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FIGURE 3. Pygofer, right lateral view. A in Revision of the genus Doratura Sahlberg (Hemiptera, Cicadellidae, Deltocephalinae) with particular regard to its distribution in Italy and description of four new species
FIGURE 3. Pygofer, right lateral view. A: Doratura stylata (Boheman), Bulgaria, Stara Planina, Barzia; B: D. butzele, Guglielmino & Bückle, Italy, Molise, Campobasso, Boiano; C: D. heterophyla Horváth, Bulgaria, North Black Sea Coast, Chernevo; D: D. rikele Guglielmino & Bückle, Paratype, Italy, Calabria, Crotone, Caccuri; E: D. homophyla (Flor), Hungary, Velence; F: D. lobele sp. nov., Greece, Arcadia, Tripoli, Kandalos.
FIGURE 38. Doratura homophyla group. Right style, dorsal view. A–D in Revision of the genus Doratura Sahlberg (Hemiptera, Cicadellidae, Deltocephalinae) with particular regard to its distribution in Italy and description of four new species
FIGURE 38. Doratura homophyla group. Right style, dorsal view. A–D: D. homophyla (Flor). A: Germany, Mecklenburg-Vorpommern, Insel Poel; B: Germany, Baden-Württemberg, Baden-Baden, Sandweier; C: Spain, Andalusia, Jaén, Cazorla; D: Irak, Bagdad.—E–G: D. caucasica Melichar. E: paratype D. arenicola Logvinenko. Azerbajan, Lenkoran, Talysh, 12.07.1970; F: paratype (?) D. arenicola Logvinenko. Azerbajan, Lenkoran, Alekseevka, 01.06.1967; G: Georgia, Tbilisi, Lac Lisi.
FIGURE. Thalictrum uncatum in the wild (Shangri-la in northwestern Yunnan, China). A. Habitat. B. Habit. C. Leaf (left: adaxial side; right: abaxial side). D. Leaflet (left: adaxial side; right: abaxial side). E. Flower. F. Sepals. G. Stamens. H. Carpels. I. Aggregate fruit (immature). J. Achenes (immature). Photographed by Y.P. Zeng. in Thalictrum spiristylum (Ranunculaceae), described from northwestern Yunnan, China, is merged with T. atriplex
FIGURE. Thalictrum uncatum in the wild (Shangri-la in northwestern Yunnan, China). A. Habitat. B. Habit. C. Leaf (left: adaxial side; right: abaxial side). D. Leaflet (left: adaxial side; right: abaxial side). E. Flower. F. Sepals. G. Stamens. H. Carpels. I. Aggregate fruit (immature). J. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE. Thalictrum uncatum in the wild (Xiaojin county in western Sichuan, China). A. Habitat. B. Habit. C. Leaf (left: adaxial side; right: abaxial side). D. Leaflet (left: adaxial side; right: abaxial side). E. Portion of inflorescence. F. Flower. G. Sepals. H. Stamens. I. Carpels. J. Aggregate fruit (immature). K. Achenes (immature). Photographed by Y.P. Zeng. in Thalictrum spiristylum (Ranunculaceae), described from northwestern Yunnan, China, is merged with T. atriplex
FIGURE. Thalictrum uncatum in the wild (Xiaojin county in western Sichuan, China). A. Habitat. B. Habit. C. Leaf (left: adaxial side; right: abaxial side). D. Leaflet (left: adaxial side; right: abaxial side). E. Portion of inflorescence. F. Flower. G. Sepals. H. Stamens. I. Carpels. J. Aggregate fruit (immature). K. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE. Thalictrum atriplex in the wild (Shangri-la county in northwestern Yunnan, China). A. Habitat. B. Habit. C. Roots. D. Portion of stem. E. Leaf (left: adaxial side; right: abaxial side). F. Leaflet (adaxial side). G. Portion of inflorescence. H. Flower. I. Sepal (left: adaxial side; right: abaxial side). J. Stamens. K. Carpels. L. Portion of infructescence. M. Aggregate fruits (immature). N. Achenes (immature). Photographed by Y.P. Zeng. in Thalictrum spiristylum (Ranunculaceae), described from northwestern Yunnan, China, is merged with T. atriplex
FIGURE. Thalictrum atriplex in the wild (Shangri-la county in northwestern Yunnan, China). A. Habitat. B. Habit. C. Roots. D. Portion of stem. E. Leaf (left: adaxial side; right: abaxial side). F. Leaflet (adaxial side). G. Portion of inflorescence. H. Flower. I. Sepal (left: adaxial side; right: abaxial side). J. Stamens. K. Carpels. L. Portion of infructescence. M. Aggregate fruits (immature). N. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE. Thalictrum atriplex in the wild (Kangding county in western Sichuan, China, the type locality). A. Habitat. B. Habit. C. Roots. D. Portion of stem. E. Leaf (left: adaxial side; right: abaxial side). F. Leaflet (adaxial side). G. Portion of inflorescence. H. Flower. I. Sepal (left: adaxial side; right: abaxial side). J. Stamens. K. Carpels. L. Aggregate fruits (immature). M. Achenes (immature). Photographed by Y.P. Zeng. in Thalictrum spiristylum (Ranunculaceae), described from northwestern Yunnan, China, is merged with T. atriplex
