilla being olfactory (Shanbhag et al., 1999). This function has been directly confirmed by electrophysiology (Clyne et al., 1997).
Small chordotonal organ of the base of the haltere, that spans the this region transversely. Original reference for these (FlyBase:FBrf0239028) is based on other flies. Chordotonal organs were not identified in Drosophila halteres by Tsubouchi et al. (2017) (FlyBase:FBrf0237124) [FBC:CP].
Sensory spiracular hair on the spiracular plate of the embryonic/larval posterior spiracles. It is chitinized and branched. There are four of these per spiracle, surrounding the spiracular opening. One sensory neuron innervates each of these sensory organs.
Trichoid sensillum 1 of the embryonic/larval posterior spiracles.
Trichoid sensillum 2 of the embryonic/larval posterior spiracles.
Trichoid sensillum 3 of the embryonic/larval posterior spiracles.
Trichoid sensillum 4 of the embryonic/larval posterior spiracles.
Sensillum that resembles a spot. One of these sensilla is found in the terminal organ of the embryo/larva.
Pit sensillum located in the dorso-lateral group of the terminal organ, on the head of the embryo/larva, located next to the dorsolateral papilla. It resembles a small pit, and houses a single dendrite that has a tubular body, indicative of mechanosensation (Rist and Thum, 2017). The bipolar neuron that innervates this sensillum has its cell body in the terminal organ ganglion.
Spot sensillum located in the distal region of the terminal organ, on the head of the embryo/larva. It is innervated by one dendrite, which ends with a tubular body, indicative of mechanosensation (Rist and Thum, 2017).
Macrochaeta of the adult mesothoracic preepisternum. There are four of these. Bryant (1978) has the plate bearing these as the episternum, not the pre-episternum.
Microchaeta that is posterior to the line of vibrissae in the adult head, below the eye.
A large, macrochaeta of the scutum located immediately posterior to the intrascutal suture (FBbt:00004602). There are two pairs of these, anterior and posterior.
Single long bristle at the end of the surstylus. Sometimes there is more than one long bristle per surstylus.
Thorn-like bristle of the surstylus. There are 25 of these arranged in a curved band.
A campaniform sensillum located on the third tarsal segment of the leg.
A campaniform sensillum located on the fifth tarsal segment of the leg.
Any bristle that is innervated by a gustatory receptor neuron. It has pores to allow food stimuli to reach the neuron.
External compound sense organ of the antenno-maxillary complex of the larval head consisting of a distal group of 11 sensilla and a dorso-lateral group of 3 sensilla. This organ is innervated by gustatory receptor neurons that fasciculate with either the larval maxillary nerve (for the dorso-lateral group) or the larval antennal nerve (for the distal group) and terminate in area 2 of the subesophageal ganglion.
Any sense organ (FBbt:00005155) that capable of some detection of temperature stimulus involved in sensory perception (GO:0050961).
The most ventral of the two campaniform sensilla of the larval thoracic ventral’ sensory cluster.
The most dorsal of the two campaniform sensilla of the larval thoracic ventral’ sensory cluster.
A campaniform sensillum located on the tibia.
A sensillum of which the external part is a seta. Note that there is some variation in usage of this term throughout entomology, with some sources using it to refer to any sensillum with a hair or bristle cuticular specialization (e.g. see Chapman, 1998 FBrf0239230). Among the Dmel model organism community it is only used for the smallest of hairs/bristle, with sensilla with larger, thicker cuticular specializations being referred to as chaetae. We follow this usage. It should be noted, however, that there is no clear dividing line between macrochaeta and microchaeta or between microchaeta and trichoid sensillum.
Olfactory sensillum of antennal segment 3 whose external sensory part is a sharply pointed hair arising from a conspicuous cylindrical base. The walls of the hair are perforated by irregularly distributed pores connecting to a lymph filled lumen containing 1-3 ORN dendrites, unbranched except occasionally near the hair tip. Morphology is consistent with these sensilla being olfactory (Shanbhag et al., 1999). This function has been directly confirmed by electrophysiology (Clyne et al., 1997).
Trichoid sensillum of the cervical membrane of the prothoracic leg. There is a group of 12.
A chordotonal organ consisting of 3 scolopidia.
One of two large campaniform sensilla at the most distal point of the wing margin of the distal costa. It is innervated by the first born of the twin sensilla neurons. This sensillum was classed as a bristle; however, both the initial reference (Murray et al., 1984) and a recent comprehensive study (Dinges et al., 2020) unambiguously describe it as a campaniform sensillum. [FlyBase:FBrf0247616]
One of two large campaniform sensilla at the most distal point of the wing margin of the distal costa. It is innervated by the second born of the twin sensilla neurons (Murray et al., 1984). This sensillum was classed as a bristle; however, both the initial reference (Murray et al., 1984) and a recent comprehensive study (Dinges et al., 2020) unambiguously describe it as a campaniform sensillum. [FlyBase:FBrf0247616]
The most dorsal of the humeral bristles.
Mono-innervated campaniform sensilla of wing vein L3. It is found close to the point where L3 connects with wing vein L2. It is a large circular sensillum, with a high profile and a distinct discontinuity between the dome and socket.
