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Figure 3 from: Schindler M, Hofmann MM, Wittmann D, Renner SS (2018) Courtship behaviour in the genus Nomada – antennal grabbing and possible transfer of male secretions. Journal of Hymenoptera Research 65: 47-59. https://doi.org/10.3897/jhr.65.24947
Figure 3 Modifications on the antennae of Nomadafucata ♂ (a) (left antenna, dorsal), N.flavoguttata ♂ (b) (right antenna, ventral) and N.lathburiana ♂ (c) (left antenna, lateral). SEM micrographs. a1 weak elevation on flagellum 6 laterally. Scale unit: 0.1 mm b1 weak elevations on flagellum 4 ventrally. Scale unit: 0.1 mm c1 nodule on flagellum 9. Scale unit: 0.1 mm a2 pores and secretions on the elevation. Scale unit: 0.01 mm b2 pores and setae on the elevations. Scale unit: 0.01 mm c2 nodule covered with secretions. Scale unit: 0.02 mm.
Figure 2 from: Schindler M, Hofmann MM, Wittmann D, Renner SS (2018) Courtship behaviour in the genus Nomada – antennal grabbing and possible transfer of male secretions. Journal of Hymenoptera Research 65: 47-59. https://doi.org/10.3897/jhr.65.24947
Figure 2 Mating of Nomadafucata (singular images of a video sequence). a ♂ mounts the ♀ and fixes its wings with its mid and hind legs. ♂ lifts the abdomen of the ♀ with its hind legs and tries to insert its genitalia in the female´s genital opening b ♂ entangles the female´s left antenna with its left flagellum c ♂ pulls its left flagellum from medial to apical along the female antenna d ♂ repeatedly entangles the female´s antennae with its left and right flagellum and pulls it off medially to apically. ♂ tries to insert its genitalia.
Figure 1 from: Schindler M, Hofmann MM, Wittmann D, Renner SS (2018) Courtship behaviour in the genus Nomada – antennal grabbing and possible transfer of male secretions. Journal of Hymenoptera Research 65: 47-59. https://doi.org/10.3897/jhr.65.24947
Figure 1 Mating of Nomadalathburiana (a, b) in the lab and of N.flavoguttata on Taraxacumofficinale s.l.. (c, d). a ♂ mounts the ♀ and fixes its wings with its mid and hind legs and tries to entangle the female´s antennae spirally with its flagella. ♂ lifts the abdomen of the ♀ with its hind legs and tries to insert its genitalia in the female´s genital opening b ♂ repeatedly spirally entangles the female´s antennae with its left and right flagellum and pulls it off medially to apically. ♂ tries to insert its genitalia repeatedly c ♂♂ patrolling at a blossom of T.officinaled Insertion phase of copulation. Antennation of ♂ as described in (b).
Supplementary material 5 from: Cahoon AB, Huffman AG, Krager MM, Crowell RM (2018) A meta-barcoding census of freshwater planktonic protists in Appalachia – Natural Tunnel State Park, Virginia, USA. Metabarcoding and Metagenomics 2: e26939. https://doi.org/10.3897/mbmg.2.26939
Table 3. Diversity Indices. :
Supplementary material 3 from: Cahoon AB, Huffman AG, Krager MM, Crowell RM (2018) A meta-barcoding census of freshwater planktonic protists in Appalachia – Natural Tunnel State Park, Virginia, USA. Metabarcoding and Metagenomics 2: e26939. https://doi.org/10.3897/mbmg.2.26939
Table 1. All Detected Taxa :
Supplementary material 1 from: Cahoon AB, Huffman AG, Krager MM, Crowell RM (2018) A meta-barcoding census of freshwater planktonic protists in Appalachia – Natural Tunnel State Park, Virginia, USA. Metabarcoding and Metagenomics 2: e26939. https://doi.org/10.3897/mbmg.2.26939
Figure 1. Sample collection sites :
Supplementary material 6 from: Cahoon AB, Huffman AG, Krager MM, Crowell RM (2018) A meta-barcoding census of freshwater planktonic protists in Appalachia – Natural Tunnel State Park, Virginia, USA. Metabarcoding and Metagenomics 2: e26939. https://doi.org/10.3897/mbmg.2.26939
Table 4. The protist genera identified in Natural Tunnel State Park organised by read count. :
Supplementary material 4 from: Cahoon AB, Huffman AG, Krager MM, Crowell RM (2018) A meta-barcoding census of freshwater planktonic protists in Appalachia – Natural Tunnel State Park, Virginia, USA. Metabarcoding and Metagenomics 2: e26939. https://doi.org/10.3897/mbmg.2.26939
Table 2. Primers and PCR Conditions. :
Figure 10 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 10 Comparison of male palp of Porrhoclubionaleucaspis (a), P.moradmandi sp. n. (b), P.laudata (c) and P.bosmansi sp. n. (d). a–d palps in the same scale a'–d' palps shown in the same size, demonstrating different proportions. Arrows point major differenced, broken inclined line reflects differences in the angle of embolic base anterior margin, ca 25°, 8°, 10.5° and 19°. Abbreviations: Eb–base of embolus, Ts–sclerotised part of tegulum.
Figure 1 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 1 General appearance of Clubionapallidula (a), Porrhoclubionalaudata (b), P.bosmansi sp. n. (c, e) and P.moradmandi sp. n. (d). a prosoma, dorsal b–d male habitus, dorsal e female habitus, dorsal.
