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FIGURE 18. Centruroides Marx, 1890, metasomal segments I and II, ventral aspect. A, D. C. rileyi Sissom, 1995, A in Systematic Revision Of The Arboreal Neotropical "Thorellii" Clade Of Centruroides Marx, 1890, Bark Scorpions (Buthidae C.L. Koch, 1837) With Descriptions Of Six New Species
FIGURE 18. Centruroides Marx, 1890, metasomal segments I and II, ventral aspect. A, D. C. rileyi Sissom, 1995, A. ♂ (CNAN SC4002), D. ♀ (CNAN SC4003). B, E. C. hamadryas, sp. nov., B. holotype ♂ (CNAN T01408), E. paratype ♀ (CNAN T01415). C, F. C. hoffmanni Armas, 1996, C. ♂, F. ♀ (CNAN SC3996). G, J. C. cuauhmapan, sp. nov., G. holotype ♂ (CNAN T01396), J. paratype ♀ (CNAN T01399). H, K. C. berstoni, sp. nov., H. holotype ♂ (CASENT 9073325), K. paratype ♀ (CASENT 9073313). I, L. C. chanae, sp. nov., I. holotype ♂ (CNAN T01403), L. paratype ♀ (CNAN T01405). M, P. C. catemacoensis, sp. nov., M. holotype ♂ (CNAN T01424), P.paratype ♀ (CNAN T01423). N, Q. C. schmidti Sissom, 1995, N. ♂ (CASENT 9073316), Q. ♀ (CASENT 9073317). O, R. C. yucatanensis, sp. nov., O. holotype ♂ (CNAN T01416), R. paratype ♀ (CNAN T01417. Scale bars = 2 mm.
FIGURE 21. Centruroides Marx, 1890, metasomal segment V, ventral aspect. A, D. C. rileyi Sissom, 1995, A in Systematic Revision Of The Arboreal Neotropical "Thorellii" Clade Of Centruroides Marx, 1890, Bark Scorpions (Buthidae C.L. Koch, 1837) With Descriptions Of Six New Species
FIGURE 21. Centruroides Marx, 1890, metasomal segment V, ventral aspect. A, D. C. rileyi Sissom, 1995, A. ♂ (CNAN SC4002), D. ♀ (CNAN SC4003). B, E. C. hamadryas, sp. nov., B. holotype ♂ (CNAN T01408), E. paratype ♀ (CNAN T01415). C, F. C. hoffmanni Armas, 1996, C. ♂, F. ♀ (CNAN SC3996). G, J. C. cuauhmapan, sp. nov., G. holotype ♂ (CNAN T01396), J. paratype ♀ (CNAN T01399). H, K. C berstoni, sp. nov., H. holotype ♂ (CASENT 9073325), K. paratype ♀ (CASENT 9073313). I, L. C. chanae, sp. nov., I. holotype ♂ (CNAN T01403), L. paratype ♀ (CNAN T01405). M, P. C. catemacoensis, sp. nov., M. holotype ♂ (CNAN T01424), P. paratype ♀ (CNAN T01423). N, Q. C. schmidti Sissom, 1995, N. ♂ (CASENT 9073316), Q. ♀ (CASENT 9073317). O, R. C. yucatanensis, sp. nov., O. holotype ♂ (CNAN T01416), R. paratype ♀ (CNAN T01417). Scale bars = 2 mm.
FIGURE 20. Centruroides Marx, 1890, metasomal segment V, dorsal aspect. A, D. C. rileyi Sissom, 1995, A in Systematic Revision Of The Arboreal Neotropical "Thorellii" Clade Of Centruroides Marx, 1890, Bark Scorpions (Buthidae C.L. Koch, 1837) With Descriptions Of Six New Species
FIGURE 20. Centruroides Marx, 1890, metasomal segment V, dorsal aspect. A, D. C. rileyi Sissom, 1995, A. ♂ (CNAN SC4002), D. ♀ (CNAN SC4003). B, E. C. hamadryas, sp. nov., B. holotype ♂ (CNAN T01408), E. paratype ♀ (CNAN T01415). C, F. C. hoffmanni Armas, 1996, C. ♂, F. ♀ (CNAN SC3996). G, J. C. cuauhmapan, sp. nov., G. holotype ♂ (CNAN T01396), J. paratype ♀ (CNAN T01399). H, K. C. berstoni, sp. nov., H. holotype ♂ (CASENT 9073325), K. paratype ♀ (CASENT 9073313). I, L. C. chanae, sp. nov., I. holotype ♂ (CNAN T01403), L. paratype ♀ (CNAN T01405). M, P. C. catemacoensis, sp. nov., M. holotype ♂ (CNAN T01424), P. paratype ♀ (CNAN T01423). N, Q. C. schmidti Sissom, 1995, N. ♂ (CASENT 9073316), Q. ♀ (CASENT 9073317). O, R. C. yucatanensis, sp. nov., O. holotype ♂ (CNAN T01416), R. paratype ♀ (CNAN T01417). Scale bars = 2 mm.
