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25 results for “distance scale”
Text-fig. 5. Mastixiopsis nyssoides KIRCHH. a, b, g–n: Organic preservation. a, b: Lignitic, unpermineralized, early Eocene Dorset Pipe clays at Arne, V. 40762. a: Ventral view (original illustration from pl. 18, fig. 1 of Chandler 1962). b: Transverse fracture, somewhat distorted by compression. c–f: Pyrite permineralization. c: Ventral view, V. 22963(1) from Sheppey, originally listed as Mastixia cantiensis. d: Lateral view, V. 22969 from Sheppey (identified as Mastixia grandis by Reid and Chandler 1933: pl. 25, fig. 8). e: Equatorial transverse physical section from (c). f: Equatorial transverse physical section from (d). g: Detail of pericarp from (e), showing endocarp formed of dense fibrous tissue, surrounded by mesocarp of anticlinally oriented larger cells. h: Detail of pericarp from (f). i–n: Type material from Eocene of Riestadt, Germany, MNB. i: Ventral view. j, k: Ventral and apical views of holotype. l: View of the transversely fractured surface from (j) showing horseshoe shaped locule. m: Equatorial transverse physical cut of the specimen in (i); note yellow resin cavity (arrow). n: Scanning electron microscopy of pericarp from (l) with locule lining at lower edge of image. Note dense endocarp tissue composed of small cells (fibres and sclereids), extending about 3/5 of distance to periphery, surrounded by mesocarp of larger, anticlinally oriented cells. Scale bars 1 cm in (a–f), (i–k), 1 mm in (g), 2 mm in (h), 3 mm in (l), m, 250 Μm in (n). Bar in (d) applies also to (c). Bar in (l) also applies to (m). Bar in (i) also applies to (j) and (k). in Mastixioid Fruits (Cornales) From The Early Eocene London Clay Flora: Morphology, Anatomy And Nomenclatural Revision
Text-fig. 5. Mastixiopsis nyssoides KIRCHH. a, b, g–n: Organic preservation. a, b: Lignitic, unpermineralized, early Eocene Dorset Pipe clays at Arne, V. 40762. a: Ventral view (original illustration from pl. 18, fig. 1 of Chandler 1962). b: Transverse fracture, somewhat distorted by compression. c–f: Pyrite permineralization. c: Ventral view, V. 22963(1) from Sheppey, originally listed as Mastixia cantiensis. d: Lateral view, V. 22969 from Sheppey (identified as Mastixia grandis by Reid and Chandler 1933: pl. 25, fig. 8). e: Equatorial transverse physical section from (c). f: Equatorial transverse physical section from (d). g: Detail of pericarp from (e), showing endocarp formed of dense fibrous tissue, surrounded by mesocarp of anticlinally oriented larger cells. h: Detail of pericarp from (f). i–n: Type material from Eocene of Riestadt, Germany, MNB. i: Ventral view. j, k: Ventral and apical views of holotype. l: View of the transversely fractured surface from (j) showing horseshoe shaped locule. m: Equatorial transverse physical cut of the specimen in (i); note yellow resin cavity (arrow). n: Scanning electron microscopy of pericarp from (l) with locule lining at lower edge of image. Note dense endocarp tissue composed of small cells (fibres and sclereids), extending about 3/5 of distance to periphery, surrounded by mesocarp of larger, anticlinally oriented cells. Scale bars 1 cm in (a–f), (i–k), 1 mm in (g), 2 mm in (h), 3 mm in (l), m, 250 Μm in (n). Bar in (d) applies also to (c). Bar in (l) also applies to (m). Bar in (i) also applies to (j) and (k).
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group. in Distribution of extracellular enzyme-producing bacteria in the digestive tracts of 4 brackish water fish species
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group.
Measures of the heights of the letters of the ostraca with scale of Iruña-Veleia, and, distances between lines and between letters of the ostraca with scale of Iruña-Veleia.
