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Figures 157–174. 157–160. Brachiacantha clara. 157 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 157–174. 157–160. Brachiacantha clara. 157) Habitus. 158) Phallobase ventral. 159) Phallobase lateral. 160) Sipho. 161–167. Brachiacantha groendali. 161) Habitus. 162) Phallobase lateral. 163) Phallobase ventral. 164) Sipho. 165) Siphonal apex dorsal. 166) Enlarged siphonal apex obliquely lateral. 167) Female genitalia. 168–174. Brachiacantha eva. 168) Habitus. 169) Protibia. 170) Phallobase ventral. 171) Phallobase lateral. 172) Sipho. 173) Enlarged siphonal apex. 174) Female genitalia.
Figures 108–127. 108–113. Brachiacantha sally. 108 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 108–127. 108–113. Brachiacantha sally. 108) Habitus. 109) Phallobase ventral. 110) Phallobase lateral. 111) Sipho. 112) Siphonal apex. 113) Enlarged siphonal apex. 114–119. Brachiacantha regina. 114) Habitus. 115) Phallobase ventral. 116) Phallobase lateral. 117) Sipho. 118) Siphonal apex dorsal. 119) Enlarged siphonal apex. 120–127. Brachiacantha darlene. 120) Habitus. 121) Protibia. 122) Phallobase ventral. 123) Phallobase lateral. 124) Sipho. 125) Enlarged siphonal apex lateral. 126) Siphonal apex dorsal. 127) Female spermathecal capsule and bursal cap.
Figures 128–138. 128–133. Brachiacantha veronica. 128 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 128–138. 128–133. Brachiacantha veronica. 128) Habitus. 129) Phallobase ventral. 130) Phallobase lateral. 131) Sipho. 132) Siphonal apex dorsal. 133) Enlarged siphonal apex lateral. 134–135. Brachiacantha lauren. 134) Habitus. 135) Female spermathecal capsule. 136–138. Brachiacantha cathy. 136) Habitus. 137) Protibia. 138) Female genitalia.
Figures 88–107. 88–94. Brachiacantha octopustulata. 88 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 88–107. 88–94. Brachiacantha octopustulata. 88) Habitus. 89) Phallobase ventral. 80) Phallobase lateral. 91) Sipho. 92) Enlarged siphonal apex lateral. 93) Enlarged siphonal apex dorsal. 94) Female genitalia. 95–102. Brachiacantha loricata. 95) Habitus. 96) Phallobase ventral. 97) Phallobase lateral. 98) Sipho. 99) Enlarged siphonal apex lateral. 100) Enlarged siphonal apex dorsal. 101) Enlarged siphonal apex dorsal. 102) Female genitalia. 103–107. Brachiacantha lynn. 103) Habitus. 104) Phallobase ventral. 104) Phallobase lateral. 106) Sipho. 107) Enlarged siphonal apex.
Figures 69–87. 69–74. Brachiacantha hazel. 69 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 69–87. 69–74. Brachiacantha hazel. 69) Habitus. 70) Protibia. 71) Phallobase ventral. 72) Phallobase lateral. 73) Sipho. 74) Enlarged siphonal apex. 75–80. Brachiacantha armandi. 75) Habitus. 76) Phallobase ventral. 77) Phallobase lateral. 78) Sipho. 79) Enlarged siphonal apex. 80) Female genitalia. 81–87. Brachiacantha margaritae. 81) Habitus. 82) Phallobase ventral. 83) Phallobase lateral. 84) Sipho. 85) Enlarged siphonal apex lateral. 86) Enlarged siphonal apex dorsal. 87) Female genitalia.
Figures 18–35. 18–23. Brachiacantha sellata. 18 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 18–35. 18–23. Brachiacantha sellata. 18) Habitus. 19) Phallobase ventral. 20) Phallobase lateral. 21) Sipho. 22) Enlarged siphonal apex. 23) Female genitalia. 24–30. Brachiacantha bruchi. 24) Habitus. 25) Phallobase ventral. 26) Phallobase lateral. 27) Sipho. 28) Enlarged siphonal apex lateral. 29) Enlarged siphonal apex dorsal. 30) Female genitalia. 31–35. Brachiacantha esther. 31) Habitus. 32) Phallobase ventral. 33) Phallobase lateral. 34) Sipho. 35) Enlarged siphonal apex.
