Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
6,999
datasets available to search
ShareScore release 0.9.0
Dataset results
6,999 results for “Provinces”
Figure 2 in Molecular detection of Borrelia anserina in Argas persicus (Acari: Argasidae) ticks collected from Lorestan province, west of Iran
Figure 2. The stereomicroscopic view of dissected salivary glands (A); ovary and uterus (B) of female Argas tick in normal saline.
Figure 5 in Classical and geometric morphometric methods reveal differences between specimens of Varroa destructor (Mesostigmata: Varroidae) from seven provinces of Iran
Figure 5. Distribution of varroa mite based on a landmark in PCA analysis. Weight matrices data are used for this analysis. Circles show the closer groups.
Figure 1 in Classical and geometric morphometric methods reveal differences between specimens of Varroa destructor (Mesostigmata: Varroidae) from seven provinces of Iran
Figure 1. Morphometric parameters measured on the ventral surface varroa mite – a: body width, b: body length, c: length of the epigynal shield, d: length of the anal shield, e: metapodal shield's width, f: metapodal shield's length.
Figure 4 in Molecular detection of Borrelia anserina in Argas persicus (Acari: Argasidae) ticks collected from Lorestan province, west of Iran
Figure 4. The phylogenetic tree inferred from flaB nucleotide sequence data of B. anserina (clade I) and other Borrelia taxa (clade II and KX171816) constructed using Neighbor-Joining (NJ) method with bootstrap test (1000 replicates). The main clade in right side of tree separated with colored rectangular shape. Taxa are as species name following GenBank accession number, taxon of the present study indicated as bold. Nodes indicated with bootstrap value. Branch lengths are proportional to evolutionary changes, the units of the number of base substitutions per site the units of the number of amino acid substitutions per site. The analysis involved 12 nucleotide sequences. All positions containing gaps and missing data were eliminated. There were a total of 500 positions in the final dataset. The more diverged Pakistani strain of B. anserina (JF693808) located inside the main B. anserina (clade I). The members of clade II and B. hermsii are as outgroup.
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021). in Floristic, Vegetation And Climate Assessment Of The Early/Middle Miocene Parschlug Flora Indicates A Distinctly Seasonal Climate
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021).
Text-fig. 4. Graphical visualization of Phytogeographic Reference Regions Assessment (PRRA) of nearest living relative genera of fossil-taxa from late Early Miocene Wiesa assemblage in eastern Germany. Analysis yields only NLRs which have modern distribution area (partly) in E and SE Asia. For relationships of fossil-taxa to nearest living relatives or ecological equivalents, see Tab. 6; taxa used for analysis marked with asterisks. Three geographic resolutions conducted: a – grid with 1.5° latitude/longitude resolution, b – grid with 2°, c – grid with 3°; similarity column indicates cooccurrences of genera of nearest living relatives in single grid box. Maximum value in our analysis: grid box marked with arrow in map a, located in western Yunnan Province, P. R. China and southern Kachin Province, NE Myanmar (east of Myitkyina city), area with 97.371 7–98.874 2° longitude and 24.586 7–25.837 5° latitude, yields 23 co-occurring species of 13 genera (Tab. 7). in Assessment Of Phytogeographic Reference Regions For Cenozoic Vegetation: A Case Study On The Miocene Flora Of Wiesa (Germany)
Text-fig. 4. Graphical visualization of Phytogeographic Reference Regions Assessment (PRRA) of nearest living relative genera of fossil-taxa from late Early Miocene Wiesa assemblage in eastern Germany. Analysis yields only NLRs which have modern distribution area (partly) in E and SE Asia. For relationships of fossil-taxa to nearest living relatives or ecological equivalents, see Tab. 6; taxa used for analysis marked with asterisks. Three geographic resolutions conducted: a – grid with 1.5° latitude/longitude resolution, b – grid with 2°, c – grid with 3°; similarity column indicates cooccurrences of genera of nearest living relatives in single grid box. Maximum value in our analysis: grid box marked with arrow in map a, located in western Yunnan Province, P. R. China and southern Kachin Province, NE Myanmar (east of Myitkyina city), area with 97.371 7–98.874 2° longitude and 24.586 7–25.837 5° latitude, yields 23 co-occurring species of 13 genera (Tab. 7).
