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158 results for “plant size”
Wood density and leaf size jointly predict woody plant growth rates across (but not within) species along a steep precipitation gradient
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A trade-off between leaf carbon economics and plant size among mangrove species in Dongzhaigang, China
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Data from: Seed size predicts global effects of small mammal seed predation on plant recruitment
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Plant species percent cover data: Seed Size and Establishment
The purpose of this experiment is to examine the importance among species differences in seed mass in determining the possibility of seedling establishment under different competitive environments. This experiment was set up in Field 61.
Maximum plant height along transects: Seed Size and Establishment
The purpose of this experiment is to examine the importance among species differences in seed mass in determining the possibility of seedling establishment under different competitive environments. This experiment was set up in Field 61.
Canopy size, gap size, plant height, and scaled height in NEAT plots at Jornada Basin LTER, Summer 2017
This data package contains estimates of vegetation indicators derived from UAV overflights and comparable field observatons at the NEAT experiment in the Jornada Basin of southern New Mexico, USA. The purpose of this study is to develop a UAV-based remote sensing method that can estimate vegetation indicators in arid and semiarid rangelands. This method was used to characterize six rangeland indicators (canopy size, bare soil gap size, plant height, scaled height, vegetation cover, and bare soil cover) in a semiarid grass-shrub ecosystem at the NEAT site. The drone-based estimates were validated with field measurements by using the standard transect methods (gap intercept, drop disk, and line-point intercept methods) in the spring and summer of 2017. Further, we use these results to show possible applications of drone-based products on arid and semiarid rangelands: the spatially explicit input of an ecological model, to detect and characterize non-stationarity, and to detect landscape anisotropy.
Data from: Evolutionary patterns in the geographic range size of Atlantic Forest plants
Species' geographic range size is arguably the single most important predictor of vulnerability to extinction and a key metric in ecology. Despite this, patterns of specific variation in range size and their underlying reasons are still poorly understood. For example, hypotheses on how evolutionary history affects range size have scarcely been tested. To address these questions, we focused on Brazil's Atlantic Forest flora, one of the most species-rich in the world, relatively well-known and highly threatened. We investigated whether and how lineages' diversification rate, number of species and age are associated with species' geographic range size. We estimated the extent of occurrence and area of occupancy of each of 13,283 plant species native to the Atlantic Forest region based on over 500,000 unique records. We used phylogenetic least squares and logistic regressions to analyze how the predictors affect the geographic range size. On average, the higher the diversification rate and number of species in the lineage, the smaller the species range size and the higher the proportion of species with vulnerably small range size. Lineage age showed no clear effect on average range size. The results support our expectations that dynamics of diversification and taxonomic richness considerably affect the species range size. Finally, this work reveals poorly known patterns of range size variation and some of the mechanisms driving variation in range size and vulnerability to extinction.
Data from: Early plant development depends on embryo damage location: the role of seed size in partial seed predation
<p>Data on 1) Observed weevil-infested acorns in the field; 2) Germination rates and times, and seedling emergence of control and embryo-damaged acorns; 3) Seedling performance and physiology of seedlings</p>
Current climate overrides historical effects on species richness and range size of freshwater plants in Europe and North America
<p>1. The latitudinal diversity gradient (LDG) hypothesis suggests that species richness should be highest at low latitudes, whereas Rapoport's rule states that largest ranges ought to be found for species at high latitudes. However, there is no consensus over these patterns and their underlying drivers in the freshwater realm.</p> <p>2. We investigated species richness and mean range size of freshwater plants in 50 km × 50 km grid cells across Europe (40°N to 71°N) and North America (25°N to 78°N), supplemented with data based on 1° latitudinal bands for mean range size. We were especially interested to find out whether there are similarities and differences in these ecogeographical patterns and their underlying drivers between the continents due to their contrasting historical characteristics, spatial extent and topography. </p> <p>3. First, we used partial regression to reveal whether species richness and mean range size of freshwater plants have a linear or quadratic relationship with latitude. Second, we employed variation partitioning based on partial regression to model relationships between plant species richness and mean range size and four explanatory variable groups (i.e., environmental features, current climate, historical climate and geographical location). Third, we utilized boosted regression tree analysis to further investigate species richness and mean range size of freshwater plants in relation to a set of explanatory variables. </p> <p>4. Our results revealed that species richness showed relatively similar patterns in relation to latitude between the continents. Similarly, mean range size trends were alike in North America whether we used 50 km x 50 km grid cell data or 1° latitudinal bands. Instead, different patterns in mean range size emerged between the used data sets in Europe. For both of species richness and mean range size, current climate (with different individual predictor variables) was the main driver in both the continents, but historical effects had a small influence on the response variables.