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Clearance effects of the Pacific oyster Crassostrea gigas on the fish-killing algae Chattonella marina and Chattonella antiqua
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00351343openalex-snapshot
Inhibitory effect of the iron chelator desferrioxamine (Desferal) on the generation of activated oxygen species by Chattonella marina
inferredcites →https://doi.org/10.1007/bf00356297openalex-snapshot
Oxygen-radical-mediated toxic effects of the red tide flagellate Chattonella marina on Vibrio alginolyticus
inferredcites →https://doi.org/10.1007/bf00393048openalex-snapshot
Ultrastructural alterations on chloride cells of the yellowtail Seriola quinqueradiata, following exposure to the red tide species Chattonella antiqua
inferredcites →https://doi.org/10.1007/bf01042181openalex-snapshot
Free radical production by the red tide alga,Chattonella antiqua
inferredcites →https://doi.org/10.1007/bf01951699openalex-snapshot
Morphological and histochemical demonstration of a glycocalyx on the cell surface ofChattonella antiqua, a ‘naked flagellate’
inferredcites →https://doi.org/10.1007/bf02118427openalex-snapshot
Generation of superoxide anions byChattonella antiqua: Possible causes for fish death caused by ‘Red Tide’
inferredcites →https://doi.org/10.1007/s002270000314openalex-snapshot
Nuclear ITS region of the alga Heterosigma akashiwo (Chromophyta: Raphidophyceae) is identical in isolates from Atlantic and Pacific basins
inferredcites →https://doi.org/10.1007/s002270050331openalex-snapshot
Lectin-induced enhancement of superoxide anion production by red tide phytoplankton
inferredcites →https://doi.org/10.1016/0003-9861(92)90133-hopenalex-snapshot
Hydroxyl radical generation by red tide algae
inferredcites →https://doi.org/10.1016/0048-9697(95)04675-4openalex-snapshot
Resistance of bivalves to anoxia as a response to pollution-induced environmental stress
inferredcites →https://doi.org/10.1016/0304-4165(94)00184-yopenalex-snapshot
Properties of hemagglutinins newly separated from toxic phytoplankton
inferredcites →https://doi.org/10.1016/0742-8413(95)02101-9openalex-snapshot
Anoxic or aerial survival of bivalves and other euryoxic invertebrates as a useful response to environmental stress—A comprehensive review
inferredcites →https://doi.org/10.1016/j.aquatox.2005.01.007openalex-snapshot
Hydrogen peroxide is not the cause of fish kills associated with Chattonella marina: Cytological and physiological evidence
inferredcites →https://doi.org/10.1016/j.jembe.2006.05.013openalex-snapshot
Antioxidant responses and lipid peroxidation in gills and erythrocytes of fish (Rhabdosarga sarba) upon exposure to Chattonella marina and hydrogen peroxide: Implications on the cause of fish kills
inferredcites →https://doi.org/10.1016/s1095-6433(01)00513-xopenalex-snapshot
Anoxic survival potential of bivalves: (arte)facts
inferredcites →https://doi.org/10.1080/20026491051695openalex-snapshot
The Effects of Harmful Algal Blooms on Aquatic Organisms
inferredcites →https://doi.org/10.1093/plankt/16.2.161openalex-snapshot
Generation of superoxide anion radicals by the marine phytoplankton organism, Chattonella antiqua
inferredcites →https://doi.org/10.1093/plankt/21.10.1809openalex-snapshot
Comparative ecophysiology of the harmful alga Chattonella marina (Raphidophyceae) form South Australian and Japanese waters
inferredcites →https://doi.org/10.1093/plankt/fbg096openalex-snapshot
Geometric models for calculating cell biovolume and surface area for phytoplankton
inferredcites →https://doi.org/10.1093/plankt/fbh085openalex-snapshot
Deleterious effect of Chattonella marina on short-necked clam (Ruditapes philippinarum); possible involvement of reactive oxygen species
inferredcites →https://doi.org/10.1096/fasebj.3.7.2565840openalex-snapshot
Brevetoxins: unique polyether dinoflagellate toxins
inferredcites →https://doi.org/10.1111/j.1444-2906.2006.01277.xopenalex-snapshot
Phylogenetic analysis of noxious red tide flagellates Chattonella antiqua, C.�marina, C.�ovata, and C.�verruculosa (Raphidophyceae) based on the rRNA gene family
inferredcites →https://doi.org/10.1111/j.1444-2906.2007.01408.xopenalex-snapshot
Genetic variation in mitochondrial genes and intergenic spacer region in harmful algae Chattonella species
inferredcites →https://doi.org/10.11233/aquaculturesci1953.49.317openalex-snapshot
Phyto-pigments in the Digestive Diverticula of Juvenile Japanese Pearl Oyster, Pinctada fucata martensii, as Indicator of Algal Diets Feeding
inferredcites →https://doi.org/10.1177/41.4.8383714openalex-snapshot
Localization of superoxide anion in the red tide alga Chattonella antiqua.
