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151 results for “Ecological scales”
Text-fig. 1. SEM images of flowers of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Flowers in lateral view showing elongated pedicel, narrowly triangular sepals and elongated protruding style (a); note the large openings in the floral tissue and pedicel (asterisks) interpreted as schizogenous secretory cavities. c: Flower in lateral view with portion of the calyx missing exposing the ovary wall and slightly raised nectariferous ring with probable stomata-like secretory structures (arrow). d: Flower in lateral view showing long pedicel and three of the five tepals; note the elongated narrowly triangular form of the sepals. e: Flower in oblique lateral view with portion of the calyx missing exposing the ovary and elongated style. f, g: Flowers in apical view showing the bases of five sepals (f) and apex of the five-parted ovary; note larger openings in the floral tissue (asterisk) interpreted as schizogenous secretory cavities. Specimens, Mira 100-S170155 (a, holotype), Mira 100-S153145 (b, c, g), Mira 100- S101267 (d), Mira 105-S100732 (e), Mira 100-S101268 (f). Scale bars = 600 µm (a–g). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications
Text-fig. 1. SEM images of flowers of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Flowers in lateral view showing elongated pedicel, narrowly triangular sepals and elongated protruding style (a); note the large openings in the floral tissue and pedicel (asterisks) interpreted as schizogenous secretory cavities. c: Flower in lateral view with portion of the calyx missing exposing the ovary wall and slightly raised nectariferous ring with probable stomata-like secretory structures (arrow). d: Flower in lateral view showing long pedicel and three of the five tepals; note the elongated narrowly triangular form of the sepals. e: Flower in oblique lateral view with portion of the calyx missing exposing the ovary and elongated style. f, g: Flowers in apical view showing the bases of five sepals (f) and apex of the five-parted ovary; note larger openings in the floral tissue (asterisk) interpreted as schizogenous secretory cavities. Specimens, Mira 100-S170155 (a, holotype), Mira 100-S153145 (b, c, g), Mira 100- S101267 (d), Mira 105-S100732 (e), Mira 100-S101268 (f). Scale bars = 600 µm (a–g).
Data from: The importance of biotic interactions in distribution models of wild bees depends on the type of ecological relations, spatial scale and range
<p>Studies have found that biotic information can play an important role in shaping the distribution of species even at large scales. However, results from species distribution models are not always consistent among studies, and the underlying factors that influence the importance of biotic information to distribution models, are unclear. 2. We studied wild bees and plants, and cleptoparasite bees and their hosts in the Netherlands to evaluate how the inclusion of their biotic interactions affects the performance of species distribution models. We assessed model performance through spatial block cross-validation and by comparing models with interactions to models where the interacting species were randomized. Finally, we evaluated how, (i) spatial resolution, (ii) taxonomic rank (genus or species), (iii) degree of specialization, (iv) distribution of the biotic factor, (v) bee body size and (vi) type of biotic interaction, affect the importance of biotic interactions in shaping the distribution of wild bee species using generalized linear models. 3. We found that the models of wild bees improved when the biotic factor was included. The model performance improved the most for parasitic bees. Spatial resolution, taxonomic rank, distribution range of the biotic factor, and degree of specialization of the modelled species all influenced the importance of the biotic interaction to the models. 4. We encourage researchers to include biotic interactions in species distribution models, especially for specialized species and when the biotic factor has a limited distribution range. However, before adding the biotic factor we suggest considering different spatial resolutions and taxonomic ranks of the biotic factor. We recommend using single species or genus data as a biotic factor in the models of specialist species and for the generalist species, we recommend using an approximate measure of interactions, such as flower richness.</p>
Рис. 6. МоΔеΛирование экоΛогических ниш коΛораΔского жука ΔΛя ΔаΛьневосточного, европейского и североамериканского ареаΛов метоΔом метрического Δвухмерного шкаΛирования с применением коэффициента Жаккара Fig. 6. Models of ecological niches of the Colorado potato beetle for the Far Eastern, European, and North-American habitats (metric multidimensional scaling, Jaccard index) in Comparative characterization of the ecology of native (Henosepilachna vigintioctomaculata) and invasive (Leptinoatrsa decemlineata) species under the conditions of the monsoon climate in the southern part of the Russian Far East
Рис. 6. МоΔеΛирование экоΛогических ниш коΛораΔского жука ΔΛя ΔаΛьневосточного, европейского и североамериканского ареаΛов метоΔом метрического Δвухмерного шкаΛирования с применением коэффициента Жаккара Fig. 6. Models of ecological niches of the Colorado potato beetle for the Far Eastern, European, and North-American habitats (metric multidimensional scaling, Jaccard index)
Figure 4 in Broad-scale ecological distribution of dominant macrozoobenthic taxa of the northern Cilician shelf, eastern Mediterranean Sea: crustaceans*
Figure 4. Abundance distribution of dominant species in each crustacean assemblage identified by CCA. Circle diameter is proportional to the abundance. The largest circle corresponds to the maximum abundance (see Appendix on the journal's website for the maximum abundance observed) of each species.
