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FIGURE 30 in Taxonomy, ecology and zoogeography of the Recent species of Rhamphostomella Lorenz, 1886 and Mixtoscutella n. gen. (Bryozoa, Cheilostomata)
FIGURE 30. Basal colony surface in some Rhamphostomella species.A. R. scabra, ZIRAS 93/50106 (Bering Island, Commander Islands, Pacific Ocean), colony fragment developed above irregular substrate, showing broken protuberances and pits formed above sponge spicules. B. R. commandorica, ZIRAS 1/50125 (Medny Island, Commander Islands, Pacific Ocean), colony fragment, showing smooth surface with rare thin protuberances. C. R. cristata, ZIRAS 2/50110 (Medny Island, Commander Islands, Pacific Ocean), colony area growing above crustose coralline algae Lithothamnion sp., showing regular series of columnar protuberances with broad bases. D. R. gigantea, ZIRAS 3/50129 (western Kamchatka shelf, Sea of Okhotsk), colony detached from internal side of broken shell of bivalve mollusc Chlamys sp. E. R. pacifica, ZIRAS 1/50124 (Kronotsky Gulf, eastern Kamchatka, Pacific Ocean), colony developed above irregular substratum. F. R. curvirostrata, NHMUK 1964.1.2.7 (Pacific coast of North America), colony margin with developing zooids, supported by long tubular processes. G. R. hincksi, USNM 11130 (Point Barrow, Alaska, Beaufort Sea), basal surface with long tubular protuberances. H. R. sibirica, ZIRAS 34/50113 (Medny Island, Commander Islands, Bering Sea), basal surface with long tubular protuberances. I. R. multirostrata, ZIRAS 1/50545 (Urup Island, Kuril Islands, Sea of Okhotsk), colony detached from a sponge, showing marginal zooids with regular series of tubular protuberances. Scale bars: 500 μm.
FIGURE 27 in Taxonomy, ecology and zoogeography of the Recent species of Rhamphostomella Lorenz, 1886 and Mixtoscutella n. gen. (Bryozoa, Cheilostomata)
FIGURE 27. Mixtoscutella ovata (Smitt, 1868). ZIRAS 36/50120 (western Kamchatka, Sea of Okhotsk). A. Colony margin with young and developing zooids (arrows, sites of ooecial development). B. Zooidal orifice, showing condyles, and suboral avicularium. C, D. Non-ovicellate zooids in young part of colony. E. Ovicellate zooids in older part of colony, showing ovicells, and suboral and adventitious avicularia. F. Ooecium covered by secondary calcification, except in proximal triangular area with pseudopores. G. Area of colony with ovicellate zooids and adventitious avicularia. H. Longitudinal section through frontal shield, showing interior of umbonulomorph suboral area and adjacent pseudoporous lepralioid shield. I. Interior of frontal shield with umbonuloid component, ring scar, areolae (smaller lateral openings in upper part of zooid), pseudopores and ooecial pore (arrow). J. Internal view of primary orifice with condyles. K. Basal surface of colony. L. Interior of frontal shield, showing blurred ring scar and exterior wall microstructure of umbonuloid component. M. Lateral view of zooid, showing frontal shield, suboral avicularium and lateral wall with mural pore chambers. Scale bars: A, D, G, K, 500 μm; B, F, I, J, 100 μm; C, E, 250 μm; H, L, 50 μm; M, 200 μm.
FIGURE 28 in Taxonomy, ecology and zoogeography of the Recent species of Rhamphostomella Lorenz, 1886 and Mixtoscutella n. gen. (Bryozoa, Cheilostomata)
FIGURE 28. Mixtoscutella ussowi (Kluge, 1908). ZIRAS 14/50567 (Korfa Gulf, eastern Kamchatka, Bering Sea). A. Colony margin with developing zooids and ooecia. B. Distal view of two zooids, showing details of orifice and suboral avicularia. C. Orifice of non-ovicellate zooid, showing condyles and suboral avicularium. D. Group of non-ovicellate zooids. E. Zooids with developing ovicells close to colony periphery. F, G. Ovicellate zooids in older part of colony, showing ovicells with ooecia covered by secondary calcification and sutures between secondary calcification arising from distal and distolateral zooids. H. Transverse section through frontal shield, showing interior of proximal margin of orifice, umbonulomorph suboral area with adjacent pseudoporous shield, and cavity of suboral avicularian chamber. I. Interior of frontal shield, showing primary orifice with condyles and elongate suboral umbonuloid component surrounded by pseudoporous lepralioid shield. J. Internal view of primary orifice. K. Basal surface of colony. L. Interior of frontal shield, showing blurred ring scar and umbonuloid component surrounded by pseudoporous lepralioid area. M. Lateral view of zooid, showing frontal shield and lateral wall with mural pore chambers. Scale bars: A, D, G, K, 500 μm; B, E, F, 250 μm; C, H–J, 100 μm; L, 50 μm; M, 200 μm.