FIGURE. Thalictrum atriplex in the wild (Kangding county in western Sichuan, China, the type locality). A. Habitat. B. Habit. C. Roots. D. Portion of stem. E. Leaf (left: adaxial side; right: abaxial side). F. Leaflet (adaxial side). G. Portion of inflorescence. H. Flower. I. Sepal (left: adaxial side; right: abaxial side). J. Stamens. K. Carpels. L. Aggregate fruits (immature). M. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE. Thalictrum spiristylum (= T. atriplex) in the wild (Ninglang county in northwestern Yunnan, China). A. Habitat. B. Habit (flowering plant). C. Habit (fruiting plant). D. Roots. E. Portion of stem. F. Leaf (left: adaxial side; right: abaxial side). G. Leaflet (adaxial side). H. Portion of inflorescence. I. Flower. J. Sepals (adaxial side). K. Stamens. L. Carpels. M. Portion of infructescence. N. Aggregate fruits (immature). O. Achenes (immature). Photographed by Y.P. Zeng. in Thalictrum spiristylum (Ranunculaceae), described from northwestern Yunnan, China, is merged with T. atriplex
FIGURE. Thalictrum spiristylum (= T. atriplex) in the wild (Ninglang county in northwestern Yunnan, China). A. Habitat. B. Habit (flowering plant). C. Habit (fruiting plant). D. Roots. E. Portion of stem. F. Leaf (left: adaxial side; right: abaxial side). G. Leaflet (adaxial side). H. Portion of inflorescence. I. Flower. J. Sepals (adaxial side). K. Stamens. L. Carpels. M. Portion of infructescence. N. Aggregate fruits (immature). O. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE. (A) Summary phylogeny showing relations between genera in tribe Phyllantheae from Bayesian and Maximum Likelihood analysis of five markers (ITS, PHYC, accD–psaI, trnS–trnG, matK), modified from Appendix 1. Classification is shown of genera (right column), subgenera (middle column) and sections (except for the genus Phyllanthus. Sections not included in phylogenetic analyses and those for the genus Flueggea were omitted. (B) summary phylogeny of the genus Phyllanthus as envisioned here with subgenera and sections of groups included in phylogenetic studies shown. in A revised phylogenetic classification of tribe Phyllantheae (Phyllanthaceae)
FIGURE. (A) Summary phylogeny showing relations between genera in tribe Phyllantheae from Bayesian and Maximum Likelihood analysis of five markers (ITS, PHYC, accD–psaI, trnS–trnG, matK), modified from Appendix 1. Classification is shown of genera (right column), subgenera (middle column) and sections (except for the genus Phyllanthus. Sections not included in phylogenetic analyses and those for the genus Flueggea were omitted. (B) summary phylogeny of the genus Phyllanthus as envisioned here with subgenera and sections of groups included in phylogenetic studies shown.
FIGURE. Fruiting heads and peduncles of C. spongifolia. A. Site WP260; two peduncles have lost heads (arrows 1 and 2), the upper part (male zone) of one spadix lies on ground (arrow 3), and six attached heads all touch ground. B–E. Site WP251; a single, detached immature head with bite marks in upper and lower ends, and torn surface at junction with peduncle (at left in D–E). Scale bars: 10 cm with 1 cm units (main image); 8 cm with 2 cm units (lower right); B–C enlarged, without scale. (Bach Ma NP, 2018). Photos: PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Fruiting heads and peduncles of C. spongifolia. A. Site WP260; two peduncles have lost heads (arrows 1 and 2), the upper part (male zone) of one spadix lies on ground (arrow 3), and six attached heads all touch ground. B–E. Site WP251; a single, detached immature head with bite marks in upper and lower ends, and torn surface at junction with peduncle (at left in D–E). Scale bars: 10 cm with 1 cm units (main image); 8 cm with 2 cm units (lower right); B–C enlarged, without scale. (Bach Ma NP, 2018). Photos: PJM.
