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738 results for “estuaries”
Figure 2 in Spatio-temporal distribution of Acartia (Copepoda: Calanoida) species along a salinity gradient in the Seomjin River estuary, South Korea
Figure 2. Monthly spatial and temporal variation in water temperature and chlorophyll a concentration in the Seomjin River Estuary: (A) temperature (°C); (B) chlorophyll a (µg l–1).
Figure 3 from: Wildish DJ, Radulovici AE (2020) Amphipods in estuaries: the sibling species low salinity switch hypothesis. Zoosystematics and Evolution 96(2): 797-805. https://doi.org/10.3897/zse.96.55896
Figure 3 Distribution of O. aestuarensis (closed circles) and O. mediterranea (open circles) in the Medway Estuary, from Wildish (1969).
FIGURE 3 in Subsphaerolaimus minor sp. n. and Micromicron cephalatum Cobb, 1920 (Nematoda) from the Yen River Estuary of Vietnam
FIGURE 3. Pictorial key for valid species of genus Subsphaerolaimus.
Data for the assessment of the detection range of acoustic listening stations in the Zeeschelde estuary, Belgium
<p>Data used to determine the detection of acoustic listening stations in an estuarine environment.</p>
Idealized estuary model data
<p>Idealized estuaries with different channel dimensions and forcing conditions</p>
Supplementary material 1 from: Katnoum C, Keetapithchayakul TS, Rahim AA, Wongkamhaeng K (2023) A new species of Cerapus (Amphipoda, Senticaudata, Ischyroceridae) from Mae Klong Estuary, with a discussion on their nesting and types of mating behaviour. Zoosystematics and Evolution 99(2): 557-574. https://doi.org/10.3897/zse.99.107974
Video of mating of Cerapus rivulus sp. nov.
Fig. 6 in Reproductive characteristics and the weight-length relationship in Anableps anableps (Linnaeus, 1758) (Cyprinodontiformes: Anablepidae) from the Amazon Estuary
Fig. 6. Monthly variation in the allometric condition factor in male and female Anableps anableps collected at the mouth of the Maracanã River, Pará State.
Distribution. Amazon River system including its estuary, Colombia, Brazil, Ecuador, and Peru. in Trichechidae
Distribution. Amazon River system including its estuary, Colombia, Brazil, Ecuador, and Peru.
Supplementary material 2 from: Naro-Maciel E, Ingala MR, Werner IE, Reid BN, Fitzgerald AM (2022) COI amplicon sequence data of environmental DNA collected from the Bronx River Estuary, New York City. Metabarcoding and Metagenomics 6: e80139. https://doi.org/10.3897/mbmg.6.80139
Tables S1,S2, Figures S1–S3
Supplementary material 1 from: Naro-Maciel E, Ingala MR, Werner IE, Reid BN, Fitzgerald AM (2022) COI amplicon sequence data of environmental DNA collected from the Bronx River Estuary, New York City. Metabarcoding and Metagenomics 6: e80139. https://doi.org/10.3897/mbmg.6.80139
Supplementary Data Files 1, 2
Coldwater fish in a warm water world: implications for predation of salmon smolts during estuary transit
<p>Predator-prey systems face intensifying pressure from human exploitation and a warming climate with implications for where and how natural resource management can successfully intervene. We hypothesized young salmon migrating to the Pacific Ocean face a seasonally intensifying predator gauntlet when warming water temperature intensifies a multiple predator effect (MPE) from Striped Bass Morone saxatilis, and Largemouth Bass Micropterus salmoides. We evaluated this hypothesis using data synthesis and simulation modeling. 2. Contemporary studies based on acoustically-tagged fish reaffirmed older observations that Chinook Salmon smolts must transit the Delta before water temperature reaches 20°C or mortality will be nearly 100%. Striped Bass attack rates on tethered smolts were insensitive to distance from shore and water temperature whereas Largemouth Bass attack rates were highest near shorelines in warm water, supporting the temporal aspect of the hypothesis. Whether the combined effects of the two predators produces an MPE remains unconfirmed due to limitations on quantifying salmon behavior. 4. We used multiple simulation models to try to reconstruct the empirical relationship between smolt survival and water temperature. Simulations reinforced attack rate results, but could not recreate the temperature dependence in smolt survival except at higher than observed temperatures. We propose three hypotheses for why and recommend discerning among them should be a focus of research. 5. We found significant linear relationships between monthly mean inflow to the Delta from each of its two largest tributaries and monthly mean water temperatures along associated salmon migration routes, but these relationships can be nonlinear, with most of the correlation occurring at low inflows when water temperature is largely controlled by air temperature and day length. As the global climate warms, changed circumstances in predator-prey relationships may present important challenges when managing species vulnerable to extinction in addition to presently more abundant species. --</p>
Supplementary material 1 from: Suklom A, Keetapithchayakul TS, Abdul Rahim A, Wongkamhaeng K (2022) Two new species of the genus Floresorchestia (Crustacea, Amphipoda, Talitridae) from Amphawa Estuary, Samut Songkhram Province, Thailand. Zoosystematics and Evolution 98(2): 285-303. https://doi.org/10.3897/zse.98.83749
Figure S1
Supplementary material 2 from: Suklom A, Keetapithchayakul TS, Abdul Rahim A, Wongkamhaeng K (2022) Two new species of the genus Floresorchestia (Crustacea, Amphipoda, Talitridae) from Amphawa Estuary, Samut Songkhram Province, Thailand. Zoosystematics and Evolution 98(2): 285-303. https://doi.org/10.3897/zse.98.83749
Figure S2
R Code for Count data, spatial data, environmental data - Dee Estuary Waders 1970-2020
<p>R Code for analysis of spatio temporal data of waders on the Dee Estuary</p>
FIGURE 1 in Four new species of Hysterocinetida (Protozoa: Ciliophora) from the digestive tract of earthworms collected to the lower Nyong estuary (South Coast, Cameroon)
FIGURE 1. Earthworm sampling sites
Figure 1 in Comparison of non-native dwarf eelgrass (Zostera japonica) and native eelgrass (Zostera marina) distributions in a northeast Pacific estuary: 1997-2014
Figure 1: Study area in Yaquina Estuary, Oregon, USA.
"Characteristics of demersal fish community structure during summer hypoxia in the Pearl River Estuary, China"
Open the record for dataset details and reuse information.
Figure 1 in First distributional record of the goby Mangarinus waterousi (Perciformes: Gobiidae) from Vellar estuary, southeast India
Figure 1. – Map showing sampling stations in the Vellar estuary (St-1–St-3) and Pazhayar fish landing centre, where Mangarinus waterousi was first recorded.
Figure 4 in First distributional record of the goby Mangarinus waterousi (Perciformes: Gobiidae) from Vellar estuary, southeast India
Figure 4. – Mangarinus waterousi, fresh specimen from Pazhayar fish land- tics were later able to be taken from those specimens, presently at ing, Tamil Nadu. Photo by H.K. Larson. Vivekananda College, Kanyakumari (Figs 3, 4). The description below is based on the seven specimens from the Vellar River estu- Table I. – Ranges and means of morphometric characteristics of the Manary and the morphometric and meristic details are given in tables I specimens from Vellar southeast India. garinus waterousi (n = 7) estuary, and II.
Figure 3 in First distributional record of the goby Mangarinus waterousi (Perciformes: Gobiidae) from Vellar estuary, southeast India
Figure 3. – Mangarinus waterousi, specimen from Pazhayar fish landing, Tamil Nadu. Photo by A. Murugan.
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International Brain Laboratory public data
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OpenNeuro
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