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Figure 8 in Presence of populations of antlions (Neuroptera: Myrmeleontidae) in Denmark correlates with presence of aeolian sand
Figure 8. Distribution of Myrmeleon bore in Denmark. Number of records in circles. a). Overall distribution. b). Detailed distribution on Skaw Spit and LaesØ. c). Detailed distribution on Bornholm.
Figure 3 in Presence of populations of antlions (Neuroptera: Myrmeleontidae) in Denmark correlates with presence of aeolian sand
Figure 3. Myrmeleon spp., adults (NHMD). Scales = 1 cm. a, b). Myrmeleon formicarius (Linnaeus, 1767). c, d). Myrmeleon bore (Tjeder, 1941), male. Red arrow = bright spot on pronotum. Green arrow = Eltringham's organ.
Figure 1 in Presence of populations of antlions (Neuroptera: Myrmeleontidae) in Denmark correlates with presence of aeolian sand
Figure 1. Euroleon nostras (Geoffroy in Fourcroy, 1785), collected in the summer 2020 on Bornholm. a). Pupa. b). Larva. c). Adult. Not to scale. Live images by Line Kraemer/Bugdex.
FIGURE 8 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 8. Comparative of head scales of Calyptommatus species from dorsal view (left) and lateral view (right). (A) C. sinebrachiatus (MTR39001); (B) C. confusionibus (MTR24343); (C) C. frontalis sp. nov. (MZUSP 106738); (D) C. leiolepis (MTR39096); (E) C. nicterus (ACG44). Scale bars correspond to 2 mm.
FIGURE 6 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 6. Habitat where Calyptommatus frontalis sp. nov. was collected, showing the typical deciduous caatinga vegetation over sandy soils present in the region during A) wet season and B) dry season.
FIGURE 9 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 9. Comparative of dorsal scales in Calyptommatus. (A) C. sinebrachiatus (MTR39001); (B) C. confusionibus (MTR24343); (C) C. frontalis sp. nov. (MZUSP 106753; MTR38962); (D) C. sp.2 (MTR18055); (E) C. leiolepis (MTR39096); (F) C. nicterus (ACG44). Scale bar corresponds to 2 mm.
FIGURE 5 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 5. Paratype of Calyptommatus frontalis sp. nov. in life from Brejo do Poção, Buritirama, state of Bahia, northeast Brazil.
FIGURE 4 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 4. Details of body scalation of the holotype of Calyptommatus frontalis sp. nov. (MZUSP 106738, field number MTR 38950): A) dorsal view at midbody; B) ventral view at midbody; C) lateral view at midbody; D) precloacal region and hindlimbs. Scale bars correspond to 2 mm.
FIGURE 3 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 3. Calyptommatus frontalis sp. nov., adult female holotype: Dorsal, lateral and ventral views of head (MZUSP 106738, field number MTR 38950).
FIGURE 2 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 2. Satellite image of the Xique-Xique dune field region showing the variation in frontal scales in Calyptommatus. Aerial image from Google Earth Pro 2021 DigitalGlobe Image Landsat/Copernicus.
FIGURE 1. A in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 1. A) Bayesian inference phylogenetic tree for Calyptommatus and outgroups based on the mtDNA data set (16S + cytb + nd4; 1,918 bp). Values on nodes refer to Bayesian posterior probabilities (pp); values above 0.95 are considered high
FIGURE S2 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE S2. Bayesian inference phylogenetic tree for Calyptommatus and outgroups based on the five loci concatenated data set (16S + cytb + nd4 + c-mos + ntf3; 2,942 bp). Values on nodes refer to Bayesian posterior probabilities (pp); values above 0.95 are considered high statistical support for clades
FIGURE S1 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE S1. Bayesian inference phylogenetic tree for Calyptommatus and outgroups based on the nuDNA data set (c-mos + ntf3; 1,024 bp). Values on nodes refer to Bayesian posterior probabilities (pp); values above 0.95 are considered high statistical support for clades.
