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226 results for “long term monitoring”

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dryad40/100

Mixed population trends inside a California protected area: Evidence from long-term community science monitoring

<p><span>Protected areas are one of the most widespread and accepted conservation interventions, yet their  population trends are rarely compared to regional trends to gain insight into their effectiveness. Here, we leverage two long-term community science datasets to demonstrate mixed effects of protected areas on long-term bird population trends. We analyzed 31 years of bird transect data recorded by community volunteers across all major habitats of Stanford University's Jasper Ridge Biological Preserve to determine the population trends for a sample of 66 species. We found that nearly a third of species experienced long-term declines, and on average, all species declined by 12%. Further, we averaged species trends by conservation status and key life history attributes to identify correlates and possible drivers of these trends. Observed increases in some cavity-nesters and declines of scrub-associated species suggest that long-term fire suppression may be a key driver, reshaping bird communities through changes in forest and chaparral structure and composition. Additionally, we compared our results to those of the North American Breeding Bird Survey's Central California Coast region (n = 55 species) to place Jasper Ridge in a broader context. Most species experienced similar directional population trends inside vs. outside of the preserve, and only eight species (14.5%) did better inside this small, protected area. Therefore, we must identify relevant management strategies for declining populations and explicitly consider how existing protected areas target and manage each species. Further, this analysis underscores the importance of local and national community science for revealing nuanced long-term bird population trends.</span></p>

opencc-zeroDec 2023View details →
zenodo40/100

Supplentary materials for: "Long-term ecosystem monitoring along the Trabocchi coast (Chieti, Italy): insights from underwater visual surveys (2011-2024)"

<p>This collection of photos and videos showcases the rich biodiversity of marine fauna and flora along the Trabocchi coast reefs in the Chieti district of Italy.</p>

opencc-by-4.0Nov 2024View details →
zenodo40/100

Data set from long-term wind and acceleration monitoring of the Gjemnessund Bridge

<p>The Gjemnessund Bridge has&nbsp;been monitored by accelerometers and anemometers for almost ten years.&nbsp;The data collected between 2013 and 2018 are now available in this open-access research entry, for free access and download. The data is collected in two h5-files (hierachical data format), with sampling rates 2 Hz and 10 Hz, downsampled from the raw sampling rate of 200 Hz. Some minimal signal processing is applied to the data in line with that applied to the Hardanger Bridge data described in Fenerci et al. (2021) and the Bergs&oslash;ysund Bridge data described in&nbsp;Kv&aring;le et al. (2022). The structure of the data is identical to that of the latter reference, which is described in a preprint appended to that research entry. The Python package opyndata available on GitHub contains useful tools compatible with the format of the dataset, for data import, processing and visualization.</p>

opencc-by-4.0Feb 2022View details →
zenodo40/100

Nocturnal flight calls dataset: long-term acoustic monitoring of birds migrating at night

