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Pathogens Of Wild And Farmed Fish
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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/jez.1402540213openalex-snapshot
A model for studying isolation mechanisms in parasite populations: The genus Lepeophtheirus (Copepoda, Caligidae)
inferredcites →https://doi.org/10.1016/0020-7519(92)90039-nopenalex-snapshot
Genetic heterogeneity within populations of Lepeophtheirus europaensis (Copepoda: Caligidae) parasitic on two host species
inferredcites →https://doi.org/10.1017/s0025315400058598openalex-snapshot
Infections with Parasitic Copepods in North Sea Marine Fishes
inferredcites →https://doi.org/10.1017/s0031182000063058openalex-snapshot
The population dynamics of Lepeophtheirus pectoralis (Müller): seasonal variation in abundance and age structure
inferredcites →https://doi.org/10.1017/s003118200006306xopenalex-snapshot
The population dynamics of Lepeophtheirus pectoralis (Müller): dispersion pattern
inferredcites →https://doi.org/10.1017/s0031182000081713openalex-snapshot
Characterization of two species ofLepeophtheirus(Copepoda, Caligidae) from flatfishes. Description ofLepeophtheirus europaensissp. nov
inferredcites →https://doi.org/10.1080/11250007809440264openalex-snapshot
La Méditerranée Creuset Ichthyologique
inferredcites →https://doi.org/10.1093/genetics/69.3.399openalex-snapshot
MORAN'S ISLAND MIGRATION MODEL
inferredcites →https://doi.org/10.1093/genetics/74.1.171openalex-snapshot
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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.5691.2.6zenodo-depositor-declared
Three new species of Lernanthropus (Copepoda: Siphonostomatoida) from Vietnam
inferred← citeshttps://doi.org/10.1002/9780470961568.chopenalex-snapshot
Introduction:Lepeophtheirus salmonis—A Remarkable Success Story
inferred← citeshttps://doi.org/10.1002/9780470961568.ch7openalex-snapshot
Salmon Louse Management on Farmed Salmon in Scotland
inferred← citeshttps://doi.org/10.1002/9781119152125.ch4openalex-snapshot
Parasitic Diseases in Aquaculture: Their Biology, Diagnosis and Control
inferred← citeshttps://doi.org/10.1006/fsim.1999.0229openalex-snapshot
Effects of sea lice (Lepeophtheirus salmonis Kröyer, 1837) infestation on macrophage functions in Atlantic salmon (Salmo salar L.)
inferred← citeshttps://doi.org/10.1006/fsim.1999.0260openalex-snapshot
Experimental exposure of rainbow trout Oncorhynchus mykiss (Walbaum) to the infective stages of the sea louseLepeophtheirus salmonis (Krøyer) influences the physiological response to an acute stressor
inferred← citeshttps://doi.org/10.1006/fsim.2001.0396openalex-snapshot
The function of Atlantic salmon (Salmo salar L.) antibodies under extremes of pH and osmolarity
inferred← citeshttps://doi.org/10.1006/jfbi.1996.0136openalex-snapshot
Hypometabolism in torpid goldsinny wrasse subjected to rapid reductions in seawater temperature
inferred← citeshttps://doi.org/10.1006/jfbi.1996.0137openalex-snapshot
Growth, diet and condition of corkwing wrasse and rock cook on the west coast of Scotland
inferred← citeshttps://doi.org/10.1006/jfbi.1996.0342openalex-snapshot
Parasites of wrasse (Labridae) in inshore waters of west Scotland stocked as cleaner fish of sea lice (Caligidae) on farmed Atlantic salmon
inferred← citeshttps://doi.org/10.1006/jmsc.2000.1040openalex-snapshot
Targeted environmental monitoring for the effects of medicines used to treat sea-lice infestation on farmed fish
inferred← citeshttps://doi.org/10.1007/0-306-47537-5_1openalex-snapshot
Why do symbiotic copepods matter?