</p> <p>5. <i>Synthesis</i>. Our findings indicated that major ecogeographical rules can strongly vary for the same taxonomic group across broad scales between continents. It is also premature to rely solely on well-known terrestrial taxonomic groups when drawing generalizations about ecogeographical rules.</p>
Data from: Testing macroecological abundance patterns: the relationship between local abundance and range size, range position and climatic suitability among European vascular plants
<p><strong>Aim: </strong>A fundamental question in macroecology centres around understanding the relationship between species' local abundance and their distribution in geographic and climatic space (i.e. the multi-dimensional climatic space or climatic niche). Here, we tested three macroecological hypotheses that link local abundance to the following range properties: (1) the abundance-range size relationship, (2) the abundance-range centre relationship, and (3) the abundance-suitability relationship.<br> <br> <strong>Location: </strong>Europe<br> <br> <strong>Taxon: </strong>Vascular plants<br> <br> <strong>Methods:</strong> Distribution range maps were extracted from the Chorological Database to derive information on the range and niche sizes of 517 European vascular plant species. To estimate local abundance, we assessed samples from 744,513 vegetation plots in the European Vegetation Archive, where local species' abundance is available as plant cover per plot. We then calculated the 'centrality', i.e. the distance between the location of the abundance observation and each species' range centre in geographic and climatic space. The climatic suitability of plot locations was estimated using coarse-grain species distribution models (SDMs). The relationships between centrality or climatic suitability with abundance were tested using linear models and quantile regression. We summarized the overall trend across species' regression slopes from linear models and quantile regression using a meta-analytical approach.<br> <br> <strong>Results: </strong>We did not detect any positive relationships between a species' mean local abundance and the size of its geographic range or climatic niche. Contrasting yet significant correlations were detected between abundance and centrality or climatic suitability among species.<br> <br> <strong>Main conclusions:</strong> Our results do not provide unequivocal support for any of the relationships tested, demonstrating that determining properties of species' distributions at large grains and extents might be of limited use for predicting local abundance, including current SDM approaches. We conclude that environmental factors influencing individual performance and local abundance are likely to differ from those factors driving plant species' distribution at coarse resolution and broad geographic extents.</p>
Data from: What does body size mean, from the "plant's eye view"?
Alternative metrics exist for representing variation in plant body size, but the vast majority of previous research for herbaceous plants has focused on dry mass. Dry mass provides a reasonably accurate and easily measured estimate for comparing relative capacity to convert solar energy into stored carbon. However, from a "plant's eye view", its experience of its local biotic environment of immediate neighbors (especially when crowded) may be more accurately represented by measures of "space occupancy" (S–O) recorded in situ—rather than dry mass measured after storage in a drying oven. This study investigated relationships between dry mass and alternative metrics of S–O body size for resident plants sampled from natural populations of herbaceous species found in Eastern Ontario. Plant height, maximum lateral canopy extent, and estimated canopy area and volume were recorded in situ (in the field)—and both fresh and dry mass were recorded in the laboratory—for 138 species ranging widely in body size and for 20 plants ranging widely in body size within each of 10 focal species. Dry mass and fresh mass were highly correlated (r2 > .95) and isometric, suggesting that for some studies, between-species (or between-plant) variation in water content may be unimportant and fresh mass can therefore substitute for dry mass. However, several relationships between dry mass and other S–O body size metrics showed allometry—that is, plants with smaller S–O body size had disproportionately less dry mass. In other words, they have higher "body mass density" (BMD) — more dry mass per unit S–O body size. These results have practical importance for experimental design and methodology as well as implications for the interpretation of "reproductive economy"—the capacity to produce offspring at small body sizes—because fecundity and dry mass (produced in the same growing season) typically have a positive, isometric relationship. Accordingly, the allometry between dry mass and S–O body size reported here suggests that plants with smaller S–O body size—because of higher BMD—may produce fewer offspring, but less than proportionately so; in other words, they may produce more offspring per unit of body size space occupancy.
