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Fig. 5. Dicranodromia foersteri Guinot, 1993 in Crabs (Crustacea, Decapoda) from the Sea off East and Southeast Asia collected by the RV Hakuhō Maru (KH-72-1 Cruise) 1. Sulu Sea and Sibutu Passage
Fig. 5. Dicranodromia foersteri Guinot, 1993, ovigerous female (NSMT-Cr 28966. CB 33.3 mm; CL 37.0 mm including rostrum). Front-orbital region with both chelipeds in ventral view (A), front-orbital region in dorsal view (B), right chela in inner view (C), right ambulatory legs in ventral view (D).
Fig. 15. A–D in Crabs (Crustacea, Decapoda) from the Sea off East and Southeast Asia collected by the RV Hakuhō Maru (KH-72-1 Cruise) 1. Sulu Sea and Sibutu Passage
Fig. 15. A–D: Oxypleurodon wilsoni Richer de Forges and Poore, 2008, full-grown male (A) (NSMT-Cr 28982. CB 10.6 mm excluding branchial tubercles; CL 16.9 mm excluding pseudorostral spines), female (B, D) (NSMT-Cr 28983. CB 6.0 mm; CL 10.1 mm), full-grown female (C) (NSMT-Cr 28984. CB 8.2 mm; CL 14.0 mm). E: Laubierinia nodosa (Rathbun, 1916), female (NSMT-Cr 28980. CB 15.0 mm excluding branchial tubercles; CL 21.4 mm excluding pseudorostral spines). F: Oxypleurodon sphenocarcinoides (Rathbun, 1916). Male (NSMT-Cr 28981. CB 7.4 mm excluding branchial tubercles; CL 11.8 mm excluding pseudorostral spines).
Fig. 9 in Crabs (Crustacea, Decapoda) from the Sea off East and Southeast Asia collected by the RV Hakuhō Maru (KH-72-1 Cruise) 1. Sulu Sea and Sibutu Passage
Fig. 9. Lysirude goekei sp. nov., male, holotype (NSMT-Cr 28969. CB 16.6 mm; CL 26.8 mm including rostrum). Dorsal (A) and ventral (B) views.
Fig. 4. Dicranodromia foersteri Guinot, 1993 in Crabs (Crustacea, Decapoda) from the Sea off East and Southeast Asia collected by the RV Hakuhō Maru (KH-72-1 Cruise) 1. Sulu Sea and Sibutu Passage
Fig. 4. Dicranodromia foersteri Guinot, 1993, ovigerous female (NSMT-Cr 28966. CB 33.3 mm; CL 37.0 mm including rostrum) in dorsal (A) and ventral (B) views.
Figures 1−5 in A new locality of Mesobuthus eupeus thersites (C. L. Koch, 1839) (Scorpiones: Buthidae) in East Kazakhstan
Figures 1−5: 1. Mesobuthus eupeus thersites (C. L. Koch, 1839) at the new locality. 2. Juvenile specimens. 3−4. The habitat at the new locality, Kyzylbel΄tau Mountains (47˚13'N, 81˚18'E), altitude 900 m. 5. Collecting localities of Mesobuthus eupeus thersites in East Kazakhstan. Circles, previous records; star, new record.
Figure 3 in Prey capture behavior in the East African scorpions Parabuthus leiosoma (Ehrenberg, 1828) and P. pallidus Pocock, 1895 (Scorpiones: Buthidae)
Figure 3: Ethogram showing the behavioral components in prey capture in Parabuthus leiosoma and P. pallidus. The behavioral components are defined in the text. Arrows indicate the direction of the prey capture sequence. The framing of the behavioral components inactive, manipulation, cheliceral activity, cleaning and travel refers to any of these behaviors observed either prior to, or after any of the others.
Рис. 3. Находки Arion subfuscus в восточной АЗии: 1–3 – Китай, по: Wiktor et al. [2000]; 4 – Приморский край у г. Фокино, по: ПроЗорова, Фоменко [2015]; 5, 6 – Курильские острова, Шикотан и Зеленый, по: ПроЗорова [2000, 2002]; 7 – г. Петропавловск-Камчатский. in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China
Рис. 3. Находки Arion subfuscus в восточной АЗии: 1–3 – Китай, по: Wiktor et al. [2000]; 4 – Приморский край у г. Фокино, по: ПроЗорова, Фоменко [2015]; 5, 6 – Курильские острова, Шикотан и Зеленый, по: ПроЗорова [2000, 2002]; 7 – г. Петропавловск-Камчатский.
Fig. 2 in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China
Fig. 2. Arion subfuscus from Kamchatka, Petropavlovsk-Kamchatsky City. Photo by O.A. Chernyagina (yellow-orange bodmucus produced by slugs is visible).
Fig. 4 in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China
Fig. 4. Location of Arion subfuscus in Petropavlovsk-Kamchatsky City near Kultuchnoye Lake. Photo by O.A. Chernyagina.
