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Gill ultrastructure and symbiotic bacteria in Codakia orbicularis (Bivalvia, Lucinidae)
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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/bf00312060openalex-snapshot
Structure and position of bacterial endosymbionts in the gill filaments of lucinidae from bermuda (Mollusca, Bivalvia)
inferredcites →https://doi.org/10.1007/bf00392747openalex-snapshot
Ultrastructure of the gill of the hydrothermal-vent mytilid Bathymodiolus sp.
inferredcites →https://doi.org/10.1007/bf00393041openalex-snapshot
Elemental sulfur in the gills of three species of clams containing chemoautotrophic symbiotic bacteria: a possible inorganic energy storage compound
inferredcites →https://doi.org/10.1007/bf00394840openalex-snapshot
Endosymbiosis in the lucinid clams Lucinoma aequizonata, Lucinoma annulata and Lucina floridana: a reexamination of the functional morphology of the gills as bacteria-bearing organs
inferredcites →https://doi.org/10.1007/bf00428126openalex-snapshot
Chemoautotrophic symbionts and translocation of fixed carbon from bacteria to host tissues in the littoral bivalve Loripes lucinalis (Lucinidae)
inferredcites →https://doi.org/10.1007/bf00689721openalex-snapshot
Sulfide oxidation and carbon fixation by the gutless clamSolemya reidi: an animal-bacteria symbiosis
inferredcites →https://doi.org/10.1016/0044-8486(84)90264-3openalex-snapshot
Potential of chemosynthesis in molluscan mariculture
inferredcites →https://doi.org/10.1016/s0022-5320(80)90053-2openalex-snapshot
Ultrastructure of the giant smooth muscle fiber of the ctenophore Beroe ovata
inferredcites →https://doi.org/10.1017/s0025315400001405openalex-snapshot
The functional morphology of the larva, and the post-larval development of Venus striatula (Da Costa)
inferredcites →https://doi.org/10.1017/s0025315400048517openalex-snapshot
Gill Symbionts in Thyasirids and Other Bivalve Molluscs
inferredcites →https://doi.org/10.1038/293291a0openalex-snapshot
Calvin-Benson cycle and sulphide oxidation enzymes in animals from sulphide-rich habitats
inferredcites →https://doi.org/10.1083/jcb.38.3.615openalex-snapshot
ULTRASTRUCTURE OF HUMAN LEUKOCYTES AFTER SIMULTANEOUS FIXATION WITH GLUTARALDEHYDE AND OSMIUM TETROXIDE AND "POSTFIXATION" IN URANYL ACETATE
inferredcites →https://doi.org/10.1098/rspb.1976.0092openalex-snapshot
Further studies on the latero-frontal tracts of bivalves
inferredcites →https://doi.org/10.1098/rstb.1958.0010openalex-snapshot
On the basic form and adaptations to habitat in the Lucinacea (Eulamellibranchia)
inferredcites →https://doi.org/10.1111/j.1749-7345.1982.tb00039.xopenalex-snapshot
MARICULTURE POTENTIAL OF SHALLOW‐WATER BAHAMIAN BIVALVES
inferredcites →https://doi.org/10.1146/annurev.mi.28.100174.001123openalex-snapshot
Inclusion Bodies of Prokaryotes
inferredcites →https://doi.org/10.1242/jcs.s2-80.319.345openalex-snapshot
On the Ciliary Mechanisms and Interrelationships of Lamellibranchs.: PART VII: Latero-frontal Cilia of the Gill Filaments and their Phylogenetic Value
inferredcites →https://doi.org/10.2307/1539582openalex-snapshot
THE HEMOGLOBIN OF THE BIVALVED MOLLUSC, PHACOIDES PECTINATUS GMELIN
inferredcites →https://doi.org/10.2307/1541289openalex-snapshot
CHEMOAUTOTROPHIC SYMBIONTS IN THE BIVALVE LUCINA FLORIDANA FROM SEAGRASS BEDS
inferredcites →https://doi.org/10.2307/3224938openalex-snapshot
Practical Methods in Electron Microscopy
inferredcites →https://doi.org/10.3109/10520297509117086openalex-snapshot
A Decalcification Method for Ultrastructure of Echinoderm Tissues
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.4196.3.2zenodo-depositor-declared
New molecular phylogeny of Lucinidae: increased taxon base with focus on tropical Western Atlantic species (Mollusca: Bivalvia)
inferred← citeshttps://doi.org/10.1002/jemt.22041openalex-snapshot
Cell proliferation and apoptosis in gill filaments of the lucinid Codakia orbiculata (Montagu, 1808) (Mollusca: Bivalvia) during bacterial decolonization and recolonization
inferred← citeshttps://doi.org/10.1002/jemt.22458openalex-snapshot
Thioautotrophic bacterial endosymbionts are degraded by enzymatic digestion during starvation: Case study of two lucinids C odakia orbicularis and C . orbiculata
