OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{GAL4-5-HT1B.Y}; 5-HT1B-M-700002; male organism; alpha/beta surface Kenyon cell; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; P{GAL4-5-HT1B.Y} expression pattern; calyx of adult mushroom body]
OutAge: Adult 5~15 days [5-HT1B-M-700003; expresses; confocal microscopy; P{GAL4-5-HT1B.Y}; male organism; FlyCircuit 1.0; gamma dorsal Kenyon cell; adult brain template JFRC2; expression pattern fragment; is part of; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; P{GAL4-5-HT1B.Y} expression pattern; calyx of adult mushroom body]
[transmission electron microscopy (TEM); 5thLN;left (L1EM:7952981); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval Pdf negative s-LNv neuron]
[transmission electron microscopy (TEM); 5thLN;right (L1EM:8717219); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval Pdf negative s-LNv neuron]
[A01c1_a1l (L1EM:4113533); transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 eIN-2 neuron]
[transmission electron microscopy (TEM); A01c1_a1r (L1EM:4936149); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 eIN-2 neuron]
[transmission electron microscopy (TEM); larval abdominal 1 A01c2 neuron; A01c2_a1l (ipsi_dendrite) (L1EM:5084467); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A01c2 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A01c2_a1r (ipsi_dendrite) (L1EM:16226512)]
[transmission electron microscopy (TEM); larval abdominal 1 eIN-3 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A01d3_a1l (L1EM:3995976)]
[transmission electron microscopy (TEM); larval abdominal 1 eIN-3 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A01d3_a1r (L1EM:17872154)]
[transmission electron microscopy (TEM); larval abdominal 1 eIN-3 neuron; A01d3_t3l (T01d3) (L1EM:14826752); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 eIN-3 neuron; A01d3_t3r (T01d3) (L1EM:4731383); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02o_a1l Wave-1 (L1EM:918889); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 Wave neuron]
[A02o_a1r Wave-1 (L1EM:18684928); transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 Wave neuron]
[transmission electron microscopy (TEM); A02o_a2l Wave-1 (L1EM:4589092); larval abdominal 2 Wave neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02o_a2r Wave-1 (L1EM:4717261); larval abdominal 2 Wave neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02o_a3l Wave-1 (L1EM:2194374); VFB CATMAID L1 CNS; larval abdominal 3 neuromere; L1 larval CNS ssTEM - Cardona/Janelia; has soma location; larval abdominal 3 Wave neuron]
[transmission electron microscopy (TEM); A02o_a3r Wave-1 (L1EM:12946335); VFB CATMAID L1 CNS; larval abdominal 3 neuromere; L1 larval CNS ssTEM - Cardona/Janelia; has soma location; larval abdominal 3 Wave neuron]
[transmission electron microscopy (TEM); larval abdominal 4 Wave neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A02o_a4l Wave-1 (L1EM:18508515)]
[transmission electron microscopy (TEM); larval abdominal 5 Wave neuron; A02o_a5l Wave-1 (L1EM:3437872); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 5 Wave neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A02o_a5r Wave-1 (L1EM:1401061)]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 6 Wave neuron; A02o_a6l Wave-1 (L1EM:754774)]
[transmission electron microscopy (TEM); larval metathoracic Wave neuron; A02o_t3l Wave-1 (L1EM:4223188); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval metathoracic Wave neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A02o_t3r Wave-1 (L1EM:5310670)]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A03a1_a1l (pre dMNs) (L1EM:4728865); larval abdominal 1 eIN-4 neuron]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 eIN-4 neuron; A03a1_a1r (pre dMNs) (L1EM:4541716)]
[transmission electron microscopy (TEM); A03a4_a1l (L1EM:8688631); larval abdominal 1 eIN-5 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 eIN-5 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A03a4_a1r (L1EM:4543281)]
[transmission electron microscopy (TEM); larval abdominal 2 eIN-5 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A03a4_a2l (L1EM:12643185)]
[transmission electron microscopy (TEM); A03a4_a2r (L1EM:13525684); larval abdominal 2 eIN-5 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A03a5 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A03a5_a1l (L1EM:5904833)]
[transmission electron microscopy (TEM); larval abdominal 1 A03a5 neuron; A03a5_a1r (L1EM:5297998); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A03g_a1l (L1EM:5309932); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A03g neuron]
[transmission electron microscopy (TEM); A03g_a1r (L1EM:10855206); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A03g neuron]
[transmission electron microscopy (TEM); A03g_t3r (T03g) (L1EM:20575657); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval metathoracic A03g neuron]
[transmission electron microscopy (TEM); A08e1_a1l (L1EM:7876385); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A08e1 local neuron]
[transmission electron microscopy (TEM); A08e1_a1r (L1EM:8198957); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A08e1 local neuron]
[transmission electron microscopy (TEM); A08e2_a1l (L1EM:12809923); larval abdominal 1 A08e2 local neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[A08e2_a1r (L1EM:8234099); transmission electron microscopy (TEM); larval abdominal 1 A08e2 local neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A08e3_a1l (L1EM:8421329); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A08e3 local neuron]
[transmission electron microscopy (TEM); A08e3_a1r (L1EM:8039617); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A08e3 local neuron]
[transmission electron microscopy (TEM); A08e3_a2l (L1EM:10413917); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 2 A08e3 local neuron]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A08e3_a2r (L1EM:10397674); larval abdominal 2 A08e3 local neuron]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; larval abdominal 1 down and back neuron; L1 larval CNS ssTEM - Cardona/Janelia; A09l_a1l (Down-and-back-1) (L1EM:12468812)]
[transmission electron microscopy (TEM); A09l_a1r (Down-and-back-1) (L1EM:4102844); VFB CATMAID L1 CNS; larval abdominal 1 down and back neuron; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A09l_a2l Down-and-back-1 (L1EM:3281615); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 2 down and back neuron]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; A09l_a2r Down-and-back-1 (L1EM:17693220); L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 2 down and back neuron]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A09l_a3l Down-and-back-1 (L1EM:2693767); larval abdominal 3 down and back neuron]
[transmission electron microscopy (TEM); A09l_a3r Down-and-back-1 (L1EM:1378190); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 3 down and back neuron]
[transmission electron microscopy (TEM); larval abdominal 4 down and back neuron; A09l_a4l Down-and-back-1 (L1EM:1371419); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 4 down and back neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A09l_a4r Down-and-back-1 (L1EM:1702280)]
[transmission electron microscopy (TEM); larval abdominal 5 down and back neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A09l_a5l_ Down-and-back-1 (L1EM:1115781)]
[transmission electron microscopy (TEM); A09l_a5r Down-and-back-1 (L1EM:3220573); larval abdominal 5 down and back neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval metathoracic down and back neuron; A09l_t3l Down-and-back-1 (L1EM:7124056); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval metathoracic down and back neuron; A09l_t3r Down-and-back-1 (L1EM:10053642); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A14b a1r (L1EM:12834795); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A18b neuron]
[transmission electron microscopy (TEM); larval abdominal 1 cholinergic lateral interneuron 2; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A18a_a1l (L1EM:10642320)]
[transmission electron microscopy (TEM); A18a_a1r (L1EM:4991402); larval abdominal 1 cholinergic lateral interneuron 2; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A18b3_a1l (L1EM:4730042); larval abdominal 1 cholinergic lateral interneuron 1]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A18b3_a1r (L1EM:16515841); larval abdominal 1 cholinergic lateral interneuron 1]
[A18b3_a2l (L1EM:12778086); larval abdominal 2 cholinergic lateral interneuron 1; transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 2 cholinergic lateral interneuron 1; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A18b3_a2r (L1EM:13121967)]
[transmission electron microscopy (TEM); A18b_a1l (L1EM:4542433); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A18b neuron]
[transmission electron microscopy (TEM); A18b_a1r (L1EM:4727546); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A18b neuron]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A18b_a2l (L1EM:10589761); larval abdominal 2 A18b neuron]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 2 A18b neuron; A18b_a2r (L1EM:16002926)]
[transmission electron microscopy (TEM); larval abdominal 1 eIN-1 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A18j_a1l (L1EM:5078760)]
[transmission electron microscopy (TEM); A18j_a1r (L1EM:16690920); larval abdominal 1 eIN-1 neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 1 A27h neuron; A27h_a1l (L1EM:10223572)]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A27h_a1r (L1EM:10398171); larval abdominal 1 A27h neuron]
[transmission electron microscopy (TEM); A27h_a2l (L1EM:10414725); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 2 A27h neuron]
[transmission electron microscopy (TEM); A27h_a2r (L1EM:10376512); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 2 A27h neuron]
[transmission electron microscopy (TEM); larval abdominal 4 A27h neuron; A27h_a4l (L1EM:4835694); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[A27h_a5r (L1EM:18628919); transmission electron microscopy (TEM); VFB CATMAID L1 CNS; larval abdominal 5 A27h neuron; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A27h_a6l (L1EM:15695112); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 6 A27h neuron]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 6 A27h neuron; A27h_a6r (L1EM:15696654)]
[larval abdominal 7 A27h neuron; transmission electron microscopy (TEM); A27h_a7l (L1EM:15756646); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 7 A27h neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A27h_a7r (L1EM:15700463)]
[transmission electron microscopy (TEM); larval abdominal 1 A14h neuron; A27k_a1l (L1EM:4213417); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A14h neuron; A27k_a1r (L1EM:10004243); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; larval abdominal 2 A14h neuron; L1 larval CNS ssTEM - Cardona/Janelia; A27k_a2l (L1EM:4038808)]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; larval abdominal 2 A14h neuron; L1 larval CNS ssTEM - Cardona/Janelia; A27k_a2r (L1EM:4113612)]
[transmission electron microscopy (TEM); A27l_a1l (L1EM:10219170); larval abdominal 1 A27l neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A27l neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A27l_a1r (L1EM:10499711)]
[A27l_a2l (L1EM:4719759); transmission electron microscopy (TEM); larval abdominal 2 A27l neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A27l_a2r (L1EM:5355175); larval abdominal 2 A27l neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 3 A27l neuron; A27l_a3l (L1EM:2111886)]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; larval abdominal 3 A27l neuron; A27l_a3r (L1EM:2072202)]
Adult uniglomerular antennal lobe projection neuron from the ad (ALad1) neuroblast lineage whose dendrites mainly innervate antennal lobe glomerulus D. This neuron is derived from the fourth larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). See FlyBase:FBrf0211729 for image.
