A02a- looper-1_a1l (L1EM:13004884) [VFB_00101565]
[transmission electron microscopy (TEM); A02a- looper-1_a1l (L1EM:13004884); VFB CATMAID L1 CNS; larval abdominal 1 A02a neuron; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02a- looper-1_a1l (L1EM:13004884); VFB CATMAID L1 CNS; larval abdominal 1 A02a neuron; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A02b neuron; A02b_a1l (L1EM:6578062); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02b_a1r (L1EM:15233041); larval abdominal 1 A02b neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A02d neuron; VFB CATMAID L1 CNS; A02d_a1l (L1EM:14046279); L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A02d neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A02d_a1r (L1EM:14046294)]
[transmission electron microscopy (TEM); larval abdominal 1 A02e neuron; VFB CATMAID L1 CNS; A02e_a1l (L1EM:7992966); L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A02e neuron; A02e_a1r (L1EM:14858626); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02f_a1l (L1EM:4071032); VFB CATMAID L1 CNS; larval abdominal 1 A02f neuron; L1 larval CNS ssTEM - Cardona/Janelia]
[A02f_a1r (L1EM:12953345); transmission electron microscopy (TEM); VFB CATMAID L1 CNS; larval abdominal 1 A02f neuron; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02g_a1l (L1EM:14866842); larval abdominal 1 A02g neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02g_a1r (L1EM:18145093); larval abdominal 1 A02g neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); A02h_a1l (L1EM:12820178); larval abdominal 1 A02h neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A02h neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A02h_a1r (L1EM:14866379)]
[transmission electron microscopy (TEM); larval abdominal 1 A02i neuron; A02i_a1l (L1EM:2798040); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A02i neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A02i_a1r (L1EM:5057361)]
[transmission electron microscopy (TEM); larval abdominal 3 A02j neuron; A02j Looper-10_a3l (L1EM:3365860); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 3 A02j neuron; A02j Looper-10_a3r (L1EM:4348665); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 1 A02j neuron; VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia; A02j_a1l (L1EM:18769231)]
[transmission electron microscopy (TEM); larval abdominal 3 A02j neuron; A02j_a3l (L1EM:16274373); VFB CATMAID L1 CNS; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval abdominal 3 A02j neuron; A02j_a3r (L1EM:7926496); 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)]
Neuromodulatory motor neuron that innervates the internal dorsal acute and oblique muscles of larval abdominal segments A1 to A7 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. These neurons have a virtually identical arborization pattern, shared with the lateral and ventral VUM neurons of A1-7. They arborize along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012). There is little or no published literature specifically on innervation in A1 and so where equivalent muscles are present between A1 and A2-7 (Landgraf et al., 1997; Schmid et al., 1999), we infer A1 motor neuron innervation patterns from those of A2-7.
Neuromodulatory motor neuron that innervates the lateral transverse muscles of larval abdominal segments A1 to A7 via type II boutons. It exits the ventral nerve cord via the segmental nerve and fasciculates with the SNa segmental nerve branches. These neurons have a virtually identical arborization pattern, shared with the dorsal and ventral VUM neurons of A1-7. They arborize along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012). There is little or no published literature specifically on innervation in A1 and so where equivalent muscles are present between A1 and A2-7 (Landgraf et al., 1997; Schmid et al., 1999), we infer A1 motor neuron innervation patterns from those of A2-7. In A2-7, these might also synapse to muscles 26 (VA1), 27 (VA2) and 29 (VA3) (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal ventral oblique and longitudinal muscles of larval abdominal segments A1 to A7 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. These neurons have a virtually identical arborization pattern, shared with the dorsal and lateral VUM neurons of A1-7. They arborize along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012). There is little or no published literature specifically on innervation in A1 and so where equivalent muscles are present between A1 and A2-7 (Landgraf et al., 1997; Schmid et al., 1999), we infer A1 motor neuron innervation patterns from those of A2-7.
Neuromodulatory motor neuron that innervates the internal dorsal acute and oblique muscles of larval abdominal segment A1 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the lateral transverse muscles of larval abdominal segment A1 via type II boutons. It exits the ventral nerve cord via the segmental nerve and fasciculates with the SNa segmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal ventral oblique and longitudinal muscles of larval abdominal segment A1 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal dorsal acute and oblique muscles of larval abdominal segment A2 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the lateral transverse muscles of larval abdominal segment A2 via type II boutons. It exits the ventral nerve cord via the segmental nerve and fasciculates with the SNa segmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal ventral oblique and longitudinal muscles of larval abdominal segment A2 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal dorsal acute and oblique muscles of larval abdominal segment A3 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the lateral transverse muscles of larval abdominal segment A3 via type II boutons. It exits the ventral nerve cord via the segmental nerve and fasciculates with the SNa segmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal ventral oblique and longitudinal muscles of larval abdominal segment A3 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal dorsal acute and oblique muscles of larval abdominal segment A4 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the lateral transverse muscles of larval abdominal segment A4 via type II boutons. It exits the ventral nerve cord via the segmental nerve and fasciculates with the SNa segmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal ventral oblique and longitudinal muscles of larval abdominal segment A4 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal dorsal acute and oblique muscles of larval abdominal segment A5 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the lateral transverse muscles of larval abdominal segment A5 via type II boutons. It exits the ventral nerve cord via the segmental nerve and fasciculates with the SNa segmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal ventral oblique and longitudinal muscles of larval abdominal segment A5 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal dorsal acute and oblique muscles of larval abdominal segment A6 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the lateral transverse muscles of larval abdominal segment A6 via type II boutons. It exits the ventral nerve cord via the segmental nerve and fasciculates with the SNa segmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal ventral oblique and longitudinal muscles of larval abdominal segment A6 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal dorsal acute and oblique muscles of larval abdominal segment A7 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the lateral transverse muscles of larval abdominal segment A7 via type II boutons. It exits the ventral nerve cord via the segmental nerve and fasciculates with the SNa segmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Neuromodulatory motor neuron that innervates the internal ventral oblique and longitudinal muscles of larval abdominal segment A7 via type II boutons. It exits the ventral nerve cord via the posterior root of the intersegmental nerve and fasciculates with the ISNb or ISNd intersegmental nerve branches. It arborizes along and dorsal to the dorsal median fascicle and laterally along the dorsal lateral fascicle, invading the next anterior neuromere. In the dorsomedial neuropil, arborizations are sent into at least two (usually three) anterior neuromeres and the adjacent posterior neuromere (Selcho et al., 2012).
