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262 results for “trematodes”
Fig. 5 in The Role Of Different Mollusk Species In Maintaining The Transmission Of Polyhostal Trematode Species In Ukrainian Polissya Waters: The Specificity Of Trematode Parthenogenetic Generations To Mollusk Hosts
Fig. 5. The distribution of polyxenic trematode species in the parthenitae host species of mollusks: A — N. attentuatus; B — L. scotiae.
Fig. 2 in Helminths Of Wild Predatory Mammals (Mammalia, Carnivora) Of Ukraine. Trematodes
Fig. 2. Structure of the trematode fauna of the racoon dog in Ukraine (original data): ALT — A. alata; MSK — M. skworzowi; EPE — E. perfoliatus; IME — I. melis; ADO — A. donicum.
Fig. 1 in Helminths Of Wild Predatory Mammals (Mammalia, Carnivora) Of Ukraine. Trematodes
Fig. 1. Structure of the trematode fauna of the red fox in Ukraine (original data): ALT — A. alata; EPE — E. perfoliatus; ADO — A. donicum; SDE — S. denticulata; MAP — M. appendiculatus; PCO — Ph. cordatum; MSK — M. skworzowi; IME — I. melis.
Reims Trematodes MSP Database V1
<p>MALDI TOF Bruker MSP database for Trematoda.</p> <p>Described in "MALDI-TOF : A new tool for the identification of <em>Schistosoma</em> cercariae and detection of hybrids" (publication pending) and Huguenin, Antoine, et al. 2019. « MALDI-TOF mass spectrometry: a new tool for rapid identification of cercariae (Trematoda, Digenea) ». <em>Parasite</em> 26 (8): 11‑13. <a href="https://doi.org/10.1051/parasite/2019011">https://doi.org/10.1051/parasite/2019011</a>.</p> <p> </p>
Fig. 1 in On the systematic position of Collyricloides massanae Vaucher, 1969 (Platyhelminthes: Digenea) with notes on distribution of this trematode species
Fig. 1 The phylogram resulting from Bayesian analysis of partial sequences of 28S rDNA gene. Posterior probabilities are expressed by the use of symbols: star (>90 % posterior probabilities) and filled square (>60 % posteriori probabilities). The arrow indicates the position of Collyricloides massanae
Fig. 7. A-B. 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. 7. A-B. A. Diphterostomun brusinae (STOSSICH, 1888) STOSSICH, 1903 from Argyrops spinifer. Ventral view. Scale 0.5 mm. B. Cirrus sac free-hand drawing
Fig. 3. 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. 3. A = Monascus filiformis (RUD., 1819) from Selaroides leptolepis. Ventral view. Scale 1 mm. B = Cirrus sac free-hand composite drawing
Fig 6 in Digenetic Trematodes From Marine Fishes Off The Coast Of Kuwait, Arabian Gulf: Fellodistomidae And Some Smaller Families, New Host And Geographic Records
Fig 6. Prosogonotrema bilabiatum PÉREZ VIGUERAS, 1940 from Epinephelus areolatus. Ventral view. Scale 1 mm
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
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. 2 in Relative competence of native and exotic fish hosts for two generalist native trematodes
Fig. 2. Mean worm size of the trematodes Telogaster opisthorchis (a) and Stegodexamene anguillae (b) in experimentally infected exotic brown trout and rainbow trout, and native longfin eel. Error bars indicate standard error.
Fig. 3 in Relative competence of native and exotic fish hosts for two generalist native trematodes
Fig. 3. Flowchart summarising the circulation and transmission dynamics of trematodes, (a) Telogaster opisthorchis and (b) Stegodexamene anguillae, in native and exotic hosts in Lake Pearson. (Native fish images; McDowall, 2000; exotic fish; Rauque et al., 2003.)
Fig. 1 in Relative competence of native and exotic fish hosts for two generalist native trematodes
Fig. 1. Mean worm size, number of eggs and egg volume of the trematodes Telogaster opisthorchis (a, c, e) and Stegodexamene anguillae (b, d, f) naturally infecting exotic salmonids (Lake Pearson) and native longfin eel (Lake Sumner). Error bars indicate standard error, ‡‡‡ Significant differences (P <0.0001).
Fig. 1 in Fluke abundance versus host age for an invasive trematode (Dicrocoelium dendriticum) of sympatric elk and beef cattle in southeastern Alberta, Canada
Fig. 1. Age–abundance profiles for the trematode, D. dendriticum in a population of elk sampled from 2009 to 2011 from Cypress Hills Park, Alberta. The solid line represents the negative binomial distribution model fit using maximum likelihood; the dashed lines represent the 95% confidence intervals.
Fig. 2 in Fluke abundance versus host age for an invasive trematode (Dicrocoelium dendriticum) of sympatric elk and beef cattle in southeastern Alberta, Canada
Fig. 2. Stacked frequency distribution of adult D. dendriticum in calf, juvenile, and adult elk collected between 1997 and 2011 from Cypress Hills Park, Alberta.
Fig. 4. Relationship between liver weight and host age for elk sampled from 2009 in Fluke abundance versus host age for an invasive trematode (Dicrocoelium dendriticum) of sympatric elk and beef cattle in southeastern Alberta, Canada
Fig. 4. Relationship between liver weight and host age for elk sampled from 2009 to 2011 from Cypress Hills Park, Alberta. Regression lines are maximum likelihood estimates.
Fig. 3 in Fluke abundance versus host age for an invasive trematode (Dicrocoelium dendriticum) of sympatric elk and beef cattle in southeastern Alberta, Canada
Fig. 3. Age–abundance profile of infection for the invasive trematode, D. dendriticum in beef cattle sampled from 2003 to 2013 from Cypress Hills Park, Alberta. The solid line represents the negative binomial distribution model fit using maximum likelihood; the dashed lines represent the 95% confidence interval.
Fig. 2 in Tegumental topography and molecular characterisation of two trematodes (Platyhelminthes: Digenea) from Clarias gariepinus (Burchell, 1822) in Kenya
Fig. 2. Scanning electron micrographs of Glossidium pedatum. (A) Round oral sucker, (B) spine surrounding the oral sucker (C) location of the genital pore and a protruding cirrus, (D) structure of the cirrus sac (abbreviations: pl-papillae like lappet; os-oral sucker; pp-papillae; dp-dome papillae; vs-ventral sucker; gp-genital pore; c -cirrus; rp-rows of small papillae).
Fig. 5 in Tegumental topography and molecular characterisation of two trematodes (Platyhelminthes: Digenea) from Clarias gariepinus (Burchell, 1822) in Kenya
Fig. 5. Phylogenetic relationships of Tylodelphys mashonensis (Sudarikov, 1971) to other Diplostomidae based on cox1. Phylogram was reconstructed using Bayesian Inference (BI) with Diplostomum spathaceum (Rudolphi, 1819) as an outgroup. Nodal values <0.90 (BI) are indicated by dashes (sequences of the present study are highlighted in bold).
Fig. 3 in Tegumental topography and molecular characterisation of two trematodes (Platyhelminthes: Digenea) from Clarias gariepinus (Burchell, 1822) in Kenya
Fig. 3. Phylogenetic relationships of Glossidium pedatum Loos, 1899 to other members of Plagiorchioidea based on 28S rDNA. Phylogram was reconstructed using Bayesian Inference (BI) with Alloglossidium corti (Lamont, 1921) as an outgroup. Nodal values <0.90 (BI) are indicated by dashes (sequences of the present study are highlighted in bold).
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Allen Brain Atlas
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