Skip to main content
Powered by ShareScore

Find research datasets worth reusing

Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.

16

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

16 results for “community respiration”

Learn how ShareScore rates datasets ↗
edi48/100

SMB01 Variation in soil respiration and bacterial community due to species-specific plant-soil history at konza prairie

We conducted a “home vs. away” plant-soil feedback greenhouse experiment using two C3 grass species (Bromus inermis and Pascopyrum smithii) grown in soil collected from Konza Prairie. We used a closed-circuit CO2 trapping method and isotopic analysis to differentiate between root-derived and SOM-derived CO2 production. We investigated how soil chemistry and soil bacterial communities differed in soils with a history of B. inermis vs soils with a history of P. smithii.

openCC0Jan 2023View details →
edi48/100

SBC LTER: Beach: CO₂ flux, wrack subsidies, invertebrate community, and consumer respiration rates for Channel Islands sandy beaches

These data result from surveys of 14 sandy beach sites on four of California’s Channel Islands from 2016 to 2018. We quantified marine macrophyte wrack subsidies, macroinvertebrates, beach physical parameters, and sediment CO2 flux at each site in order to elucidate the role of marine wrack subsidies and wrack consumers on sandy beach sediment CO2 flux. We also measured the respiration rates of the six most common wrack consumer species in the laboratory. Data are contained in two tables: 1) Mean wrack cover, invertebrate community composition (species richness, abundance, and biomass), beach physical parameters, and sediment CO2 flux, and 2) respiration rates and biomass of each replicate individual for each of the six species.

openCC (other)Sep 2025View details →
zenodo44/100

Data set: Can ocean community production and respiration be determined by measuring high-frequency oxygen profiles from autonomous floats?

<p>Relevant autonomous float data for&nbsp;<a href="https://doi.org/10.5194/bg-17-4119-2020">Gordon et al. (2020)</a>. Following a similar structure to the Argo network&#39;s &quot;synthetic&quot; profile files, one file per float is produced with all relevant variables (temperature, salinity, chlorophyll, backscatter, dissolved oxygen) on a common depth and time grid. The &nbsp;Electro-Magnetic Autonomous Profiling Explorer (EM-APEX) floats were deployed in the northern Gulf of Mexico in May 2017 - see&nbsp;<a href="https://doi.org/10.1109/CWTM43797.2019.8955168">Shay et al. (2019)</a>&nbsp;for more information.&nbsp;</p> <p>The data published here contains a timestamp for each data point. Another version of this data which contains some additional variables is hosted on&nbsp;<a href="https://data.gulfresearchinitiative.org/data/R5.x275.281:0001">GRIIDC</a>, but does not contain a timestamp for each data point, but rather for each profile.&nbsp;</p>

opencc-by-4.0Jun 2020View details →
edi44/100

Substrate Induced Respiration (SIR) from 26 sites across vegetation community gradient in and near sensor network, 2017

In alpine ecosystems, small-scale variations in topography determine the spatial and temporal “patchiness” of snow accumulation, snowmelt, vegetation, and biological activity. In the Niwot Ridge Long-term Ecological Research Program VII proposal, Suding and colleagues specifically articulate a need to determine how asynchronous responses across a landscape affect catchment-scale export of water and nutrients in the context of changing climate (H4). Accordingly, we must develop an understanding of how asynchronous responses in patch-scale behavior including microbial activity and decomposition are connected hydrologically, how they aggregate at the catchment scale, and how those relationships may change in the future. To address this, we measured substrate induced respiration (SIR; analogous to microbial biomass) from alpine tundra soils at 26 locations across a soil moisture and corresponding vegetation community composition gradient that included NWT sensor network nodes 6 through 21 in the Saddle stream catchment. These data help to constrain interactions between patch-scale alpine biogeochemical and hydrological processes over space and time.

openCC (other)Jan 2022View details →
zenodo40/100

Data for "Temporal and vertical variability in phytoplankton primary production and microbial community respiration in the North Pacific Subtropical Gyre"