Female version of the adult dorsal posterior Ilp7 neuron. This is a glutamatergic motor neuron that innervates the oviduct. There are 4 of these neurons, in a dorsal cluster. These cells are generated by post-embryonic neurogenesis in the late third instar larva. Unlike the male version, this cell does not produce serotonin. These neurons express fruitless (FBgn0004652) but not doublesex (FBgn0000504). The expression of Bruchpilot was used to reveal presynaptic terminals (Castellanos et al., 2013).
Adult doublesex aDN neuron of the female (Nojima et al., 2021). Its lateral (input) neurites are mainly found in the posterior part of the superior lateral protocerebrum, with minor processes in the superior clamp and ventrolateral protocerebrum (Nojima et al., 2021). It receives multimodal sensory information, including inputs from a range of antennal lobe projection neurons (Nojima et al., 2021). It also receives substantial input from the oviposition excitatory and inhibitory neurons and is involved in egg-laying site selection (Nojima et al., 2021).
Adult doublesex aDN neuron of the male (Nojima et al., 2021). Its lateral (input) arbor is mainly restricted to the anterior optic tubercle, where it receives input from LC10a neurons (Nojima et al., 2021). It is involved in approaching and facing the female during courtship (Nojima et al., 2021).
Doublesex-expressing neuron of the adult that has its soma in the anterodorsal region of the superior protocerebrum (Lee et al., 2002). There are two of these cells per hemisphere in both males and females (Nojima et al., 2021). In both sexes, their neurites are all ipsilateral, with a medial arbor in the superior medial protocerebrum containing mainly presynaptic sites (Nojima et al., 2021). Lateral arborization, containing mainly postsynaptic sites, is sexually-dimorphic (Nojima et al., 2021). These neurons are glutamatergic (Pavlou et al., 2016). Lee et al. (2002) and Robinett et al. (2010) state that they do not see aDN in the female, but Rideout et al., 2010 and Pavlou et al., 2016 show that they are present in the female. These neurons do not express fruitless (Pavlou et al., 2016).
Adult gustatory neuron of the leg that detects female pheromones (Thistle et al., 2012; Kallman et al., 2015). It can be distinguished from male-pheromone-detecting cells based on its expression of ppk25 (Kallman et al., 2015). It is glutamatergic (Kallman et al., 2015). These cells do not ascend to the brain (Kallman et al., 2015).
Neuron located in the adult female ventral nerve cord. It arborizes one of the two ppk23-positive cells in each leg chemosensory bristle (the ppk25 positive one) from the three leg neuromeres. It does not extend into the brain. This neuron is involved in the detection of female pheromones.
Adult doublesex AbN neuron of the adult female that also expresses vGlut. There are approximately 100 of these cells in the female and a smaller number in the male. Some of these neurons innervate the internal genitalia, including muscles of the uterus, spermathecal and parovarian ducts. Some of these neurons appear to be synapsed by the GABAergic AbN neurons (Pavlou et al., 2016).
Adult doublesex AbN neuron of the adult male that also expresses vGlut. There are approximately 80 of these cells in the male and a larger number in the female. This class encompasses all of the neurons innervating phallic and periphallic musculature. Some of these neurons appear to be synapsed by the GABAergic AbN neurons (Pavlou et al., 2016).
Any glutamatergic neuron (FBbt:00100291) that is part of some adult nervous system (FBbt:00003559).
Large field neuron of the central complex that is intrinsic to the protocerebral bridge (Lin et al., 2013; Wolff et al., 2015). It has dendritic arbors in 18 glomeruli, and axon terminals distributed in two glomeruli spaced seven glomeruli apart (Wolff et al., 2015). There are three subtypes that differ on the location of the axon terminals (Lin et al., 2013). One subtype has terminals in the ipsilateral glomerulus 7 and contralateral glomerulus 2; another with terminals in the ipsilateral glomerulus 6 and contralateral glomerulus 3; and the last with terminals in the ipsilateral glomerulus 5 and contralateral glomerulus 4 (Lin et al., 2013; Wolff et al., 2015). Discrepancy between Lin et al. (2013) and Wolff et al. (2015) due to discovery of additional medial PB glomerulus in either hemisphere.
Large field protocerebral bridge intrinsic neuron that has dendritic arbors in all 18 glomeruli and axon terminals distributed in three glomeruli that are seven glomeruli apart (Lin et al., 2013; Wolff et al., 2015). Its axonal terminals are in ipsilateral glomerulus 8 and contralateral glomeruli 1 and 9 (Lin et al., 2013; Wolff et al., 2015).
Large field neuron of the central complex that is intrinsic to the protocerebral bridge (PB) with dendritic arbors in all 18 glomeruli and axon terminals in glomeruli that are seven glomeruli apart (Lin et al., 2013; Wolff et al., 2015). There are four subtypes, collectively having presynaptic terminals in all glomeruli (Wolff et al., 2015). They have inhibitory output onto E-PG neurons in their output glomeruli and receive input from E-PG neurons of other PB regions (Turner-Evans et al., 2020). They are glutamatergic (Turner-Evans et al., 2020).
Subtype of the protocerebral bridge 18 glomeruli type 2 neuron that has axonal terminals in the ipsilateral glomerulus 5 and contralateral glomerulus 4.
Subtype of the protocerebral bridge 18 glomeruli type 2 neuron that has axonal terminals in the ipsilateral glomerulus 6 and contralateral glomerulus 3.
Subtype of the protocerebral bridge 18 glomeruli type 2 neuron that has axonal terminals in the ipsilateral glomerulus 7 and contralateral glomerulus 2.
Adult neuron that has a large cluster of dendrites in the antennal mechanosensory and motor center and a commissural projection in the superior brain (Guo et al., 2022). It receives substantial input from Johnston organ neurons and makes substantial inhibitory (glutamatergic) connections to DNg11 (Guo et al., 2022). There is one of these cells per hemisphere (Guo et al., 2022).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the BLAd2 (SIPa1) ventral hemilineage (Bates et al., 2020). There are five of these neurons per hemisphere and they are glutamatergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the AV6 primary neurite tract (Schlegel et al., 2021). There are around three of these cells per hemisphere and they are glutamatergic (Schlegel et al., 2021). Neurotransmitter predicted based on hemilineage (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 (Dolan et al., 2019). There are five of these neurons per hemisphere and they are glutamatergic (Dolan et al., 2019).
Adult lateral horn local neuron that fasciculates with the PD3 primary neurite tract (Dolan et al., 2019). These neurons are glutamatergic (Dolan et al., 2019).
Adult lateral horn local neuron that fasciculates with the PD3 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the DPLm2 (LHd2) dorsal hemilineage (Bates et al., 2020). There are nine of these neurons per hemisphere and they are glutamatergic (Dolan et al., 2019). Bates et al. (2020) classify this as an output neuron.
