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.
685
datasets available to search
ShareScore release 0.7.1
Dataset results
685 results for “biotic”
Fig. 5 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 5 Shanggang. Detailed stratigraphic log of the studied interval of the Shanggang section showing the distribution of conodont taxa and the δ13Crecord throughout the Smithian and Spathian part of the Luolou Formation. The LMHs and UAZ are indicated. Note the gap because of low carb angle faulting in the upper part of the black shales
Fig. 6 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 6 Lilong. Detailed stratigraphic log of the studied interval of the Lilong section showing the distribution of conodont taxa and the δ13Ccarb record throughout the late Smithian and Early Spathian part of the Luolou Formation. The LMHs and UAZs are indicated
Fig. 7 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 7 Youping Cascade. Detailed stratigraphic log of the studied interval of the Youping Cascade section showing the distribution of conodont taxa and the δ13Crecord throughout the late Smithian and Early Spathian part of the Luolou Formation. The LMHs and UAZs are indicated carb
Fig. 9 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 9 Position of the UAZs in the studied sections Qiakong, Laren, Shanggang, Lilong and Youping Cascade. The lithological units are simplified and represented from unit III to unit Vc. Note the ammonoid zones recorded from Laren, Shanggang, Lilong and Youping Cascade
Fig. 4 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 4 Laren. Detailed stratigraphic log of the studied interval of the Laren section showing the distribution of conodont taxa and the δ13Ccarb record throughout the Smithian and Spathian part of the Luolou Formation. The LMHs and UAZs are indicated
Fig. 2 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 2 Pictures from four of the five studied sections in the Nanpanjiang basin. A Qiakong, B Shanggang, C Laren (Kuang Guodun for scale), D Lilong (Hugo Bucher for scale)
Fig. 3 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 3 Qiakong. Detailed stratigraphic log of the studied interval of the Qiakong section showing the distribution of conodont taxa and the δ13Ccarb record throughout the middle Smithian part of the Daye Formation and the late Smithian to Spathian Luolou Formation. The LMHs and UAZs are indicated
Fig. 3 in Quantitative Biogeographic Characterization Of Hungary Based On The Distribution Data Of Land Snails (Mollusca,Gastropoda): A Case Of Nestedness Of Species Ranges With Extensive Overlap Of Biotic Elements
Fig. 3. Distribution maps of four biotic elements found by PRABCLUS: (a) highland species, (b) general species, (c) localizes species distributed in the northern and (d) south–eastern parts of Hungary. The different shadings indicate the areas where>70%,>30%, and>0% of the species of an ele-
Fig. 1 in Quantitative Biogeographic Characterization Of Hungary Based On The Distribution Data Of Land Snails (Mollusca,Gastropoda): A Case Of Nestedness Of Species Ranges With Extensive Overlap Of Biotic Elements
Fig. 1. Biogeographic classification of Hungary based on distribution data of land snails according to the (a) hierarchical clustering of the (b) spatial units (ca. 50 km × 50 km). For clustering, the Sørensen–index and Ward–Orlóci fusion method was used. Shades of grey indicate main partitions of the cluster hierarchy, circled numbers 1–6 indicate lower level partitions mentioned in the text, numbers 1–49 identify spatial units (a) in the cluster foot and (b) in the map. Capital letters correspond to IndVal species groups listed in the text and in Appendix, lines associated to letters refer to
Fig. 2 in Quantitative Biogeographic Characterization Of Hungary Based On The Distribution Data Of Land Snails (Mollusca,Gastropoda): A Case Of Nestedness Of Species Ranges With Extensive Overlap Of Biotic Elements
Fig. 2. First two dimensions of the metric multidimensional scaling of the range data of the Hungarian land snail species. 1–4: biotic elements found by PRABCLUS; N: noise component.
