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Figure 8 from: Nefediev PS, Farzalieva GS, Tuf IH, Nedoev KK, Niyazov ST (2018) Millipede and centipede assemblages on the northern and southern slopes of the lowland Altais, southwestern Siberia, Russia (Diplopoda, Chilopoda). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 219-254. https://doi.org/10.3897/zookeys.741.21936
Figure 8 The species diversity of millipedes on the southern and northern slopes.
Figure 12 from: Nefediev PS, Farzalieva GS, Tuf IH, Nedoev KK, Niyazov ST (2018) Millipede and centipede assemblages on the northern and southern slopes of the lowland Altais, southwestern Siberia, Russia (Diplopoda, Chilopoda). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 219-254. https://doi.org/10.3897/zookeys.741.21936
Figure 12 The seasonal dynamics of Diplopoda density on study slopes.
Figure 1 from: Nefediev PS, Farzalieva GS, Tuf IH, Nedoev KK, Niyazov ST (2018) Millipede and centipede assemblages on the northern and southern slopes of the lowland Altais, southwestern Siberia, Russia (Diplopoda, Chilopoda). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 219-254. https://doi.org/10.3897/zookeys.741.21936
Figure 1 Map of study locality (shown by the red spot).
Figure 14 from: Nefediev PS, Farzalieva GS, Tuf IH, Nedoev KK, Niyazov ST (2018) Millipede and centipede assemblages on the northern and southern slopes of the lowland Altais, southwestern Siberia, Russia (Diplopoda, Chilopoda). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 219-254. https://doi.org/10.3897/zookeys.741.21936
Figure 14 The distribution of myriapods along soil profile on both slopes.
Figure 2 from: de Oliveira Dias C, de Araujo AV, Bonecker SLC (2018) Vertical distribution and structure of copepod (Arthropoda: Copepoda) assemblages in two different seasons down to 1,200 m in the tropical Southwestern Atlantic. Zoologia 35: 1-11. https://doi.org/10.3897/zoologia.35.e13886
Figure 2 Study area showing sampling stations.
Figure 10 from: Souza CD, Batista VS, Fabré NN (2018) What are the main local drivers determining richness and fishery yields in tropical coastal fish assemblages? Zoologia 35: 1-12. https://doi.org/10.3897/zoologia.35.e12898
Figure 10 - Frequency and direction of winds in each sampled month on the coast of Alagoas.
Figure 11 from: Souza CD, Batista VS, Fabré NN (2018) What are the main local drivers determining richness and fishery yields in tropical coastal fish assemblages? Zoologia 35: 1-12. https://doi.org/10.3897/zoologia.35.e12898
Figure 11 - PCA of species abundance associated to precipitation and wind speed.
Figure 3 in Does the location of coastal brackish waters determine diversity and abundance of zooplankton assemblages?
Figure 3. Abundance (ind. dm–3) of zooplankton in the Vistula Lagoon and Lake Łebsko in 2010–2011.
Fig. 2G in Enumeration of Herpetofaunal assemblage of Surajpur Wetland, National Capital Region (India)
Fig. 2G. Indian Garden Lizard Calotes versicolor.
Fig. 2F in Enumeration of Herpetofaunal assemblage of Surajpur Wetland, National Capital Region (India)
Fig. 2F. Indian Flapshell Turtle Lissemys punctata.
Fig. 2C in Enumeration of Herpetofaunal assemblage of Surajpur Wetland, National Capital Region (India)
Fig. 2C. Skittering Frog Euphlyctis cyanophlyctis.
Fig. 2J in Enumeration of Herpetofaunal assemblage of Surajpur Wetland, National Capital Region (India)
Fig. 2J. Spotted Supple Skink Lygosoma punctata.
Fig. 2N in Enumeration of Herpetofaunal assemblage of Surajpur Wetland, National Capital Region (India)
Fig. 2N. Checkered Keelback Xenochrophis piscator.
Figure 2 in Postmucilage status of teleost fish assemblages in the Sea of Marmara
Figure 2. Evaluation of retained catch.
Figure 1 in Water quality assessment in an irrigation pond based on adult caddisfly (Insecta: Trichoptera) assemblages
Figure 1. Sampling site for adult Trichoptera and water quality variables.