Fig. 12 in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 12. Toxotoma gonzalezi sp. nov. A. Holotype (MNHW), ♂, abdomen. B. Paratype (MNHW), ♀, abdomen. C. Holotype (MNHW), ♂, tergite VIII. D. Holotype (MNHW), ♂, ventrite 6. E. Paratype (MNHW), ♀, tergite VIII. F. Paratype (MNHW), ♀, ventrite 6. G. Holotype (MNHW), penis, lateral view. H. Holotype (MNHW), penis tip, lateral view. I. Holotype (MNHW), penis tip, inner view. J. Paratype (MNHW), ♀ genitalia, ventral view. K. Holotype (MNHW), ♂, segments IX and X, dorsal view. L. Holotype (MNHW), tegmen, lateral view. M. Holotype (MNHW), tegmen, inner view.
Fig. 13 in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 13. Hyperaspis rutai sp. nov. A. Holotype (MNHW), ♂, abdomen. B. Holotype (MNHW), ♂, tergite VIII. C. Paratype (MNHW), ♀, abdomen. D. Paratype (MNHW), ♀, tergite VIII. E. Paratype (MNHW), ♀, ventrite 6. F. Holotype (MNHW), ♂, segments IX and X, dorsal view. G. Holotype (MNHW), penis, lateral view. H. Paratype (MNHW), female genitalia, ventral view. I. Holotype (MNHW), penis tip, lateral view. J. Holotype (MNHW), penis tip, inner view. K. Holotype (MNHW), tegmen, inner view. L. Holotype (MNHW), tegmen, lateral view.
Fig. 11. Epilachna obtusiforma Gordon, 1975 in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 11. Epilachna obtusiforma Gordon, 1975, ♂ (MIZ). A. Ventrite 6. B. Tergite VIII. C. Penis, lateral view. D. Penis tip, lateral view. E. Penis tip, inner view. F. Segments IX and X, dorsal view. G. Tegmen, lateral view. H. Tegmen, inner view.
Fig. 9 in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 9. Siola atra González, 2015 (MIZ). A. Penis, lateral view. B. Penis tip, lateral view. C. Tegmen, inner. D. ♂, segments IX and X, dorsal view. E. Tegmen, lateral view. F. ♀, spermatheca. G. ♀, genitalia, ventral view.
Fig. 8 in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 8. Exoplectra misahualli sp. nov., ♂, holotype (MNHW). A. Abdomen. B. Inner surface of abdomen. C. Segment VIII, ventral view. D. Penis, lateral view. E. Penis tip, lateral view. F. Segments IX and X, dorsal view. G. Tegmen, inner view. H. Tegmen, lateral view. I. Penis guide apex, lateral view. J. Paramere apex, inner. view.
Fig. 7 in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 7. Chnoodes yanayacu sp. nov. A. Paratype (MNHW), ♀, abdomen. B. Holotype (MNHW), ♂, abdomen. C. Paratype (MNHW), ♀, tergite VIII. D. Paratype (MNHW), ♀, sternite VIII. E. Holotype (MNHW), ♂, tergite VIII. F. Holotype (MNHW), ♂, sternite VIII. G. Paratype (MNHW), spermatheca. H. Paratype (MNHW), ♀, genitalia, ventral. I. Holotype (MNHW), penis, lateral. J. Holotype (MNHW), penis tip, inner view. K. Holotype (MNHW), penis tip, lateral view. L. Holotype (MNHW), ♂, segments IX and X, dorsal view. M. Holotype (MNHW), tegmen, lateral view. N. Holotype (MNHW), tegmen, inner view.
Fig. 5. Habitus. A–C in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 5. Habitus. A–C. Eupalea borowieci sp. nov., ♂, holotype (MNHW). A. Dorsal view. B. Lateral view. C. Frontal view. D–F. Psyllobora marshalli Crotch, 1874, sex (MNHW). D. Dorsal view. E. Lateral view. F. Frontal view. G–I. Chnoodes yanayacu sp. nov., ♂, holotype (MNHW). G. Dorsal view. H. Lateral view. I. Frontal view. J–L. Exoplectra misahualli sp. nov., ♂, holotype (MNHW). J. Dorsal view. K. Lateral view. L. Frontal view.
