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1,445 results for “species richness.”

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zenodo32/100

Figure 5 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)

Figure 5. Annual cyclic pattern of the proportion of the effectively specialized fauna (squares) and singleton species (circles) for the total number of hemipteran species from each sampling period.

opennotspecifiedNov 2011View details →
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Figure 3 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)

Figure 3. Mean number of individuals (from SIMPER analysis) of dominant hemipteran species, during each sampling period, for most plant species.

opennotspecifiedNov 2011View details →
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Figure 1 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)

Figure 1. Interactions between plant species sampled and sampling period for (A) abundance (number of individuals) per plant and (B) species richness per plant (standard error bars are shown).

opennotspecifiedNov 2011View details →
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Figure 6 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)

Figure 6. Relationship between the effectively specialized fauna (squares) and singleton species (circles) for the number of hemipteran species from each sampling period and for the entire collection. An exponential decay equation is fitted for effectively specialized fauna, y = 2.973∗ exp (−0.00575∗ x) + (−1.478), R2 = 0.7598, and for singleton species, y = 22.53∗exp (−0.08466∗x) + 0.2614, R2 = 0.9873.

opennotspecifiedNov 2011View details →
dryad32/100

Vegetation changes from private forestland management can increase species richness and abundance

<p>Conservation efforts on private lands are important for biodiversity conservation. On private lands in South Carolina, forestry management practices (prescribed burning, thinning, herbicide application) are used to improve upland pine habitat for wildlife and timber harvest and are incentivized through United States Department of Agriculture Farm Bill cost-share programs. Because many forest-dependent bird species have habitat requirements created primarily through forest management, data are needed on the effectiveness of these management activities. We studied privately-owned loblolly pine (Pinus taeda) stands in the South Carolina Piedmont region. Our objective was to understand how management practices influence avian species richness and abundance at local (forest stand) and landscape levels in relatively small stands (average ~28 hectares). We surveyed 49 forest stands during two bird breeding seasons with traditional point counts and vegetation surveys. We evaluated the effects of management on pine stand characteristics, avian species richness, and abundance of state-designated bird species of concern. Repeated burning and thinning shifted stand conditions to open pine woodlands with reduced basal area and herbaceous understories. Stands with lower basal area supported greater avian species richness. Some species increased in abundance in response to active management (e.g., Brown-headed Nuthatch, Sitta pusilla, and Indigo Bunting, Passerina cyanea), but relationships varied. Some species responded positively to increases in forest quantity at a landscape scale (1–5 km, e.g., Northern Bobwhite, Colinus virginianus). We found species-rich avian communities and species of conservation concern on working timber lands, indicating that incentivized forest management on private lands can provide valuable habitat for wildlife.   </p>

opencc-zeroAug 2021View details →
zenodo32/100

Figure 1 in The freshwater crustaceans (Cladocera: Copepoda) of Bering Island (Commander Islands, Russian Far East): species richness and taxocene structure

Figure 1. Location of the sampled stations in inner water bodies on the map of Bering Island, and its geographical position.

opennotspecifiedDec 2015View details →
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Figure 3. Haplotype networks for cytochrome oxidase I in Bythinella Moquin-Tandon, 1856 (Gastropoda: Rissooidea: Bythinellidae) in Romania: species richness in a glacial refugium

Figure 3. Haplotype networks for cytochrome oxidase I (COI), computed with TCS 1.21; square and ellipse size reflects haplotype frequency; connection limit excluding homoplastic changes was set to 95% (hence excluding some haplotypes from network); haplotypes in squares have biggest outgroup weights.

opennotspecifiedNov 2009View details →
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Figure 1 in Bythinella Moquin-Tandon, 1856 (Gastropoda: Rissooidea: Bythinellidae) in Romania: species richness in a glacial refugium

Figure 1. Sampling localities of Bythinella in Romania. Figure produced using Cartografx Professional Software.