<p>This ALOHA_GOP&amp;R.xslx data set provides measurements of biological rates conducted between April 2015 and July 2020 at different depths in the euphotic zone at or in the vicinity of Station ALOHA (22&deg; 45' N, 158&deg; W), the long-term sampling site of the Hawaii Ocean Time-series (HOT) program, within the North Pacific Subtropical Gyre.&nbsp;</p> <p>The file ALOHA_GOP&amp;R.xslx contains incubation-based measurements of gross oxygen production and community respiration that were measured in the same incubation bottles by applying the&nbsp;<sup>18</sup>O-water method and tracking net changes in oxygen to argon ratios during dawn to dusk in situ incubations, following Ferr&oacute;n et al. (2016). The samples were measured using membrane inlet mass spectrometry. Rates were measured at 6 depths within the euphotic zone: 5, 25, 45, 75, 100, 125 m, except in a few occasions in which there were no measurements made at 125 m.</p> <p>Data description</p> <table> <tbody> <tr> <td> <p>Variable</p> </td> <td> <p>Description</p> </td> <td> <p>Units</p> </td> </tr> <tr> <td> <p>Date&nbsp;</p> </td> <td> <p>Date of sampling and start of incubation (UTC -10 hours)</p> </td> <td> <p>&nbsp;</p> </td> </tr> <tr> <td> <p>Cruise ID</p> </td> <td> <p>Cruise identification</p> </td> <td> <p>#</p> </td> </tr> <tr> <td> <p>Latitude</p> </td> <td> <p>Latitude</p> </td> <td> <p>degrees N</p> </td> </tr> <tr> <td> <p>Longitude</p> </td> <td> <p>Longitude</p> </td> <td> <p>degrees E</p> </td> </tr> <tr> <td>Stn ALOHA&nbsp;</td> <td>Whether the data are from Station ALOHA (yes/no)</td> <td>&nbsp;</td> </tr> <tr> <td>IncT</td> <td> <p>Incubation time</p> </td> <td> <p>hours</p> </td> </tr> <tr> <td> <p>Depth</p> </td> <td>Nominal depth of sampling and incubation&nbsp;</td> <td> <p>meters</p> </td> </tr> <tr> <td>GOP</td> <td>Gross oxygen production&nbsp;</td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td>CR</td> <td>Estimate of community respiration&nbsp;</td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td> <p>Flag GOP</p> </td> <td>Flag identification for gross oxygen production (good=1,questionable=2)</td> <td> <p>#</p> </td> </tr> <tr> <td> <p>Flag CR</p> </td> <td> <p>Flag identification for community respiration (good=1,questionable=2)</p> </td> <td> <p>#</p> </td> </tr> </tbody> </table> <p>&nbsp;</p> <p>The Light-dark_ALOHA_rates.xlsx file contains metabolic rates measured by the ligth-dark oxygen method between June 2005 and June 2007 at different depths in the euphotic zone at Station ALOHA (22&deg; 45' N, 158&deg; W). Rates of net community production, communnity respiration, and gross oxygen production were measured at 6 depths within the euphotic zone (5, 25, 45, 75, 100, 125 m)&nbsp; in dawn to dawn incubations, following Williams et al. (2004).&nbsp;</p> <p>Data description</p> <table> <tbody> <tr> <td> <p>Variable</p> </td> <td> <p>Description</p> </td> <td> <p>Units</p> </td> </tr> <tr> <td> <p>HOT</p> </td> <td>HOT cruise number</td> <td> <p>#</p> </td> </tr> <tr> <td> <p>Date</p> </td> <td>Date of sampling and start of incubation (UTC -10)</td> <td> <p>&nbsp;</p> </td> </tr> <tr> <td> <p>Depth</p> </td> <td>Nominal depth of sampling and incubation&nbsp;</td> <td> <p>meters</p> </td> </tr> <tr> <td>GOP</td> <td>Gross oxygen production, average of 8 replicates</td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td>GOP SE</td> <td>Gross oxygen production standard error&nbsp;</td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td>CR</td> <td> <p>Dark community respiration, average of 8 replicates</p> </td> <td> <p>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></p> </td> </tr> <tr> <td> <p>CR SE</p> </td> <td>Dark community respiration standard error</td> <td> <p>meters</p> </td> </tr> <tr> <td>NCP</td> <td>Net community production,average of 8 replicates&nbsp;</td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td>NCP SE</td> <td>Net community production standard error&nbsp;</td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> </tbody> </table> <p>&nbsp;</p>

opencc-by-4.0Oct 2024View details →
edi40/100

McMurdo Dry Valleys Community Respiration Rates : Quantifying the Activity of the Electron Transport System (ETS)