Data from: The importance of biotic interactions in distribution models of wild bees depends on the type of ecological relations, spatial scale and range
<p>Studies have found that biotic information can play an important role in shaping the distribution of species even at large scales. However, results from species distribution models are not always consistent among studies, and the underlying factors that influence the importance of biotic information to distribution models, are unclear. 2. We studied wild bees and plants, and cleptoparasite bees and their hosts in the Netherlands to evaluate how the inclusion of their biotic interactions affects the performance of species distribution models. We assessed model performance through spatial block cross-validation and by comparing models with interactions to models where the interacting species were randomized. Finally, we evaluated how, (i) spatial resolution, (ii) taxonomic rank (genus or species), (iii) degree of specialization, (iv) distribution of the biotic factor, (v) bee body size and (vi) type of biotic interaction, affect the importance of biotic interactions in shaping the distribution of wild bee species using generalized linear models. 3. We found that the models of wild bees improved when the biotic factor was included. The model performance improved the most for parasitic bees. Spatial resolution, taxonomic rank, distribution range of the biotic factor, and degree of specialization of the modelled species all influenced the importance of the biotic interaction to the models. 4. We encourage researchers to include biotic interactions in species distribution models, especially for specialized species and when the biotic factor has a limited distribution range. However, before adding the biotic factor we suggest considering different spatial resolutions and taxonomic ranks of the biotic factor. We recommend using single species or genus data as a biotic factor in the models of specialist species and for the generalist species, we recommend using an approximate measure of interactions, such as flower richness.</p>
Fig. 1 in Assessment of Odonate assemblages in the Agro Pontino (Latina, Central Italy) using two biotic indices (Insecta: Odonata)
Fig. 1 – Geographical location of the study area (Lazio, central Italy). On the right: geographical location within Italy
Fig. 26 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 26 Cornudininae from Qiakong, Laren and Shanggang. Magnification is × 80. The scale bar is 400 μm. All elements are considered to be P1 elements if not specifically identified otherwise. A–W Urdyella unicorna n. gen. n. sp.; A LAR225, PIMUZ 39345; B LAR225, PIMUZ 39346; C LAR229, PIMUZ 39347; D LAR227, PIMUZ 39348; E LAR229, PIMUZ 39349; F LAR229, PIMUZ 39350; G LAR225, PIMUZ 39351; H LAR229, PIMUZ 39352; I QIA123, PIMUZ 39353; J LAR227, PIMUZ 39354; K QIA123, PIMUZ 39355; L QIA123, PIMUZ 39356; M LAR227, PIMUZ 39357; N LAR225, PIMUZ 39358; O QIA120, PIMUZ 39359; P LAR225, PIMUZ 39360; Q QIA121, PIMUZ 39361; R LAR232, PIMUZ 39362; S LAR232, PIMUZ 39363; T QIA124, PIMUZ 39364; U LAR232, PIMUZ 39365; V QIA123, PIMUZ 39366; W SHA341, PIMUZ 39367. X-AA Urdyella tridenta n. gen. n. sp.; X LAR227, PIMUZ 39341; Y LAR227, PIMUZ 39342; Z LAR227, PIMUZ 39343; AA LAR227, PIMUZ 39344. AB, AC Discretella? n. sp. D; AB QIA124, PIMUZ 39118; AC QIA123, PIMUZ 39119. AD Neostrachanognathus n. sp. A; LAR232, PIMUZ 39183. AE Urdyella n. sp. A; LAR232, PIMUZ 39340