The upper canines of the male Sulawesi Babirusa grow upwards through the snout and continue to grow in a backward-curving spiral. They are too brittle and shallow rooted to be used in fighting and theirfunction, if any, is unknown. Until recently, all babirusas were classified as a single species. The genus has now been split into at least three species, based on features of their skulls and teeth and the amount of hair on their bodies. The Sulawest Babirusa has nearly naked skin. The name Babyrousa celebensis specifically refers to animals from north Sulawesi and the taxonomic identity of babirusas onthe rest of the island remains undecided. Unlike other pig species, babirusas do not have noses adapted for rooting. Babyrousa celebensis Lore Lindu National Park, Sulawesi. Photo: Berndt Fischer/ photolibrary.com in Suidae
The upper canines of the male Sulawesi Babirusa grow upwards through the snout and continue to grow in a backward-curving spiral. They are too brittle and shallow rooted to be used in fighting and theirfunction, if any, is unknown. Until recently, all babirusas were classified as a single species. The genus has now been split into at least three species, based on features of their skulls and teeth and the amount of hair on their bodies. The Sulawest Babirusa has nearly naked skin. The name Babyrousa celebensis specifically refers to animals from north Sulawesi and the taxonomic identity of babirusas onthe rest of the island remains undecided. Unlike other pig species, babirusas do not have noses adapted for rooting. Babyrousa celebensis Lore Lindu National Park, Sulawesi. Photo: Berndt Fischer/ photolibrary.com
Distribution. Bolivian lowlands (NE to the Chiquitano Mts and SW to the piedmont elevations in the subandean region) and SW Brazilian Amazon in the upper Madeira River, and the Beni, Ichilo, Marmoré, Ipurupuru, Iboré, Baré, Abuna, and Iténez (= Guaporé) rivers and their tributaries, all of which drain into the Madeira; recently also recorded below Santo Antonio falls between the cities of Porto Velho and Borba. in Iniidae
Distribution. Bolivian lowlands (NE to the Chiquitano Mts and SW to the piedmont elevations in the subandean region) and SW Brazilian Amazon in the upper Madeira River, and the Beni, Ichilo, Marmoré, Ipurupuru, Iboré, Baré, Abuna, and Iténez (= Guaporé) rivers and their tributaries, all of which drain into the Madeira; recently also recorded below Santo Antonio falls between the cities of Porto Velho and Borba.
Distribution. Mainly in Guadalupe I, off the W coast of C Baja California (Mexico), recently has expanded SE to San Benito Is near the Baja California coast, and N to Channel Is (San Miguel I) and other S California islands and to Farallon Is off N California, USA. Wandering individuals have reached as far N as Washington State and one individual to SC Alaska. in Otariidae
Distribution. Mainly in Guadalupe I, off the W coast of C Baja California (Mexico), recently has expanded SE to San Benito Is near the Baja California coast, and N to Channel Is (San Miguel I) and other S California islands and to Farallon Is off N California, USA. Wandering individuals have reached as far N as Washington State and one individual to SC Alaska.
Distribution. Aru Is and lowlands of S New Guinea in Merauke and Western provinces and Avera (= Avela), Aroa River,in the E; recently, two specimens were obtained in the Trans-Fly region near Serki Village. in Dasyuridae
Distribution. Aru Is and lowlands of S New Guinea in Merauke and Western provinces and Avera (= Avela), Aroa River,in the E; recently, two specimens were obtained in the Trans-Fly region near Serki Village.