Ventral-most cibarial gustatory sense organ near the upper end of the posterior cibarial plate of the adult pharynx, and innervated by the pharyngeal nerve (Demerec, 1994; Nayak and Singh, 1983). It is flanked distally and proximally by the ventral row bristles and the dorsal row bristles, respectively. It comprises three sensilla (distal, middle and proximal), containing in total about 8 gustatory receptor neurons. Nayak & Singh (1983) claim the ventral cibarial sense organ is composed of two sensilla: the ventral and the dorsal sensilla. In contrast, Montell (2009), Vosshall & Stocker (2007), and Stocker & Schorderet (1981) report three sensilla: the proximal, the middle and the distal sensilla. This is shown via enhancer trap activity in Gendre et al., 1994. We follow the report of three sensilla. Similarly, the number of chemosensory neurons varies: both Nayak & Singh (1983), and Stocker (1994) report 6, whilst Gendre et al., (1994), Montell (2009), and Vosshall & Stocker (2007) report 8. We follow the latter.
Ventral compartment of chamber III of the sacculus. It contains sensillum of the type grooved sensillum 1 (Shanbhag et al., 1995).
Bristle located in the ventral double row.
Bristle of the ventral posterior head, ventrolateral to the neck and medial to the ventral postorbital bristles (Eichler et al., 2023). There are approximately 15 of these on each side (Eichler et al., 2023). Based on position and numbers, this group in Eichler et al. (2023) appears to include the postgenal bristles, postgenal trichoid sensilla and the proximal rostral trichoid sensilla from Haynie and Bryant (1986).
External compound sense organ of the antenno-maxillary complex of the larval head, located amongst the cirri. It contains three ‘knob-like’ sensilla, one bi-dendritic and two mono-dendritic. Neurons of the ventral organ connect with the larval maxillary nerve and terminate in area 2 of the subesophageal ganglion. Evidence for maxillary segment origin comes from Schmidt-Ott et al., 1994. There is some disagreement about the number of sensilla in the ventral organ: Campos-Ortega and Hartenstein, 1997, mention only 3 - one with two neurons and the other two with one each; Singh and Singh, 1984, provide evidence for 5 sensilla, 4 innervated by one neuron, the other by four neurons. This ontology follows Singh and Singh, 1984.
Any external sensillum (FBbt:00007231) that is part of some ventral organ (FBbt:00002707).
Sensillum of the ventral organ innervated by 4 dendrites.
Mono-dendritic sensillum of the ventral organ.
Mono-dendritic sensillum of the ventral organ, linked to the exterior by a pore. Putative taste sensillum (Singh, 1997).
Mono-dendritic sensillum of the ventral organ.
Mono-dendritic sensillum of the ventral organ.
A campaniform sensillum that is one of around 46 sensilla arranged in 10 transverse rows on the ventral side of the pedicel. It is elliptical with a low profile and socket (type 5). The central cuticular specialization has a raised profile, and the sockets are fused to the sockets of adjacent sensilla in the same row. It is around 3.5-4 micrometers in length.
Postorbital bristle with a relatively ventral position that is innervated by a mechanosensory neuron that fasciculates with the eye nerve (Eichler et al., 2023). There are approximately 12 of these on each side (Eichler et al., 2023).
One of 12-15 singly innervated small bristles of the ventral row of the cibarial fish-trap bristle, ventral to the ventral cibarial sense organ. They are innervated by mechanosensory neurons. Disambiguation: these bristles are sometimes referred to as the ‘ventral row’ (Stocker and Schorderet, 1981; Nayak and Singh, 1983), which may be confused with the ‘ventral row’ sensilla of the anterior wing margin (Bate and Martinez Arias, 1991). Also referred to as the lower/distal fishtrap bristles (Gendre et al., 2004).
One of 4-5 elliptical socketed campaniform sensilla with a high profile (type 5) arranged in a diamond shape on the ventral side of the scabellum. It is around 4 micrometers in diameter.
The most ventral of the sternopleural bristles of the adult mesothoracic preepisternum.
Bristle of the ventral triple row.
Large bristle on top of the adult head, immediately medial to the eye. There are two pairs of these.
Posteriormost vertical bristle (Eichler et al., 2023). It is small and relatively lateral (Eichler et al., 2023).
Second-most posterior vertical bristle (Eichler et al., 2023). It is small and relatively medial (Eichler et al., 2023).
Curved bristle of head capsule, located under the eyes and above the mouthparts.
A chordotonal organ associated with the anterior of abdominal sternite 2. It is visible externally as a raised patch of smooth cuticle without trichomes or bristles. It consists of two clusters of scolopidia (FBbt:00005217), one on either side of the ventral midline (Smith and Shepherd, 1996). The sensory neurons of Wheeler’s organ project through the second segmental nerve of the abdomen and then through the abdominal neuromeres via dorso-lateral tract of the ventral fasciculus (DLV), to terminate in the prothoracic neuromere (Smith and Shepherd, 1996).
Campaniform sensillum of the wing.
Any chaeta (FBbt:00005177) that is part of some wing margin (FBbt:00005378).
Bristle of the anterior wing margin that is innervated by a mechanosensory neuron and can detect mechanical stimuli.
Curved bristle of the anterior wing margin that is innervated by a chemosensory neuron.
Any sensillum (FBbt:00007152) that is part of some wing (FBbt:00004729).
Ommatidial subtype with stochastic distribution throughout the retina making up about 70% of all ommatidia. This ommatidial subtype is specialized to detect longer wavelengths (far UV + green). The yellow ommatidium expresses the far ultraviolet-specific opsin Rh4 (FBgn0003250) in photoreceptor R7 cells and the green-sensitive Rh6 (FBgn0019940) in photoreceptor R8 cells (Wernet and Desplan, 2004).