<p><strong>General Description:</strong></p> <p>This is a development set used in the experiments in the Ph.D. thesis: &quot;Nowe metody akustycznej identyfikacji ptak&oacute;w migrujących nocą&quot; (<em>&quot;Novel methods of acoustic identification of birds migrating at night&quot;</em>) by Hanna Pamula. The project focuses on the detection (and - partially - classification) of passerine birds&#39; calls from long-term audio recordings collected during bird autumn migration between 2016 and 2019. The dataset consists of &gt;56,5 hours of recordings with annotations of nocturnal flight calls of passerine birds migrating along the Baltic Sea coast, Poland.</p> <p>&nbsp;</p> <p><strong>Folder Structure</strong></p> <p>Development_Set_3.1.zip</p> <p>|_Development_Set_3.1/</p> <p>&nbsp;&nbsp;&nbsp; |__Training_Set/</p> <p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; |____*.wav</p> <p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; |____*.txt</p> <p>&nbsp;&nbsp; &nbsp;|__Validation_Set/</p> <p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; |____*.wav</p> <p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; |____*.txt</p> <p>&nbsp;&nbsp;&nbsp; |__Testing_Set/</p> <p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; |____*.wav</p> <p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; |____*.txt</p> <p>Training Set: 86 recordings</p> <p>Validation Set: 8 recordings</p> <p>Testing set: 18 recordings (BUT: uploaded 20 recordings, as in the previous version of the dataset - version 3, two additional recordings were used. Then, they were deleted in the final version of development set 3.1. Two additional recordings are: &#39;BUK5_20161101_002104a and BUK5_20161101_002104b)</p> <p>Names of waveforms and annotations are matching.</p> <p><strong>Waveforms:</strong></p> <p>The whole dataset consists of 114 recordings. One hundred thirteen recordings are about 30 minutes long (29min56s &ndash; 29min 59s), one recording is 1min20s. All data were recorded at 44,100 Hz sampling rate, one channel, with SM2 Wildlife Acoustics recorders + SMX-NFC microphone. The recording sessions were performed at night (starting time and date denoted in a file name) on the Baltic Sea coast in Poland (Dąbkowice, near Darłowo).</p> <p><strong>Annotations:</strong></p> <p>Transcriptions were produced using Audacity 2.4.1: https://www.audacityteam.org/ by an experienced birdwatcher, Hanna Pamula. While every effort has been made to ensure the quality and accuracy of the labels, some errors may occur, taking into account the difficulty of nocturnal call recognition and transcription tasks in general.</p> <p>Transcription format:</p> <p>[Starting time (sec)] [Ending time (sec)] [Label]</p> <p><strong>Meaning of the labels:</strong></p> <p>1. Positive classes &ndash; migrating passerine birds:</p> <ul> <li>&#39;s&#39; &ndash; song thrush call (Turdus philomelos)</li> <li>&#39;k&#39; &ndash; blackbird call (Turdus merula)</li> <li>&#39;d&#39; &ndash; redwing call (Turdus iliacus)</li> <li>&#39;r&#39; &ndash; robin call (Erithacus rubecula)</li> <li>&lsquo;kwiczol&rsquo; &ndash; fieldfare call (Turdus pilaris)</li> <li>&lsquo;skowronek&rsquo; &ndash; skylark call (Alauda arvensis)</li> <li>Each of the above labels could also have a question mark &#39;?&#39;, e.g. &#39;r?&#39;, &#39;k?&#39; &ndash; meaning that it&#39;s not a sure label. In a bird call detection task, they are regarded as positive chunks containing bird call(s).</li> <li>&#39;ni&#39; &ndash; non identified bird call (distant/quiet/not recognized)</li> </ul> <p>Only the supposed calls of migrating passerine birds were labeled; other sounds of species were ignored (e.g., robin&#39;s tik-calling, which can be often heard at dusk, and may be regarded as warning sounds).</p> <p>2. Negative classes &ndash; other marked sound events:</p> <ul> <li>&#39;g&#39; &ndash; other bird calls/songs/sounds. Sounds that could confuse the model; for example, sounds of migrating geese, cranes, plovers calls, etc.</li> <li>&#39;gh&#39; &ndash; human voices</li> <li>&#39;t&#39; &ndash; cracks, clicks, raindrops, other noise</li> <li>&lsquo;puszczyk&rsquo; &ndash; tawny owl voice (Strix aluco)</li> <li>&#39;czapla&#39; &ndash; grey heron voice (Ardea cinerea)</li> </ul> <p>Not all occurrences of the negative sounds were labeled &ndash; only some chosen examples to represent the possible noises/negative samples. Thus these annotations can&#39;t be used for entirely different detection / classification tasks than intended, e.g., detecting migrating cranes or human voices in long-term recordings.</p> <p>3. Labels to be excluded from analysis:</p> <ul> <li>&#39;???&#39;, &#39;??? mysz&#39;, &#39;??? high freq&#39; &ndash; unknown, not sure if the sound event is a birds&#39; call or not. Uncertainty about belonging to a positive/negative class in the detection task.</li> </ul>

opencc-by-4.0May 2022View details →
zenodo40/100

Data and results for manuscript "Imaging groundwater infiltration dynamics in karst vadose zone with long-term ERT monitoring"