Adult uniglomerular antennal lobe projection neuron from the dorsal hemilineage of the lateral neuroblast (ALl1) whose dendrites mainly innervate antennal lobe glomerulus DA1 (Bates et al., 2020). The axons of these neurons innervate a small area at the anterior edge of the lateral horn. There are around eight of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the lateral antennal lobe neuroblast (ALl1) dorsal hemilineage whose dendrites mainly innervate antennal lobe glomerulus DA2 (Bates et al., 2020). The axons of these neurons innervate the posteriomedial region of the lateral horn. There are around 5 of these per hemisphere, they project through the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage (embryonic born) whose dendrites mainly innervate antennal lobe glomerulus DA3. Neurons of this class are born during the 2nd larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage with dendrites that mainly innervate antennal lobe glomerulus DA4l. This neuron is born from the fifth division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020).
Unilateral, uniglomerular antennal lobe (AL) projection neuron whose dendrites mainly innervate glomerulus DA4m (Tanaka et al., 2012). It develops from the ALad1 neuroblast (Bates et al., 2020) and has its soma in the ventral part of the cell body rind around the AL (Tanaka et al., 2012). It bifurcates in the AL hub, with one branch forming glomerular arborizations in DA4m, with some additional neurites around the glomerulus, and one branch joining the medial antennal lobe tract (Tanaka et al., 2012). Collateral branches innervate the central area of the mushroom body calyx and the ventral area of the lateral horn (Tanaka et al., 2012). One of the lateral horn branches turns ventrally and projects via the lateral section of the posterior lateral fascicle to reach the anterior posterior lateral protocerebrum (Tanaka et al., 2012). There is one of these per hemisphere and it is cholinergic (Bates et al., 2020). This was the only example of a medial antennal lobe projection neuron 3 found by Tanaka et al., 2012.
Adult uniglomerular antennal lobe projection neuron from the neuroblast ALad1 (FBbt:00067346) lineage whose dendrites mainly innervate antennal lobe glomerulus DC1. This neuron is born from the 11th division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). Its boutons in the mushroom body calyx are widely distributed, mostly within the dorsal half (Li et al., 2020). It is the only uniglomerular projection neuron to receive input in DC1 (Li et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage whose dendrites mainly innervate antennal lobe glomerulus DC2. This neuron is derived from the third larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage whose dendrites mainly innervate antennal lobe glomerulus DC3. Neurons of this class are derived from the sixth larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). The axons of these neurons innervate a small area at the anterior edge of the lateral horn, in a similar region to VL2a and VA1lm PNs. There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage whose dendrites mainly innervate antennal lobe glomerulus DC4 (Ai et al., 2013; Bates et al., 2020). It follows the medial antennal lobe tract to innervate the mushroom body and lateral horn (Ai et al., 2013). Its axon bifurcates to form stereotypical dorsal and ventral branches in the anterior medial region of the lateral horn (Ai et al., 2013). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). Ai et al. (2013) found 2-3 of these cells, but only one in Bates et al. (2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage whose dendrites mainly innervate antennal lobe glomerulus DL1. Neurons of this class are derived from the first larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). The axons of these neurons innervate a small area at the ventroposterior edge of the lateral horn. There are around two of these per hemisphere and they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage with dendrites that mainly innervate antennal lobe glomerulus DL2d. Neurons of this class are derived from the 23rd larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around five of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage whose dendrites mainly innervate antennal lobe glomerulus DL2v. Neurons of this class are derived from the 22nd larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around four of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the lateral neuroblast (ALl1) dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus DL3 (Bates et al., 2020). The axons of these neurons innervate the lateral horn. There are around five of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron of the ad neuroblast (ALad1) lineage with dendrites that mainly innervate antennal lobe glomerulus DL4. Neurons of this class are born during the 20th and final division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). It innervates the posteriomedial region of the lateral horn and the mushroom body calyx. There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron of the ad neuroblast (ALad1) with dendrites that mainly innervate antennal lobe glomerulus DL5. This neuron is born from the 16th division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) lineage with dendrites that mainly innervate antennal lobe glomerulus DL5 (Bates et al., 2020). There is one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the lateral neuroblast (ALl1) dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus DM1 (Bates et al., 2020). The axons of these neurons innervate a small area at the dorsoposterior edge of the lateral horn. There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). Its boutons in the mushroom body calyx are widely distributed, mostly within the ventral half (Li et al., 2020). It is the only uniglomerular projection neuron to receive input in DM1 (Li et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the lateral neuroblast (ALl1) dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus DM2 (Bates et al., 2020). The axons of these neurons innervate the lateral horn. There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus DM3. Neurons of this class are born during the 18th division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus DM4. This neuron is born from the 15th division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ALl1 dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus DM5 (Bates et al., 2020). The axons of these neurons innervate the lateral horn. There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus DM6. Neurons of this class are derived from the 12th larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ALad1 neuroblast (FBbt:00067346) lineage with dendrites that mainly innervate antennal lobe glomerulus DP1l. There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). ‘DP1l adPN’ is not listed in Yu et al., 2010, which claims to account for all adPNs. Probably equivalent to one of those identified by Yu et al., but with disagreement over target glomerulus name.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus DP1m. This is the first neuron born from the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). The axonal terminals in the lateral horn branch extensively and occupy large regions of this neuropil (Ai et al., 2013). There is one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Ai et al., 2013; Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VA1d. Neurons of this class are derived from the seventh larval division of the ALad1 neuroblast (FBbt:00067346) and their axons innervate the anterior/ventral region of the lateral horn (Marin et al., 2002, Tanaka et al., 2004). There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VA1 ventral compartment. Neurons of this class are derived from the 13th larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). Their axons innervate the ventral half of the lateral horn (Marin et al., 2002). There are around four of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VA2. This neuron is born from the 14th division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729. Bates et al. (2020) supplement lists this as an AL-mlPN1, but this is probably a mistake as it is inconsistent with lineage information.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VA3. Neurons of this class derive from the fifth larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ALl1 dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus VA4 (Bates et al., 2020). The axons of these neurons innervate a small area at the dorsoposterior edge of the lateral horn. There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the lateral neuroblast (ALl1) dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus VA5 (Bates et al., 2020). The axons of these neurons innervate the lateral horn. There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VA6. This neuron is born during the eighth division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis. The axons of these neurons innervate a small area at the ventroposterior edge of the lateral horn. There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VA7l. This neuron is born from the 13th division of neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the lateral neuroblast (ALl1) dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus VA7m (Bates et al., 2020). The axons of these neurons innervate the lateral horn. There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ALl1 dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus VC1 (Bates et al., 2020). It connects to the mushroom body and lateral horn via the inner antennocerebral tract (medial antennal lobe tract) (Lin et al., 2012). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ALl1 dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus VC2 (Bates et al., 2020). The axons of these neurons innervate the lateral horn. There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). Existence confirmed by Greg Jefferis (personal communication).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VC3l. Neurons of this class are derived from the 17th larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around four of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729. Only VC3-innervating adPN in Bates et al. (2020) is VC3l adPN.
Adult uniglomerular antennal lobe projection neuron from the ALlv1 neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VC3m (Bates et al., 2020). There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VC4. Neurons of this class are derived from the 14th larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult unilateral, uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage with dendrites that mainly innervate antennal lobe glomerulus VC5 (Bates et al., 2020). It receives primarily olfactory input (Marin et al., 2020). This neuron is born from the seventh division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is approximately one of these cells per hemisphere, it is cholinergic and it fasciculates with the medial antennal lobe tract to project to the mushroom body calyx and lateral horn (Bates et al., 2020; Marin et al., 2020). For image, see FlyBase:FBrf0211729. Yu et al. (2010) classify this neuron as uniglomerular. Also classified as uniglomerular by Bates et al. (2020), who clarify that it mainly innervates VC5, with some additional branches in other glomeruli (uni+ class).
Adult uniglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) lineage with dendrites that mainly innervate antennal lobe glomerulus VC5 in both hemispheres (Bates et al., 2020; Marin et al., 2020). It receives primarily olfactory input (Marin et al., 2020). It fasciculates with the ipsilateral medial antennal lobe tract to innervate the lateral horn (Marin et al., 2020). There are approximately two of these cells per hemisphere and they are cholinergic (Bates et al., 2020; Marin et al., 2020).
Adult unilateral, multiglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) lineage with dendrites that mainly innervate antennal lobe glomerulus VC5 (Bates et al., 2020; Marin et al., 2020). It receives primarily olfactory input (Marin et al., 2020). It fasciculates with the medial antennal lobe tract to innervate the lateral horn (Marin et al., 2020). There is one of these cells per hemisphere and it is cholinergic (Bates et al., 2020; Marin et al., 2020).
