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828 results for “species trait”
FIGURES 1–2. Gibocercus and Biguembia relationships. 1 in Gibocercus Szumik and Biguembia Szumik (Embioptera, Archembiidae): new species and the potentiality of female traits
FIGURES 1–2. Gibocercus and Biguembia relationships. 1. According to Szumik (1997); 2. According to the phylogeny of Embioptera in Szumik et al. (2008).
Supplementary material 2 from: Grimm A, Ramírez AMP, Moulherat S, Reynaud J, Henle K (2014) Life-history trait database of European reptile species. Nature Conservation 9: 45-67. https://doi.org/10.3897/natureconservation.9.8908
Comments on taxonomy and species coverage: Explanation note: The supplementary material consists of several tables that explain differences between our updated list of species names to the lists used by Sillero et al. (2014) in their new SEH list of species and the list of Speybroeck et al. (2010).
Supplementary material 1 from: Grimm A, Ramírez AMP, Moulherat S, Reynaud J, Henle K (2014) Life-history trait database of European reptile species. Nature Conservation 9: 45-67. https://doi.org/10.3897/natureconservation.9.8908
Species names used in our database and used in the Societas Europaea Herpetologica (SEH) atlas: Explanation note: The table matches the species names in the SEH atlas with the updated speceis names used in our database. It thus provides the two species list that can be used to search the database.
FIGURE 6. Hyalella montana n in A new species of Hyalella (Crustacea: Amphipoda: Hyalellidae) from Itatiaia National Park, Brazil: an epigean freshwater amphipod with troglobiotic traits at 2,200 meters of altitude
FIGURE 6. Hyalella montana n. sp., Itatiaia National Park (22°22′13,3″S –44°42′32,6″W), Minas Gerais state, Itamonte municipality, Brazil. Holotype, male, 5.8 mm, CRFFP 87. Scale bars: 0.1 mm for T; 0.2 mm for U1–3; 0.5 mm for the remainder.
FIGURE 5. Hyalella montana n in A new species of Hyalella (Crustacea: Amphipoda: Hyalellidae) from Itatiaia National Park, Brazil: an epigean freshwater amphipod with troglobiotic traits at 2,200 meters of altitude
FIGURE 5. Hyalella montana n. sp., Itatiaia National Park (22°22′13,3″S –44°42′32,6″W), Minas Gerais state, Itamonte municipality, Brazil. Holotype, male, 5.8 mm, CRFFP 87; paratype, female, 5.0 mm, CRFFP 88. Scale bars: 0.1 mm for Pl; 0.2 mm for Mp; 0.5 mm for the remainder.
FIGURE 4. Hyalella montana n in A new species of Hyalella (Crustacea: Amphipoda: Hyalellidae) from Itatiaia National Park, Brazil: an epigean freshwater amphipod with troglobiotic traits at 2,200 meters of altitude
FIGURE 4. Hyalella montana n. sp., Itatiaia National Park (22°22′13,3″S –44°42′32,6″W), Minas Gerais state, Itamonte municipality, Brazil. Holotype, male, 5.8 mm, CRFFP 87; paratype, female, 5.0 mm, CRFFP 88. Scale bars: 0.1 mm for LL; 0.5 mm for the remainder.
FIGURE 3. Hyalella montana n in A new species of Hyalella (Crustacea: Amphipoda: Hyalellidae) from Itatiaia National Park, Brazil: an epigean freshwater amphipod with troglobiotic traits at 2,200 meters of altitude
FIGURE 3. Hyalella montana n. sp., Itatiaia National Park (22°22′13,3″S –44°42′32,6″W), Minas Gerais state, Itamonte municipality, Brazil. Paratype, male, 5.8 mm, CRFFP 87. Scale bars: 0.5 mm for A1–2; 0.2 mm for rMd; 0.1 mm for the remainder.
FIGURE 2. Hyalella montana n in A new species of Hyalella (Crustacea: Amphipoda: Hyalellidae) from Itatiaia National Park, Brazil: an epigean freshwater amphipod with troglobiotic traits at 2,200 meters of altitude
FIGURE 2. Hyalella montana n. sp., Itatiaia National Park (22°22′13,3″S–44°42′32,6″W), Minas Gerais state, Itamonte municipality, Brazil. Holotype, male, 5.7 mm, CRFFP 86; paratype, female, 5.0 mm, CRFFP 88. Scale bars: 1.0 mm.
FIGURE 1 in A new species of Hyalella (Crustacea: Amphipoda: Hyalellidae) from Itatiaia National Park, Brazil: an epigean freshwater amphipod with troglobiotic traits at 2,200 meters of altitude
FIGURE 1. Collection site of H. montana n. sp. A: Itatiaia National Park, Minas Gerais state, Itamonte municipality, Brazil; B: Small stream next to the Alsene river, (22°22′13,3″S–44°42′32,6″W—Type locality); C and D: screening of specimens on a styrofoam tray.
