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4,669 results for “Environment;”
Province of Cremona - Environment and Territory Department - Online digital library database
<p>The province of Cremona lies in Northern Italy, along the left bank of the River Po floodplain. This is the database of the online digital library of the Province Administration Environment and Territory Department. At present the library comprises 610 contributions concerning the environment, ecology, geography, history and landscape of the province, of the Po basin at large and of other areas as well. Most contributions have a short or extended abstract in English. Each publication in the library is freely downloadable as a PDF file from the library website http://bibliotecadigitale.provincia.cremona.it.</p> <p>The database fields are as follows: Publication code, Publication series, Publication title in Italian, Publication title in English, Publication type (magazine or monograph), ISSN number (if assigned), Issue number, Issue year, Contribution type (article, report or short note, monograph etc.), Title in Italian<em>,</em> Title in English, Topic, Subtopic 1, Subtopic 2, Pages, Author 1, Author 2, …, Author 16, Link to the file of each publication issue on the digital library website, Notes.</p> <p>Further information on the digital library and the database can be found in the open access article (in English) in V. 2 N. 1 (2022) of BORNH (Bullettin of Regional Natural History of the Società dei Naturalisti in Napoli): <a href="https://serena.sharepress.it/index.php/bornh/issue/view/653">https://serena.sharepress.it/index.php/bornh/issue/view/653</a></p> <p>Please note that upon opening the file with LibreOffice (and perhaps other softwares) it might be necessary to select Windows 1252 as the character type and the comma as the separator.</p>
Validation of MUISCA for Blockchain Interoperability: A Case Study in a Healthcare Environment
<p>This repository contains the questions asked to the 31 experts who participated in the study “Validation of MUISCA for Blockchain Interoperability: A Case Study in a Healthcare Environment”. It also contains the spreadsheet with the recorded answers.</p>
Outdoor NB-IoT and 5G coverage and channel information data in urban environments
<p>This dataset includes data for NB-IoT and 5G networks as collected in two cities: Oslo, Norway (NB-IoT only) and Rome, Italy (both NB-IoT and 5G).</p> <p>Data were collected using the Rohde & Schwarz TSMA6 mobile network scanner. 7 measurement campaigns are provided for Oslo, and 6 for Rome. Additional data collected in Rome are provided in the following large-scale dataset, focusing on the two major mobile network operators: <a href="https://ieee-dataport.org/documents/large-scale-dataset-4g-nb-iot-and-5g-non-standalone-network-measurements">https://ieee-dataport.org/documents/large-scale-dataset-4g-nb-iot-and-5g-non-standalone-network-measurements</a> </p> <p>The dataset includes a metadata file providing the following information for each campaign: </p> <ul> <li>date of collection;</li> <li>start time and end time of collection;</li> <li>length;</li> <li>type (walking/driving).</li> </ul> <p>Two additional metadata files are provided: two .kml files, one for each city, allowing the import of coordinates of data points organized by campaign in a GIS engine, such as Google Earth, for interactive visualization.</p> <p>The dataset contains the following data for NB-IoT:</p> <ul> <li>Raw data for each campaign, stored in two .csv files. For a generic campaign <X>, the files are: <ul> <li>NB-IoT_coverage_C<X>.csv including a geo-tagged data entry in each row. Each entry provides information on a Narrowband Physical Cell Identifier (NPCI), with data related to the time stamp the NPCI was detected, GPS information, network (NPCI, Operator, Country Code, eNodeB-ID) and RF signal (RSSI, SINR, RSRP and RSRQ values);</li> <li> NB-IoT_RefSig_cir_C<X>.csv, also including a geo-tagged data entry in each row. Each entry provides information on a NPCI, with data related to the time stamp the NPCI was detected, GPS information, network (NPCI, Operator ID, Country Code, eNodeB-ID) and Channel Impulse Response (CIR) statistics, including the maximum delay.</li> </ul> </li> <li>Processed data, stored in a Matlab workspace (.mat) file for each city: data are grouped in data points, identified by <Latitude, longitude> pairs. Each data point provides RF and CIR maximum delay measurements for each <NPCI, Operator ID, eNodeB-ID> unique combination detected at the coordinates of the data point.