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Translocation of fixed carbon from symbiotic bacteria to host tissues in the gutless bivalve Solemya reidi
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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/bf00406001openalex-snapshot
CO2 fixation in tissues of marine oligochaetes (Phallodrilus leukodermatus and P. planus) containing symbiotic, chemoautotrophic bacteria
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(66)90028-4openalex-snapshot
Carbon dioxide fixation in marine invertebrates—V. Rate and pathway in the oyster
inferredcites →https://doi.org/10.1016/b978-0-12-751402-4.50017-0openalex-snapshot
Biochemical Interactions between Molluscs and Their Algal and Bacterial Symbionts11These studies were supported in part by National Science Foundation grants OCE78-08933 and OCE78-08852 to James Childress, and OCE78-08853, PCM80-01949, and OCE80-24251 to George Somero, and Deutsche…
inferredcites →https://doi.org/10.1016/s0021-9258(19)73766-1openalex-snapshot
Carbon Dioxide Fixation in Marine Invertebrates
inferredcites →https://doi.org/10.1016/s0076-6879(71)23129-3openalex-snapshot
[53] Ribulose diphosphate carboxylase from spinach leaves
inferredcites →https://doi.org/10.1017/s0025315400044131openalex-snapshot
Bacterial Symbionts in Pogonophora
inferredcites →https://doi.org/10.1038/2271155b0openalex-snapshot
Synthesis of a Mucous Cuticle by a Zoanthid
inferredcites →https://doi.org/10.1038/293616a0openalex-snapshot
Bacterial symbionts and low 13C/12C ratios in tissues of Pogonophora indicate unusual nutrition and metabolism
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.42.2.404openalex-snapshot
CHLOROPLASTS AS FUNCTIONAL ORGANELLES IN ANIMAL TISSUES
inferredcites →https://doi.org/10.1093/icb/24.1.57openalex-snapshot
How Do Benthic Organisms Withstand Moving Water?
inferredcites →https://doi.org/10.1111/j.1469-7998.1965.tb02025.xopenalex-snapshot
THE MANTLE AND SHELL OF SOLEMYA PARKINSONI (PROTOBRANCHIA: BIVALVIA)
inferredcites →https://doi.org/10.1111/j.1469-7998.1973.tb03121.xopenalex-snapshot
On the utilization of photosynthetic products from zooxanthellae and of a dissolved amino acid in Tridacna maxima f. elongata (Mollusca: Bivalvia)*
inferredcites →https://doi.org/10.1126/science.203.4381.648openalex-snapshot
Carbon-13 Depletion in a Hydrothermal Vent Mussel: Suggestion of a Chemosynthetic Food Source
inferredcites →https://doi.org/10.1126/science.207.4437.1345openalex-snapshot
Deep-Sea Primary Production at the Galápagos Hydrothermal Vents
inferredcites →https://doi.org/10.1126/science.213.4505.336openalex-snapshot
Chemoautotrophic Potential of the Hydrothermal Vent Tube Worm, Riftia pachyptila Jones (Vestimentifera)
inferredcites →https://doi.org/10.1126/science.213.4505.338openalex-snapshot
Hydrothermal Vent Clam and Tube Worm 13 C/ 12 C: Further Evidence of Nonphotosynthetic Food Sources
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/10.1126/science.219.4582.295openalex-snapshot
Sulfide Binding by the Blood of the Hydrothermal Vent Tube Worm Riftia pachyptila
inferredcites →https://doi.org/10.1126/science.229.4715.713openalex-snapshot
Hydrothermal Vent Animals: Distribution and Biology
inferredcites →https://doi.org/10.1136/jcp.36.5.609-dopenalex-snapshot
Theory and Practice of Histological Techniques
inferredcites →https://doi.org/10.1139/z80-050openalex-snapshot
