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168 results for “Parasite communities”
Parasite communities of Coregonus spp. from Swiss and Norwegian Lakes
<p>Data on the parasite communities of Coregonus spp. from 5 lakes in Switzerland and 2 lakes in northern Norway. These data represent 15 communities from Switzerland and 5 from Norway that were used in the Host sampling completeness analysis in Llopis‐Belenguer, C., J. A. Balbuena, I. Blasco‐Costa, A. Karvonen, V. Sarabeev, and J. Jokela. 2022. Sensitivity of bipartite network analyses to incomplete sampling and taxonomic uncertainty. Ecology.</p>
Fig. 2 in New Geographic Record Of Myxobolus portulacalensis (Saraiva & Molnar, 1990) And Spinitectus Inermis (Zeder, 1800) In European Eel (Anguilla Anguilla) Parasite Communities From Latvia Freshwaters
Fig. 2. Male Spinitectus inermis (Zeder, 1800) body from stomach of European eel (Anguilla anguilla) caught in Lake Usma, Latvia (100 x magnification). A - anterior end; B – posterior end.
Fig. 1 in New Geographic Record Of Myxobolus portulacalensis (Saraiva & Molnar, 1990) And Spinitectus Inermis (Zeder, 1800) In European Eel (Anguilla Anguilla) Parasite Communities From Latvia Freshwaters
Fig. 1. Spores of Myxobolus portucalensis (Saraiva and Molnar, 1990) from fins of European eel (Anguilla anguilla) caught in Lake Usma, Latvia (600 x magnification).
Fig. 2 in Helminths Of Antarctic Rockcod Notothenia Coriiceps (Perciformes, Nototheniidae) From The Akademik Vernadsky Station Area (Argentine Islands, West Antarctica): New Data On The Parasite Community
Fig. 2. Average number of cysts of Corynosoma spp. in the body cavity of Notothenia coriiceps of five size groups.
Fig. 1 in Helminths Of Antarctic Rockcod Notothenia Coriiceps (Perciformes, Nototheniidae) From The Akademik Vernadsky Station Area (Argentine Islands, West Antarctica): New Data On The Parasite Community
Fig. 1. Prevalence (in %) and mean intensity of helminth species found in Notothenia coriiceps in the waters surrounding the Ukrainian Antarctic station "Akademik Vernadsky" in 2014–2015.
Fig. 3 in Gastrointestinal Parasite Community In A New Population Of The Przewalski'S Horse (Equus Ferus Przewalskii) In The Orenburg State Reserve, Russia
Fig. 3. Distribution of strongylid species from the Przewalski's horses in Pre-Urals Steppe, Orenburg State Reserve, on ten prevalence classes.
Fig. 1 in Species Composition And Structure Of The Communities Of Plant-Parasitic And Free-Living Soil Nematodes In The Greenhouses Of Botanical Gardens Of Ukraine
Fig. 1. Dendrogram of similarity of the nematode communities in the greenhouses of botanical gardens of Ukraine (amalgamation by the method of complete linkage). Explanation of the abbreviations is given in table 2. Рис. 1. Дендрограмма сходства нематодных сообществ в оранжереях ботанических садов Украины (объединение по методу полной связи). Расшифровка сокращений дана в таблице 2.
Fig. 2 in Species Composition And Structure Of The Communities Of Plant-Parasitic And Free-Living Soil Nematodes In The Greenhouses Of Botanical Gardens Of Ukraine
Fig. 2. Dendrogram of similarity of plant-parasitic nematodes' communities in the greenhouses of botanical gardens of Ukraine (amalgamation by the method of complete linkage). Explanation of the abbreviations is given in table 2.
Fig. 6 Seasonal parasite transmission along the lower Mbam river showing a in ONCHOCERCA VOLVULUS transmission in the Mbam valley of Cameroon following 16 years of annual community-directed treatment with ivermectin, and the description of a new cytotype of SIMULIUM SQUAMOSUM
Fig. 6 Seasonal parasite transmission along the lower Mbam river showing a combined parity and infection rates for flies dissected at Bayomen and Nyamongo I riverside sites (L1–L2 = percentage of flies infected with developing parasite stages only, L3H = percentage of flies containing L3 stages in the head), and b monthly transmission potentials at Bayomen, Nyamongo I, and Egona II estimated based on dissection data only. Ondouano not shown since no larvae were found in dissected flies
Figure 2. Dendrogram resulting from a in Host specificity and the structure of helminth parasite communities of fishes in a Neotropical river in Mexico
Figure 2. Dendrogram resulting from a similarity matrix based on the Sørensen measure for component communities of adult autogenic helminth parasites of 10 fish species from Apazapan, Río La Antigua, Veracruz, Mexico. Host species are: Amex, A. mexicanus; Rgua, R. guatemalensis; Smar, S. marmoratus; Hbim, P. bimaculata; Pmex, Poecilia mexicana; Pgra, Poeciliosis gracilis; Psph, Poecilia sphenops; Xell, X. helleri; Tell, T. ellioti; Vfen, V. fenestrata.
