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.
1,287
datasets available to search
ShareScore release 0.7.1
Dataset results
1,287 results for “species identity”
Figs 179–186 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 179–186. Tituboea paykullii species group, head of males. 179–182 – frontal view: 179 – Tituboea fasciata Lefèvre, 1872; 180 – T. femoralis Medvedev, 1962; 181 – T. laticollis (Olivier, 1808); 182 – T. paykullii (Lacordaire, 1848). 183–186 – lateral view: 183 – Tituboea fasciata; 184 – T. femoralis; 185 – T. laticollis; 186 – T. paykullii.
Figs 35–39. 35–37 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 35–39. 35–37 – Tituboea fasciata Lefèvre, 1872: 35 – aedeagus (dorsal, lateral and ventral views); 36 – spermatheca; 37 – right male protarsus. 38–39 – Tituboea paykullii (Lacordaire, 1848): 38 – aedeagus (dorsal, lateral and ventral views); 39 – right male protarsus. Scale bars: 1 mm for Figs 37 and 39; 0.5 mm for Figs 35, 36 and 38.
Figs 173–178 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 173–178. Tituboea paykullii species group, habitus: 173 – Tituboeafasciata Lefèvre, 1872 (male, 9.5 mm); 174 – T. femoralis Medvedev, 1962 (male, 11.5 mm); 175 – T. laticollis (Olivier, 1808) (male, 11.9 mm); 176–178 – males of T. paykullii (Lacordaire, 1848) from Morocco, illustrating the color variability (lengths: 176 – 9.5 mm, 177 – 7.8 mm, 178 – 8.8 mm).
Figs 7–10. 7–8 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 7–10. 7–8 – Coptocephala normandi Pic, 1914: 7 – aedeagus (dorsal, lateral and ventral views); 8 – spermatheca. 9–10 – Coptocephala perrisi (Desbrochers des Loges, 1870): 9 – aedeagus (dorsal, lateral and ventral views); 10 – spermatheca. Scale bars: 1 mm for Fig. 9, 0.5 mm for Fig. 7, 0.25 mm for Figs 8 and 10.
Figs 87–92. Coptocephala normandi Pic, 1914 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 87–92. Coptocephala normandi Pic, 1914: 87 – habitus of male (5.2 mm); 88 – habitus of female (4.4 mm); 89 – head of male; 90 – head of female; 91 – habitus of syntype (female, 4.2 mm); 92 – labels of syntype.
Figs 19–25. 19–21 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 19–25. 19–21 – Tituboea arabica (Olivier, 1808): 19 – aedeagus (dorsal, lateral and ventral views); 20 – spermatheca; 21 – right male protarsus. 22–25 – Tituboea atriceps Pic, 1924: 22 – aedeagus (dorsal and lateral views, from Egypt); 23 – aedeagus (dorsal and lateral views, from Israel); 24 – spermatheca; 25 – right male protarsus. Scale bars: 1 mm for Figs 21 and 25; 0.5 mm for Figs 19, 20, 22 and 23, 0.25 mm for Fig. 24.
Figs 155–164. Tituboea atriceps Pic, 1924. 155–157 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 155–164. Tituboea atriceps Pic, 1924. 155–157 – Invalid type of T. minor var. atriceps (female, 5.2 mm): 155 habitus; 156 – head; 157 – labels. 158–160 – Holotype of T. minor var. decemmaculata Pic, 1937 (female, 3.9 mm): 158 – habitus; 159 – head; 160 – labels. 161 – male (4.4 mm); 162 – head of male. 163–164 – Holotype of Antipa israelita Medvedev, 1992 (male, Romantsov orig.): 163 – habitus; 164 – labels.
Figs 145–154 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 145–154. Tituboea arabica (Olivier, 1808). 145–146 – syntype of Clytra arabica Olivier, 1808 (unsexed): 145 – habitus; 146 – labels. 147–148 – syntype of T. mokattamensis Pic, 1912 (female, 6.0 mm): 147 – habitus; 148 – labels. 149–150 – syntype of T. subabbreviata Pic, 1912 (male, 6.5 mm); 149 – habitus; 150 – labels. 151 – male (Iran, 8.2 mm); 152 – male (Syria, 8.0 mm); 153 – head of male (Iran); 154 – head of male (Syria).
