Find research datasets worth reusing

opencc-by-4.0Nov 2003View details →

Fig. 2. A in Digenetic Trematodes From Marine Fishes Off The Coast Of Kuwait, Arabian Gulf: Fellodistomidae And Some Smaller Families, New Host And Geographic Records

Fig. 2. A = Complexobursa vjetnamensis OSHMARIN e t MAMAEV, 1963, from Terapon theraps. Ventrolateral view. Scale 1 mm. B. Cirrus sac free-hand drawing

opencc-by-4.0Nov 2003View details →

Fig. 1. A in Digenetic Trematodes From Marine Fishes Off The Coast Of Kuwait, Arabian Gulf: Fellodistomidae And Some Smaller Families, New Host And Geographic Records

Fig. 1. A = Lintonium vibex (LINTON, 1900) STUNKARD e t NIGRELLI, 1930, from Lagocephalus lunaris. Ventral view. Scale 1 mm. B = Cirrus sac free-hand composite drawing

Fig. 6 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey

Fig. 6. Prevalence (broken line) (❍: D. cornu, ∆: D. difformis) and mean intensity (solid line) of the parasite species (●: D. cornu, ▲: D. difformis) on Vimba vimba and Scardinius erythrophthalmus in

Fig. 3 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey

Fig. 3. Prevalence (broken line) and mean intensity (solid line) of D. crucifer on R. rutilus in Lake Manyas over two years

Fig. 2 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey

Fig. 2. Prevalence (broken line) and mean intensity (solid line) of D. sphyrna on B. bjoerkna in Lake Manyas over two years, and the water temperature (*) of the Lake during the study period (surface)

Fig. 5 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey

Fig. 5. Prevalence (broken line) (❍: D. sphyrna, ∆: D. crucifer) and mean intensity (solid line) of the parasite species (●: D. sphyrna, ▲: D. crucifer) on Blicca bjoerkna and Rutilus rutilus in relation to

Fig. 4 in Occurrence Of Dactylogyrus Infection Linked To Seasonal Changes And Host Fish Size On Four Cyprinid Fishes In Lake Manyas, Turkey

Fig. 4. Prevalence (broken line) (❍: D. cornu, ∆: D. difformis) and mean intensity (solid line) of the parasite species (●: D. cornu, ▲: D. difformis) on Vimba vimba and Scardinius erythropthalmus in Lake Manyas over two years

opencc-by-4.0Sep 2008View details →

Fig. 2 in Host Ant Use Of Maculinea Teleius In The Carpathian Basin (Lepidoptera: Lycaenidae)

Fig. 2. The mean number (± SE) of M. teleius specimens found in nests of the different Myrmica ant species combining all data. Standard errors are based on a General Linear Model with negative bino-

opencc-by-4.0Sep 2008View details →

Fig. 1 in Host Ant Use Of Maculinea Teleius In The Carpathian Basin (Lepidoptera: Lycaenidae)

Fig. 1. The investigated sites and the proportion of M. teleius specimens found in nests of different Myrmica species (see Table 2 for more details and for a key to site codes)

opencc-by-4.0Nov 2023View details →

Supplementary Data for 'Crossing host boundaries: the evolutionary drivers and correlates of viral host jumps'

This version provides the raw maximum likelihood trees with ancestral host states annotated, as described in Tan et al. 2024 (https://doi.org/10.1038/s41559-024-02353-4).    Tip labels are formatted as {genbank accession}|{host}|{collection_date}|{country}. Nodel labels are formatted as follows: <ul> <li>rooted_trees_simplified: {node name}|{host}, where {host} is the most likely ancestral state (i.e., highest ancestral state likelihood)</li> </ul> <ul> <li>rooted_trees: {node name}|{host1}:{likelihood1}|{host2}:{likelihood2}...|{hostn}:{likelihoodn}, which provides the raw ancestral state likelihoods for each host state. </li> <li>All node names correspond to those provided in the Supplementary Tables in Tan et al. 2024.</li> </ul>

Fig. 1 in Choosy Outsiders? Satellite Males Associate With Sexy Hosts In The European Tree Frog Hyla Arborea

