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Mitogenomic analysis of Montipora cactus and Anacropora matthai (cnidaria; scleractinia; acroporidae) indicates an unequal rate of mitochondrial evolution among Acroporidae corals

https://doi.org/10.1007/s00338-005-0499-x
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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/bf00164024openalex-snapshot
Evolution and structural conservation of the control region of insect mitochondrial DNA
inferredcites →https://doi.org/10.1007/pl00006245openalex-snapshot
Molecular evolution of a portion of the mitochondrial 16S ribosomal gene region in scleractinian corals
inferredcites →https://doi.org/10.1007/pl00006321openalex-snapshot
Mitochondrial DNA of the coral sarcophyton glaucum contains a gene for a homologue of bacterial muts: A possible case of gene transfer from the nucleus to the mitochondrion
inferredcites →https://doi.org/10.1007/pl00006429openalex-snapshot
Sequence Analysis of the Mitochondrial Genome of Sarcophyton glaucum: Conserved Gene Order Among Octocorals
inferredcites →https://doi.org/10.1007/s00239-001-0075-0openalex-snapshot
The Mitochondrial Genome of Acropora tenuis (Cnidaria; Scleractinia) Contains a Large Group I Intron and a Candidate Control Region
inferredcites →https://doi.org/10.1007/s003380100169openalex-snapshot
Unexpectedly high coral coverage in Chinwan Inner Bay, Pescadores: a proposed site for a Marine Protection Area
inferredcites →https://doi.org/10.1007/s101269900018openalex-snapshot
Universal Primers for Amplification of Mitochondrial Small Subunit Ribosomal RNA-Encoding Gene in Scleractinian Corals
inferredcites →https://doi.org/10.1016/b978-0-444-82235-2.50029-1openalex-snapshot
Mitochondrial Genomes of Anthozoa (Cnidaria)
inferredcites →https://doi.org/10.1016/s0074-7696(08)62066-5openalex-snapshot
Animal Mitochondrial DNA: Structure and Evolution
inferredcites →https://doi.org/10.1016/s1055-7903(02)00008-8openalex-snapshot
Analysis of the mitochondrial 12S rRNA gene supports a two-clade hypothesis of the evolutionary history of scleractinian corals
inferredcites →https://doi.org/10.1038/369684a0openalex-snapshot
Long PCR
inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01526.xopenalex-snapshot
The highly cross‐fertile coral species,Acropora hyacinthusandAcropora cytherea, constitute statistically distinguishable lineages
inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01652.xopenalex-snapshot
Slow mitochondrial DNA sequence evolution in the Anthozoa (Cnidaria)
inferredcites →https://doi.org/10.1071/9780643101388openalex-snapshot
Staghorn Corals of the World
inferredcites →https://doi.org/10.1073/pnas.89.18.8750openalex-snapshot
Class-level relationships in the phylum Cnidaria: evidence from mitochondrial genome structure.
inferredcites →https://doi.org/10.1073/pnas.93.11.5619openalex-snapshot
Two mitochondrial group I introns in a metazoan, the sea anemone Metridium senile: one intron contains genes for subunits 1 and 3 of NADH dehydrogenase.
inferredcites →https://doi.org/10.1093/bioinformatics/17.12.1244openalex-snapshot
MEGA2: molecular evolutionary genetics analysis software
inferredcites →https://doi.org/10.1093/genetics/121.3.551openalex-snapshot
Molecular population genetics of mtDNA size variation in crickets.
inferredcites →https://doi.org/10.1093/genetics/135.2.599openalex-snapshot
Simple methods for testing the molecular evolutionary clock hypothesis.
inferredcites →https://doi.org/10.1093/genetics/148.3.1091openalex-snapshot
The Mitochondrial Genome of the Sea Anemone Metridium senile (Cnidaria): Introns, a Paucity of tRNA Genes, and a Near-Standard Genetic Code
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003916openalex-snapshot
The Evolutionary History of the Coral Genus Acropora (Scleractinia, Cnidaria) Based on a Mitochondrial and a Nuclear Marker: Reticulation, Incomplete Lineage Sorting, or Morphological Convergence?