<p>Measures of the heights of the letters of the ostraca with scale of Iruña-Veleia, and, distances between lines and between letters of the ostraca with scale of Iruña-Veleia.</p>
Data from: Odor source distance is predictable from time-histories of odor statistics for large scale outdoor plumes
<p>Odor plumes in turbulent environments are intermittent and sparse. Lab-scaled experiments suggest that information about the source distance may be encoded in odor signal statistics, yet it is unclear whether useful and continuous distance estimates can be made under real-world flow conditions. Here we analyze odor signals from outdoor experiments with a sensor moving across large spatial scales in desert and forest environments to show that odor signal statistics can yield useful estimates of distance. We show that achieving accurate estimates of distance requires integrating statistics from 5-10 seconds, with a high temporal encoding of the olfactory signal of at least 20 Hz. By combining distance estimates from a linear model with wind-relative motion dynamics, we achieved source distance estimates in a 60x60 m<sup>2</sup> search area with median errors of 3-8 meters, a distance at which point odor sources are often within visual range for animals such as mosquitoes.</p>
Data from: Odor source distance is predictable from time-histories of odor statistics for large scale outdoor plumes
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Pairwise distance demarcation of species in the family Coronaviridae. a, Diagonal matrix of PPDs of 2,505 viruses clustered according to 49 coronavirus species, 39 established and 10 pending or tentative, and ordered from the most to least populous species, from left to right; green and white, PPDs smaller and larger than the inter-species threshold, respectively. Areas of the green squares along the diagonal are proportional to the virus sampling of the respective species, and virus prototypes of the five most sampled species are specified to the left; asterisks indicate species that include viruses whose intra-species PPDs crossed the inter-species threshold (threshold 'violators'). b, Maximal intra-species PPDs (x axis, linear scale) plotted against virus sampling (y axis, log scale) for 49 species (green dots) of the Coronaviridae. Indicated are the acronyms of virus prototypes of the seven most sampled species. Green and blue plot sections represent intra-species and intra-subgenera PPD ranges. The vertical black line indicates the inter-species threshold. c, Shown are the PDs of non-identical residues (y axis) for four viruses representing three major phylogenetic lineages (clades) of the species Severe acute respiratorysyndrome-related coronavirus (panel b) and all pairs of the 256 viruses of this species ('all pairs'). The PD values were derived from pairwise distances in the MSA that were calculated using an identity matrix. Panels a and b were adopted from the DEmARC v.1.4 output. in The species Severe acute respiratory syndromerelated coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2
Pairwise distance demarcation of species in the family Coronaviridae. a, Diagonal matrix of PPDs of 2,505 viruses clustered according to 49 coronavirus species, 39 established and 10 pending or tentative, and ordered from the most to least populous species, from left to right; green and white, PPDs smaller and larger than the inter-species threshold, respectively. Areas of the green squares along the diagonal are proportional to the virus sampling of the respective species, and virus prototypes of the five most sampled species are specified to the left; asterisks indicate species that include viruses whose intra-species PPDs crossed the inter-species threshold (threshold 'violators'). b, Maximal intra-species PPDs (x axis, linear scale) plotted against virus sampling (y axis, log scale) for 49 species (green dots) of the Coronaviridae. Indicated are the acronyms of virus prototypes of the seven most sampled species. Green and blue plot sections represent intra-species and intra-subgenera PPD ranges. The vertical black line indicates the inter-species threshold. c, Shown are the PDs of non-identical residues (y axis) for four viruses representing three major phylogenetic lineages (clades) of the species Severe acute respiratorysyndrome-related coronavirus (panel b) and all pairs of the 256 viruses of this species ('all pairs'). The PD values were derived from pairwise distances in the MSA that were calculated using an identity matrix. Panels a and b were adopted from the DEmARC v.1.4 output.