inferred← citeshttps://doi.org/10.1007/bf00353264openalex-snapshot
Gill structure in Lucina pectinata (Bivalvia: Lucinidae) with reference to hemoglobin in bivalves with symbiotic sulphur-oxidizing bacteria
inferred← citeshttps://doi.org/10.1007/bf02536990openalex-snapshot
Long-term history of chemoautotrophic clam-dominated faunas of petroleum seeps in the Northwestern Gulf of Mexico
inferred← citeshttps://doi.org/10.1007/s00203-010-0627-zopenalex-snapshot
Effects of the antibiotic growth promoters flavomycin and florfenicol on the autochthonous intestinal microbiota of hybrid tilapia (Oreochromis niloticus ♀ × O. aureus ♂)
inferred← citeshttps://doi.org/10.1007/s00227-002-0921-7openalex-snapshot
Interspecific infection of aposymbiotic juveniles of Codakia orbicularis by various tropical lucinid gill-endosymbionts
inferred← citeshttps://doi.org/10.1007/s00227-004-1350-6openalex-snapshot
Anatomical and experimental evidence for particulate feeding in Lucinoma aequizonata and Parvilucina tenuisculpta (Bivalvia: Lucinidae) from the Santa Barbara Basin
inferred← citeshttps://doi.org/10.1007/s00227-008-0962-7openalex-snapshot
In situ characterization of sulphur in gill-endosymbionts of the shallow water lucinid Codakia orbicularis (Linné, 1758) by high-pressure cryofixation and EFTEM microanalysis
inferred← citeshttps://doi.org/10.1007/s00253-011-3819-9openalex-snapshot
On the evolutionary ecology of symbioses between chemosynthetic bacteria and bivalves
inferred← citeshttps://doi.org/10.1007/s00435-007-0034-4openalex-snapshot
Structural and ultrastructural analysis of the gills in the bacterial-bearing species Thyasira falklandica (Bivalvia, Mollusca)
inferred← citeshttps://doi.org/10.1016/j.acthis.2007.11.001openalex-snapshot
Easy flat embedding of oriented samples in hydrophilic resin (LR White) under controlled atmosphere: Application allowing both nucleic acid hybridizations (CARD-FISH) and ultrastructural observations
inferred← citeshttps://doi.org/10.1016/j.cbpa.2010.04.004openalex-snapshot
Identification and molecular characterization of a mucosal lectin (MeML) from the blue mussel Mytilus edulis and its potential role in particle capture
inferred← citeshttps://doi.org/10.1016/j.fsi.2007.03.009openalex-snapshot
The three-dimensional structure of codakine and related marine C-type lectins
inferred← citeshttps://doi.org/10.1016/j.jembe.2013.07.015openalex-snapshot
Endosymbiotic bacteria in the bivalve Loripes lacteus: Localization, characterization and aspects of symbiont regulation
inferred← citeshttps://doi.org/10.1016/j.jip.2009.11.008openalex-snapshot
Identification and characterization of the pathogenic effect of a Vibrio parahaemolyticus-related bacterium isolated from clam Meretrix meretrix with mass mortality
inferred← citeshttps://doi.org/10.1016/s0742-8413(00)00100-6openalex-snapshot
Reproductive characteristics and strategies of reducing-system bivalves
inferred← citeshttps://doi.org/10.1016/s0967-0637(02)00010-9openalex-snapshot
Lucinoma kazani n. sp. (Mollusca: Bivalvia): evidence of a living benthic community associated with a cold seep in the Eastern Mediterranean Sea
inferred← citeshttps://doi.org/10.1017/s002531540100371xopenalex-snapshot
Bacterial symbiosis in Loripes lucinalis (Mollusca: Bivalvia) with comments on reproductive strategy
inferred← citeshttps://doi.org/10.1017/s0025315407054409openalex-snapshot
Evolutionary relationships of the bivalve family Thyasiridae (Mollusca: Bivalvia), monophyly and superfamily status
inferred← citeshttps://doi.org/10.1017/s1477200005001672openalex-snapshot
Cryptic diversity of chemosymbiotic bivalves: A systematic revision of worldwide Anodontia (Mollusca: Bivalvia: Lucinidae)
inferred← citeshttps://doi.org/10.1038/nmicrobiol.2016.193openalex-snapshot
Nitrogen fixation in a chemoautotrophic lucinid symbiosis
inferred← citeshttps://doi.org/10.1042/bc20080051openalex-snapshot
Raman microspectrometry sulfur detection and characterization in the marine ectosymbiotic nematode Eubostrichus dianae (Desmodoridae, Stilbonematidae)
inferred← citeshttps://doi.org/10.1054/tice.2000.0169openalex-snapshot