Adult uniglomerular antennal lobe projection neuron with its soma in the lateral subesophageal zone and dendrites that mainly innervate antennal lobe glomerulus VL1 (Tanaka et al., 2012; Bates et al., 2020). It bifurcates below the esophagus and has roughly symmetrical innervation in both hemispheres (Tanaka et al., 2012). It follows the mALT, sending branches to the central part of the mushroom body calyx and the posterior ventral lateral horn (Tanaka et a., 2012; Bates et al., 2020). There is one of these per hemisphere and it is cholinergic (Bates et al., 2020). Corresponds to AL-mPN2 from Tanaka et al. (2012) (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VL2a. This neuron is born from the tenth division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). It innervates the antero-ventral lateral horn (Grosjean et al., 2011). Its terminals in this region overlap extensively with the terminals of DA1 and VA1lm projection neurons, which have been implicated in a pheromone-sensing pathway (Jefferis et al., 2007). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage (embryonic born) with dendrites that mainly innervate antennal lobe glomerulus VL2p. This neuron is born in the third division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the lateral antennal lobe neuroblast (ALl1) dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus VM1 (Bates et al., 2020). The axons of these neurons innervate the lateral horn. There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage with dendrites that mainly innervate antennal lobe glomerulus VM2. Neurons of this class are derived from the 11th larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). The axons of these neurons innervate a small area at the dorsoposterior edge of the lateral horn. There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage (embryonic born) with dendrites that mainly innervate antennal lobe glomerulus VM3. Neurons of this class are born during the 17th and 19th divisions of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VM4. This neuron is born from the sixth division of the neuroblast ALad1 (FBbt:00067346) during embryogenesis (Yu et al., 2010). There is around one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) lineage with dendrites that mainly innervate antennal lobe glomerulus VM4 (Bates et al., 2020). There are two of these per antennal lobe, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage with dendrites that mainly innervate antennal lobe glomerulus VM5d. Neurons of this class are derived from the 15th larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around four of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast (ALad1) lineage with dendrites that mainly innervate antennal lobe glomerulus VM5v. Neurons of this class are derived from the 16th larval division of the neuroblast ALad1 (FBbt:00067346) (Yu et al., 2010). There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VM7d (Grabe et al., 2016). There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ad neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VM7v (also known as glomerulus 1). Neurons of this class derive from the ninth larval division of the ALad1 neuroblast (FBbt:00067346). There are around two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020). For image, see FlyBase:FBrf0211729.1 adPN has been renamed to VM7v to be consistent with the change of glomerulus name from glomerulus 1 to glomerulus VM7v.
Adult unilateral, multiglomerular antennal lobe projection neuron from the dorsal hemilineage of the lateral neuroblast (ALl1) whose dendrites innervate antennal lobe glomerulus VP1d (Bates et al., 2020; Marin et al., 2020). It receives primarily olfactory input (Marin et al., 2020). It fasciculates with the medial antennal lobe tract to innervate the mushroom body calyx, in some cases continuing to the lateral horn (Marin et al., 2020). There are around five of these per hemisphere and they are cholinergic (Marin et al., 2020; Bates et al., 2020). Unlike Marin et al. (2020), Bates et al. (2020) distinguish one of these (#1 in Marin et al., 2020) as a separate type that is pan-glomerular. Mapped to M_lPNm11D based on body IDs in Marin et al. (2020) supplement and notes in neuprint.
Adult unilateral, uniglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VC3l (Bates et al., 2020; Marin et al., 2020). There are around three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020; Marin et al., 2020). It projects to the superior medial protocerebrum and superior lateral protocerebrum (Marin et al., 2020).
Adult uniglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VC3l, with a branch extending to the contralateral antennal lobe (Bates et al., 2020; Marin et al., 2020). There is one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020; Marin et al., 2020). It projects to the ipsilateral superior medial protocerebrum, superior lateral protocerebrum and lateral horn (Marin et al., 2020). Mapped to M_lvPNm36 based on body ID in Marin et al. (2020) supplement and neuprint notes.
Adult unilateral, panglomerular antennal lobe projection neuron from the dorsal hemilineage of the lateral neuroblast (ALl1) with substantial dendritic innervation of antennal lobe glomerulus VP1l (Bates et al., 2020; Marin et al., 2020). It receives primarily olfactory input (Marin et al., 2020). It fasciculates with the medial antennal lobe tract to innervate the mushroom body calyx, before curving ventrally to innervate the posterior lateral protocerebrum (Marin et al., 2020). There is around one of these per hemisphere and it is cholinergic (Marin et al., 2020; Bates et al., 2020). Mapped to M_lPNm11B based on body ID in Marin et al. (2020) supplement and notes in neuprint.
Adult unilateral, multiglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) neuroblast lineage with dendrites that innervate antennal lobe glomerulus VP1m (Bates et al., 2020; Marin et al., 2020). There is one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020; Marin et al., 2020). It projects to the mushroom body calyx and lateral horn (Marin et al., 2020).
Adult unilateral, multiglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) neuroblast lineage with dendrites that innervate antennal lobe glomeruli VP1m and VP2 (Bates et al., 2020; Marin et al., 2020). There are three of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020; Marin et al., 2020). It projects to the mushroom body calyx and lateral horn (Marin et al., 2020).
Adult uniglomerular antennal lobe projection neuron that develops from the ALad1 neuroblast and has dendrites that mainly innervate antennal lobe glomerulus VP2 (Stocker et al., 1990; Marin et al., 2020). It projects via the medial antennal lobe tract to arborize in the mushroom body calyx, lateral accessory calyx and the lateral horn (Stocker et al., 1990; Marin et al., 2020). There is one of these per hemisphere and it is cholinergic (Marin et al., 2020).
Adult uniglomerular antennal lobe projection neuron that develops from the ALad1 neuroblast and has dendrites that mainly innervate antennal lobe glomerulus VP2, but also has several antennal lobe arborizations outside of VP2 (Marin et al., 2020). It projects via the medial antennal lobe tract to arborize in the mushroom body calyx and the lateral protocerebrum (Marin et al., 2020). There is one of these per hemisphere and it is cholinergic (Marin et al., 2020).
Adult multiglomerular antennal lobe projection neuron from the ALlv1 neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VP2 (Bates et al., 2020; Marin et al., 2020). It receives mainly olfactory input (Marin et al., 2020). It fasciculates with the medial antennal lobe tract, then curves ventrally to innervate the posterior lateral protocerebrum (Marin et al., 2020). There is one of these per hemisphere and it is cholinergic (Bates et al., 2020; Marin et al., 2020). Bates et al. (2020) class this as panglomerular, but does not look it in Marin et al. (2020). Bates et al. (2020) also group this in the same morphological class as another ‘panglomerular’ PN mainly innervating DA2. One of two M_lvPNm47 cells mapped to VP2++ lvPN in Marin et al. (2020) supplement and neuprint notes.
Adult uniglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) neuroblast lineage with dendrites that mainly innervate the ipsilateral antennal lobe glomerulus VP2 and the medial subesophageal zone (Bates et al., 2020; Marin et al., 2020). There are one or two of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020; Marin et al., 2020). It projects to the mushroom body calyx and the lateral horn (Marin et al., 2020). Mapped to VP2+Z_lvPN based on body ID in Marin et al. (2020) supplement and neuprint notes.
Adult unilateral, uniglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) neuroblast lineage with dendrites that mainly innervate antennal lobe glomerulus VP2 and also extend into the dorsal subesophageal zone (Bates et al., 2020; Marin et al., 2020). There is one of these per hemisphere, it fasciculates with the medial antennal lobe tract and it is cholinergic (Bates et al., 2020; Marin et al., 2020). It projects to the mushroom body calyx and the lateral horn (Marin et al., 2020). Mapped to MZ_lvPN based on body ID in Marin et al. (2020) supplement and notes in neuprint.
Adult unilateral, multiglomerular antennal lobe projection neuron from the ALlv1 (BAlp4) neuroblast lineage with dendrites that innervate antennal lobe glomeruli VP2 and VP5 (Bates et al., 2020; Marin et al., 2020). There may be four of these per hemisphere, they fasciculate with the medial antennal lobe tract and they are cholinergic (Bates et al., 2020; Marin et al., 2020). It projects to the mushroom body calyx and along the ventral part of the lateral horn to the posterior lateral protocerebrum (Marin et al., 2020). Mapped to M_lvPNm48 based on body IDs in Marin et al. (2020) supplement and neuprint notes.
Adult antennal lobe projection neuron from the lateral antennal lobe (ALl1) neuroblast dorsal hemilineage with dendrites that mainly innervate antennal lobe glomerulus VP4, but also have substantial arborization in other glomeruli (Marin et al., 2020). A projection also crosses the midline to innervate the contralateral antennal lobe (Marin et al., 2020). It fasciculates with the medial antennal lobe tract and reaches the lateral horn, then turns ventrally and descends to the inferior posterior slope (Marin et al., 2020). There are around three of these per hemisphere and they are cholinergic (Marin et al., 2020). Mapped to M_lPNm11A based on body IDs in Marin et al. (2020) supplement and notes in neuprint.
Auditory system neuron of the adult brain that preferentially responds to male pulse, rather than sine, courtship song (Baker et al., 2022). Its main innervation is in the anterior ventrolateral protocerebrum and posterior ventrolateral protocerebrum and it crosses the midline (Baker et al., 2022). It is cholinergic (Baker et al., 2022). Cell type identified at light level and in EM data (Baker et al., 2022). Neurotransmitter predicted from EM data (Baker et al., 2022).