Figure 1 in Host specificity and the structure of helminth parasite communities of fishes in a Neotropical river in Mexico
Figure 1. Patterns of relative abundance of 24 species of helminths in 11 component communities of freshwater fishes from Río Apazapan, Río La Antigua basin, Mexico (fish species: Am, A. mexicanus; Rg, Rhamdia guatemalensis; Hb, Pseudoxiphophorus bimaculata; Pm, Poecilia mexicana; Ps, P. sphenops; Pg, Poeciliopsis gracilis; Xh, Xiphophorus helleri; Te, Thorichthys helleri; Vf, Vieja fenestrata; Sm, Sicydium gymnogaster).
Fig. 1 in Experimental manipulation reveals few subclinical impacts of a parasite community in juvenile kangaroos
Fig. 1. Mean faecal egg counts for control and anthelmintic-treated juvenile eastern grey kangaroos in two periods post-capture (12–33 days) and initial treatment (40– 90 days) at the Anglesea Golf Club, Victoria, Australia, from March to May 2012. Bars indicate standard errors. It was not always possible to sample each individual in each period; numbers on columns indicate sample size for each time period.
Fig. 4 in Parasite community dynamics in an invasive vole ‾ From focal introduction to wave front
Fig. 4. Statistical associations between ectoparasites and endoparasites infecting bank voles, Myodes glareolus. All associations are due to the presence of a coinfecting species, positive relationships are shown in black and negative relationships are in grey. The predicted absolute percentage change (see Methods for definition) of the dependent variable is given for each interaction. Parentheses identify whether the relationship is based on body mass (BM), host sex (S) or at the mid-point along the invasion wave (WM). Lice had a prevalence of less than 10% so were excluded from analyses.
Fig. 1 in Parasite community dynamics in an invasive vole ‾ From focal introduction to wave front
Fig. 1. Sampling sites of the invasive bank vole, Myodes glareolus, across the Republic of Ireland. Curraghchase and Adare are the focal point of introduction, Gort, Nenagh and Cashel are mid-wave, and Tuam, Birr and New Ross represent the invasion front. For all trapping sites along the invasion gradient (black = focal point of introduction, grey = mid-wave, and white = invasion front), bar charts depict the prevalence of each parasite and boxplots indicate the mean parasite abundance (log x +1), where boxes indicate the mean, and lines the 95% confidence intervals.
Fig. 3 in Parasite community dynamics in an invasive vole ‾ From focal introduction to wave front
Fig. 3. Parasite interactivity index from eight sampling sites at three points along an invasion gradient (black = focal point of introduction, grey = mid-wave, and white = invasion front) in the Republic of Ireland. Boxes represent upper and lower quartile, with median indicated, with bars representing maximum and minimum range.
Fig. 2 in Parasite community dynamics in an invasive vole ‾ From focal introduction to wave front
Fig. 2. Parasite abundance of the invasive bank vole, Myodes glareolus, from eight locations at three points along an invasion gradient (black = focal point of introduction, grey = mid-wave, and white = invasion front) in the Republic of Ireland. Boxes represent upper and lower quartile, with median indicated, with bars representing maximum and minimum range.
Fig. 3 in Parasite community structure as a predictor of host population structure: An example using Callorhinchus capensis
Fig. 3. Randomized individual-based species accumulation curve of parasites infecting Callorhinchus capensis (n = 259) caught off the West and South Coasts of South Africa between 2010 and 2015.
Fig. 1 in Parasite community structure as a predictor of host population structure: An example using Callorhinchus capensis
Fig. 1. Map showing sample locations (St Helena Bay, False Bay and trawl locations shown by diamond symbols) in which Callorhinchus capensis were caught (dashed line indicates 200 m depth contour). The inset shows the distribution range of Callorhinchus capensis (IUCN, 2012).
Fig. 2. a–d in Parasite community structure as a predictor of host population structure: An example using Callorhinchus capensis
Fig. 2. a–d: Four metazoan parasites found infecting Callorhinchus capensis caught in False Bay, South Africa in 2013. Photos taken by T. Morris.
Fig. 7 in Altered parasite community structure in an endangered marsupial following translocation
Fig. 7. Mean trypanosome prevalence over time (with 95% CI) in translocated and resident woylies within Dryandra. TRAN: time of translocation.
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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)
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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.