inferred← citeshttps://doi.org/10.1007/0-306-47537-5_35openalex-snapshot
Annual changes in the population size of the salmon louse Lepeophtheirus salmonis (Copepoda: Caligidae) on high-seas Pacific Salmon (Oncorhynchus spp.), and relationship to host abundance
inferred← citeshttps://doi.org/10.1007/978-1-4020-8835-3_10openalex-snapshot
A Synopsis of Environmental Issues Associated with Salmon Aquaculture in Canada
inferred← citeshttps://doi.org/10.1007/978-3-030-42484-8_10openalex-snapshot
Evolutionary History of Crustaceans as Parasites
inferred← citeshttps://doi.org/10.1007/978-94-007-1189-1_10openalex-snapshot
Farmed Atlantic Salmon in Nature
inferred← citeshttps://doi.org/10.1007/978-94-007-5383-9_5openalex-snapshot
Injuries and deformities in fish: their potential impacts upon aquacultural production and welfare
inferred← citeshttps://doi.org/10.1007/bf00121626openalex-snapshot
Variation in sea lice infestation on Atlantic salmon smolts in Killary Harbour, West Coast of Ireland
inferred← citeshttps://doi.org/10.1007/s00436-011-2724-6openalex-snapshot
Lernanthropus kroyeri (Van Beneden and Hesse 1851) parasitic Copepoda (Siphonostomatoidae, Lernanthropidae) of European cultured sea bass Dicentrarchus labrax (Linnaeus 1758) from Corsica: ecological and morphological study
inferred← citeshttps://doi.org/10.1007/s10695-011-9557-1openalex-snapshot
Injuries and deformities in fish: their potential impacts upon aquacultural production and welfare
inferred← citeshttps://doi.org/10.1007/s10739-011-9299-zopenalex-snapshot
Science, Salmon, and Sea Lice: Constructing Practice and Place in an Environmental Controversy
inferred← citeshttps://doi.org/10.1007/s11071-019-05088-1openalex-snapshot
Dynamic analysis of a biocontrol of sea lice by age-structured model
inferred← citeshttps://doi.org/10.1007/s11160-010-9169-3openalex-snapshot
A review of the use of copepods in marine fish larviculture
inferred← citeshttps://doi.org/10.1007/s12601-012-0018-2openalex-snapshot
Seasonal occurrence and microhabitat of the hyperparasitic monogenean Udonella fugu on the caligid Copepod Pseudocaligus fugu infecting the grass puffer Takifugu niphobles in the Seto Inland Sea, Japan
inferred← citeshttps://doi.org/10.1007/s41208-018-0088-8openalex-snapshot
The Life Cycle of Caligus minimus on Seabass (Lates calcarifer) from Floating Cage Culture
inferred← citeshttps://doi.org/10.1016/0022-0981(96)00008-1openalex-snapshot
Observations on mating and reproductive behaviour of Lepeophtheirus salmonis, Krøyer (Copepoda: Caligidae)
inferred← citeshttps://doi.org/10.1016/0044-8486(94)00331-hopenalex-snapshot
The use of cleaner-fish to control sea lice on two Irish salmon (Salmo salar) farms with particular reference to wrasse behaviour in salmon cages
inferred← citeshttps://doi.org/10.1016/0044-8486(95)01245-1openalex-snapshot
Use of cleaner-wrasse (Centrolabrus exoletus (L.) and Ctenolabrus rupestris (L.)) to control infestations of Caligus elongatus Nordmann on farmed Atlantic salmon
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2004.07.021openalex-snapshot
Carbon and nitrogen stable isotopes: a tool to differentiate between Lepeophtheirus salmonis and different salmonid host species?
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2004.07.030openalex-snapshot
Individual variation in sea lice (Lepeophtheirus salmonis) infection on Atlantic salmon (Salmo salar)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2004.12.027openalex-snapshot
A review of the Norwegian ‘National Action Plan Against Salmon Lice on Salmonids’: The effect on wild salmonids
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2006.02.043openalex-snapshot
Use of hydrogen peroxide against the fish pathogen Tenacibaculum maritimum and its effect on infected turbot (Scophthalmus maximus)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2006.12.039openalex-snapshot
A proposed life history strategy for the salmon louse, Lepeophtheirus salmonis in the subarctic Pacific
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2007.03.020openalex-snapshot
Risk assessment for metazoan parasites of yellowtail kingfish Seriola lalandi (Perciformes: Carangidae) in South Australian sea-cage aquaculture
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2007.05.025openalex-snapshot
Behavioural studies of host, non-host and mate location by the Sea Louse, Caligus rogercresseyi Boxshall & Bravo, 2000 (Copepoda: Caligidae)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2008.04.016openalex-snapshot
Evaluation of testing strategies for infectious salmon anaemia and implications for surveillance and control programs
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2008.12.005openalex-snapshot
The settlement and survival of the salmon louse, Lepeophtheirus salmonis (Krøyer, 1837), on atypical hosts
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2009.03.006openalex-snapshot
Susceptibility of Atlantic salmon and rainbow trout to the salmon lice Lepeophtheirus salmonis
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2009.06.028openalex-snapshot