Auditory system neuron of the adult brain that responds similarly to male sine and pulse courtship song (Baker et al., 2022). Its main innervation is in the anterior ventrolateral protocerebrum, it also innervates the posterior ventrolateral protocerebrum and inferior clamp (Baker et al., 2022). It is cholinergic (Baker et al., 2022). Cell type identified at light level and in EM data (Baker et al., 2022). Neurotransmitter predicted from EM data (Baker et al., 2022).
Auditory system neuron of the adult brain that preferentially responds to male pulse, rather than sine, courtship song (Baker et al., 2022). Its main innervation is in the anterior ventrolateral protocerebrum, it also innervates the inferior clamp and superior intermediate protocerebrum and it crosses the midline (Baker et al., 2022). It is cholinergic (Baker et al., 2022). Cell type identified at light level and in EM data (Baker et al., 2022). Neurotransmitter predicted from EM data (Baker et al., 2022).
Auditory system neuron of the adult brain that preferentially responds to male sine, rather than pulse, courtship song (Baker et al., 2022). Its main innervation is in the anterior ventrolateral protocerebrum and it crosses the midline (Baker et al., 2022). It is cholinergic (Baker et al., 2022). Cell type identified at light level and in EM data (Baker et al., 2022). Neurotransmitter predicted from EM data (Baker et al., 2022).
Auditory system neuron of the adult brain that preferentially responds to male sine, rather than pulse, courtship song (Baker et al., 2022). Its main innervation is in the anterior ventrolateral protocerebrum and it crosses the midline (Baker et al., 2022). It is cholinergic (Baker et al., 2022). Cell type identified at light level and in EM data (Baker et al., 2022). Neurotransmitter predicted from EM data (Baker et al., 2022).
Auditory system neuron of the adult brain that preferentially responds to male sine, rather than pulse, courtship song (Baker et al., 2022). Its main innervation is in the anterior ventrolateral protocerebrum and it does not cross the midline (Baker et al., 2022). It is cholinergic (Baker et al., 2022). Cell type identified at light level and in EM data (Baker et al., 2022). Neurotransmitter predicted from EM data (Baker et al., 2022).
Auditory system neuron of the adult brain that preferentially responds to male pulse, rather than sine, courtship song (Baker et al., 2022). Its main innervation is in the anterior ventrolateral protocerebrum (Baker et al., 2022). It is cholinergic (Baker et al., 2022). Cell type identified at light level and in EM data (Baker et al., 2022). Neurotransmitter predicted from EM data (Baker et al., 2022).
Adult lateral horn input neuron that has its dendrites predominantly within the anterior ventrolateral protocerebrum (Dolan et al., 2019). It is a secondary neuron that is part of the BLP1 (VPNp&v) posterior hemilineage (Bates et al., 2020). There are ten of these neurons per hemisphere and they are cholinergic and GABAergic (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Any cholinergic neuron (FBbt:00007173) that is part of some adult nervous system (FBbt:00003559).
Doublesex-expressing neuron of the female that is part of a cluster in the posterior medial region of the protocerebrum. There are fewer of these cells in the female than pC1 (male) cells in the male (approximately 50) (Zhou et al., 2014; Kimura et al., 2015; Pavlou et al., 2016). They are generally more active in virgin females than mated females (Wang et al., 2020). Subclasses can be distinguished by their characteristic branching patterns (Wang et al., 2020). They are cholinergic (Wang et al., 2020). Some of these cells are derived from the DM4 neuroblast (Ren et al., 2016). Kimura et al. (2015) report around 27 pC1 (female) cells per hemisphere, Zhou et al. (2014) and Pavlou et al. (2016) report around 8, Wang et al. (2020) report 5.
Adult doublesex pC1 neuron of the female that, similar to pC1d and pC1e, has a contralateral projection that extends further laterally than that of pC1b and pC1c and lacks a characteristic branch into the dorsal ipsilateral superior lateral protocerebrum (Wang et al., 2020). Its contralateral branch crosses the midline at the level of the superior medial protocerebrum (Wang et al., 2020). Unlike pC1d and pC1e, it does not project ventromedially towards the esophageal foramen (Wang et al., 2020). It is strongly synapsed by and activated by sex peptide abdominal ganglion neurons (Wang et al., 2020).
Adult doublesex pC1 neuron of the female that, similar to pC1c, has a relatively short contralateral projection compared to pC1a, pC1d and pC1e and has a characteristic branch into the dorsal ipsilateral superior lateral protocerebrum (Wang et al., 2020). Its contralateral branch crosses the midline at the level of the superior medial protocerebrum, but unlike pC1c, it does not have a ventrally-directed branch on each side of this crossing point (Wang et al., 2020).
Adult doublesex pC1 neuron of the female that, similar to pC1b, has a relatively short contralateral projection compared to pC1a, pC1d and pC1e and has a characteristic branch into the dorsal ipsilateral superior lateral protocerebrum (Wang et al., 2020). Its contralateral branch crosses the midline at the level of the superior medial protocerebrum, but unlike pC1b, it has a ventrally-directed branch on each side of this crossing point (Wang et al., 2020).
Adult doublesex pC1 neuron of the female that, similar to pC1a and pC1e, has a contralateral projection that extends further laterally than that of pC1b and pC1c and lacks a characteristic branch into the dorsal ipsilateral superior lateral protocerebrum (Wang et al., 2020). Its contralateral branch crosses the midline at the level of the superior medial protocerebrum (Wang et al., 2020). Unlike pC1a, it projects ventromedially towards the esophageal foramen, with more extensive and more ventral arborization than pC1e (Wang et al., 2020).
Adult doublesex pC1 neuron of the female that, similar to pC1a and pC1d, has a contralateral projection that extends further laterally than that of pC1b and pC1c and lacks a characteristic branch into the dorsal ipsilateral superior lateral protocerebrum (Wang et al., 2020). Its contralateral branch crosses the midline at the level of the superior medial protocerebrum (Wang et al., 2020). Unlike pC1a it projects ventromedially towards the esophageal foramen, but has less extensive arborization and does not extend as far ventrally as pC1d (Wang et al., 2020).
Doublesex-expressing neuron of the male that is part of a cluster in the superior medial protocerebrum (Rideout et al., 2010). It is cholinergic and also expresses fruitless (Jung et al., 2020). There are more of these cells in the male (approximately 16) than pCd (female) neurons in the female (approximately 12) (Robinett et al., 2010; Kimura et al., 2015). They are required for long-term normal increases in mating behavior and aggression in some social contexts (Zhang et al., 2019; Jung et al., 2020). Some of these cells arise from the DM2 (DPMpm1) neuroblast and some arise from the CP3 (DL2) neuroblast (Ren et al., 2016).
Doublesex-expressing neuron of the male that is part of a larger, more dorsal subcluster within the pCd cluster (Kimura et al., 2015). There are approximately 12 of these cells per hemisphere (Kimura et al., 2015).
Doublesex-expressing neuron of the male that is part of a smaller, more ventral subcluster within the pCd cluster (Kimura et al., 2015). There are approximately 4 of these cells per hemisphere (Kimura et al., 2015).
Doublesex-expressing neuron of the adult female with its cell body in the posterior medial protocerebrum, ventral to the pC1 cluster (Kimura et al., 2015). There is one of these cells per hemisphere, it is cholinergic, and its activity stimulates vaginal plate opening (Wang et al., 2020). Its dendrites arborize in the superior lateral protocerebrum and its axons project to multiple regions of the ventral nerve cord, including the abdominal ganglion (Wang et al., 2020). It receives input from the pulse song-responsive (inhibitory) vpoINs and (excitatory) vpoENs (Wang et al., 2020), and it is activated in response to conspecific male pulse song (Deutsch et al., 2019; Wang et al., 2020). It also receives input from the pC1 cells, which convey mating status information and increase the excitability of pMN2 (Wang et al., 2020). Robinett et al. (2010) - FBrf0210735 state that pMN2 cells are not sexually dimorphic. Kimura et al. (2015) show that these neurons are gender-specific, with males having what they refer to as pMN3 neurons and females having what they refer to as pMN2 in a similar location. These are different cells, as genetic manipulations can result in both cell types being present in one fly (Kimura et al., 2015). Thought to be involved in oviposition based on correlation with non-specific activation in Kimura et al. (2015), but shown to be involved in vaginal plate opening by more specific activation in Wang et al. (2020).
Small field neuron of the central complex with dendritic arbors in the inner, outer and posterior layers of half or a full ellipsoid body slice, and axon terminals in the dorsal gall and one odd-numbered protocerebral bridge glomerulus (except glomerulus 9) (Lin et al., 2013; Wolff et al., 2015).
Small field neuron of the central complex with dendritic and axonal arbors in the inner, outer and posterior layers of either a half or a full ellipsoid body (EB) slice (wedge), and axon terminals in the dorsal or ventral gall and a single protocerebral bridge glomerulus (excluding glomerulus 9) (Lin et al., 2013; Wolff et al., 2015). Neurons that target odd or even numbered protocerebral bridge glomeruli target the dorsal or ventral gall, respectively (Lin et al., 2013; Wolff et al., 2015). These neurons receive inhibitory input from delta 7 (PB 18 glomeruli) neurons and they are cholinergic (Turner-Evans et al., 2020). These cells output to P-EN1 neurons and P-EG neurons of the same glomerulus in the protocerebral bridge, and form less specific ‘hyper-local’ feedback loops with P-EN1 neurons in the EB (Turner-Evans et al., 2020). It also receives input from R4d ring neurons and P-EN2 neurons in the EB (Turner-Evans et al., 2020). Based on images/diagrams in Lin et al. (2013), Wolff et al. (2015) and Turner-Evans et al. (2020), these appear to innervate the ipsilateral PB and contralateral gall, but could not find confirmation of this [FBC:CP].