</li> <li>Estimated positions of eNodeBs, stored in a csv file for each city;</li> <li>A matlab script and a function to extract and generate processed data from the raw data for each city.</li> </ul> <p>The dataset contains the following data for 5G:</p> <ul> <li>Raw data for each campaign, stored in two .xslx files. For a generic campaign <X>, the files are: <ul> <li>5G_coverage_C<X>.xslx including a geo-tagged data entry in each row. Each entry provides information on a Physical Cell Identifier (PCI), with data related to the time stamp the PCI was detected, GPS information, network (PCI, Beamforming Index, Operator, Country Code) and RF data (SSB-RSSI, SSS-SINR, SSS-RSRP and SSS-RSRQ values, and similar information for the PBCH signal);</li> <li> 5G_RefSig_cir_C<X>.csv, also including a geo-tagged data entry in each row. Each entry provides information on a PCI, with data related to the time stamp the PCI was detected, GPS information, network (PCI, Beamforming Index, Operator ID, Country Code) and Channel Impulse Response (CIR) statistics, including the maximum delay.</li> </ul> </li> <li>Processed data, stored in a Matlab workspace (.mat) file: data are grouped in data points, identified by <Latitude, longitude> pairs. Each data point provides RF and CIR maximum delay measurements for each <PCI, Beamforming Index, Operator ID> unique combination detected at the coordinates of the data point.</li> <li>A matlab script and a supporting function to extract and generate processed data from the raw data.</li> </ul> <p>In addition, in the case of the Rome data additional matlab workspaces are provided, containing interpolated data in the feature dimensions according to two different approaches:</p> <ul> <li>A campaign-by-campaign linear interpolation (both NB-IoT and 5G);</li> <li>A bidimensional interpolation on all campaigns combined (NB-IoT only).</li> </ul> <p>A function to interpolate missing data in the original data according to the first approach is also provided for each technology. The interpolation rationale and procedure for the first approach is detailed in:</p> <p>L. De Nardis, G. Caso, Ö. Alay, U. Ali, M. Neri, A. Brunstrom and M.-G. Di Benedetto, "Positioning by Multicell Fingerprinting in Urban NB-IoT networks," Sensors, Volume 23, Issue 9, Article ID 4266, April 2023. <span>DOI: </span><a href="https://doi.org/10.3390/s23094266" target="_blank" rel="noopener"><span>10.3390/s23094266</span></a>.</p> <p>The second interpolation approach is instead introduced and described in:</p> <p>L. De Nardis, M. Savelli, G. Caso, F. Ferretti, L. Tonelli, N. Bouzar, A. Brunstrom, O. Alay, M. Neri, F. Elbahhar and M.-G. Di Benedetto, " Range-free Positioning in NB-IoT Networks by Machine Learning: beyond WkNN", under major revision in IEEE Journal of Indoor and Seamless Positioning and Navigation.</p> <p>Positioning using the 5G data was furthermore in investigated in: </p> <p>K. Kousias, M. Rajiullah, G. Caso, U. Ali, Ö. Alay, A. Brunstrom, L. De Nardis, M. Neri, and M.-G. Di Benedetto, "A Large-Scale Dataset of 4G, NB-IoT, and 5G Non-Standalone Network Measurements," <span>IEEE Communications Magazine, Volume 62, Issue 5, pp</span><span>. 44-49, May</span><span> 202</span><span>4</span><span>. DOI: </span><a href="https://doi.org/10.1109/MCOM.011.2200707" target="_blank" rel="noopener"><span>10.1109/MCOM.011.2200707</span></a><span>.</span></p> <p><span>G. Caso, M. Rajiullah, K. Kousias, U. Ali, N. Bouzar, L. De Nardis, A. Brunstrom, Ö. Alay, M. Neri and M.-G. Di Benedetto,"The Chronicles of 5G Non-Standalone: An Empirical Analysis of Performance and Service Evolution", IEEE Open Journal of the Communications Society, Volume 5, pp. 7380 - 7399, 2024. DOI: <a href="https://doi.org/10.1109/OJCOMS.2024.3499370" target="_blank" rel="noopener"><span>10.1109/OJCOMS.2024.3499370</span></a>.</span></p> <p>Please refer to the above publications when using and citing the dataset. </p>
Paper dataset of "ARAMIS: a Martian radiative environment model built from GEANT4 simulations"
<p>Supplementary materila dataset concerning the article : <a href="https://doi.org/10.1051/swsc/2024032">https://doi.org/10.1051/swsc/2024032 .</a></p> <p>In the version v1, the proton flux where not giving for both cone and total view which is corrected here. Beside there was a wrong upload file for proton_aramis_2015_2016.dat, which has been corrected as well.</p>
Dataset: Ambient BTEX concentrations during the COVID-19 lockdown in a peri-urban environment (Orléans, France)
<p>The dataset of the manuscript "Ambient BTEX concentrations during the COVID-19 lockdown in a peri-urban environment (Orléans, France)" are presented here</p>
Pelt biting as a practical indicator of social and environment stress in farmed red deer