Adult lateral horn output neuron that fasciculates with the PD3 primary neurite tract (Bates et al., 2020). It is a secondary neuron that is part of the DPLm2 (LHd2) dorsal hemilineage (Bates et al., 2020). It is glutamatergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PD3 primary neurite tract (Bates et al., 2020). It is a secondary neuron that is part of the DPLm2 (LHd2) dorsal hemilineage (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PD3 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLm2 (LHd2) dorsal hemilineage (Schlegel et al., 2021). There are approximately two of these cells per hemisphere and they are glutamatergic (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 PD3 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLm2 (LHd2) dorsal hemilineage (Schlegel et al., 2021). There are approximately two of these cells per hemisphere and they are glutamatergic (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 PD3 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLm2 (LHd2) dorsal hemilineage (Schlegel et al., 2021). There is approximately one of these cells per hemisphere and it is glutamatergic (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 local neuron that fasciculates with the PV4 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Bates et al., 2020). It is glutamatergic (Dolan et al., 2019; Bates et al., 2020). There are approximately 8 neurons that are of PV4a1-5 types (Dolan et al., 2019). Bates et al. (2020) classify this as an output neuron.
Adult lateral horn local neuron that fasciculates with the PV4 primary neurite tract (Frechter et al., 2019). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Bates et al., 2020). It is glutamatergic (Bates et al., 2020). Bates et al. (2020) classify this as an output neuron.
Adult lateral horn local neuron that fasciculates with the PV4 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Bates et al., 2020). It is glutamatergic (Dolan et al., 2019; Bates et al., 2020). There are approximately 8 neurons that are of PV4a1-5 types (Dolan et al., 2019). Bates et al. (2020) classify this as an output neuron.
Adult lateral horn local neuron that fasciculates with the PV4 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Bates et al., 2020). It is glutamatergic (Dolan et al., 2019; Bates et al., 2020). There are approximately 8 neurons that are of PV4a1-5 types (Dolan et al., 2019). Bates et al. (2020) classify this as an output neuron.
Adult lateral horn local neuron that fasciculates with the PV4 primary neurite tract (Frechter et al., 2019). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Bates et al., 2020). It is glutamatergic (Bates et al., 2020). Bates et al. (2020) classify this as an output neuron.
Adult lateral horn local neuron that fasciculates with the PV4 primary neurite tract (Frechter et al., 2019; Dolan et al., 2019). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Bates et al., 2020). There are three of these neurons per hemisphere and they are glutamatergic (Dolan et al., 2019). Bates et al. (2020) classify this as an output neuron.
Adult lateral horn output neuron that fasciculates with the PV4 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Bates et al., 2020). There is one of these neurons per hemisphere and it is glutamatergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV4 primary neurite tract (Bates et al., 2020). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Bates et al., 2020). It is glutamatergic (Bates et al., 2020).
Adult lateral horn local neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is glutamatergic (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 local neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Schlegel et al., 2021). There is one of these cells per hemisphere and it is glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Schlegel et al., 2021). There is one of these cells per hemisphere and it is glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Schlegel et al., 2021). There is one of these neurons per hemisphere and it is glutamatergic (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 PV4 primary neurite tract (Bates et al., 2020). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Bates et al., 2020). It is glutamatergic (Bates et al., 2020).
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). There are five of these neurons per hemisphere and they are glutamatergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV4 primary neurite tract (Dolan et al., 2019). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Bates et al., 2020). There are seven of these neurons per hemisphere and they are glutamatergic (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). There are nine of these neurons per hemisphere and they are glutamatergic (Dolan et al., 2019).
Adult lateral horn output neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There are approximately 3-4 of these neurons per hemisphere and they are glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There are approximately 1-2 of these cells per hemisphere and they are glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There are approximately 1-2 of these neurons per hemisphere and they are glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There are approximately 2-3 of these neurons per hemisphere and they are glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There is one of these neurons per hemisphere and it is glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is glutamatergic (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 PV4 primary neurite tract (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 glutamatergic (Bates et al., 2020).
Adult lateral horn output neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Schlegel et al., 2021). There are approximately 3-4 of these cells per hemisphere and they are glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There is approximately one of these cells per hemisphere and it is glutamatergic (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 local neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There are roughly 1-3 of these neurons per hemisphere and they are glutamatergic (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 local neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There is approximately one of these cells per hemisphere and it is glutamatergic (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 local neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There are roughly 4-5 of these neurons per hemisphere and they are glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There is around one of these cells per hemisphere and it is glutamatergic (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 neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There are roughly 2-3 of these neurons per hemisphere and they are glutamatergic (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). Schlegel et al. (2021) list 1 individual each of LHLN and LHON.
Adult lateral horn local neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There are roughly 2-3 of these neurons per hemisphere and they are glutamatergic (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 local neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There is one of these cells per hemisphere and it is glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There is approximately one of these cells per hemisphere and it is glutamatergic (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 local neuron that fasciculates with the PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that develops from the BLP4 (LHp1) neuroblast (Schlegel et al., 2021). There is one of these neurons per hemisphere and it is glutamatergic (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 PV4 primary neurite tract (Schlegel et al., 2021). It is a secondary neuron that is part of the DPLp2 (SLPp&v1) posterior hemilineage (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is glutamatergic (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 is a secondary neuron and is part of the secondary LHp1 (BLP4) lineage (Schlegel et al., 2021). There is approximately one of these neurons per hemisphere and it is glutamatergic (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). Listed with PV4 neurons as being part of the LHp1 lineage despite PV5 in name (Schlegel et al., 2021).
Adult lateral horn output neuron that is a secondary neuron and is part of the secondary LHp1 (BLP4) lineage (Schlegel et al., 2021). There is around one of these cells per hemisphere and it is glutamatergic (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). Listed with PV4 neurons as being part of the LHp1 lineage despite PV5 in name (Schlegel et al., 2021).
Adult lateral horn output neuron that fasciculates with the PV5 primary neurite tract (Dolan et al., 2019). There are four of these neurons per hemisphere and they are glutamatergic (Dolan et al., 2019). It is a fan-shaped body tangential neuron that innervates layer 2 (Dolan et al., 2019; Hulse et al., 2020). Hulse et al. (2020) - doi:10.1101/2020.12.08.413955 say this likely corresponds to what they call FB2H_a, FB2H_b and/or FB2I_b.
Any adult octopaminergic neuron (FBbt:00058203) that capable of some glutamate secretion, neurotransmission (GO:0061535). Approximately 70 of these (of 100 OA neurons) in the male (Sherer et al., 2020).