inferredcites →https://doi.org/10.1267/ahc.16.232openalex-snapshot
Effects of sea bloom, chattonella antiqua, on gill primary lamellae of the young yellowtail, seriola quinqueradiata.
inferredcites →https://doi.org/10.1271/bbb.58.957openalex-snapshot
Hydrogen Peroxide Production by the Red-tide FlagellateChattonella marina
inferredcites →https://doi.org/10.1271/bbb.59.2044openalex-snapshot
Catalase- and Superoxide Dismutase-induced Morphological Changes and Growth Inhibition in the Red Tide PhytoplanktonChattonella marina
inferredcites →https://doi.org/10.1271/bbb.61.1658openalex-snapshot
Generation of Reactive Oxygen Species by Raphidophycean Phytoplankton
inferredcites →https://doi.org/10.1289/ehp.02110465openalex-snapshot
New fish-killing alga in coastal Delaware produces neurotoxins.
inferredcites →https://doi.org/10.2216/08-98.1openalex-snapshot
Taxonomic revision ofChattonella antiqua, C. marinaandC. ovata(Raphidophyceae) based on their morphological characteristics and genetic diversity
inferredcites →https://doi.org/10.2216/i0031-8884-35-3-239.1openalex-snapshot
A toxicological study of the marine phytoflagellate, Chattonella antiqua (Raphidophyceae)
inferredcites →https://doi.org/10.2216/i0031-8884-41-1-15.1openalex-snapshot
Rapid identification of marine algae (Raphidophyceae) using three-primer PCR amplification of nuclear internal transcribed spacer (ITS) regions from fresh and archived material
inferredcites →https://doi.org/10.2307/1352736openalex-snapshot
The Eastern Oyster, "Crassostrea virginica"
inferredcites →https://doi.org/10.2331/fishsci.64.875openalex-snapshot
Comparison of Physiological Responses to Exposure to Chattonella marina in Yellowtail, Red Sea Bream and Japanese Flounder
inferredcites →https://doi.org/10.2331/fishsci.65.248openalex-snapshot
Effects of Harmful Dinoflagellates, Gymnodinium mikimotoi and Heterocapsa circularisquama, Red-tide on Filtering Rate of Bivalve Molluscs
inferredcites →https://doi.org/10.2983/0730-8000(2008)27[567:dpofap]2.0.co;2openalex-snapshot
Differential Production of Feces and Pseudofeces by the Oyster Crassostrea ariakensis When Exposed to Diets Containing Harmful Dinoflagellate and Raphidophyte Species
inferredcites →https://doi.org/10.3354/meps166163openalex-snapshot
Effects of natural and anthropogenic stressors on lysosomal destabilization in oysters Crassostrea virginica
inferredcites →https://doi.org/10.3354/meps312141openalex-snapshot
Sublethal cellular effects of short-term raphidophyte and brevetoxin exposures on the eastern oyster Crassostrea virginica
inferredcites →https://doi.org/10.3354/meps339083openalex-snapshot
Allelopathic interactions between the bacillariophyte Skeletonema costatum and the raphidophyte Heterosigma akashiwo
inferredcites →https://doi.org/10.3800/pbr.1.71openalex-snapshot
Eutrophication and occurrences of harmful algal blooms in the Seto Inland Sea, Japan
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/neobiota.102.148326zenodo-depositor-declared
Eating contest between native and non-indigenous bivalve species: Estimating capture efficiencies and clearance rates using natural seston
inferred← citeshttps://doi.org/10.1002/lno.11433openalex-snapshot
Adaptive feeding in the American oyster Crassostrea virginica : Complex impacts of pulsatile flow during pseudofecal ejection events
inferred← citeshttps://doi.org/10.1007/s10811-020-02167-4openalex-snapshot
Seaweed single cell detritus effects on the digestive enzymes activity and microbiota of the oyster Crassostrea gigas
inferred← citeshttps://doi.org/10.1007/s40071-019-00244-0openalex-snapshot
Phytoplankton uptake and growth rate in the Japanese egg cockle Fulvia mutica
inferred← citeshttps://doi.org/10.1016/j.rsma.2021.101968openalex-snapshot
Climate warming promotes Pacific oyster (Magallana gigas) production in a subarctic lagoon and bay, Japan: Projection of future trends using a three dimensional physical-ecosystem coupled model
inferred← citeshttps://doi.org/10.3354/ab00374openalex-snapshot
Effects of hydrogen sulfide on the feeding activity of Manila clam Ruditapes philippinarum
inferred← citeshttps://doi.org/10.3800/pbr.8.102openalex-snapshot
Dietary effects of the red-tide raphidophyte Heterosigma akashiwo on growth of juvenile Manila clams, Ruditapes philippinarum
inferred← citeshttps://doi.org/10.7837/kosomes.2018.24.7.967openalex-snapshot
Molecular Phylogeny of Chattonella (Raphidophyceae) Species from Deungnyang Bay, Korea Using Single-Cell PCR
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