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Differential occupation of axial morphospace

https://doi.org/10.1016/j.zool.2013.10.006
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What this work says

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

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Why do almost all mammals have seven cervical vertebrae? Developmental constraints, Hox genes, and cancer
inferredcites →https://doi.org/10.1002/(sici)1097-4687(199909)241:3<217::aid-jmor4>3.0.co;2-mopenalex-snapshot
Testing an inference of function from structure: Snake vertebrae do the twist
inferredcites →https://doi.org/10.1002/aja.1002030302openalex-snapshot
Stages of embryonic development of the zebrafish
inferredcites →https://doi.org/10.1002/dvdy.10387openalex-snapshot
Developmental morphology of the axial skeleton of the zebrafish, Danio rerio (Ostariophysi: Cyprinidae)
inferredcites →https://doi.org/10.1002/jez.b.21029openalex-snapshot
Evolution of the vertebral formulae in mammals: A perspective on developmental constraints
inferredcites →https://doi.org/10.1002/jez.b.21305openalex-snapshot
Developmental control of segment numbers in vertebrates
inferredcites →https://doi.org/10.1002/jez.b.21353openalex-snapshot
From fetus to adult—an allometric analysis of the giraffe vertebral column
inferredcites →https://doi.org/10.1002/jmor.1051390302openalex-snapshot
Developmental and adult morphology of the vertebral column in the plethodontid salamander Eurycea bislineata, with comments on vertebral evolution in the amphibia
inferredcites →https://doi.org/10.1002/jmor.1051950304openalex-snapshot
Reevaluation of the caudal skeleton of some actinopterygian fishes: II. Hiodon, Elops, and Albula
inferredcites →https://doi.org/10.1002/jmor.1062openalex-snapshot
Vertebral column and associated elements in dipnoans and comparison with other fishes: Development and homology
inferredcites →https://doi.org/10.1002/jmor.11034openalex-snapshot
Regional variation in morphology of vertebral centra and intervertebral joints in striped bass, Morone saxatilis
inferredcites →https://doi.org/10.1002/mmng.201100003openalex-snapshot
Morphology of the anterior vertebral region in elasmobranchs: special focus, Squatiniformes
inferredcites →https://doi.org/10.1007/978-3-319-27613-7_2openalex-snapshot
Evolution of the Vertebral Column
inferredcites →https://doi.org/10.1016/0925-4773(95)00455-6openalex-snapshot
Teleost HoxD and HoxA genes: comparison with tetrapods and functional evolution of the HOXD complex
inferredcites →https://doi.org/10.1016/j.cub.2012.10.044openalex-snapshot
Evolutionary Shift from Fighting to Foraging in Blind Cavefish through Changes in the Serotonin Network
inferredcites →https://doi.org/10.1016/j.cub.2013.05.003openalex-snapshot
Evolutionary Origin of the Turtle Shell
inferredcites →https://doi.org/10.1016/j.ydbio.2009.04.031openalex-snapshot
Axial patterning in snakes and caecilians: Evidence for an alternative interpretation of the Hox code
inferredcites →https://doi.org/10.1016/j.ymeth.2014.03.033openalex-snapshot
Developmental Biology
inferredcites →https://doi.org/10.1016/j.zool.2008.05.003openalex-snapshot
Building an evolutionary innovation: Differential growth in the modified vertebral elements of the zebrafish Weberian apparatus
inferredcites →https://doi.org/10.1016/j.zool.2013.03.001openalex-snapshot
A revised metric for quantifying body shape in vertebrates
inferredcites →https://doi.org/10.1038/nature07020openalex-snapshot
Control of segment number in vertebrate embryos
inferredcites →https://doi.org/10.1038/nrg2320openalex-snapshot
Segmental patterning of the vertebrate embryonic axis
inferredcites →https://doi.org/10.1073/pnas.1300592110openalex-snapshot
Role of a polymorphism in a Hox/Pax-responsive enhancer in the evolution of the vertebrate spine
inferredcites →https://doi.org/10.1080/00222935508655673openalex-snapshot
LXXIII.—A preliminary revision of the fishes of the genusAulostomus
inferredcites →https://doi.org/10.1093/icb/icq029openalex-snapshot
Axial Elongation in Fishes: Using Morphological Approaches to Elucidate Developmental Mechanisms in Studying Body Shape
inferredcites →https://doi.org/10.1093/icb/icq057openalex-snapshot
Disentangling the Functional Roles of Morphology and Motion in the Swimming of Fish
inferredcites →https://doi.org/10.1093/icb/icq075openalex-snapshot
Elongation of the Body in Eels
inferredcites →https://doi.org/10.1097/00005053-193111000-00026openalex-snapshot
STUDIES ON THE STRUCTURE AND DEVELOPMENT OF VERTEBRATES
inferredcites →https://doi.org/10.1098/rspb.2012.0784openalex-snapshot
Tetrapod-like axial regionalization in an early ray-finned fish
inferredcites →https://doi.org/10.1111/j.1095-8312.2007.00714.xopenalex-snapshot
Evolution of axial patterning in elongate fishes
inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01823.xopenalex-snapshot
Jordan’s and other ecogeographical rules, and the vertebral number in fishes
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01491.xopenalex-snapshot
VERTEBRAL EVOLUTION AND THE DIVERSIFICATION OF SQUAMATE REPTILES
inferredcites →https://doi.org/10.1111/jeb.12128openalex-snapshot
Phylogenetic patterns of skeletal morphometrics and pelvic traits in relation to locomotor mode in frogs
inferredcites →https://doi.org/10.1126/science.1085672openalex-snapshot
Hox10 and Hox11 Genes Are Required to Globally Pattern the Mammalian Skeleton
inferredcites →https://doi.org/10.1126/science.76.1982.583openalex-snapshot
On the Locomotion of Snakes
inferredcites →https://doi.org/10.1139/f75-283openalex-snapshot
Pleomerism, the Widespread Tendency Among Related Fish Species for Vertebral Number to be Correlated with Maximum Body Length
inferredcites →https://doi.org/10.1186/1742-9994-10-17openalex-snapshot
‘Monster… -omics’: on segmentation, re-segmentation, and vertebrae formation in amphibians and other vertebrates
inferredcites →https://doi.org/10.1242/dev.063735openalex-snapshot
Patterning embryos with oscillations: structure, function and dynamics of the vertebrate segmentation clock
inferredcites →https://doi.org/10.1242/dev.121.2.333openalex-snapshot
Hox genes and the evolution of vertebrate axial morphology
inferredcites →https://doi.org/10.1242/dev.129.16.3851openalex-snapshot
Segmental relationship between somites and vertebral column in zebrafish
inferredcites →https://doi.org/10.1671/0272-4634(2001)021[0061:ssiji]2.0.co;2openalex-snapshot
Swimming styles in Jurassic ichthyosaurs
inferredcites →https://doi.org/10.2307/1441916openalex-snapshot
Vertebrate Paleontology
inferredcites →https://doi.org/10.2307/1443620openalex-snapshot
Evolutionary Relationships of the Sea Moths (Teleostei: Pegasidae) with a Classification of Gasterosteiform Families
inferredcites →https://doi.org/10.5479/si.00963801.14-845.107openalex-snapshot
Relations of temperature to vertebrae among fishes
inferredcites →https://doi.org/10.5860/choice.36-4487openalex-snapshot
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inferredcites →https://doi.org/10.5962/bhl.title.57348openalex-snapshot
A manual of zoology
inferredcites →https://doi.org/10.5962/p.184688openalex-snapshot
Deep sea fishes of the Bermuda oceanographic expeditions. Family Nemichthyidae

