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1,133 results for “wetlands”

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zenodo20/100

Table 3 in Temperate grassy wetlands of South Africa: Description, classification and explanatory environmental factors

<p><b>Table 3</b> Indicator species for the broad clusters of temperate grassy wetlands, indicating the Indicator Values and p-values. Only species where the p-value is smaller than 0.05 and the Indicator Value larger than 20 are listed. Alien species are marked with an asterisk.</p><table><tbody><tr><th>Number</th><th>No. of plots</th><th>Dominants</th><th>Where</th><th>Indicator species</th><th>Indicator value</th><th>p - Value</th></tr></tbody><tbody><tr><th>1</th><td>242</td><td>Eleocharis dregeana, Leersia dregeana</td><td>Throughout the country</td><td>Eleocharis dregeana</td><td>47.7</td><td>0.001</td></tr><tr><th>2</th><td>53</td><td><i>Carex acutiformis</i></td><td>Highveld, Kwazulu-Natal</td><td>Carex acutiformis</td><td>75</td><td>0.001</td></tr><tr><th>3</th><td>36</td><td>Aristida junciformis, Helichrysum aureonitens</td><td>Highveld, Kwazulu-Natal</td><td>Fuirena pubescens</td><td>40</td><td>0.001</td></tr><tr><td>Aristida junciformis</td><td>32.7</td><td>0.001</td></tr><tr><td></td><td>Helichrysum aureonitens</td><td>24.3</td><td>0.001</td></tr><tr><th>4</th><td>162</td><td>Cyperus denudatus, Schoenoplectus brachyceras,</td><td>Highveld</td><td><i>Eragrostis curvula</i></td><td>46.7</td><td>0.001</td></tr><tr><td><i>Juncus effusus</i></td><td><i>Hyparrhenia hirta</i></td><td>50.3</td><td>0.001</td></tr><tr><td>Schoenoplectus brachyceras</td><td>88.8</td><td>0.001</td></tr><tr><td>Juncus effusus</td><td>63.8</td><td>0.001</td></tr><tr><td>Cyperus denudatus</td><td>62.3</td><td>0.001</td></tr><tr><th>5</th><td>31</td><td>Eragrostis planiculmis</td><td>Highveld</td><td>Eragrostis planiculmis</td><td>56.7</td><td>0.001</td></tr><tr><th>6</th><td>63</td><td>Arundinella nepalensis, Leucosidea sericea</td><td>Highveld, particularly Drakensberg</td><td>Arundinella nepalensis</td><td>33.7</td><td>0.001</td></tr><tr><td>Leucosidea sericea</td><td>79.7</td><td>0.001</td></tr><tr><td>Searsia dentata</td><td>52.8</td><td>0.001</td></tr><tr><td>Cliffortia nitidula</td><td>36.9</td><td>0.001</td></tr><tr><td>Euclea crispa</td><td>29.2</td><td>0.001</td></tr><tr><th>7</th><td>114</td><td><i>Hemarthria altissima</i>, Cyperus marginatus,</td><td>Mostly Highveld</td><td>Hemarthria altissima</td><td>37.6</td><td>0.001</td></tr><tr><td><i>Paspalum dilatatum</i></td><td>Cyperus marginatus</td><td>63.8</td><td>0.001</td></tr><tr><td><i>Cynodon dactylon</i></td><td>30.6</td><td>0.001</td></tr><tr><td><i>Plantago lanceolata</i></td><td>29.7</td><td>0.001</td></tr><tr><td>Paspalum dilatatum</td><td>26.4</td><td>0.001</td></tr><tr><td><i>Trifolium repens</i></td><td>26.2</td><td>0.001</td></tr><tr><th>8</th><td>65</td><td><i>Themeda triandra</i></td><td>Highveld</td><td>Themeda triandra</td><td>52.4</td><td>0.001</td></tr><tr><th>9</th><td>77</td><td>Cyperus fastigiatus</td><td>Throughout the country</td><td>Cyperus fastigiatus</td><td>62.8</td><td>0.001</td></tr><tr><th>10</th><td>136</td><td><i>Imperata cylindrica</i></td><td>Throughout the country</td><td>Imperata cylindrica</td><td>41.1</td><td>0.001</td></tr><tr><td>Senecio achilleifolius</td><td>54.2</td><td>0.001</td></tr><tr><td>Pulicaria scabra</td><td>47.3</td><td>0.001</td></tr><tr><td>Andropogon eucomus</td><td>42.2</td><td>0.001</td></tr><tr><td><i>Fimbristylis ferruginea</i></td><td>41.6</td><td>0.001</td></tr><tr><td><i>Paspalum urvillei</i></td><td>34.9</td><td>0.001</td></tr><tr><td>Pycreus betschuanus</td><td>26.8</td><td>0.001</td></tr><tr><td>Chamaecrista stricta</td><td>26.4</td><td>0.001</td></tr><tr><td>Kyllinga alba</td><td>31.8</td><td>0.001</td></tr><tr><td>Miscanthus junceus</td><td>28.9</td><td>0.001</td></tr><tr><td>Phymaspermum athanasoides</td><td>26.6</td><td>0.001</td></tr><tr><td>Wahlenbergia undulata</td><td>26.4</td><td>0.001</td></tr><tr><th>11</th><td>138</td><td><i>Eragrostis plana</i></td><td>Throughout the country</td><td>Eragrostis plana</td><td>29.8</td><td>0.001</td></tr><tr><th>12</th><td>107</td><td>Typha capensis</td><td>Throughout the country</td><td>Typha capensis</td><td>51.9</td><td>0.001</td></tr><tr><th>13</th><td>90</td><td><i>Phragmites australis</i></td><td>Throughout the country</td><td>Phragmites australis</td><td>39.5</td><td>0.001</td></tr></tbody></table>