Carabid beetle assemblages at Silwood Park, UK
<p>Anthropogenically created habitat edges have long been known to affect communities of adjacent habitats. This data is curated from a collection of studies where pitfall-trapping were used to compare changes in ground beetle (Coleoptera Carabidae) assemblages along transects marking the transition between different types of habitats: grassland to woodland, grassland to farmland and farmland to woodland. </p> <p>Studies were part of undergraduate or Master degree projects, thus the methods used between years are not the same. Students original data and reports are available.</p> <p>The study site is the Silwood Park Campus from Imperial College London, Buckhurst Road, Ascot, Berkshire SL5 7PY, United Kingdom. The campus, with 75 ha, contains grasslands, scrubland, ancient woodlands and few decades old oak-dominated woodlands. Woodlands in Silwood Park used in these studies developed from natural succession from about 1960’s. They are the typical species-poor type found in lowland southern Britain, classified as (W10a) with common tree species like Pedunculated Oak (Quercus robur), Silver birch (Betula pendula) and with Bramble (Rubus fruticosus), Common Nettle (Urtica dioica) and Bracken (Pteridium aquilinum) dominating the field layer. Grasslands are species-poor on sandy, acidic soil of the Bagshot Series, MG5 Cynosurus cristatus/ Centaurea debeauxii, Danthonia decumbens subcommunity (United Kingdome National Vegetation Classification, https://jncc.gov.uk/).<br> <br>Farmland used are former arable plots abandoned since the 1970's and maintained by cutting vegetation, ploughing and rotovating the soil in October every year. </p> <p>Silwood Park experiences an average annual rainfall of 698mm with little seasonal pattern. Mean hourly temperature is 10oC with July max of 23 oC and January min of 1.4 oC (Means from Silwood Weather Station,1987-2022, https://www.imperial.ac.uk/silwood-park/research/field-experiments/silwood-weather/).</p> <p>Methods</p> <p>Data 2016: Three grassland to woodland 64m transects were placed perpendicular to the habitats edge at each site; 32m extending into the woodland, 32m extending into the grassland and the midpoint of the transect at the edge. One pitfall trap was placed at each of the following distances each side of the edge: 2m, 4m, 8m, 16m, 32m, and another was placed at 0m. Overall carabids were collected over a total of 21 trap-days divided in seven sampling periods of three days each. Abundance of carabid species collected in each pitfall trap is reported for each three-day collection period. </p> <p>Data 2017: Two transects were set in each habitat transition: grassland to woodland and grassland to farmland. Three 5x5m2 plots were placed at 5m intervals, along a 25m transect, across each site. In each plot, five dry pitfall traps were set 1m apart in the diagonal line of the plot (Fig.1). Traps were plastic cups of 7 cm diameter buried at ground level. Pitfall traps were set 14 times in each plot and examined after 24h. Carabid beetles found were identified, marked with nail polish using color codes and released in the same location. After 24h pitfall traps were examined again, and the number of captures and recaptures recorded. Data are number of carabid beetles of each species found in pitfall traps for the whole plot in a given 48 sampling period.</p> <p>Data 2019: Three replicate transects were set up along two habitat edges: Agriculture field to woodland and acid grassland to woodland. Transects were at a minimum distance of 20m from any other edge. The transects were separated by the maximum possible distance of 14m. Each replicate transect was composed of five plots ranging from 20m within the woodland interior to 20m into the matrix (grassland/agricultural field), using the central traps as reference for measures of distance. Each plot contained nine pitfall traps arranged in 2x2m grids resulting in a total of 270 traps. Simple “Barber” pitfall traps were composed of 2 stacked 200ml plastic cups with an open diameter of 7.2cm and buried at ground level. Beetle collection occurred over a period of 24 days (April 14 to May 8, 2019). Traps were emptied at three-day intervals for six of the eight sampling events, with one sampling event occurring after two days, and another after four days due to organizational complications. Samples were grouped by plot rather than by individual trap, resulting in the collection of 30 samples per sampling event. Specimens were conserved in 40% ethanol solution and stored for later identification.</p>
Data from: Long-term monitoring dataset of fish assemblages impinged at nuclear power plants in northern Taiwan
The long-term species diversity patterns in marine fish communities are garnering increasing attention from ecologists and conservation biologists. However, current databases on quantitative abundance information lack consistent long-term time series, which are particularly important in exploring the possible underlying mechanism of community changes and evaluating the effectiveness of biodiversity conservation measures. Here we describe an impinged fish assemblage dataset containing 1, 283, 707 individuals from 439 taxa. Once a month over 19 years (1987–1990 and 2000–2014), we systematically collected the fish killed by impingement upon cooling water intake screens at two nuclear power plants on the northern coast of Taiwan. Because impingement surveys have low sampling errors and can be carried out over many years, they serve as an ideal sampling tool for monitoring how fish diversity and community structure vary over an extended period of time.