Figs 126–132. 126–127 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 126–132. 126–127 – Otiothraea rotroui (Kocher, 1961) (male, 4.0 mm): 126 – habitus; 127 – head. 128–129 – Otiothraea riffensis Romantsov, 2011 (holotype, male, Romantsov orig.): 128 – habitus; 129 – head. 130–132 Smaragdina ssavicollis (Charpentier, 1825) (syntype of Gynandrophthalma amasina Pic, 1897, female, 4.5 mm): 130 – habitus; 131 – head; 132 – labels.
Figs 26–29. 26–27 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 26–29. 26–27 – Tituboea chobauti (Pic, 1896): 26 – aedeagus (dorsal and lateral views); 27 – spermatheca. 28–29 – Tituboea cingulata (Lefèvre, 1884): 28 – aedeagus (dorsal, lateral and ventral views); 29 – right male protarsus. Scale bars: 1 mm for Fig. 29; 0.5 mm for Figs 26–28.
Figs 229–235 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 229–235. Tituboea tredecimpunctata (Desbrochers des Loges, 1870): 229 – habitus of male (Israel, 8.4 mm); 230 – head of male; 231 – habitus of female (Tunisia, 8.1 mm); 232 – head of female. 233–235 – syntype of T. peyerimhofþ Pic, 1902(female, 6.6 mm): 233 – habitus; 234 – habitusin lateral view; 235 – labels.
Figs 66–70. 66–67 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 66–70. 66–67 – Tituboea tredecimpunctata (Desbrochers des Loges, 1870): 66 – aedeagus (dorsal and lateral views); 67 – spermatheca. 68–70 – Tituboea biguttata (Olivier, 1791): 68 – aedeagus (dorsal and lateral views); 69 – spermatheca (from Greece); 70– spermatheca (from Spain). Scale bars: 0.5 mm for Figs 66 and 68–70; 0.25 mm for Fig. 67.
Figs 57–62. 57–60 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 57–62. 57–60 – Tituboea saadensis (Pic, 1894): 57 – aedeagus (dorsal and lateral views, from Algeria); 58 – aedeagus (dorsal and lateral views, from Mali); 59 – spermatheca; 60 – right male protarsus. 61–62 – Tituboea carmelica (Lopatin & Chikatunov, 2001): 61 – aedeagus (dorsal and lateral views); 62 – right male protarsus. Scale bar: 0.5 mm.
Figs 30–34. 30–31 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 30–34. 30–31 – Tituboea femoralis Medvedev, 1962: 30 – aedeagus (dorsal, lateral and ventral views); 31 right male protarsus. 32–34 – Tituboea laticollis (Olivier, 1808): 32 – aedeagus (dorsal, lateral and ventral views); 33 – right male protarsus; 34 – spermatheca. Scale bars: 1 mm for Figs 31–33; 0.5 mm for Figs 30 and 34.
Figs 51–56. 51–53 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 51–56. 51–53 – Tituboea mecheriensis Pic, 1895: 51 – aedeagus (dorsal and lateral views); 52 –spermatheca; 53 – right male protarsus. 54–56 – Tituboea octopunctata (Fabricius, 1787): 54 – aedeagus (dorsal and lateral views); 55 – spermatheca; 56 – right male protarsus. Scale bars: 1 mm for Figs 53, 54 and 56; 0.5 mm for Figs 51, 52 and 55.
Figs 40–45. 40–42 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 40–45. 40–42 – Tituboea lacordairei (Pic, 1929): 40 – aedeagus (dorsal, lateral and ventral views); 41 – spermatheca; 42 – right male protarsus. 43–45 – Tituboea ogloblini (Medvedev, 1962): 43 – aedeagus (dorsal, lateral and ventral views); 44 – spermatheca; 45 – right male protarsus. Scale bars: 1 mm for Figs 42 and 45; 0.5 mm for Figs 40 and 43, 0.25 mm for Figs 41 and 44.
Figs 208–213. Tituboea mecheriensis Pic, 1895 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 208–213. Tituboea mecheriensis Pic, 1895: 208 – male (7.1 mm); 209 – head of male; 210 – female (5.9 mm); 211 – head of female. 212–213 – Syntype of Tituboea octopunctata var. mecheriensis Pic, 1895 (male, 7.1 mm): 212 – habitus; 213 – labels.
