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Correlations of geographic distribution and temperature of embryonic development with the nuclear DNA content in the Salamandridae (Urodela, Amphibia)

https://doi.org/10.1139/g07-010
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What this work says

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

inferredcites →https://doi.org/10.1002/jez.1135openalex-snapshot
The evolution of genome size: What can be learned from anuran development?
inferredcites →https://doi.org/10.1006/bcmd.2001.0457openalex-snapshot
The Bigger the C-Value, the Larger the Cell: Genome Size and Red Blood Cell Size in Vertebrates
inferredcites →https://doi.org/10.1006/jtbi.1997.0629openalex-snapshot
Buffering: a Possible Passive-homeostasis Role for Redundant DNA
inferredcites →https://doi.org/10.1006/tpbi.2002.1605openalex-snapshot
Mutational Equilibrium Model of Genome Size Evolution
inferredcites →https://doi.org/10.1007/978-94-009-3127-5openalex-snapshot
Temperature Biology of Animals
inferredcites →https://doi.org/10.1007/bf00596625openalex-snapshot
Die Entwicklung vonTriton alpestris bei verschiedenen Temperaturen, mit Normentafel
inferredcites →https://doi.org/10.1007/bf01938475openalex-snapshot
Evolution of the genome and cell sizes in salamanders
inferredcites →https://doi.org/10.1007/bf02101640openalex-snapshot
Evolution of the genome size inAkodon (Rodentia, Cricetidae)
inferredcites →https://doi.org/10.1007/s000180050343openalex-snapshot
Amphibian sex determination and sex reversal
inferredcites →https://doi.org/10.1007/s10577-007-1205-3openalex-snapshot
Evolutionary cytogenetics in salamanders
inferredcites →https://doi.org/10.1007/s10577-008-1197-7openalex-snapshot
Cytogenetic analysis of the Asian Plethodontid salamander, Karsenia koreana: Evidence for karyotypic conservation, chromosome repatterning, and genome size evolution
inferredcites →https://doi.org/10.1016/0305-0491(91)90089-vopenalex-snapshot
Genome size and metabolic rate in salamanders
inferredcites →https://doi.org/10.1016/j.biolcel.2003.11.005openalex-snapshot
Genome size in Echinops L. and related genera (Asteraceae, Cardueae): karyological, ecological and phylogenetic implications
inferredcites →https://doi.org/10.1016/j.tig.2005.09.003openalex-snapshot
Genome size is negatively correlated with effective population size in ray-finned fish
inferredcites →https://doi.org/10.1016/j.ympev.2006.05.008openalex-snapshot
A molecular assessment of phylogenetic relationships and lineage accumulation rates within the family Salamandridae (Amphibia, Caudata)
inferredcites →https://doi.org/10.1016/s0168-9525(00)02157-0openalex-snapshot
Evolution of genome size: new approaches to an old problem
inferredcites →https://doi.org/10.1017/s1464793100005595openalex-snapshot
Coincidence, coevolution, or causation? DNA content, cell size, and the C-value enigma
inferredcites →https://doi.org/10.1023/a:1016032400147openalex-snapshot
Genome size and developmental complexity
inferredcites →https://doi.org/10.1038/35016000openalex-snapshot
The genetic legacy of the Quaternary ice ages
inferredcites →https://doi.org/10.1038/417070aopenalex-snapshot
Effects of size and temperature on developmental time
inferredcites →https://doi.org/10.1046/j.1095-8312.2003.00191.xopenalex-snapshot
Variation across amphibian species in the size of the nuclear genome supports a pluralistic, hierarchical approach to the C-value enigma
inferredcites →https://doi.org/10.1073/pnas.49.6.897openalex-snapshot
A RELATIONSHIP BETWEEN DNA CONTENT, NUCLEAR VOLUME, AND MINIMUM MITOTIC CYCLE TIME
inferredcites →https://doi.org/10.1073/pnas.91.11.4796openalex-snapshot
Cell size predicts morphological complexity in the brains of frogs and salamanders.