Figure 1 in Broad-scale ecological distribution of dominant macrozoobenthic taxa of the northern Cilician shelf, eastern Mediterranean Sea: crustaceans*
Figure 1. Study area and Turkish part of the Cilician Basin (transects: M: Mersin, I: İskenderun, A: Anamur) and location of the sampling stations (depth code: 1: 10 m, 2: 25 m, 3: 50 m, 4: 75 m, 5: 100 m, 6: 150 m, and 7: 200 m) visited in November 2005, March 2006, July 2006, and January 2007.
Data from: Fractal triads efficiently sample ecological diversity and processes across spatial scales
<p>The relative influence of ecological assembly processes, such as environmental filtering, competition, and dispersal, vary across spatial scales. Changes in phylogenetic and taxonomic diversity across environments provide insight into these processes, however, it is challenging to assess the effect of spatial scale on these metrics. Here, we outline a nested sampling design that fractally spaces sampling locations to concentrate statistical power across spatial scales in a study area. We test this design in northeast Utah, at a study site with distinct vegetation types (including sagebrush steppe and mixed conifer forest), that vary across environmental gradients. We demonstrate the power of this design to detect changes in community phylogenetic diversity across environmental gradients and assess the spatial scale at which the sampling design captures the most variation in empirical data. We find clear evidence of broad-scale changes in multiple features of phylogenetic and taxonomic diversity across aspect. At finer scales, we find additional variation in phylodiversity, highlighting the power of our fractal sampling design to efficiently detect patterns across multiple spatial scales. Thus, our fractal sampling design and analysis effectively identify important environmental gradients and spatial scales that drive community phylogenetic structure. We discuss the insights this gives us into the ecological assembly processes that differentiate plant communities found in northeast Utah.</p>
Data for: Zebra finch song ecology: monitoring of breeding, observational transects, focal and year-round acoustic recordings, and a large-scale simultaneous playback experiment
<p class="MsoNormal">Male songbirds sing to establish territories and to attract mates. However, increasing reports of singing in non-reproductive contexts and by females show that song use is more diverse than previously considered. Therefore, alternative functions of song, such as social cohesion and synchronisation of breeding, by and large were overlooked even in such well-studied species as the zebra finch (<em>Taeniopygia guttata</em>). In these social songbirds only the males sing and pairs breed synchronously in loose colonies following aseasonal rain events in their arid habitat. As males are not territorial, and pairs form long-term monogamous bonds early in life, conventional theory predicts that zebra finches should not sing much at all; yet they do and their song is the focus of hundreds of lab-based studies. We hypothesise that zebra finch song functions to maintain social cohesion and to synchronise breeding. Here we test this idea using data from five years of field studies, including observational transects, focal and year-round audio recordings, and a large-scale playback experiment. We show that zebra finches frequently sing while in groups, that breeding status influences song output at the nest and at aggregations, that they sing year-round, and that they predominantly sing when with their partner, suggesting that song remains important after pair formation. Our playback reveals that song actively features in social aggregations as it attracts conspecifics. Together, these results demonstrate that birdsong has important functions beyond territoriality and mate choice, illustrating its importance in coordination and cohesion of social units within larger societies.</p>
Data from: The spatial patterns of community composition, their environmental drivers and their spatial scale dependence vary markedly between fungal ecological guilds