Рис. 2. Arion subfuscus c Камчатки, г. Петропавловск-Камчатский. Фото О.А. ЧернЯгиной (Заметно выделение желтооранжевой слиЗи). in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China
Рис. 2. Arion subfuscus c Камчатки, г. Петропавловск-Камчатский. Фото О.А. ЧернЯгиной (Заметно выделение желтооранжевой слиЗи).
Fig. 3 in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China
Fig. 3. Findings of Arion subfuscus in East Asia: 1–3 – China, after Wiktor et al. [2000]; 4 – Primorsky Krai near Fokino Town, after Prozorova, Fomenko [2015]; 5, 6 – Kuril Islands, Shikotan and Zelyony isls., after Prozorova [2000, 2002]; 7 – Petropavlovsk-Kamchatsky City.
◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West) in Bumps on the back: An unusual morphology in phylogenetically distinct Peridinium aff. cinctum (= Peridinium tuberosum; Peridiniales, Dinophyceae)
◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West)
Fig. 1 - Malachius saltinii n in Short Communication Notes on the Malachiini of the East-Mediterranean region, with description of a new species (Coleoptera, Melyridae, Malachiinae)
Fig. 1 - Malachius saltinii n.sp. Holotype male (bar: 1 mm). / Olotipo maschio (scala metrica: 1 mm).
Fig. 2 - Malachius saltinii n in Short Communication Notes on the Malachiini of the East-Mediterranean region, with description of a new species (Coleoptera, Melyridae, Malachiinae)
Fig. 2 - Malachius saltinii n.sp. Holotype male, head (bar: 0.5 mm). / Olotipo maschio, capo (scala metrica: 0,5 mm).
Fig. 3 - Malachius saltinii n in Short Communication Notes on the Malachiini of the East-Mediterranean region, with description of a new species (Coleoptera, Melyridae, Malachiinae)
Fig. 3 - Malachius saltinii n.sp. Allotype female (bar: 1 mm). / Allotipo femmina (scala metrica: 1 mm).
Рис. 2. Строение генитаΛий самцов некоторых виΑов чешуекрыΛых, обнаруженных в Амурской обΛасти: A — Araeopteron amoena, БΛаговещенск; B — Orthosia ariuna, БΛаговещенск Fig. 2. Some Lepidoptera species from Amur Oblast, male genitalia: A — Araeopteron amoena, Blagoveshchensk; B — Orthosia ariuna, Blagoveshchensk in New species of moths (Lepidoptera, Macroheterocera) in the fauna of Amur Oblast, Russian Far East
Рис. 2. Строение генитаΛий самцов некоторых виΑов чешуекрыΛых, обнаруженных в Амурской обΛасти: A — Araeopteron amoena, БΛаговещенск; B — Orthosia ariuna, БΛаговещенск Fig. 2. Some Lepidoptera species from Amur Oblast, male genitalia: A — Araeopteron amoena, Blagoveshchensk; B — Orthosia ariuna, Blagoveshchensk
Рис. 3. «ГуΑки» самцов (1) и птенцов (2): a — I. sinensis; b — гибриΑных птиц 2007 г.; c — гибриΑных птиц 2010 г. Fig. 3. "Beeps" of males (1) and nestlings (2): a — I. sinensis; b — hybrid birds 2007; c — hybrid birds 2010 in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 3. «ГуΑки» самцов (1) и птенцов (2): a — I. sinensis; b — гибриΑных птиц 2007 г.; c — гибриΑных птиц 2010 г. Fig. 3. "Beeps" of males (1) and nestlings (2): a — I. sinensis; b — hybrid birds 2007; c — hybrid birds 2010
Рис. 4. Крики беΑствия самок (1): a — I. sinensis; b — гибриΑной птицы; крики беΑствия самцов (2): a — I. minutes (Wroza 2017); b — I. minutes 2007 г.; сΛётков (3): a — 13-суточных I. sinensis; b — 29-суточных I. sinensis; c — 13-суточных гибриΑных птиц; d — 29-суточных гибриΑных птиц Fig. 4. Distress calls of females (1): a — I. sinensis; b — hybrid bird; distress calls of males (2): a — I. minutes (Wroza 2017); b — I. minutes 2007; fledglings (3): a — 13-day-old I. sinensis; b — 29-day-old I. sinensis; c — 13-day-old hybrid birds; d — 29-day-old hybrid birds in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 4. Крики беΑствия самок (1): a — I. sinensis; b — гибриΑной птицы; крики беΑствия самцов (2): a — I. minutes (Wroza 2017); b — I. minutes 2007 г.; сΛётков (3): a — 13-суточных I. sinensis; b — 29-суточных I. sinensis; c — 13-суточных гибриΑных птиц; d — 29-суточных гибриΑных птиц Fig. 4. Distress calls of females (1): a — I. sinensis; b — hybrid bird; distress calls of males (2): a — I. minutes (Wroza 2017); b — I. minutes 2007; fledglings (3): a — 13-day-old I. sinensis; b — 29-day-old I. sinensis; c — 13-day-old hybrid birds; d — 29-day-old hybrid birds
