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1,254 results for “PANs”

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zenodo40/100

Fig. 1 in Aquatic invertebrate communities of perennial pans in Mpumalanga, South Africa: a diversity and functional approach

Fig. 1. Location of the various pans included in the study. Pans 1, 2 and 8 are influenced by mining activities, pan 3 by agricultural activities, and pans 4–7 and 9 are located in an area with few anthropogenic activities.

opencc-by-4.0Dec 2012View details →
zenodo40/100

Fig. 3 in Aquatic invertebrate communities of perennial pans in Mpumalanga, South Africa: a diversity and functional approach

Fig. 3. MDS ordination of the community traits of the selected pans with similarities based on agglomerative cluster analysis overlain. Numbers 1–9 represent the different pans, while repeated numbers represent the various sampling occasions.

opencc-by-4.0Dec 2012View details →
zenodo40/100

FIGURE 2 in Dating the origin and diversiFIcation of Pan-Chelidae (Testudines, Pleurodira) under multiple molecular clock approaches

FIGURE 2 Opening of Tasman Sea; Pal., Paleocene; P, Pliocene; Pe, Pelomedusa; Pel, Pelusios; Pelt, Peltocephalus; (cont.) Ph, Phrynops; Pl, Platemys; Ple, Pleurodira; Po, Podocnemis; Ps, Pseudemydura; Q, Quaternary; R, Rheodytes; Rh, Rhinemys. *, constrained nodes based on the TE MP topology; †, extinct taxa; ↑, origin of total groups Pan-Chelidae and Pan-Pelomedusioides. Downloaded from Brill.com10/07/2022 07:36:56PM via free access

opencc-by-4.0Feb 2020View details →
zenodo40/100

FIGURE 3 in Dating the origin and diversiFIcation of Pan-Chelidae (Testudines, Pleurodira) under multiple molecular clock approaches

FIGURE 3 Comparison of the three dating analyses performed in this study (simplified trees). Node number as in table 2. Abbreviations of analyses as in table 1. Abbreviations of geological events as in fig. 2. Abbrevia- tions of genera as in figs. 1 and 2. * constrained nodes based on the MP topologies; ↑, origin of total groups Pan-Chelidae and Pan- Pelomedusioides.

opencc-by-4.0Feb 2020View details →
zenodo40/100

FIGURE 4 in Dating the origin and diversiFIcation of Pan-Chelidae (Testudines, Pleurodira) under multiple molecular clock approaches

FIGURE 4 Comparison of dates produced by the three analyses of this study and four previous molecular clock studies. Abbreviations: Dea (2011), Dornburg et al. (2011); Jea (2013), Joyce et al. (2013); Pea (2017), Pereira et al. (2017); TS-M TD, This study morphological tip-dating; TS- ND, This study node-dating; TS-TE TD, This study total-evidence tip- dating; R&DF (2016), Rodrigues & Diniz-Filho (2016). Node numbers as in table 2.

opencc-by-4.0Feb 2020View details →
zenodo40/100

Pan-cancer snRandom-seq datasets

<p>The integrated UMI matrices and metadata for paper: "<strong>Pan-cancer transcriptomic profiling reveals lncRNA-associated cell heterogeneity</strong>"</p>

opencc-by-4.0Oct 2023View details →
dryad40/100

Drivers of interspecific spatial segregation in two closely related seabird species at a pan-Atlantic scale

Open the record for dataset details and reuse information.

publicNov 2024View details →
dryad40/100

Data from: Chimpanzees (Pan troglodytes) strategically manipulate their environment to deny conspecifics access to food

Open the record for dataset details and reuse information.

publicAug 2024View details →
dryad40/100

Data from: Pan-European phylogeography of the European roe deer (Capreolus capreolus)

Open the record for dataset details and reuse information.

publicJun 2023View details →
dryad40/100

Quantitative estimates of glacial refugia for chimpanzees (Pan troglodytes) since the Last Interglacial (120,000 BP)

Open the record for dataset details and reuse information.

publicAug 2021View details →
dryad40/100

Pan Arctic Species List (PASL) matching script

Open the record for dataset details and reuse information.

publicNov 2023View details →
edi40/100

Soil temperatures, lake temperature, lake depth, and evaporation pan depth and pan water temperature data from Toolik Field Station, Toolik Lake, Alaska for 2000.

Weather data file for Arctic Tundra LTER site at Toolik Lake. Only the sensors that are measured every 10 minutes and averaged every three hours are include, i.e. soil temperatures, lake temperature, lake depth, and evaporation pan depth and pan water temperature.

openOpenMar 2016View details →
edi40/100

Soil temperatures, lake temperature, lake depth, and evaporation pan depth and pan water temperature data from Toolik Field Station, Toolik Lake, Alaska for 1993.