Aspects of the biology of a gutless species of Solemya (Bivalvia: Protobranchia)
inferredcites →https://doi.org/10.1242/jcs.s3-102.57.15openalex-snapshot
A Note on the Habits and Nutrition of Solemya parkinsoni (Protobranchia: Bivalvia)
inferredcites →https://doi.org/10.2307/1307765openalex-snapshot
Chemosynthetic Primary Production at East Pacific Sea Floor Spreading Centers
inferredcites →https://doi.org/10.2307/1541117openalex-snapshot
OBSERVATIONS ON THE SYMBIOSIS WITH ZOOXANTHELLAE AMONG THE TRIDACNIDAE (MOLLUSCA, BIVALVIA)
inferredcites →https://doi.org/10.2307/1541289openalex-snapshot
CHEMOAUTOTROPHIC SYMBIONTS IN THE BIVALVE LUCINA FLORIDANA FROM SEAGRASS BEDS
inferredcites →https://doi.org/10.2307/1541384openalex-snapshot
SYMBIOTIC ASSIMILATION OF CO2IN TWO HYDROTHERMAL VENT ANIMALS, THE MUSSELBATHYMODIOLUS THERMOPHILUSAND THE TUBE WORMRIFTIA PACHYPTILA
inferredcites →https://doi.org/10.2307/1541396openalex-snapshot
SULFIDE OXIDATION OCCURS IN THE ANIMAL TISSUE OF THE GUTLESS CLAM,SOLEMYA REIDI
inferredcites →https://doi.org/10.3354/meps005353openalex-snapshot
The Gutless Marine Oligochaete Phallodrilus leukodermatus. Structural Studies on an Aberrant Tubificid Associated with Bacteria
inferredcites →https://doi.org/10.3354/meps024113openalex-snapshot
Significance of the occurrence of chemoautotrophic bacterial endosymbionts in lucinid clams from Bermuda
inferredcites →https://doi.org/10.3354/meps028233openalex-snapshot
13C/12C ratios in marine invertebrates from reducing sediments: confirmation of nutricional importance of chemoautotrophic endosymbiotic bacteria
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/zookeys.1198.112618zenodo-depositor-declared
A new chemosymbiotic bivalve species of the genus Acharax Dall, 1908 (Bivalvia, Solemyida, Solemyidae) from the Haima cold seep of the South China Sea
inferred← citeshttps://doi.org/10.1002/jez.1402490202openalex-snapshot
Hydrogen sulfide oxidation by abundant nonhemoglobin heme compounds in marine invertebrates from sulfide‐rich habitats
inferred← citeshttps://doi.org/10.1002/jez.1402560203openalex-snapshot
Aerobic metabolism is maintained in animal tissue during rapid sulfide oxidation in the symbiont‐containing clam Solemya reidi
inferred← citeshttps://doi.org/10.1007/0-387-30741-9_18openalex-snapshot
Marine Chemosynthetic Symbioses
inferred← citeshttps://doi.org/10.1007/978-1-4757-2191-1_53openalex-snapshot
Prokaryotic Symbionts of Marine Invertebrates
inferred← citeshttps://doi.org/10.1007/978-3-642-30194-0_21openalex-snapshot
Marine Chemosynthetic Symbioses
inferred← citeshttps://doi.org/10.1007/978-981-99-1494-4_6openalex-snapshot
Symbioses from Cold Seeps
inferred← citeshttps://doi.org/10.1007/bf00171889openalex-snapshot
The presence, nature, and role of gut microflora in aquatic invertebrates: A synthesis
inferred← citeshttps://doi.org/10.1007/bf00346178openalex-snapshot
Characterization and site description of Solemya borealis (Bivalvia; Solemyidae), another bivalve-bacteria symbiosis
inferred← citeshttps://doi.org/10.1007/bf00349283openalex-snapshot
Digestive enzymes in marine invertebrates from hydrothermal vents and other reducing environments
inferred← citeshttps://doi.org/10.1007/bf00397769openalex-snapshot
Association of bacteria with larvae of the gutless protobranch bivalve Solemya reidi (Cryptodonta: Solemyidae)
inferred← citeshttps://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)