Female-specific adult Ilp7 neuron. There are 3 to 4 of these neurons, in a ventral cluster of the abdominal neuromere with the dMP2 Ilp7 neurons. It is a glutamatergic motor neuron that fasciculates with the abdominal nerve trunk and innervates the oviduct muscle. These cells are generated by post-embryonic neurogenesis in the late third instar larva. The expression of Bruchpilot was used to reveal presynaptic terminals. These neurons express fruitless (FBgn0004652), but not doublesex (FBgn0000504) (Castellanos et al., 2013).
Adult interneuron that receives a large amount of input from bitter-sensing gustatory neurons in the subesophageal zone and sends inhibitory (predicted glutamatergic) input to feeding premotor neurons (Shiu et al., 2022). Neurotransmitter prediction based on machine learning classification (Shiu et al., 2022). Named based on resemblance to an inverted scapula bone and proximity to clavicle neuron (Shiu et al., 2022).
Allatostatin A-expressing neuron of the adult that has its cell body in the superior lateral protocerebrum (Ni et al., 2019). These neurons are glutamatergic and express the Allatostatin A neuropeptide (Ni et al., 2019). Their activation increases sleep upstream of ExFl2 neurons, to which they synapse in the superior medial protocerebrum (Ni et al., 2019). Synapsing shown by GRASP and functional data (Ni et al., 2019).
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; Cha-F-000078; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli 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; Cha-F-000089; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; 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; 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 [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 [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 [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 [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 [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; Cha-F-200130; overlaps]
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; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-200148; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; adult brain template JFRC2; expression pattern fragment; is part of; female organism; Cha-F-200165; JRC2018Unisex; adult brain; overlaps]
OutAge: Adult 5~15 days [Cha-F-200257; 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; adult brain; overlaps]
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; Cha-F-300149; adult brain; overlaps]
OutAge: Adult 5~15 days [Cha-F-300196; expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli 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; Cha-F-300236; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli 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; Cha-F-300305; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; 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; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; Cha-F-300324; 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; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-400031]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; posterior ventrolateral protocerebrum; confocal microscopy; Cha-F-600053; 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; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-600063]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-600066]
OutAge: Adult 5~15 days [expresses; confocal microscopy; P{ChAT-GAL4.7.4} expression pattern; FlyCircuit 1.0; P{ChAT-GAL4.7.4}; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; adult brain template JFRC2; expression pattern fragment; is part of; female organism; JRC2018Unisex; adult brain; Cha-F-700075; overlaps]
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-700192]
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; female organism; JRC2018Unisex; adult brain; overlaps; Cha-F-900016; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
[transmission electron microscopy (TEM); VFB CATMAID Adult Brain (FAFB); is part of; female organism; JRC2018Unisex; adult brain; Delta7-1R9R8L#1 (FAFB:803916); adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
[transmission electron microscopy (TEM); VFB CATMAID Adult Brain (FAFB); adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; is part of; female organism; JRC2018Unisex; adult brain; Delta7-2R7L#1 (FAFB:6454109)]
[transmission electron microscopy (TEM); Delta7-5R4L#1 (FAFB:3017999); VFB CATMAID Adult Brain (FAFB); is part of; female organism; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
[transmission electron microscopy (TEM); Delta7-5R4L#2 (FAFB:676155); VFB CATMAID Adult Brain (FAFB); is part of; female organism; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
[transmission electron microscopy (TEM); VFB CATMAID Adult Brain (FAFB); Delta7-6R3L#1 (FAFB:632638); adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; is part of; JRC2018Unisex; adult brain]
[Delta7-6R3L#2 (FAFB:6102788); transmission electron microscopy (TEM); VFB CATMAID Adult Brain (FAFB); adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; is part of; JRC2018Unisex; adult brain]
[transmission electron microscopy (TEM); VFB CATMAID Adult Brain (FAFB); adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; is part of; female organism; JRC2018Unisex; adult brain; Delta7-7R2L#1 (FAFB:6254861)]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L1L9R8_R (FlyEM-HB:5813061383); adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L1L9R8_R (FlyEM-HB:881221166); adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L1L9R8_R (FlyEM-HB:911574261); adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L1L9R8_R (FlyEM-HB:911911004); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; Delta7(PB15)_L1L9R8_R (FlyEM-HB:911919917); neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L2R7_R (FlyEM-HB:911470352); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; Delta7(PB15)_L2R7_R (FlyEM-HB:911574041); neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; neuronbridge; is part of; female organism; Delta7(PB15)_L2R7_R (FlyEM-HB:911578496); Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L2R7_R (FlyEM-HB:911911699)]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L2R7_R (FlyEM-HB:942522378); adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L3R6_R (FlyEM-HB:910783961); JRC_FlyEM_Hemibrain; focussed ion beam scanning electron microscopy (FIB-SEM); neuronbridge; is part of; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); Delta7(PB15)_L3R6_R (FlyEM-HB:911565419); JRC_FlyEM_Hemibrain; neuronbridge; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; is part of; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L3R6_R (FlyEM-HB:911906936); neuronbridge; is part of; female organism; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L3R6_R (FlyEM-HB:941469087); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; is part of; female organism; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; Delta7(PB15)_L4R5_R (FlyEM-HB:880880259); female organism; is part of; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L4R5_R (FlyEM-HB:910442723); neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; is part of; female organism; Delta7(PB15)_L4R5_R (FlyEM-HB:911129339); Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L4R5_R (FlyEM-HB:911134009); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L4R5_R (FlyEM-HB:911138168); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L4R6_R (FlyEM-HB:910442782)]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L4R6_R (FlyEM-HB:911901802); adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L5R4_L (FlyEM-HB:5813048042); adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L5R4_L (FlyEM-HB:880530613); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L5R4_L (FlyEM-HB:880875736); neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L5R4_L (FlyEM-HB:910796989); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L5R4_L (FlyEM-HB:910801332); neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 5 and 4 neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; Delta7(PB15)_L6R3_L (FlyEM-HB:734581598); is part of; Neuprint web interface - hemibrain:v1.1; adult brain; JRC2018Unisex]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L6R3_L (FlyEM-HB:911919044); neuronbridge; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; is part of; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; Delta7(PB15)_L6R3_L (FlyEM-HB:941482720); adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; is part of; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L6R3_L (FlyEM-HB:941814787); focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; is part of; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 6 and 3 neuron; female organism; is part of; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L6R3_L (FlyEM-HB:973959177)]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L6R4_L (FlyEM-HB:911211196)]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L6R4_L (FlyEM-HB:911241750); adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L7R2_L (FlyEM-HB:1158747783)]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; Delta7(PB15)_L7R2_L (FlyEM-HB:911129204); adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-glomeruli 7 and 2 neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; Delta7(PB15)_L7R2_L (FlyEM-HB:912243353)]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Delta7(PB15)_L7R3_L (FlyEM-HB:941810314); Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L8R1R9_L (FlyEM-HB:910442752); adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [Delta7(PB15)_L8R1R9_L (FlyEM-HB:910783731); JRC_FlyEM_Hemibrain; focussed ion beam scanning electron microscopy (FIB-SEM); adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; Delta7(PB15)_L8R1R9_L (FlyEM-HB:910783883); adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); Delta7(PB15)_L8R1R9_L (FlyEM-HB:911578595); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
tracing status-Roughly traced, cropped-False [focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; Delta7(PB15)_L8R1R9_L (FlyEM-HB:911911193); neuronbridge; is part of; female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
Distal medullary wide-field amacrine neuron whose cell body is located in the anterior region of the cell body rind of the medulla. It branches extensively at the distal surface of the medulla forming a moderately broad arbor with each branch making a distinctive bouton-like terminal in the region between M1 and M2 (in the same sublayer as Dm18, and more proximal than Dm9 and Dm10 in M1), from which short, fine terminal branches project (Morante and Desplan, 2008; Fischbach and Dittrich, 1989). The arbor varies in shape between cells, covering around 20-30 columns, but with these areas overlapping. The size of the terminals of Dm1 is smaller than those of Dm18. There are around 40 Dm1 neurons per hemisphere. They are glutamatergic (Davis et al., 2020). Pre- versus postsynaptic innervation judged by scoring of terminal morphology from figures in Fischbach and Dittrich (1989) as assessed by FlyBrain Neuron DB.