<p>Data sets used in the analyses of paper title "Pelt biting as a practical indicator of social and environment stress in farmed red deer"</p>
Genetic divergence and local adaptation of Liriodendron driven by heterogeneous environments
<p><span>Ecological adaptive differentiation alters both the species diversity and intraspecific genetic diversity in forests, thus affecting the stability of forest ecosystems. Therefore, knowledge of the genetic underpinnings of the ecological adaptive differentiation of forest species is critical for effective species conservation. In this study, single-nucleotide polymorphisms (SNPs) from population transcriptomes were used to investigate the spatial distribution of genetic variation in <i>Liriodendron</i> to assess whether environmental variables can explain genetic divergence. We examined the contributions of environmental variables to population divergence and explored the genetic underpinnings of local adaptation using a landscape genomic approach. Niche models and statistical analyses showed significant niche divergence between <i>L. chinense</i> and <i>L. tulipifera</i>, suggesting that ecological adaptation may play a crucial role in driving interspecific divergence. We detected a new fine-scale genetic structure in <i>L. chinense</i>, and divergence of the six groups occurred during the late Pliocene to early Pleistocene. Redundancy analysis (RDA) revealed significant associations between genetic variation and multiple environmental variables. Environmental association analyses identified 67 environmental association loci (EALs; nonsynonymous SNPs) that underwent interspecific or intraspecific differentiation, 28 of which were associated with adaptive genes. These 28 candidate adaptive loci provide substantial evidence for local adaptation in <i>Liriodendron</i>. Our findings reveal ecological adaptive divergence pattern between <i>Liriodendron</i> species and provide novel insight into the role of heterogeneous environments in shaping genetic structure and driving local adaptation among populations, informing future <i>L. chinense</i> conservation efforts. </span></p>
Local thermal environment and warming influence supercooling and drive widespread shifts in the metabolome of diapausing Pieris rapae butterflies
<p>Global climate change has the potential to negatively impact biological systems as organisms are exposed to novel temperature regimes. Increases in annual mean temperature have been accompanied by disproportionate rates of change in temperature across seasons, and winter is the season warming most rapidly. Yet, we know relatively little about how warming will alter the physiology of overwintering organisms. Here, we simulated future warming conditions by comparing diapausing <i>Pieris rapae</i> butterfly pupae collected from disparate thermal environments and by exposing <i>P. rapae </i>pupae to acute and chronic increases in temperature. First, we compared internal freezing temperatures (supercooling points) of diapausing pupae that were developed in common-garden conditions but whose parents were collected from northern Vermont, USA, or North Carolina, USA. Matching the warmer winter climate of North Carolina, North Carolina pupae had significantly higher supercooling points than Vermont pupae. Next, we measured the effects of acute and chronic warming exposure in Vermont pupae and found that warming induced higher supercooling points. We further characterized the effects of chronic warming by profiling the metabolomes of Vermont pupae via untargeted LC-MS metabolomics. Warming caused significant changes in abundance of hundreds of metabolites across the metabolome. Notably, there were warming-induced shifts in key biochemical pathways, such as pyruvate metabolism, fructose and mannose metabolism, and β-alanine metabolism, suggesting shifts in energy metabolism and cryoprotection. These results suggest that warming affects various aspects of overwintering physiology in <i>P. rapae</i> and may be detrimental depending on the frequency and variation of winter warming events. Further research is needed to ascertain the extent to which the effects of warming are felt among a broader set of populations of <i>P. rapae</i>,<i> </i>and among other species, in order to better predict how insects may respond to changes in winter thermal environments.</p>
Living room environment
