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56 results for “Long term data monitoring”
Data from: Long-term monitoring of <em>Ziphius cavirostris</em> behavior using 3D tracking from fixed hydrophone arrays off Southern California
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Data for: Large-scale long-term passive-acoustic monitoring reveals spatiotemporal activity patterns of boreal bats
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Data from: evaluating the use of lake sedimentary DNA in palaeolimnology: a comparison with long-term microscopy-based monitoring of the phytoplankton community
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Small mammals surveys, 1981 - 1996, Adirondack Long-Term Ecological Monitoring Program Project No. 10 by Adirondack Ecological Center of the State University of New York College of Environmental Science and Forestry, Newcomb, New York. Environmental Data Initiative
Small mammals are important in forested ecosystems: they are key predators on seeds and invertebrates, provide food for larger predators and act as disease vectors. The objective of this study was to document small mammal abundance and population changes in managed and unmanaged forests of Huntington Wildlife Forest (HWF). Seven sites were sampled from 1981-1996. Fifty traps per site (250 total) were deployed for 4 nights and checked in the mornings. All captured small mammals were identified, sexed, weighed, and measured for reproductive condition, tagged, and brought into the lab for processing. Females with embryos or placental scars were noted in the lab. Over a five-year period, 671 deer mice; 261 woodland jumping mice, 594 southern redbacked voles, 248 short-tailed shrews, 373 masked shrews, 75 smoky shrews and small numbers of other species were captured and sexed/aged. According to Prachar and Sage (1988), weights of deer mice, redbacked voles, woodland jumping mice, short-tailed shrews, masked shrews and smoky shrews differed among years and age classes for 1983-1987. Weights differed between sexes for mice and voles but not shrews. Placental scar/embryo counts of mice and voles did not differ among years, habitats, mammal age classes or sexes. Reproductive rates of shrews exhibited patterns of fluctuation from 1983-1987.
Songbird surveys , 1952 - 1964, 1983 - 2008 Adirondack Long-Term Ecological Monitoring Program Project No. 2 Breeding Birds by Adirondack Ecological Center of the State University of New York College of Environmental Science and Forestry, Newcomb, New York. Environmental Data Initiative.
Study objectives were to (1) Document long-term trends in relative abundance and diversity of breeding forest birds (songbirds) in forest stands with different harvest histories and (2) Identify bird species that can be used as indicators of habitat change or degradation. Declines in neotropical migrants have been linked to changes in habitat quantity and quality across species' range. Songbirds that nest and forage in different habitat types or at different heights in the forest canopy may not be affected equally by forest change or management. We detected breeding songbirds using point-counts at Huntington Wildlife Forest (HWF) in the central Adirondack Mountains of New York during 1983-2000 and modeled on an original songbird point count dataset from Webb et al. (1977). Relative abundance (RA, the number of individual birds/count) was measured in sites with differing management histories, from an unmanaged >300-year-old stand to a stand cut with the shelterwood/overstory removal method just prior to sampling in 1983). Over eighty bird species were detected during the study duration. Songbird ecology and habitat characteristics can be used to understand long-term changes in relative abundance as related to forest change.