Distal medullary wide-field amacrine neuron whose cell body is located in the dorsal region of the cell body rind of the medulla. Its primary neurite extends beyond M6A layer, and then turns back, forming recurrent processes from M6A to M1, and into the first optic chiasm. The arbor varies in shape between cells, covering around 9 columns and showing tiling. The terminals in M6A layer occupy the whole layer, whereas in the other layers the processes are thin, occupying only one column, and being associated with R7 and R8 photoreceptor axons. There are around 70 Dm11 neurons per hemisphere. They are glutamatergic (Davis et al., 2020).
Distal medullary wide-field amacrine neuron whose cell body is located in the cell body rind of the medulla. Its primary neurite extends into the M6 layer, and then turns back to project to M3B. The arbor is circular in shape, overlapping and covering around 15-20 columns. The arbor is located in a peripheral intracolumnar position. There are around 120 Dm12 neurons per hemisphere. They are glutamatergic (Davis et al., 2020).
Distal medullary wide-field amacrine neuron whose cell body is located in the cell body rind of the medulla. It projects asymmetrically along layers M2 and M3A forming mixed morphology arborizations (Morante and Desplan, 2008; Fischbach and Dittrich, 1989). The arborization is proximal to that of Dm15 in M2 and distal to Dm4, Dm12 and Dm20 in M3B. Its arbor has a distinct narrow and elongated shape, covering one column wide and 10 columns long. The arbors overlap significantly between cells, aligning with rows of medulla columns, and extending in one of two orthogonal orientations. It is a glutamatergic neuron (Raghu and Borst, 2011). The neurotransmitter was assessed by labelling cells with a vGlut[CNSIII]-GAL4 driver [FBti0129148] (Raghu and Borst, 2011). Pre- versus postsynaptic innervation judged by scoring of terminal morphology from figures in Fischbach and Dittrich (1989) as assessed by FlyBrain Neuron DB.
Dm3 neuron with posterior-ventrally oriented dendrites (Ozel et al., 2021). It can be distinguished from Dm3b based on its lack of bi expression (Ozel et al., 2021).
Dm3 neuron with posterior-dorsally oriented dendrites (Ozel et al., 2021). It can be distinguished from Dm3a based on its expression of bi (Ozel et al., 2021).
Distal medullary wide-field amacrine neuron whose cell body is located in the anterior region of the cell body rind of the medulla. The main neurite extends into M6, and then turns back to arborize in the boundary between M5 and M6, and in M3B, with mixed morphology arborizations. The arbor varies in shape between cells, covering around 21 columns, but with these areas tiling. It is located in a central position in the column, surrounded by the terminal of photoreceptors R7 and R8, with the cell boundaries following the column boundaries. There are around 40 Dm4 neurons per hemisphere. They are glutamatergic (Davis et al., 2020). Classified as columnar based on first stretch of main projection being limited to a single column, but as it then bends and projects along the plane of M5/M6 where it arborizes, this is clearly an edge case. Pre- versus postsynaptic innervation were judged by scoring of terminal morphology from figures in Fischbach and Dittrich (1989) as assessed by FlyBrain Neuron DB.
Distal medullary wide-field amacrine neuron that has a moderately broad, fine terminal arborization in layers M4-6. It is a glutamatergic neuron (Raghu and Borst, 2011). The neurotransmitter was assessed by labelling cells with a vGlut[CNSIII]-GAL4 driver [FBti0129148] (Raghu and Borst, 2011). Pre- versus postsynaptic innervation judged by scoring of terminal morphology from figures in Fischbach and Dittrich (1989) as assessed by FlyBrain Neuron DB.
Glutamatergic (Gao et al., 2008; Karuppudurai et al., 2014) distal medullary amacrine neuron that branches extensively in medulla layer M6A (Fischbach and Dittrich, 1989; Takemura et al., 2013; Nern et al., 2015), spanning approximately 16 medulla columns (Karuppudurai et al., 2014), with centrifugal projections back to layer M4 (Takemura et al., 2013; Nern et al., 2015). The highest arbor density is found in the center of the cell, within one column, with these regions tiling, while the rest of the arbor overlaps with other Dm8 cells considerably (Gao et al., 2008; Nern et al., 2015). In layer M6, it is postsynaptic to several R7 photoreceptor cells and presynaptic to Tm5c (Gao et al., 2008; Takemura et al., 2013; Karuppudurai et al., 2014). The contacts with Tm5c are clustered in one column at the center of the dendritic field of Dm8 (Karuppudurai et al., 2014). It is involved in UV preference (Gao et al., 2008). Connectivity inferred from EM reconstructions from a single EM section. The neurotransmitter was assessed in cells labelled with a glutamate GAL4 driver P{GawB}vGlut[OK371] [FBti0076967] (Gao et al., 2008), RT-PCR and by immunohistochemistry (Karuppudurai et al., 2014). Connectivity with R7 was assessed by EM reconstruction of a single medulla column (Gao et al., 2008) or reconstruction of serial-section TEM (Takemura et al., 2013).