opennotspecifiedNov 2009View details →
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Figure 2. Bayesian phylogram computed for cytochrome oxidase I in Bythinella Moquin-Tandon, 1856 (Gastropoda: Rissooidea: Bythinellidae) in Romania: species richness in a glacial refugium

Figure 2. Bayesian phylogram computed for cytochrome oxidase I (COI) sequences with MRBAYES, Bayesian probabilities for branches are given.

opennotspecifiedNov 2009View details →
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FIG. 3 in The barnacles of Astreopora (Cirripedia, Pyrgomatini/ Scleractinia, Acroporidae): organization plans, host speci®city, species-richness and geographic range

FIG. 3. Hiroa stubbingsi Ross and Newman, 1973 from Astreopora myriophthalma Lamarck, 1816 from Sulawesi, Indonesia (RMNH C 2276): (A) labrum and outlines of mandibular palps; (B) mandibular palp; (C) mandible; (D) maxilla I; (E) maxilla II. Scale bar= 0.1 mm.

opennotspecifiedDec 2010View details →
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FIG. 1 in The barnacles of Astreopora (Cirripedia, Pyrgomatini/ Scleractinia, Acroporidae): organization plans, host speci®city, species-richness and geographic range

FIG. 1. Distribution of Astreopora (shaded, after Veron 1986, 1993) and known occurrences of Cantellius euspinulosa (D), C. iwayama (E), C. tredecimus, (D) C. pallidus (L), Hiroa stubbingsi (H), Cionophora soongi (*) and C. guillaumae sp. nov. (+). Localities, for sites of collection see results: 1, Red Sea, Gulf of Elat or Aqaba; 2, Red Sea; 3, Red Sea,Yemen; 4, Kenya; 5, Tanzania; 6, Mozambique, Inhaca Island; 7, Seychelles; 8, Mauritius; 9, Reunion; 10, Maldive Islands; 11, Vietnam; 12, Indonesia, Sabah; 13, Indonesia, Sulawesi; 14, Philippines; 15, Taiwan (Soong and Chang, 1983); 16, Japan, Okinawa (Ogawa and Matsuzaki, 1990; Asami and Yamaguchi, 1997); 17, Japan, Kushimoto, 18, Truk Islands (Ollan Island, type locality of Hiroa stubbingsi); 19, Australia, Western Australia; 20, Australia, Darwin; 21, 22, Australia, Great Barrier Reef; 23, Australia, Lord Howe Island; 24, New Caledonia (type locality of Cionophora guillaumae); 25, Vanuatu; 26, Marshall Islands, Enewetok Atoll; 27, Gilbert Islands; 28, Tonga Islands.

opennotspecifiedDec 2010View details →
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FIG. 2 in The barnacles of Astreopora (Cirripedia, Pyrgomatini/ Scleractinia, Acroporidae): organization plans, host speci®city, species-richness and geographic range

FIG. 2. Scanning electron micrographs of shell and opercular plates of Hiroa stubbingsi Ross and Newman, 1973: (A) exterior of specimen from Sulawesi, Indonesia (RMNH C 2276) with opercular plates in place [see (D) for enlargement of area outlined on (A), and (E) for enlargement of the opercular region]; (B) carinal plate and portion of basis of specimen from Sabah (Borneo) showing grooves in basis into which the radial septa of the wall insert; (C) interior of partially disarticulated wall showing four parietal plates (note the rostrum contributes substantially less to the sheath than the carina despite their comparable widths); (D) radial ridge and marginal teeth of radial septum engaging a longitudinal groove of the basis [enlargement of outlined area in (A)]; (E) enlargement of the opercular plates in situ, illustrating interlocking of the teeth of the occludent margins of the scuta and the rows of pores; (F) articulate opercular valves of a specimen from New Caledonia illustrating the relationships of the large area for insertion of tergal depressor muscles and the relatively large spur of the tergum to the large, dependent limbus adductorum (adductor ridge) of the scutum (a, outer view; b, inner view); (G) disarticulated scuta and terga of a specimen from Sulawesi Indonesia (RMNH C 2276) (a and b, scuta; c and d, terga). Scale bars: (A±C, F, G)= 1 mm; (D, E)=0.1 mm.