Data from: New Olonbulukia material and its related assemblage reveal an early radiation of stem Caprini along the north of the Tibetan Plateau
Living Caprini are dominant bovids in the pan-Tibetan area that are strongly adapted to dry steppe and high mountain meadow habitats. Some taxa with Holarctic distributions, such as Ovis, were thought to originate on the Tibetan Plateau and subsequently dispersed elsewhere, which was depicted as an "out of Tibet" story. However, except for some information on a stem caprine assemblage from the Qaidam Basin, the early evolution of Caprini around the Tibetan Plateau is poorly known. Here, we report new material of Olonbulukia tsaidamensis, which was a member of this stem caprine assemblage, from the Wuzhong region, northern China, confirming similarity of the Wuzhong Fauna and 'Qaidam Fauna'. Based on a metric study of horncores from the 'Qaidam' and Wuzhong faunas, we recognized six taxa from this stem caprine assemblage: Olonbulukia tsaidamensis, Olonbulukia sp., Qurliqnoria cheni, Tossunnoria pseudibex, ? Protoryx cf. enanus, and cf. Pachytragus sp. Among these taxa, Qurliqnoria and Tossunnoria are probably related to some extant Tibetan endemic species, such as Tibetan antelope (Pantholops hodgsonii) and Himalayan tahr (Hemitragus jemlahicus), and others might be ancestral to the Turolian caprine assemblages and even possibly gave rise to the extant Caprina. This work reveals an early radiation of stem caprines along the northern side of the rising Tibetan Plateau and indicates a mixed pattern of pan-Tibetan stem caprine evolution prior to their dispersal out of the Tibetan Plateau.
Data from: A Tournaisian (earliest Carboniferous) conglomerate-preserved non-marine faunal assemblage and its environmental and sedimentological context
A conglomerate bed from the Tournaisian Ballagan Formation of Scotland preserves a rich array of vertebrate and other non-marine fossils providing an insight into the wider ecosystem and palaeoenvironment that existed during this pivotal stage of Earth history. It challenges hypotheses of a long-lasting post-extinction trough following the end-Devonian extinction event. The fauna recovered includes a wide size range of tetrapods, rhizodonts and dipnoans, from tiny juveniles or small-bodied taxa up to large adults, and more than one taxon of each group is likely. Some fauna, such as actinopterygians and chondrichthyans, are rare as macrofauna but are better represented in the microfossil assemblage. The fauna provides evidence of the largest Carboniferous lungfish ever found. The specimens are preserved in a localised, poorly-sorted conglomerate which was deposited in the deepest part of a river channel, the youngest of a group of channels. In addition to the fossils (micro- and macro-), the conglomerate includes locally-derived clasts of palaeosols and other distinctive elements of the surrounding floodplains. Charcoal fragments represent stem and possible trunk tissue from arborescent pteridosperms. Preservation of the fossils indicates some aerial exposure prior to transport, with abrasion from rolling. The findings presented here contrast with other published trends in vertebrate size that are used to interpret a reduction in maximum sizes during the Tournaisian. The richness of the fauna runs counter to the assumption of a depauperate non-marine fauna following the end-Devonian Hangenberg event, and charcoal content highlights the occurrence of fire, with the requisite levels of atmospheric oxygen during that stage.
Figure 2 in Variation in dung beetle (Coleoptera: Scarabaeidae: Scarabaeinae) assemblages in a tropical forest remnant from a Mexican National Park
Figure 2. Species accumulation curve of the total richness captured in a tropical forest remnant in the Cañón del Sumidero National Park, Chiapas.
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.