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.
6,859
datasets available to search
ShareScore release 0.7.1
Dataset results
6,859 results for “parasite”
Figure 6 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 6. Acanthochondria krishnai sp. n., non-type male from Uranoscopus guttatus Cuvier. A. Habitus lateral view. B. Antennule. C. Antenna. D. Mandible. E. Maxillule. F. Maxilla. G. Maxilliped. H. Leg 1. I. Leg 2. J. Lateral view of genito-abdomen. K. Ventral view of genito-abdomen.
Figure 7. A, B in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 7. A, B. Site of attachment of Chondracanthus kabatai sp. n. (arrows) on its host fish Zenopsis conchifer Lowe.
Figure 5 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 5. Acanthochondria krishnai sp. n., non-type male from Uranoscopus guttatus Cuvier. A. Habitus lateral view. B. Antennule. C. Antenna.
Figure 4 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 4. Acanthochondria krishnai sp. n., paratype, female from Uranoscopus guttatus Cuvier. A. Mandible. B. Maxillule. C. Maxilla. D. Maxilliped. E. Maxilliped apex. F. Leg 1. G. Leg 2. H, I. Genito-abdomen with rami, ventral and ventro-lateral views. J. Rami.
Figure 2 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 2. Acanthochondria krishnai sp. n., holotype, female from Uranoscopus guttatus Cuvier. A. Dorsal view. B. Ventral view. C, D. Cephalon, dorsal and ventral views. E. Antennule. F. Antenna.
Figure 1 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 1. Acanthochondria krishnai sp. n., female from Uranoscopus guttatus Cuvier. A, B. Dorsal view. C. Ventral view.
Figure 3 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 3. Acanthochondria krishnai sp. n., non-type female from Uranoscopus guttatus Cuvier. A. Cephalon ventral view showing cephalic appendages. B. Antennule (arrow). C. Antennules (arrows). D. Cephalic appendages. E. Leg 1. F. Leg 2. G–J. Genitoabdomen. G. Lateral view with rami. H. Ventral view with rami. I. Dorsal view with male. J. With rami. (a1- antennule, a2- antenna, mxp- maxilliped, max- maxilla; L1- leg 1, L2- leg 2, m- male, r- rami).
Figure 14 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 14. Chondracanthus kabatai sp. n., paratype male from Zenopsis conchifer Lowe. A. Habitus, lateral view. B. Antennule. C. Antenna. D. Mandible. E. Maxillule. F. Maxilla. G. Maxilliped. H. Leg 1. I. Leg 2. J. Lateral view of genito-abdomen. K. Rami.
Figure 8 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 8. Chondracanthus kabatai sp. n. from Zenopsis conchifer Lowe. A–C. Holotype, female, dorsal, ventral and lateral views. D–F. Paratype, female, dorsal, ventral and dorso-lateral views.
Fig. 3 in Prevalence and genetic diversity of haematozoa in South American waterfowl and evidence for intercontinental redistribution of parasites by migratory birds
Fig. 3. Bayesian phylogenetic tree of haematozoa mitochondrial DNA cytochrome b haplotypes obtained from infected waterfowl. Trees were rooted with mammalian Plasmodium outgroups. Node tips are labeled with parasite genus (Haem = Haemoproteus, Leuc = Leucocytozoon, and Plas = Plasmodium), followed by the lineage name, GenBank accession number for each sequence, host order (passerine/waterfowl), and the country/state from which the samples were collected. All haplotypes identified in this study are highlighted in red. Numbers on branches represent posterior probabilities from the analysis. Asterisks after node tip labels indicate sequences from our study that were identical to lineages previously found in non-waterfowl hosts. All reference sequences were obtained from the National Center for Biotechnology Information website.
Fig. 2. Minimum spanning network for haematozoa mitochondrial DNA cytochrome b in Prevalence and genetic diversity of haematozoa in South American waterfowl and evidence for intercontinental redistribution of parasites by migratory birds
Fig. 2. Minimum spanning network for haematozoa mitochondrial DNA cytochrome b haplotypes detected in South American waterfowl. Shaded circles represent unsampled nodes. All circles are drawn proportional to the frequency at which haplotypes were observed. Lines separating nodes are drawn to scale based on the number of nucleotide mutations, unless otherwise indicated by hash marks. Only haplotypes with a length of 358 bp or greater were included. Haplotype name abbreviations are as follows: Haem = Haemoproteus, Leuc = Leucocytozoon, and Plas = Plasmodium.
Fig. 1 in Prevalence and genetic diversity of haematozoa in South American waterfowl and evidence for intercontinental redistribution of parasites by migratory birds
Fig. 1. Map of sampling locations in Peru and Argentina. The number of waterfowl blood samples collected at each site is provided in parentheses.
Fig. 1 in (macro-) Evolutionary ecology of parasite diversity: From determinants of parasite species richness to host diversification
Fig. 1. Expression of the basic transmission rate (R0) for the case of microparasites (i.e. viruses) and macroparasites (i.e. helminths with direct transmission) (for derivations of these expressions see Morand and Deter, 2008), emphasizing the importance of two host traits, longevity and density, as likely determinants of parasite invasion and then parasite species richness. In the right panel, relationships showing that both density and longevity are in allometry with host body mass (after Brown, 1995).