Phylogenetic divergence and ecophysiological variation in the disjunct Kalmia buxifolia (Sand-myrtle, Ericaceae)
<p><em>Kalmia buxifolia</em> (sand-myrtle, Ericaceae) is disjunctly distributed across the high-elevation rock outcrops of the southern Appalachians, upper monadnocks and pine savannas of the Carolina Piedmont and Coastal Plain, and the New Jersey Pine Barrens. Here, we sampled plants from each region and reconstructed the phylogeographic history of <em> K</em>. <em>buxifolia</em> to test a rock-outcrop Pleistocene refugium hypothesis, estimate the potential direction(s) and timing of migration, and date divergence from its alpine sister species, <em>K. procumbens</em>. We also assess whether isolation in these different environments has led to variation in intrinsic water-use efficiency (IWUE). Dating analysis challenges the current hypothesis that rock-outcrop species are relics of Pleistocene refugia (<18,000 ybp), placing the divergence of <em>K. buxifolia</em> and <em>K. procumbens</em> much earlier, in the late-Miocene (9.40 Ma). Chloroplast haplotype analysis indicates four potential refugial sites, with the most ancient on Mount LeConte in the Great Smoky Mountains, and point to an Appalachian corridor as the likely Pine Barrens colonization route. The sister species divergence time and population level divergences within <em>K. buxifolia</em> generally coincide with major climatic shifts from the late-Miocene to mid-Pleistocene. Results from CID indicate that plant water-use varies geographically within <em>K. buxifolia</em>, as does leaf morphology, although it is unclear whether this variation is due to genetic adaptation or phenotypic plasticity. These patterns of phylogenetic divergence and resulting ecophysiological diversity within <em>K. buxifolia</em> are significant for clarifying long-held questions about the biogeographic history and trait differentiation within this species. Further, our results suggest that high-elevation rock outcrop communities may have been inhabitated by northern-affinity species for much longer than previously assumed, and that subsequent population disjunction and isolation may have resulted in ecophysioloigcal differentiation in these communities.</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: 3. Idaho Pocket Gopher (Thomomys idahoensis); 4. Wyoming Pocket Gopher (Thomomys clusius); 5. Northern Pocket Gopher (Thomomys talpoides); 6. Camas Pocket Gopher (Thomomys bulbivorus), 7. Townsend's Pocket Gopher (Thomomys townsend); 8. Southern Pocket Gopher (Thomomys umbrinus); 9. Sierra Madre Occidental Pocket Gopher (Thomomys sheldoni); 10. Black-and-Brown Pocket Gopher (Thomomys atrovarius), 11. Nayar Pocket Gopher (Thomomys nayarensis); 12. Botta's Pocket Gopher (Thomomys bottae); 13. Plains Pocket Gopher (Geomys bursarius); 14. Hall's Pocket Gopher (Geomys jugossicularis); 15. Sand Hills Pocket Gopher (Geomys lutescens); 16. Desert Pocket Gopher (Geomys arenarius); 17. Jones's Pocket Gopher (Geomys knoxjonesi); 18. Attwater''s Pocket Gopher (Geomys attwateri); 19. Texas Pocket Gopher (Geomys personatus); 20. Strecker's Pocket Gopher (Geomys streckeri); 21. Tropical Pocket Gopher (Geomys tropicalis); 22. Llano Pocket Gopher (Geomys texensis); 23. Baird's Pocket Gopher (Geomys breviceps); 24. South-eastern Pocket Gopher (Geomys pinetis). in Geomyidae
On following pages: 3. Idaho Pocket Gopher (Thomomys idahoensis); 4. Wyoming Pocket Gopher (Thomomys clusius); 5. Northern Pocket Gopher (Thomomys talpoides); 6. Camas Pocket Gopher (Thomomys bulbivorus), 7. Townsend's Pocket Gopher (Thomomys townsend); 8. Southern Pocket Gopher (Thomomys umbrinus); 9. Sierra Madre Occidental Pocket Gopher (Thomomys sheldoni); 10. Black-and-Brown Pocket Gopher (Thomomys atrovarius), 11. Nayar Pocket Gopher (Thomomys nayarensis); 12. Botta's Pocket Gopher (Thomomys bottae); 13. Plains Pocket Gopher (Geomys bursarius); 14. Hall's Pocket Gopher (Geomys jugossicularis); 15. Sand Hills Pocket Gopher (Geomys lutescens); 16. Desert Pocket Gopher (Geomys arenarius); 17. Jones's Pocket Gopher (Geomys knoxjonesi); 18. Attwater''s Pocket Gopher (Geomys attwateri); 19. Texas Pocket Gopher (Geomys personatus); 20. Strecker's Pocket Gopher (Geomys streckeri); 21. Tropical Pocket Gopher (Geomys tropicalis); 22. Llano Pocket Gopher (Geomys texensis); 23. Baird's Pocket Gopher (Geomys breviceps); 24. South-eastern Pocket Gopher (Geomys pinetis).