Data from: Geographic range size is predicted by plant mating system
Species' geographic ranges vary enormously, and even closest relatives may differ in range size by several orders of magnitude. With data from hundreds of species spanning 20 genera in 15 families, we show that plant species that autonomously reproduce via self-pollination consistently have larger geographic ranges than their close relatives that generally require two parents for reproduction. Further analyses strongly implicate autonomous self-fertilisation in causing this relationship, as it is not driven by traits such as polyploidy or annual life history whose evolution is sometimes correlated with selfing. Furthermore, we find that selfers occur at higher maximum latitudes and that disparity in range size between selfers and outcrossers increases with time since their evolutionary divergence. Together, these results show that autonomous reproduction—a critical biological trait that eliminates mate limitation and thus potentially increases the probability of establishment—increases range size.
Data from: Revising traditional theory on the link between plant body size and fitness under competition: evidence from old-field vegetation
The selection consequences of competition in plants have been traditionally interpreted based on a "size-advantage" hypothesis – that is, under intense crowding/competition from neighbors, natural selection generally favors capacity for a relatively large plant body size. However, this conflicts with abundant data, showing that resident species body size distributions are usually strongly right-skewed at virtually all scales within vegetation. Using surveys within sample plots and a neighbor-removal experiment, we tested: (1) whether resident species that have a larger maximum potential body size (MAX) generally have more successful local individual recruitment, and thus greater local abundance/density (as predicted by the traditional size-advantage hypothesis); and (2) whether there is a general between-species trade-off relationship between MAX and capacity to produce offspring when body size is severely suppressed by crowding/competition – that is, whether resident species with a larger MAX generally also need to reach a larger minimum reproductive threshold size (MIN) before they can reproduce at all. The results showed that MIN had a positive relationship with MAX across resident species, and local density – as well as local density of just reproductive individuals – was generally greater for species with smaller MIN (and hence smaller MAX). In addition, the cleared neighborhoods of larger target species (which had relatively large MIN) generally had – in the following growing season – a lower ratio of conspecific recruitment within these neighborhoods relative to recruitment of other (i.e., smaller) species (which had generally smaller MIN). These data are consistent with an alternative hypothesis based on a 'reproductive-economy-advantage' – that is, superior fitness under competition in plants generally requires not larger potential body size, but rather superior capacity to recruit offspring that are in turn capable of producing grand-offspring – and hence transmitting genes to future generations – despite intense and persistent (cross-generational) crowding/competition from near neighbors. Selection for the latter is expected to favor relatively small minimum reproductive threshold size and hence – as a tradeoff – relatively small (not large) potential body size.
Data from: Habitat diversity associated with island size and environmental filtering control the species richness of rock-savanna plants in neotropical inselbergs
Disentangling the multiple factors controlling species diversity is a major challenge in ecology. Island biogeography and environmental filtering are two influential theories emphasizing respectively island size and isolation, and the abiotic environment, as key drivers of species richness. However, few attempts have been made to quantify their relative importance and investigate their mechanistic basis. Here, we applied structural equation modelling, a powerful method allowing test of complex hypotheses involving multiple and indirect effects, on an island-like system of 22 French Guianan neotropical inselbergs covered with rock-savanna. We separated the effects of size (rock-savanna area), isolation (density of surrounding inselbergs), environmental filtering (rainfall, altitude) and dispersal filtering (forest-matrix openness) on the species richness of all plants and of various ecological groups (terrestrial versus epiphytic, small-scale versus large-scale dispersal species). We showed that the species richness of all plants and terrestrial species was mainly explained by the size of rock-savanna vegetation patches, with increasing richness associated with higher rock-savanna area, while inselberg isolation and forest-matrix openness had no measurable effect. This size effect was mediated by an increase in terrestrial-habitat diversity, even after accounting for increased sampling effort. The richness of epiphytic species was mainly explained by environmental filtering, with a positive effect of rainfall and altitude, but also by a positive size effect mediated by enhanced woody-plant species richness. Inselberg size and environmental filtering both explained the richness of small-scale and large-scale dispersal species, but these ecological groups responded in opposite directions to altitude and rainfall, that is positively for large-scale and negatively for small-scale dispersal species. Our study revealed both habitat diversity associated with island size and environmental filtering as major drivers of neotropical inselberg plant diversity and showed the importance of plant species growth form and dispersal ability to explain the relative importance of each driver.