FIGURE. Stem, roots, and buds of C. spongifolia. A. Cross section of stem in B, showing clear, gummy exudate. B. Mature stem with decumbent part at left, erect part at right, roots and rootlets, brown leaf scars, and single adaxial buds (arrows). C. Young stem, with single, adaxial bud revealed. Scale bars = 2 cm (Bach Ma NP, 2018, 2021). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Stem, roots, and buds of C. spongifolia. A. Cross section of stem in B, showing clear, gummy exudate. B. Mature stem with decumbent part at left, erect part at right, roots and rootlets, brown leaf scars, and single adaxial buds (arrows). C. Young stem, with single, adaxial bud revealed. Scale bars = 2 cm (Bach Ma NP, 2018, 2021). Photos: NVD and PJM.
Left hepatectomy with concomitant the right hepatic artery and the portal vein resection
<p>The supplemental video shows our procedure for HAR in PHCC (supplemental video). The first step of the surgical procedure for HAR was similar to the standard resection for PHCC surgery: lymphadenectomy (skeletonization) for the hepatoduodenal ligament and distal bile duct resection just above the posterior superior pancreatic duodenal artery. We usually pick up the right hepatic artery (or posterior branch) at Rouviere’s sulcus before skeletonization around the proper hepatic artery to confirm resectability. Hepatic artery reconstruction is usually performed as the final step after bile duct and portal vein resection and reconstruction.</p>
Subspecies and Distribution. pos sagitta Pallas, 1773 — S Russia (Altai Krai) and right bank of Irtysh River in Kazakhstan (Pavlodar and East Kazakhstan regions). D.s.aksuensisWangSung,1964—NWChina(NTarimBasininXinjiang). D.s.austrouralensisShenbrot,1991—NWKazakhstan(WestKazakhstan,Atyrau,andAktoberegionsbetweenUralandEmbarivers). D.s.bulganensisShenbrot,1991—EKazakhstan(ELakeZaysaninEastKazakhstanRegion),NWChina(DzungarianBasininXinjiang),andMongolia(SKhovdandSWGovi-Altai). D.s.deasyiBarret-Hamilton,1900—NWChina(STarimBasininXinjiangandS&WQaidamBasininQinghai). D. s. fuscocanus Wang Sung, 1964 — W China (S foothills of E Tian Shan in Xinjiang). D. s. halli Sowerby, 1920 — China (NE Inner Mongolia [= Nei Mongol], SW Heilongjiang, NWJilin, and N Liaoning) and SE Mongolia (Stikhbaatar). D. s. innae Ognev, 1930 — S Russia (Astrakhan Region E of Volga River) and NW Kazakhstan (West Kazakhstan and Atyrau regions W of Ural River). D. s. lagopus Lichtenstein, 1823 — WC Kazakhstan (E of Emba and N of Syrdarya rivers). D. s. megacranius Shenbrot, 1991 — SE Kazakhstan (Moinkum Sands in Jambyl Region). D. s. nogai Satunin, 1907 — S European Russia (Volgograd and Astrakhan regions E of Volga River, Kalmykia, and Dagestan). D. s. sowerbyi Thomas, 1908 — N China (NE Xinjiang, N Qaidam Basin in Qinghai, Gansu, SW Inner Mongolia, N Ningxia, and N Shaanxi) and Mongolia. D. s. turanicus Shenbrot, 1991 — SW Kazakhstan (S Kyzylorda S of Syrdarya River and Mangystau regions), Uzbekistan, and Turkmenistan; it probably occurs in adjacent W Afghanistan. D. s. ubsanensis Bannikov, 1947 — NW Mongolia (N Uvs) and adjacent Russia (extreme S Tuva). D. s. usuni Shenbrot, 1991 — SE Kazakhstan (Almaty Region); it probably occurs in adjacent China (sands of Ili Valley of W Xinjiang). D. s. zaissanensis Selevin, 1934 — E Kazakhstan (NW Lake Zaysan Basin on the left bank of Irtysh River). Isolated population in N Iran (Turan Desert in E Semnan Province) may belong to turanicus or correspond to a yet undescribed subspecies. in Dipodidae
