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Gill structure in Lucina pectinata (Bivalvia: Lucinidae) with reference to hemoglobin in bivalves with symbiotic sulphur-oxidizing bacteria

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What this work says

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

inferredcites →https://doi.org/10.1001/jama.1953.02940280072039openalex-snapshot
Histochemistry: Theoretical and Applied
inferredcites →https://doi.org/10.1002/jez.1402490202openalex-snapshot
Hydrogen sulfide oxidation by abundant nonhemoglobin heme compounds in marine invertebrates from sulfide‐rich habitats
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/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/bf00397934openalex-snapshot
Gill ultrastructure and symbiotic bacteria in Codakia orbicularis (Bivalvia, Lucinidae)
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/bf00569130openalex-snapshot
Ultrastructure of the gill of the hydrothermal vent bivalveCalyptogena magnifica, with a discussion of its nutrition
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/10.1016/0010-406x(61)90195-5openalex-snapshot
Histochimie et cytochimie animales
inferredcites →https://doi.org/10.1016/0010-406x(65)90342-7openalex-snapshot
The characterization of the hemoglobins of the bivalve mollusc Phacoides pectinatus (Gmelin)
inferredcites →https://doi.org/10.1016/0044-8486(84)90264-3openalex-snapshot
Potential of chemosynthesis in molluscan mariculture
inferredcites →https://doi.org/10.1016/s0021-9258(17)46185-0openalex-snapshot
Hemoglobins of the Lucina pectinata/bacteria symbiosis. I. Molecular properties, kinetics and equilibria of reactions with ligands.
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/s0025315400048517openalex-snapshot
Gill Symbionts in Thyasirids and Other Bivalve Molluscs
inferredcites →https://doi.org/10.1017/s0025315400048529openalex-snapshot
Chemoautotrophy in Bivalve Molluscs of the Genus Thyasira
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/10.1038/302058a0openalex-snapshot
Symbiotic chemoautotrophic bacteria in marine invertebrates from sulphide-rich habitats
inferredcites →https://doi.org/10.1083/jcb.44.3.513openalex-snapshot
HEMOGLOBIN UPTAKE BY RAT HEPATOCYTES AND ITS BREAKDOWN WITHIN LYSOSOMES
inferredcites →https://doi.org/10.1098/rspb.1986.0021openalex-snapshot
Chemoautotrophic symbionts in the gills of the bivalve mollusc Lucinoma borealis and the sediment chemistry of its habitat
inferredcites →https://doi.org/10.1111/j.1749-7345.1982.tb00039.xopenalex-snapshot
MARICULTURE POTENTIAL OF SHALLOW‐WATER BAHAMIAN BIVALVES
inferredcites →https://doi.org/10.1126/science.213.4505.340openalex-snapshot
Prokaryotic Cells in the Hydrothermal Vent Tube Worm Riftia pachyptila Jones: Possible Chemoautotrophic Symbionts
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/10.2307/3226036openalex-snapshot
Practical Methods in Electron Microscopy, Vol. 6
inferredcites →https://doi.org/10.3354/meps023085openalex-snapshot
Sulphur-oxidising bacteria and haemoglobin in gills of the bivalve mollusc Myrtea spinifera
inferredcites →https://doi.org/10.3354/meps024113openalex-snapshot
Significance of the occurrence of chemoautotrophic bacterial endosymbionts in lucinid clams from Bermuda