Effects of experimental infection by Caligus rogercresseyi (Copepoda: Caligidae) on the common jollytail, Galaxias maculatus (Osmeriforme: Galaxiidae) (Jenyns, 1842) in Chile
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2010.10.037openalex-snapshot
Salmon lice-induced mortality of Atlantic salmon postsmolts experiencing episodic acidification and recovery in freshwater
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2010.11.020openalex-snapshot
Environmental drivers of Atlantic salmon behaviour in sea-cages: A review
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2011.01.029openalex-snapshot
A baseline method for benchmarking mortality losses in Atlantic salmon (Salmo salar) production
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2011.02.014openalex-snapshot
Disease interaction and pathogens exchange between wild and farmed fish populations with special reference to Norway
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2011.03.032openalex-snapshot
The spatial distribution patterns of Caligus rogercresseyi and C. elongatus on Atlantic salmon hosts (Salmo salar)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2012.03.029openalex-snapshot
Confidence in assessing the effectiveness of bath treatments for the control of sea lice on Norwegian salmon farms
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2013.04.010openalex-snapshot
Effects of temperature, diet, and bivalve size on the ingestion of sea lice (Lepeophtheirus salmonis) larvae by various filter-feeding shellfish
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2013.11.027openalex-snapshot
Assessment of sea lice (Lepeophtheirus salmonis) management in New Brunswick, Canada using deltamethrin (AlphaMax®) through clinical field treatment and laboratory bioassay responses
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2014.09.009openalex-snapshot
Factors affecting the abundance of Caligus rogercresseyi (Boxshall and Bravo) on farmed salmonids in Chile in the period 2006–2007
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2015.03.011openalex-snapshot
The effect of chemotherapeutic drugs used to control sea lice on the hatching viability of egg strings from Caligus rogercresseyi
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2015.08.009openalex-snapshot
Multivariate evaluation of the effectiveness of delousing treatment efficacy of azamethiphos (Salmosan®) against the salmon louse ( Lepeophtheirus salmonis ) in Atlantic salmon ( Salmo salar ) using wellboat, skirt and tarpaulin treatment modalities
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2020.735170openalex-snapshot
More than bubbles: In vivo assessment and transcriptome modulation of Caligus rogercresseyi and Atlantic salmon exposed to hydrogen peroxide (PARAMOVE®)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.742007openalex-snapshot
Exposures to hydrogen peroxide impact healing, redox and oxygen transport differentially from immune mechanisms in the gill of Atlantic Salmon (Salmo salar)
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2008.05.005openalex-snapshot
Antifouling enzymes and the biochemistry of marine settlement
inferred← citeshttps://doi.org/10.1016/j.cbd.2011.04.001openalex-snapshot
Differentiating size-dependent responses of juvenile pink salmon (Oncorhynchus gorbuscha) to sea lice (Lepeophtheirus salmonis) infections
inferred← citeshttps://doi.org/10.1016/j.exppara.2009.08.017openalex-snapshot
Cytochrome oxidase I sequences reveal possible cryptic diversity in the cosmopolitan symbiotic copepod Nesippus orientalis Heller, 1868 (Pandaridae: Siphonostomatoida) on elasmobranch hosts from the KwaZulu-Natal coast of South Africa
inferred← citeshttps://doi.org/10.1016/j.exppara.2009.12.001openalex-snapshot
The reproductive output of sea lice Caligus rogercresseyi under controlled conditions
inferred← citeshttps://doi.org/10.1016/j.fishres.2005.06.007openalex-snapshot
Sea lice on adult Pacific salmon in the coastal waters of Central British Columbia, Canada
inferred← citeshttps://doi.org/10.1016/j.fsi.2005.11.010openalex-snapshot
The effects of Lepeophtheirus salmonis infections on the stress response and immunological status of Atlantic salmon (Salmo salar)
inferred← citeshttps://doi.org/10.1016/j.fsi.2007.12.013openalex-snapshot
Transcriptional analysis of the common carp (Cyprinus carpio L.) immune response to the fish louse Argulus japonicus Thiele (Crustacea: Branchiura)
inferred← citeshttps://doi.org/10.1016/j.icesjms.2005.10.009openalex-snapshot
Diseases of gadoid fish in cultivation: a review
inferred← citeshttps://doi.org/10.1016/j.icesjms.2006.04.011openalex-snapshot
Exceptional marine survival of pink salmon that entered the marine environment in 2003 suggests that farmed Atlantic salmon and Pacific salmon can coexist successfully in a marine ecosystem on the Pacific coast of Canada
inferred← citeshttps://doi.org/10.1016/j.icesjms.2006.04.017openalex-snapshot
A review of the biology and genetics of sea lice
inferred← citeshttps://doi.org/10.1016/j.ijpara.2004.02.004openalex-snapshot
Molecular characterisation of five trypsin-like peptidase transcripts from the salmon louse (Lepeophtheirus salmonis) intestine
