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Anisakid infection in the European shag Phalacrocorax aristotelis aristotelis

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/mmnz.19590350107openalex-snapshot
Revision der vogelparasitischen Nematoden Mitteleuropas I. Die Gattung Porrocaecum Railliet & Henry, 1912 (Ascaridoidea)
inferredcites →https://doi.org/10.1007/978-94-009-9972-5openalex-snapshot
Helminths of Fish-Eating Birds of the Palaearctic Region
inferredcites →https://doi.org/10.1007/bf00009787openalex-snapshot
Morphological study of Contracaecum magnicollare (Nematoda, Anisakidae) from Anous minutus (Aves, Laridae)
inferredcites →https://doi.org/10.1007/bf00011888openalex-snapshot
Systematic implications of male caudal morphology in ascaridoid nematode parasites
inferredcites →https://doi.org/10.1007/bf00012194openalex-snapshot
Technology as applied to museum collections: the collection, fixation and conservation of helminths
inferredcites →https://doi.org/10.1007/bf00012195openalex-snapshot
Basic techniques involved in helminth preservation
inferredcites →https://doi.org/10.1007/bf00260308openalex-snapshot
[Contracaecum septentrionale, a new parasite from the cormorant; its life cycle, as well as reports on the development of Anisakinae. (Contribution to the knowledge of parasitic nematodes XVI.)].
inferredcites →https://doi.org/10.1016/0020-7519(88)90074-4openalex-snapshot
Patterns of caudal papillae in Contracaecum osculatum (Nematoda) and some related species from different regions of the world
inferredcites →https://doi.org/10.1016/0020-7519(93)90103-6openalex-snapshot
Three sibling species within Contracaecum osculatum (nematoda, ascaridida, ascaridoidea) from the atlantic arctic-boreal region: Reproductive isolation and host preferences
inferredcites →https://doi.org/10.1016/0020-7519(94)90084-1openalex-snapshot
Two new members in the Contracaecum osculatum complex (nematoda, ascaridoidea) from the antarctic
inferredcites →https://doi.org/10.1016/0021-9975(69)90043-7openalex-snapshot
Larval nematodes from fish of the subfamily anisakinae and gastro-intestinal lesions in mammals
inferredcites →https://doi.org/10.1016/0169-4758(93)90182-fopenalex-snapshot
Nematode parasites of vertebrates. Their development and transmission
inferredcites →https://doi.org/10.1016/0169-5347(87)90072-3openalex-snapshot
Conservation biology: The science of scarcity and diversity
inferredcites →https://doi.org/10.1016/0198-0149(81)90045-5openalex-snapshot
Diseases of marine animals
inferredcites →https://doi.org/10.1016/c2013-0-06260-3openalex-snapshot
Cellular Pathology Technique
inferredcites →https://doi.org/10.1016/s0065-2881(08)60141-8openalex-snapshot
Competition between Fisheries and Seabird Communities
inferredcites →https://doi.org/10.1017/s0022149x00030650openalex-snapshot
An outbreak of Parasitic Necrosis in Turkeys caused by Plagiorchis laricola (Skrjabin)
inferredcites →https://doi.org/10.1017/s0031182000075788openalex-snapshot
Introduction: Ecological impact of parasitism on wildlife host populations
inferredcites →https://doi.org/10.1038/scientificamerican0673-22openalex-snapshot
The Anchovy Crisis
inferredcites →https://doi.org/10.1079/9780851994215.0000openalex-snapshot
Nematode parasites of vertebrates: their development and transmission
inferredcites →https://doi.org/10.1093/oso/9780198548935.005.0002openalex-snapshot
Collection and quantification of avian helminths and protozoa
inferredcites →https://doi.org/10.1111/j.1463-6409.1987.tb00047.xopenalex-snapshot
A redescription of the pinniped parasite Contracaecum ogmorhini (Nematoda, Ascaridoidea), with an assessment of its antiboreal circumpolar distribution
inferredcites →https://doi.org/10.1111/j.1463-6409.1992.tb00315.xopenalex-snapshot
Morphological distinction between adult Contracaecum radiaturn and Contracaecum osculatum (Nematoda, Anisakidae) from the Weddell seal (Leptonychotes weddelli)
inferredcites →https://doi.org/10.1111/j.1523-1739.1988.tb00332.xopenalex-snapshot
Conservation and Disease
inferredcites →https://doi.org/10.1136/pgmj.62.727.417openalex-snapshot
Cellular Pathology Technique
inferredcites →https://doi.org/10.1139/f92-106openalex-snapshot
Ascaridoid Nematodes from the Stomach of Harp Seals, Phoca groenlandica, from Newfoundland and Labrador
inferredcites →https://doi.org/10.1139/z57-023openalex-snapshot
NEMATODE PARASITES OF SEALS IN THE EASTERN CANADIAN ARCTIC
inferredcites →https://doi.org/10.20506/rst.7.4.380openalex-snapshot
Research on wildlife diseases: is a reappraisal necessary ?