Fig. 1. Box plots for snout-urostyle length of sampled males of Hyla arborea, classified as satellites, callers or hosts. Boxes represent standard error of mean and whiskers represent standard deviation. Small squares represent mean

Fig. 5 in Parasitoids Of The Bedeguar Gall (Diplolepis Rosae): Effect Of Host Scale On Density And Prevalence

Fig. 5. Parasitoid prevalence per shrubs (dots) and galls (triangles) as a function of rose shrub densities per 50 m × 50 m plot and gall densities per shrub (nested linear fixed effect ANCOVA)

Fig. 2. a in Parasitoids Of The Bedeguar Gall (Diplolepis Rosae): Effect Of Host Scale On Density And Prevalence

Fig. 2. a) Parasitoid number per shrub; b) parasitoid prevalence per shrub; c) parasitoid number per gall; d) parasitoid prevalence per gall as a function of rose shrub density per 50 m × 50 m plot (linear regressions). The dotted lines represent the 95% CI, while the dashed lines the prediction intervals

Fig. 1 in Parasitoids Of The Bedeguar Gall (Diplolepis Rosae): Effect Of Host Scale On Density And Prevalence

Fig. 1. Gall density per shrub as a function of rose shrub density per 50 m × 50 m plot (linear regression). The dotted lines represent the 95% CI, while the dashed lines represent the prediction intervals

Fig. 4. a in Parasitoids Of The Bedeguar Gall (Diplolepis Rosae): Effect Of Host Scale On Density And Prevalence

Fig. 4. a) Parasitoid numbers per shrubs (dots) and galls (triangles); b) parasitoid prevalences per shrubs (dots) and galls (triangles) versus gall numbers per shrub (nested linear fixed effect ANCOVA)

Fig. 3. a in Parasitoids Of The Bedeguar Gall (Diplolepis Rosae): Effect Of Host Scale On Density And Prevalence

Fig. 3. a) Parasitoid numbers per shrubs (dots) and galls (triangles); b) parasitoid prevalences per shrubs (dots) and galls (triangles) versus rose shrub density per 50 m × 50 m plot (nested linear fixed effect ANCOVA)

opencc-by-4.0Dec 2020View details →

Figure 3 in Host conservation through their parasites: molecular surveillance of vector-borne microorganisms in bats using ectoparasitic bat flies

Figure 3. Comparison of detected microorganism prevalence (prevalence of infection) between bats and bat flies. Different bars represent hosts (black), all bat flies (dark grey), and consensus fly results, meaning that at least one infected fly individual was present on the host (light grey).

opencc-by-4.0Nov 2021View details →

Figure 4 in A new order of fishes as hosts of blood flukes (Aporocotylidae); description of a new genus and three new species infecting squirrelfishes (Holocentriformes, Holocentridae) on the Great Barrier Reef

Figure 4. Relationships between species of Holocentricola and other members of the Aporocotylidae based on phylogenetic analysis of the 28S dataset. Bayesian inference posterior probabilities values are shown above the nodes and maximum likelihood bootstrap support shown below; values of <85 and <0.85 not shown. The scale-bar indicates expected number of substitutions per site.

opencc-by-4.0Nov 2021View details →

Figure 3 in A new order of fishes as hosts of blood flukes (Aporocotylidae); description of a new genus and three new species infecting squirrelfishes (Holocentriformes, Holocentridae) on the Great Barrier Reef

Figure 3. Species of Holocentricola from Great Barrier Reef Holocentridae, terminal genitalia, dorsal views; spines illustrated are ventral. (A) Holocentricola rufus n. sp. ex Sargocentron rubrum from off Heron Island (paratype, QM G239440); (B) Holocentricola exilis n. sp. ex Neoniphon sammara from off Lizard Island (paratype, QM G239119); (C) Holocentricola coronatus n. sp. ex Sargocentron diadema from off Lizard Island (paratype, QM G239126). Abbreviations: CS, cirrus-sac; ER, egg reservoir; FGP, female genital pore; MGP, male genital pore; Od, oviduct; Oö, oötype; Ov, ovary; PP, pars prostatica; SV, seminal vesicle; Ut, uterus; VD, vas deferens; VitD, vitelline duct. Scale-bars: A–C, 100 µm.