Data from: Long-term monitoring of seed dispersal by Asian elephants in a Sundaland rainforest
<p><span><span><span><span><span><span><span><span><span><span><span>Asian elephants (<i>Elephas maximus</i>) have inhabited almost all forests in tropical Asia until recently, yet little is known about their role in ecological processes, particularly in the Sundaic forests of Southeast Asia. These forests are peculiar in their phenology, with supra-annual and highly irregular episodes of mast fruiting. Here we present a long-term (six-year) monitoring of the seeds dispersed by elephants in dipterocarp forests of northern Peninsular Malaysia. We conducted monthly dung surveys at two mineral licks (11.3 km apart) frequently visited by elephants. Additionally, we recorded haphazard observations of seeds and seedlings in elephant dung at other locations. We recorded a minimum of 48 morphospecies from at least 25 plant families dispersed by elephants. Elephant seed dispersal was very heterogenous in space, with only 30.3 % of the morphospecies dispersed at both sites (Jaccard dissimilarity index = 0.48). Temporally, elephants dispersed seeds in sporadic pulses of abundance and diversity, without any apparent seasonality (seeds appeared in 19.1 % of 1,284 dung piles and 57.1 % of the 63 months in which we found dung) and with long periods without any seed being dispersed. Nearly half (48 %) of the plants dispersed by elephants belong to a megafaunal dispersal syndrome. Our long-term approach allowed us to unravel an important aspect of Asian elephants' role and effectiveness in the seed dispersal cycle. Sundaland's forests are undergoing a rapid loss of their previously common megaherbivores (rhinos and elephants), with profound and long-term consequences for ecosystem functioning.</span></span></span></span></span></span></span></span></span></span></span></p>
Improving citizen science data for long-term monitoring of plant species
<p>In 2012, a new volunteer-based recording scheme for vascular plants was launched in the Netherlands. Its purpose is to track the changes in the number of occupied 1-km grid cells for as many native plant species as possible between survey rounds of 8 years. We did not prescribe a strict field protocol to minimize variation in observer effort, but instead chose to statistically correct for this variation with occupancy models. These models require replicated visits to a grid cell per season, which was implemented by having two independent observers survey grid cells and record all plant species observed. Now that a first survey round has ended (2012–2019), we evaluate our approach, i.e. we tested whether the scheme has the potential to produce proper trend estimates. The number of occupied grid cells in the first round was estimated per species, using an occupancy model with day of year, visit duration and observer experience as covariates for detection. The detection probability, which was 0.43 on average, strongly depended on visit duration and day of year. It was possible to estimate the number of occupied grid cells quite precisely for several hundreds of species, such that the statistical power is expected to be high enough to detect changes of 10% between survey rounds. For rare species, however, the power to detect changes is expected to be quite low. We conclude that the approach works well, but further improvements are suggested.</p>
Data from: The role of exotic ladybeetles in the decline of native ladybeetle populations: evidence from long-term monitoring
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Data from: Long-term monitoring of seed dispersal by Asian elephants in a Sundaland rainforest
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Data and code for: Leveraging long-term data to improve biodiversity monitoring with species distribution models
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Data for: Understanding post-fire vegetation recovery in Southern California ecosystems with the aid of pre-fire observations from long term monitoring
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Monitoring long-term vegetation dynamics over the Yangtze River Basin, China, using multi-temporal remote sensing data
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Improving citizen science data for long-term monitoring of plant species
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Ruffed grouse (Bonasa umbellus) drumming surveys, 1987-2017, Adirondack Long-Term Ecological Monitoring Program Project No. 9 by Adirondack Ecological Center of the State University of New York College of Environmental Science and Forestry, Newcomb, New York. Environmental Data Initiative
The objective is to document long-term population trends of ruffed grouse in a northern hardwood ecosystem. The survey area is the Huntington Wildlife Forest, a 6,000 ha field station which receives no hunting pressure. Routes are surveyed starting an hour prior to sunrise on 2-5 mornings each year between April 14 and May 9 (occasionally later), on days when wind and rain are minimal to absent. Counts are standardized relative to weather conditions and timing. Observers count the number of individual ruffed grouse heard drumming (""drummers"") at 32-50 route stations during a 4-minute period. Trends at stations over time as well as overall drummer index are calculated and compared to independent datasets.