inferredcites →https://doi.org/10.2307/1366091openalex-snapshot
Model Estimation of Energy Flow in Oregon Coastal Seabird Populations
inferredcites →https://doi.org/10.2307/2402446openalex-snapshot
The Relationship Between the Presence of Larval Anisakine Nematodes in Cod and Marine Mammals in British Home Waters
inferredcites →https://doi.org/10.2307/3221805openalex-snapshot
The Nematode Parasites of Vertebrates
inferredcites →https://doi.org/10.2307/3284227openalex-snapshot
Parasitology Meets Ecology on Its Own Terms: Margolis et al. Revisited
inferredcites →https://doi.org/10.2307/3546970openalex-snapshot
Sex-Biased Parasitism of Avian Hosts: Relations to Blood Parasite Taxon and Mating System
inferredcites →https://doi.org/10.2307/4082462openalex-snapshot
Nematodes in Birds of the Order Pelecaniformes
inferredcites →https://doi.org/10.2307/4082504openalex-snapshot
Heavy Nematode Infestation of White Pelican
inferredcites →https://doi.org/10.2307/5339openalex-snapshot
Regulation and Stability of a Free-Living Host-Parasite System: Trichostrongylus tenuis in Red Grouse. II. Population Models
inferredcites →https://doi.org/10.3354/dao032227openalex-snapshot
Macroparasites in cetaceans stranded on the northwestern Spanish Atlantic coast
inferredcites →https://doi.org/10.3354/meps008243openalex-snapshot
Interactions Between Breeding Seabird and Pelagic Fish Populations in the Southern Benguela Region
inferredcites →https://doi.org/10.7589/0090-3558-7.3.198openalex-snapshot
CONTRACAECIASIS IN PELICANIFORM BIRDS

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/zootaxa.5256.1.3zenodo-depositor-declared
The genus Contracaecum Raillet & Henry (Nematoda: Anisakidae): host and geographical distribution on Neotropical and Antarctic species
inferred← citeshttps://doi.org/10.1002/ece3.1192openalex-snapshot
Parasitism in early life: environmental conditions shape within‐brood variation in responses to infection
inferred← citeshttps://doi.org/10.1007/978-3-031-00303-5_13openalex-snapshot
Anisakiasis
inferred← citeshttps://doi.org/10.1007/978-3-7091-1782-8_11openalex-snapshot
Anisakiasis
inferred← citeshttps://doi.org/10.1007/s00300-013-1391-8openalex-snapshot
New data on gastrointestinal helminths in shags (Phalacrocorax verrucosus) at Kerguelen Archipelago
inferred← citeshttps://doi.org/10.1007/s00436-005-1366-yopenalex-snapshot
Genetic evidence for the existence of sibling species within Contracaecum rudolphii (Hartwich, 1964) and the validity of Contracaecum septentrionale (Kreis, 1955) (Nematoda: Anisakidae)
inferred← citeshttps://doi.org/10.1007/s00436-005-1372-0openalex-snapshot
Nematode parasites of the digestive tract in Neotropic cormorant chicks (Phalacrocorax brasilianus) from the River Cruces Ramsar site in southern Chile
inferred← citeshttps://doi.org/10.1007/s00436-009-1424-yopenalex-snapshot
Genetic and morphological evidences for the existence of sibling species within Contracaecum rudolphii (Hartwich, 1964) (Nematoda: Anisakidae) in Australia
inferred← citeshttps://doi.org/10.1007/s00436-023-08050-8openalex-snapshot
Multidisciplinary approach to the diagnosis of Contracaecum magnipapillatum infections in Australian black noddies, Anous minutus (Charadriiformes: Laridae)