<p><strong><span>Aim</span></strong></p> <p><span>How community composition varies in space and what governs the variation has been extensively investigated in macroorganisms. However, we have only limited knowledge for microorganisms, especially fungi, despite their ecological and economic significance. Based on previous research, we define and test a series of hypotheses regarding the composition of fungal communities, its most influential drivers and their spatial scale dependence. </span></p> <p><strong><span>Location</span></strong></p> <p><span>Czech Republic.</span></p> <p><strong><span>Time period</span></strong></p> <p><span>Present.</span></p> <p><strong><span>Taxa studied</span></strong></p> <p><span>Fungi.</span></p> <p><strong><span>Methods</span></strong></p> <p><span>We analyzed the distance decay relationships, community composition and its drivers (physical distance, litter and soil chemistry, tree composition, climate) in fungi, using multivariate analyses. We compared the results across three fungal ecological guilds (ectomycorrhizal fungi, saprotrophs and yeasts), two forest microhabitats (litter and bulk soil) and six spatial scales (from 5 m to 80 km) that comprehensively cover the Czech Republic.</span></p> <p><strong><span>Results</span></strong></p> <p><span>We found that, similar to macroorganisms, the ectomycorrhizal fungi and saprotrophs showed marked distance-decay relationships</span><span>,</span><span> and their community composition was driven mainly by vegetation and dispersal at local scales, but at regional scales, by environmental effects. In contrast, the third fungal guild, the unicellular yeasts, showed little distance decay, suggesting extraordinary spatial homogeneity, as often seen in microorganisms, such as bacteria.</span></p> <p><strong><span>Main conclusions</span></strong></p> <p><span>Our results underscore the remarkable variation in the community ecology of fungi, which seems to range well-known patterns both from the macro- and the microworld. Knowledge of these patterns advances our understanding of the ecology of fungi, rather understudied organisms of significant ecological and economic importance, which our findings identify as a potentially suitable model for bridging the gaps between the biogeography of micro- and macroorganisms. </span></p>
Data from: A framework to apply trait-based ecological restoration at large scales
<p>R scripts and data to run the proposed framework at</p> <p>Coutinho, A. G., Carlucci, M. B., Cianciaruso, M. V. (2023) A framework to apply trait-based ecological restoration at large scales. Journal of Applied Ecology.</p>
Distribution System Environmental and Sequencing Datasets for Assessing the Impacts of Lead Corrosion Control on the Microbial Ecology and Abundance of Drinking Water Associated Pathogens in a Full-Scale Drinking Water Distribution System
<p>The dataset of environmental parameters and sequence fastqs used to create figures and do analysis in the paper <strong>Assessing the Impacts of Lead Corrosion Control on the Microbial Ecology and Abundance of Drinking Water Associated Pathogens in a Full-Scale Drinking Water Distribution System </strong>submitted to Environmental Science & Technology</p>
Data from: The importance of biotic interactions in distribution models of wild bees depends on the type of ecological relations, spatial scale and range
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Data from: Fractal triads efficiently sample ecological diversity and processes across spatial scales
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Ecological and evolutionary drivers of stingless bee honey variation at the global scale
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Data for: Zebra finch song ecology: monitoring of breeding, observational transects, focal and year-round acoustic recordings, and a large-scale simultaneous playback experiment
Open the record for dataset details and reuse information.
Data from: The spatial patterns of community composition, their environmental drivers and their spatial scale dependence vary markedly between fungal ecological guilds
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Data set for 'Lunge filter feeding biomechanics constrain rorqual foraging ecology across scale'...