Svalbard reindeer winter diets (1995–2012) dataset
<p>Arctic ecosystems are changing dramatically with warmer and wetter conditions resulting in complex interactions between herbivores and their forage. We investigated how Svalbard reindeer (<em>Rangifer tarandus platyrhynchus</em>) modify their late winter diets in response to long-term trends and interannual variation in forage availability and accessibility. By reconstructing their diets and foraging niches over a 17-year period (1995–2012) using serum δ<sup>13</sup>C and δ<sup>15</sup>N values, we found strong support for a temporal increase in the proportions of graminoids in the diets with a concurrent decline in the contributions of mosses. This dietary shift corresponds with graminoid abundance increases in the region and was associated with increases in population density, warmer summer temperatures and more frequent rain-on-snow (ROS) in winter. In addition, the variance in isotopic niche positions, breadths and overlaps also supported a temporal shift in the foraging niche and a dietary response to extreme ROS events. Our long-term study highlights the mechanisms by which winter and summer climate changes cascade through vegetation shifts and herbivore population dynamics to alter the foraging niche of Svalbard reindeer. Although i<span>t has been anticipated that climate changes in the Svalbard region of the Arctic would be detrimental to this unique ungulate</span>, our study suggests that environmental change is in a phase where conditions are improving for this subspecies at the northernmost edge of the <em>Rangifer</em> distribution.</p>
Text-fig. 4. Type specimens of Magnolia allasoniae MARTINETTO sp. nov. from the Pliocene locality Ca' Viettone. a1–a4: Holotype (MGPT-PU141081) in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 5) in a black and white print (a1), in a new digital photograph in basal view (a2), ventral view (a3) and dorsal view (a4); b1–b4: Paratype MGPT-PU141082 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 4) in a black and white print (b1), in a new digital photograph in basal view (b2), ventral view (b3) and dorsal view (b4); c1–c4: Paratype MGPT-PU141083 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 6) in a black and white print (c1), in a new digital photograph in basal view (c2), ventral view (c3) and dorsal view (c4); d1–d4: Paratype MGPT-PU141084 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 7) in a black and white print (d1), in a new digital photograph in basal view (d2), ventral view (d3) and internal view (d4). Scale bars 1 mm. in Late Messinian Flora From The Post-Evaporitic Deposits Of The Piedmont Basin (Northwest Italy)
Text-fig. 4. Type specimens of Magnolia allasoniae MARTINETTO sp. nov. from the Pliocene locality Ca' Viettone. a1–a4: Holotype (MGPT-PU141081) in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 5) in a black and white print (a1), in a new digital photograph in basal view (a2), ventral view (a3) and dorsal view (a4); b1–b4: Paratype MGPT-PU141082 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 4) in a black and white print (b1), in a new digital photograph in basal view (b2), ventral view (b3) and dorsal view (b4); c1–c4: Paratype MGPT-PU141083 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 6) in a black and white print (c1), in a new digital photograph in basal view (c2), ventral view (c3) and dorsal view (c4); d1–d4: Paratype MGPT-PU141084 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 7) in a black and white print (d1), in a new digital photograph in basal view (d2), ventral view (d3) and internal view (d4). Scale bars 1 mm.