What points at this work

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

inferred← citeshttps://doi.org/10.1093/zoolinnean/zlae005zenodo-depositor-declared
Revision of the genus Robbea (Stilbonematinae: Desmodoridae), worldwide abundant marine nematodes with chromophoric Fe–Br inclusions and the description of a new stilbonematine genus
inferred← citeshttps://doi.org/10.1002/9781394316946.ch11openalex-snapshot
Thiomargarita magnifica
inferred← citeshttps://doi.org/10.1002/bip.23427openalex-snapshot
SAXS structure of homodimeric oxyHemoglobin III from bivalve Lucina pectinata
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/10.1007/3-540-33774-1_2openalex-snapshot
Bacterial Sulfur Globules: Occurrence, Structure and Metabolism
inferred← citeshttps://doi.org/10.1007/978-3-030-60173-7_2openalex-snapshot
Bacterial Intracellular Sulphur Globules
inferred← citeshttps://doi.org/10.1007/978-3-319-99194-8_7openalex-snapshot
Bivalve Chemosymbioses on Mudflats
inferred← citeshttps://doi.org/10.1007/978-90-481-9572-5_5openalex-snapshot
Chemosymbiotic Bivalves
inferred← citeshttps://doi.org/10.1007/978-94-017-8721-5_3openalex-snapshot
Relationships of Internal Shell Features to Chemosymbiosis, Life Position, and Geometric Constraints Within the Lucinidae (Bivalvia)
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/s00227-003-1103-yopenalex-snapshot
Mollusc feeding guilds on sandy beaches in S�o Paulo State, Brazil
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/s00227-015-2727-4openalex-snapshot
Temporal variation in chemoautotrophic symbiont abundance in the thyasirid bivalve Thyasira cf. gouldi
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/10.1007/s00435-007-0035-3openalex-snapshot
Gill-symbiosis in mytilidae associated with wood fall environments
inferred← citeshttps://doi.org/10.1007/s13199-021-00801-4openalex-snapshot
Bacterial ectosymbionts colonizing gills of two Caribbean mangrove crabs
inferred← citeshttps://doi.org/10.1016/bs.ampbs.2026.06.003openalex-snapshot
Biochemistry and transcriptional regulation of bacterial sulfur oxidation
inferred← citeshttps://doi.org/10.1016/j.dsr.2008.02.001openalex-snapshot
Metabolic rates and thermal tolerances of chemoautotrophic symbioses from Lau Basin hydrothermal vents and their implications for species distributions
inferred← citeshttps://doi.org/10.1016/j.ejop.2017.11.002openalex-snapshot
Thioautotrophic ectosymbiosis in Pseudovorticella sp., a peritrich ciliate species colonizing wood falls in marine mangrove
inferred← citeshttps://doi.org/10.1016/j.fsi.2018.11.041openalex-snapshot
Gill symbionts of the cold-seep mussel Bathymodiolus platifrons: Composition, environmental dependency and immune control
inferred← citeshttps://doi.org/10.1016/j.marenvres.2008.11.006openalex-snapshot
Sunken wood habitat for thiotrophic symbiosis in mangrove swamps
inferred← citeshttps://doi.org/10.1016/j.marenvres.2010.02.001openalex-snapshot
Raman microspectrometry as a powerful tool for a quick screening of thiotrophy: An application on mangrove swamp meiofauna of Guadeloupe (F.W.I.)
inferred← citeshttps://doi.org/10.1016/j.marenvres.2013.03.007openalex-snapshot
Dynamics of wood fall colonization in relation to sulfide concentration in a mangrove swamp
inferred← citeshttps://doi.org/10.1016/s0025-326x(01)00113-8openalex-snapshot
Oxygen, Sulphide and Nutrient Uptake of the Mangrove Mud Clam Anodontia edentula (Family: Lucinidae)
inferred← citeshttps://doi.org/10.1016/s0065-2881(01)40003-4openalex-snapshot
Biology of mangroves and mangrove Ecosystems
inferred← citeshttps://doi.org/10.1016/s0141-1136(01)00112-xopenalex-snapshot
DNA damage and apoptosis in the mussel Mytilus galloprovincialis
inferred← citeshttps://doi.org/10.1016/s0378-1097(98)00041-xopenalex-snapshot
Putative environmental transmission of sulfur-oxidizing bacterial symbionts in tropical lucinid bivalves inhabiting various environments
inferred← citeshttps://doi.org/10.1016/s0742-8413(00)00100-6openalex-snapshot
Reproductive characteristics and strategies of reducing-system bivalves
inferred← citeshttps://doi.org/10.1017/s0025315401004337openalex-snapshot
Different energy sources for three symbiont-dependent bivalve molluscs at the Logatchev hydrothermal site (Mid-Atlantic Ridge)
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/10.1021/bi400745aopenalex-snapshot
Reactivity and Dynamics of H2S, NO, and O2 Interacting with Hemoglobins from Lucina pectinata
inferred← citeshttps://doi.org/10.1038/nmicrobiol.2016.195openalex-snapshot
Chemosynthetic symbionts of marine invertebrate animals are capable of nitrogen fixation
inferred← citeshttps://doi.org/10.1038/s41396-018-0318-3openalex-snapshot
Taxonomic and functional heterogeneity of the gill microbiome in a symbiotic coastal mangrove lucinid species
inferred← citeshttps://doi.org/10.1042/bc20040502openalex-snapshot
In situ localization of sulphur in the thioautotrophic symbiotic model Lucina pectinata (Gmelin, 1791) by cryo‐EFTEM microanalysis
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/10.1080/10409238.2023.2299381openalex-snapshot