<p>An audio-visual model for virtual reality of the living room laboratory at the CvO university Oldenburg. The model has been created for a highly accurate acoustic rendering over loudspeaker arrays and headphones and for visual representation in virtual reality. The package encompasses an accurate spatial geometric model of the living room and adjacent kitchen, which can be used for acoustic simulations, and a visual model for virtual reality. It further includes a definition of two acoustic scenes for the purpose of audiology and hearing research together with the associated measurements of the acoustic impulse responses using a binaural recording system (binaural room impulse responses), a spherical microphone array, and omnidirectional microphones.</p>
Methylation and gene expression data from: Differential DNA methylation across environments has no effect on gene expression in the eastern oyster
<p>1. It has been hypothesized that environmentally induced changes to gene body methylation could facilitate adaptive transgenerational responses to changing environments.</p> <p>2. We compared patterns of global gene expression (Tag-seq) and gene body methylation (reduced representation bisulfite sequencing) in 80 eastern oysters (<i>Crassostrea virginica</i>) from six full-sib families, common gardened for 14 months at two sites in the northern Gulf of Mexico that differed in mean salinity.</p> <p>3. At the time of sampling, oysters from the two sites differed in mass by 60% and in parasite loads by nearly two orders of magnitude. They also differentially expressed 35% of measured transcripts. However, we observed differential methylation at only 1.4% of potentially methylated loci in comparisons between individuals from these different environments, and little correspondence between differential methylation and differential gene expression.</p> <p>4. Instead, methylation patterns were largely driven by genetic differences among families, with a PERMANOVA analysis indicating nearly a two orders of magnitude greater number of genes differentially methylated between families than between environments.</p> <p>5. An analysis of CpG observed/expected values (CpG O/E ) across the <i>C. virginica</i> genome showed a distinct bimodal distribution, with genes from the first cluster showing the lower CpG O/E values, greater methylation, and higher, and more stable gene expression, while genes from the second cluster showed lower methylation, and lower and more variable gene expression.</p> <p>6. Taken together, the differential methylation results suggest that only a small portion of the <i>C. virginica</i> genome is affected by environmentally induced changes in methylation. At this point, there is little evidence to suggest that environmentally induced methylation states would play a leading role in regulating gene expression responses to new environments.</p>
Host traits and environment interact to drive persistence of bat populations impacted by white-nose syndrome
<p>Emerging infectious diseases have resulted in severe population declines across diverse taxa. In some instances, despite attributes associated with high extinction risk, disease emergence and host declines are followed by host stabilization for unknown reasons. While host, pathogen, and the environment are recognized as important factors that interact to determine host-pathogen coexistence, they are often considered independently. Here, we use a translocation experiment to disentangle the role of host traits and environmental conditions in driving the persistence of remnant bat populations a decade after they declined 70-99% due to white-nose syndrome and subsequently stabilized. While survival was significantly higher than during the initial epidemic within all sites, protection from severe disease only existed within a narrow environmental space, suggesting host traits conducive to surviving disease are highly environmentally dependent. Ultimately, population persistence following pathogen invasion is the product of host-pathogen interactions that vary across a patchwork of environments.</p>
PACs concentrations in traffic-related environments
<p>The data are the PACs concentrations during the sampling periods in three traffic-related receptor environments.</p>
Leaf economics in a three‐dimensional environment: Testing leaf trait responses in vascular epiphytes to land use, climate, and tree zone