Distribution. Australia, in recent times recorded only in the deserts along the borders of S Northern Territory, CN South Australia, and SW Queensland; formerly more widespread in W & S Australia. in Dasyuridae
Distribution. Australia, in recent times recorded only in the deserts along the borders of S Northern Territory, CN South Australia, and SW Queensland; formerly more widespread in W & S Australia.
Distribution. Southern Hemisphere (E South America from S Brazil to Tierra del Fuego, Falkland Is (= Malvinas), South Georgia Is, Kerguelen Is, Heard I, Macquarie I, Auckland Is, and Tasmania). Although previously thought to be exclusively coastal, like other members of the genus, recent sightings in oceanic waters of the Antarctic and subantarctic zones suggest that the species actually has a circumpolar distribution and may be largely oceanic. in Phocoenidae
Distribution. Southern Hemisphere (E South America from S Brazil to Tierra del Fuego, Falkland Is (= Malvinas), South Georgia Is, Kerguelen Is, Heard I, Macquarie I, Auckland Is, and Tasmania). Although previously thought to be exclusively coastal, like other members of the genus, recent sightings in oceanic waters of the Antarctic and subantarctic zones suggest that the species actually has a circumpolar distribution and may be largely oceanic.
Subspecies and Distribution. I.a.auratusRamsay,1887—NWKimberleyandseveralsmallislandsoffKimberleycoast. I.a.arnhemensisLyne&Mort,1981—CapeArnhem,NENorthernTerritory. I. a. barrowensis Thomas, 1901 — Barrow I and Middle I, Western Australia. Occurs also (subspecies uncertain) on Marchinbar I, in Wessel Group, Northern Territory, and introduced recently to two further islands in Wessel Group. Barrow I race barrowensis introduced to nearby Hermite I, to Doole I (in Exmouth Gulf), and to Lorna Glen (mainland of C Western Australia) in recentyears. in Peramelidae
Subspecies and Distribution. I.a.auratusRamsay,1887—NWKimberleyandseveralsmallislandsoffKimberleycoast. I.a.arnhemensisLyne&Mort,1981—CapeArnhem,NENorthernTerritory. I. a. barrowensis Thomas, 1901 — Barrow I and Middle I, Western Australia. Occurs also (subspecies uncertain) on Marchinbar I, in Wessel Group, Northern Territory, and introduced recently to two further islands in Wessel Group. Barrow I race barrowensis introduced to nearby Hermite I, to Doole I (in Exmouth Gulf), and to Lorna Glen (mainland of C Western Australia) in recentyears.
Distribution. Brazilian Amazon, S of the Rio Amazonas, between the Tapajos/Juruena system and the Tocantins/Araguaia river system to the E, in the Brazilian states of Para and Mato Grosso; the exact S limit ofits distribution is unclear, but it seems likely that it coincides with the transition between the Amazon rainforest and the cerrado savannas of C Brazil; this ecotone encompasses headwaters of the Xingu and Tapajos river systems in N Mato Grosso. Vieira's Titi (C. vieirai) is also known to occur in this region, but there are too few records to confirm whether their distributions intergrade, or in fact where the exact limits of their distributions are. One recent study also found that the Red-bellied Titi may be absent from or present at extremely low densities in large areas of the Tocantins-Xingu interfluvium. Given the overall lack of records, while it is clear that the Red-bellied Titi occurs over a vast area of the SE Amazon Basin, the exact limits of its distribution within this area remain unclear. in Phitheciidae
Distribution. Brazilian Amazon, S of the Rio Amazonas, between the Tapajos/Juruena system and the Tocantins/Araguaia river system to the E, in the Brazilian states of Para and Mato Grosso; the exact S limit ofits distribution is unclear, but it seems likely that it coincides with the transition between the Amazon rainforest and the cerrado savannas of C Brazil; this ecotone encompasses headwaters of the Xingu and Tapajos river systems in N Mato Grosso. Vieira's Titi (C. vieirai) is also known to occur in this region, but there are too few records to confirm whether their distributions intergrade, or in fact where the exact limits of their distributions are. One recent study also found that the Red-bellied Titi may be absent from or present at extremely low densities in large areas of the Tocantins-Xingu interfluvium. Given the overall lack of records, while it is clear that the Red-bellied Titi occurs over a vast area of the SE Amazon Basin, the exact limits of its distribution within this area remain unclear.