Рис. 1. ЧешуекрыΛые, обнаруженные в Амурской обΛасти: внешний виΑ гусеницы посΛеΑнего возраста (A) и имаго (B–O): A — Sphecodina caudata; B — Mirina christophi, самец; C — Paracolax fentoni, самка; D — Pangrapta costaemacula, самка; E — P. suaveola, самец; F — Araeopteron amoena, самец; G — Sinocharis korbae, самец; H — Nacna malachitis, самец; I — Sarbanissa venusta, самец; J — Plusilla rosalia, самец; K — Xylopolia bellula, самец; L — Xestia efflorescens, самец; M — Orthosia satoi, самец; N, O — O. ariuna (N — самец, O — самка). Места сбора: A, F, H, J, N, O — окрестности БΛаговещенска; B, G, L — Архаринский район, окрестности станции Тарманчукан; C, M — окрестности станции Рачи; D, E, I – окрестности с. Грибовка; K — БΛаговещенский район, окрестности с. Новопетровка. Масштабная Λинейка 5 мм Fig. 1. Lepidoptera species from Amur Oblast: habitus of last instar larva (A) and adult (B–O): A — Sphecodina caudata; B — Mirina christophi, male; C — Paracolax fentoni, female; D — Pangrapta costaemacula, female; E — P. suaveola, male; F — Araeopteron amoena, male; G — Sinocharis korbae, male; H — Nacna malachitis, male; I — Sarbanissa venusta, male; J — Plusilla rosalia, male; K — Xylopolia bellula, male; L — Xestia efflorescens, male; M —Orthosia satoi, male; N, O — O. ariuna (N — male, O — female). Localities: A, F, H, J, N, O — environs of Blagoveshchensk; B, G, L — Arkhara District, vicinity of Tarmanchukan; C, M — vicinity of Rachi; D, E, I — vicinity of Gribovka; K — Blagoveshchensk District, vicinity of Novopetrovka. Scale bar 5 mm in New species of moths (Lepidoptera, Macroheterocera) in the fauna of Amur Oblast, Russian Far East
Рис. 1. ЧешуекрыΛые, обнаруженные в Амурской обΛасти: внешний виΑ гусеницы посΛеΑнего возраста (A) и имаго (B–O): A — Sphecodina caudata; B — Mirina christophi, самец; C — Paracolax fentoni, самка; D — Pangrapta costaemacula, самка; E — P. suaveola, самец; F — Araeopteron amoena, самец; G — Sinocharis korbae, самец; H — Nacna malachitis, самец; I — Sarbanissa venusta, самец; J — Plusilla rosalia, самец; K — Xylopolia bellula, самец; L — Xestia efflorescens, самец; M — Orthosia satoi, самец; N, O — O. ariuna (N — самец, O — самка). Места сбора: A, F, H, J, N, O — окрестности БΛаговещенска; B, G, L — Архаринский район, окрестности станции Тарманчукан; C, M — окрестности станции Рачи; D, E, I – окрестности с. Грибовка; K — БΛаговещенский район, окрестности с. Новопетровка. Масштабная Λинейка 5 мм Fig. 1. Lepidoptera species from Amur Oblast: habitus of last instar larva (A) and adult (B–O): A — Sphecodina caudata; B — Mirina christophi, male; C — Paracolax fentoni, female; D — Pangrapta costaemacula, female; E — P. suaveola, male; F — Araeopteron amoena, male; G — Sinocharis korbae, male; H — Nacna malachitis, male; I — Sarbanissa venusta, male; J — Plusilla rosalia, male; K — Xylopolia bellula, male; L — Xestia efflorescens, male; M —Orthosia satoi, male; N, O — O. ariuna (N — male, O — female). Localities: A, F, H, J, N, O — environs of Blagoveshchensk; B, G, L — Arkhara District, vicinity of Tarmanchukan; C, M — vicinity of Rachi; D, E, I — vicinity of Gribovka; K — Blagoveshchensk District, vicinity of Novopetrovka. Scale bar 5 mm
Рис. 1. Брачные крики и их инΑивиΑуаΛьная изменчивость у разных виΑов воΛчков: a — I. m. minutes (Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) Fig. 1. Mating calls and their individual variability in different bittern species: a — I. m.minutes Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 1. Брачные крики и их инΑивиΑуаΛьная изменчивость у разных виΑов воΛчков: a — I. m. minutes (Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) Fig. 1. Mating calls and their individual variability in different bittern species: a — I. m.minutes Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016)
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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.