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Рис.5. СоотношениеразΛичныхгнезΑовыхтиповопорв 2018–2019 гг. поаΑминистративным районам (Λевый график) и в цеΛом по Амурской обΛасти (правый график) Fig. 5. The ratio of different types of nesting supports in 2018–2019 by administrative districts (right graph) and in general in the Amur region (left graph) in Oriental stork (Ciconia boyciana Swinhoe) breeding population survey in the Amur region in 2018-2019
Рис.5. СоотношениеразΛичныхгнезΑовыхтиповопорв 2018–2019 гг. поаΑминистративным районам (Λевый график) и в цеΛом по Амурской обΛасти (правый график) Fig. 5. The ratio of different types of nesting supports in 2018–2019 by administrative districts (right graph) and in general in the Amur region (left graph)
Рис. 4. Фотографии жиΛых гнезΑ в заказнике «Амурский» на искусственных гнезΑовых треногах (сΛева — «активное», справа — «засеΛенное») Fig. 4. Photos of inhabited nests in the Amursky wildlife reserve that are located on artificial nesting structures ("active" on the left and "inhabited" on the right) in Oriental stork (Ciconia boyciana Swinhoe) breeding population survey in the Amur region in 2018-2019
Рис. 4. Фотографии жиΛых гнезΑ в заказнике «Амурский» на искусственных гнезΑовых треногах (сΛева — «активное», справа — «засеΛенное») Fig. 4. Photos of inhabited nests in the Amursky wildlife reserve that are located on artificial nesting structures ("active" on the left and "inhabited" on the right)
→ Fig. 2. Representative skeletal elements of ornithosuchid archosaur Dynamosuchus collisensis gen. et sp. nov. (CAPPA/UFSM 0248) from Janner outcrop, Carnian, Late Triassic. A. Selected skull bones in left lateral view. B. Reconstruction of the skull. C. Skull in ventral view. D. Left quadrate and quadratojugal in posterodorsal view. E. Parabasisphenoid in left lateral view. F. Neural arch of an anterior cervical vertebra in anterior view. G. Centrum of a cervical vertebra in left lateral view. H. Right osteoderm in dorsal view. I. Neural arch of an anterior dorsal vertebra in left lateral view. J. Left ilium in lateral view. L. Right humerus in anterior view. M. Right forearm in medial view. N. Left manus in dorsal view. O. Right (reversed) pubis in lateral view. P. Left femur in anterior view. Q. Left fibula in lateral view. Some unpreserved portions are modified from Baczko et al. in press, for the reconstruction of the skeleton of CAPPA/UFSM 0248 (preserved elements indicated in orange) (K). Scale bars 20 mm. in The first ornithosuchid from Brazil and its macroevolutionary and phylogenetic implications for Late Triassic faunas in Gondwana
→ Fig. 2. Representative skeletal elements of ornithosuchid archosaur Dynamosuchus collisensis gen. et sp. nov. (CAPPA/UFSM 0248) from Janner outcrop, Carnian, Late Triassic. A. Selected skull bones in left lateral view. B. Reconstruction of the skull. C. Skull in ventral view. D. Left quadrate and quadratojugal in posterodorsal view. E. Parabasisphenoid in left lateral view. F. Neural arch of an anterior cervical vertebra in anterior view. G. Centrum of a cervical vertebra in left lateral view. H. Right osteoderm in dorsal view. I. Neural arch of an anterior dorsal vertebra in left lateral view. J. Left ilium in lateral view. L. Right humerus in anterior view. M. Right forearm in medial view. N. Left manus in dorsal view. O. Right (reversed) pubis in lateral view. P. Left femur in anterior view. Q. Left fibula in lateral view. Some unpreserved portions are modified from Baczko et al. in press, for the reconstruction of the skeleton of CAPPA/UFSM 0248 (preserved elements indicated in orange) (K). Scale bars 20 mm.