<p>1. The study of functional traits offers predictive power for community ecology. Particularly in cases where individual species are difficult to study, known properties of trait spectra, such as the leaf economics spectrum (LES), and trait-environment relationships can provide crucial generalizable information that can contribute to forecasts of distributional shifts in response to the abiotic effects of climate and land use changes.</p> <p>2. Vascular epiphytes have been proposed as indicators of environmental change, but we know little about the ecology of most species. Key functional trait assumptions are based on terrestrial plants; testing these in epiphytes verifies their universality and will inform applying functional traits in predicting epiphyte responses to climate and land use change.</p> <p>3. In this study, we use functional traits from 37 vascular epiphyte species from forests and shade coffee farms at two sites in northern Nicaragua. We compare correlations among traits and intraspecific trait variances with those of terrestrial plants and among epiphyte taxonomic groups. We also test trait responses to environmental differences between sites and land use types, and within zones of the tree.</p> <p>4. We find that epiphyte leaf traits fall toward the slower end of the LES, but with about one-third lower leaf nitrogen per change in specific leaf area (SLA) relative to terrestrial herbaceous plants. Bromeliads show less relationship between these traits than other epiphyte groups and also deviate in other trait interrelationships, suggesting unique leaf construction.</p> <p>5. Trait-environment relationships varied most strongly along vertical gradients within trees, but some traits, including SLA and carbon isotope ratio, also responded to land use and site differences.</p> <p>6. We present evidence that trait relationships established for terrestrial plants appear to translate to epiphytes, but identify some possible caveats. Strong trait response to vertical gradients within trees suggests that within-canopy shifts could provide resilience to climate and land use changes for some epiphyte species.</p>
Data from: Rapid radiation in a highly diverse marine environment
<p>Rapid diversification is often observed when founding species invade isolated or newly formed habitats that provide ecological opportunity for adaptive radiation. However, most of the Earth's diversity arose in diverse environments where ecological opportunities appear to be more constrained. Here, we present a striking example of a rapid radiation in a highly diverse marine habitat. The hamlets, a group of reef fishes from the wider Caribbean, have radiated into a stunning diversity of color patterns but show low divergence across other ecological axes. Although the hamlet lineage is approximately 26 million years old, the radiation appears to have occurred within the last 10,000 generations in a burst of diversification that ranks among the fastest in fishes. As such, the hamlets provide a compelling backdrop to uncover the genomic elements associated with phenotypic diversification and an excellent opportunity to build a broader comparative framework for understanding the drivers of adaptive radiation. The analysis of 170 genomes suggests that color pattern diversity is generated by different combinations of alleles at a few large-effect loci. Such a modular genomic architecture of diversification has been documented before in <em>Heliconius</em> butterflies, capuchino finches and munia finches, three other tropical radiations that took place in highly diverse and complex environments. The hamlet radiation also occurred in a context of high effective population size, which is typical of marine populations. This allows for the accumulation of new variants through mutation and the retention of ancestral genetic variation, both of which appear to be important in this radiation.</p>
Supporting code, tables and data for: Megafrugivores as fading shadows of the past: Extant frugivores and the abiotic environment as the most important determinants of the distribution of palms in Madagascar
<p>The extinction of all Madagascar's megafrugivores ca. 1000 years ago, may have left its signature on the current distribution of vertebrate-dispersed plants across the island, due to the loss of effective seed dispersal. In this study, we dissect the roles of extinct and extant frugivore distributions, abiotic variables, human impact and spatial predictors on the compositional turnover, or beta-diversity, of palm (Arecaceae) species and their fruit sizes across 40 assemblages on Madagascar. Variation partitioning showed that palm beta-diversity is mostly shaped by the distribution of extant frugivores (8 lemur, 3 bird, 2 rodent and 1 bat species) and the abiotic environment (e.g., forest cover, slope and temperature), and to a lesser extent by the distribution of extinct frugivores (5 giant lemur and 3 elephant bird<i> </i>species)<i>. </i>However, the contribution of these variables differed between dry western assemblages and wet eastern assemblages, with a more prominent