Cytological effects of experimental exposure to Hg on the gill epithelium of the European flat oyster Ostrea edulis: ultrastructural and quantitative changes related to bioaccumulation
inferred← citeshttps://doi.org/10.1080/07924259.1997.9672577openalex-snapshot
Storage tissue and reproductive strategy inLucina pectinata(Gmelin), a tropical lucinid bivalve adapted to a reducing sulfur-rich, mangrove environment
inferred← citeshttps://doi.org/10.1080/07924259.1998.9652656openalex-snapshot
Gill filament differentiation and experimental colonization by symbiotic bacteria in aposymbiotic juveniles ofCodakia orbicularis(Bivalvia: Lucinidae)
inferred← citeshttps://doi.org/10.1081/pb-120015458openalex-snapshot
ELECTROPHORETIC SEPARATION OF GILL PROTEINS OF THE CLAMCODAKIA ORBICULARIS
inferred← citeshttps://doi.org/10.1093/mollus/70.2.187openalex-snapshot
MOLECULAR PHYLOGENY OF THE LUCINOIDEA (BIVALVIA): NON‐MONOPHYLY AND SEPARATE ACQUISITION OF BACTERIAL CHEMOSYMBIOSIS
inferred← citeshttps://doi.org/10.1093/mollus/eyaa037openalex-snapshot
Regulation of mucosal lectins in the oyster Crassostrea virginica in response to food availability and environmental factors
inferred← citeshttps://doi.org/10.1093/mollus/eyac025openalex-snapshot
Closing the gap: a new phylogeny and classification of the chemosymbiotic bivalve family Lucinidae with molecular evidence for 73% of living genera
inferred← citeshttps://doi.org/10.1093/mollus/eyp009openalex-snapshot
Ctenidial structure and three bacterial symbiont morphotypes in Anodontia (Euanodontia) ovum (Reeve, 1850) from the Great Barrier Reef, Australia (Bivalvia: Lucinidae)
inferred← citeshttps://doi.org/10.1093/mollus/eyv001openalex-snapshot
Embryonic and larval development of the New Zealand bivalvePaphies ventricosaGray, 1843 (Veneroida: Mesodesmatidae) at a range of temperatures
inferred← citeshttps://doi.org/10.1111/1574-6941.12366openalex-snapshot
Comparative modifications in bacterial gill-endosymbiotic populations of the two bivalvesCodakia orbiculataandLucina pensylvanicaduring bacterial loss and reacquisition
inferred← citeshttps://doi.org/10.1111/gbi.12093openalex-snapshot
The isotopic biosignatures of photo‐ vs. thiotrophic bivalves: are they preserved in fossil shells?
inferred← citeshttps://doi.org/10.1111/j.1096-3642.2006.00261.xopenalex-snapshot
Lucinidae (Bivalvia)–the most diverse group of chemosymbiotic molluscs
inferred← citeshttps://doi.org/10.1111/j.1096-3642.2011.00700.xopenalex-snapshot
Molecular phylogeny and classification of the chemosymbiotic bivalve family Lucinidae (Mollusca: Bivalvia)
inferred← citeshttps://doi.org/10.1111/j.1439-0485.2010.00413.xopenalex-snapshot
Characterization of bacterial symbioses in Myrtea sp. (Bivalvia: Lucinidae) and Thyasira sp. (Bivalvia: Thyasiridae) from a cold seep in the Eastern Mediterranean
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2012.02748.xopenalex-snapshot
Plasticity of symbiont acquisition throughout the life cycle of the shallow‐water tropical lucinid Codakia orbiculata (Mollusca: Bivalvia)
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2008.00839.xopenalex-snapshot
A GIANT LUCINID BIVALVE FROM THE EOCENE OF JAMAICA – SYSTEMATICS, LIFE HABITS AND CHEMOSYMBIOSIS (MOLLUSCA: BIVALVIA: LUCINIDAE)
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2008.00626.xopenalex-snapshot
Lack of endosymbiont release by two Lucinidae (Bivalvia) of the genus Codakia: consequences for symbiotic relationships
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2010.00989.xopenalex-snapshot
Lucinidae/sulfur-oxidizing bacteria: ancestral heritage or opportunistic association? Further insights from the Bohol Sea (the Philippines)
inferred← citeshttps://doi.org/10.1128/aem.01683-06openalex-snapshot
Characterization of the Population of the Sulfur-Oxidizing Symbiont ofCodakia orbicularis(Bivalvia, Lucinidae) by Single-Cell Analyses
inferred← citeshttps://doi.org/10.1128/aem.02659-08openalex-snapshot
Effects of Long-Term Starvation on a Host Bivalve (Codakia orbicularis, Lucinidae) and Its Symbiont Population
inferred← citeshttps://doi.org/10.1128/aem.62.7.2324-2330.1996openalex-snapshot
Environmental transmission of a sulfur-oxidizing bacterial gill endosymbiont in the tropical lucinid bivalve Codakia orbicularis
inferred← citeshttps://doi.org/10.1128/aem.69.10.6264-6267.2003openalex-snapshot