Does conspicuousness scale linearly with colour distance? a test using reef fish
<p><span><span><span><span><span><span><span><span><span><span><span>To be effective, animal colour signals must attract attention – and therefore need to be conspicuous. To understand signal function, it is useful to evaluate their conspicuousness to relevant viewers under various environmental conditions, including when visual scenes are cluttered by objects of varying colour. A widely used metric of colour difference (ΔS) is based on the Receptor Noise Limited (RNL) model, which was originally proposed to determine when two similar colours appear different from one another, termed the discrimination threshold (or JND, just noticeable difference). Estimates of the perceptual distances between colours that exceed this threshold – termed 'suprathreshold' colour differences – often assumes that a colour's conspicuousness scales linearly with colour distance, and that this scale is independent of direction in colour space. Currently, there is little behavioural evidence to support these assumptions. This study evaluated the relationship between ΔS and conspicuousness in suprathreshold colours using an Ishihara-style test with a coral reef fish, <i>Rhinecanthus aculeatus</i>. As our measure of conspicuousness, we tested whether fish, when presented with two colourful targets, preferred to peck at the one with a greater ΔS from the average distractor colour. We found the relationship between ΔS and conspicuousness followed a sigmoidal function, with high ΔS colours perceived as equally conspicuous. We found that the relationship between ΔS and conspicuousness varied across colour space (i.e. for different hues). The sigmoidal detectability curve was little affected by colour variation in the background or when colour distance was calculated using a model that does not correct for receptor noise. These results suggest that the RNL model may provide accurate estimates for perceptual distance for small suprathreshold distance colours, even in complex viewing environments, but must be used with caution with perceptual distances exceeding 10 ΔS.</span></span></span></span></span></span></span></span></span></span></span></p>
Data from: Gauging scale effects and biogeographical signals in similarity distance decay analyses: an Early Jurassic ammonite case study
In biogeography, the similarity distance decay (SDD) relationship refers to the decrease in compositional similarity between communities with geographical distance. Although representing one of the most widely used relationships in biogeography, a review of the literature reveals that: (1) SDD is influenced by both spatial extent and sample size; (2) the potential effect of the phylogenetic level has yet to be tested; (3) the effect of a marked biogeographical structuring upon SDD patterns is largely unknown; and (4) the SDD relationship is usually explored with modern, mainly terrestrial organisms, whereas fossil taxa are seldom used in that perspective. Using this relationship, we explore the long-distance dispersal of the Early Jurassic (early Pliensbachian, c. 190.8 Ma to 187.6 Ma) ammonites of the western Tethys and adjacent areas, in a context of marked provincialism. We show that the long-distance dispersal of these ammonites is not related to shell size and shape, but rather to the environmental characteristics of the province to which they belong. This suggests that their long-distance dispersal may have been essentially driven by passive planktonic drift during early juvenile, post-hatching stages. Furthermore, it seems that the SDD relationship is not always an appropriate method to characterize the existence of a biogeographical structuring. We conducted SDD analyses at various spatial, sampling and phylogenetic scales in order to evaluate their sensitivity to scale effects. This multi-scale approach indicates that the sampling scale may influence SDD rates in an unpredictable way and that the phylogenetic level has a major impact on SDD patterns.
Data from: The large-scale drivers of population declines in a long-distance migratory shorebird
Migratory species can travel tens of thousands of kilometers each year, spending different parts of their annual cycle in geographically distinct locations. Understanding the drivers of population change is vital for conserving migratory species, yet the challenge of collecting data over entire geographic ranges has hindered attempts to identify the processes leading to observed population changes. Here, we use remotely sensed environmental data and count data to investigate the factors driving variability in abundance in two subspecies of a long-distance migratory shorebird, the bar-tailed godwit (Limosa lapponica). We compiled a spatially and temporally explicit dataset of three environmental variables to identify the conditions experienced by each subspecies in each stage of their annual cycle (breeding, non-breeding and staging). We used a Bayesian N-mixture model to analyze 18 years of monthly count data from 21 sites across Australia and New Zealand in relation to the remote sensing datasets. We found that the abundance of one subspecies (L. l. menzbieri) in their non-breeding range was related to climate conditions in breeding grounds, and detected sustained population declines between 1995 and 2012 in both subspecies (L. l. menzbieri, -6.7% and L. l. baueri, -2.1% year-1). To investigate the possible causes of the declines, we quantified changes in habitat extent at 22 migratory staging sites in the Yellow Sea, East Asia, over a 25-year period and found -1.7% and -1.2% year-1 loss of habitat at staging sites used by L. l. menzbieri and L. l baueri, respectively. Our results highlight the need to identify environmental and anthropogenic drivers of population change across all stages of migration to allow the formulation of effective conservation strategies across entire migratory ranges.