inferred← citeshttps://doi.org/10.1007/bf01313266openalex-snapshot
Role of filter-feeding in the nutritional biology of a deep-sea mussel with methanotrophic symbionts
inferred← citeshttps://doi.org/10.1007/bf03179969openalex-snapshot
Cell proliferation and growth inZoothamnium niveum (Oligohymenophora, Peritrichida) — Thiotrophic bacteria symbiosis
inferred← citeshttps://doi.org/10.1007/s00227-005-1630-9openalex-snapshot
Allometry of gill weights, gill surface areas, and foot biomass δ13C values of the chemoautotroph–bivalve symbiosis Solemya velum
inferred← citeshttps://doi.org/10.1007/s00227-007-0709-xopenalex-snapshot
Persistence, morphology, and nutritional state of a gastropod hosted bacterial symbiosis in different levels of hydrothermal vent flux
inferred← citeshttps://doi.org/10.1007/s002270050187openalex-snapshot
Methanotrophic symbiont location and fate of carbon incorporated from methane in a hydrocarbon seep mussel
inferred← citeshttps://doi.org/10.1007/s002270050722openalex-snapshot
An autoradiographic examination of carbon fixation, transfer and utilization in the Riftia pachyptila symbiosis
inferred← citeshttps://doi.org/10.1007/s00343-022-2217-8openalex-snapshot
The first complete mitogenome of Acharax sp. (Protobranchia, Solemyida, Solemyidae): comparisons with other Solemyidae bivalves and deep-sea adaptive characteristics
inferred← citeshttps://doi.org/10.1007/s10482-006-9086-6openalex-snapshot
Bacterial endosymbioses in Solemya (Mollusca: Bivalvia)—Model systems for studies of symbiont–host adaptation
inferred← citeshttps://doi.org/10.1007/s13199-017-0525-0openalex-snapshot
Life and death in facultative chemosymbioses: control of bacterial population dynamics in the Thyasiridae
inferred← citeshttps://doi.org/10.1007/s13199-021-00801-4openalex-snapshot
Bacterial ectosymbionts colonizing gills of two Caribbean mangrove crabs
inferred← citeshttps://doi.org/10.1007/springerreference_3633openalex-snapshot
Marine Chemosynthetic Symbioses
inferred← citeshttps://doi.org/10.1016/0022-0981(91)90215-iopenalex-snapshot
Abundance, growth and production of the bivalve Solemya sp., a food source for juvenile rock lobsters in a seagrass community in Western Australia
inferred← citeshttps://doi.org/10.1016/0022-0981(92)90309-xopenalex-snapshot
Ammonium and free amino acids as nitrogen sources for the chemoautotrophic symbiosis Solemya reidi Bernard (Bivalvia : Protobranchia)
inferred← citeshttps://doi.org/10.1016/0077-7579(89)90040-9openalex-snapshot
Chemoautotrophic metabolism of intracellular gill bacteria in the marine bivalve Spisula subtruncata (da Costa)
inferred← citeshttps://doi.org/10.1016/0146-6380(92)90054-2openalex-snapshot
Gulf of Mexico hydrocarbon seep communities—IX. Sterol biosynthesis of seep mussels and its implications for host-symbiont association
inferred← citeshttps://doi.org/10.1016/0198-0149(88)90049-0openalex-snapshot
Microhabitat variation in the hydrothermal vent mussel, Bathymodiolus thermophilus, at the Rose Garden vent on the Galapagos Rift
inferred← citeshttps://doi.org/10.1016/0300-9629(94)00211-bopenalex-snapshot
Feeding and digestive adaptations of bivalve molluscs to sulphide-rich habitats
inferred← citeshttps://doi.org/10.1016/0305-0491(91)90188-jopenalex-snapshot
The effects of sulfide on the anaerobic metabolism of two congeneric species of mudflat clams
inferred← citeshttps://doi.org/10.1016/0305-1978(89)90025-2openalex-snapshot