inferred← citeshttps://doi.org/10.1016/j.ijpara.2009.04.004openalex-snapshot
Functional characterisation of the maternal yolk-associated protein (LsYAP) utilising systemic RNA interference in the salmon louse (Lepeophtheirus salmonis) (Crustacea: Copepoda)
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2008.12.009openalex-snapshot
A new generation of biocides for control of crustacea in fish farms
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2005.02.001openalex-snapshot
Sea lice treatments on salmon farms have no adverse effects on zooplankton communities: a case study
inferred← citeshttps://doi.org/10.1016/j.parint.2006.12.003openalex-snapshot
Metazoan parasite assemblages of wild Seriola lalandi (Carangidae) from eastern and southern Australia
inferred← citeshttps://doi.org/10.1016/j.parint.2009.08.009openalex-snapshot
Establishment and characterisation of salmon louse (Lepeophtheirus salmonis (Krøyer 1837)) laboratory strains
inferred← citeshttps://doi.org/10.1016/j.prevetmed.2006.09.006openalex-snapshot
Hydrographics and the timing of infectious salmon anemia outbreaks among Atlantic salmon (Salmo salar L.) farms in the Quoddy region of Maine, USA and New Brunswick, Canada
inferred← citeshttps://doi.org/10.1016/j.pt.2006.08.006openalex-snapshot
Ecology of sea lice parasitic on farmed and wild fish
inferred← citeshttps://doi.org/10.1016/j.rvsc.2007.09.007openalex-snapshot
The first report of phototaxis of fish ectoparasite, Argulus japonicus
inferred← citeshttps://doi.org/10.1016/j.toxicon.2006.04.019openalex-snapshot
Accumulation of tetrodotoxin (TTX) in Pseudocaligus fugu, a parasitic copepod from panther puffer Takifugu pardalis, but without vertical transmission—Using an immunoenzymatic technique
inferred← citeshttps://doi.org/10.1016/j.toxicon.2007.06.021openalex-snapshot
Isolation and characterization of bacteria from the copepod Pseudocaligus fugu ectoparasitic on the panther puffer Takifugu pardalis with the emphasis on TTX
inferred← citeshttps://doi.org/10.1016/j.vetpar.2009.06.016openalex-snapshot
Selected parasitosis in cultured and wild fish
inferred← citeshttps://doi.org/10.1016/j.vetpar.2011.08.008openalex-snapshot
Caligidae infestation in Asian seabass, Lates calcarifer, Bloch 1790 cultured at different salinity in Malaysia
inferred← citeshttps://doi.org/10.1016/j.vetpar.2012.02.003openalex-snapshot
Prevalence, mean intensity and site preference of Caligus rotundigenitalis Yü, 1933 (Copepoda: Caligidae) on cage cultured crimson snapper (Lutjanus erythropterus Bloch, 1790) from Bukit Tambun, Penang, Malaysia
inferred← citeshttps://doi.org/10.1016/j.ympev.2007.02.004openalex-snapshot
Extraordinary host switching in siphonostomatoid copepods and the demise of the Monstrilloida: Integrating molecular data, ontogeny and antennulary morphology
inferred← citeshttps://doi.org/10.1016/s0020-7519(98)00175-1openalex-snapshot
Egg development, hatching and early life-history of Dissonus manteri (Copepoda),parasitic on the gills of coral trout, Plectropomus leopardus
inferred← citeshttps://doi.org/10.1016/s0022-0981(96)02696-2openalex-snapshot
Genetic differentiation of populations of the copepod sea louse Lepeophtheirus salmonis (Krøyer) ectoparasitic on wild and farmed salmonids around the coasts of Scotland: Evidence from RAPD markers
inferred← citeshttps://doi.org/10.1016/s0022-0981(98)00081-1openalex-snapshot
An assessment of the acute impact of the sea lice treatment ivermectin on a benthic community
inferred← citeshttps://doi.org/10.1016/s0044-8486(00)00308-2openalex-snapshot
Seasonal population dynamics of parasitic copepods, Sinergasilus spp. on farmed fish in China
inferred← citeshttps://doi.org/10.1016/s0044-8486(00)00309-4openalex-snapshot
Selection of host sample number and design of a monitoring programme for ectoparasitic sea lice (Copepoda: Caligidae) on farmed Atlantic salmon, Salmo salar
inferred← citeshttps://doi.org/10.1016/s0044-8486(02)00189-8openalex-snapshot
The effect of artificial light treatment and depth on the infestation of the sea louse Lepeophtheirus salmonis on Atlantic salmon (Salmo salar L.) culture
inferred← citeshttps://doi.org/10.1016/s0044-8486(02)00339-3openalex-snapshot
Determination of reduced sensitivity in sea lice (Lepeophtheirus salmonis Krøyer) against the pyrethroid deltamethrin using bioassays and probit modelling
inferred← citeshttps://doi.org/10.1016/s0044-8486(02)00512-4openalex-snapshot
Life cycle of Caligus rogercresseyi, (Copepoda: Caligidae) parasite of Chilean reared salmonids
inferred← citeshttps://doi.org/10.1016/s0044-8486(03)00454-xopenalex-snapshot
A comparison of sea louse (Lepeophtheirus salmonis) infection levels in farmed and wild Atlantic salmon (Salmo salar L.) stocks
inferred← citeshttps://doi.org/10.1016/s0044-8486(96)01267-7openalex-snapshot
The efficacy of hydrogen peroxide for the treatment of farmed Atlantic salmon, Salmo salar L. infested with sea lice (Copepoda: Caligidae)
inferred← citeshttps://doi.org/10.1016/s0044-8486(97)00037-9openalex-snapshot
The effects of hydrogen peroxide on the gill tissues of Atlantic salmon, Salmo solar L.