inferredcites →https://doi.org/10.1080/00087114.1973.10796525openalex-snapshot
Quantitative Variations in the Nuclear DNA and Phylogenesis of the Amphibia
inferredcites →https://doi.org/10.1083/jcb.19.2.279openalex-snapshot
THE BASE COMPOSITION OF RIBONUCLEIC ACID IN LAMPBRUSH CHROMOSOMES, NUCLEOLI, NUCLEAR SAP, AND CYTOPLASM OF TRITURUS OOCYTES
inferredcites →https://doi.org/10.1086/282588openalex-snapshot
Temperature Adaptations of Amphibian Embryos
inferredcites →https://doi.org/10.1086/physzool.45.3.30152501openalex-snapshot
Temperature Adaptation of Embryonic Development Rate among Frogs
inferredcites →https://doi.org/10.1086/physzool.48.4.30155661openalex-snapshot
Embryonic Temperature Adaptation in Development Rate of Frogs
inferredcites →https://doi.org/10.1086/physzool.63.6.30152638openalex-snapshot
Incubation Time and Rate of Embryonic Development in Amphibians: The Influence of Ovum Size, Temperature, and Reproductive Mode
inferredcites →https://doi.org/10.1093/jhered/esi061openalex-snapshot
Genome Size Evolution in New Zealand Triplefin Fishes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040260openalex-snapshot
Body temperature, rate of biosynthesis, and evolution of genome size.
inferredcites →https://doi.org/10.1098/rspb.1992.0093openalex-snapshot
Variation across species in the size of the nuclear genome supports the junk-DNA explanation for the C-value paradox
inferredcites →https://doi.org/10.1098/rspb.1997.0085openalex-snapshot
An evolutionary correlate of genome size change in plethodontid salamanders
inferredcites →https://doi.org/10.1098/rspb.2004.2776openalex-snapshot
Genome size and extinction risk in vertebrates
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02457.xopenalex-snapshot
Is genome size influenced by colonization of new environments in dipteran species?
inferredcites →https://doi.org/10.1111/j.1439-0469.1978.tb00931.xopenalex-snapshot
Nuclear DNA amounts and developmental rate in holarctic anura
inferredcites →https://doi.org/10.1111/j.1469-7998.2000.tb01087.xopenalex-snapshot
The relationship of neonate mass and incubation temperature to embryonic development time in a range of animal taxa
inferredcites →https://doi.org/10.1111/j.1558-5646.1987.tb02463.xopenalex-snapshot
DEVELOPMENTAL CORRELATES OF GENOME SIZE IN PLETHODONTID SALAMANDERS AND THEIR IMPLICATIONS FOR GENOME EVOLUTION
inferredcites →https://doi.org/10.1111/j.1601-5223.2003.01766.xopenalex-snapshot
C-value estimates for 31 species of ladybird beetles (Coleoptera: Coccinellidae)
inferredcites →https://doi.org/10.1126/science.1061967openalex-snapshot
Effects of Size and Temperature on Metabolic Rate
inferredcites →https://doi.org/10.1139/g90-092openalex-snapshot
Genome elimination in diploid and triploid Rana esculenta males: cytological evidence from DNA flow cytometry
inferredcites →https://doi.org/10.1139/g98-117openalex-snapshot
Genome in toto
inferredcites →https://doi.org/10.1139/gen-42-2-361openalex-snapshot
Genome in toto
inferredcites →https://doi.org/10.1159/000074174openalex-snapshot
Reptiles: a group of transition in the evolution of genome size and of the nucleotypic effect
inferredcites →https://doi.org/10.1159/000113321openalex-snapshot
Genome Size, Secondary Simplification, and the Evolution of the Brain in Salamanders
inferredcites →https://doi.org/10.1163/15685380152770354openalex-snapshot
Cryptic speciation in Pelobates fuscus (Anura, Pelobatidae): evidence from DNA flow cytometry
inferredcites →https://doi.org/10.1163/156853805774408685openalex-snapshot
Taxonomic status of Triturus vittatus (Amphibia: Salamandridae) in western Turkey: trunk vertebrae count, genome size and allozyme data