role, albeit still small, of extinct megafrugivores in the west. These results suggest that palm distributions in the dry west of Madagascar, where megafrugivores were probably most abundant in the past, still show signatures of past interactions. With a fourth-corner analysis we observed that the distribution of palm species with relatively large fruits and seeds was negatively associated with home range of extant mammalian frugivores and frugivore richness of both past and extant communities, and positively associated with the hand-wing index (HWI) – a proxy for dispersal ability - of extant bird communities. This suggests that palm species with relatively large fruits tend to occur in places with fewer, small-ranged mammalian frugivores, which may indicate dysfunctional seed dispersal, although a few wide-ranging bird species may compensate this loss by dispersing the seeds of small-to medium-sized palm fruits. Our results shed new light on anachronisms in Madagascar, and how defaunation and past interactions may underlie current plant distributions.</p>
Data file for consumer moral identity effects on engagement in sustainable consumption in personal life and workplace environments project
<p>The survey data was collected in year 2018 to identify effects of moral identity on consumer engagement in sustainable consumption. Two environments were considered when collecting data for the project - work and home environments. The data contains survey responses to a number of questions which measure consumer engagement in sustainable consumption at home, consumer engagement in sustainable consumption at work, two dimensions of moral identity and offers demographic data about the respondents. </p>
Data for Klaes et al. High-resolution stalagmite stratigraphy supports the Late Holocene tephrochronology of southernmost Patagonia. Comms. Earth Environ. (2022)..
<p>This data set comprises the LA-ICP-MS, ICP-MS, EPMA and NanoSIMS measurements as well as SEM imagery presented in the research paper 'High-resolution stalagmite stratigraphy supports the Late Holocene tephrochronology of southernmost Patagonia' by Klaes et al. The Th-U data of the revised chronology of stalagmite MA1 with the calculated correction values according to Budsky et al. (2016) are also included. In addition, stable isotope data from Schimpf et al. (2011) with the revised version of the age-depth model are given. For detailed information on the analyses (e.g., instruments used), the user is kindly referred to the methods section of the article. </p>
Understanding parapatry: How do environment and competitive interactions shape Iberian vipers' distributions?
<p><b>Aim</b>: To assess if the parapatry of the three viper species present in the Iberian Peninsula is mainly caused by environmental conditions, historical events, interspecific competition among them, or a combination of these factors.</p> <p><b>Location</b>: The Iberian Peninsula</p> <p><b>Taxon</b>: <i>Vipera aspis</i>, <i>V. latastei,</i> and <i>V. seoanei</i>.</p> <p><b>Methods</b>: We applied the concept of favourability of occurrence to produce commensurate distribution units unaffected by the prevalence of different species in the Iberian Peninsula. We compared the favourability of each species individually with the favourability of occurrence of more than one species co-occurring in their overlapping ranges, and identified the areas in which sympatric coexistence, environmental segregation, and competitive exclusion are predicted to occur.</p> <p><b>Results</b>:<i> </i>The main driver of the parapatric pattern was competitive exclusion, which was mediated by gradual changes in the environmental conditions favouring each species.<i> </i>The para-Mediterranean<i> V. aspis </i>presented fragmented favourable areas outside its range that seemed to be unoccupied due to competitive exclusion by the other vipers. The Mediterranean <i>V. latastei</i> appeared to be limited by competition with the other viper species and by the environment in northwestern Iberia. <i>V. seoanei</i> prevented the other two species becoming established in the north-western quarter of the Iberian Peninsula due to its better adaption to the humid conditions in this region. Some areas of sustainable coexistence were detected, mainly in the upper reaches of the River Ebro.</p> <p><b>Main conclusions</b>: Each species is better adapted to particular conditions. However, the existence of ecotones forces them to occur sympatrically and compete for resources. The parapatric pattern is a result of the evolutionary history of the species and of strong competitive interactions between them, which form 'competitive-exclusion barriers'. However, these barriers are environmentally dependent, so changes in the environment could rapidly affect the limits of the species distribution.</p>