opennotspecifiedNov 2017View details →
zenodo20/100

FIG. 2 in Factors Influencing Anuran Wetland Occupancy in an Agricultural Landscape

FIG. 2.—Amphibian occupancy by species and life stage in Iowa during 2015 (light gray) and 2016 (dark gray). A. americanus ¼ Anaxŋrus americanus (American Toads); Hŋla spp. ¼ Hŋla Ʋersicolor and Hŋla chrŋsocelis (Gray Treefrogs and Cope̕s Gray Treefrogs, respectively); L. pipiens ¼ Lithobates pipiens (Northern Leopard Frogs); and P. maculata ¼ Pseudacris maculata (Boreal Chorus Frogs). Error bars represent 95% confidence intervals. Estimates are from the model with the most support (see Table 3).

opennotspecifiedMar 2019View details →
dryad20/100

Remote sensing spectral vegetation indices for 2011 NWCA wetland sites

Open the record for dataset details and reuse information.

publicJun 2019View details →
geo16/100

Using Gene Expression to Assess the Status of Fish from Anthropogenically Influenced Estuarine Wetlands

GEO Series GSE28695. Gillichthys mirabilis. 60 samples. Type: Expression profiling by array.

openGEO-OpenApr 2011View details →
zenodo16/100

The grain size endmembers of Tengchongbeihai wetland sediments over the past 46 ka

<p>&nbsp;Here, we present a grain size end-member analysis for Tengchongbeihai wetland sediments from southwestern China to investigate the paleo-hydroclimate changes since the late MIS3. The overall low fine silt (EM2) content before ~16.5 cal ka BP resulted from weak catchment erosion indicating weak ISM during cold glacial while the increasing trend thereafter indicates the ISM strengthened during the last deglaciation and Holocene. Such an orbital ISM evolution resembles to the insolation gradient between 25°N and 25°S during the boreal summer periods, which implies the transequatorial insolation difference could be an alternative explanation for the orbital scale low latitude hydroclimate changes. The striking peaks of coarse component (EM3) around ~12,&nbsp;16, 24, 29, 32 and 39 cal ka BP were related to significant water level descending indicating the millennial ISM collapse corresponding to the YD and Heinrich events. However, the absence of sawtooth feature as the NGRIP δ18O and the well correspondence to the Indian Ocean sea surface temperatures (SSTs) of the ISM collapses evidence the complementary role of low latitude climate for the North Atlantic climate on the millennial scale hydroclimate variabilities.</p>