Рис. 1. Раковины Mya truncata (А–Г) (Белое море) и Laternula elliptica (А'–Г') (Зал. Прюдс): А, А' – обЩий вид; Б, Г' – внутреннЯЯ поверхность левых створок; В, В' – вид хондрофора со стороны дорсального краЯ; Г, Б' – внутреннЯЯ поверхность правых створок. ОбоЗначениЯ: пК – передний край раковины; ЗК – Задний край; дК – дорсальный край; м – макушка; мщ – макушечнаЯ (умбональнаЯ) Щель; Кс – концентрическаЯ скульптура; сКп – складки периостракума; хр – хондрофор; ппЛ – поддерживаюЩаЯ пластинка; син – синус; ОмЗ – отпечаток мускула-ЗамыкателЯ. Fig. 1. Shells of Mya truncata (А–Г) (White Sea) and Laternula elliptica (А'–Г') (Prydz Bay): A, A' – general view; Б, Г' – internal view of left valves; В, В' – dorsal view on chondrophores; Г, Б' – internal view of right valves. Notes: пК – anterior margin; ЗК – posterior margin; дК – dorsal margin; м – umbo; мщ – umbonal crack; Кс – concentric sculpture; сКп – periostracal wrinkles; хр – chondrophore; ппЛ – buttress; син – sinus; ОмЗ – trace of retractor muscle. in Species of warm-water origin Laternula elliptica (King, 1832) (Mollusca: Bivalvia: Laternulidae), a widespread mollusk in recent Antarctica
Рис. 1. Раковины Mya truncata (А–Г) (Белое море) и Laternula elliptica (А'–Г') (Зал. Прюдс): А, А' – обЩий вид; Б, Г' – внутреннЯЯ поверхность левых створок; В, В' – вид хондрофора со стороны дорсального краЯ; Г, Б' – внутреннЯЯ поверхность правых створок. ОбоЗначениЯ: пК – передний край раковины; ЗК – Задний край; дК – дорсальный край; м – макушка; мщ – макушечнаЯ (умбональнаЯ) Щель; Кс – концентрическаЯ скульптура; сКп – складки периостракума; хр – хондрофор; ппЛ – поддерживаюЩаЯ пластинка; син – синус; ОмЗ – отпечаток мускула-ЗамыкателЯ. Fig. 1. Shells of Mya truncata (А–Г) (White Sea) and Laternula elliptica (А'–Г') (Prydz Bay): A, A' – general view; Б, Г' – internal view of left valves; В, В' – dorsal view on chondrophores; Г, Б' – internal view of right valves. Notes: пК – anterior margin; ЗК – posterior margin; дК – dorsal margin; м – umbo; мщ – umbonal crack; Кс – concentric sculpture; сКп – periostracal wrinkles; хр – chondrophore; ппЛ – buttress; син – sinus; ОмЗ – trace of retractor muscle.
Рис. 2. A, B. Modiolus (Modiolus) kurilensis Bernard, 1983: леваЯ створка снаружи (A), иЗнутри (B). Длина раковины 26.4 мм, высота – 47.3 мм; C, D. Gari (Gobraeus) kazusensis (Yokoyama, 1922): леваЯ створка снаружи (C), иЗнутри (D). Длина раковины 71.0 мм, высота – 39.9 мм. E, F. Panomya norvegica (Spengler, 1973): леваЯ створка снаружи (E), праваЯ створка иЗнутри (F). Длина раковины 70.8 мм, высота – 44.5 мм, толЩина – 36.7 мм. Fig. 2. A, B. Modiolus (Modiolus) kurilensis Bernard, 1983: left valve (A) outside, (B) inside. Shell length 26.4 mm, height – 47.3 mm. C, D. Gari (Gobraeus) kazusensis (Yokoyama, 1922): left valve (C) outside, (D) inside. Shell length 71.0 mm, height – 39.9 mm. E, F. Panomya norvegica (Spengler, 1973): left valve (E) outside, right valve (F) inside. Shell length 70.8 mm, height – 44.5 mm, thickness – 36.7 mm. in On the species composition of marine bivalves of the Sikhote-Alin Reserve (northern Primorye, Japan/East Sea)
Рис. 2. A, B. Modiolus (Modiolus) kurilensis Bernard, 1983: леваЯ створка снаружи (A), иЗнутри (B). Длина раковины 26.4 мм, высота – 47.3 мм; C, D. Gari (Gobraeus) kazusensis (Yokoyama, 1922): леваЯ створка снаружи (C), иЗнутри (D). Длина раковины 71.0 мм, высота – 39.9 мм. E, F. Panomya norvegica (Spengler, 1973): леваЯ створка снаружи (E), праваЯ створка иЗнутри (F). Длина раковины 70.8 мм, высота – 44.5 мм, толЩина – 36.7 мм. Fig. 2. A, B. Modiolus (Modiolus) kurilensis Bernard, 1983: left valve (A) outside, (B) inside. Shell length 26.4 mm, height – 47.3 mm. C, D. Gari (Gobraeus) kazusensis (Yokoyama, 1922): left valve (C) outside, (D) inside. Shell length 71.0 mm, height – 39.9 mm. E, F. Panomya norvegica (Spengler, 1973): left valve (E) outside, right valve (F) inside. Shell length 70.8 mm, height – 44.5 mm, thickness – 36.7 mm.