Data from: Soil organic carbon stability in forests: distinct effects of tree species identity and traits
Rising atmospheric CO2 concentrations have increased interest in the potential for forest ecosystems and soils to act as carbon (C) sinks. While soil organic C contents often vary with tree species identity, little is known about if, and how, tree species influence the stability of C in soil. Using a 40‐year‐old common garden experiment with replicated plots of eleven temperate tree species, we investigated relationships between soil organic matter (SOM) stability in mineral soils and 17 ecological factors (including tree tissue chemistry, magnitude of organic matter inputs and their turnover, microbial community descriptors, and soil physico‐chemical properties). We measured five SOM stability indices, including heterotrophic respiration, C in aggregate‐occluded particulate organic matter (POM) and mineral‐associated SOM, and bulk SOM δ15N and ∆14C. The stability of SOM varied substantially among tree species and this variability was independent of the amount of organic C in soils. Thus, when considering forest soils as C sinks, the stability of C stocks must be considered in addition to their size. Further, our results suggest tree species regulate soil C stability via the composition of their tissues, especially roots. Stability of SOM appeared to be greater (as indicated by higher δ15N and reduced respiration) beneath species with higher concentrations of nitrogen and lower amounts of acid‐insoluble compounds in their roots, while SOM stability appeared to be lower (as indicated by higher respiration and lower proportions of C in aggregate‐occluded POM) beneath species with higher tissue calcium contents. The proportion of C in mineral‐associated SOM and bulk soil ∆14C, though, were negligibly dependent on tree species traits, likely reflecting an insensitivity of some SOM pools to decadal‐scale shifts in ecological factors. Strategies aiming to increase soil C stocks may thus focus on particulate C pools, which can more easily be manipulated and are most sensitive to climate change.
Data from: Preserved collagen reveals species identity in archaeological marine turtle bones from Caribbean and Florida sites
Advancements in molecular science are continually improving our understanding of marine turtle biology and evolution. However, there are still considerable gaps in our understanding, such as past marine turtle distributions, which can benefit from advanced zooarchaeological analyses. Here we apply collagen fingerprinting to 130 archaeological marine turtle bone samples up to 2500 years old from the Caribbean and Florida's Gulf Coast for faunal identification, finding the vast majority of samples (88%) to contain preserved collagen despite deposition in the tropics. All samples can be identified to species-level with the exception of the Kemp's ridley (Lepidochelys kempii) and olive ridley (L. olivacea) turtles, which can be separated to genus level, having diverged from one another only ~5 million years ago. Additionally, we identify a single homologous peptide that allows the separation of archaeological green turtle samples, Chelonia spp., into two distinct groups, which potentially signifies a difference in genetic stock. The majority of the archaeological samples are identified as green turtle (Chelonia spp.; 63%), with hawksbill (Eretmochelys imbricata; 17%) and ridley turtles (Lepidochelys spp.; 3%) making up smaller proportions of the assemblage. There were no molecular identifications of the loggerhead turtle (Caretta caretta) in the assemblage despite 9% of the samples being morphologically identified as such, highlighting the difficulties in relying on morphological identifications alone in archaeological remains. Finally, we present the first marine turtle molecular phylogeny using collagen (I) amino acid sequences and find our analyses match recent phylogenies based on nuclear and mitochondrial DNA. Our results highlight the advantage of using collagen fingerprinting to supplement morphological analyses of turtle bones and support the usefulness of this technique for assessing their past distributions across the Caribbean and Florida's Gulf Coast, especially in these tropical environments where DNA preservation may be poor.
FIGURES 1 – 8. Lopheucoila anastrephae. 1 in Eucoilinae species (Hymenoptera: Cynipoidea: Figitidae) parasitoids of fruitinfesting dipterous larvae in Brazil: identity, geographical distribution and host associations
FIGURES 1 – 8. Lopheucoila anastrephae. 1. Head, anterior view (183 x, 100 m); 2. Female antenna (58 x, 250 m); 3. Flagellomerous 1 and 2 of male (170 x, 100 m); 4. Pronotal plate (160 x, 100 m); 5. Head, mesosoma and anterior part of metasoma, lateral view (74 x, 250 m); 6. Mesosoma, dorsal view (172 x, 100 m); 7. Forewing (10 x, 0,5 mm); 8. Metacoxa (163 x, 100 m).
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.