Fig. 2 in (macro-) Evolutionary ecology of parasite diversity: From determinants of parasite species richness to host diversification
Fig. 2. (A) Variability of ectoparasite species richness among 113 families of mammals (20 orders) (data from Kim, 1985;see Poulin and Morand, 2004). (B) Ectoparasite species richness is related to mammal diversification. The statistical analysis follows Nunn et al. (2004), where the change in the number of descendent clades is related to the change in the number of ectoparasite species, estimated using a modified version of the independent contrast method (Agapow and Isaac, 2002), for each node of the mammal phylogeny (from Binida-Emonds et al., 2007).
Fig. 1. a in First report on Phyllobothrium delphini infection and Crassicauda sp. parasitism resulting in osseous metaplasia in a Cuvier's beaked whale (Ziphius cavirostris) from the Brazilian region
Fig. 1. a Infected adipous tissue. Phyllobothrium delphini located in the center of the well-delimited parasitic cyst. Inset: Phyllobothrium delphini displaying a whitish coloration and shiny appearance. Bar, 2 cm b Thoracic aorta artery displaying bone metaplasia. Radiographic image highlighting the strong radiopacity, similar to bone radiopacity, observed along all the artery walls. Bar, 15 cm c Parasitic cyst located in adipose tissue. Proliferating and reacting fibrous tissue with a moderate number of lymphocytes and plasmocytes located along the parasitic cyst wall. Numerous activated macrophages and multinucleated giant cell (black arrow) are visible around the P. delphini specimen displaying a degenerated cuticle (red arrow). Insert: Hight power field of inflammatory infiltrate with lymphocytes (black arrow) and plasma cells (red arrow). d Thoracic aorta artery displaying bone metaplasia. Mature bone tissue is organized as circumferential lamellae and cement line (red arrow). Note the erythrocytes within the blood vessel and adipose tissue in the medullar region of the detected bone metaplasia. Inset: Hight power field of bone metaplasia with osteocytes allocated in lacunae (black arrow). e Parasitized kidney. Crassicauda sp. involved by reactive fibrous tissue associated with inflammatory infiltrate. f Parasitized Kidney. High power field of nephritis associated with Crassicauda sp. Note the fibrosis and inflammatory infiltrate formed by macrophages (red arrow) and plasma cells (black arrow).. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Figure 1. A in Contribution to the fauna of bat-parasitizing ticks in Bosnia and Herzegovina
Figure 1. A. Distribution of haplotypes obtained in this research and earlier studies. L and C markings represent the location and country, respectively. The locations are marked with numbers from 1 to 6, whereby (1) denotes Zvornik, (2) Šipovo, (3) Dimitrov grad, (4) Zlot, (5) Rijeka Crnojevića, and (6) Jama Šutonjića cave; B. Dorsal surface of tick sample; C. Ventral surface of tick sample.
Figure 2 in Rediscovery and redescription of Entoniscus creplinii Giard and Bonnier, 1887 (Isopoda: Bopyroidea: Entoniscidae) parasitizing Polyonyx gibbesi Haig, 1956 (Decapoda: Anomura: Porcellanidae), a symbiotic crab from the tubes of Chaetopterus cf. variopedatus (Annelida), from North Carolina and Florida, U. S. A.
Figure 2. Entoniscus creplinii Giard and Bonnier, 1887 (USNM 1660598). A) Mature female, lateral view. B) Close-up of side of pleomere 3 showing scales. C) Terminal segment of pleon. D) Female cephalon with host sheath surrounding, en face view. E) Female cephalon with host sheath surrounding, lateral view. F) Female cephalon with host sheath removed, en face view. G) Female cephalon with host sheath removed, lateral view. H) Pleon of female with host sheath partially removed, asterisk showing position of first pleopods still covered by host sheath; stippled region shows channel within which second pleopods lay. Abbreviations: ce = cephalon; he = heart; 2–4 = pleopods 2 to 4. Scales = 0.5 mm (A, D–H); 10 µm (B, C).
Figure 1 in Rediscovery and redescription of Entoniscus creplinii Giard and Bonnier, 1887 (Isopoda: Bopyroidea: Entoniscidae) parasitizing Polyonyx gibbesi Haig, 1956 (Decapoda: Anomura: Porcellanidae), a symbiotic crab from the tubes of Chaetopterus cf. variopedatus (Annelida), from North Carolina and Florida, U. S. A.
Figure 1.Entoniscus creplinii Giard and Bonnier, 1887 (USNM 1660598). A) Mature female, dorsal view. B) Mature female, dorsal view. C) Mature female, lateral view. D) Pleon of female extending to opening at the merus-carpus articulation of the third right walking leg of host Polyonyx gibbesi Haig, 1956. Abbreviations: ce = cephalon; he = heart; 1o–5o = oostegites 1 to 5; 1p–5p = pleomeres 1 to 5; pl = pleural lamellae. Scales = 0.5 mm (A); 1 mm (B–D).
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).
ScienceDex guides
Understand access before you commit
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.