inferred← citeshttps://doi.org/10.1016/s0044-8486(97)00209-3openalex-snapshot
Environmental risk from dissolved ivermectin to marine organisms
inferred← citeshttps://doi.org/10.1016/s0044-8486(97)00210-xopenalex-snapshot
Acute toxicity of ivermectin to the lugworm Arenicola marina
inferred← citeshttps://doi.org/10.1016/s0044-8486(98)00211-7openalex-snapshot
Environmental risk of ivermectin to sediment dwelling organisms
inferred← citeshttps://doi.org/10.1016/s0044-8486(98)00301-9openalex-snapshot
Native sea lice (Copepoda: Caligidae) infestation of salmonids reared in netpen systems in southern Chile
inferred← citeshttps://doi.org/10.1016/s0044-8486(99)00282-3openalex-snapshot
Differential infectivity of Caligus flexispina (Copepoda, Caligidae) in three farmed salmonids in Chile
inferred← citeshttps://doi.org/10.1016/s0044-8486(99)00374-9openalex-snapshot
Field trials to evaluate the efficacy of emamectin benzoate in the control of sea lice, Lepeophtheirus salmonis (Krøyer) and Caligus elongatus Nordmann, infestations in Atlantic salmon Salmo salar L.
inferred← citeshttps://doi.org/10.1016/s0065-308x(07)65005-2openalex-snapshot
A Review of the Biology of the Parasitic Copepod Lernaeocera branchialis (L., 1767) (Copepoda: Pennellidae)
inferred← citeshttps://doi.org/10.1016/s0065-308x(08)60233-xopenalex-snapshot
Sealice on Salmonids: Their Biology and Control
inferred← citeshttps://doi.org/10.1016/s0144-8609(98)00020-xopenalex-snapshot
Use of mesocosms in larval rearing of saithe [Pollachius virens (L.)], goldsinny [Ctenolabrus rupestris (L.)], and corkwing [Crenilabrus melops (L.)]
inferred← citeshttps://doi.org/10.1016/s0145-305x(01)00039-8openalex-snapshot
The occurrence and mechanisms of innate immunity against parasites in fish
inferred← citeshttps://doi.org/10.1016/s0304-4017(99)00039-4openalex-snapshot
Parasites in cultured and feral fish
inferred← citeshttps://doi.org/10.1016/s0924-7963(97)00046-8openalex-snapshot
Copepod reproductive strategies: life-history theory, phylogenetic pattern and invasion of inland waters
inferred← citeshttps://doi.org/10.1016/s0924-7963(97)00056-0openalex-snapshot
Distant water sailors: parasitic Copepoda of the open ocean
inferred← citeshttps://doi.org/10.1016/s1054-3139(03)00088-2openalex-snapshot
Differing susceptibility of anadromous brown trout (Salmo trutta L.) populations to salmon louse (Lepeophtheirus salmonis (Krøyer, 1837)) infection
inferred← citeshttps://doi.org/10.1016/s1546-5098(05)24007-4openalex-snapshot
Behavioural Physiology of Fish Migrations: salmon as a model approach
inferred← citeshttps://doi.org/10.1017/s0022149x00015388openalex-snapshot
Benedeniine capsalid monogeneans from Australian fishes: pathogenic species, site-specificity and camouflage
inferred← citeshttps://doi.org/10.1017/s0025315400029064openalex-snapshot
Planktonic Dispersion of Larval Salmon-Lice,Lepeophtheirus Salmonis, Associated with Cultured Salmon,Salmo Salar, in Western Ireland
inferred← citeshttps://doi.org/10.1017/s002531540003825xopenalex-snapshot
Experimental Evidence for Aggregation of Salmon Louse Copepodids (Lepeophtheirus Salmonis) in Step Salinity Gradients
inferred← citeshttps://doi.org/10.1017/s0025315400044830openalex-snapshot
Planktonic Distribution of Sea Lice Larvae, Lepeophtheirus Salmonis, in Killary Harbour, West Coast of Ireland
inferred← citeshttps://doi.org/10.1017/s0031182000085097openalex-snapshot
Niche restriction in parasites: proximate and ultimate causes
inferred← citeshttps://doi.org/10.1017/s003118201100014xopenalex-snapshot
Determinants of life-history traits in a fish ectoparasite: a hierarchical analysis
inferred← citeshttps://doi.org/10.1023/a:1013139212227openalex-snapshot
Why do symbiotic copepods matter?