Subspecies and Distribution. C.a.ammophilusOsgood,1907—NWMexico(restrictedtoSantaMargaritaI,SWBaja C.a. Sur). . C.a.dalquestiRoth,1976—NWMexico(SPacificcoastandC.a.RegionofBajaC.forniaSur). C. a. sublucidus Nelson & Goldman, 1929 — NW Mexico (coast S & E of the Bahia de la Paz, except the El Magote sand spit, S Baja C.a. Sur). in Heteromyidae
Subspecies and Distribution. C.a.ammophilusOsgood,1907—NWMexico(restrictedtoSantaMargaritaI,SWBaja C.a. Sur). . C.a.dalquestiRoth,1976—NWMexico(SPacificcoastandC.a.RegionofBajaC.forniaSur). C. a. sublucidus Nelson & Goldman, 1929 — NW Mexico (coast S & E of the Bahia de la Paz, except the El Magote sand spit, S Baja C.a. Sur).
Data set for: Effects of microstructure evolution on compressive strength of silica sand-enhanced oil well cement at a wide temperature range
<p><span>The influence of microstructure of silica-enhanced cement on the mechanical performance of cement is difficult to be described. In this study, we used the scanning electron microscope and image processing method to investigate the relationship between the complicity of cement microstructure and compressive strength under various temperature and curing time conditions. Fractal dimension was applied to describe the complicity of cement. The relationships among compressive strength, fractal dimension, temperature, curing time and pore structure of cement were identified. The results show that curing time of cement directly control the complicity of cement microstructure and compressive strength by altering the pore orientation and macropore ratio in cement. The curing temperature affects the complicity of cement microstructure and compressive strength indirectly by changing the ratio of micropore and small pore. The fractal dimension of silica-enhanced cement shows good correlation with compressive strength. Pore size distribution is the most important factor that influence the complicity of cement matrix and compressive strength of silica-enhanced cement. When building up the macroscopic mechanical performance model of cement, we should consider the influence of pore size distribution in cement under different curing temperatures and times on the complicity of cement microstructure. </span></p>
On following pages: 347. Plains Mouse (Pseudomys australis); 348. Bolam''s Mouse (Pseudomys bolami); 349. Kakadu Pebble Mouse (Pseudomys calabyi); 350. Western Pebble Mouse (Pseudomys chapmani); 351. Desert Mouse (Pseudomys desertor); 352. Shark Bay Mouse (Pseudomys field); 353. Australian Smoky Mouse (Pseudomys fumeus); 354. Eastern Chestnut Mouse (Pseudomys gracilicaudatus); 355. Sandy Inland Mouse (Pseudomys hermannsburgensis); 356. Long-tailed Mouse (Pseudomys higginsi); 357. Central Pebble Mouse (Pseudomys johnson); 358. Western Chestnut Mouse (Pseudomys nanus); 359. New Holland Mouse (Pseudomys novaehollandiae); 360. Western Mouse (Pseudomys occidentalis); 361. Hastings River Mouse (Pseudomys oralis); 362. Eastern Pebble Mouse (Pseudomys patrius); 363. Heath Mouse (Pseudomys shortridgel); 364. Common Australian Rock Rat (Zyzomys argurus); 365. Arnhem Land Rock Rat (Zyzomys maini); 366. Carpentarian Rock Rat (Zyzomys palatalis); 367. Central Australian Rock Rat (Zyzomys pedunculatus); 368. Kimberley Rock Rat (Zyzomys woodward); 369. Malayan Tree Rat (Pithecheir parvus); 370. Red Tree Rat (Pithecheir melanurus); 371. Bornean Tree Rat (Pithecheirops otion); 372. Cutch Rat (Cremnomys cutchicus); 373. Elvira Rat (Cremnomys elvira); 374. Crump's Rat (Diomys crumpi); 375. White-tailed Wood Rat (Madromys blanfordi); 376. Sand-colored Soft-furred Rat (Millardia gleadowi); 377. Kondana Soft-furred Rat (Millardia kondana); 378. Common Soft-furred Rat (Millardia in Muridae