<p>Fundamental scaling relationships influence the physiology of vital rates, which in turn shape the ecology and evolution of organisms. For diving mammals, benefits conferred by large body size include reduced transport costs and enhanced breath-holding capacity, thereby increasing overall foraging efficiency. Rorqual whales feed by engulfing a large mass of prey-laden water at high speed and filter it through baleen plates. However, as engulfment capacity increases with body length across species (Engulfment Volume ∝ Body Length <sup>3.57</sup>), the surface area of the baleen filter does not increase proportionally (Baleen Area ∝ Body Length<sup>1.82</sup>), and thus the filtration time of larger rorquals predictably increases because the baleen surface area must filter a disproportionally large amount of water. We predicted that filtration time should scale with body length to the power of 1.75 (Filter Time ∝ Body Length<sup>1.75</sup><i>)</i>. We tested this hypothesis on four rorqual species using multi-sensor tags with corresponding unoccupied aerial systems (UAS) -based body length estimates. We found that filter time scales with body length to the power of 1.79 (95% CI: 1.61 - 1.97). This result highlights a scale-dependent trade-off between engulfment capacity and baleen area that creates a biomechanical constraint to foraging through increased filtration time. Consequently, larger whales must target high density prey patches commensurate to the gulp size to meet their increased energetic demands. If these optimal patches are absent, larger rorquals may experience reduced foraging efficiency compared to smaller whales if they do not match engulfment capacity to the size of targeted prey aggregations.</p>
Large-scale patterns of green turtle trophic ecology in the eastern Pacific Ocean
<p><span><span><span><span><span><span><span><span><span><span><span>Trophic position and niche width are fundamental components of a species' ecology, reflecting resource use, and influencing key demographic parameters such as somatic growth, maturation, and survival. The present data file contains results of stable isotope analysis (stable-carbon, δ<sup>13</sup>C; stable-nitrogen, δ<sup>15</sup>N values) that was conducted on bulk skin tissue of 718 green sea turtles (<i>Chelonia mydas</i>) distributed among 16 foraging areas in the eastern Pacific from the US to Chile, a range spanning ~10,000 km. These study sites </span></span></span></span></span></span></span></span></span></span></span>were distributed across a latitudinal range from 33.736 °N to 23.098°S in the Eastern Pacific (Site Code): Long Beach, USA (LB); San Diego Bay, USA (SDB); north Gulf of Ulloa, Mexico (NGU); Magdalena Bay, Mexico (BMA); Los Angeles Bay, Mexico (BLA); Infiernillo Channel, Mexico (CIN); Navachiste Bay, Mexico (NAV); Dulce Gulf, Costa Rica (DUL); Cocos Island, Costa Rica (COC); Gorgona Island, Colombia (GOR); Punta Espinosa, Galapagos Islands, Ecuador (IGP); Bahia Elizabeth, Galapagos Islands, Ecuador (IGE); Caleta Derek, Galapagos Islands, Ecuador (IGD); oceanic waters, Peru (PPE); Pisco Paracas Bay, Peru (PAR); and Mejillones Bay, Chile (MEJ). <span><span><span><span><span><span><span><span><span><span><span>Substantial variability in bulk tissue δ<sup>13</sup>C and δ<sup>15</sup>N values was found within and among sites. These data were also used to calculate the isotope niche space (used as a proxy for ecological niche space) using the Bayesian ellipse approach, and we found that isotope niche space varied among sites, likely influenced by the diversity of prey types and relative input of terrestrial- vs. marine-derived nutrients. In addition to providing additional spatial resolution for δ<sup>13</sup>C and δ<sup>15</sup>N isoscapes in the eastern Pacific, especially in coastal habitats, this study and resultant dataset further establish stable isotope analysis as an effective tool to study the trophic ecology of sea turtles across a variety of food webs and habitats. </span></span></span></span></span></span></span></span></span></span></span></p>
Data from: Ecological differentiation facilitates fine-scale coexistence of sexual and asexual Boechera
Premise of the study: Ecological differentiation (ED) between sexual and asexual organisms may permit the maintenance of reproductive polymorphism. Several studies of sexual/asexual ED in plants have shown that the geographic ranges of asexuals extend beyond those of sexuals, often in areas of higher latitude or elevation. But very little is known about ED at fine scales, wherein coexistence of sexuals and asexuals may be permitted by differential niche occupation. Methods: We used 149 populations of sexual and apomictic lineages in the genus Boechera (rock cress) collected across a portion of this mustard's vast range. We characterized reproductive mode, ploidy, and species identity or hybrid parentage of each individual, and then used a multi-pronged statistical approach to 1) identify ED between sexuals and asexuals; 2) investigate the impacts of two confounding factors, polyploidy and hybridization, on ED; and 3) determine the environmental variables underlying ED. Key results: We found that sexuals and asexuals are significantly ecologically differentiated across the landscape, despite fine-scale interdigitation of these two reproductive forms. Asexual reproduction was strongly associated with greater disturbance, reduced slope, and greater environmental variability. Although ploidy had little effect on the patterns observed, hybridization has a unique impact on the relationships between asexual reproduction and specific environmental variables. Conclusions: Ecological differentiation along the axes of disturbance, slope, and climatic variability, as well as the effects of heterozygosity, may contribute to the maintenance of sexuality and asexuality across the landscape, ultimately impacting the establishment and spread of asexual lineages.