РИС. 8. Примеры проблем с иЗображением при работе на СЭМ. А, В. Засветка раЗличных частей раковин глохидиев (А. Anodonta anatina (=Colletopterum), оЗ. Красное, ХакасиЯ. В. Inversiunio reinianus, оЗ. Бива, о-в Хонсю, ЯпониЯ). C. РаЗнаЯ скорость сканированиЯ (слева – очень быстраЯ, справа – медленнаЯ) наружной поверхности глохидиЯ (Anodonta cygnea, р. Ялма, МосковскаЯ обл.). D. Артефакты в виде гориЗонтальных полос вследствие накоплениЯ отрицательного ЗарЯда при недостаточном напылении внутренней поверхности глохидиЯ (Nodularia douglasiae, ПетровскаЯ протока, бассейн р. Амур, Хабаровский кр.). МасШтаб 50 мкм (А, В), 2 мкм (С), 5 мкм (D). Микроскопы Zeiss EVO 40 (А, С, D), Zeiss MERLIN (В), напыление углеродом (А, С), хромом (В, D). FIG. 8. Illustration of different problems with SEM images. A, B. Overall illumination of some glochidia shells parts (A. Anodonta anatina (= Colletopterum), Krasnoe Lake, Khakassia. B. Inversiunio reinianus, Biwa Lake, Honshu Island, Japan). C. Different scanning speed (faster on the left and slower on the right) of the exterior glochidia valve (Anodonta cygnea, Yalma River, Moscow Oblast). D. Artifacts as horizontal stripes because of additional accumulation of a negative charge due to insufficient coating of the interior glochidia valve (Nodularia douglasiae, Petrovskaya channel, Amur River basin, Khabarovsk Krai). Scale bars 50 μm (A, B), 2 μm (C), 5 μm (D). Zeiss EVO 40 (A, C, D) and Zeiss MERLIN (B) microscopes, sputter coating with carbon (A, C) and chromium (B, D). in Методика подготовки раковин глохидиев (Bivalvia, Unionidae) длЯ работы на сканируюЩем Электронном микроскопе
РИС. 8. Примеры проблем с иЗображением при работе на СЭМ. А, В. Засветка раЗличных частей раковин глохидиев (А. Anodonta anatina (=Colletopterum), оЗ. Красное, ХакасиЯ. В. Inversiunio reinianus, оЗ. Бива, о-в Хонсю, ЯпониЯ). C. РаЗнаЯ скорость сканированиЯ (слева – очень быстраЯ, справа – медленнаЯ) наружной поверхности глохидиЯ (Anodonta cygnea, р. Ялма, МосковскаЯ обл.). D. Артефакты в виде гориЗонтальных полос вследствие накоплениЯ отрицательного ЗарЯда при недостаточном напылении внутренней поверхности глохидиЯ (Nodularia douglasiae, ПетровскаЯ протока, бассейн р. Амур, Хабаровский кр.). МасШтаб 50 мкм (А, В), 2 мкм (С), 5 мкм (D). Микроскопы Zeiss EVO 40 (А, С, D), Zeiss MERLIN (В), напыление углеродом (А, С), хромом (В, D). FIG. 8. Illustration of different problems with SEM images. A, B. Overall illumination of some glochidia shells parts (A. Anodonta anatina (= Colletopterum), Krasnoe Lake, Khakassia. B. Inversiunio reinianus, Biwa Lake, Honshu Island, Japan). C. Different scanning speed (faster on the left and slower on the right) of the exterior glochidia valve (Anodonta cygnea, Yalma River, Moscow Oblast). D. Artifacts as horizontal stripes because of additional accumulation of a negative charge due to insufficient coating of the interior glochidia valve (Nodularia douglasiae, Petrovskaya channel, Amur River basin, Khabarovsk Krai). Scale bars 50 μm (A, B), 2 μm (C), 5 μm (D). Zeiss EVO 40 (A, C, D) and Zeiss MERLIN (B) microscopes, sputter coating with carbon (A, C) and chromium (B, D).