inferred← citeshttps://doi.org/10.1007/s11230-007-9116-4openalex-snapshot
Contracaecum bioccai n. sp. from the brown pelican Pelecanus occidentalis (L.) in Colombia (Nematoda: Anisakidae): morphology, molecular evidence and its genetic relationship with congeners from fish-eating birds
inferred← citeshttps://doi.org/10.1007/s12639-025-01842-yopenalex-snapshot
Report on nematode parasites in spot-billed pelicans (Pelecanus philippensis) and painted storks (Mycteria leucocephala) from Telineelapuram, Srikakulam District, AP, India
inferred← citeshttps://doi.org/10.1016/j.exppara.2022.108335openalex-snapshot
Parasite identification in mullet fish (Mugil curema) from Chautengo Lagoon, Guerrero, Mexico, based on morphology and molecular analysis
inferred← citeshttps://doi.org/10.1016/j.mcp.2006.08.004openalex-snapshot
Practical PCR tools for the delineation of Contracaecum rudolphii A and Contracaecum rudolphii B (Ascaridoidea: Anisakidae) using genetic markers in nuclear ribosomal DNA
inferred← citeshttps://doi.org/10.1016/j.mcp.2013.02.004openalex-snapshot
Sequence variation in four mitochondrial genes among sibling species within Contracaecum rudolphii sensu lato
inferred← citeshttps://doi.org/10.1016/j.vetpar.2009.08.002openalex-snapshot
Larval Contracaecum sp. (Nematoda: Anisakidae) in the Great Cormorant [Phalacrocorax carbo (L., 1758)] from north-eastern Poland: A morphological and morphometric analysis
inferred← citeshttps://doi.org/10.1016/j.vprsr.2024.101106openalex-snapshot
First record of Contracaecum australe (Nematoda: Anisakidae) infecting Neotropic cormorant (Phalacrocorax brasilianus) (Aves: Phalacrocoracidae) in southern Brazil with a phylogenetic analysis
inferred← citeshttps://doi.org/10.1017/s0022149x11000046openalex-snapshot
Levels of infection of gastric nematodes in a flock of great cormorants (Phalacrocorax carbo) from Lake Biwa, Japan
inferred← citeshttps://doi.org/10.1017/s0022149x20000644openalex-snapshot
A new species ofContracaecum(Nematoda: Anisakidae) found parasitizingNannopterum brasilianus(Suliformes: Phalacrocoracidae) andHoplias argentinensis(Characiformes: Erythrinidae) in South America: morphological and molecular characterization of larval and adult stages
inferred← citeshttps://doi.org/10.1017/s0022149x25101120openalex-snapshot
New Contracaecum species (Nematoda, Anisakidae) parasitizing Ardea cocoi Linnaeus (Aves, Ardeidae) in a mixed infection: morphological and molecular studies in Argentina
inferred← citeshttps://doi.org/10.1017/s0022149x26101163openalex-snapshot
Diversity of helminths parasitising North-East Atlantic and Antarctic seabirds
inferred← citeshttps://doi.org/10.1017/s003118200700251xopenalex-snapshot
Genetic characterization of members of the genusContracaecum(Nematoda: Anisakidae) from fish-eating birds from west-central Florida, USA, with evidence of new species
inferred← citeshttps://doi.org/10.1017/s0031182016001700openalex-snapshot
Between-individual variation in nematode burden among juveniles in a wild host
inferred← citeshttps://doi.org/10.1017/s0031182020001341openalex-snapshot
