Academic literature on the topic 'Chelicerate evolution'

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Journal articles on the topic "Chelicerate evolution"

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van der Hammen, L. "Functional morphology and affinities of extant Chelicerata in evolutionary perspective." Earth and Environmental Science Transactions of the Royal Society of Edinburgh 76, no. 2-3 (1985): 137–46. http://dx.doi.org/10.1017/s0263593300010403.

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ABSTRACTA survey is given of the functional morphology of extant Chelicerata with special reference to segmentation of the body, segmentation and articulation of the legs, coxal glands, mouthparts and ingestion, respiratory organs, sperm transfer, and development. This is followed by a discussion of primitive types, evolution and diversity, the transition from aquatic to terrestrial life, and the affinities of extant chelicerate groups.
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Rehm, Peter, Christian Pick, Janus Borner, Jürgen Markl, and Thorsten Burmester. "The diversity and evolution of chelicerate hemocyanins." BMC Evolutionary Biology 12, no. 1 (2012): 19. http://dx.doi.org/10.1186/1471-2148-12-19.

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Ballesteros, Jesús A., and Prashant P. Sharma. "A Critical Appraisal of the Placement of Xiphosura (Chelicerata) with Account of Known Sources of Phylogenetic Error." Systematic Biology 68, no. 6 (2019): 896–917. http://dx.doi.org/10.1093/sysbio/syz011.

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AbstractHorseshoe crabs (Xiphosura) are traditionally regarded as sister group to the clade of terrestrial chelicerates (Arachnida). This hypothesis has been challenged by recent phylogenomic analyses, but the non-monophyly of Arachnida has consistently been disregarded as artifactual. We re-evaluated the placement of Xiphosura among chelicerates using the most complete phylogenetic data set to date, expanding outgroup sampling, and including data from whole genome sequencing projects. In spite of uncertainty in the placement of some arachnid clades, all analyses show Xiphosura consistently ne
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Wheeler, Ward C., and Cheryl Y. Hayashi. "The Phylogeny of the Extant Chelicerate Orders." Cladistics 14, no. 2 (1998): 173–92. http://dx.doi.org/10.1111/j.1096-0031.1998.tb00331.x.

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Van Leeuwen, Thomas, and Wannes Dermauw. "The Molecular Evolution of Xenobiotic Metabolism and Resistance in Chelicerate Mites." Annual Review of Entomology 61, no. 1 (2016): 475–98. http://dx.doi.org/10.1146/annurev-ento-010715-023907.

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Abzhanov, Arhat, Aleksandar Popadic, and Thomas C. Kaufman. "Chelicerate Hox genes and the homology of arthropod segments." Evolution and Development 1, no. 2 (1999): 77–89. http://dx.doi.org/10.1046/j.1525-142x.1999.99014.x.

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CHEN, JUNYUAN, DIETER WALOSZEK, and ANDREAS MAAS. "A new ‘great-appendage’ arthropod from the Lower Cambrian of China and homology of chelicerate chelicerae and raptorial antero-ventral appendages." Lethaia 37, no. 1 (2004): 3–20. http://dx.doi.org/10.1080/00241160410004764.

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Cartwright, Paulyn, Matthew Dick, and Leo W. Buss. "HOM/Hox Type Homeoboxes in the Chelicerate Limulus polyphemus." Molecular Phylogenetics and Evolution 2, no. 3 (1993): 185–92. http://dx.doi.org/10.1006/mpev.1993.1019.

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CHETVERIKOV, P.E. "EVOLUTIONARY PLASTICITY OF HIGHLY SPECIALIZED ORGANISMS: EVOLUTION OF ERIOPHYOID MITES (ACARIFORMES: ERIOPHYOIDEA) ON PLANTS." Acta entomologica serbica 20, no. 1 (2015): 151–61. https://doi.org/10.5281/zenodo.44649.

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Eriophyoids are highly specialized plant-feeding acarifom mites. As a result of miniaturization and adaptation to phytoparasitism they lacked III and IV pairs of legs and acquired elongated vermiform body, unique structure of gnathosoma and peculiar anatomy. Despite the high degree of specialization eriophyoid mites demonstrate remarkable evolutionary plasticity which manifests itself in numerous morphoilogical reversia, parallelisms and modifications associated with occupying of a variety of niches, processes of gall formation, transitions to new groups of hosts and various adaptations to cli
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Veenstra, Jan A. "Neuropeptide evolution: Chelicerate neurohormone and neuropeptide genes may reflect one or more whole genome duplications." General and Comparative Endocrinology 229 (April 2016): 41–55. http://dx.doi.org/10.1016/j.ygcen.2015.11.019.

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Dissertations / Theses on the topic "Chelicerate evolution"

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Barnett, Austen Alan. "KEY DEVELOPMENTAL EVENTS IN THE ORIBATID MITE, ARCHEGOZETES LONGISETOSUS, AND THE EVOLUTION OF CHELICERATE BODY PLANS." OpenSIUC, 2013. https://opensiuc.lib.siu.edu/dissertations/754.