opennotspecifiedDec 2010View details →
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FIGURE 29. Zoosphaerium aureum n in Unexplored richness: discovery of 31 new species of Giant Pill-Millipedes endemic to Madagascar, with a special emphasis on microendemism (Diplopoda, Sphaerotheriida)

FIGURE 29. Zoosphaerium aureum n. sp. posterior telopods, paratype, A: posterior telopods, anterior view; B: left posterior telopod, posterior view. Abbreviations: AL = anal lobes; cr-t = crenulated teeth; IH = inner horns; ml = membranous lobe. Scale bars = 1 mm.

opennotspecifiedMay 2009View details →
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Figure 17 in An integrative approach to reveal speciation and species richness in the genus Diasporus (Amphibia: Anura: Eleutherodactylidae) in eastern Panama

Figure 17. Diasporus tinker: A, B, Pirre mountain range (PM), Pirre ridge (MHCH 2864); C, F, PM, Pirre ridge (SMF 97324); G, H, Jingurudo-Sapo mountain range (JSM), showing metachrosis (same specimen); G, night coloration; H, day coloration.

opennotspecifiedSep 2016View details →
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Figure 11 in An integrative approach to reveal speciation and species richness in the genus Diasporus (Amphibia: Anura: Eleutherodactylidae) in eastern Panama

Figure 11. Holotype of Diasporus majeensis sp. nov.: A, B, frontal and lateral view, respectively; C, left foot ventrally; D, right hand ventrally.

opennotspecifiedSep 2016View details →
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Figure 14 in An integrative approach to reveal speciation and species richness in the genus Diasporus (Amphibia: Anura: Eleutherodactylidae) in eastern Panama

Figure 14. Color variation of the new Diasporus species: A, B, Diasporus darienensis sp. nov. (SMF 97305); C, D, Diasporus majeensis sp. nov. (SMF 97658); E, F, Diasporus pequeno sp. nov. (MHCH 2830); G, H, Diasporus sapo sp. nov. (G, not collected; H, MHCH 2854).

opennotspecifiedSep 2016View details →
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Figure 12 in An integrative approach to reveal speciation and species richness in the genus Diasporus (Amphibia: Anura: Eleutherodactylidae) in eastern Panama

Figure 12. Holotype of Diasporus pequeno sp. nov.: A, B, frontal and lateral view, respectively; C, ventral view; D, flanks.

opennotspecifiedSep 2016View details →
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Figure 10 in An integrative approach to reveal speciation and species richness in the genus Diasporus (Amphibia: Anura: Eleutherodactylidae) in eastern Panama

Figure 10. Holotype of Diasporus darienensis&gt; sp. nov.: A, frontal view; B, ventral view; C, left foot ventrally; D, right hand ventrally; E, flanks; F, posterior side of thighs and rear.

opennotspecifiedSep 2016View details →
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Figure 8 in An integrative approach to reveal speciation and species richness in the genus Diasporus (Amphibia: Anura: Eleutherodactylidae) in eastern Panama

Figure 8. Bayesian consensus tree of the genus Diasporus based on 16S, COI, and RAG1 genes. Out-groups are not shown (Pristimantis caryophyllaceus, Craugastor gollmeri, Craugastor fitzingeri, Colostethus pratti, Eleutherodactylus planirostris, and Eleutherodactylus thorectes). Asterisks on nodes indicate estimated posterior probabilities: P ≥ 0.90.

opennotspecifiedSep 2016View details →
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Figure 4 in An integrative approach to reveal speciation and species richness in the genus Diasporus (Amphibia: Anura: Eleutherodactylidae) in eastern Panama

Figure 4. Discriminant function analyses of the acoustic characters of Diasporus species. Variables included in the analysis: note duration, note interval, dominant frequency (DF, corrected by snout-vent length), low frequency, high frequency, and call rate (temporal characters are corrected for temperature).

opennotspecifiedSep 2016View 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)

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.

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