Small field neuron of the central complex with dendritic arbors in the inner, outer and posterior layers of half or a full ellipsoid body slice, and axon terminals in the ventral gall and one even-numbered protocerebral bridge glomerulus (Lin et al., 2013; Wolff et al., 2015). The ventral spindle body is located in the dorsolateral region of the inferior dorsofrontal protocerebrum (IDFP) and corresponds to the ventral gall (Ito et al., 2014, Lin et al., 2013, Wolff et al., 2015).
Adult ellipsoid body-protocerebral bridge-gall neuron that has its protocerebral bridge terminals in glomerulus 1 (Wolff et al., 2015). It has its ellipsoid body terminals in slice (wedge) 8 in the opposite hemisphere (Wolff et al., 2015).
Adult ellipsoid body-protocerebral bridge-gall neuron that has its protocerebral bridge terminals in glomerulus 2 (Lin et al., 2013; Wolff et al., 2015). It has its ellipsoid body terminals in slice (wedge) 6 in the opposite hemisphere (Wolff et al., 2015). The ventral spindle body is located in the dorsolateral region of the inferior dorsofrontal protocerebrum (IDFP) and corresponds to the ventral gall (Ito et al., 2014, Lin et al., 2013, Wolff et al., 2015).
Adult ellipsoid body-protocerebral bridge-gall neuron that has its protocerebral bridge terminals in glomerulus 3 (Lin et al., 2013; Wolff et al., 2015). It has its ellipsoid body terminals in slice (wedge) 4 in the opposite hemisphere (Wolff et al., 2015).
Adult ellipsoid body-protocerebral bridge-gall neuron that has its protocerebral bridge terminals in glomerulus 4 (Lin et al., 2013; Wolff et al., 2015). It has its ellipsoid body terminals in slice (wedge) 2 in the opposite hemisphere (Wolff et al., 2015). The ventral spindle body is located in the dorsolateral region of the inferior dorsofrontal protocerebrum (IDFP) and corresponds to the ventral gall (Ito et al., 2014, Lin et al., 2013, Wolff et al., 2015).
Adult ellipsoid body-protocerebral bridge-gall neuron that has its protocerebral bridge terminals in glomerulus 5 (Lin et al., 2013; Wolff et al., 2015). It has its ellipsoid body terminals in slice (wedge) 1 in the same hemisphere (Wolff et al., 2015).
Adult ellipsoid body-protocerebral bridge-gall neuron that has its protocerebral bridge terminals in glomerulus 6 (Lin et al., 2013; Wolff et al., 2015). It has its ellipsoid body terminals in slice (wedge) 3 in the same hemisphere (Wolff et al., 2015). The ventral spindle body is located in the dorsolateral region of the inferior dorsofrontal protocerebrum (IDFP) and corresponds to the ventral gall (Ito et al., 2014, Lin et al., 2013, Wolff et al., 2015).
Adult ellipsoid body-protocerebral bridge-gall neuron that has its protocerebral bridge terminals in glomerulus 7 (Lin et al., 2013; Wolff et al., 2015). It has its ellipsoid body terminals in slice (wedge) 5 in the same hemisphere (Wolff et al., 2015).
Adult ellipsoid body-protocerebral bridge-gall neuron that has its protocerebral bridge terminals in glomerulus 8 (Lin et al., 2013; Wolff et al., 2015). It has its ellipsoid body terminals in slice (wedge) 7 in the same hemisphere (Wolff et al., 2015). The ventral spindle body is located in the dorsolateral region of the inferior dorsofrontal protocerebrum (IDFP) and corresponds to the ventral gall (Ito et al., 2014, Lin et al., 2013, Wolff et al., 2015).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). There are five of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019). AD1e1 referred to as a fruitless aSP-g neuron in Dolan et al. (2019) and class renamed to aSP-g1 in neuprint (neuprint.janelia.org) hemibrain 1.1 data. Bates (2020) lists two different neuroblasts of origin (DPLal2 and DPLal3) for different individuals.
Adult lateral horn input neuron that has its dendrites predominantly within the gnathal ganglion (Dolan et al., 2019). It is a secondary neuron that develops from the VESa1 (BAla3) neuroblast (Bates et al., 2020). There is one of these neurons per hemisphere and it is cholinergic (Dolan et al., 2019).
Cholinergic interneuron of the subesophageal ganglion that receives input from Gr43a/Gr46a-expressing sweet taste neurons of the pharynx, but not the Gr5a-expressing neurons of the labellum (Yapici et al., 2016). Sugar must therefore be ingested for these neurons to be activated (Yapici et al., 2016). Activation increases feeding in hungry flies (Yapici et al., 2016). There are 12 of these cells, whose processes cross the midline to arborize in both the ipsilateral and contralateral sides of the subesophageal zone (Yapici et al., 2016). Synapsing shown by GRASP (Yapici et al., 2016).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the DPLal3 (SLPal2) ventral hemilineage and it is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). These neurons are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Frechter et al., 2019). It is a secondary neuron that is part of the DPLal2 (LHl2) medial hemilineage and it is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the DPLal2 (LHl2) medial hemilineage (Bates et al., 2020). There are around twelve of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019; Li et al., 2020).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the LHl2 (DPLal2) medial hemilineage (Schlegel et al., 2021). There are approximately three of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the LHl2 (DPLal2) medial hemilineage (Schlegel et al., 2021). There are approximately three of two neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the DPLal2 (LHl2) medial hemilineage (Bates et al., 2020). There are nine of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the DPLal1 (SLPal1) neuroblast (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Lineage based on shared primary neurite tract with LHAD1f1 and LHAD1f4 (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the DPLal1 (SLPal1) neuroblast (Schlegel et al., 2021). There are approximately five of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Lineage based on shared primary neurite tract with LHAD1f1 and LHAD1f4 (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract. It is a secondary neuron that develops from the DPLal1 (SLPal1) neuroblast and it is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the DPLal1 (SLPal1) neuroblast (Schlegel et al., 2021). There is roughly one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Lineage based on shared primary neurite tract with LHAD1f1 and LHAD1f4 (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the DPLal1 (SLPal1) neuroblast (Schlegel et al., 2021). There is around one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Lineage based on shared primary neurite tract with LHAD1f1 and LHAD1f4 (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Bates et al., 2020). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There is around one of these cells per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There is approximately one of these cells per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There are approximately two of these cells per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Dolan et al., 2019). There are five of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There is around one of these neurons per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There is around one of these cells per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There is around one of these cells per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There is around one of these cells per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There is around one of these cells per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). There is around one of these cells per hemisphere (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AD3 primary neurite tract (Schlegel et al., 2021). It develops from the DPLd (LHd1) neuroblast and it is cholinergic (Schlegel et al., 2021). Assumed same lineage as LHAD3a1, LHAD3a10 and LHAD3a8 based on shared primary neurite tract (ADL17) (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV1 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the BLVp2 (VLPl&p1) anterior hemilineage (Bates et al., 2020). There are four of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AV1 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the BLVp2 (VLPl&p1) anterior hemilineage (Bates et al., 2020). There are six of these neurons per hemisphere and they are cholinergic and GABAergic (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AV1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the BLVp1 (VLPl&p2) lateral hemilineage (Schlegel et al., 2021). There is around one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the BLVp1 (VLPl&p2) lateral hemilineage (Schlegel et al., 2021). There are approximately 1-2 of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the BLVp1 (VLPl&p2) lateral hemilineage (Schlegel et al., 2021). There is approximately one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV1 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the BLVp1 (VLPl&p2) lateral hemilineage (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the BLAv2 (VLPl2) dorsal hemilineage (Bates et al., 2020). It is GABAergic (Dolan et al., 2019) and cholinergic (Dolan et al., 2019; Bates et al., 2020). There are approximately 3 neurons that belong to either the AV2b1 or AV2b2 types (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the BLAv2 (VLPl2) dorsal hemilineage (Bates et al., 2020). It is GABAergic (Dolan et al., 2019) and cholinergic (Dolan et al., 2019; Bates et al., 2020). There are approximately 3 neurons that belong to either the AV2b1 or AV2b2 types (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There is around one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are around two of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn local neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are around three of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are around three of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There is around one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately three of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately two of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There is around one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately three of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately four of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately two of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately eight of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately three of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately two of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV2 primary neurite tract (Schlegel et al., 2021). There are approximately three of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV3 primary neurite tract (Schlegel et al., 2021). There is approximately one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the BLAd1 (LHa1) medial hemilineage (Bates et al., 2020). There are seven of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the BLAd1 (LHa1) medial hemilineage (Schlegel et al., 2021). There are approximately three of these per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021). Assuming shared hemilineage with LHAV6a1, LHAV6a10 and LHAV6a3 based on shared primary neurite tract (ADL13) in Schlegel et al. (2021).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the BLAd1 (LHa1) medial hemilineage (Schlegel et al., 2021). There are around three of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021). Assuming shared hemilineage with LHAV6a1, LHAV6a10 and LHAV6a3 based on shared primary neurite tract (ADL13) in Schlegel et al. (2021).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the BLAd1 (LHa1) medial hemilineage (Schlegel et al., 2021). There are around two of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021). Assuming shared hemilineage with LHAV6a1, LHAV6a10 and LHAV6a3 based on shared primary neurite tract (ADL13) in Schlegel et al. (2021).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the BLAd1 (LHa1) medial hemilineage (Schlegel et al., 2021). There are around four of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021). Assuming shared hemilineage with LHAV6a1, LHAV6a10 and LHAV6a3 based on shared primary neurite tract (ADL13) in Schlegel et al. (2021).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the AV7 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that develops from the DAL1l (AOTUv2) neuroblast (Bates et al., 2020). There are four of these neurons per hemisphere and they are cholinergic and glutamatergic (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PD2 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the DPLl2 (VLPd&p1) dorsal hemilineage (Bates et al., 2020). There are approximately 5 of these neurons and they are cholinergic (Dolan et al., 2018). A large portion of its input is from antennal lobe projection neurons and it responds to olfactory stimuli (Dolan et al., 2018). Some of these cells receive input from mushroom body vertical lobe arborizing neuron 2 alpha (MBON-alpha2sc) and they may be involved in memory (Dolan et al., 2018).