Data from: Form–function relationships in a marine foundation species depend on scale: a shoot to global perspective from a distributed ecological experiment
Form-function relationships in plants underlie their ecosystem roles in supporting higher trophic levels through primary production, detrital pathways, and habitat provision. For widespread, phenotypically-variable plants, productivity may differ not only across abiotic conditions, but also from distinct morphological or demographic traits. A single foundation species, eelgrass (Zostera marina), typically dominates north temperate seagrass meadows, which we studied across 14 sites spanning 32-61° N latitude and two ocean basins. Body size varied by nearly two orders of magnitude through this range, and was largest at mid-latitudes and in the Pacific Ocean. At the global scale, neither latitude, site-level environmental conditions, nor body size helped predict productivity (relative growth rate 1-2% d-1 at most sites), suggesting a remarkable capacity of Z. marina to achieve similar productivity in summer. Furthermore, among a suite of stressors applied within sites, only ambient leaf damage reduced productivity; grazer reduction and nutrient addition had no effect on eelgrass size or growth. Scale-dependence was evident in different allometric relationships within and across sites for productivity and for modules (leaf count) relative to size. Z. marina provides a range of ecosystem functions related to both body size (habitat provision, water flow) and growth rates (food, carbon dynamics). Our observed decoupling of body size and maximum production suggests that geographic variation in these ecosystem functions may be independent, with a future need to resolve how local adaptation or plasticity of body size might actually enable more consistent peak productivity across disparate environmental conditions.
Data from: Boreal tree growth exhibits decadal-scale ecological memory to drought and insect defoliation, but no negative response to their interaction
1. Interactions between drought and insect defoliation may dramatically alter forest function under novel climate and disturbance regimes, but remain poorly understood. We empirically tested two important hypotheses regarding tree responses to drought and insect defoliation: 1) trees exhibit delayed, persistent, and cumulative growth responses to these stressors; 2) physiological feedbacks in tree responses to these stressors exacerbate their impacts on tree growth. These hypotheses remain largely untested at a landscape scale, yet are critical for predicting forest function under novel future conditions given the connection between tree growth and demographic processes such as mortality and regeneration. 2. We developed a Bayesian hierarchical model to quantify the ecological memory of tree growth to past water deficits and insect defoliation events, derive antecedent variables reflecting the persistent and cumulative effects of these stressors on current growth, and test for their interactive effects. The model was applied to extensive tree growth, weather, and defoliation survey data from western and eastern regions of the Canadian boreal forest impacted by recent drought and defoliation events and characterized by contrasting tree compositions, climates, and insect defoliators. 3. Results revealed persistent negative tree growth responses to past water (all trees) and defoliation (host trees) stress lasting 3-6 and 10-12 years, respectively, depending on study region. Accounting for the ecological memory of tree growth to water and defoliation stress allowed for detection of interactions not previously demonstrated. Contrary to expectations, we found evidence for positive interactions among non-host trees likely due to reduced water stress following defoliation events. Regional differences in ecological memory to water stress highlight the role of climate in shaping forest responses to drought. 4. Synthesis. Study results suggest negative feedbacks in tree responses to drought and insect attack may be weaker than predicted for defoliator-dominated boreal forest systems. Instead, insect defoliation may offset the impacts of water deficit on boreal tree growth by reducing transpirational water demand. This offset mimics increased resistance to drought following forest thinning and may lessen growth and mortality losses due to increased aridity and more severe insect damage forecast for the boreal forest under global change.
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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
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.