Рис. 6. Ювенильные раковины Laternula elliptica: А1, А3 – левые створки, внешний вид, H×L=3.0×4.4 мм; А2 – вид со стороны дорсального краЯ на сдвоенные створки, обраЗуюЩие по Заднему краю ЗиЯние; А4 – Замок, соединЯюЩий фрагменты раЗрушенных створок (штриховка); Б1 – праваЯ створка, внешний вид, H×L=8.5×14.0 мм; Б2 – внутреннЯЯ поверхность правой створки. Фрагменты раковины вЗрослого моллюска (L=69.7 мм): В1 – вид со стороны дорсального краЯ; В2 – фрагмент правой створки, вид сбоку. ОбоЗначениЯ: ЗК – Задний край; дК – дорсальный край; сКп – складки периостракума; м – макушка; мщ – макушечнаЯ Щель; пр – продиссоконх; хр – хондрофор; ппЛ – поддерживаюЩаЯ пластинка; дпЛ – дополнительнаЯ пластинка; син – синус. Fig. 6. Juvenile shells of Laternula elliptica: A1, A3 – left valves, external view, H×L=3.0×4.4 mm; A2 – paired valves, dorsal view, showing gape through which the siphon project; A4 – hinge with chondrophore and buttress, internal view; Б1– right valve, external view, H×L=8.5×14.0 mm; Б2 – right valve, internal view. Adult shell (L=69.7 мм): B1 – fragment of right valve, dorsal view; B2 – fragment of right valve, lateral view on umbo. Notes: ЗК – posterior margin; дК – dorsal margin; сКп – periostracal wrinkles; м – umbo; мщ – umbonal crack; пр – prodissoconch; хр – chondrophore; ппЛ – buttress; дпЛ – additional supporting plate; син – sinus. in Species of warm-water origin Laternula elliptica (King, 1832) (Mollusca: Bivalvia: Laternulidae), a widespread mollusk in recent Antarctica
Рис. 6. Ювенильные раковины Laternula elliptica: А1, А3 – левые створки, внешний вид, H×L=3.0×4.4 мм; А2 – вид со стороны дорсального краЯ на сдвоенные створки, обраЗуюЩие по Заднему краю ЗиЯние; А4 – Замок, соединЯюЩий фрагменты раЗрушенных створок (штриховка); Б1 – праваЯ створка, внешний вид, H×L=8.5×14.0 мм; Б2 – внутреннЯЯ поверхность правой створки. Фрагменты раковины вЗрослого моллюска (L=69.7 мм): В1 – вид со стороны дорсального краЯ; В2 – фрагмент правой створки, вид сбоку. ОбоЗначениЯ: ЗК – Задний край; дК – дорсальный край; сКп – складки периостракума; м – макушка; мщ – макушечнаЯ Щель; пр – продиссоконх; хр – хондрофор; ппЛ – поддерживаюЩаЯ пластинка; дпЛ – дополнительнаЯ пластинка; син – синус. Fig. 6. Juvenile shells of Laternula elliptica: A1, A3 – left valves, external view, H×L=3.0×4.4 mm; A2 – paired valves, dorsal view, showing gape through which the siphon project; A4 – hinge with chondrophore and buttress, internal view; Б1– right valve, external view, H×L=8.5×14.0 mm; Б2 – right valve, internal view. Adult shell (L=69.7 мм): B1 – fragment of right valve, dorsal view; B2 – fragment of right valve, lateral view on umbo. Notes: ЗК – posterior margin; дК – dorsal margin; сКп – periostracal wrinkles; м – umbo; мщ – umbonal crack; пр – prodissoconch; хр – chondrophore; ппЛ – buttress; дпЛ – additional supporting plate; син – sinus.