Adult lateral horn output neuron that fasciculates with the PD2 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PD2 primary neurite tract (Schlegel et al., 2021). There is around one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PD2 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the DPLl2 (VLPd&p1) dorsal hemilineage (Bates et al., 2020). It has dendrites in the mushroom body calyx, as well as in the lateral horn (Dolan et al., 2018). A large portion of its input is from antennal lobe projection neurons and it responds to olfactory stimuli (Dolan et al., 2018). There are approximately 2 of these neurons and they are cholinergic (Dolan et al., 2018). Some of these cells receive input from mushroom body vertical lobe arborizing neuron 2 alpha (MBON-alpha2sc) and they may be involved in memory (Dolan et al., 2018).
Adult lateral horn output neuron that fasciculates with the PD2 primary neurite tract (Schlegel et al., 2021). There are around four of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV2 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the DPLpv (VLPp&l1) dorsal hemilineage (Bates et al., 2020). There are nine of these neurons per hemisphere and they are cholinergic and GABAergic (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV3 primary neurite tract (Schlegel et al., 2021). There are around two of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV3 primary neurite tract (Schlegel et al., 2021). There are around two of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV3 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV3 primary neurite tract (Bates et al., 2020). It is a secondary neuron that is part of the BLD5 (VPNp1) posterior hemilineage (Bates et al., 2020). It is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PV3 primary neurite tract (Dolan et al., 2019). There are five of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV4 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Bates et al., 2020). It is cholinergic (Bates et al., 2020). There are approximately 11 neurons that belong to either the PV4b1 or PV4b2 types and some of these are glutamatergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019) There are twelve of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019). They are secondary neurons that develop from the CP3 (DL2) neuroblast, but different cells of this type may belong to the dorsal or lateral hemilineages (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). There are eight of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract and is part of the CP3 (DL2) dorsal hemilineage (Schlegel et al., 2021). There are two of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Bates et al., 2020). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Bates et al., 2020). It is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). There are eleven of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the CP2 (DL1) dorsal hemilineage (Bates et al., 2020). There are eight of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the CP2 (DL1) dorsal hemilineage (Bates et al., 2020). There are seven of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Schlegel et al., 2021). There are approximately three of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Schlegel et al., 2021). There are approximately 1-2 of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Schlegel et al., 2021). There are approximately 4-5 of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). There are twelve of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that is part of the CP2 (DL1) dorsal hemilineage (Bates et al., 2020). There are five of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019). It is a secondary neuron that is part of the CP2 (DL1) dorsal hemilineage (Bates et al., 2020). It is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the CP2 (DL1) dorsal hemilineage (Schlegel et al., 2021). There is one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Frechter et al., 2019). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Bates et al., 2020). It is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Schlegel et al., 2021). There is one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Bates et al., 2020). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Bates et al., 2020). It is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is part of the DL1 (CP2) dorsal hemilineage (Schlegel et al., 2021). There is one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract and is part of the DL1 (CP2) dorsal hemilineage (Schlegel et al., 2021). There is one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Schlegel et al., 2021). There is one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Bates et al., 2020). It is cholinergic (Dolan et al., 2019; Bates et al., 2020). There are approximately 5 neurons that belong to either the PV5g1 or PV5g2 types (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the CP3 (DL2) dorsal hemilineage (Bates et al., 2020). It is cholinergic (Dolan et al., 2019; Bates et al., 2020). There are approximately 5 neurons that belong to either the PV5g1 or PV5g2 types (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the CP2 (DL1) dorsal hemilineage (Schlegel et al., 2021). There is one of these neurons per hemisphere and it is cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the CP2 (DL1) dorsal hemilineage (Schlegel et al., 2021). There are one or two of these neurons per hemisphere and they are cholinergic (Schlegel et al., 2021). Cell type found in both hemibrain and FAFB (Schlegel et al., 2021). Neurotransmitter predicted based on lineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the DPLp1 (LHp2) medial hemilineage (Bates et al., 2020). There are six of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the DPLp1 (LHp2) medial hemilineage (Bates et al., 2020). There are five of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the DPLp1 (LHp2) medial hemilineage (Bates et al., 2020). There is one of these neurons per hemisphere and it is cholinergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). There are approximately two of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). There are approximately two of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). There are approximately two of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). It is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). There are approximately two of these cells per hemisphere and they are cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). There is approximately one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Bates et al., 2020). It is a secondary neuron that is part of the BLP1 (VPNp&v1) posterior hemilineage (Bates et al., 2020). It is cholinergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PV6 primary neurite tract (Schlegel et al., 2021). There is approximately one of these cells per hemisphere and it is cholinergic (Schlegel et al., 2021).
Adult lateral horn input neuron that has its dendrites predominantly within the lobula (Dolan et al., 2019). It is part of the VLPp&l1 (DPLpv) ventral hemilineage (Bates et al., 2020). There are seven of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult lateral horn input neuron that has its dendrites predominantly within the lobula (Dolan et al., 2019). It is part of the VLPp&l1 (DPLpv) ventral hemilineage (Bates et al., 2020). There are three of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Doublesex-expressing neuron of the adult male that has its cell body in the abdominal neuromere, dendrites around the male external genitalia and ascending projections to the superior medial protocerebrum (Zhang et al., 2019). It is involved in the regulation of male mating drive (Zhang et al., 2019). There are around 25 of these neurons and they are cholinergic (Zhang et al., 2019).
Adult lateral horn input neuron that has its dendrites predominantly within the posterior lateral protocerebrum (Dolan et al., 2019). It is a secondary neuron that is part of the BLP1 (VPNp&v1) posterior hemilineage (Bates et al., 2020). There are two of these neurons per hemisphere and they are cholinergic (Dolan et al., 2019).
Adult cholinergic interneuron of hemilineage 10B with its soma in the prothoracic neuromere that receives input from a directionally-tuned femoral chordotonal organ (FeCO) club neuron and responds to tibial vibrations and tibial movements in both directions (Agrawal et al., 2020). These cells innervate multiple neuromeres and a subset ascend to the brain, where they innervate the antennal mechanosensory and motor center (Agrawal et al., 2020). Its activation causes pausing behaviour in walking flies (Agrawal et al., 2020).