What points at this work

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

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Regional differentiation of felid vertebral column evolution: a study of 3D shape trajectories
inferred← citeshttps://doi.org/10.1002/ar.25653openalex-snapshot
Modularity and integration of the neural arch and vertebral centrum in primates
inferred← citeshttps://doi.org/10.1002/jmor.20733openalex-snapshot
Trunk elongation and ontogenetic changes in the axial skeleton of Triturus newts
inferred← citeshttps://doi.org/10.1002/jmor.20833openalex-snapshot
Patterns of growth in the presacral vertebral column of the leopard gecko (Eublepharis macularius)
inferred← citeshttps://doi.org/10.1002/jmor.21776openalex-snapshot
Precaudal Vertebrae in the Postcranial Region of Moray Eels Form Ventral Processes
inferred← citeshttps://doi.org/10.1007/s10914-020-09506-9openalex-snapshot
Evolution of the Mammalian Neck from Developmental, Morpho-Functional, and Paleontological Perspectives
inferred← citeshttps://doi.org/10.1016/b978-0-12-416678-3.00059-8openalex-snapshot
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Axial systems and their actuation: new twists on the ancient body of craniates
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Angles and waves: intervertebral joint angles and axial kinematics of limbed lizards, limbless lizards, and snakes
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Mosaic adaptive peak shifts underlie body shape diversification in pelagiarian fishes (Acanthomorpha: Percomorpha)
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Convergent Evolution of Elongate Forms in Craniates and of Locomotion in Elongate Squamate Reptiles
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Ontogenetic Allometry in Shape and Flexibility Underlies Life History Patterns of Labrid Cleaning Behavior
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Different Evolutionary Pathways Lead to Incomplete Convergence of Elongate Body Shapes in Carnivoran Mammals
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Relationships between Fecundity and the Number of Vertebrae in Common Roach Rutilus rutilus in the Rybinsk Reservoir
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Vertebral number is highly evolvable in salamanders and newts (family Salamandridae) and variably associated with climatic parameters
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Relationship between Fecundity and the Number of Vertebrae in the Roach Rutilus rutilus of the Rybinsk Reservoir
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Additional file 1 of The neck as a keystone structure in avian macroevolution and mosaicism
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Additional file 2 of The neck as a keystone structure in avian macroevolution and mosaicism
inferred← citeshttps://doi.org/10.7287/peerj.14800v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Scaling patterns of body plans differ among squirrel ecotypes (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14800v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Scaling patterns of body plans differ among squirrel ecotypes (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14800v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Scaling patterns of body plans differ among squirrel ecotypes (v0.1)"
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Peer Review #1 of "Scaling patterns of body plans differ among squirrel ecotypes (v0.2)"
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Peer Review #2 of "Scaling patterns of body plans differ among squirrel ecotypes (v0.2)"
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Peer Review #3 of "Scaling patterns of body plans differ among squirrel ecotypes (v0.2)"
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Scaling patterns of body plans differ among squirrel ecotypes
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