Рис. 3. Àневные чешуекрыΛые Ботчинского заповеΑника в прироΑе. Фото И. В. Костомаровой: 1 — Vanessa cardui; 2 — Euphydryas intermedia, самец; 3 — Melitaea arcesia, самка; 4 — Mellicta ambigua, самец; 5 — Nephargynnis anadyomene ella, самка; 6 — Damora sagana, самец; 7 — Erebia ligea eumonia (сΛева) и Erebia ajanensis (справа), самцы; 8 — Erebia wanga, самец Fig. 3. Diurnal butterflies of the Botchinsky reserve in nature. Photos by I. V. Kostomarova: 1 — Vanessa cardui; 2 — Euphydryas intermedia, males; 3 — Melitaea arcesia, female; 4 — Mellicta ambigua, male; 5 — Nephargynnis anadyomene ella, female; 6 — Damora sagana, male; 7 — Erebia ligea eumonia (left) and Erebia ajanensis (right), males; 8 — Erebia wanga, male in Hesperioidea And Papilionoidea (Lepidoptera) Of Coniferous Forests From The Nature Reserve Botchinskii
Рис. 3. Àневные чешуекрыΛые Ботчинского заповеΑника в прироΑе. Фото И. В. Костомаровой: 1 — Vanessa cardui; 2 — Euphydryas intermedia, самец; 3 — Melitaea arcesia, самка; 4 — Mellicta ambigua, самец; 5 — Nephargynnis anadyomene ella, самка; 6 — Damora sagana, самец; 7 — Erebia ligea eumonia (сΛева) и Erebia ajanensis (справа), самцы; 8 — Erebia wanga, самец Fig. 3. Diurnal butterflies of the Botchinsky reserve in nature. Photos by I. V. Kostomarova: 1 — Vanessa cardui; 2 — Euphydryas intermedia, males; 3 — Melitaea arcesia, female; 4 — Mellicta ambigua, male; 5 — Nephargynnis anadyomene ella, female; 6 — Damora sagana, male; 7 — Erebia ligea eumonia (left) and Erebia ajanensis (right), males; 8 — Erebia wanga, male
Fig. 1 in A new record of right eyed deep-sea flat fish Poecilopsetta colorata Gunther, 1880 (Pleuronectiformes: Pleuronectidae) from the Arabian Sea
Fig. 1 — Poecilopsetta colorata Gunther, 1880, specimen (SL: 118 mm): a) Lateral view of the adult specimen, and b) Lateral view of the juvenile P. colorata; collected in Southeastern Arabian Sea, Sakthikulangara fishing port, Kerala coast, India; depth of 200 – 300 m
SI Figure 4: SEM images of either unwashed (left) or washed (right) E. antarcticus nematodes. A. Unwashed head region with arrows pointing to attached material and possible fungal hyphae. B. Washed head region with arrows pointing to the remaining attached material. C. Unwashed annules with arrows pointing to commonly attached foreign material. D. Washed annules with arrows pointing to remaining attached material. E. Unwashed somatic pore with arrows pointing to the common organic material. F. Washed vulva with an arrow pointing to remaining attached organic material. G. Unwashed cuticle with arrows showing a possible biofilm. H. Washed cuticle showing single attached cells indicated with arrows. I. Unwashed cuticle showing an off-axis line of attached material. J. Washed cuticle showing a similar off-axis line of material (as indicated with arrow) but reduced in quantity compared to the unwashed. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 4: SEM images of either unwashed (left) or washed (right) E. antarcticus nematodes. A. Unwashed head region with arrows pointing to attached material and possible fungal hyphae. B. Washed head region with arrows pointing to the remaining attached material. C. Unwashed annules with arrows pointing to commonly attached foreign material. D. Washed annules with arrows pointing to remaining attached material. E. Unwashed somatic pore with arrows pointing to the common organic material. F. Washed vulva with an arrow pointing to remaining attached organic material. G. Unwashed cuticle with arrows showing a possible biofilm. H. Washed cuticle showing single attached cells indicated with arrows. I. Unwashed cuticle showing an off-axis line of attached material. J. Washed cuticle showing a similar off-axis line of material (as indicated with arrow) but reduced in quantity compared to the unwashed.
FIG. 55. Morphotype 50, VMNH 49790. A, B. Habitus. C. Right hind leg. D. Right foreleg and middle leg. E in Remarkable Diversity Of Beetles (Coleoptera) In The Late Triassic (Norian) "Solite Deposit" Of Virginia And North Carolina
FIG. 55. Morphotype 50, VMNH 49790. A, B. Habitus. C. Right hind leg. D. Right foreleg and middle leg. E. Left foreleg and middle leg. Scale bars: A, B: 1 mm; C–E: 0.25 mm.