Fig. 3. SEM images. A–D in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 3. SEM images. A–D. Eupalea borowieci sp. nov., paratype (MIZ). E. Hyperaspis rutai sp. nov., paratype (MIZ). F. Hinda ecuadorica Gordon & Canepari, 2013, ♂, (MIZ). A. Head and pronotum. B. Head, ventral. C. Prosternum and mesoventrite. D. Habitus, ventral view. E. Head, dorsal view. F. Distal part of abdomen, ventral view.
Fig. 2 in New Coccinellidae (Coleoptera, Coccinelloidea) from Napo Province in Ecuador
Fig. 2. Cyrea mcclarini sp. nov. A. Paratype (MIZ), ♀, abdomen. B. Holotype (MNHW), ♂, abdomen. C. Holotype (MNHW), ♂, tergite VIII. D. Paratype (MIZ), ♀, genitalia, ventral view. E. Paratype (MIZ), ♀, genitalia, lateral view. F. Paratype (MIZ), coxites apices, ventral view. G. Holotype (MNHW), ♂, segments IX and X, dorsal. H. Holotype (MNHW), penis, lateral. I. Holotype (MNHW), penis tip, lateral. J. Holotype (MNHW), penis tip, inner. K. Holotype (MNHW), tegmen, lateral view. L. Holotype (MNHW), tegmen, inner view.
Fig. 8 in Two new species of the genus Macrothele Ausserer, 1871 from Yunnan Province, China (Araneae: Macrothelidae)
Fig. 8. Macrothele auriculata sp. nov., paratype, ♀ (Ma-kh-m01). A. Body. B. Cuspules and sternum. C. Left chelicera, ventral view. D. Genitalia, dorsal view.
Fig. 7 in Two new species of the genus Macrothele Ausserer, 1871 from Yunnan Province, China (Araneae: Macrothelidae)
Fig. 7. Macrothele auriculata sp. nov., holotype, ♂ (Ma-kh-m01). A–C. Left palp tibia. A. Inside view. B. Dorsal view. C. Lateral view. D–G. Left palpal embolus. D. Inside view. E. Dorsal view. F. Lateral view. G. The end.
Fig. 4 in Two new species of the genus Macrothele Ausserer, 1871 from Yunnan Province, China (Araneae: Macrothelidae)
Fig. 4. Macrothele nullispine sp. nov., paratype, ♀ (Mn-hy-f01). A. Body. B. Left chelicera, ventral view. C. Cuspules and sternum. D. Genitalia, dorsal view.
Fig. 1 in Two new species of the genus Macrothele Ausserer, 1871 from Yunnan Province, China (Araneae: Macrothelidae)
Fig. 1. Distribution of Macrothele nullispine sp. nov. and Macrothele auriculata sp. nov. (red triangles) (the green triangles show other species of Macrothele spiders distributed in Yunnan Province, China, with a total of 15 species, including M. bannaensis Xu & Yin, 2001, M. cangshanensis Z.B. Yang, Zhao, Zhang & Z.Z. Yang, 2018, M. jingzhao Chen, Jiang & Yang, 2020, M. jinlin Z.B. Yang, Zhao, Zhang & Z.Z. Yang, 2018, M. menglunensis Li & Zha, 2013, M. multispine Wang, Li & Yang, 2019, M. yani Xu, Yin & Griswold, 2002, M. yongshengensis Z.B. Yang, Zhao & Z.Z. Yang, 2019, M. yunlingensis Z.B. Yang, Zhao & Z.Z. Yang, 2019, M. sanheensis Tang, Zhao & Yang, 2020, M. undata Tang, Zhao & Yang, 2020, M. arcuata Tang, Zhao & Yang, 2020, M. mingsheng Wu & Z.Z. Yang, 2022, M. washanensis Wu & Z.Z. Yang, 2022 and M. wuliangensis Wu & Z.Z. Yang, 2022).
Fig. 3 in Two new species of the genus Macrothele Ausserer, 1871 from Yunnan Province, China (Araneae: Macrothelidae)
Fig. 3. Macrothele nullispine sp. nov., holotype, ♂ (Mn-hy-m01). A. Left palp tibia, inside view. B. Same, dorsal view. C. Same, lateral view. D–G. Left palpal embolus. D. Inside view. E. Dorsal view. F. Lateral view. G. The end.
ScienceDex guides
Understand access before you commit
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.