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026094openalex-snapshot
Gene content and organization in a segment of the mitochondrial genome of the scleractinian coral Acropora tenuis: major differences in gene order within the anthozoan subclass zoantharia Citation]
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026360openalex-snapshot
The Complete Mitochondrial DNA Sequence of the Horseshoe Crab Limulus polyphemus
inferredcites →https://doi.org/10.1098/rspb.1999.0619openalex-snapshot
Atypically low rate of cytochrome b evolution in the scleractinian coral genus Acropora
inferredcites →https://doi.org/10.1098/rspb.2002.2014openalex-snapshot
Sympatric populations of the highly cross-fertile coral speciesAcropora hyacinthusandAcropora cythereaare genetically distinct
inferredcites →https://doi.org/10.1126/science.1069524openalex-snapshot
Hybridization and the Evolution of Reef Coral Diversity
inferredcites →https://doi.org/10.2108/zsj.15.689openalex-snapshot
Phylogenetic Relationships in the Coral Family Acroporidae, Reassessed by Inference from Mitochondrial Genes
inferredcites →https://doi.org/10.5860/choice.33-2723openalex-snapshot
Corals in space and time: the biogeography and evolution of the Scleractinia

What points at this work

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

inferred← citeshttps://doi.org/10.21425/fob.19.174247zenodo-depositor-declared
Global biogeography of zoantharians indicates a weak genetic differentiation between the Atlantic and Indo-Pacific oceans, and distinct communities in tropical and temperate provinces
inferred← citeshttps://doi.org/10.1007/978-3-319-31305-4_4openalex-snapshot
The New Systematics of Scleractinia: Integrating Molecular and Morphological Evidence
inferred← citeshttps://doi.org/10.1007/s00227-015-2657-1openalex-snapshot
Massively parallel sequencing (MPS) assays for sequencing mitochondrial genomes: the phylogenomic implications for Acropora staghorn corals (Scleractinia; Acroporidae)
inferred← citeshttps://doi.org/10.1007/s00239-006-0015-0openalex-snapshot
Mitochondrial Genome of Savalia savaglia (Cnidaria, Hexacorallia) and Early Metazoan Phylogeny
inferred← citeshttps://doi.org/10.1007/s00239-006-0279-4openalex-snapshot
Novel Group I Introns Encoding a Putative Homing Endonuclease in the Mitochondrial cox1 Gene of Scleractinian Corals
inferred← citeshttps://doi.org/10.1007/s00239-008-9069-5openalex-snapshot
Slow Mitochondrial COI Sequence Evolution at the Base of the Metazoan Tree and Its Implications for DNA Barcoding
inferred← citeshttps://doi.org/10.1007/s00338-011-0797-4openalex-snapshot
Comparison of morphological and genetic analyses reveals cryptic divergence and morphological plasticity in Stylophora (Cnidaria, Scleractinia)
inferred← citeshttps://doi.org/10.1007/s10126-008-9093-xopenalex-snapshot
Unique Mitogenomic Features in the Scleractinian Family Pocilloporidae (Scleractinia: Astrocoeniina)
inferred← citeshttps://doi.org/10.1007/s10126-008-9129-2openalex-snapshot
Comparative Analyses of Coding and Noncoding DNA Regions Indicate that Acropora (Anthozoa: Scleractina) Possesses a Similar Evolutionary Tempo of Nuclear vs. Mitochondrial Genomes as in Plants
inferred← citeshttps://doi.org/10.1016/j.gene.2007.07.006openalex-snapshot
The mitochondrial genome of Pocillopora (Cnidaria: Scleractinia) contains two variable regions: The putative D-loop and a novel ORF of unknown function
inferred← citeshttps://doi.org/10.1016/j.gene.2016.05.034openalex-snapshot
Complete mitochondrial genome sequences of Atlantic representatives of the invasive Pacific coral species Tubastraea coccinea and T. tagusensis (Scleractinia, Dendrophylliidae): Implications for species identification
inferred← citeshttps://doi.org/10.1016/j.ympev.2006.08.016openalex-snapshot
The complete mitochondrial genome of the black coral Chrysopathes formosa (Cnidaria:Anthozoa:Antipatharia) supports classification of antipatharians within the subclass Hexacorallia
inferred← citeshttps://doi.org/10.1016/j.ympev.2007.09.013openalex-snapshot