Subspecies and Distribution. pos sagitta Pallas, 1773 — S Russia (Altai Krai) and right bank of Irtysh River in Kazakhstan (Pavlodar and East Kazakhstan regions). D.s.aksuensisWangSung,1964—NWChina(NTarimBasininXinjiang). D.s.austrouralensisShenbrot,1991—NWKazakhstan(WestKazakhstan,Atyrau,andAktoberegionsbetweenUralandEmbarivers). D.s.bulganensisShenbrot,1991—EKazakhstan(ELakeZaysaninEastKazakhstanRegion),NWChina(DzungarianBasininXinjiang),andMongolia(SKhovdandSWGovi-Altai). D.s.deasyiBarret-Hamilton,1900—NWChina(STarimBasininXinjiangandS&WQaidamBasininQinghai). D. s. fuscocanus Wang Sung, 1964 — W China (S foothills of E Tian Shan in Xinjiang). D. s. halli Sowerby, 1920 — China (NE Inner Mongolia [= Nei Mongol], SW Heilongjiang, NWJilin, and N Liaoning) and SE Mongolia (Stikhbaatar). D. s. innae Ognev, 1930 — S Russia (Astrakhan Region E of Volga River) and NW Kazakhstan (West Kazakhstan and Atyrau regions W of Ural River). D. s. lagopus Lichtenstein, 1823 — WC Kazakhstan (E of Emba and N of Syrdarya rivers). D. s. megacranius Shenbrot, 1991 — SE Kazakhstan (Moinkum Sands in Jambyl Region). D. s. nogai Satunin, 1907 — S European Russia (Volgograd and Astrakhan regions E of Volga River, Kalmykia, and Dagestan). D. s. sowerbyi Thomas, 1908 — N China (NE Xinjiang, N Qaidam Basin in Qinghai, Gansu, SW Inner Mongolia, N Ningxia, and N Shaanxi) and Mongolia. D. s. turanicus Shenbrot, 1991 — SW Kazakhstan (S Kyzylorda S of Syrdarya River and Mangystau regions), Uzbekistan, and Turkmenistan; it probably occurs in adjacent W Afghanistan. D. s. ubsanensis Bannikov, 1947 — NW Mongolia (N Uvs) and adjacent Russia (extreme S Tuva). D. s. usuni Shenbrot, 1991 — SE Kazakhstan (Almaty Region); it probably occurs in adjacent China (sands of Ili Valley of W Xinjiang). D. s. zaissanensis Selevin, 1934 — E Kazakhstan (NW Lake Zaysan Basin on the left bank of Irtysh River). Isolated population in N Iran (Turan Desert in E Semnan Province) may belong to turanicus or correspond to a yet undescribed subspecies.
On following pages: 2. North Pacific Right Whale (Eubalaena japonica); 3. Southern Right Whale (Eubalaena australis); 4. Bowhead Whale (Balaena mysticetus). in Balaenidae
On following pages: 2. North Pacific Right Whale (Eubalaena japonica); 3. Southern Right Whale (Eubalaena australis); 4. Bowhead Whale (Balaena mysticetus).
FIGURE. Sanicula orthacantha in the wild (China, Chongqing, Nanchuan, Jinfo Shan, the type locality of S. nanchuanensis). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit. J. Mericarps. in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha in the wild (China, Chongqing, Nanchuan, Jinfo Shan, the type locality of S. nanchuanensis). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit. J. Mericarps.
FIGURE. Sanicula orthacantha in the wild (China, Jiangxi, Jiujiang, Lushan, the type locality of S. orthacantha). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha in the wild (China, Jiangxi, Jiujiang, Lushan, the type locality of S. orthacantha). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps
FIGURE. Sanicula orthacantha var. brevispina in the wild (China, Sichuan, Emei Shan, the type locality of S. orthacantha var. brevispina and S. orthacantha var. stolonifera). A. Habitat and habit. B. Rhizome. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps. in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha var. brevispina in the wild (China, Sichuan, Emei Shan, the type locality of S. orthacantha var. brevispina and S. orthacantha var. stolonifera). A. Habitat and habit. B. Rhizome. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps.
Distribution. Poorly known, but it is believed to extend from the S (right) bank of the upper reaches of the Rio Purus in SE Peru, W into the Rio Urubamba Valley in the Cuzco Department, including the upper Rio Madre de Dios, S and E as far the Tambopata Basin, and extending into NW Bolivia. in Cebidae
Distribution. Poorly known, but it is believed to extend from the S (right) bank of the upper reaches of the Rio Purus in SE Peru, W into the Rio Urubamba Valley in the Cuzco Department, including the upper Rio Madre de Dios, S and E as far the Tambopata Basin, and extending into NW Bolivia.