<p>This data set contains raw and inverted data from an Electrical Resistivity Tomography (ERT) monitoring experiment conducted over a period of three years at the Rochefort Cave Laboratory (RCL) site in South Belgium. It highlights variable hydrodynamics in the karst vadose zone of Lorette Cave. More conventional hydrological measurements (drip discharge monitoring, soil moisture and water conductivity data sets) are also included in the package, which aims at provide a thorough understanding of the groundwater infiltration. Seasonal changes affect all the imaged areas leading to increases in resistivity in spring/summer attributed to enhanced evapotranspiration, whereas winter is characterised by a general decrease in resistivity associated with a groundwater recharge of the vadose zone. This study provides detailed images of the sources of drip discharge spots traditionally monitored in caves and aims to support modelling approaches of karst hydrological processes.</p>

opencc-by-4.0Jan 2018View details →
zenodo40/100

Supplementary Data for "Development of a General Calibration Model and Long-Term Performance Evaluation of Low-Cost Sensors for Air Pollutant Gas Monitoring" (abridged version)

<p>This is a supplementary data set associated with the publication &quot;Development of a General Calibration Model and Long-Term Performance Evaluation of Low-Cost Sensors for Air Pollutant Gas Monitoring&quot; from the Center for Atmospheric Particle Studies, submitted to Atmospheric Measurement Techniques. This is an abbreviated version which does not include the calibrated models; these models must be re-generated by running the codes contained with the data set.</p> <p>&nbsp;</p>

opencc-by-4.0Nov 2018View details →
zenodo40/100

Linked collectors and determiners for: Long-term monitoring of Azorean forest arthropods: the BALA Project (1997-2022).

Natural history specimen data linked to collectors and determiners held within, "Long-term monitoring of Azorean forest arthropods: the BALA Project (1997-2022)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/8a4be36d-18cd-484c-b8ce-f67194cf4bac">https://bionomia.net/dataset/8a4be36d-18cd-484c-b8ce-f67194cf4bac</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/8a4be36d-18cd-484c-b8ce-f67194cf4bac">https://gbif.org/dataset/8a4be36d-18cd-484c-b8ce-f67194cf4bac</a>. Formatted as a Frictionless Data package.

opencc-zeroOct 2024View details →
zenodo40/100

Long-term snow chemical composition monitoring - Hansbreen glacier (Hornsund) - raw data

<p>During the accumulation season, snow samples were taken on Hansbreen Glacier. Several times per season. Snow samples were collected in polyethylene sterile bags and transported to the Polish Polar Station Hornsund. After melting at room temperature, the pH, conductivity and chemical composition (major ions) were analysed in the chemical laboratory of the Polish Polar Station.<br> Snow chemical composition: major ions, HCO3-, pH, conductivity</p> <p>Presented data from 2015 to 2019</p> <p>The data has not been checked, which means that it is raw data.</p> <p>Principal Investigator (PI) Adam Nawrot</p>

opencc-by-4.0Dec 2022View details →
zenodo40/100

Long-term atmospheric precipitation monitoring in Hornsund region (Fuglebekken) - raw data

<p>Since 2004, snow and rain samples have been collected in the Fuglebekken catchment in close vicinity of the Polish Polar Station Hornsund. The rain and snow samples are collected after every event. The pH, conductivity and chemical composition (major ions) are analysed at the Polish Polar Station&rsquo;s chemical laboratory. The rain gauge is checked approximately once a day.</p> <p>Presented data from 2016 to 2022</p> <p>The data has not been checked, which means that it is raw data.</p>

opencc-by-4.0Dec 2022View details →
dryad40/100

Data for: Large-scale long-term passive-acoustic monitoring reveals spatiotemporal activity patterns of boreal bats