inferredcites →https://doi.org/10.1163/156853897x00260openalex-snapshot
Flow cytometry in biodiversity surveys: methods, utility, and constraints
inferredcites →https://doi.org/10.1163/156853898x00016openalex-snapshot
Embryonic development of the newt Triturus italicus in relation to temperature
inferredcites →https://doi.org/10.1242/jcs.63.1.135openalex-snapshot
C value and cell volume: Their significance in the evolution and development of amphibians
inferredcites →https://doi.org/10.2307/1442021openalex-snapshot
DNA and Amphibian Life History
inferredcites →https://doi.org/10.2307/1443555openalex-snapshot
Genome Size and Nuclear Size in Palaearctic Frogs (Rana)
inferredcites →https://doi.org/10.2307/1564180openalex-snapshot
Normal Development in Newts (Triturus) and Its Arrest as a Consequence of an Unusual Chromosomal Situation
inferredcites →https://doi.org/10.2307/1930439openalex-snapshot
Temperature Tolerance and Rates of Development in the Eggs of Amphibia
inferredcites →https://doi.org/10.2307/2425927openalex-snapshot
Embryonic Development and Temperature Tolerance in Diploid and Polyploid Salamanders (Genus Ambystoma)
inferredcites →https://doi.org/10.30906/1026-2296-2001-8-1-74-76openalex-snapshot
Natural Autotriploidy in the Danube Newt, Triturus dobrogicus (Salamandridae)
inferredcites →https://doi.org/10.5281/zenodo.16146089openalex-snapshot
NUCLEAR DNA AND DEVELOPMENTAL RATE IN FROGS

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.3682.3.5zenodo-depositor-declared
A revised taxonomy of crested newts in the Triturus karelinii group (Amphibia: Caudata: Salamandridae), with the description of a new species
inferred← citeshttps://doi.org/10.1002/ece3.71835openalex-snapshot
NewtCap : An Efficient Target Capture Approach to Boost Genomic Studies in Salamandridae (True Salamanders and Newts)
inferred← citeshttps://doi.org/10.1007/978-1-4939-2495-0_1openalex-snapshot
Variation in Salamanders: An Essay on Genomes, Development, and Evolution
inferred← citeshttps://doi.org/10.1007/s10577-007-1205-3openalex-snapshot
Evolutionary cytogenetics in salamanders
inferred← citeshttps://doi.org/10.1007/s10577-008-1197-7openalex-snapshot
Cytogenetic analysis of the Asian Plethodontid salamander, Karsenia koreana: Evidence for karyotypic conservation, chromosome repatterning, and genome size evolution
inferred← citeshttps://doi.org/10.1016/b978-0-12-374984-0.00639-2openalex-snapshot
Genome Size
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2023.103474openalex-snapshot
Higher Temperature Induces Oxidative Stress in Hybrids But Not in Parental Species: A Case Study of Crested Newts
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2026.104479openalex-snapshot
Variation in thermal plasticity of larval morphology among crested newt species and their reciprocal hybrids (Salamandridae: Triturus)
inferred← citeshttps://doi.org/10.1038/s41598-020-62408-xopenalex-snapshot
The transcriptome of the newt Cynops orientalis provides new insights into evolution and function of sexual gene networks in sarcopterygians
inferred← citeshttps://doi.org/10.1038/srep24051openalex-snapshot
Molecular Inversion Probes for targeted resequencing in non-model organisms
inferred← citeshttps://doi.org/10.1080/00222930802585794openalex-snapshot
Interspecific differences in early life‐history traits in crested newts (Triturus cristatussuperspecies, Caudata, Salamandridae) from the Balkan Peninsula
inferred← citeshttps://doi.org/10.1080/24750263.2020.1747558openalex-snapshot
Shedding light upon the complex net of genome size, genome composition and environment in chordates
inferred← citeshttps://doi.org/10.1093/gbe/evaf155openalex-snapshot