Distal medullary wide-field amacrine neuron whose cell body is located in the ventral region of the cell body rind of the medulla. It as a tubular shape, and extends between the distal M1 and M6A layers. The arbors overlap in M1 and M6A, but otherwise tile. The processes in M2 and M5 occupy a central column position and are closely associated with R7 and R8 photoreceptor axons, covering around 7 columns. There are around 110 Dm9 neurons per hemisphere. They are glutamatergic (Davis et al., 2020).
Distal medullary amacrine neuron that branches extensively in medulla layers M1 to M4, with blob-like protrusions at the terminals. It is a glutamatergic neuron (Raghu and Borst, 2011). The neurotransmitter was assessed by labelling cells with a vGlut[CNSIII]-GAL4 driver (Raghu and Borst, 2011).
Dm11#1, FBbt:00111272 [transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; Dm11#1 (FAFB:11450453); VFB CATMAID Adult Brain (FAFB); adult brain; distal medullary amacrine neuron Dm11]
Dm11#2, FBbt:00111272 [transmission electron microscopy (TEM); is part of; Dm11#2 (FAFB:11444398); female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain; distal medullary amacrine neuron Dm11]
Dm11#3, FBbt:00111272 [transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain; distal medullary amacrine neuron Dm11; Dm11#3 (FAFB:11455071)]
Dm11#4, FBbt:00111272 [transmission electron microscopy (TEM); is part of; Dm11#4 (FAFB:17161735); female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain; distal medullary amacrine neuron Dm11]
Dm8#1, FBbt:00013774 [transmission electron microscopy (TEM); is part of; Dm8#1 (FAFB:10109586); female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#10, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; Dm8#10 (FAFB:10410432); JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#11, FBbt:00013774 [Dm8#11 (FAFB:10196189); transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#12, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; Dm8#12 (FAFB:10245571); JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#13, FBbt:00013774 [transmission electron microscopy (TEM); is part of; Dm8#13 (FAFB:10971698); female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#14, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain; Dm8#14 (FAFB:11445681)]
Dm8#15, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain; Dm8#15 (FAFB:10995248)]
Dm8#2, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain; Dm8#2 (FAFB:11453021)]
Dm8#3, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain; Dm8#3 (FAFB:10411811)]
Dm8#4, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; Dm8#4 (FAFB:10208775); JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#5, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; Dm8#5 (FAFB:11453311); VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#6, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain; Dm8#6 (FAFB:11500071)]
Dm8#7, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; Dm8#7 (FAFB:11523807); distal medullary amacrine neuron Dm8; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#8, FBbt:00013774 [transmission electron microscopy (TEM); is part of; female organism; Dm8#8 (FAFB:10419714); JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm8#9, FBbt:00013774 [Dm8#9 (FAFB:11447520); transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; distal medullary amacrine neuron Dm8; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm9#1, FBbt:00111271 [transmission electron microscopy (TEM); is part of; distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain; Dm9#1 (FAFB:11452427)]
Dm9#10, FBbt:00111271 [transmission electron microscopy (TEM); is part of; Dm9#10 (FAFB:10655888); distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm9#11, FBbt:00111271 [transmission electron microscopy (TEM); is part of; distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain; Dm9#11 (FAFB:14933802)]
Dm9#12, FBbt:00111271 [transmission electron microscopy (TEM); is part of; Dm9#12 (FAFB:14310274); distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm9#2, FBbt:00111271 [transmission electron microscopy (TEM); is part of; distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain; Dm9#2 (FAFB:11447061)]
Dm9#3, FBbt:00111271 [transmission electron microscopy (TEM); is part of; Dm9#3 (FAFB:11450495); distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm9#4, FBbt:00111271 [transmission electron microscopy (TEM); is part of; Dm9#4 (FAFB:11484679); distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm9#5, FBbt:00111271 [transmission electron microscopy (TEM); is part of; distal medullary amacrine neuron Dm9; female organism; Dm9#5 (FAFB:11454714); JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm9#6, FBbt:00111271 [transmission electron microscopy (TEM); is part of; Dm9#6 (FAFB:11444386); female organism; distal medullary amacrine neuron Dm9; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm9#7, FBbt:00111271 [transmission electron microscopy (TEM); is part of; distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain; Dm9#7 (FAFB:11916195)]
Dm9#8, FBbt:00111271 [transmission electron microscopy (TEM); is part of; Dm9#8 (FAFB:12013129); distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Dm9#9, FBbt:00111271 [transmission electron microscopy (TEM); Dm9#9 (FAFB:10657500); is part of; distal medullary amacrine neuron Dm9; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Neuromodulatory motor neuron developing from the VUM midline precursor. It innervates the dorsal oblique and acute muscles. Following Landgraf et al., 1997, larval motor neurons are named according to the muscle they innervate. The same caveats therefore apply regarding inference of serial homology from nomenclature as for the muscles: Following Bate (1993), larval hypodermal muscles are named for their orientation and numbered based on their order from dorsal to ventral or anterior to posterior. So, except where musculature is essentially identical between segments (as for A1-7, with a couple of exceptions for A1), serial homology should not be assumed on the basis of a shared name. VUM neurons are found in thoracic and abdominal segments (Schmid et al., 1999).