<p class="MsoNormal"><span>The distribution ranges and spatio-temporal patterns in the occurrence and activity of boreal bats are yet largely unknown due to their cryptic lifestyle and lack of suitable and efficient study methods. We approached the issue by establishing a permanent passive-acoustic sampling setup spanning the area of Finland to gain an understanding on how latitude affects bat species composition and activity patterns in northern Europe. The recorded bat calls were semi-automatically identified for three target taxa; <em>Myotis</em> spp., <em>Eptesicus nilssonii</em> or <em>Pipistrellus nathusii</em> and the seasonal activity patterns were modeled for each taxa across the seven sampling years (2015–2021). We found an increase in activity since 2015 for <em>E. nilssonii</em> and <em>Myotis </em>spp. For <em>E. nilssonii</em> and <em>Myotis</em> spp. we found significant latitude -dependent seasonal activity patterns, where seasonal variation in patterns appeared stronger in the north. Over the years, activity of <em>P. nathusii</em> increased during activity peak in June and late season but decreased in mid season. We found the passive-acoustic monitoring </span><span>network to be an effective and cost-efficient method for gathering b</span><span>at activity data to analyze spatio-temporal patterns. Long-term data on the composition and dynamics of bat communities facilitates better estimates of abundances and population trend directions for conservation purposes and predicting the effects of cli</span><span>mate change.</span></p>

opencc-zeroFeb 2023View details →
dryad40/100

Assessment of the nesting population demography of loggerhead turtles (Caretta caretta) in La Roche Percée: first long-term monitoring in New Caledonia.

<p><span>Population monitoring is essential to assess, manage and protect threatened species. Although the South Pacific loggerhead turtle subpopulation is classified as critically endangered by the IUCN, monitoring data are scarce. </span></p> <p><span>This study reports the results of the first long-term monitoring of the nesting population of loggerhead turtles held by Bwärä Tortues Marines on La Roche Percée beach, New Caledonia. </span><span>From 2006 to 2020, Capture Mark Recapture was used to identify nesting individuals. Time and nesting success were recorded on site.</span></p> <p><span>A total of 452 different females were observed and tagged over 14 years. The number of different nesting individuals observed each year showed a significant increase along the timeframe of the study. A remigration interval of 3.34 years was observed and the overall nesting success was 59.02%. This study also reports the inter-nesting intervals, monthly and hourly variabilities in the visits at the nesting site.</span></p> <p><span>The conservation actions led by Bwärä Tortues Marines seem to be correlated with a higher nesting success. This study provides encouraging results and highlights the need to pursue the monitoring and conservation actions implemented by Bwärä Tortues Marines. Further management recommendations are also provided.</span></p>

opencc-zeroApr 2023View details →
zenodo40/100

Data set from long-term wave, wind and response monitoring of the Bergsøysund Bridge

<p>Wind, wave, displacement and acceleration data have been collected in a measurement campaign on the Bergs&oslash;ysund Bridge between the years 2014 and 2018. The data set is now available in this open-access research entry, for free access and download. The data is collected in two h5-files (hierachical data format), with sampling rates 2 Hz and 10 Hz, downsampled from the raw sampling rate of 200 Hz. Note that the data has undergone some minimal signal processing and adjustment, in line with that applied to the Hardanger Bridge data described in Fenerci et al. (2021). Tools and examples for import, data visualization and initial analysis are given in the opyndata Python package available on GitHub (Kv&aring;le, 2022). Furthermore, a document briefly describing the hierarchy and structure of the data, is given. For more details on the measurement system and the bridge, it is referred to Kv&aring;le and &Oslash;iseth (2017).</p> <p>The updated, copyrighted version of the appended&nbsp;preprint is published by&nbsp;ASCE&nbsp;with the following&nbsp;DOI:&nbsp;<a href="https://doi.org/10.1061/JSENDH.STENG-12095">10.1061/JSENDH.STENG-12095</a></p>

opencc-by-4.0Jan 2022View details →
dryad40/100

Data from: evaluating the use of lake sedimentary DNA in palaeolimnology: a comparison with long-term microscopy-based monitoring of the phytoplankton community