Figure 6 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 6 Male palp of Porrhoclubionalaudata (a–c) and P.leucaspis (d–f). a, d ventral b, f prolateral c, e retrolateral. Abbreviations: At–anterior part of tegulum, Pt–prolateral tibial apophysis, St–subtegulum.
Figure 9 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 9 Endogyne and bulb of Porrhoclubionabosmansi sp. n. (a), P.moradmandi sp. n. (b, d) and P.leucaspis (c). a–b endogyne, dorsal c–d macerated tegulum, ventral, showing course of sperm duct. Abbreviations: Eb–base of embolus, Dl–loop of copulatory duct, Ts–sclerotised part of tegulum, St–subtegulum.
Figure 5 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 5 SEM micrographs of the male palp of Porrhoclubionabosmansi sp. n. (a, g), P.moradmandi sp. n. (b, d, e) and P.leucaspis (c, f). a–c modified cymbial setae d proximal part of cymbium with modified short setae e–f tibial apophysis g basoretrolateral part of cymbium showing tutaculum and tegular groove. Abbreviations: Fl–filamentous extension, Ms–modified short setae, Sb–basal part of setae, Tg–tegular groove, Tu–tutaculum.
Figure 7 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 7 Male palp of Porrhoclubionamoradmandi sp. n. (a–c) and P.bosmansi sp. n. (d–f). Abbreviations: Pt–prolateral tibial apophysis, St–subtegulum.
Figure 3 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 3 SEM micrographs of the female leg I of Porrhoclubionabosmansi sp. n. a whole leg, prolateral b metatarsus, subventral c distal part of tarsus, lateral, showing tarsal organ d femur, showing bold areas and spine e tibia, showing spines with locking mechanism f tarsus, subventral, showing spines lacking locking mechanism g trichobothrium. Abbreviations: Ba–bald areas, Lm–locking mechanism, To–tarsal organ.
Figure 8 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 8 Epigyne of Porrhoclubionamoradmandi sp. n. (a–c), P.bosmansi sp. n. (d–f) and P.leucaspis (g–i). a, d, g intact, ventral a, d, g intact, ventral b, e, h macerated, ventral c, f, i macerated, dorsal. Abbreviations: Dl–loop of copulatory duct, Hr–hyaline (secondary) receptacle, Sr–sclerotized (primary) receptacle.
Figure 4 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 4 SEM micrographs of the male palp of Porrhoclubionabosmansi sp. n. (a–c), P.moradmandi sp. n. (d–f) and P.leucaspis (g–i). a, d, g retrolateral b, e retro-ventral h ventral c, i tibia and proximal part of bulb and cymbium; retrolateral f cymbium and part of tegulum, retrolateral. Abbreviations: At–anterior part of tegulum, Eb–base of embolus, Fl–filamentous extension, Pt–prolateral tibial apophysis, St–subtegulum, Tg–tegular groove, Ts–sclerotised part of tegulum, Tu–tutaculum.
Figure 2 from: Marusik YM, Omelko MM (2018) A survey of the Porrhoclubiona Lohmander, 1944 from Central Asia (Araneae, Clubiondae). ZooKeys 802: 19-38. https://doi.org/10.3897/zookeys.802.30236
Figure 2 Somatic characters of Porrhoclubionabosmansi sp. n. (a–d, j) and Clubionapallidula (e, f–i). a, h anterior part of male prosoma, ventral, showing mouth parts b, f left male chelicera, mesal c, g left male chelicera, posterior e female tibia–tarsus I, prolateral d female leg I, prolateral i–j maxilla and labium, ventral.
Figures 8-10 from: De Assis JE, Souza JRB, Lima MM, Lima GV, Cordeiro RTS, Pérez CD (2019) Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13. https://doi.org/10.3897/zoologia.36.e28714
Figures 8-10 (8) Corallum morphology of Stylopathesadinocrada; (9) pinnulation pattern of S.adinocrada, showing the "worm run"; (10) organization of spines in S.adinocrada. Scale bars: 8–9 = 10 mm, 10: 100 µm.
Figures 2-7 from: De Assis JE, Souza JRB, Lima MM, Lima GV, Cordeiro RTS, Pérez CD (2019) Association between deep-water scale-worms (Annelida: Polynoidae) and black corals (Cnidaria: Antipatharia) in the Southwestern Atlantic. Zoologia 36: 1-13. https://doi.org/10.3897/zoologia.36.e28714
Figures 2-7 (2) Benhamypolynoecf.antipathicola on the branches of Stylopathesadinocrada: (3) median chaetigers of B.antipathicola showing elytrophores, elytra and dorsal cirri; (4) head of B.antipathicola showing the prostomium, palps and antennae; (5) posterior chaetigers of B.antipathicola showing the ventral cirrus and neuropodia; (6) neurochaetae from posterior chaetigers, showing a faint serration; (7) detail of distal tip of neurochaetae. (ch) chaetae, (dc) dorsal cirrus, (el) elytra, (et) elytrophore, (ct) cirratophore, (la) lateral antennae; (ma) median antennae, (ne) neuropodium, (pa) parapodium, (pl) palp, (pr) prostomium, (tc) tentacular cirrus. Scale bars: 2–4: 1 mm, 5 = 200 µm, 6 = 100 µm, 7 = 10 µm.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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International Brain Laboratory public data
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OpenNeuro
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