Island biogeography at the meso-scale: distance from forest edge affects choice of patch size by ovipositing treefrogs
<p>Diversity in habitat patches is partly driven by variation in patch size, which affects extinction, and isolation, which affects immigration. Patch size also affects immigration as a component of patch quality. In wetland ecosystems, where variation in patch size and inter-patch distance is ubiquitous, relationships between size and isolation may involve trade-offs. We assayed treefrog oviposition at three patch sizes in arrays of two types, one where size increased with distance from forest (dispersed), and one with all patches equidistant from forest (equidistant), testing directly for an interaction between patch size and distance, which was highly significant. Medium patches in dispersed arrays received more eggs than those in equidistant arrays as use of typically preferred larger patches was reduced in dispersed arrays. Our results demonstrate a habitat selection trade-off between preferred large and less-preferred medium patches across small-scale variation in isolation. Such patch size/isolation relationships are critical to community assembly and to understanding how diversity is maintained within a metapopulation and metacommunity framework, especially as wetland habitat becomes increasingly rare and fragmented. These results bring lessons of Island Biogeography, writ large, to bear on questions at small scales where ecologists often work, and where habitat restoration is most often focused.</p>
Long distance migration is a major factor driving local adaptation at continental scale in a Pacific Salmon
<p><span>Inferring the genomic basis of local adaptation is a long-standing goal of evolutionary biology. Beyond its fundamental evolutionary implications, such knowledge can guide conservation decisions for populations of conservation and management concern. Here, we investigated the genomic basis of local adaptation in the Coho salmon (<i>Oncorhynchus kisutch</i>) across its entirety North American range. We hypothesized that extensive spatial variation in environmental conditions and the species' homing behavior may promote the establishment of local adaptation. We genotyped 7,829 individuals representing 217 sampling locations at more than 100,000 high-quality RADseq loci to investigate how recombination might affect the detection of loci putatively under selection and took advantage of the precise description of the demographic history of the species from our previous work to draw accurate population genomic inferences about local adaptation. Results indicated that genetic differentiation scans and genetic-environment association analyses were both significantly affected by variation in recombination rate as low recombination regions displayed increased rate of outliers. By taking these confounding factors into consideration, we revealed that migration distance was the primary selective factor driving local adaptation and partial parallel divergence among distant populations. Moreover, we identified several candidates SNP associated with long distance migration and altitude including gene known to be involved in adaptation to altitude in other species. The evolutionary implications of our findings are discussed along with conservation applications.</span></p>
How to enhance the inverse distance weighting method to detect the precipitation pattern in a large-scale watershed
<p>These datasets provide precipitation data over Central Plateau watershed of Iran. Four different variants of the Inverse Distance Weighting (IDW) method are utilized to create these datasets. Two out of four IDW variants are proposed and developed by the authors to enhance the performance of the available standard models.</p> <p> </p> <p>Data Format: xlsx</p> <p>Spatial Resolution: ~0.08˚ & 0.25˚</p> <p>Spatial Coverage: Central Plateau watershed, Iran (48˚07'E to 61˚25'E - 26˚33'N to 37˚27'N)</p> <p>Temporal Resolution: Monthly</p> <p>Temporal Coverage: 2005 - 2015 (Inclusively)</p> <p> </p> <p><strong>How to cite:</strong></p> <p><strong>Arash Ghomlaghi, Mohsen Nasseri & Bardia Bayat (2022): How to enhance the inverse distance weighting method to detect the precipitation pattern in a large-scale watershed, Hydrological Sciences Journal, DOI: 10.1080/02626667.2022.2124874</strong></p>
FIG. 2. Nonmetric multidimensional scaling calculated with the Bray-Curtis distance metric using a in Spatial Variation of False Map Turtle (Graptemys pseudogeographica) Bacterial Microbiota in the Lower Missouri River, United States
FIG. 2. Nonmetric multidimensional scaling calculated with the Bray-Curtis distance metric using a square root transformation and Wisconsin double-standardization. Location is represented by color, and sex is represented by shape. Stress of fit for the ordination is reported at 0.145. Axis titles represent the two dimensions to which the data have been ordinated.
Data from: The large-scale drivers of population declines in a long-distance migratory shorebird
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Island biogeography at the meso-scale: distance from forest edge affects choice of patch size by ovipositing treefrogs
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Data from: Mother-offspring distances reflect sex differences in fine-scale genetic structure of eastern grey kangaroos
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Long distance migration is a major factor driving local adaptation at continental scale in a Pacific Salmon
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Data from: Fine-scale sampling reveals distinct isolation by distance patterns in chum salmon (Oncorhynchus keta) populations occupying a glacially dynamic environment
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Does conspicuousness scale linearly with colour distance? a test using reef fish
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Data from: Gauging scale effects and biogeographical signals in similarity distance decay analyses: an Early Jurassic ammonite case study
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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.