An important part of the McMurdo Long Term Ecological Research (LTER) is monitoring of spatial and temporal patterns, and processes that control net primary production (carbon dynamics) in perennial ice-covered lakes. One of the primary losses of carbon fixed by phytoplankton is through respiration, directly by the phytoplankton themselves and secondarily through the metabolic contributions of heterotrophic organisms such as bacterioplankton and protozoa. The coupling of low metabolic activity and supersaturated gases in the water column prohibits a direct measurement of respiration. Therefore, we measure the respiratory electron transport system (ETS) activity which drives oxidative phosphorylation, and hence oxygen consumption in all aerobic organisms (Packard 1985). This data set addresses this core area of research and estimates a community-wide respiration rate at specific depths in McMurdo Dry Valley lakes (Hoare, Fryxell and Bonney).

openOpenNov 2014View details →
dryad36/100

Plankton community respiration and POC in the Kuroshio east of Taiwan

<p><span>This dataset contains data </span>collected from six shipboard measurements taken from the R/V <em>Ocean Researcher I</em> between April 2014 and November 2015, which covered the entire season: April, July, September, and November 2014 and March, June, September, and November 2015 in the Kuroshio, east of Taiwan described in the paper: "Chung-Chi Chen, Pei-Ji Meng, Chih-hao Hsieh, Sen Jan (2022). Plankton community respiration and particulate organic carbon in the Kuroshio, east of Taiwan. <em>Plants</em>".</p> <p><span>The main results of this study included seven figures, which show: 1). The sampling stations; 2). Typical depth profile contour plots of temperature, nitrate, chlorophyll a and particulate organic carbon within 250 m water depth along the KTV1 transect in September 2015; 3). Temporal and spatial variations of the mean values of nitrate and phosphate across the KTV1 transect of the Kuroshio; 4). Temporal and spatial variations of the mean values of chlorophyll a, particulate organic carbon, and plankton community respiration across the KTV1 transect of the Kuroshio; 5). Relationships between the concentration of plankton community respiration vs. particulate organic carbon, chlorophyll a, heterotrophic bacterioplankton, and all picophytoplankton; 6). Relationships between the concentration of particulate organic carbon vs. chlorophyll a and picophytoplankton for all pooled data; and 7). Temporal and spatial variations of the mean values of picophytoplankton in terms of abundance and biomass across the KTV1 transect of the Kuroshio.</span></p>

opencc-zeroNov 2022View details →
dryad36/100

Plankton community respiration and POC in the Kuroshio east of Taiwan

Open the record for dataset details and reuse information.

publicNov 2022View details →
edi36/100

In situ soil respirations throughout the 2020 growing season across an N fertilization gradient:Nutrient Network. A cross-site investigation of bottom-up control over herbaceous plant community dynamics and ecosystem function.

This experiment is one implementation of a globally distributed experiment, known as the Nutrient Network. At Cedar Creek, as in over 70 other sites in grasslands around the world, the experiment aims to describe impacts of increased nutrients (nitrogen, phosphorus, potassium, sulfur and other metals) and decreased herbivory (removal of mammals by fencing). Two overarching questions are being explored with these manipulations: 1. To what extent are plant production and diversity co-limited by multiple nutrients in herbaceous-dominated communities? 2. Under what conditions do grazers or fertilization control plant biomass, diversity, and composition? By utilizing identical protocols at diverse grassland sites around the world, NutNet aims to uncover both the generalities in ecosystem functioning, and the contingencies or differences which can obscure those common mechanisms. In addition to the standard NutNet protocol, e247 includes an additional low Nitrogen gradient (1 gram Nitrogen per meter squared per year and 5 grams Nitrogen per meter squared per year in addition to the standard 10 grams Nitrogen per meter squared per year).

openCC0May 2022View details →
dryad32/100

Data from: Exposure to dairy manure leads to greater antibiotic resistance and increased mass-specific respiration in soil microbial communities