Interneuron that has dendrites in a single protocerebral bridge (PB) glomerulus, and axon terminals in one tile domain of the ellipsoid body (EB) and either the dorsal or ventral gall (Wolff et al., 2015). PB arbors may spill into neighboring glomeruli (Wolff and Rubin, 2018) and EB terminals may spread slightly into neighboring tiles (Wolff et al., 2015). Neurons that target odd or even numbered PB slices target the dorsal or ventral gall, respectively, with arbors filling the region (Wolff et al., 2015). These neurons are cholinergic (Turner-Evans et al., 2020). They are synapsed by E-PG neurons of the same PB glomerulus and output onto P-EN2 neurons in the EB (Turner-Evans et al., 2020). Its soma is located close to the PB glomerulus it innervates (Wolff et al., 2015). Collectively, all 9 protocerebral bridge glomeruli are targeted by cells of this type (Wolff and Rubin, 2018). Thought not to arborize in PB G9 by Wolff et al. (2015), this was amended in Wolff and Rubin (2018) and they changed the name from PBG1-8.s-EBt.b-D/V GA.b to PBG1-9.s-EBt.b-D/V GA.b. This neuron was not identified by Lin et al. (2013) (FBrf0221742) and does not correspond to PB1-glomerulus->EBC-IDFPDBSB or any other Lin et al. (2013) type (Wolff and Rubin, 2018).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron (PEN) that is activated in phase with adult ellipsoid body-protocerebral bridge-gall neuron (EPG) neurons (Green et al., 2017). It is cholinergic (Turner-Evans et al., 2020). These cells receive input from EPG neurons of the same glomerulus in the protocerebral bridge, and form less specific ‘hyper-local’ feedback loops with EPG neurons in the ellipsoid body (Turner-Evans et al., 2020).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron (PEN) that is activated out of phase with ellipsoid body-protocerebral bridge-gall neuron (EPG) neurons (Green et al., 2017). It is cholinergic (Turner-Evans et al., 2020). In the ellipsoid body, it receives input from protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron (PEG) neurons and outputs onto EPG neurons (Turner-Evans et al., 2020). In the protocerebral bridge, it receives strong input from the delta7 (protocerebral bridge 18 glomeruli) neurons (Turner-Evans et al., 2020).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 1 (Wolff et al., 2015). In the ellipsoid body, its output terminals are in the ventralmost (6:00) tile and it projects to the dorsal gall (Wolff et al., 2015).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 1 (FBbt:00049803) that receives synaptic input in region some protocerebral bridge glomerulus 2 (FBbt:00003670).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 2 (FBbt:00049804) that receives synaptic input in region some protocerebral bridge glomerulus 2 (FBbt:00003670).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 2 (Wolff et al., 2015). In the ellipsoid body, its output terminals are in the ventrolateral tile of the opposite hemisphere and it projects to the ventral gall (Wolff et al., 2015).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 3 (Wolff et al., 2015). In the ellipsoid body, its output terminals are in the lateralmost tile in the opposite hemisphere and it projects to the dorsal gall (Wolff et al., 2015).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 1 (FBbt:00049803) that receives synaptic input in region some protocerebral bridge glomerulus 3 (FBbt:00003671).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 2 (FBbt:00049804) that receives synaptic input in region some protocerebral bridge glomerulus 3 (FBbt:00003671).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 1 (FBbt:00049803) that receives synaptic input in region some protocerebral bridge glomerulus 4 (FBbt:00003672).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 2 (FBbt:00049804) that receives synaptic input in region some protocerebral bridge glomerulus 4 (FBbt:00003672).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 4 (Wolff et al., 2015). In the ellipsoid body, its output terminals are in the dorsolateral tile of the opposite hemisphere and it projects to the ventral gall (Wolff et al., 2015).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 5 (Wolff et al., 2015). In the ellipsoid body, its output terminals are in the dorsalmost (12:00) tile and it projects to the dorsal gall (Wolff et al., 2015).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 1 (FBbt:00049803) that receives synaptic input in region some protocerebral bridge glomerulus 5 (FBbt:00003673).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 2 (FBbt:00049804) that receives synaptic input in region some protocerebral bridge glomerulus 5 (FBbt:00003673).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 1 (FBbt:00049803) that receives synaptic input in region some protocerebral bridge glomerulus 6 (FBbt:00003674).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 2 (FBbt:00049804) that receives synaptic input in region some protocerebral bridge glomerulus 6 (FBbt:00003674).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 6 (Wolff et al., 2015). In the ellipsoid body, its output terminals are in the dorsolateral tile of the same hemisphere and it projects to the ventral gall (Wolff et al., 2015).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 7 (Wolff et al., 2015). In the ellipsoid body, its output terminals are in the lateralmost tile in the same hemisphere and it projects to the dorsal gall (Wolff et al., 2015).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 1 (FBbt:00049803) that receives synaptic input in region some protocerebral bridge glomerulus 7 (FBbt:00003675).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 2 (FBbt:00049804) that receives synaptic input in region some protocerebral bridge glomerulus 7 (FBbt:00003675).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 1 (FBbt:00049803) that receives synaptic input in region some protocerebral bridge glomerulus 8 (FBbt:00003676).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 2 (FBbt:00049804) that receives synaptic input in region some protocerebral bridge glomerulus 8 (FBbt:00003676).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 8 (Wolff et al., 2015). In the ellipsoid body, its output terminals are in the ventrolateral tile of the same hemisphere and it projects to the ventral gall (Wolff et al., 2015).
Adult protocerebral bridge 1 glomerulus-ellipsoid body tile-gall neuron that receives its input mainly in protocerebral bridge glomerulus 9 (Wolff and Rubin, 2018). In the ellipsoid body, its output terminals are in the ventralmost tile and it projects to the dorsal gall (Wolff and Rubin, 2018).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 1 (FBbt:00049803) that receives synaptic input in region some protocerebral bridge glomerulus 9 (FBbt:00003677).
Any adult protocerebral bridge 1 glomerulus-ellipsoid body tile-nodulus 1 neuron 2 (FBbt:00049804) that receives synaptic input in region some protocerebral bridge glomerulus 9 (FBbt:00003677).
Adult feeding initiation premotor neuron that receives input from gustatory system neurons in the subesophageal zone (Shiu et al., 2022). It is predicted to be cholinergic (Shiu et al., 2022). Neurotransmitter prediction based on machine learning classification (Shiu et al., 2022).
Adult premotor neuron that receives input from gustatory system neurons in the subesophageal zone (Shiu et al., 2022). It is predicted to be cholinergic (Shiu et al., 2022). Neurotransmitter prediction based on machine learning classification (Shiu et al., 2022).
Female-specific adult ascending neuron that regulates female receptivity to mating (Feng et al., 2014). There are two of these cells per female, with their somas on either side of the midline, variably found on either the dorsal or ventral surface of the abdominal ganglion (Feng et al., 2014). It arborizes extensively within the abdominal ganglion, in the same region as the adult sex peptide sensory neuron, and sends an ascending projection along the dorsal midline into the brain (Feng et al., 2014). There, it projects ipsilaterally in the periesophageal region and bilaterally in the dorsal protocerebrum, including the pars intercerebralis (Feng et al., 2014). In the brain, it synapses onto and can activate doublesex pC1a neurons (Wang et al., 2020). It is cholinergic (Wang et al., 2020). These neurons express doublesex (FBgn0000504), but not fruitless (FBgn0004652) (Feng et al., 2014).
Adult uniglomerular antennal lobe projection neuron that arborizes in both V glomeruli and has its soma in the lateral subesophageal zone (Stocker et al., 1990; Bracker et al., 2013; Bates et al., 2020). It sends a posterior projection towards the midline, where it bifurcates, branching into both hemispheres with a symmetrical morphology (Stocker et al., 1990; Bracker et al., 2013). After receiving input in the V glomerulus, it follows the lateral antennal lobe tract, bifurcates, and sends processes into the mushroom body calyx and the lateral horn (Bracker et al., 2013). In the calyx, it synapses to multiple types of Kenyon cell (Bracker et al., 2013). There is one of these per hemisphere and it is cholinergic (Bracker et al., 2013; Bates et al., 2020). It responds to carbon dioxide (Lin et al., 2013) and is required for carbon dioxide avoidance in starved, but not fed flies (Bracker et al., 2013). Equivalent to the biVPN in Bracker et al. (2013), as these two neurons have matching descriptions and only one corresponding type found by Bates et al. (2020) in a comprehensive EM analysis.
Adult lateral horn input neuron that has its dendrites predominantly within the ventral nerve cord (Dolan et al., 2019). It is cholinergic (Dolan et al., 2019).
Auditory system neuron of the adult brain that preferentially responds to male sine, rather than pulse, courtship song (Baker et al., 2022). Its main innervation is in the wedge, it also innervates the posterior lateral protocerebrum and it crosses the midline (Baker et al., 2022). It is cholinergic (Baker et al., 2022). Cell type identified at light level and in EM data (Baker et al., 2022). Neurotransmitter predicted from EM data (Baker et al., 2022).
Adult neuron that has dendritic arborizations in the wedge and lateral horn and also has an axon in the lateral horn, extending into a neighboring region (Dolan et al., 2019; Bates et al., 2020). It is a secondary neuron that develops from the WEDa2 (BAlp3) neuroblast (Bates et al., 2020). There are five of these neurons per hemisphere and they are cholinergic and GABAergic (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Adult neuron that has dendritic arborizations in the wedge and lateral horn and also has an axon in the lateral horn, extending into a neighboring region (Dolan et al., 2019; Bates et al., 2020). It is a secondary neuron that develops from the WEDa2 (BAlp3) neuroblast (Bates et al., 2020). There are seven of these neurons per hemisphere and they are cholinergic and GABAergic (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Adult neuron that has dendritic arborization in the wedge and an axon projecting to the lateral horn (Dolan et al., 2019; Bates et al., 2020). It is a secondary neuron that develops from the WEDa2 (BAlp3) neuroblast (Bates et al., 2020). There are five of these neurons per hemisphere and they are cholinergic and GABAergic (Dolan et al., 2019). Both neurotransmitters detected by antibody staining (Dolan et al., 2019).
Adult subesophageal local neuron with its soma in the ventral gnathal ganglion (Shiu et al., 2022). It receives gustatory input, mainly from sugar-sensing neurons and its activation results in proboscis extension (Shiu et al., 2022). It is bilateral, but most of its innervation is in the ipsilateral hemisphere (Shiu et al., 2022). It is predicted to be cholinergic (Shiu et al., 2022). Neurotransmitter prediction based on machine learning classification (Shiu et al., 2022). Named based on ‘Z’ morphology of proximal neurite (Shiu et al., 2022).
Alpha/beta mushroom body neuron that has dendrites in the main calyx, with its axons occupying the core layer of the peduncle, alpha and beta lobes (Strausfeld et al., 2003; Tanaka et al., 2008). They can be subdivided into inner and outer core cells (Tanaka et al., 2008; Takemura et al., 2017). There are around 400 of these neurons in each hemisphere (Aso et al., 2014; Takemura et al., 2017). Li et al. (2020) only class ~ 250 cells as alpha/beta core, these may correspond to the inner core group.
Kenyon cell of the inner part of the alpha/beta lobe core stratum (Tanaka et al., 2008). There are around 260 of these cells per hemisphere (Takemura et al., 2017). Based on cell numbers, these may correspond to the alpha/beta core neurons of Li et al. (2020) - FlyBase:FBrf0248215.