Detection of the Free-Living Forms of Sulfide-Oxidizing Gill Endosymbionts in the Lucinid Habitat ( Thalassia testudinum Environment)
inferred← citeshttps://doi.org/10.1128/aem.70.7.4144-4150.2004openalex-snapshot
Respiration Strategies Utilized by the Gill Endosymbiont from the Host Lucinid Codakia orbicularis (Bivalvia: Lucinidae)
inferred← citeshttps://doi.org/10.1128/msystems.01135-23openalex-snapshot
SoxY gene family expansion underpins adaptation to diverse hosts and environments in symbiotic sulfide oxidizers
inferred← citeshttps://doi.org/10.1144/gsl.sp.2000.177.01.12openalex-snapshot
Functional anatomy, chemosymbiosis and evolution of the Lucinidae
inferred← citeshttps://doi.org/10.1385/abab:125:1:041openalex-snapshot
Application of Recombinant Phage Display Antibody System in Study of Codakia orbicularis Gill Proteins
inferred← citeshttps://doi.org/10.25135/rnp.295.2108.2194openalex-snapshot
A New Short Chain Acetamide from the Biosphere and Bioactive Glycerolipids Extracted from the Marine Bibalve Codakia orbicularis (Lucinidae).
inferred← citeshttps://doi.org/10.3389/fevo.2022.846586openalex-snapshot
Developmental Integration of Endosymbionts in Insects
inferred← citeshttps://doi.org/10.3390/jmse12050847openalex-snapshot
The Complete Mitochondrial Genome of the Chemosymbiotic Lucinid Bivalve Pillucina pisidium (Dunker, 1860) Occurring in Seagrass Zostera marina Bed in a Lagoon in Jeju Island, Korea
inferred← citeshttps://doi.org/10.3897/zookeys.620.9569openalex-snapshot
Pleurolucina from the western Atlantic and eastern Pacific Oceans: a new intertidal species from Curaçao with unusual shell microstructure (Mollusca, Bivalvia, Lucinidae)
inferred← citeshttps://doi.org/10.4002/040.058.0201openalex-snapshot
Comparative Anatomy of Selected Marine Bivalves from the Florida Keys, with Notes on Brazilian Congeners (Mollusca: Bivalvia)
inferred← citeshttps://doi.org/10.47749/t/unicamp.2020.1149134openalex-snapshot
Investigating the Thyasiridae Dall, 1901 (Bivalvia, Mollusca) from the Southwestern Atlantic Ocean
inferred← citeshttps://doi.org/10.5194/bg-10-3241-2013openalex-snapshot
An overview of chemosynthetic symbioses in bivalves from the North Atlantic and Mediterranean Sea
inferred← citeshttps://doi.org/10.53846/goediss-4153openalex-snapshot
Chemosynthetische Endosymbiosen an rezenten und fossilen Cold Seep-Standorten
inferred← citeshttps://doi.org/10.70675/48868752zf06cz4b3dzbdadzf9d2bdfc3c5bopenalex-snapshot
Plasticité tissulaire et cellulaire du filament branchial des Lucinidae symbiotiques côtiers Codakia orbiculata et Lucine pensylvanica
inferred← citeshttps://doi.org/10.70675/4ee99161z14aaz44d3z8af4z90881d646bd0openalex-snapshot
La flexibilité des symbioses entre bivalves et bactéries chimiotrophes : mécanismes, régulation et résilience
inferred← citeshttps://doi.org/10.70675/ab5f7116z8190z4e5fz9245z3b3dcf9d82cdopenalex-snapshot
The bacterial symbiont in the shallow water lucinids Codakia orbicularis and C. orbiculata analyzed by physiological proteogenomics
inferred← citeshttps://doi.org/10.7287/peerj.9326v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Microbial community analysis in the gills of abalones suggested possible dominance of epsilonproteobacterium in Haliotis gigantea (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.9326v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Microbial community analysis in the gills of abalones suggested possible dominance of epsilonproteobacterium in Haliotis gigantea (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.9326v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Microbial community analysis in the gills of abalones suggested possible dominance of epsilonproteobacterium in Haliotis gigantea (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.9326v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Microbial community analysis in the gills of abalones suggested possible dominance of epsilonproteobacterium in Haliotis gigantea (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.9326openalex-snapshot
Microbial community analysis in the gills of abalones suggested possible dominance of epsilonproteobacterium in Haliotis gigantea
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