Understory and canopy phenology, I/Io, solar radiation, and temperature related to Trelease Woods, Urbana, IL, USA from 1995–2022
<p>This study used phenological field observations made year-round for 15 dominant canopy tree species (1995-2022), understory saplings of three species (1995-2022), and 33 herb species (1995-2017) in Trelease Woods, a mature old-growth deciduous forest remnant near Urbana, Illinois, USA. The phenological data sets are paired with basal-area data, mid-day light transmission data from 21 days in 2002, daily solar radiation data from a NOAA (SURFRAD) site at Bondville, Illinois, and daily temperature data from a nearby weather station in Champaign, Illinois. These datasets were used to parameterize models of canopy light transmittance and understory plant light interception.</p> <p>These data sets were used to test the mismatch hypothesis, viz, whether canopy trees or understory plants are more sensitive to climate change, thus changing through time the relative amount of transmitted light understory species intercept. We estimated how four factors (understory phenology, cold temperatures, canopy phenology, and sunlight) individually limit the potential light interception of each understory species.</p>
Fig. 3 in A new species of the deep-sea porter crab genus Gordonopsis Guinot & Richer de Forges, 1995 (Crustacea, Decapoda, Brachyura, Homolidae) from the South China Sea
Fig. 3. Gordonopsis mazupo, new species, holotype male (33.4 × 24.3 mm) (SY353B6), South China Sea. A, lateral view of cephalothorax; B, left third maxilliped; C, frontal view of cephalothorax; D, ventral view showing buccal cavity, epistome, antennae and antennules; E, dorsal view of carpus of left cheliped; F, dorsal view of carpus of right cheliped; G, outer view of right chela; H, outer view of right chela; I, inner view of right chela.
Fig. 5 in A new species of the deep-sea porter crab genus Gordonopsis Guinot & Richer de Forges, 1995 (Crustacea, Decapoda, Brachyura, Homolidae) from the South China Sea
Fig. 5. Gordonopsis mazupo, new species, holotype male (33.4 × 24.3 mm) (SY353B6), South China Sea. A, left P2–P4 coxae and basisischia (denuded); B, right P2–P4 coxae (denuded); C, sternopleonal cavity with right G1 and G2 in situ; D, G, left G1 (ventral view); E, H, left G1 (dorsal view); F, I, left G2 (ventral view). G–I, drawn to same scale. Scale bars = 5 mm.
Fig. 1 in A new species of the deep-sea porter crab genus Gordonopsis Guinot & Richer de Forges, 1995 (Crustacea, Decapoda, Brachyura, Homolidae) from the South China Sea
Fig. 1. Gordonopsis mazupo, new species, holotype male (33.4 × 24.3 mm) (SY353B6), South China Sea. Colour in life. Scale bars = 10.0 mm. Photographs by Yadong Zhou.
Fig. 2 in A new species of the deep-sea porter crab genus Gordonopsis Guinot & Richer de Forges, 1995 (Crustacea, Decapoda, Brachyura, Homolidae) from the South China Sea
Fig. 2. Gordonopsis mazupo, new species, holotype male (33.4 × 24.3 mm) (SY353B6), South China Sea. A, overall habitus (legs detached); B, dorsal view of carapace; C, dorso-frontal view of carapace.
Fig. 4 in A new species of the deep-sea porter crab genus Gordonopsis Guinot & Richer de Forges, 1995 (Crustacea, Decapoda, Brachyura, Homolidae) from the South China Sea
Fig. 4. Gordonopsis mazupo, new species, holotype male (33.4 × 24.3 mm) (SY353B6), South China Sea. A, dorsal view of carapace showing relative P5 length; B, ventral view of cephalothorax showing pleon; C–F, right P2–P5, respectively (all to same scale); G, right P5 pseudochela; H, left P5 pseudochela; I, proximal part of right P2 merus (lateral view); J, proximal part of right P3 merus (lateral view); K, proximal part of right P4 merus (lateral view); L, proximal part of right P4 merus (view from flexor margin showing median spine on lateral surface).
Fig. 14. The provannid gastropod Provanna antiqua Squires, 1995 in Mollusks and a crustacean from early Oligocene methane-seep deposits in the Talara Basin, northern Peru
Fig. 14. The provannid gastropod Provanna antiqua Squires, 1995, from early Oligocene seep deposits at Cerro La Salina (block 1, A, F; block 4, H; block 6, B, C, D, G; block 8, E), Talara Basin, northern Peru. A. NRM Mo187044, specimen with distinctive axial and spiral sculpture, in abapertural view. B. NRM Mo187045, specimen with distinctive sculpture and showing the basal groove, in apertural view. C. NRM Mo187046, specimen with weak axial sculpture in the upper whorl, in apertural view. D. NRM Mo187047, fragmentary specimen with mainly spiral sculpture, in apertural view. E. NRM Mo187048, nearly smooth specimen showing slightly sinuous growth lines, in apertural view. F. NRM Mo187049, specimen with small shoulder and sculpture mainly in upper part of whorls, in apertural view. G. NRM Mo187050, specimen with faint axial and spiral sculpture, in apertural view. H. NRM Mo187051, two specimens with small shoulder and sculpture mainly in upper part of whorls..