Intensifying livestock production to meet the demands of a growing global population coincides with increases in both the administration of veterinary antibiotics and manure inputs to soils. These trends have the potential to increase antibiotic resistance in soil microbial communities. The effect of maintaining increased antibiotic resistance on soil microbial communities and the ecosystem processes they regulate is unknown. We compare soil microbial communities from paired reference and dairy manure-exposed sites across the USA. Given that manure exposure has been shown to elicit increased antibiotic resistance in soil microbial communities, we expect that manure-exposed sites will exhibit (i) compositionally different soil microbial communities, with shifts toward taxa known to exhibit resistance; (ii) greater abundance of antibiotic resistance genes; and (iii) corresponding maintenance of antibiotic resistance would lead to decreased microbial efficiency. We found that bacterial and fungal communities differed between reference and manure-exposed sites. Additionally, the β-lactam resistance gene ampC was 5.2-fold greater under manure exposure, potentially due to the use of cephalosporin antibiotics in dairy herds. Finally, ampC abundance was positively correlated with indicators of microbial stress, and microbial mass-specific respiration, which increased 2.1-fold under manure exposure. These findings demonstrate that the maintenance of antibiotic resistance associated with manure inputs alters soil microbial communities and ecosystem function.

opencc-zeroDec 2016View details →
dryad32/100

Data from: Partitioning the effect of composition and diversity of tree communities on leaf litter decomposition and soil respiration

Open the record for dataset details and reuse information.

publicNov 2016View details →
dryad32/100

Data from: The influence of soil communities on the temperature sensitivity of soil respiration

Open the record for dataset details and reuse information.

publicJul 2019View details →
dryad32/100

Data from: Exposure to dairy manure leads to greater antibiotic resistance and increased mass-specific respiration in soil microbial communities

Open the record for dataset details and reuse information.

publicFeb 2017View details →
zenodo28/100

Soil trenching – are microbial communities alike in experimental peatland plots measuring total and heterotrophic respiration?

<p>&nbsp;</p> <table> <tbody> <tr> <td>Data obtained within a project financed by LIFE Programme of the European Union &lsquo;Demonstration of climate change mitigation potential of nutrients rich organic soils in Baltic States and Finland (LIFE OrgBalt, LIFE18 CCM/LV/001158)</td> </tr> <tr></tr> </tbody> </table>

embargoedcc-by-4.0Nov 2024View details →
zenodo28/100

High benthic community respiration and ecosystem response to phytodetrital input in a sub-polar fjord on the West Antarctic Peninsula

<p><span>Glaciomarine fjords dominate the coastal margin of the West Antarctic Peninsula. Studies in similar habitats in the Arctic have shown that benthic biodiversity and ecosystem functioning in inner and middle fjord basins are reduced by turbidity and sedimentation disturbance caused by climate-warming-enhanced glacial melting. In contrast, the inner and middle fjord basins along the West Antarctic Peninsula are characterised as productivity and biodiversity hotspots, but benthic ecosystem functions remain unevaluated.</span> <span>In 2015-2016, we conducted sediment-respiration and <sup>13</sup>C pulse-chase experiments to assess benthic ecosystem functions along a five-station transect at ~500-600 m depths from the inner Andvord Bay fjord, through to Gerlache Strait, and onto the open continental shelf. Incubation samples from the inner and middle basins of Andvord Bay showed peaks in background seafloor respiration, benthic biomass, and uptake of labeled algal biomass compared to more outlying stations; the continental shelf exhibited the lowest levels of these variables, as well as dissolved inorganic carbon production. Macrofaunal community uptake was responsible for most of the C processing in the inner and middle parts of the fjord (&gt;45%) while dissolved inorganic carbon was the dominant repository of processed C near the fjord mouth and on the continental shelf (&gt;80%). The inner parts of Andvord Bay are hotspots of benthic C-cycling and metabolism, in addition to biodiversity. Ongoing climate warming is likely to negatively impact these inner-fjord hotspots by increasing meltwater input and sedimentation disturbance, yielding a reduction in the input and recycling of labile detritus at the seafloor in the inner-middle fjord.</span></p>

opencc-by-4.0Sep 2024View details →
ClinicalTrials.gov24/100

Children's Automated Respiration Monitor (ChARM) for Child Pneumonia Diagnosis by Community Health Workers in Mali

ClinicalTrials.gov study NCT03457519. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record