Mushroom body neuron that bifurcates at the anterior end of the pedunculus and projects into the alpha and beta lobes of the adult mushroom body (Lee et al., 1999). The alpha/beta neurons are the last born of the Kenyon cells, generated during the pupal stage (Lee et al., 1999). In the pedunculus, the alpha/beta neurons occupy the core stratum with the alpha'/beta' neurons in the intermediate stratum and the gamma neurons at the periphery (Tanaka et al., 2008; Li et al., 2020). They are cholinergic neurons (Pankova & Borst, 2017; Barnstedt et al., 2016). There are around 900-1000 of these cells per hemisphere (Aso et al., 2014; Li et al., 2020). Neuron was assessed to be cholinergic by Pankova & Borst (2017), based on anti-HA antibody detection of HA-tagged VAChT expression; Barnstedt et al. (2016) show that Kenyon cells express ChAT and VAChT proteins, and that antagonism of nicotinic ACh receptors or reduction of ACh processing in Kenyon cells impairs Kenyon cell-evoked responses in mushroom body output neurons.
Kenyon cell of the outer part of the alpha/beta lobe core stratum (Tanaka et al., 2008). There are around 130 of these cells per hemisphere (Takemura et al., 2017). Based on cell numbers, these may belong to the alpha/beta middle group of Li et al. (2020) FlyBase:FBrf0248215.
Alpha/beta mushroom body neuron that has its dendrites in the dorsal accessory calyx, with no arborization in the main calyx (Aso et al., 2014; Li et al., 2020). It occupies the outermost stratum and the posterior layer at the tip of the alpha and beta lobes (Tanaka et al., 2008). In the shaft region of the alpha lobe, alpha/beta posterior Kenyon cell form mesh-like arrangements, with one or two nodes where axons appear to gather. In the pedunculus, their axons form several bundles, which run through the outermost layer of the central zone. They are the first-born alpha/beta Kenyon cells (Aso et al., 2014). There are around 60-90 of these neurons in each hemisphere (Aso et al., 2014; Takemura et al., 2017; Li et al., 2020). They receive visual input in the dorsal accessory calyx, but this is mainly from local visual interneurons, rather than visual projection neurons (Li et al., 2020). Li, Mahoney et al. (2020) - FBrf0246721 claim that these are the only KC subtype in the dACA, but this is not the case as it is also innervated by some gamma-s cells (Li et al., 2020 - FBrf0248215).
Alpha/beta mushroom body neuron that has dendrites in the main calyx and projects axons to the surface layer of the alpha and beta lobes, where they form a continuous layer surrounding the alpha/beta core (Aso et al., 2014). There are around 500 of these neurons in each hemisphere (Aso et al., 2014; Takemura et al., 2017). Li et al.(2020) - FlyBase:FBrf0248215 only class ~220 cells as surface, rest likely to be ‘middle’ group.
Alpha/beta mushroom body neuron that has dendrites in the main calyx and whose axons form concentrically layered regions of the alpha and beta lobes (Takemura et al., 2017). They are born after the alpha/beta posterior neurons and are organized by birth order, with later-born neurons located more centrally (Takemura et al., 2017; Li et al., 2020). There are around 800-900 of these neurons in each hemisphere (Aso et al., 2014; Takemura et al., 2017; Li et al., 2020). Sizes of layers are inconsistent between papers: ~500 surface, ~130 outer core, ~260 inner core in Tanaka et al. (2008); Aso et al. (2014); Takemura et al. (2017), ~220 surface, ~350 middle, ~250 core in Li et al. (2020).
tracing status-Roughly traced, cropped-False [aSP-g1_R (FlyEM-HB:485430434); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult fruitless aSP-g1 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult fruitless aSP-g (female) neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult fruitless aSP-g1 neuron; aSP-g1_R (FlyEM-HB:485775679); neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult fruitless aSP-g (female) neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult fruitless aSP-g1 neuron; aSP-g1_R (FlyEM-HB:610916994); neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult fruitless aSP-g (female) neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult fruitless aSP-g1 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult fruitless aSP-g (female) neuron; aSP-g1_R (FlyEM-HB:887148641)]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult fruitless aSP-g1 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; aSP-g1_R (FlyEM-HB:949534412); JRC2018Unisex; adult brain; adult fruitless aSP-g (female) neuron]
[transmission electron microscopy (TEM); adult fruitless aSP-g1 neuron; VFB CATMAID Adult Brain (FAFB); is part of; female organism; JRC2018Unisex; adult brain; adult fruitless aSP-g (female) neuron; aSP-g1b#1 (FAFB:2477473)]
[transmission electron microscopy (TEM); adult fruitless aSP-g1 neuron; VFB CATMAID Adult Brain (FAFB); JRC2018Unisex; adult brain template JFRC2; aSP-g1b#2 (FAFB:1149437)]
[transmission electron microscopy (TEM); adult AVLP-PN1 lateral horn input neuron; VFB CATMAID Adult Brain (FAFB); JRC2018Unisex; adult brain template JFRC2; AVLP560#1 (FAFB:8927505)]
Bract#1, FBbt:00051861 [transmission electron microscopy (TEM); is part of; female organism; adult bract subesophageal neuron; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain; Bract#1 (FAFB:17024882)]
Bract#2, FBbt:00051861 [transmission electron microscopy (TEM); is part of; female organism; Bract#2 (FAFB:17542353); adult bract subesophageal neuron; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
OutAge: Adult 5~15 days [expresses; confocal microscopy; Cha-F-000003; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000011; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; Cha-F-000022; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2; Cha-F-000024]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000034; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body]
OutAge: Adult 5~15 days [expresses; Cha-F-000035; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000037; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body]
OutAge: Adult 5~15 days [alpha/beta posterior Kenyon cell; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000038; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; lobula columnar neuron LC6; Cha-F-000039; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps]
OutAge: Adult 5~15 days [expresses; confocal microscopy; Cha-F-000046; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000057; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; Cha-F-000073; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; Cha-F-000075; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; expression pattern fragment; is part of; female organism; adult brain template JFRC2; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; expression pattern fragment; is part of; female organism; Cha-F-000076; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000092; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000094; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2; Cha-F-000102]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; Cha-F-000104; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; expression pattern fragment; is part of; female organism; adult brain template JFRC2; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; Cha-F-000111; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000113; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; Cha-F-000114; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; posterior ventrolateral protocerebrum; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; Cha-F-000126; female organism; JRC2018Unisex; adult brain; overlaps]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; posterior ventrolateral protocerebrum; confocal microscopy; adult brain; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; Cha-F-000138; overlaps]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000141; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; Cha-F-000143; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; Cha-F-000151; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; pedunculus of adult mushroom body; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; Cha-F-000157; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000172; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; Cha-F-000182; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; Cha-F-000187; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; expression pattern fragment; is part of; female organism; adult brain template JFRC2; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; confocal microscopy; Cha-F-000213; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000217; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; gamma dorsal Kenyon cell; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; Cha-F-000228; medial lobe of adult mushroom body; overlaps]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2; Cha-F-000288]
OutAge: Adult 5~15 days [Cha-F-000323; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; adult ellipsoid body-protocerebral bridge glomerulus 8-ventral gall neuron; Cha-F-000327; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000336; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps]
OutAge: Adult 5~15 days [Cha-F-000337; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult protocerebral bridge glomerulus 1-ellipsoid body tile-dorsal gall neuron; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; expression pattern fragment; Cha-F-100004; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; Cha-F-100035; alpha/beta core Kenyon cell; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; Cha-F-100040; adult brain; overlaps]
OutAge: Adult 5~15 days [alpha/beta posterior Kenyon cell; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; Cha-F-100043; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; Cha-F-100045; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-100049; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; Cha-F-100070; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2; Cha-F-100074]
OutAge: Adult 5~15 days [adult crepine; expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; pedunculus of adult mushroom body; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; Cha-F-100076; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [Cha-F-100080; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; Cha-F-100096; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; Cha-F-100097; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-100107; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; pedunculus of adult mushroom body; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; Cha-F-100110; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; superior lateral protocerebrum; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; Cha-F-100115; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; Cha-F-100120; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; Cha-F-100140; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [Cha-F-100159; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; Cha-F-100160; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [Cha-F-100178; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; gamma dorsal Kenyon cell; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-100187; medial lobe of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; Cha-F-100188; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; Cha-F-100200; FlyCircuit 1.0; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; Cha-F-100209; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-100220; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; Cha-F-100222; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; adult brain; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; Cha-F-100227; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; expression pattern fragment; Cha-F-100232; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; pedunculus of adult mushroom body; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; Cha-F-100243; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; Cha-F-100251; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [Cha-F-100283; alpha/beta posterior Kenyon cell; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; medial lobe of adult mushroom body; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; adult ellipsoid body-protocerebral bridge glomerulus 3-dorsal gall neuron; female organism; JRC2018Unisex; adult brain; Cha-F-100322; overlaps]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; Cha-F-100323; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-100334; calyx of adult mushroom body]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; posterior ventrolateral protocerebrum; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-100342]
OutAge: Adult 5~15 days [Cha-F-100347; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult brain template JFRC2; expression pattern fragment; alpha/beta core Kenyon cell; is part of; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; vertical lobe of adult mushroom body; P{ChAT-GAL4.7.4} expression pattern; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; Cha-F-100360; female organism; JRC2018Unisex; adult brain; overlaps; calyx of adult mushroom body]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-200004; alpha/beta surface Kenyon cell; P{ChAT-GAL4.7.4}; FlyCircuit 1.0; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; adult brain template JFRC2]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; gamma dorsal Kenyon cell; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; Cha-F-200017; adult brain; overlaps; medial lobe of adult mushroom body]