<p>Palaeolimnological records provide valuable information about how phytoplankton respond to long-term drivers of environmental change. Traditional palaeolimnological tools such as microfossils and pigments are restricted to taxa that leave sub-fossil remains, and a method that can be applied to the wider community is required. Sedimentary DNA (sedDNA), extracted from lake sediment cores, shows promise in palaeolimnology, but validation against data from long-term monitoring of lake water is necessary to enable its development as a reliable record of past phytoplankton communities. To address this need, 18S rRNA gene amplicon sequencing was carried out on lake sediments from a core collected from Esthwaite Water (English Lake District) spanning ~105 years. This sedDNA record was compared with concurrent long-term microscopy-based monitoring of phytoplankton in the surface water. Broadly comparable trends were observed between the datasets, with respect to the diversity and relative abundance and occurrence of chlorophytes, dinoflagellates, ochrophytes and bacillariophytes. Up to 20% of genera were successfully captured using both methods, and sedDNA revealed a previously undetected community of phytoplankton. These results suggest that sedDNA can be used as an effective record of past phytoplankton communities, at least over timescales of less than 100 years. However, a substantial proportion of genera identified by microscopy were not detected using sedDNA, highlighting the current limitations of the technique that require further development such as reference database coverage. The taphonomic processes which may affect its reliability, such as the extent and rate of deposition and DNA degradation, also require further research.</p>

opencc-zeroSep 2023View details →
zenodo40/100

Figure 10. - Different fish abundance dynamic profiles between 1983 and 2014 in Long term monitoring of coral and fish assemblages (1983-2014) in Tiahura reefs, Moorea, French Polynesia

Figure 10. - Different fish abundance dynamic profiles between 1983 and 2014 on the outer slope at Tiahura sector in Moorea.

opencc-by-4.0Jan 2016View details →
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Figure 6 in Long term monitoring of coral and fish assemblages (1983-2014) in Tiahura reefs, Moorea, French Polynesia

Figure 6. - Commercial fish abundance at Tiahura sector in Moorea for the barrier reef and outer slope. Second-degree polynomial models were fitted to data (*: 0.01 &lt;p ≤ 0.05, **: 0.001 &lt;p≤ 0.01).

opencc-by-4.0Jan 2016View details →
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Figure 4 in Long term monitoring of coral and fish assemblages (1983-2014) in Tiahura reefs, Moorea, French Polynesia

Figure 4. - Total fish abundance at Tiahura sector in Moorea for the fringing reef. Second degree polynomial models were fitted to data (*: 0.01 &lt;p ≤ 0.05, **: 0.001 &lt;p ≤ 0.01).

opencc-by-4.0Jan 2016View details →
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Figure 9 in Long term monitoring of coral and fish assemblages (1983-2014) in Tiahura reefs, Moorea, French Polynesia

Figure 9. - Herbivorous fish species richness at Tiahura sector in Moorea for the three habitats. Linear models were fitted to data (**: 0.001 &lt;p ≤ 0.01; ***: p ≤ 0.001).

opencc-by-4.0Jan 2016View details →
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Figure 5 in Long term monitoring of coral and fish assemblages (1983-2014) in Tiahura reefs, Moorea, French Polynesia

Figure 5. - Total fish species richness at Tiahura sector in Moorea for the fringing reef. Linear models were fitted to data (***: p ≤ 0.001).

opencc-by-4.0Jan 2016View details →
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Figure 8 in Long term monitoring of coral and fish assemblages (1983-2014) in Tiahura reefs, Moorea, French Polynesia

Figure 8. - Herbivorous fish abundance at Tiahura sector in Moorea for the barrier reef and outer slope. Linear models were fitted to data (**: 0.001 &lt;p ≤ 0.01).

opencc-by-4.0Jan 2016View details →
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Figure 3 in Long term monitoring of coral and fish assemblages (1983-2014) in Tiahura reefs, Moorea, French Polynesia

Figure 3. - Temporal dynamics in coral percentage cover on the outer slope of Tiahura sector from 1979 to 2011. Stars denote the five main disturbances that affected the reef over the study period (COTS: Acanthaster planci outbreak). Dotted lines correspond to linear interpolation of coral percentage cover.

opencc-by-4.0Jan 2016View details →

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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.

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