Distribution. NE Brazil (NE Para and NW Maranhao states); the precise distribution is unknown but is suspected to include an area of at least 15,000 km? from the Rio Tocantins in Para to the right bank of the Rio Grajau in Maranhao. in Cebidae
Distribution. NE Brazil (NE Para and NW Maranhao states); the precise distribution is unknown but is suspected to include an area of at least 15,000 km? from the Rio Tocantins in Para to the right bank of the Rio Grajau in Maranhao.
Subspecies and Distribution. C.o.olivaceusSchomburgk,1848—mightberestrictedtotheVenezuelanAmazonBasinfromtheupperRioOrinoco,andthroughouttheOrinocosavannaabovethemouthoftheRioMeta,asfarNandWastheSierradePerijaandtheVenezuelanC.o.dela C.o. (C.o. Range), to the left bank of the Rio Essequibo in W Guyana, in forests of the Guiana Shield; distributional limits separating the two subspecies are not well known. C. o. castaneus 1. Geoffroy Saint-Hilaire, 1851 — Guianas (possibly from the Rio Essequibo in Guyana E through Suriname and French Guiana) and N Brazil, where its distributional limits are not well known but are possibly marked by the rios Negro and Branco and Catrimani (right bank affluent of the Rio Branco) in the W, the Rio Amazonas in the S, and the Atlantic coast in the E, and it also occurs on Caviana and Mexiana Is in the estuary of the Rio Amazonas. Small numbers introduced as pets are now feral on Margarita I off the Venezuelan coast. in Cebidae
Subspecies and Distribution. C.o.olivaceusSchomburgk,1848—mightberestrictedtotheVenezuelanAmazonBasinfromtheupperRioOrinoco,andthroughouttheOrinocosavannaabovethemouthoftheRioMeta,asfarNandWastheSierradePerijaandtheVenezuelanC.o.dela C.o. (C.o. Range), to the left bank of the Rio Essequibo in W Guyana, in forests of the Guiana Shield; distributional limits separating the two subspecies are not well known. C. o. castaneus 1. Geoffroy Saint-Hilaire, 1851 — Guianas (possibly from the Rio Essequibo in Guyana E through Suriname and French Guiana) and N Brazil, where its distributional limits are not well known but are possibly marked by the rios Negro and Branco and Catrimani (right bank affluent of the Rio Branco) in the W, the Rio Amazonas in the S, and the Atlantic coast in the E, and it also occurs on Caviana and Mexiana Is in the estuary of the Rio Amazonas. Small numbers introduced as pets are now feral on Margarita I off the Venezuelan coast.
Subspecies and Distribution. P.i.wrrorataGray,1842—Brazil(fromtheriosJurua-TarauacaEtotheriosTapajos-Juruena,andStotheRioGuaporé),NBolivia(NoftheRioMadredeDios),andSEPeru(fromtheupperRioPurus,WoftheRioUrubamba,andStotheRioTambopata);itdoesnotoccurbetweenthelowerPurusandtheRioJurua,thedomainoftheBuftySaki(P.albicans). P. i. vanzolinii Hershkovitz, 1987 — First described from Santa Cruz on the Rio Eiru (S tributary of the Rio Jurua), and believed to occur between the S (right) bank of the upper Rio Jurua and the S bank of the Rio Tarauaca in the SW of the Amazonas and Acre states, but there are very few documented locations. in Phitheciidae
Subspecies and Distribution. P.i.wrrorataGray,1842—Brazil(fromtheriosJurua-TarauacaEtotheriosTapajos-Juruena,andStotheRioGuaporé),NBolivia(NoftheRioMadredeDios),andSEPeru(fromtheupperRioPurus,WoftheRioUrubamba,andStotheRioTambopata);itdoesnotoccurbetweenthelowerPurusandtheRioJurua,thedomainoftheBuftySaki(P.albicans). P. i. vanzolinii Hershkovitz, 1987 — First described from Santa Cruz on the Rio Eiru (S tributary of the Rio Jurua), and believed to occur between the S (right) bank of the upper Rio Jurua and the S bank of the Rio Tarauaca in the SW of the Amazonas and Acre states, but there are very few documented locations.
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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.