Figure 10. Right manual phalanx 1 in Phylogenetic relationships of the Cretaceous Gondwanan theropods Megaraptor and Australovenator: the evidence afforded by their manual anatomy
Figure 10. Right manual phalanx 1 of digit I in ventral view and schematic representations of Megaraptor (A, C), Australovenator (B,D). Scale bar: 2 cm. Note the well-developed longitudinal ventral furrow.
Figure 7. Right metacarpals II and I in Phylogenetic relationships of the Cretaceous Gondwanan theropods Megaraptor and Australovenator: the evidence afforded by their manual anatomy
Figure 7. Right metacarpals II and I in dorsal view of A, Acrocanthosaurus (modified from Currie and Carpenter, 2000); B, Torvosaurus (modified from Galton and Jensen, 1979); C, Megaraptor; D, Deinonychus (modified from Ostrom, 1969); E, Guanlong (modified from Xu et al., 2009). Not to scale. Abbreviations: ep, extensor pit; pdp, proximomedial process; ps, proximolateral surface.
Figure 10. Anthropodyptes gilli holotype right humerus, NMV P17167 in A review of Australian fossil penguins (Aves: Sphenisciformes)
Figure 10. Anthropodyptes gilli holotype right humerus, NMV P17167: A, dorsal view; B, ventral view.
Figure 8. Sphenisciformes indet. partial right humerus, SAM P10863 in A review of Australian fossil penguins (Aves: Sphenisciformes)
Figure 8. Sphenisciformes indet. partial right humerus, SAM P10863: A, dorsal view; B, ventral view.
Figure. Cross-sections of ovaries of Heliconia psittacorum (A,B) and Musa velutina (C,D). Polyethylene glycol–embedded ovaries are on the left (A,C). Paraffin-embedded ovaries are on the right (B,D). Scale bars: 1 mm. Images obtained by Anastasia Romanov (A and C) and Bruce Kirchoff (B and D). in USE OF POLYETHYLENE GLYCOL (PEG, CARBOWAX) AS AN EMBEDDING MEDIUM PRODUCES RESULTS COMPARABLE TO PARAFFIN
Figure. Cross-sections of ovaries of Heliconia psittacorum (A,B) and Musa velutina (C,D). Polyethylene glycol–embedded ovaries are on the left (A,C). Paraffin-embedded ovaries are on the right (B,D). Scale bars: 1 mm. Images obtained by Anastasia Romanov (A and C) and Bruce Kirchoff (B and D).
Figure 2 in The tangled nomenclatural history of Haplopelia forbesi Salvadori, 1904: were Forbes and Robinson right all along?
Figure 2. Specimens of Lemon Doves Columba (Aplopelia) larvata in the Vertebrate Zoology collection at World Museum, National Museums Liverpool. From left to right (subspecies according to labels): bronzina (NML-VZ T13165), forbesi (NML-VZ D3567b), larvata (NML-VZ D4217), johnstoni (NML-VZ T18511), larvata (NML-VZ T16271), larvata (NML-VZ T8168) (© National Museums Liverpool [World Museum Liverpool] / John-James Wilson)
Figure 1 in The tangled nomenclatural history of Haplopelia forbesi Salvadori, 1904: were Forbes and Robinson right all along?
Figure 1. Forbes' Lemon Dove Haplopelia forbesi (NML-VZ D3567b) (top) and Caribbean Dove Leptotila jamaicensis (NML-VZ D3567a) (bottom) bequeathed by the 13th Earl of Derby to the people of Liverpool and now in the Vertebrate Zoology collection at World Museum, National Museums Liverpool (© National Museums Liverpool [World Museum Liverpool] / John-James Wilson)
Figure 4 in The tangled nomenclatural history of Haplopelia forbesi Salvadori, 1904: were Forbes and Robinson right all along?
Figure 4. Sub-tree (of a larger tree produced by Neighbor Joining) showing the four Lemon Dove Columba (Aplopelia) larvata cytochrome sequences in NCBI GenBank aligned by BLAST with the sequence from Forbes' Lemon Dove Haplopelia forbesi (NML-VZ D3567b). Sequences are annotated with the collection locality followed by the GenBank accession no.
Figure 3 in The tangled nomenclatural history of Haplopelia forbesi Salvadori, 1904: were Forbes and Robinson right all along?
Figure 3. The second specimen identified as Haplopelia forbesi Salvadori, now at the Natural History Museum at Tring (NHMUK 1896.10.22.1) (© Trustees of the Natural History Museum, London / A. Bond)
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.