inferred← citeshttps://doi.org/10.1023/a:1013154403992openalex-snapshot
Annual changes in the population size of the salmon louse Lepeophtheirus salmonis (Copepoda: Caligidae) on high-seas Pacific Salmon (Oncorhynchus spp.), and relationship to host abundance
inferred← citeshttps://doi.org/10.1038/srep43465openalex-snapshot
Parasitism perturbs the mucosal microbiome of Atlantic Salmon
inferred← citeshttps://doi.org/10.1039/9781839165795-00179openalex-snapshot
GABAergic Neurotransmission and Toxicity 2: Macrocyclic Lactones
inferred← citeshttps://doi.org/10.1039/9781849733007-00427openalex-snapshot
Macrocyclic Lactone Endectocides
inferred← citeshttps://doi.org/10.1039/9781849735483-00150openalex-snapshot
Veterinary Products Containing Pesticide Active Ingredients
inferred← citeshttps://doi.org/10.1039/b913772fopenalex-snapshot
Biomimetic silica encapsulation of enzymes for replacement of biocides in antifouling coatings
inferred← citeshttps://doi.org/10.1046/j.1365-2109.2000.00515.xopenalex-snapshot
Juvenile Lepeophtheirus salmonis (Krøyer) affect the skin and gills of rainbow trout Oncorhynchus mykiss (Walbaum) and the host response to a handling procedure
inferred← citeshttps://doi.org/10.1051/alr/2012007openalex-snapshot
Sea caged Atlantic salmon display size-dependent swimming depth
inferred← citeshttps://doi.org/10.1079/9781800629066.0017openalex-snapshot
Fisheries for cleaner fish species in Europe
inferred← citeshttps://doi.org/10.1080/00222899709600843openalex-snapshot
Editorial Policy and Instructions for Authors
inferred← citeshttps://doi.org/10.1080/00222930902993757openalex-snapshot
Developmental stages and growth ofPseudocaligus fuguYamaguti, 1936 (Copepoda: Siphonostomatoida: Caligidae) host-specific to Puffer
inferred← citeshttps://doi.org/10.1080/00222933.2012.738830openalex-snapshot
Localization and transcription patterns of LsVasa, a molecular marker of germ cells inLepeophtheirus salmonis(Krøyer)
inferred← citeshttps://doi.org/10.1080/00222933.2015.1022615openalex-snapshot
Parasitic copepods of marine fish cultured in Japan: a review
inferred← citeshttps://doi.org/10.1080/10641260500207109openalex-snapshot
The Effects of Water Temperature, Salinity, and Currents on the Survival and Distribution of the Infective Copepodid Stage of Sea Lice ( Lepeophtheirus Salmonis ) Originating on Atlantic Salmon Farms in the Broughton Archipelago of British Columbia, Canada
inferred← citeshttps://doi.org/10.1093/icb/icp033openalex-snapshot
Parasitic crustaceans as vectors of viruses, with an emphasis on three penaeid viruses
inferred← citeshttps://doi.org/10.1093/icb/icw084openalex-snapshot
Parasite Rates of Discovery, Global Species Richness and Host Specificity
inferred← citeshttps://doi.org/10.1093/icesjms/fsab069openalex-snapshot
The effect of a warmer climate on the salmon lice infection pressure from Norwegian aquaculture
inferred← citeshttps://doi.org/10.1093/icesjms/fsl029openalex-snapshot
Differences in risks and consequences of salmon louse, Lepeophtheirus salmonis (Krøyer), infestation on sympatric populations of Atlantic salmon, brown trout, and Arctic charr within northern fjords
inferred← citeshttps://doi.org/10.1093/icesjms/fsx222openalex-snapshot
Salmon lice evasion, susceptibility, retention, and development differ amongst host salmonid species
inferred← citeshttps://doi.org/10.1093/icesjms/fsy015openalex-snapshot
Production, mortality, and infectivity of planktonic larval sea lice, Lepeophtheirus salmonis (Krøyer, 1837): current knowledge and implications for epidemiological modelling
inferred← citeshttps://doi.org/10.1093/icesjms/fsz256openalex-snapshot
Prediction of the salmon lice infestation pressure in a Norwegian fjord
inferred← citeshttps://doi.org/10.1093/plankt/20.11.2129openalex-snapshot
Perception of inert particles by calanoid copepods: behavioral observations and a numerical model
inferred← citeshttps://doi.org/10.1093/plankt/fbl060openalex-snapshot
Water flow around a fish mimic attracts a parasitic and deters a planktonic copepod
inferred← citeshttps://doi.org/10.1093/plankt/fbu025openalex-snapshot
The chemical ecology of copepods
inferred← citeshttps://doi.org/10.1098/rstb.1998.0232openalex-snapshot
Preface to the Themed Discussion on ‘Mating biology of copepod crustaceans’
inferred← citeshttps://doi.org/10.1098/rstb.1998.0241openalex-snapshot