[transmission electron microscopy (TEM); larval mushroom body feed across neuron 10; FAN-10 (L1EM:9103732); VFB CATMAID L1 CNS; is part of; embryonic/larval nervous system; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); larval mushroom body feed across neuron 10; VFB CATMAID L1 CNS; is part of; embryonic/larval nervous system; L1 larval CNS ssTEM - Cardona/Janelia; FAN-10 (L1EM:9238937)]
[transmission electron microscopy (TEM); adult lateral horn PV5k1 neuron; VFB CATMAID Adult Brain (FAFB); JRC2018Unisex; adult brain template JFRC2; FB2H#1 (FAFB:1546454)]
effector genotype: ‘10xUAS-IVS-mCD8::GFP’ [confocal microscopy; TI{GAL4(DBD)::Zip-}dsx[GAL4-DBD] ∩ P{dVP16AD}VGlut[OK371-dVP16AD] expression pattern; Female_aDN; expression pattern fragment; is part of; adult doublesex aDN (female) neuron; female organism; JRC2018Unisex; adult brain]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; confocal microscopy; Gad1-F-000038; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; P{Gad1-GAL4.3.098} expression pattern; JRC2018Unisex; adult brain; overlaps; P{Gad1-GAL4.3.098}]
OutAge: Adult 5~15 days [expresses; confocal microscopy; FlyCircuit 1.0; adult intrinsic protocerebral bridge 18 glomeruli-2 glomeruli neuron; adult brain template JFRC2; Gad1-F-400111; expression pattern fragment; is part of; female organism; P{Gad1-GAL4.3.098} expression pattern; JRC2018Unisex; adult brain; overlaps; P{Gad1-GAL4.3.098}]
OutAge: Adult 5~15 days [Gad1-F-500016; expresses; confocal microscopy; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; P{Gad1-GAL4.3.098} expression pattern; female organism; JRC2018Unisex; adult brain; overlaps; P{Gad1-GAL4.3.098}; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
OutAge: Adult 5~15 days [expresses; confocal microscopy; Gad1-F-700035; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; P{Gad1-GAL4.3.098} expression pattern; JRC2018Unisex; adult brain; overlaps; P{Gad1-GAL4.3.098}; adult intrinsic protocerebral bridge 18 glomeruli-3 glomeruli neuron]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; posterior ventrolateral protocerebrum; confocal microscopy; Gad1-F-800054; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; P{Gad1-GAL4.3.098} expression pattern; female organism; JRC2018Unisex; adult brain; overlaps; P{Gad1-GAL4.3.098}]
OutAge: Adult 5~15 days [lobula columnar neuron LC4; expresses; confocal microscopy; Gad1-F-800081; FlyCircuit 1.0; adult brain template JFRC2; expression pattern fragment; is part of; female organism; P{Gad1-GAL4.3.098} expression pattern; JRC2018Unisex; adult brain; overlaps; P{Gad1-GAL4.3.098}]
[transmission electron microscopy (TEM); GlulOLP;left (L1EM:8700125); VFB CATMAID L1 CNS; optic lobe pioneer neuron 2; L1 larval CNS ssTEM - Cardona/Janelia]
[transmission electron microscopy (TEM); VFB CATMAID L1 CNS; optic lobe pioneer neuron 2; L1 larval CNS ssTEM - Cardona/Janelia; GlulOLP;right (L1EM:7897051)]
Glutamatergic local interneuron of the adult antennal lobe. The minority of local interneurons of the adult antennal lobe fall into this class. Most of the cell bodies of these interneurons belong to the ventral neuroblast lineage, and a few to the lateral neuroblast lineage. Inferred to be glutamatergic based on vesicular glutamate transporter (vGlut) expression detected by antibody (Chou et al., 2010).
Glutamatergic midline interneuron of the ventral nerve cord whose cell body is dorsal to the VUM and MNB cells. It develops from the MP3 precursor. Neurotransmitter was assessed by the expression of the vesicular glutamate transporter (vGlut) (FBgn0031424) (Wheeler et al., 2006).
Any hemilineage B (Notch OFF) neuron that develops from neuroblast NB5-7 during the postembryonic phase of neurogenesis. It is glutamatergic (Lacin et al., 2019).
Any hemilineage A (Notch ON) neuron that develops from neuroblast NB4-3 during the postembryonic phase of neurogenesis.
Any hemilineage B (Notch OFF) neuron that develops from neuroblast NB4-3 during the postembryonic phase of neurogenesis.
Any hemilineage B (Notch OFF) neuron that develops from neuroblast NB5-4 during the postembryonic phase of neurogenesis. It is glutamatergic (Lacin et al., 2019).
Any hemilineage A (Notch ON) neuron that develops from neuroblast NB3-3 during the postembryonic phase of neurogenesis. It is glutamatergic (Lacin et al., 2019).
Any hemilineage B (Notch OFF) neuron that develops from neuroblast NB3-5 during the postembryonic phase of neurogenesis. It is glutamatergic (Lacin et al., 2019).
tracing status-Roughly traced, cropped-False [ventral giant horizontal cell HSS; focussed ion beam scanning electron microscopy (FIB-SEM); JRC_FlyEM_Hemibrain; neuronbridge; is part of; HSS LPTC (FlyEM-HB:2179731270); female organism; Neuprint web interface - hemibrain:v1.1; JRC2018Unisex; adult brain]
L1#1, FBbt:00003719 [lamina monopolar neuron L1; transmission electron microscopy (TEM); is part of; L1#1 (FAFB:11472940); female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
L1#2, FBbt:00003719 [lamina monopolar neuron L1; transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; L1#2 (FAFB:10108985); VFB CATMAID Adult Brain (FAFB); adult brain]
L1#3, FBbt:00003719 [lamina monopolar neuron L1; transmission electron microscopy (TEM); is part of; L1#3 (FAFB:11472770); female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
L1#4, FBbt:00003719 [lamina monopolar neuron L1; transmission electron microscopy (TEM); is part of; female organism; L1#4 (FAFB:11470178); JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
L1#5, FBbt:00003719 [L1#5 (FAFB:11915725); lamina monopolar neuron L1; transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
L1#6, FBbt:00003719 [lamina monopolar neuron L1; transmission electron microscopy (TEM); is part of; female organism; L1#6 (FAFB:10654562); JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
L1#7, FBbt:00003719 [L1#7 (FAFB:12019444); lamina monopolar neuron L1; transmission electron microscopy (TEM); is part of; female organism; JRC2018Unisex; VFB CATMAID Adult Brain (FAFB); adult brain]
Intrinsic neuron of the lamina with arborizations spanning the proximal and distal lamina, whose cell body lies proximal to the lamina (Fischbach and Dittrich, 1989; Meinertzhagen and Sorra, 2001). It has extensive arborizations and forms a substantial number of presynaptic terminals with columnar neuron T1 and epithelial glia (Rivera-Alba et al., 2011). It receives strong input from each of photoreceptors R1-R6, and from lamina wide-field cells (Rivera-Alba et al., 2011). It is a glutamatergic neuron (Davis et al., 2020). Cell connectivity in the lamina was determined by analysis of semi-automated EM reconstruction of 749 serial sections of 21 complete lamina cartridges. The number of synaptic connections for Lai (presynaptic/postsynaptic) in a single lamina cartridge with each cell type was the following: R1 (-/36), R2 (1/39), R3 (-/39), R4 (2/37), R5 (2/35), R6 (-/40), L1 (1/-), L2 (1/-), L3 (10/-), L4 (4/2), L5 (4/-), Lai (1), T1 (54/1), C2 (1/5), C3 (1/9), Lawf (-/24) and epithelial glia (87/-) (Rivera-Alba et al., 2011).