Stresses affect inbreeding depression in complex ways: Disentangling stress-specific genetic effects from effects of initial size in plants
<p>The magnitude of inbreeding depression (ID) varies unpredictably among environments. ID often increases in stressful environments suggesting that these expose more deleterious alleles to selection or increase their effects. More simply, ID could increase under conditions that amplify phenotypic variation (CV²), e.g. by accentuating size hierarchies among plants. These mechanisms are difficult to distinguish when stress increases both ID and phenotypic variation. We grew in- and outbred progeny of <i>Mimulus guttatus</i> under six abiotic stress treatments (control, waterlogging, drought, nutrient deficiency, copper addition and clipping) with and without competition by the grass <i>Poa palustris</i>. ID differed greatly among stress treatments with δ varying from 7% (control) to 61% (waterlogging) but did not consistently increase with stress intensity. <i>Poa</i> competition increased ID under nutrient deficiency but not other stresses. Analyzing effects of initial size on performance of outbred plants suggests that under some conditions (low N, clipping) competition increased ID by amplifying initial size differences. In other cases (e.g., high ID under waterlogging), particular environments amplified the deleterious genetic effects of inbreeding suggesting differential gene expression. Interestingly, conditions that increased the phenotypic variability of inbred progeny regularly increased ID whereas variability among outbred progeny showed no relationship to ID. Our study reconciles the stress- and phenotypic variability hypotheses by demonstrating how specific conditions (rather than stress <i>per se</i>) act to increase ID. Analyzing CV² separately in inbred and outbred progeny while including effects of initial plant size improve our ability to predict how ID and gene expression vary across environments.</p>
FIGURE. Puccinia klugkistiana on Ligustrum obtusifolium (A–F, N, O, P) and Cleistogenes hackelii (G–N). A. Plant hedges producing spermogonia and aecia in the field. B. Spermogonia on the upper leaf surface. C. Vertical section of an aecium surrounded with peridia. D. Aecia on the lower leaf surface. E. Vertical section of a spermogonium. F. Aeciospores. G. Uredinia on the leaf surface. H. Vertical section of a uredinium. I. Urediniospores. J, K. Telia on the leaf surface. L. Teliospores. M. Urediniospore observed under SEM. N. Vertical section of an uredinium observed under SEM. O. Aecium observed under SEM. P. Aeciospores with various sizes of verrucae on the surface observed under SEM. Scale bars: C = 100 μm, E, F = 20 μm, H, I = 30 μm, M = 5 μm, P = 10 μm, H, L, O = 40 μm. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China
FIGURE. Puccinia klugkistiana on Ligustrum obtusifolium (A–F, N, O, P) and Cleistogenes hackelii (G–N). A. Plant hedges producing spermogonia and aecia in the field. B. Spermogonia on the upper leaf surface. C. Vertical section of an aecium surrounded with peridia. D. Aecia on the lower leaf surface. E. Vertical section of a spermogonium. F. Aeciospores. G. Uredinia on the leaf surface. H. Vertical section of a uredinium. I. Urediniospores. J, K. Telia on the leaf surface. L. Teliospores. M. Urediniospore observed under SEM. N. Vertical section of an uredinium observed under SEM. O. Aecium observed under SEM. P. Aeciospores with various sizes of verrucae on the surface observed under SEM. Scale bars: C = 100 μm, E, F = 20 μm, H, I = 30 μm, M = 5 μm, P = 10 μm, H, L, O = 40 μm.
FIGURE. Individuals in two Populations of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the variation in plant size and rhizome character (each line represents a population). A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS). in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Individuals in two Populations of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the variation in plant size and rhizome character (each line represents a population). A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS).
FIGURE. Cauline Leaves of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the size and shape of leaves within and between populations (each line represents a plant individual). A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS). in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Cauline Leaves of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the size and shape of leaves within and between populations (each line represents a plant individual). A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS).
Leaf traits, plant size and environment data of a common tree species Clausena dunniana in a subtropical broad-leaved forest
<p>This dataset contains the leaf traits, plant size and environment data of 262 individuals of a widespread species <em>Clausena dunniana</em> in the subtropical broad-leaved forests in Maolan National Nature Reserve in the karst region of southwestern China. The 262 individuals of <em>C. dunniana</em> are distributed at two major topographic habitat types, the slope and the hilltop, within the forests of six sites evenly distributed in two regions within the Maolan reserve. The measured individual plant level leaf traits include specific leaf area (SLA), leaf area, leaf dry-matter content (LDMC) and leaf thickness. The plant size represents the first principal component of plant basal diameter and plant height, and the environmental factors include topographic habitat, canopy height, and rock-bareness rate.</p>
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
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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.
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
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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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