Data from: Long-term monitoring data provide evidence of declining species richness in a river valued for biodiversity conservation
Free-flowing river segments provide refuges for many imperiled aquatic biota that have been extirpated elsewhere in their native ranges. These biodiversity refuges are also foci of conservation concerns because species persisting within isolated habitat fragments may be particularly vulnerable to local environmental change. We have analyzed long-term (14- and 20-year) survey data to assess evidence of fish species declines in two southeastern U.S. rivers where managers and stakeholders have identified potentially detrimental impacts of current and future land uses. The Conasauga River (Georgia and Tennessee) and the Etowah River (Georgia) form free-flowing headwaters of the extensively dammed Coosa River system. These rivers are valued in part because they harbor multiple species of conservation concern, including three federally endangered and two federally threatened fishes. We have used data sets comprising annual surveys for fish species at multiple, fixed sites located at river shoals to analyze occupancy dynamics and temporal changes in species richness. Our analyses incorporate repeated site-specific surveys in some years to estimate and account for incomplete species detection, and test for species-specific (rarity, mainstem-restriction) and year-specific (elevated frequencies of low- or high-flow days) covariates on occupancy dynamics. In the Conasauga River, analysis of 26 species at 13 sites shows evidence of temporal declines in colonization rates for nearly all taxa, accompanied by declining species richness. Four taxa (including one federally endangered species) have reduced occupancy across the Conasauga study sites, with three of these taxa apparently absent for at least the last 5 years of the study. In contrast, a similar fauna of 28 taxa at 10 sites in the Etowah River shows no trends in species persistence, colonization or occupancy. None of the tested covariates show strong effects on persistence or colonization rates in either river. Previous studies and observations identify contaminants, nutrient loading, or changes in benthic habitat as possible causes for fish species declines in the Conasauga River. Our analysis provides baseline information that could be used to assess effectiveness of future management actions in the Conasauga or Etowah rivers, and illustrates the use of dynamic occupancy models to evaluate evidence of faunal decline from time-series data.
Data from: Long-term environmental monitoring for assessment of change: measurement inconsistencies over time and potential solutions
The importance of long-term environmental monitoring and research for detecting and understanding changes in ecosystems and human impacts on natural systems is widely acknowledged. Over the last decades a number of critical components for successful long-term monitoring have been identified. One basic component is quality assurance/quality control protocols to ensure consistency and comparability of data. In Norway, the authorities require environmental monitoring of the impacts of the offshore petroleum industry on the Norwegian continental shelf, and in 1996 a large-scale regional environmental monitoring program was established. As a case study, we used a sub-set of data from this monitoring to explore concepts regarding best practices for long-term environmental monitoring. Specifically, we examined data from physical and chemical sediment samples and benthic macro-invertebrate assemblages from 11 stations from six sampling occasions during the period 1996-2011. Despite the established quality assessment and quality control protocols for this monitoring program, we identified several data challenges, such as, missing values and outliers, discrepancies in variable and station names, changes in procedures without calibration, and different taxonomic resolution. Furthermore, we show that the use of different laboratories over time makes it difficult to draw conclusions with regard to some of the observed changes. We offer recommendations to facilitate comparison of data over time. We also present a new procedure to handle different taxonomic resolution so valuable historical data is not discarded. These topics have a broader relevance and application than for our case study.
Data from: Challenges of NGS in conservation management: insights from long-term monitoring of corridor effects on the genetic diversity of mouse lemurs in a fragmented landscape
Long-term genetic monitoring of populations is essential for efforts aimed at preserving genetic diversity of endangered species. Here, we employ a framework of long-term genetic monitoring to evaluate the effects of fragmentation and the effectiveness of the establishment of corridors in restoring population connectivity and genetic diversity of mouse lemurs Micocebus ganzhorni. To this end, we supplement estimates of neutral genetic diversity with the assessment of adaptive genetic variability of the MHC. In addition, we address the challenges of long-term genetic monitoring of functional diversity by comparing the genotyping performance and estimates of MHC variability generated by SSCP/Sanger-sequencing with those obtained by high throughput sequencing (NGS, Illumina), an issue that is particularly relevant when previous work serves as a baseline for planning management strategies that aim to ensure the viability of a population. We report that SSCP greatly underestimates individual diversity and that discrepancies in estimates of MHC diversity attributable to the comparisons of traditional and NGS genotyping techniques can influence the conclusions drawn from conservation management scenarios. Evidence of migration among fragments in Mandena suggests that mouse lemurs are robust to the process of fragmentation and that the effect of corridors is masked by ongoing gene flow. Nonetheless, results based on a larger number of shared private alleles at neutral loci between fragment pairs found after the establishment of corridors in Mandena suggest that gene flow is augmented as a result of enhanced connectivity. Our data points out that despite low effective population size, M. ganzhorni maintains high individual heterozygosity at neutral loci and at MHC II DRB gene and that selection plays a predominant role in maintaining MHC diversity. These findings highlight the importance of long-term genetic monitoring in order to disentangle between the processes of drift and selection maintaining adaptive genetic diversity in small populations.