A lamina monopolar neuron with short collaterals that project radially from the main projection in the lamina and arborizes in medulla layers M1 and M5 (Fischbach and Dittrich, 1989). In the lamina, these short collaterals are strongly postsynaptic to the terminals of photoreceptors R1-6 (Rivera-Alba et al., 2011). In the medulla, it makes strong reciprocal synaptic connections with lamina monopolar cell L5 and centrifugal neuron C2, as well as substantial output synapses to C3, Mi1 and Tm3 cells (Takemura et al., 2013). It is also electrically synapsed to lamina monopolar neuron L2 (Joesch et al., 2010). It is a glutamatergic neuron (Gao et al., 2008; Takemura et al., 2011). The neurotransmitter was assessed by labelling cells with a vGlut[OK371]-dVP16AD-GAL4 driver [FBti0129742] (Gao et al., 2008) or by single cell RT-PCR with specific primers (Takemura et al., 2011). Cell connectivity in the lamina was determined by analysis of semi-automated EM reconstruction of 749 serial sections of 21 complete lamina cartridges. The number of synaptic connections for L1 (presynaptic/postsynaptic) in a single lamina cartridge with each cell type was the following: R1 (-/40), R2 (-/43), R3 (-/37), R4 (-/38), R5 (-/38), R6 (-/45), L2 (-/3), Lai (-/1), C3 (-/3) and Lawf (-/1) (Rivera-Alba et al., 2011). Connectivity in the medulla was extrapolated from serial EM of 7 columns from a single sample (Takemura et al., 2013). Electrical connectivity was shown by dye labelling (Joesch et al., 2010).
Larval Pdf neuron of the abdominal neuromere with a larger cell body than the small Pdf neurons that are located more posteriorly (Helfrich-Forster, 1997).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is late-born in the NB2-1 Notch OFF primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron additionally turns back ventrally, close to the midline, at the end of the loop (Schneider-Mizell et al., 2016; Kohsaka et al., 2019). It receives input from the ipsilateral dorsal bipolar neuron dbp and outputs to the ipsilateral A27j neuron and A02b neurons of both hemineuromeres (Schneider-Mizell et al., 2016). These neurons were identified in a EM reconstruction of a volume that includes the posterior half of abdominal segment 2 and abdominal segment 3, of a 12-24h old first instar larva. The number of connections was estimated from the publication figures. The number of input synapses was the following (number in brackets left/right; ipsi- and contralateral connections separated by comma): from dbp (35/35), A02b (5/10). The number of output synapses was the following: to A27j (15/10), A02b (8, 18/20, 18) (Schneider-Mizell et al., 2016). Looper-1 synonym from catmaid.
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is late-born in the NB2-1 Notch OFF primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has a relatively large amount of dendritic arborization around the midline, crossing into the contralateral hemineuromere (Schneider-Mizell et al., 2016; Kohsaka et al., 2019). It receives input from the proprioceptors dmd1 (dda1), ddaD and vbp, and outputs onto the ipsilateral A03a1 (eIN-4) (axo-axonic connection) and RP2 motor neuron (Schneider-Mizell et al., 2016). These neurons were identified in a EM reconstruction of a volume that includes the posterior half of abdominal segment 2 and abdominal segment 3, of a 12-24h old first instar larva. The number of connections was estimated from the publication figures. The number of input synapses was the following (number in brackets left/right; ipsi- and contralateral connections separated by comma): from dda1 (15, 15/15, 15), ddaD (10, 4/15, 15), vbp (15, 8/15, 10), A02a (8, 18/20, 18). The number of output synapses was the following: to A03a1 (15/20), A02a (5/10), A1-7 dorsal motor neuron (12/12) (Schneider-Mizell et al., 2016).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is late-born in the NB2-1 Notch OFF primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has a bifurcation in the ventral part of the loop that produces a branch that extends back medially (Kohsaka et al., 2019).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is late-born in the NB2-1 Notch OFF primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has a bifurcation proximal to the loop, producing a branch that extends to the lateral contralateral neuropil (Kohsaka et al., 2019).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is late-born in the NB2-1 Notch ON primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has relatively dense arborization at the lateral and dorsal parts of the loop, where it has postsynapses and presynapses, respectively (Kohsaka et al., 2019). It is a premotor neuron (Burgos et al., 2018), targeting motor neurons in the same segment (Kohsaka et al., 2019). These neurons are activated in waves during forwards and backwards fictive locomotion (Kohsaka et al., 2019).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is late-born in the NB2-1 Notch ON primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has a bifurcation in the lateral part of the loop that produces a ventrally-extending branch, and the loop is relatively small, as the neurites do not travel far back medially (Kohsaka et al., 2019). It receives direct input from sensory neurons (Kohsaka et al., 2019) and it is a premotor neuron (Zarin et al., 2019).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is late-born in the NB2-1 Notch ON primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has relatively dense arborization at the lateral (postsynaptic) and dorsal (presynaptic) parts of the loop, and the loop is relatively small, as the neurites do not travel far back medially (Kohsaka et al., 2019). It receives direct input from sensory neurons (Kohsaka et al., 2019) and it is a premotor neuron (Burgos et al., 2018), targeting motor neurons in the same segment (Kohsaka et al., 2019).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is late-born in the NB2-1 Notch ON primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has a bifurcation in the lateral part of the loop that produces a relatively long ventrally-extending branch, and the loop is relatively small, as the neurites do not travel far back medially (Kohsaka et al., 2019). It receives direct input from sensory neurons (Kohsaka et al., 2019) and it is a premotor neuron (Zarin et al., 2019).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is early-born in the NB2-1 Notch ON primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has relatively dense arborization at the ventral and dorsal parts of the loop and extends into anterior segments (Kohsaka et al., 2019). It is a premotor neuron (Zarin et al., 2019).
Larval period-positive median segmental interneuron (PMSI) (Kohsaka et al., 2019) that is early-born in the NB2-1 Notch ON primary hemilineage (Mark et al., 2021). Like other PMSIs it has a ventral soma and it extends dorsally, close to the midline, then forms a loop in the dorsal neuropil (Kohsaka et al. , 2019). This neuron has relatively dense arborization at the lateral and dorsal parts of the loop and extends a long projection anteriorly (Kohsaka et al., 2019). It outputs to GDL neurons of the two segments anterior to itself, and motor neurons of its own segment (Fushiki et al., 2016). These neurons were identified in a EM reconstruction of the full CNS of a 6h old first instar larva. The number of output synapses was the following (number in brackets left/right): to GDL - one segment posterior (7), to GDL - two segments posterior (4/2), to A02l (2/-) (Fushiki et al., 2016).
Any larval A02a neuron (FBbt:00111662) that has soma location some larval abdominal 1 neuromere (FBbt:00111033).
Any larval A02b neuron (FBbt:00111664) that has soma location some larval abdominal 1 neuromere (FBbt:00111033).