Genetic variability of the Lucinidae:Loripes lucinalis,Lucinella divaricata and Lucinoma borealis minor (Mollusca: Bivalvia) from Brittany, France
inferred← citeshttps://doi.org/10.1016/b978-0-12-751411-6.50019-9openalex-snapshot
The Structure and Function of Molluscan Digestive Systems
inferred← citeshttps://doi.org/10.1016/j.bbalip.2025.159617openalex-snapshot
Methyl-end desaturases determine the capability for de novo biosynthesis of polyunsaturated fatty acids in bivalves
inferred← citeshttps://doi.org/10.1016/j.dsr.2005.01.006openalex-snapshot
Live foraminiferal faunas from a 2800 m deep lower canyon station from the Bay of Biscay: Faunal response to focusing of refractory organic matter
inferred← citeshttps://doi.org/10.1016/j.dsr.2006.05.010openalex-snapshot
Hydrothermal vent meiobenthos associated with mytilid mussel aggregations from the Mid-Atlantic Ridge and the East Pacific Rise
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2018.03.007openalex-snapshot
Modelling the interactions of the hydrothermal mussel Bathymodiolus azoricus with vent fluid
inferred← citeshttps://doi.org/10.1016/j.palaeo.2012.10.033openalex-snapshot
Cretaceous methane-seep deposits from New Zealand and their fauna
inferred← citeshttps://doi.org/10.1016/j.palaeo.2014.11.020openalex-snapshot
Late Cretaceous (Maastrichtian) shallow water hydrocarbon seeps from Snow Hill and Seymour Islands, James Ross Basin, Antarctica
inferred← citeshttps://doi.org/10.1016/s1095-6433(00)00254-3openalex-snapshot
Respiration in the burrowing brittlestar, Hemipholis elongata Say (Echinodermata, Ophiuroidea): a study of the effects of environmental variables on oxygen uptake
inferred← citeshttps://doi.org/10.1038/s41396-018-0069-1openalex-snapshot
NanoSIMS and tissue autoradiography reveal symbiont carbon fixation and organic carbon transfer to giant ciliate host
inferred← citeshttps://doi.org/10.1086/741341openalex-snapshot
Ultrastructural Bacteriocyte Characterization among Chemosymbiotic Alviniconcha Snails from Hydrothermal Vents in the Indo-Pacific Oceans
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2000.tb00007.xopenalex-snapshot
The adoral sense organ in protobranch bivalves (Mollusca): comparative fine structure with special reference toNucula nucleus
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2002.tb00128.xopenalex-snapshot
Methane‐based symbiosis in a mussel, Bathymodiolus platifrons, from cold seeps in Sagami Bay, Japan
inferred← citeshttps://doi.org/10.1111/mec.12460openalex-snapshot
Characterizing the plasticity of nitrogen metabolism by the host and symbionts of the hydrothermal vent chemoautotrophic symbioses R idgeia piscesae
inferred← citeshttps://doi.org/10.1126/science.240.4848.78openalex-snapshot
Mussel Growth Supported by Methane as Sole Carbon and Energy Source
inferred← citeshttps://doi.org/10.1128/aem.01522-19openalex-snapshot
Hydrogen Does Not Appear To Be a Major Electron Donor for Symbiosis with the Deep-Sea Hydrothermal Vent Tubeworm Riftia pachyptila
inferred← citeshttps://doi.org/10.1128/aem.56.8.2436-2440.1990openalex-snapshot
Description of a Novel Symbiotic Bacterium from the Brittle Star, Amphipholis squamata
inferred← citeshttps://doi.org/10.1186/s40645-025-00768-6openalex-snapshot
Nitrogen isotopic composition of amino acids reveals a variety of trophic ecology of organisms inhabiting chemosynthesis-based ecosystems