On following pages: 347. Plains Mouse (Pseudomys australis); 348. Bolam''s Mouse (Pseudomys bolami); 349. Kakadu Pebble Mouse (Pseudomys calabyi); 350. Western Pebble Mouse (Pseudomys chapmani); 351. Desert Mouse (Pseudomys desertor); 352. Shark Bay Mouse (Pseudomys field); 353. Australian Smoky Mouse (Pseudomys fumeus); 354. Eastern Chestnut Mouse (Pseudomys gracilicaudatus); 355. Sandy Inland Mouse (Pseudomys hermannsburgensis); 356. Long-tailed Mouse (Pseudomys higginsi); 357. Central Pebble Mouse (Pseudomys johnson); 358. Western Chestnut Mouse (Pseudomys nanus); 359. New Holland Mouse (Pseudomys novaehollandiae); 360. Western Mouse (Pseudomys occidentalis); 361. Hastings River Mouse (Pseudomys oralis); 362. Eastern Pebble Mouse (Pseudomys patrius); 363. Heath Mouse (Pseudomys shortridgel); 364. Common Australian Rock Rat (Zyzomys argurus); 365. Arnhem Land Rock Rat (Zyzomys maini); 366. Carpentarian Rock Rat (Zyzomys palatalis); 367. Central Australian Rock Rat (Zyzomys pedunculatus); 368. Kimberley Rock Rat (Zyzomys woodward); 369. Malayan Tree Rat (Pithecheir parvus); 370. Red Tree Rat (Pithecheir melanurus); 371. Bornean Tree Rat (Pithecheirops otion); 372. Cutch Rat (Cremnomys cutchicus); 373. Elvira Rat (Cremnomys elvira); 374. Crump's Rat (Diomys crumpi); 375. White-tailed Wood Rat (Madromys blanfordi); 376. Sand-colored Soft-furred Rat (Millardia gleadowi); 377. Kondana Soft-furred Rat (Millardia kondana); 378. Common Soft-furred Rat (Millardia
On following pages: 141. Shaw's Jird (Meriones shawii); 142. Tristram's Jird (Meriones tristrami); 143. Dahl's Jird (Meriones dahl); 144. Vinogradov's Jird (Meriones vinogradovi); 145. Buxton's Jird (Meriones sacrament); 146. King Jird (Meriones rex); 147. Arabian Jird (Meriones arimalius); 148. Persian Jird (Meriones persicus); 149. Zarudny's Jird (Meriones zarudnyi); 150. Indian Desert Jird (Meriones hurrianae); 151. Cheng''s Jird (Meriones cheng); 152. Midday Jird (Meriones meridianus); 153. Tamarisk Jird (Meriones tamariscinus); 154. Mongolian Jird (Meriones unguiculatus); 155. Przewalski's Jird (Brachiones przewalskii); 156. Fat Sand Rat (Psammomys obesus); 157. Lesser Sand Rat (Psammomys vexillaris), 158. Great Gerbil (Rhombomys opimus); 159. Bittner's African Forest Mouse (Leimacomys buettneri); 160. Maned Rat (Lophiomys imhausi). in Muridae
On following pages: 141. Shaw's Jird (Meriones shawii); 142. Tristram's Jird (Meriones tristrami); 143. Dahl's Jird (Meriones dahl); 144. Vinogradov's Jird (Meriones vinogradovi); 145. Buxton's Jird (Meriones sacrament); 146. King Jird (Meriones rex); 147. Arabian Jird (Meriones arimalius); 148. Persian Jird (Meriones persicus); 149. Zarudny's Jird (Meriones zarudnyi); 150. Indian Desert Jird (Meriones hurrianae); 151. Cheng''s Jird (Meriones cheng); 152. Midday Jird (Meriones meridianus); 153. Tamarisk Jird (Meriones tamariscinus); 154. Mongolian Jird (Meriones unguiculatus); 155. Przewalski's Jird (Brachiones przewalskii); 156. Fat Sand Rat (Psammomys obesus); 157. Lesser Sand Rat (Psammomys vexillaris), 158. Great Gerbil (Rhombomys opimus); 159. Bittner's African Forest Mouse (Leimacomys buettneri); 160. Maned Rat (Lophiomys imhausi).
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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
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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.
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