The complete mitochondrial genomes of needle corals, Seriatopora spp. (Scleractinia: Pocilloporidae): An idiosyncratic atp8, duplicated trnW gene, and hypervariable regions used to determine species phylogenies and recently diverged populations
inferred← citeshttps://doi.org/10.1080/23802359.2017.1419100openalex-snapshot
The complete mitochondrial genome of the Montipora peltiformi (Scleractinia: Acroporidae)
inferred← citeshttps://doi.org/10.1080/23802359.2025.2499129openalex-snapshot
Complete mitochondrial genome of the brain coral Platygyra daedalea (Ellis & Solander, 1786)
inferred← citeshttps://doi.org/10.1080/23802359.2025.2512867openalex-snapshot
Complete mitochondrial genome and phylogenetic analysis of Podabacia crustacea (Pallas, 1766)
inferred← citeshttps://doi.org/10.1093/icb/icq081openalex-snapshot
Phylogenetic Signal in Mitochondrial and Nuclear Markers in Sea Anemones (Cnidaria, Actiniaria)
inferred← citeshttps://doi.org/10.1111/j.1471-8286.2007.01996.xopenalex-snapshot
DNA BARCODING: Barcoding corals: limited by interspecific divergence, not intraspecific variation
inferred← citeshttps://doi.org/10.1111/maec.12388openalex-snapshot
Inter‐ and intra‐colonial genotypic diversity in hermatypic hydrozoans of the family Milleporidae
inferred← citeshttps://doi.org/10.1111/zoj.12060openalex-snapshot
The evolutionary history of the order Antipatharia (Cnidaria: Anthozoa: Hexacorallia) as inferred from mitochondrial and nuclear DNA: implications for black coral taxonomy and systematics
inferred← citeshttps://doi.org/10.1186/1471-2148-6-24openalex-snapshot
No variation and low synonymous substitution rates in coral mtDNA despite high nuclear variation
inferred← citeshttps://doi.org/10.1371/journal.pone.0094774openalex-snapshot
The “Naked Coral” Hypothesis Revisited – Evidence for and Against Scleractinian Monophyly
inferred← citeshttps://doi.org/10.1371/journal.pone.0098406openalex-snapshot
A Phylogeny of the Family Poritidae (Cnidaria, Scleractinia) Based on Molecular and Morphological Analyses
inferred← citeshttps://doi.org/10.1371/journal.pone.0107366openalex-snapshot
Identification of Scleractinian Coral Recruits Using Fluorescent Censusing and DNA Barcoding Techniques
inferred← citeshttps://doi.org/10.3109/19401736.2014.1003845openalex-snapshot
The complete mitochondrial genomes of Pseudosiderastrea spp (Cnidaria, Scleractinia, Siderastreidae)
inferred← citeshttps://doi.org/10.3109/19401736.2014.926506openalex-snapshot
Complete mitochondrial genome of disc coral Turbinaria peltata (Scleractinia, Dendrophylliidae)
inferred← citeshttps://doi.org/10.3109/19401736.2015.1082092openalex-snapshot
The complete mitochondrial genome of Acropora aculeus (cnidaria, scleractinia, acroporidae)
inferred← citeshttps://doi.org/10.3354/meps08879openalex-snapshot
Evolutionary history of the seagrass genus Posidonia
inferred← citeshttps://doi.org/10.3755/galaxea.11.21openalex-snapshot
The partial mitochondrial genome of Leiopathes glaberrima (Hexacorallia: Antipatharia) and the first report of the presence of an intron in COI in black corals
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.3/reviews/1openalex-snapshot
Peer Review #1 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.3)"
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.3/reviews/2openalex-snapshot
Peer Review #2 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.3)"
inferred← citeshttps://doi.org/10.7287/peerj.13451v0.3/reviews/3openalex-snapshot
Peer Review #3 of "Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific (v0.3)"
inferred← citeshttps://doi.org/10.7717/peerj.13451openalex-snapshot
Population genetics and demography of the coral-killing cyanobacteriosponge, Terpios hoshinota, in the Indo-West Pacific
inferred← citeshttps://doi.org/10.7717/peerj.4074openalex-snapshot
Resurrecting a subgenus to genus: molecular phylogeny of Euphyllia and Fimbriaphyllia (order Scleractinia; family Euphyllidae; clade V)
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