Adaptive and non-adaptive plasticity in changing environments: implications for sexual species with different life history strategies
<p>Populations adapt to novel environmental conditions by genetic changes or phenotypic plasticity. Plastic responses are generally faster and can buffer fitness losses under variable conditions. Plasticity is typically modelled as random noise and linear reaction norms that assume simple one-to-one genotype-phenotype maps and no limits to the phenotypic response. Most studies on plasticity have focused on its effect on population viability. However, it is not clear, whether the advantage of plasticity depends solely on environmental fluctuations or also on the genetic and demographic properties (life histories) of populations. Here we present an individual-based model and study the relative importance of adaptive and non-adaptive plasticity for populations of sexual species with different life histories experiencing directional stochastic climate change. Environmental fluctuations were simulated using differentially autocorrelated climatic stochasticity or noise color, and scenarios of directional climate change. Non-adaptive plasticity was simulated as a random environmental effect on trait development, while adaptive plasticity as a linear, saturating, or sinusoidal reaction norm. The last two imposed limits to the plastic response and emphasized flexible interactions of the genotype with the environment. Interestingly, this assumption led to (i) smaller phenotypic than genotypic variance in the population (many-to-one genotype-phenotype map) and the coexistence of polymorphisms, and (ii) the maintenance of higher genetic variation – compared to linear reaction norms and genetic determinism – even when the population was exposed to a constant environment for several generations. Limits to plasticity led to genetic accommodation, when costs were negligible, and to the appearance of cryptic variation when limits were exceeded. We found that adaptive plasticity promoted population persistence under red environmental noise and was particularly important for life histories with low fecundity. Populations producing more offspring could cope with environmental fluctuations solely by genetic changes or random plasticity, unless environmental change was too fast.</p>
Supplementary data to "Alternative reproductive tactics are associated with sperm performance in invasive round goby from two different salinity environments"
<p>During male-male competition, evolution can favor alternative reproductive tactics. This often results in a dominant morph that holds a resource, such as a nest for egg laying, competes with a smaller sneaker morph that reproduces by stealing fertilizations. The salinity environment can influence male growth rates, e.g. via osmoregulatory costs, which in turn may influence the use of sneaker tactics for small males competing for mating opportunities. Salinity can also affect sperm directly; however, little is known of how salinity influences sneaker tactics through sperm performance. We sampled males of the invasive round goby (<i>Neogobius melanostomus</i>) from two environments, a freshwater river and a brackish estuary. This fish has two male morphs: nest-holding dark males and non-nest-holding light males. We examined the role of water salinity of 0, 8 and 16 on sperm performance and found that in estuarine males, a salinity of 0 reduced sperm velocity compared to a salinity of 8 and 16. Riverine males had low velocity in all salinities. Sperm viability also decreased by over 30 % in 0 salinity, compared to 8 and 16, for fish from both environments. Gobies produce ejaculate contents in specialized glands that could in theory shield sperm in an adverse environment. However, gland contents did not improve sperm performance in our tests. Body mass and age estimates indicate that riverine males invested more in somatic growth compared to estuarine males. Estuarine light morph males had a high enough gonadosomatic index to indicate sneaker tactics. We propose that when sperm performance is low, such as for the riverine males, sneaker tactics are ineffective, and will be selected against or phenotypically suppressed. Instead, we interpret the increased investment in somatic growth found in riverine males as a life-history decision that is advantageous when defending a nest in the next reproductive season.</p>
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.