Hemoglobin wonders: a fascinating gas transporter dive into molluscs
inferred← citeshttps://doi.org/10.1093/femsle/fnx172openalex-snapshot
First description of a new uncultured epsilon sulfur bacterium colonizing marine mangrove sediment in the Caribbean: Thiovulum sp. strain karukerense
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/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/eyp052openalex-snapshot
Abyssogena: a new genus of the family Vesicomyidae (Bivalvia) from deep-water vents and seeps
inferred← citeshttps://doi.org/10.1093/mollus/eys031openalex-snapshot
Bacterial symbiosis in Syssitomya pourtalesiana Oliver, 2012 (Galeommatoidea: Montacutidae), a bivalve commensal with the deep-sea echinoid Pourtalesia
inferred← citeshttps://doi.org/10.1098/rsbl.2023.0573openalex-snapshot
Discovery of deep-sea acoels from a chemosynthesis-based ecosystem
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/bij.12208openalex-snapshot
Diversification of chemosymbiotic bivalves: origins and relationships of deeper water Lucinidae
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.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.1744-7410.2007.00086.xopenalex-snapshot
Rapid induction and disappearance of electron‐dense organelles following sulfide exposure in the marine annelid Branchioasychis americana
inferred← citeshttps://doi.org/10.1111/maec.12296openalex-snapshot
Diet of Haplognathia ruberrima (Gnathostomulida) in a Caribbean marine mangrove
inferred← citeshttps://doi.org/10.1111/pala.12046openalex-snapshot
Exceptional preservation of a novel gill grade in large C retaceous inoceramids: systematic and palaeobiological implications
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.02129-20openalex-snapshot
The Symbiotic “All-Rounders”: Partnerships between Marine Animals and Chemosynthetic Nitrogen-Fixing Bacteria
inferred← citeshttps://doi.org/10.1139/cjm-2021-0101openalex-snapshot
Candidatus Thiovulum sp. strain imperiosus: the largest free-living Epsilonproteobacteraeota Thiovulum strain lives in a marine mangrove environment
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/10.11646/zootaxa.3859.1.1openalex-snapshot
Bivalves from the latest Jurassic-earliest Cretaceous hydrocarbon seep carbonates from central Spitsbergen, Svalbard
inferred← citeshttps://doi.org/10.1264/jsme2.13.203openalex-snapshot
Bacterial flora in mangroves and their biological role.
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.27183.1openalex-snapshot
The chromosomal genome sequence of Loripinus fragilis (R.A.Philippi, 1836) (Lucinida: Lucinidae) and its associated microbial metagenome sequences
inferred← citeshttps://doi.org/10.1371/journal.pone.0117832openalex-snapshot
Two New Beggiatoa Species Inhabiting Marine Mangrove Sediments in the Caribbean
inferred← citeshttps://doi.org/10.1371/journal.pone.0127625openalex-snapshot
First Description of Sulphur-Oxidizing Bacterial Symbiosis in a Cnidarian (Medusozoa) Living in Sulphidic Shallow-Water Environments
inferred← citeshttps://doi.org/10.21203/rs.3.rs-561495/v1openalex-snapshot
Chemoautotrophy at the Expense of Thiosulphate: A Supplementary Nutritional Source to the Mangrove Clam-Polymesoda Erosa
inferred← citeshttps://doi.org/10.21411/cbm.a.f82628c6openalex-snapshot
Extracellular bacterial association in gills of «wood mussels»
inferred← citeshttps://doi.org/10.2307/1542719openalex-snapshot
Bacterial Endosymbionts in the Gills of the Deep-Sea Wood-Boring Bivalves Xylophaga atlantica and Xylophaga washingtona
inferred← citeshttps://doi.org/10.31390/gradschool_theses.1970openalex-snapshot
Characterization of the lucinid bivalve-bacteria symbiotic system: the significance of the geochemical habitat on bacterial symbiont diversity and phylogeny
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1491485openalex-snapshot
A novel open-source cultivation system helps establish the first full cycle chemosynthetic symbiosis model system involving the giant ciliate Zoothamnium niveum
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/10.5194/bg-10-3241-2013openalex-snapshot
An overview of chemosynthetic symbioses in bivalves from the North Atlantic and Mediterranean Sea
inferred← citeshttps://doi.org/10.70675/1155c3dcz2499z47b7z9519zef7ce6fd1052openalex-snapshot
Consommation de bivalves marins et pollution à l'arsenic : le risque lié à deux espèces comestibles en Martinique
inferred← citeshttps://doi.org/10.70675/41e55b04z3b86z40e2z8a9fzfe4762d615f4openalex-snapshot
Analyse statistique par balayage et prévision de l'évolution spatio-temporelle d'indices de fragilité
inferred← citeshttps://doi.org/10.70675/47314edez9a2az4f92z90ddz099451da5877openalex-snapshot
Symbioses bactériennes chez les protistes ciliés des sédiments réduits de mangroves de Guadeloupe.
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/ab5f7116z8190z4e5fz9245z3b3dcf9d82cdopenalex-snapshot
The bacterial symbiont in the shallow water lucinids Codakia orbicularis and C. orbiculata analyzed by physiological proteogenomics
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