Relevant bibliographies by topics / Reciprocal monophyly

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Academic literature on the topic 'Reciprocal monophyly'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Reciprocal monophyly"

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Zhu, Sha, James H. Degnan, and Mike Steel. "Clades, clans, and reciprocal monophyly under neutral evolutionary models." Theoretical Population Biology 79, no. 4 (2011): 220–27. http://dx.doi.org/10.1016/j.tpb.2011.03.002.

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Vanderlaan, Tegan A., Malte C. Ebach, David M. Williams, and John S. Wilkins. "Defining and redefining monophyly: Haeckel, Hennig, Ashlock, Nelson and the proliferation of definitions." Australian Systematic Botany 26, no. 5 (2013): 347. http://dx.doi.org/10.1071/sb13031.

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The various existing definitions of monophyly have resulted in confusion within the systematics community. The divergence in terminology started with the work of Willi Hennig who attempted to introduce a precise definition of phylogenetic relationship in 1950, a term that he had synonymised with monophyly by 1953, thereby creating a new definition. In 1965, Hennig introduced paraphyly to distinguish his version of monophyly from groups based on symplesiomorphies or stem groups. In attempting to resolve the confusion, Ashlock synonymised Hennig’s monophyly as holophyly, resulting in another new
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Thacker, Robert W., and Valerie J. Paul. "Morphological, Chemical, and Genetic Diversity of Tropical Marine Cyanobacteria Lyngbya spp. and Symploca spp. (Oscillatoriales)." Applied and Environmental Microbiology 70, no. 6 (2004): 3305–12. http://dx.doi.org/10.1128/aem.70.6.3305-3312.2004.

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ABSTRACT Although diverse natural products have been isolated from the benthic, filamentous cyanobacterium Lyngbya majuscula, it is unclear whether this chemical variation can be used to establish taxonomic relationships among disparate collections. We compared morphological characteristics, secondary-metabolite compositions, and partial 16S ribosomal DNA (rDNA) sequences among several collections of L. majuscula Gomont, Lyngbya spp., and Symploca spp. from Guam and the Republic of Palau. The morphological characteristics examined were cell length, cell width, and the presence or absence of a
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Mehta, Rohan S., and Noah A. Rosenberg. "The probability of reciprocal monophyly of gene lineages in three and four species." Theoretical Population Biology 129 (October 2019): 133–47. http://dx.doi.org/10.1016/j.tpb.2018.04.004.

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5

Souza, Mateus S., Andréa T. Thomaz, and Nelson J. R. Fagundes. "River capture or ancestral polymorphism: an empirical genetic test in a freshwater fish using approximate Bayesian computation." Biological Journal of the Linnean Society 131, no. 3 (2020): 575–84. http://dx.doi.org/10.1093/biolinnean/blaa140.

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Abstract A headwater or river capture is a phenomenon commonly invoked to explain the absence of reciprocal monophyly of genetic lineages among isolated hydrographic basins in freshwater fish. Under the assumption of river capture, a secondary contact between populations previously isolated in different basins explains the observed genetic pattern. However, the absence of reciprocal monophyly could also arise under population isolation through the retention of ancestral of polymorphisms. Here, we applied an approximate Bayesian computation (ABC) framework for estimating the relative probabilit
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Padilla-Jacobo, Gabriela, Tiberio Cesar Monterrubio-Rico, Horacio Cano Camacho, and María Guadalupe Zavala-Páramo. "USE OF PHYLOGENETIC ANALYSIS TO IDENTIFY EVOLUTIONARILY SIGNIFICANT UNITS FOR THE ORANGE-FRONTED PARAKEET (EUPSITTULA CANICULARIS) IN MEXICO." Ornitología Neotropical 26, no. 4 (2016): 325–35. http://dx.doi.org/10.58843/ornneo.v26i4.68.