Weather data file for Arctic Tundra LTER site at Toolik Lake. Only the sensors that are measured every 10 minutes and averaged every three hours are include, i.e. soil temperatures, lake temperature, lake depth, and evaporation pan depth and pan water temperature.

openOpenMar 2016View details →
dryad36/100

Data for: Evaluating the impact of physical frailty during ageing in wild chimpanzees (Pan troglodytes schweinfurthii)

<p>While declining physical performance is an expected consequence of aging, human clinical research has placed increasing emphasis on physical frailty as a predictor of death and disability in the elderly. We examined non-invasive measures approximating frailty in a richly-sampled longitudinal dataset on wild chimpanzees. Using urinary creatinine to assess lean body mass, we demonstrated moderate but significant declines in physical condition with age in both sexes. While older chimpanzees spent less of their day in the trees and feeding, they did not alter activity budgets with respect to travel or resting. There was little evidence that declining lean body mass had negative consequences independent of age. Old chimpanzees with poor lean body mass rested more often but did not otherwise differ in activity. Males, but not females, in poor condition were more likely to exhibit respiratory illness. Poor muscle mass was associated acutely with death in males, but it did not predict future mortality in either sex. While there may be some reasons to suspect biological differences in the susceptibility to frailty in chimpanzees versus humans, our data are consistent with recent reports from humans that lean, physically active individuals can successfully combat frailty.</p>

opencc-zeroJan 2020View details →
dryad36/100

Autopolyploidy-driven range expansion of a temperate-originated plant to pan-tropic under global change

<p>Angiosperms are believed to have emerged initially in the tropics and expanded their distribution range polewards through diverse mechanisms, for example polyploidization-driven cold-tolerance evolution. Reversed expansion from temperate to pantropic climate through a polyploidization-driven shift in heat-tolerance remains largely unknown. Here, we found autopolyploidy in relation to the global expansion of <i>Solidago canadensis</i> from its temperate-climate native range in North American to hot-summer climate in an introduced range. Our cytogeographical study of 2062 accessions from 471 locations worldwide demonstrates that ploidy levels correlates negatively with latitude and positively with average temperature. An isotherm-dependent shift of the climate niches at the threshold of 20-24ºC between geo-cytotypes can be attributed mainly to autopolyploidy-driven differentiation of heat tolerance; only polyploids and not diploids are able to complete sexual reproduction, germinate and grow in the hot-summer climate of low latitudes. Ploidy-dependent fertility appears to play a key role in the hot-summer introduced range in the northern hemisphere through both pre-adaptation and rapid post-introduction adaptive evolution of delayed flowering and improved heat-tolerance during embryo development. MaxEnt model predicts continuous expansion of this weed under global change. These results provide new insights into the mechanisms governing autopolyploidy-driven backward range-expansion of plant species from temperate origins.</p>

opencc-zeroOct 2020View details →
zenodo36/100

Figure S2 in Surveys of the bee (Hymenoptera: Apiformes) community in a Neotropical savanna using pan traps

Figure S2. Habitat view of the point of each trail (trails in lines) used to collect bees using pan traps at Rio Preto State Park, Minas Gerais, Brazil. Pictures were taken in March 2014.

opencc-by-nc-4.0Jul 2020View details →
zenodo36/100

Figure 2 in Surveys of the bee (Hymenoptera: Apiformes) community in a Neotropical savanna using pan traps

Figure 2. Species richness (A) and abundance (B) of bees collected by pan traps in each trail (1-5) during five consecutive days in October 2013 and March 2014 at Rio Preto State Park, Minas Gerais, Brazil.

opencc-by-nc-4.0Jul 2020View details →
zenodo36/100

Figure 1 in Surveys of the bee (Hymenoptera: Apiformes) community in a Neotropical savanna using pan traps

Figure 1.Species accumulation curves (mean + SD) and richness estimator Chao 1 values for the bees captured by pan traps in the Rio Preto State Park, Minas Gerais, Brazil,during five consecutive days of samplings in October 2013 and March 2014.

opencc-by-nc-4.0Jul 2020View details →
zenodo36/100

Figure S3 in Surveys of the bee (Hymenoptera: Apiformes) community in a Neotropical savanna using pan traps

Figure S3. Landscape aerial images of the five trails and the five points at each trail used to collect bees using pan traps at Rio Preto State Park, Minas Gerais, Brazil. Satellite images from Google Earth. Scale bar = 100 meters.

opencc-by-nc-4.0Jul 2020View details →
zenodo36/100

Figure S1 in Surveys of the bee (Hymenoptera: Apiformes) community in a Neotropical savanna using pan traps

Figure S1. Map of the study site in the Rio Preto State Park, Minas Gerais, Brazil, and the schematic drawing illustrating the trail design (one of the 5 trails) and the position of the three colored traps (white, yellow and blue) in the trail.

opencc-by-nc-4.0Jul 2020View details →

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Allen Brain Atlas

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DANDI Archive for NWB datasets

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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.

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OpenNeuro

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Last verified 2026-04-29Open record