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The chelicerates (e.g., spiders, mites, scorpions, harvestmen and horseshoe crabs) are oneof the oldest arthropod clades, arising in the Cambrian. The chelicerates display a conserved body plan comprising of an anterior prosoma and a posterior opisthosoma. The prosoma comprises the segments bearing the chelicerae, pedipalps and the four pairs of walking legs. The opisthosoma is more variable, and either contains no appendages (e.g., in harvestmen), or extremely derived appendages (e.g., the spinnerets of spiders and the pectines of scorpions). Recent evolutionary developmental (evo devo) studi
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Pace, Ryan M., Miodrag Grbić, and Lisa M. Nagy. "Composition and genomic organization of arthropod Hox clusters." BioMed Central, 2016. http://hdl.handle.net/10150/615123.

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Moore, Rachel A. "The origin and early evolution of the Chelicerata." Thesis, University of Bristol, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.411078.

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Books on the topic "Chelicerate evolution"

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Chelicerate palaeobiology and evolution. Royal Society of Edinburgh, 2004.

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Book chapters on the topic "Chelicerate evolution"

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Weygoldt, Peter. "Evolution and systematics of the Chelicerata." In Ecology and Evolution of the Acari. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-017-1343-6_1.

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Sharma, Prashant P. "Duplication and Evolution of Hox Clusters in Chelicerata (Arthropoda)." In Hox Modules in Evolution and Development. CRC Press, 2023. http://dx.doi.org/10.1201/9781003057215-4.

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Schram, Frederick R., and Stefan Koenemann. "Pancrustacea." In Evolution and Phylogeny of Pancrustacea. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780195365764.003.0051.

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The understanding the evolution of Arthropoda has depended on fossils from localities of unusual preservation, Lagerstätten. Science still tends to view the ever-growing arthropod record in the Cambrian in the shadows cast by the living forms. Stem forms appear to lead to the living Euarthropoda. The living lineages also contain fossils of importance. For example, trilobites may or may not be related to taxa such as chelicerates and pycnogonids. A superclade, Mandibulata, unites the terrestrial myriapods and the pancrustaceans. The origin of the former has problems, but a possible sister group
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Brusca, Richard C., Gonzalo Giribet, and Wendy Moore. "Panarthropoda and the Emergence of the Arthropods." In Invertebrates. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780197554418.003.0020.

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This chapter looks into the clade Panarthropoda which comprises three phyla of Arthropoda, Onychophora, and Tardigrada. The clade Panarthropoda is characterized by metamerism, reduced coeloms and a hemocoel, ecdysis, muscles isolated in bands, and paired ventrolateral segmental appendages with terminal claws. The chapter then features illustrations that show the body plan of members of Arthropoda, Onychophora, and Tardigrada. The phylum Arthropoda is unprecedented for its diversity with its four distinguished subphylas of Crustacea, Hexapoda, Myriapoda, and Chelicerata. The chapter also provid
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Greenfield, Michael D. "Sound and Vibration and the Mechanical Channel." In Signalers and Receivers. Oxford University PressNew York, NY, 2002. http://dx.doi.org/10.1093/oso/9780195134520.003.0004.

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Abstract Communication along the mechanical channel is highly developed in only two animal phyla, the arthropods and the chordates. In arthropods as a whole, sound and vibration are not the pre-eminent modalities for signaling, but they nonetheless play vital functions in diverse taxa distributed among seven major insect orders, several minor ones. and some groups of chelicerates and crustaceans (Table 4.1). In these arthropod species, sound and vibration serve as sexual advertisement, courtship, aggression, defense, and social recruitment signals. Moreover, certain of these communication syst
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Crandalla, Keith A., Megan L. Porterc, and Marcos Pérez-Losada. "Crabs, shrimps, and lobsters (Decapoda)." In The Timetree of Life. Oxford University PressOxford, 2009. http://dx.doi.org/10.1093/oso/9780199535033.003.0036.

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Abstract Crustaceans comprise the fourth most species-rich group of metazoans on the planet, following insects, chelicerates, and mollusks. But in terms of morphological diversity (disparity), they are unrivaled (see 1, 2). Foremost among the crustaceans in number and diversity are the decapods. With over 15,000 described species they include those crustaceans most familiar to the general public—shrimp, lobsters, crabs (Fig. 1), and crayAsh— but also lesser known and unusual groups (3). themost recent classification (2) partitions 62,000 species of extant Crustacea among 849 families (compared
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Conference papers on the topic "Chelicerate evolution"

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Lamsdell, James. "DEVELOPMENTAL PARALLELISMS AND PAEDOMORPHOSIS DROVE CONVERGENT EVOLUTION BETWEEN CHASMATASPIDID AND EURYPTERID CHELICERATES." In GSA Connects 2022 meeting in Denver, Colorado. Geological Society of America, 2022. http://dx.doi.org/10.1130/abs/2022am-378866.

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Bingham, Joseph, James C. Lamsdell, Ron Meyer, and Gerald Gunderson. "EARLY EVOLUTION OF SEA SCORPIONS: EURYPTERIDS (CHELICERATA: EURYPTERIDA) OF THE BIG HILL LAGERSTÄTTE." In GSA Connects 2024 Meeting in Anaheim, California. Geological Society of America, 2024. http://dx.doi.org/10.1130/abs/2024am-401218.

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