New insights into the coexistence ofContracaecum rudolphiiA andContracaecum rudolphiiB (Nematoda: Anisakidae) inPhalacrocorax carbosinensis from Sardinia: genetic variability and phylogenetic analysis
inferred← citeshttps://doi.org/10.1017/s003118202200138xopenalex-snapshot
Large-scale genetic investigation of nematode diversity and their phylogenetic patterns in New Zealand's marine animals
inferred← citeshttps://doi.org/10.1017/s0031182023000902openalex-snapshot
Molecular and morphological studies onContracaecum rudolphiiA andC. rudolphiiB in great cormorants (Phalacrocorax carbo sinensis) from Italy and Israel
inferred← citeshttps://doi.org/10.1021/acs.est.0c03021openalex-snapshot
Interactions between Environmental Contaminants and Gastrointestinal Parasites: Novel Insights from an Integrative Approach in a Marine Predator
inferred← citeshttps://doi.org/10.1098/rspb.2018.0489openalex-snapshot
The energetic cost of parasitism in a wild population
inferred← citeshttps://doi.org/10.1111/2041-210x.12015openalex-snapshot
Endoscopy as a novel method for assessing endoparasite burdens in free‐ranging European shags (Phalacrocorax aristotelis)
inferred← citeshttps://doi.org/10.1134/s2075111720010129openalex-snapshot
Expansion of the Great Cormorant (Phalacrocorax carbo L. 1758) to the Northwest of Russia as a Possibility of the Spread of Parasites
inferred← citeshttps://doi.org/10.1242/jeb.190066openalex-snapshot
The role of parasitism in the energy management of a free-ranging bird
inferred← citeshttps://doi.org/10.1371/journal.pone.0032236openalex-snapshot
Impacts of Parasites in Early Life: Contrasting Effects on Juvenile Growth for Different Family Members
inferred← citeshttps://doi.org/10.1515/biolog-2015-0022openalex-snapshot
Parasitic helminths in grey heron (Ardea cinerea) chicks
inferred← citeshttps://doi.org/10.1515/ohs-2017-0017openalex-snapshot
Occurrence of Nematodes in the alimentary tract of great cormorants [Phalacrocorax carbo (Linnaeus, 1758)] in colonies located in the upper and lower Vistula River
inferred← citeshttps://doi.org/10.15446/ga.v24n2.97356openalex-snapshot
Contracaecum sp. (Nematode: Anisakidae) en peces de interés comercial en el golfo de Morrosquillo, Sucre - Colombia
inferred← citeshttps://doi.org/10.1590/s0101-81752006000400046openalex-snapshot
Contracaecum rudolphii Hartwich (Nematoda, Anisakidae) from the Neotropical Cormorant, Phalacrocorax brasilianus (Gmelin) (Aves, Phalacrocoracidae) in southern Brazil
inferred← citeshttps://doi.org/10.1590/s1984-29612023039openalex-snapshot
Morphological and molecular characterization of Contracaecum australe (Nematoda: Anisakidae) parasitizing Phalacrocorax brasilianus (Aves: Phalacrocoracidae) on the north coast of Brazil
inferred← citeshttps://doi.org/10.1645/ge-1369.1openalex-snapshot
A New Anisakid Species Parasitizing the Imperial Cormorant Phalacrocorax atriceps From the North Patagonian Coast, Argentina
inferred← citeshttps://doi.org/10.1645/ge-2450.1openalex-snapshot
Genetic and Morphological Evidences for the Existence of a New Species of Contracaecum (Nematoda: Anisakidae) Parasite of Phalacrocorax brasilianus (Gmelin) From Chile and Its Genetic Relationships with Congeners From Fish-Eating Birds
inferred← citeshttps://doi.org/10.1645/ge-2473.1openalex-snapshot