inferred← citeshttps://doi.org/10.1242/jeb.049023openalex-snapshot
The metabolic demands of endosymbiotic chemoautotrophic metabolism on host physiological capacities
inferred← citeshttps://doi.org/10.1242/jeb.076711openalex-snapshot
Intracapsular algae provide fixed carbon to developing embryos of the salamanderAmbystoma maculatum
inferred← citeshttps://doi.org/10.1242/jeb.133.1.1openalex-snapshot
Net Uptake of CO2 Driven by Sulphide and Thiosulphate Oxidation in the Bacterial Symbiont-Containing Clam Solemya Reidi
inferred← citeshttps://doi.org/10.1242/jeb.149.1.133openalex-snapshot
Production of thiosulphate during sulphide oxidation by mitochondria of the symbiont-containing bivalve Solemya reidi
inferred← citeshttps://doi.org/10.1242/jeb.199.6.1343openalex-snapshot
Sulfide May Directly Modify Cytoplasmic Hemoglobin Deoxygenation in Solemya Reidi Gills
inferred← citeshttps://doi.org/10.1242/jeb.200.21.2797openalex-snapshot
The effects of exposure to ammonia on ammonia and taurine pools of the symbiotic clam Solemya reidi
inferred← citeshttps://doi.org/10.1242/jeb.202.3.289openalex-snapshot
Pathways of inorganic nitrogen assimilation in chemoautotrophic bacteria–marine invertebrate symbioses: expression of host and symbiont glutamine synthetase
inferred← citeshttps://doi.org/10.1264/microbes1986.3.73openalex-snapshot
The Symbiotic Relationship between Bacteria and a Mesogastropod Snail, Alviniconcha hessleri, collected from Hydrothermal Vents of the Mariana Back-Arc Basin
inferred← citeshttps://doi.org/10.2307/1541730openalex-snapshot
Gill Hemoglobin May Deliver Sulfide to Bacterial Symbionts ofSolemya velum(Bivalvia, Mollusca)
inferred← citeshttps://doi.org/10.2307/1542263openalex-snapshot
Hydrogen Sulfide Reduction of Symbiont Cytochrome c552 in Gills of Solemya reidi (Mollusca)
inferred← citeshttps://doi.org/10.2307/1542437openalex-snapshot
Sulfide-Driven Autotrophic Balance in the Bacterial Symbiont-Containing Hydrothermal Vent Tubeworm, Riftia pachyptila Jones
inferred← citeshttps://doi.org/10.3354/meps086145openalex-snapshot
Suspension feeding on phytoplankton by Solemya velum, a symbiont-containing clam
inferred← citeshttps://doi.org/10.3354/meps231115openalex-snapshot
Glycogen storage in the Riftia pachyptila trophosome: contribution of host and symbionts
inferred← citeshttps://doi.org/10.3389/fmicb.2014.00145openalex-snapshot
The giant ciliate Zoothamnium niveum and its thiotrophic epibiont Candidatus Thiobios zoothamnicoli: a model system to study interspecies cooperation
inferred← citeshttps://doi.org/10.3390/microorganisms12040652openalex-snapshot
Environmental Transmission of Symbionts in the Mangrove Crabs Aratus pisonii and Minuca rapax: Acquisition of the Bacterial Community through Larval Development to Juvenile Stage
inferred← citeshttps://doi.org/10.4002/040.051.0202openalex-snapshot
North Pacific Species of the GenusSolemyaLamarck, 1818 (Bivalvia: Solemyidae), with Notes onAcharax johnsoni(Dall, 1891)
inferred← citeshttps://doi.org/10.4236/ojms.2017.71010openalex-snapshot
Molecular Phylogenetic Analysis of Chemosymbiotic Solemyidae and Thyasiridae
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/10.70675/97084483z1169z4f01z8bd5z453590e95ec1openalex-snapshot
Fonctionnement et dynamique des écosystèmes hydrothermaux : vers un premier modèle
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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