Data from: Long-term genetic monitoring reveals contrasting changes in the genetic composition of newly established populations of the intertidal snail Bembicium vittatum
Newly established populations are susceptible to founder events that reduce genetic variation. This may be counterbalanced by gene flow after populations become established or founders coming from genetically different populations. However, initial gains in genetic diversity may be short-lived if there is limited mixing between lineages and subsequent inbreeding or if one lineage sweeps to fixation through selection or genetic drift. Here, we report on the genetic changes taking place within two newly established populations of intertidal snail over a 15-year period (~ 10 generations). Each translocation was set up using multiple, genetically distinct source populations. Our data show that higher levels of variation in the translocated populations compared to the source populations were maintained over time for both nuclear (microsatellite) and mitochondrial genes. Small changes in allele and haplotype frequencies were observed in the source populations and in one of the translocated populations, but marked changes were evident in the other, where there was a dramatic shift towards the genetic make-up of one of the source populations. These genetic changes occurred despite relatively large numbers of founders (200- 374 adults) and no evidence of the population experiencing a severe reduction in effective population size. Our study shows that the genetic composition of newly established populations can vary greatly over time and that genetic outcomes can be highly variable, and significantly different to expectations, even when they are established using high numbers of individuals and involve source populations from the same geographic regions.
Data from: Long-term effective population size dynamics of an intensively monitored vertebrate population
Long-term genetic data from intensively monitored natural populations are important for understanding how effective population sizes (Ne) can vary over time. We therefore genotyped 1622 common buzzard (Buteo buteo) chicks sampled over 12 consecutive years (2002–2013 inclusive) at 15 microsatellite loci. This data set allowed us to both compare single-sample with temporal approaches and explore temporal patterns in the effective number of parents that produced each cohort in relation to the observed population dynamics. We found reasonable consistency between linkage disequilibrium-based single-sample and temporal estimators, particularly during the latter half of the study, but no clear relationship between annual Ne estimates (hdy201667e1gif(239)1917) and census sizes. We also documented a 14-fold increase in hdy201667e2gif(239)1917 between 2008 and 2011, a period during which the census size doubled, probably reflecting a combination of higher adult survival and immigration from further afield. Our study thus reveals appreciable temporal heterogeneity in the effective population size of a natural vertebrate population, confirms the need for long-term studies and cautions against drawing conclusions from a single sample.
Long-term snow chemical composition monitoring - Ariebreen glacier (Hornsund) - raw data
<p>Since 2020, snow samples have been taken from the Ariebreen glacier several times a season during the accumulation season. The snow samples are collected in polyethylene sterile bags and transported to the Polish Polar Station Hornsund. After melting at room temperature, they are analysed in the chemical laboratory of the Polish Polar Station for pH, conductivity and chemical composition (major ions).<br> <br> Site Information Ariebreen - 0.5 km long glacier between Skoddefjellet and the northern part of Ariekammen, southernmost in Wedel Jarlsberg Land.</p> <p>Presented data from 2020 to 2022</p> <p>The data has not been checked, which means that it is raw data.</p> <p>Principal investigator (PI) Adam Nawrot</p>
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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.