Identification of Y-chromosome Turnover in Newts Fails to Support a Sex Chromosome Origin for the Triturus Balanced Lethal System
inferred← citeshttps://doi.org/10.1093/iob/obad020openalex-snapshot
Post-Diapause DNA Replication during Oogenesis in a Capital-Breeding Copepod
inferred← citeshttps://doi.org/10.1098/rspb.2019.1780openalex-snapshot
Ecological constraints associated with genome size across salamander lineages
inferred← citeshttps://doi.org/10.1111/1755-0998.70019openalex-snapshot
Linkage Mapping vs. Association: A Comparison of Two RADseq ‐Based Approaches to Identify Markers for Homomorphic Sex Chromosomes in Large Genomes
inferred← citeshttps://doi.org/10.1111/j.1439-0469.2011.00633.xopenalex-snapshot
The evolution of the adult body form of the crested newt (Triturus cristatussuperspecies, Caudata, Salamandridae)
inferred← citeshttps://doi.org/10.1111/j.1469-7998.2010.00760.xopenalex-snapshot
Ontogeny of body form and metamorphosis: insights from the crested newts
inferred← citeshttps://doi.org/10.1134/s1062359025700463openalex-snapshot
Genome Size Variation in Diploid and Polyploid Rock Lizards of the Genus Darevskia (Lacertidae, Squamata)
inferred← citeshttps://doi.org/10.1155/2012/740605openalex-snapshot
A Phenotypic Point of View of the Adaptive Radiation of Crested Newts (Triturus cristatus Superspecies, Caudata, Amphibia)
inferred← citeshttps://doi.org/10.1159/000444429openalex-snapshot
Transposons, Genome Size, and Evolutionary Insights in Animals
inferred← citeshttps://doi.org/10.1163/15685381-bja10082openalex-snapshot
Consequences of hybridization on life history and growth in postmetamorphic Triturus macedonicus
inferred← citeshttps://doi.org/10.1163/18759866-07802001openalex-snapshot
Early ontogeny shows the same interspecific variation as natural history parameters in the crested newt (Triturus cristatus superspecies) (Caudata, Salamandridae)
inferred← citeshttps://doi.org/10.1242/jeb.242196openalex-snapshot
Genome size influences adaptive plasticity of water loss, but not metabolic rates, in lungless salamanders
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.24257.1openalex-snapshot
The genome sequence of the great crested newt, Triturus cristatus (Laurenti, 1768)
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.27692.1openalex-snapshot
The genome sequence of the Smooth Newt, Lissotriton vulgaris (Linnaeus, 1758) (Caudata: Salamandridae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0109831openalex-snapshot
A Transcriptome for the Study of Early Processes of Retinal Regeneration in the Adult Newt, Cynops pyrrhogaster
inferred← citeshttps://doi.org/10.1534/g3.117.041178openalex-snapshot
Linkage Map ofLissotritonNewts Provides Insight into the Genetic Basis of Reproductive Isolation
inferred← citeshttps://doi.org/10.2298/abs200328026vopenalex-snapshot
Reproductive characteristics of two Triturus species (Amphibia: Caudata)
inferred← citeshttps://doi.org/10.31857/s0044513424110032openalex-snapshot
Genome size variation in diploid and polyploid mountain lizards of the genus Darevskia (Lacertidae, Squamata)
inferred← citeshttps://doi.org/10.3390/ani12040443openalex-snapshot
The Reproductive Success of Triturus ivanbureschi × T. macedonicus F1 Hybrid Females (Amphibia: Salamandridae)
inferred← citeshttps://doi.org/10.5358/hsj.32.89openalex-snapshot
Chromosomal Localization of the 18S and 28S Ribosomal RNA Genes Using Fish and AgNO3Banding inHynobiusquelpaertensis, H. tsuensisandOnychodactylus koreanus(Urodela: Hynobiidae)
inferred← citeshttps://doi.org/10.5735/086.051.0505openalex-snapshot
The Roles of Phylogeny and Climate in Shaping Variation in Life-History Traits of the Newt GenusTriturus(Caudata, Salamandridae)
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