Fig. 18 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 18 Novispathodinae from Laren and Lilong. Magnification is × 80. The scale bar is 400 μm. All elements are considered to be P1 elements if not specifically identified otherwise. A, B, D, F, L–N, Q, S, T Novispathodus praebrevissimus n. sp.; A LIL506, PIMUZ 39274; B LAR207, PIMUZ 39275; D LIL508, PIMUZ 39276; F LIL507, PIMUZ 39277; L LIL507, PIMUZ 39278; M LIL509, PIMUZ 39279; N LIL507, PIMUZ 39280; Q LIL507, PIMUZ 39281; S LIL507, PIMUZ 39282; T LIL507, PIMUZ 39283. C, O, R Novispathodus?praebrevissimus n. sp.; C LAR204, PIMUZ 39284; O LIL507, PIMUZ 39285; R LIL507, PIMUZ 39286. E, I Novispathodus ex gr. pingdingshanensis (Zhao & Orchard); E LIL507, PIMUZ 39232, I LIL507, PIMUZ 39233. G Triassospathodus aff. symmetricus (Orchard); LIL507, PIMUZ 39309. H Novispathodus ex gr. abruptus (Orchard); LIL507, PIMUZ 39212. J, K Novispathodus praebrevissimus (juvenile) n. sp.; J LIL507, PIMUZ 39287; K LIL507, PIMUZ 39288. P Novispathodus robustispinus (Zhao & Orchard); LIL507, PIMUZ 39290
Fig. 20 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 20 Novispathodinae from Qiakong, Laren and Lilong. Magnification is × 80. The scale bar is 400 μm. All elements are considered to be P1 elements if not specifically identified otherwise. A–G, K–M, Q, X Novispathodus ex gr. abruptus (Orchard); A LAR212, PIMUZ 39213; B LAR207, PIMUZ 39214; C LAR205, PIMUZ 39215; D LAR202, PIMUZ 39216; E LAR202, PIMUZ 39217; F LIL506, PIMUZ 39218; G LAR210, PIMUZ 39219; K LIL505, PIMUZ 39220; L LIL506, PIMUZ 39221; M LIL505, PIMUZ 39222; Q LAR203, PIMUZ 39223; X QIA136, PIMUZ 39224. H, V Novispathodus sp. indet.; H QIA136, PIMUZ 39291; V, QIA134, PIMUZ 39292. I, J, P, AA Novispathodus n. sp. Z; I QIA138, PIMUZ 39247; J QIA138, PIMUZ 39248; P LIL506, PIMUZ 39249; AA QIA136, PIMUZ 39250. N, O, S Novispathodus ex gr. pingdingshanensis (Zhao & Orchard); N LIL506, PIMUZ 39234; O LIL505, PIMUZ 39235; S QIA136, PIMUZ 39236. R sp. indet.; LIL511, PIMUZ 39296. T, Y, Z Novispathodus n. sp. A; T QIA134, PIMUZ 39256, Y QIA135, PIMUZ 39257; Z QIA134, PIMUZ 39258. U Novispathodus expansus (Zhao & Orchard); QIA134, PIMUZ 39242. W Novispathodus gryphus n. sp.; QIA135, PIMUZ 39246
Fig. 16 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 16 Neogondolellinae, Novispathodinae and Mullerinae from Shanggang and Youping cascade. Magnification is × 80. The scale bar is 400 μm. All elements are considered to be P1 elements if not specifically identified otherwise. A, F, M Discretella? n. sp. C; A YC16, PIMUZ 39115; F YC16, PIMUZ 39116; M SHA342C, PIMUZ 39117. B Discretella? n. sp. B; YC16, PIMUZ 39113. C Discretella aff. discreta (MÜller); YC22, PIMUZ 39106. D, S Discretella discreta (MÜller); D YC16, PIMUZ 39110; S SHA304C, PIMUZ 39111. E Novispathodus ex gr. abruptus (Orchard); YC41, PIMUZ 39225. G–I, K, L, N, O Discretella pseudodieneri n. sp.; G YC16, PIMUZ 39124; H YC25, PIMUZ 39125; I SHA304C, PIMUZ 39126; K YC22, PIMUZ 39127, L YC25, PIMUZ 39128; N SHA304C, PIMUZ 39129; O SHA343C, PIMUZ SQL54979. J Guangxidella bransoni (MÜller); YC16, PIMUZ 39140. P–R Neospathodus bevelledi n. sp.; P SHA 304C, PIMUZ 39178; Q SHA333C, PIMUZ 39179; R YC12, PIMUZ 39180