Patterns of pair formation and mating in an ectoparasitic caligid copepod Lepeophtheirus salmonis (Krøyer 1837): implications for its sensory and mating biology
inferred← citeshttps://doi.org/10.1101/026583openalex-snapshot
A Model For Sea Lice (Lepeophtheirus salmonis) Dynamics In A Seasonally Changing Environment)
inferred← citeshttps://doi.org/10.1111/are.12460openalex-snapshot
Effects ofCaligus rogercresseyi(Boxshall & Bravo 2000) chalimus stage condition (dead, moribund, live) on the estimates of Cypermethrin BETAMAX®efficacy
inferred← citeshttps://doi.org/10.1111/ede.12000openalex-snapshot
The lunule of caligid copepods: an evolutionarily novel structure
inferred← citeshttps://doi.org/10.1111/j.1095-8649.1996.tb00004.xopenalex-snapshot
Exposure of goldsinny, rock cook and corkwing wrasse to low temperature and low salinity: survival, blood physiology and seasonal variation
inferred← citeshttps://doi.org/10.1111/j.1365-2109.2004.01097.xopenalex-snapshot
Management actions in relation to the controversy about salmon lice infections in fish farms as a hazard to wild salmonid populations
inferred← citeshttps://doi.org/10.1111/j.1523-1739.2008.01128.xopenalex-snapshot
Sea‐Cage Aquaculture, Sea Lice, and Declines of Wild Fish
inferred← citeshttps://doi.org/10.1111/j.1749-7345.1998.tb00676.xopenalex-snapshot
Modification of Walleyes Stizostedion vitreum Tolerance to Hydrogen Peroxide Bath Treatment
inferred← citeshttps://doi.org/10.1111/jfd.13141openalex-snapshot
The filter‐feeding bivalve Mytilus chilensis capture pelagic stages of Caligus rogercresseyi: A potential controller of the sea lice fish parasites
inferred← citeshttps://doi.org/10.1139/d98-021openalex-snapshot
Diseases and parasites in wild Atlantic salmon (Salmo salar) populations
inferred← citeshttps://doi.org/10.1139/f04-069openalex-snapshot
Population genetic differentiation of sea lice (Lepeophtheirus salmonis) parasitic on Atlantic and Pacific salmonids: analyses of microsatellite DNA variation among wild and farmed hosts
inferred← citeshttps://doi.org/10.1139/f09-094openalex-snapshot
Monitoring and potential control of sea lice using an LED-based light trap
inferred← citeshttps://doi.org/10.1139/z95-009openalex-snapshot
Life cycle of a sea louse, Caligus elongatus von Nordmann, 1832 (Copepoda, Siphonostomatoida, Caligidae)
inferred← citeshttps://doi.org/10.1139/z96-161openalex-snapshot
The developmental stages of Caligus elongatus von Nordmann, 1832 (Copepoda: Caligidae)
inferred← citeshttps://doi.org/10.1163/20021975-99990187openalex-snapshot
WHY INFESTATION BY LEPEOPHTHEIRUS SALMONIS (COPEPODA:CALIGIDAE) IS NOT A PROBLEM IN THE COHO SALMON FARMING INDUSTRY IN JAPAN
inferred← citeshttps://doi.org/10.1163/ej.9789004174252.i-354.30openalex-snapshot
Recent Advances In The Biology Of The Parasitic Copepod Pseudocaligus Fugu (Siphonostomatoida, Caligidae), Host Specific To Pufferfishes Of The Genus Takifugu (Actinopterygii, Tetraodontidae)
inferred← citeshttps://doi.org/10.11646/zootaxa.3920.2.8openalex-snapshot
New records of sea lice (Copepoda: Caligidae) from marine fishes in Jaramijó, an area with potential for sea-cage aquaculture in Ecuador
inferred← citeshttps://doi.org/10.1186/1471-2164-9-126openalex-snapshot
Salmon louse (Lepeophtheirus salmonis) transcriptomes during post molting maturation and egg production, revealed using EST-sequencing and microarray analysis
inferred← citeshttps://doi.org/10.1186/1746-6148-9-258openalex-snapshot
Multivariate evaluation of the effectiveness of treatment efficacy of cypermethrin against sea lice (Lepeophtheirus salmonis) in Atlantic salmon (Salmo salar)
inferred← citeshttps://doi.org/10.1186/1756-3305-6-336openalex-snapshot
Multiple gene analyses of caligid copepods indicate that the reduction of a thoracic appendage in Pseudocaligus represents convergent evolution
inferred← citeshttps://doi.org/10.1242/jeb.203.11.1649openalex-snapshot
Ontogenetic Changes in Visual Sensitivity of The Parasitic Salmon Louse Lepeophtheirus Salmonis
inferred← citeshttps://doi.org/10.12782/sd.17.2.201openalex-snapshot
Records of Adult Caligiform Copepods (Crustacea: Copepoda: Siphonostomatoida) in Marine Plankton from East Asia, Including Descriptions of Two New Species of Caligus (Caligidae)
inferred← citeshttps://doi.org/10.1300/j028v14n03_03openalex-snapshot
Stability of Hydrogen Peroxide in Aquaria as a Fish Disease Treatment
inferred← citeshttps://doi.org/10.1371/journal.pone.0001549openalex-snapshot