restrictedcc-by-4.0Dec 2023View details →
zenodo16/100

FIGURE 30 in Shallow-water Demospongiae (Porifera) from Sodwana Bay, iSimangaliso Wetland Park, South Africa

FIGURE 30. Psammocinia alba sp. nov. A. In situ; B &amp; C. Skeletal architecture (B, x5; C, x10)

opennotspecifiedApr 2019View details →
zenodo12/100

ESM Chapter 2 - Drivers of vegetation development, biomass production and the initiation of peat formation in a newly constructed wetland

<p>Electronic supplementary material&nbsp; to&nbsp;Chapter 2 &quot;Drivers of vegetation development, biomass production and the initiation of peat formation in a newly constructed wetland&quot; of&nbsp;PhD thesis from Ciska Overbeek, &quot;Peat formation on a former landfill - Production and decomposition of aquatic pioneer vegetation&quot;.&nbsp;</p>

restrictedJun 2019View details →
zenodo12/100

Linking functional diversity, trait composition, invasion, and environmental drivers in boreal wetland plant assemblages

<p>These datasets contain information for the the species occurrence, trait, and wetland site characteristics used in this manuscript.</p>

restrictedAug 2021View details →
zenodo12/100

The refined annual 10-m wetland maps of Dongting Lake wetland during 2015~2021

<p>The wetland maps include 8 wetland classes and 5 non-wetland classes, with a spatial resolution of 10m.</p>

restrictedNov 2022View details →
zenodo8/100

Data from: The Restoration of Wetlands Dominated by Habitat Modifiers

<p>Unpublished data to chapters 3 till 7 from:</p> <p>Temmink, R.J.M. 2020. The Restoration of Wetlands Dominated by Habitat Modifiers.&nbsp;PhD thesis, Radboud Universiteit, Nijmegen, the Netherlands.</p> <p>&nbsp;</p>

restrictedAug 2020View details →
zenodo8/100

A water-table-dependent net warming effect of global wetlands from potent greenhouse gases

<p>A database of the annual greenhouse gase fluxes across global wetlands. In total, the database comprised 2,455 observations of annual net ecosystem exchange of CO<sub>2 </sub>(NEE; net gaseous CO<sub>2</sub> exchange between land and atmosphere), 2,342 observations of annual CH<sub>4 </sub>fluxes and 850 observations of annual N<sub>2</sub>O fluxes.</p>

restrictedJan 2022View details →
zenodo8/100

Success of coastal wetlands restoration is driven by sediment availability

<p>Shorelines and their ecosystems are endangered by sea-level rise. Nature-based coastal protection is becoming a global strategy to enhance coastal resilience through the cost-effective creation, restoration and sustainable use of coastal wetlands. However, the resilience to sea-level rise of coastal wetlands created under Nature-based solution has been assessed largely on a regional scale. Here we assess, using a meta-analysis, the difference in accretion, elevation, and sediment deposition rates between natural and restored coastal wetlands across the world. Our results show that restored coastal wetlands can trap more sediment and that the effectiveness of these restoration projects is primarily driven by sediment availability, not by wetland elevation, tidal range, local rates of sea-level rise, and significant wave height. Our results suggest that Nature-based Solutions can mitigate coastal wetland vulnerability to sea-level rise, but are effective only in coastal locations where abundant sediment supply is available.</p>

restrictedJan 2021View details →
zenodo8/100

Movement and competition ecology of African lions in semi-arid and wetland ecosystems

<p>GPS dataset of lion tracking data.</p>

restrictedOct 2021View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

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abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record