Population Biology of Contracaecum rudolphii Sensu Lato (Nematoda) in the Great Cormorant (Phalacrocorax carbo) from Northeastern Poland
inferred← citeshttps://doi.org/10.1645/ge-875r1.1openalex-snapshot
FURTHER STUDY OF CONTRACAECUM PELAGICUM (NEMATODA: ANISAKIDAE) IN SPHENISCUS MAGELLANICUS (AVES: SPHENISCIDAE) FROM ARGENTINEAN COASTS
inferred← citeshttps://doi.org/10.20350/digitalcsic/8810openalex-snapshot
Cormorán moñudo – Phalacrocorax aristotelis (Linnaeus, 1761)
inferred← citeshttps://doi.org/10.2478/acve-2024-0032openalex-snapshot
Pathological and Parasitological Findings in Serbian Great Cormorants Infected by Contracoecum rudolphii Sensu Lato
inferred← citeshttps://doi.org/10.2478/helm-2023-0034openalex-snapshot
Impact of anthropogenous environmental factors on the marine ecosystem of trophically transmitted helminths and hosting seabirds: Focus on North Atlantic, North Sea, Baltic and the Arctic seas
inferred← citeshttps://doi.org/10.2478/s11687-007-0013-9openalex-snapshot
Life cycle of the nematode Contracaecum rudolphii Hartwig, 1964 (sensu lato) from northern Poland under laboratory conditions
inferred← citeshttps://doi.org/10.2478/s11687-011-0006-6openalex-snapshot
Pathology associated with Contracaecum rudolphii (Nematoda: Anisakidae) infection in the great cormorant Phalacrocorax carbo (L. 1758)
inferred← citeshttps://doi.org/10.2478/s11756-012-0012-2openalex-snapshot
Black cormorant Phalacrocorax carbo (L., 1758) as a vector of fungi and parasites occurring in the gastrointestinal tract
inferred← citeshttps://doi.org/10.2478/s13545-014-0129-8openalex-snapshot
In vitro infection experiments with eggs of the nematode Contracaecum rudolphii Hartwich, 1964 (sensu lato) targeting aquatic insect larvae (Odonata: Coenagrionidae and Libellulidae; Trichoptera: Integripalpia) as possible intermediate hosts
inferred← citeshttps://doi.org/10.2478/v10009-008-0013-1openalex-snapshot
Infestation of the black cormorants (Phalacrocorax carbo sinensis L. 1758) from the colony on the Selment Wielki, with the nematode Contracaecum rudolphii Hartwich, 1964 (Nematoda, Anisakidae)
inferred← citeshttps://doi.org/10.3389/fvets.2023.1122291openalex-snapshot
Genetic diversity of Contracaecum rudolphii sp. A (Nematoda: Anisakidae) parasitizing the European Shag Phalacrocorax aristotelis desmarestii from the Spanish Mediterranean coast
inferred← citeshttps://doi.org/10.3390/parasitologia5030032openalex-snapshot
Gastrointestinal Helminths of Suliformes Birds from the Southern Coast of São Paulo, Brazil
inferred← citeshttps://doi.org/10.35537/10915/4323openalex-snapshot
Taxonomía y evaluación de la especificidad hospedatoria de nematodos Anisakidae parásitos de aves marinas en el área de Península Valdés, Chubut, Argentina
inferred← citeshttps://doi.org/10.5433/1679-0359.2020v41n4p1439openalex-snapshot
Seabirds: studies with parasitofauna and potential indicator for environmental anthropogenic impacts
inferred← citeshttps://doi.org/10.56714/bjrs.50.1.3openalex-snapshot
Recording of three species of the Contracaecum genus in Phalacrocorax pygmaeus and Phalacrocorax carbo in Basrah province
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