Fig. 13 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 13 Gladigondolellinae, Neogondolellinae and Cornudininae from Qiakong, Laren, Shanggang and Lilong. Magnification is × 80. The scale bar is 400 μm. All elements are considered to be P1 elements if not specifically identified otherwise. A Borinella buurensis (Dagis), LAR212, PIMUZ 39103. B, C, G Gladigondolella laii (morphotype A); B LAR231C, PIMUZ 39132; C BAN2, PIMUZ 39133; G LAR227C, PIMUZ 39134. D, sp. indet.(P2 element?), SHA319, PIMUZ 39293. E, F, H, I Gladigondolella laii (morphotype B); E LIL510, PIMUZ 39135; F LIL512, PIMUZ 39136; H QIA140, PIMUZ 39137; I LIL510, PIMUZ 39138. J–L, O, Spathicuspus spathi (Sweet); J QIA141, PIMUZ 39300; K QIA144, PIMUZ 39301; L BAN1, PIMUZ 39302; O SHA322, PIMUZ 39303. M, P Spathicuspus n. sp. A; M QIA144, PIMUZ 39297; P, QIA143, PIMUZ 39298. N, R Spathicuspus spathi (juvenile) (Sweet); N, LIL515D, PIMUZ 39304; R QIA143, PIMUZ 39305. Q Spathicuspus n. sp. B; LAR226C, PIMUZ 39299
Fig. 17 in A Unitary Association-based conodont biozonation of the Smithian-Spathian boundary (Early Triassic) and associated biotic crisis from South China
Fig. 17 Novispathodinae from Qiakong, Laren, Shanggang, and Lilong. Magnification is × 80. The scale bar is 400 μm. All elements are considered to be P1 elements if not specifically identified otherwise. A–C, J, T, AA Novispathodus ex gr. pingdingshanensis (Zhao & Orchard); A, QIA138, PIMUZ 39226; B QIA138, PIMUZ 39227; C LAR202, PIMUZ 39228; J QIA136, PIMUZ 39229; T LIL504, PIMUZ 39230; AA LIL508, PIMUZ 39231. D–F, M–P, R, S, U, X, AB, AD Novispathodus pingdingshanensis (Zhao & Orchard); D QIA135, PIMUZ 39259; E LIL508, PIMUZ 39260; F LIL506, PIMUZ 39261; M LIL506, PIMUZ 39262; N LIL506, PIMUZ 39263; O LIL507, PIMUZ 39264; P LIL506, PIMUZ 39265; R LIL508, PIMUZ 39266; S LAR204, PIMUZ 39267; U LIL507, PIMUZ 39268; X LIL508, PIMUZ 39269; AB LIL508, PIMUZ 39270; AD LIL508, PIMUZ 39271. G, I, Q Novispathodus cf.?gryphus n. sp.; G QIA136, PIMUZ 39204; I QIA136, PIMUZ 39205; Q QIA135, PIMUZ 39206. H, K, L Novispathodus gryphus n. sp.; H QIA135, PIMUZ 39243; K LIL506, PIMUZ 39244; L LIL506, PIMUZ 39245. V Novispathodus praebrevissimus n. sp.; LIL507, PIMUZ 39273. W, Y, Z, AE Novispathodus ex gr. abruptus (Orchard); W LIL505, PIMUZ 39208; Y SHA346, PIMUZ 39209; Z LIL506, PIMUZ 39210; AE SHA346, PIMUZ 39211. AC sp. indet.; LIL504, PIMUZ 39295. AF Novispathodus pingdingshanensis (P1 cluster) (Zhao & Orchard); QIA136, PIMUZ 39272
FIG. 3. — Microphotina viridula n in Les mantes (Dictyoptera, Mantodea) du massif du Mitaraka (Guyane), in Touroult J. (ed.), "Our Planet Reviewed" 2015 large-scale biotic survey in Mitaraka, French Guiana.
FIG. 3. — Microphotina viridula n. sp., holotype mâle: A, vue dorsale; B, vue ventrale de l'avant-corps; C, étiquettes. Échelles: A, 1 cm; B, 5 mm. Photos M. Depraetere.
FIG. 4. — Microphotina viridula n in Les mantes (Dictyoptera, Mantodea) du massif du Mitaraka (Guyane), in Touroult J. (ed.), "Our Planet Reviewed" 2015 large-scale biotic survey in Mitaraka, French Guiana.
FIG. 4. — Microphotina viridula n. sp.: A, plaque sous-génitale d'un paratype; B, genitalia de l'holotype en vue ventrale avec en plus grand l'apex de l'épiphallus gauche (D) et sa variabilité chez un paratype (C). Échelles: A, B, 1 mm; C, D, 0,5 mm.
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.