Figures 51–68. 51–55. Brachiacantha joanne. 51 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 51–68. 51–55. Brachiacantha joanne. 51) Habitus. 52) Phallobase ventral. 53) Phallobase lateral. 54) Sipho. 55) Enlarged siphonal apex. 56–62. Brachiacantha juanita. 56) Habitus. 57) Phallobase ventral. 58) Phallobase lateral. 59) Sipho. 60) Enlarged siphonal apex lateral. 61) Enlarged siphonal apex dorsal. 62) Female genitalia. 63–68. Brachiacantha anita. 63) Habitus. 64) Phallobase ventral. 65) Phallobase lateral. 66) Sipho. 67) Enlarged siphonal apex. 68) Female genitalia.
Figures 36–50. 36–40. Brachiacantha pauline. 36 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 36–50. 36–40. Brachiacantha pauline. 36) Habitus. 37) Phallobase ventral. 38) Phallobase lateral. 39) Sipho. 40) Enlarged siphonal apex. 41–45. Brachiacantha emma. 41) Habitus. 42) Phallobase ventral. 43) Phallobase lateral. 44) Sipho (basal 2/3). 45) Female spermathecal capsule and bursal cap. 46–50. Brachiacantha jamie. 46) Habitus. 47) Phallobase ventral. 48) Phallobase lateral. 49) Sipho. 50) Enlarged siphonal apex.
Figures 1–17. 1–6. Brachiacantha bistripustulata. 1 in South American Coccinellidae (Coleoptera), Part XVI: systematic revision of Brachiacantha Dejean (Coccinellinae: Hyperaspidini)
Figures 1–17. 1–6. Brachiacantha bistripustulata. 1) Habitus. 2) Phallobase ventral. 3) Phallobase lateral. 4) Sipho. 5) Enlarged siphonal apex. 6) Female genitalia. 7–12. Brachiacantha buckleyi. 7) Habitus. 8) Phallobase ventral. 9) Phallobase lateral. 10) Sipho. 11) Enlarged siphonal apex. 12) Female spermathecal capsule. 13–17. Brachiacantha charlotte. 13) Habitus. 14) Phallobase ventral. 15) Phallobase lateral. 16) Sipho. 17) Enlarged siphonal apex.
Figures 11–20 in Systematic revision of the genus Trichonotuloides Balthasar, 1945 with description of two new Mexican species (Coleoptera: Scarabaeidae: Aphodiinae)
Figures 11–20. Trichonotuloides hansferyi, new species (Los Laureles, Ixhuacán de los Reyes, Veracruz, Mexico). 11) Epipharynx. 12–13) Habitus (length ideogram and morphological details). 14–15) Aedeagus (dorsal and lateral views). Trichonotuloides latecrenatus (Bates, 1887) (Totonicapam, Guatemala). 16) Epipharynx. 17–18) Habitus (morphological details and length ideogram). 19–20) Aedeagus (dorsal and lateral views).
Figures 1–10 in Systematic revision of the genus Trichonotuloides Balthasar, 1945 with description of two new Mexican species (Coleoptera: Scarabaeidae: Aphodiinae)
Figures 1–10. Trichonotuloides alfonsinae, new species (Pico de Orizaba, Veracruz, Mexico). 1) Epipharynx. 2–3) Habitus (length ideogram and morphological details). 4–5) Aedeagus (dorsal and lateral views). Trichonotuloides glyptus (Bates, 1887) (Toluca, México, Mexico). 6) Epipharynx. 7–8) Habitus (morphological details and length ideogram). 9–10) Aedeagus (dorsal and lateral views).
Figure 2 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 2. The tadpole of Adenomera sp. Above: lateral view of the left side (scale bar: 4.0 mm). Below: detail of the oral apparatus (scale bar: 0.5 mm). Specimen from Uberlândia (MG, Brazil).