Data for: Phenotypic variation of hydraulic traits for woody species
<p>Hydraulic traits are major determinants of plant fitness, thus exerting control over vegetation structure, function and distribution. Yet it remains unclear whether and how hydraulic traits respond to environmental stimuli (i.e., phenotypic variation of hydraulic traits; PVHT), and if the coordination between different hydraulic traits and the trait-climate relationship are affected by PVHT.</p> <p>Here, we synthesized data of PVHT (maximum hydraulic conductivity and water potential inducing 50% loss of hydraulic conductivity) as well as potentially related morphological and anatomical traits (e.g. sapwood density, branch Huber value, mean and hydraulic weighted conduit diameter). We analyzed the magnitude, direction and source of variation of the plastic response, as well as the influence of environmental factors on trait coordination. Additionally, we compared the intra- and inter- specific variation between key hydraulic traits and climate metrics (mean annual precipitation and mean annual temperature) at the site of growth, as well as across the population range.</p> <p>PVHT was highly variable in both magnitude and direction, which was contingent on the environmental factor. The variation in PVHT mainly occurred at high taxonomic levels (i.e., family and genus), whereas phenology explained little variation for PVHT. Despite the high variability, trait correlation remained robust in the presence of environmental stimuli. Moreover, trait-climate relationships differed at inter-specific and intra-specific levels. The intra-specific variation of hydraulic traits in most species showed no correlation with climate metrics compared with the high correlation of hydraulic traits with climate metrics across species.</p> <p>Our findings suggest that the high variability of PVHT does not affect the trait correlation which may be valuable in predicting vegetation dynamics under varying environments. The distinct trait-climate relationships highlight the need to unravel the driving force of PVHT, as well as the adaptive strategy across populations.</p>
Data and code for "Tree species abundance changes at the edges of their climatic distribution: an interplay between climate change, plant traits, and forest management"
<p>## Secondary data and code to accompany the research entitled "Tree species abundance changes at the edges of their climatic distribution: an interplay between climate change, plant traits, and forest management" by Padullés Cubino et al. (2024).</p> <p># There are four folders with (1) "raw data", (2) "processed data", (3) "results", and (4) "scripts".</p> <p># The raw and processed data folders contain the CSV and XLSX files with all the data used for analysis and produced from them</p> <p># The "results" folder contains the figures and table presented in the manuscript.</p> <p># The "scripts" folder contains four scripts for the analyses described in the manuscript:</p> <p> 01_preparation_ClimEdge.R -> data cleaning and processing</p> <p> 02_script_Fig1.R -> code to produce Fig1</p> <p> 03_script_Fig2.R -> code to produce Fig2</p> <p> 04_script_Table1_Fig3.R -> code to produce Table 1 and Fig3</p> <p># If anything is unclear, please contact the corresponding author for clarification (padullesj@gmail.com).</p>
Fig. 3 in A species-level trait dataset of bats in Europe and beyond
Fig. 3 Number of trait categories (genetic composition, physiology, morphology, acoustic signature, climatic associations, foraging habitat, roost type, diet, spatial behaviour, life history, pathogens, phenology, and distribution) provided at the country level across all species. For sake of clarity and for highlighting gaps in geographic coverage, we did not consider in this map traits provided across a given species' range or at regional level. Details on each trait category are provided in Supplementary Material 4.
Fig. 1 in A species-level trait dataset of bats in Europe and beyond
Fig. 1 Number of peer-reviewed studies per year (a) and per geographic area (b) that implemented a traitbased approach to study bats15–91. Data were extracted from a systematic literature search conducted in Web of Science and Google Scholar on the 15th of November 2021 using the following search string terms: (Bat* OR Chiroptera) AND ("trait-base*" OR "trait diversity" OR "functional diversity" OR trait*). The black solid line represents the LOESS (locally weighted scatterplot smoothing) fit to the observed relationship. See raw data and details in Supplementary Material 1.