Distribution. NE Madagascar, extremely limited distribution in the far N of the island, just to the S of Antsiranana (= Diégo-Suarez), it was formerly believed to inhabit both dry and humid forests from the Montagne d' Ambre region S to the Mahavavy River near Ambilobe in the W, and probably to the Fanambana River S of Vohémarin the E. However, with the recognition of the Ankarana Sportive Lemur (L. ankaranensis) as a distinct species, the range of the Sahafary Sportive Lemur was reduced to a handful of very small remnant forest patches nearthe villages of Madirobe and Ankarongana in the Sahafary region, and in the immediate vicinity of Andrahona, a small mountain rising out of the surrounding lowlands about 30 km south of Antsiranana and E of the RN6 main road. Recent faunal surveys in the Montagne des Francais, a calcareous massif of c.6114 ha approximately 12 km SE of Antsiranana, listed the Sahafary Sportive Lemur as one of the species occurring there, but this needs to be confirmed; it may be widerranging than the Ankarana Sportive Lemur. in Lepilemuridae
Distribution. NE Madagascar, extremely limited distribution in the far N of the island, just to the S of Antsiranana (= Diégo-Suarez), it was formerly believed to inhabit both dry and humid forests from the Montagne d' Ambre region S to the Mahavavy River near Ambilobe in the W, and probably to the Fanambana River S of Vohémarin the E. However, with the recognition of the Ankarana Sportive Lemur (L. ankaranensis) as a distinct species, the range of the Sahafary Sportive Lemur was reduced to a handful of very small remnant forest patches nearthe villages of Madirobe and Ankarongana in the Sahafary region, and in the immediate vicinity of Andrahona, a small mountain rising out of the surrounding lowlands about 30 km south of Antsiranana and E of the RN6 main road. Recent faunal surveys in the Montagne des Francais, a calcareous massif of c.6114 ha approximately 12 km SE of Antsiranana, listed the Sahafary Sportive Lemur as one of the species occurring there, but this needs to be confirmed; it may be widerranging than the Ankarana Sportive Lemur.
Distribution. CE & SE Madagascar; until recently restricted to the SC portion of the country's rainforests including Ranomafana and Andringitra national parks, Ambositra-Vondrozo Corridor and isolated forests between and to the E ofthese localities (e.g. Ambolomavo, Ifanadiana, Kianjavato), and one locality N of the Manampatrana River (Evendra); recent surveys have now confirmed its presence in the forests of Torotorofotsy, in the region of Andasibe-Mantadia, and 18 sites in and around the Ankeniheny-Zahamena Corridor, and at five additional sites around the Marolambo forest corridor and as far N as Zahamena National Park, and it extends to near the Midongy du Sud National Park in the S, 670 km S of Zahamena. Reports of large bamboo lemursfitting this species' description have been filtering in from various other remote sites (e.g. Mananara region). in Lemuridae
Distribution. CE & SE Madagascar; until recently restricted to the SC portion of the country's rainforests including Ranomafana and Andringitra national parks, Ambositra-Vondrozo Corridor and isolated forests between and to the E ofthese localities (e.g. Ambolomavo, Ifanadiana, Kianjavato), and one locality N of the Manampatrana River (Evendra); recent surveys have now confirmed its presence in the forests of Torotorofotsy, in the region of Andasibe-Mantadia, and 18 sites in and around the Ankeniheny-Zahamena Corridor, and at five additional sites around the Marolambo forest corridor and as far N as Zahamena National Park, and it extends to near the Midongy du Sud National Park in the S, 670 km S of Zahamena. Reports of large bamboo lemursfitting this species' description have been filtering in from various other remote sites (e.g. Mananara region).
Distribution. NW Australia, patchily across the Kimberley region in Western Australia, from Kalumburu in the N to North Derby in the S, including Bigge and Boongaree Is. The species was recently confirmed to occur in the East Kimberley (Cockburn Ranges) for the first time since its initial scientific discovery in 1917. in Phalangeridae
Distribution. NW Australia, patchily across the Kimberley region in Western Australia, from Kalumburu in the N to North Derby in the S, including Bigge and Boongaree Is. The species was recently confirmed to occur in the East Kimberley (Cockburn Ranges) for the first time since its initial scientific discovery in 1917.