Figure 1 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 1. Rainfall in the municipality of Uberlândia. Lines represent median values over the last 21 years; columns represent values accumulated over the pitfall sampling period (seasons 1999/2000 and 2000/2001). Data from meteorological station of the Universidade Federal de Uberlândia (Campus Santa Mônica).
Figure 4 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 4. Oscillogram (first row), audiospectrogram (second and fourth rows) and power spectrum (third row) of the advertisement call of Adenomera sp. The first three rows are representations of single notes, the fourth represents a sequence of three notes. Recording files: first column, Adenomspmg2AAGd (17 December 2003, 17:00 h, air 24°C, unvouchered recording); second column, AdenomspmgAAGd (10 December 2003, 20:10 h, air 26°C, unvouchered recording); fourth row, AdenomspmgAAG21 (5 October 1999, 19:40 h, air 21°C, voucher AAG-UFU 2633).
Figure 3 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 3. Monthly variation in abundance of adults (males and females) and juveniles of Adenomera sp. in pitfall traps in two localities at the municipality of Uberlândia, Minas Gerais, Brazil. Above: Caça e Pesca sample (N572 adults, 32 juveniles). Below: Panga sample (N513 adults and 13 juveniles). Sampling period from October 1999 to October 2001. The monthly samples are not independent, since the trapped specimens were removed from the environment.
Figure 5 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 5. Territorial call of Adenomera sp. Above left: audiospectrogram of a sequence of three calls. Above right: oscillogram of single note. Below left: audiospectrogram of single note. Below right: power spectrum of single note. Record file AdenomspmgbAAG27, 14 November 2002, 20:30 h, air 23.0°C (unvouchered).
Figure 1 in Redescription and systematic status of the Antarctic genus Abietinella Levinsen, 1913 (Lafoeidae, Hydrozoa, Cnidaria)
Figure 1. Abietinella operculata (Jäderholm, 1903), holotype SMNH 5708. (A) Apical portion of colony; (B) hydrotheca with dish-shaped operculum and basal lateral nematothecae; (C) lateral view of hydrotheca and apophysis; (D) hydrotheca and hydranth with abcauline triangular caecum; (E) hydrothecal diaphragm; (F) origin of lateral branch; (G) hydrothecal rim renovation; (H) basal hydrotheca without nematothecae. Scale bars: 2 mm (A); 200 Mm (B–D, H); 50 Mm (E, G); 400 Mm (F).
Figure 14 in Systematics and zoogeography of the deep-sea hyperbenthic family Arietellidae (Copepoda: Calanoida) collected from the Sulu Sea
Figure 14. Cladogram of arietellid genera including the two new genera, Metacalanalis and Protoparamisophria. Main habitat and depth range provided only for hyperbenthic genera, excluding two truly pelagic genera, Arietellus and Paraugaptilus.
Figure 1. Metacalanalis hakuhoae n. gen., n in Systematics and zoogeography of the deep-sea hyperbenthic family Arietellidae (Copepoda: Calanoida) collected from the Sulu Sea
Figure 1. Metacalanalis hakuhoae n. gen., n. sp., female (holotype). (A) Habitus, dorsal; (B) habitus, lateral; (C) rostrum, ventral; (D) last compound pedigerous somite and genital double-somite, lateral; (E) genital doublesomite, ventral; (F) left antennule; (G) terminal segments of left antennule; (H) right antennule; (I) terminal segment of right antennule; (J) terminal segments of antennary endopod; (K) antennary exopod, terminal segments missing. Scale bars in mm.
Figure 13. Sarsarietellus suluensis n in Systematics and zoogeography of the deep-sea hyperbenthic family Arietellidae (Copepoda: Calanoida) collected from the Sulu Sea
Figure 13. Sarsarietellus suluensis n. sp., male (holotype). (A) Leg 1, anterior; (B) endopod of leg 1, anterior; (C) leg 2, anterior; (D) outer distal corner of second endopodal segment of leg 2; (E) leg 3, anterior; (F) leg 4, posterior; (G) leg 5, posterior. Scale bars in mm.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.