Body length trait values from the BETSI database, on all Collembola species, all literature sources, requested on 01-06-2017
<p><strong>This table gathers 'Body length' trait values extracted from the BETSI database, on all Collembola species, all literature sources, on 01/06/2017 (DD/MM/YYYY).</strong><br> <br> The BETSI database hosts soil invertebrates trait data.<br> The BETSI database is available here: <a href="http://betsi.cesab.org">http://betsi.cesab.org</a><br> The BETSI database is regularly updated. Please follow the link and contact its administrators if you want to obtain the most up-to-date data ; or contact the dataset's author if you need information on how to use the present dataset.</p> <p><br> <strong>Information in this table</strong><br> <em>BETSI coder</em>: First name and family name of the person that provided the trait value and uploaded it into the BETSI database<br> <em>Collembola species</em>: Collembola species name, taxonomy according to Fauna Europaea<br> <em>Body length value</em>: Trait value, in mm<br> <em>Literature source</em>: Literature source in which the trait value was collected by the BETSI coder<br> <br> This dataset was created, used, and shared with the approval of all concerned BETSI coders (data collectors) and administrators (data managers).</p> <p> </p> <p><strong>If you aim to re-use this dataset:</strong><br> <br> - please cite <strong>Bonfanti et al. (2018) <em>Functional ecology </em></strong><a href="https://doi.org/10.1111/1365-2435.13194">https://doi.org/10.1111/1365-2435.13194</a>, study for which this dataset was originally requested and compiled ;<br> - please give appropriate credit to the concerned BETSI coders and administrators, BETSI database project, and to the authors of the literature sources mentioned in the dataset.</p>
Fig. 2 in Gut-content analysis in four species, combined with comparative analysis of trophic traits, suggests an araneophagous habit for the entire family Palpimanidae (Araneae)
Fig. 2 Comparison of relative 1 conspeccfics spcders cnsects 1 frequency of conspecifics (can- A B nibalism), heterospecific spiders 0.9 0.9 (araneophagy), and insects in 0.8 0.8 the gut of P . gibbulus A, P . 0.7 0.7 potteri B , Diaphorocellus C and frequency Otiothops D . Proportions are 0.6 0.6 estimated per all individuals in e 0.5 0.5 a class (male, female, juvenile). 0.4 0.4 Frequency of cannibalism can be overestimated (see "Discus- Rela 0.3 0.3 sion" for more details), thus 0.2 0.2 should be interpreted with 0.1 0.1 caution 0 0 male female female juvencle adult juvencle adult
Fig. 3 in Gut-content analysis in four species, combined with comparative analysis of trophic traits, suggests an araneophagous habit for the entire family Palpimanidae (Araneae)
Fig. 3 Phylogeny of Palpimanidae plus three other families on the genus level, with estimates of the probabilities of each of five traits at nodes. The fuller the symbol, the higher the probability of a presence of the trait. For trait values at terminals see Table S7
FIG. 3 in Thermal Traits of Anurans Database for the Southeastern United States (TRAD): A Database of Thermal Trait Values for 40 Anuran Species
FIG. 3. Adult trait completeness, or number of traits with at least one trait value in the literature, varies among and within anuran genera (A) and families (B). Each y-axis is ordered by the group with the highest trait completion to group with the lowest trait completion. Points represent individual species. Boxplots indicate standard delineations of median, 25th, and 75th percentiles, and lines indicate the lesser of largest or smallest values or 1.5 times the interquartile range.
FIG. 2 in Thermal Traits of Anurans Database for the Southeastern United States (TRAD): A Database of Thermal Trait Values for 40 Anuran Species
FIG. 2. Species' thermal trait data, measured as sources with unique species and trait combinations (points), have increased since 1945.
FIG. 1 in Thermal Traits of Anurans Database for the Southeastern United States (TRAD): A Database of Thermal Trait Values for 40 Anuran Species
FIG. 1. Counts of adult thermal trait values found within the literature for 37 species of frogs and toads (anurans) within the southeastern United States. Species Pseudacris brimleyi, Pseudacris nigrita, and Pseudacris ocularis are not shown due to no trait values reported. States indicated in gray in the inset map of the conterminous United States are considered the southeastern United States for this database. Trait Name is ordered based on type of trait: warm colored traits are mass and physiological traits, and cool colored traits are behavioral traits. Physiological traits include critical thermal maximum (CTmax), critical thermal minimum (CTmin), and Tpref (preferred temperature). Behavioral traits include basking temperature (Tbask), foraging temperature limits (Tforage_min and Tforage_max), emergence temperature (Tmerge), and activity. An * indicates a species of conservation concern. Conservation status, as defined by the International Union for the Conservation of Nature Red List, was determined on 15 August 2020 (International Union for Conservation of Nature, 2017).
FIG. 4 in Thermal Traits of Anurans Database for the Southeastern United States (TRAD): A Database of Thermal Trait Values for 40 Anuran Species
FIG. 4. The number of traits with at least one trait value in the literature (trait completeness) increases with range size for adults (A) and for all life stages (B) for 37 anurans native to the southeastern United States. Maximum trait completeness is 9 for adults and 22 for all life stages. Each point represents a species that has at least one trait value in the TRAD database, with the symbol and shade in (B) representing the total number of life stages (egg/embryo, tadpole, metamorph, juvenile, and adults) with trait data.
ScienceDex guides
Understand access before you commit
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.