Fig. 2. Cleomenes modicatus Fig. 3. Cleomenes Fig. 4. Cleomenes longipennis tristriatus Holzschuh 1995 in Two New Taxa Of Cleomenes Thomson, 1864 (Coleoptera: Cerambycidae) From China And Vietnam
Fig. 2. Cleomenes modicatus Fig. 3. Cleomenes Fig. 4. Cleomenes longipennis tristriatus Holzschuh 1995, holotype katrinae sp. nov. Gressitt, 1951, holotype (Berzak 2020). (Berzak 2020).
Figure 1 in The first record of the jumping bristletail Pedetontus gershneri Allen, 1995 (Microcoryphia: Machilidae) from Alabama, USA significantly extends its known range
Figure 1. Map showing the known distribution of Pedetontus gershneri Allen 1995. Square represents the previous distribution records from the type locality of Magazine Mountain, Arkansas. Star represents the new record reported here from Bankhead National Forest, Alabama.
Fig. 1. Cyrtohymena australis Foissner, 1995 in Morphological redescriptions of three Cyrtohymena ciliates (Ciliophora: Sporadotrichida: Oxytrichidae) new to Korea
Fig. 1. Cyrtohymena australis Foissner, 1995 from live (A, D, E, F) and protargol-impregnated specimens (B, C, G). A, D. Ventral view of a typical individual. B, G. Ventral view of general infraciliature and nuclear apparatus. C. Showing dorsal kineties and caudal cirri. E. Flexible body. F. Cortical granules on dorsal side. Scale bar=100 µm.
Figure 1. Maximum margin hyper-plane (Cortes & Vapnik, 1995).-Cognitive Development Optimization Algorithm Based Support Vector Machines for Determining Diabetes
<p>In other words, it aims to find the state in which the distance between the two classes is the maximum. The hallmarks of this classification reasoning are the support vectors chosen from the training set, and they are located on the closest points of both classes (Javed, Ayyaz, & Mehmood, 2007). In Figure 1, an example of support vectors and a maximum margin hyper-plane (in other words, an optimum separating hyper- plane) is shown (Cortes & Vapnik, 1995).</p>
Fig. 28 in Semi-aquatic Epilamprinae cockroaches (Blattodea: Blaberidae) in Cameroon: towards a revision of continental African species of Rhabdoblatta Kirby, 1903 and Africalolampra Roth, 1995
Fig. 28. Rhabdoblatta lyncea (Gerstaecker, 1883), paratype, juvenile (ZIMG-II 27341). Habitus in dorsal and ventral views, with labels. Photographed by Lara Lopardo (ZIMG). Scale bar = 5 mm.
Fig. 25 in Semi-aquatic Epilamprinae cockroaches (Blattodea: Blaberidae) in Cameroon: towards a revision of continental African species of Rhabdoblatta Kirby, 1903 and Africalolampra Roth, 1995
Fig. 25. Rhabdoblatta pluriramosa (Karny, 1915), juvenile specimen (MNHN-EP7605), habitus in dorsal and ventral views. Scale bar = 5 mm.
Fig. 31 in Semi-aquatic Epilamprinae cockroaches (Blattodea: Blaberidae) in Cameroon: towards a revision of continental African species of Rhabdoblatta Kirby, 1903 and Africalolampra Roth, 1995
Fig. 31. Unidentified female specimen (MNHN-EP7602). A. Habitus in dorsal and ventral views. B. Pronotum. C. Head. D. Hindleg with close-up on tarsi and serrated claws, ventral view. E. Subgenital plate and cerci. F. Front femur. Scale bars: A = 5 mm; B–F = 1 mm.
Fig. 22 in Semi-aquatic Epilamprinae cockroaches (Blattodea: Blaberidae) in Cameroon: towards a revision of continental African species of Rhabdoblatta Kirby, 1903 and Africalolampra Roth, 1995
Fig. 22. Rhabdoblatta pluriramosa (Karny, 1915), male specimen (MNHN-EP7616). A. Habitus in dorsal and ventral views. B. Pronotum. C. Front femur. D. Subgenital plate. E. Supra-anal plate. F. Tarsi and claws of hind leg. Scale bars: A = 5 mm; B–F = 1 mm.
ScienceDex guides
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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.