The Efficacy of Emamectin Benzoate against Infestations of Lepeophtheirus salmonis on Farmed Atlantic Salmon (Salmo salar L) in Scotland, 2002–2006
inferred← citeshttps://doi.org/10.1371/journal.pone.0077832openalex-snapshot
Identification of a Sex-Linked SNP Marker in the Salmon Louse (Lepeophtheirus salmonis) Using RAD Sequencing
inferred← citeshttps://doi.org/10.14295/cs.v7i1.1248openalex-snapshot
Gyrodactylus anguillae and Vibrio vulnificus infections affecting cultured eel, Anguilla anguilla
inferred← citeshttps://doi.org/10.14411/fp.2003.049openalex-snapshot
Observations on the metazoan parasites of the Atlantic salmon (Salmo salar) after its reintroduction into the Elbe River basin in the Czech Republic
inferred← citeshttps://doi.org/10.14411/fp.2015.004openalex-snapshot
Developmental stages and fecundity of Lepeophtheirus simplex (Copepoda: Caligidae) parasitic on bullseye puffer fish (Sphoeroides annulatus)
inferred← citeshttps://doi.org/10.1577/1548-8667(2002)014<0095:ateoih>2.0.co;2openalex-snapshot
Assessing the Effects of Increasing Hydrogen Peroxide Dosage on Rainbow Trout Gills Utilizing a Digitized Scoring Methodology
inferred← citeshttps://doi.org/10.1577/1548-8667(2002)014<0154:qsogpo>2.0.co;2openalex-snapshot
Quantitative Scoring of Gill Pathology of Walleyes Exposed to Hydrogen Peroxide
inferred← citeshttps://doi.org/10.15832/tbd.71968openalex-snapshot
Clavellotis briani (Copepoda, Lernaeopodidae) Infestation on Striped Seabream, Lithognathus mormyrus (Sparidae) from the Northeast Mediterranean Sea, Turkey
inferred← citeshttps://doi.org/10.1590/s1519-69842004000100019openalex-snapshot
Community ecology of the metazoan parasites of white sea catfish, Netuma barba (Osteichthyes: Ariidae), from the coastal zone of the state of Rio de Janeiro, Brazil
inferred← citeshttps://doi.org/10.1590/s1984-29612012000300031openalex-snapshot
First record of Caligus mutabilis (Copepoda: Caligidae), in sea-farmed Mycteroperca microlepis (Perciformes: Serranidae) in Brazil
inferred← citeshttps://doi.org/10.2108/zsj.18.423openalex-snapshot
Occurrence of Caligus lalandei Barnard, 1948 (Copepoda, Siphonostomatoida) on Amberjacks (Seriola spp.) in the Western North Pacific
inferred← citeshttps://doi.org/10.2331/suisan.73.693openalex-snapshot
Prevalence, intensity and reproduction of copepods parasitic on temperate bass Lateolabrax japonicus collected from Ariake Sea
inferred← citeshttps://doi.org/10.2527/af.2014-0004openalex-snapshot
Lepeophtheirus salmonis: a persisting challenge for salmon aquaculture
inferred← citeshttps://doi.org/10.3147/jsfp.31.129openalex-snapshot
Two Species of Caligidae(Copepoda) Parasitic on Cultured Rabbit Fish(Siganus fuscescens) in Taiwan.
inferred← citeshttps://doi.org/10.3354/meps303225openalex-snapshot
Polyandry in the ectoparasitic copepod Lepeophtheirus salmonis despite complex precopulatory and postcopulatory mate-guarding
inferred← citeshttps://doi.org/10.3390/ani10071166openalex-snapshot
Fin Erosion of Salmo salar (Linnaeus 1758) Infested with the Parasite Caligus rogercresseyi (Boxshall & Bravo 2000)
inferred← citeshttps://doi.org/10.3390/parasitologia6050058openalex-snapshot
Detection of Tenacibaculum spp. in Caligus rogercresseyi: Evidence of Potential Pathogen Carriage in Salmon Aquaculture
inferred← citeshttps://doi.org/10.3390/pathogens12030460openalex-snapshot
Are We Ready to Get Rid of the Terms “Chalimus” and ”Preadult” in the Caligid (Crustacea: Copepoda: Caligidae) Life Cycle Nomenclature?
inferred← citeshttps://doi.org/10.3390/vaccines12070732openalex-snapshot
Transforming Aquaculture through Vaccination: A Review on Recent Developments and Milestones
inferred← citeshttps://doi.org/10.3750/aip2004.34.2.01openalex-snapshot
Opercular lesion in wild black drum, Pogonias cromis (Linnaeus, 1766), associated with attachment of the sea louse Sciaenophilus tenuis (Copepoda: Siphonostomatoida: Caligidae)
inferred← citeshttps://doi.org/10.3800/pbr.20.s202openalex-snapshot
A checklist of the parasitic copepods of Taiwanese aquatic animals (1930–2024), with a note on Ju-shey Ho’s contribution to clarifying the parasitic copepod fauna of Taiwan
inferred← citeshttps://doi.org/10.3800/pbr.3.202openalex-snapshot
Descriptions of caligiform copepods in plankton samples collected from East Asia: Accidental occurrences or a new mode of life cycle?
Editorial review for independent work. ICSAC — the Institute for Complexity
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