Distribution. SW Western Australia, restricted to coast from S of Bunbury to Waychinicup National Park (near Albany) and in suitable habitat inland, most notably at Perup Nature Reserve and surrounding state forest near Manjimup; recently found near the Harvey River and Collie (NE Bunbury). in Pseudocheiridae
Distribution. SW Western Australia, restricted to coast from S of Bunbury to Waychinicup National Park (near Albany) and in suitable habitat inland, most notably at Perup Nature Reserve and surrounding state forest near Manjimup; recently found near the Harvey River and Collie (NE Bunbury).
Distribution. NE Vietnam (Cao Bang and Vinh Phuc provinces), also S China (recently found in Yunnan and Jiangxi). in Talpidae
Distribution. NE Vietnam (Cao Bang and Vinh Phuc provinces), also S China (recently found in Yunnan and Jiangxi).
Distribution. Restricted and patchy range in NE Madagascar that includes the humid forest belt extending from the Marojejy Massif and the Andapa Basin to Maroantsetra; the Androranga River may be the NE distributional limit in the Tsaratanana Corridor, although further surveys are needed to confirm this, and the Antainambalana River in the Makira Forest protected area is currently regarded as the S boundary. Currently, Marojejy represents the N limit ofits distribution, although historic range maps suggest that it once occurred as far N as the Bemarivo River near Sambava. The NE distributional limit in Makira was only recently established, when a few groups were found in the Antohaka Lava Forest, but informal reports suggest that the unprotected Maherivaratra Forest, outside NE Makira, may also contain Silky Sifakas. in Indriidae
Distribution. Restricted and patchy range in NE Madagascar that includes the humid forest belt extending from the Marojejy Massif and the Andapa Basin to Maroantsetra; the Androranga River may be the NE distributional limit in the Tsaratanana Corridor, although further surveys are needed to confirm this, and the Antainambalana River in the Makira Forest protected area is currently regarded as the S boundary. Currently, Marojejy represents the N limit ofits distribution, although historic range maps suggest that it once occurred as far N as the Bemarivo River near Sambava. The NE distributional limit in Makira was only recently established, when a few groups were found in the Antohaka Lava Forest, but informal reports suggest that the unprotected Maherivaratra Forest, outside NE Makira, may also contain Silky Sifakas.
Distribution. NE & E Madagascar from the Mananara River in the N to the Mangoro and Onive rivers in the S; although the precise distributional limits are unknown, the Diademed Sifaka is thought to be the most widely distributed of the sifakas, occurring throughout Madagascar's E rainforests. Historically, its distribution extended farther N to just S of the Antainambalana River, but it has not been found in recent years during fairly extensive studies of that region. in Indriidae
Distribution. NE & E Madagascar from the Mananara River in the N to the Mangoro and Onive rivers in the S; although the precise distributional limits are unknown, the Diademed Sifaka is thought to be the most widely distributed of the sifakas, occurring throughout Madagascar's E rainforests. Historically, its distribution extended farther N to just S of the Antainambalana River, but it has not been found in recent years during fairly extensive studies of that region.
Distribution. NE & E Madagascar from the Bemarivo River in the N to the Mangoro/Nesivolo rivers in the S; prior to the recent taxonomic splitting of this species, it was thought to range almost the entire length of E Madagascar's rainforests from the Ankarana Massif in the extreme N to the Tolagnaro (= Fort-Dauphin) region in the extreme S. in Indriidae
Distribution. NE & E Madagascar from the Bemarivo River in the N to the Mangoro/Nesivolo rivers in the S; prior to the recent taxonomic splitting of this species, it was thought to range almost the entire length of E Madagascar's rainforests from the Ankarana Massif in the extreme N to the Tolagnaro (= Fort-Dauphin) region in the extreme S.
Dataset presented in the recently submitted AGU manuscript "A multi-resolution finite-element approach for global electromagnetic induction modeling with application to southeast China coastal geomagnetic observatory studies"
<p>Dataset presented in the recently submitted AGU paper "A multi-resolution finite-element approach for global electromagnetic induction modeling with application to southeast China coastal geomagnetic observatory studies"</p>
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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.