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In avian conservation biology, the subspecies concept based on reciprocal monophyly has been successfully applied to define priority populations through Evolutionarily Significant Units (ESUs). In México, the Orange-fronted Parakeet (Eupsittula canicularis) ranks first in illegal parrot trade. Its distribution ranges from southern Sonora to Chiapas on the Pacific slope, with populations representing three subspecies: E. c. canicularis, E. c. eburnirostrum, and E. c. clarae. To identify and propose ESUs to assist in conservation proposals for different populations, we assessed subspecific recip
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Kizirian, David, and Maureen A. Donnelly. "The criterion of reciprocal monophyly and classification of nested diversity at the species level." Molecular Phylogenetics and Evolution 32, no. 3 (2004): 1072–76. http://dx.doi.org/10.1016/j.ympev.2004.05.001.

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8

Hiller, Alexandra, and Bernd Werding. "Description of a new species of the Petrolisthes galathinus complex from the Caribbean Sea, and resurrection of Petrolisthes occidentalis from the East Pacific (Crustacea, Anomura, Porcellanidae)." ZooKeys 1191 (February 16, 2024): 391–407. http://dx.doi.org/10.3897/zookeys.1191.111570.

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The Petrolisthes galathinus complex currently consists of six American species distributed in the West Atlantic, including the amphi-American P. galathinus. All species in the complex are similar in their adult morphology but differ in colour, size, larval morphology, and shape of the adult sternal plate. The West Atlantic species have different geographic ranges, which overlap in the southern Caribbean. Previously published molecular data support the monophyly of the complex, and the reciprocal monophyly of each described species and further clades corresponding to different colour morphs. He
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Hiller, Alexandra, and Bernd Werding. "Description of a new species of the Petrolisthes galathinus complex from the Caribbean Sea, and resurrection of Petrolisthes occidentalis from the East Pacific (Crustacea, Anomura, Porcellanidae)." ZooKeys 1191 (February 16, 2024): 391–407. https://doi.org/10.3897/zookeys.1191.111570.

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The <i>Petrolisthes galathinus</i> complex currently consists of six American species distributed in the West Atlantic, including the amphi-American <i>P. galathinus</i>. All species in the complex are similar in their adult morphology but differ in colour, size, larval morphology, and shape of the adult sternal plate. The West Atlantic species have different geographic ranges, which overlap in the southern Caribbean. Previously published molecular data support the monophyly of the complex, and the reciprocal monophyly of each described species and further clades corresponding to different col
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10

Chen, Chien-Lin, Joseph W. Goy, Heather D. Bracken-Grissom, Darryl L. Felder, Ling Ming Tsang, and Tin-Yam Chan. "Corrigendum to: Phylogeny of Stenopodidea (Crustacea : Decapoda) shrimps inferred from nuclear and mitochondrial genes reveals non-monophyly of the families Spongicolidae and Stenopididae and most of their composite genera." Invertebrate Systematics 30, no. 6 (2016): 650. http://dx.doi.org/10.1071/is16024_co.

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The infraorder Stenopodidea is a relatively small group of marine decapod crustaceans including the well known cleaner shrimps, but their higher taxonomy has been rather controversial. This study provides the most comprehensive molecular phylogenetic analyses of Stenopodidea using sequence data from two mitochondrial (16S and 12S rRNA) and two nuclear (histone H3 and sodium–potassium ATPase ?-subunit (NaK)) genes. We included all 12 nominal genera from the three stenopodidean families in order to test the proposed evolutionary hypothesis and taxonomic scheme of the group. The inferred phylogen
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Book chapters on the topic "Reciprocal monophyly"

1

"Biology, Management, and Conservation of Lampreys in North America." In Biology, Management, and Conservation of Lampreys in North America, edited by Margaret F. Docker. American Fisheries Society, 2009. http://dx.doi.org/10.47886/9781934874134.ch4.

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&lt;em&gt;Abstract&lt;/em&gt;.—In most lamprey genera, “paired” species exist in which the larvae (which are microphagous filter feeders) are morphologically similar but the adults differ dramatically, becoming parasitic on teleost fishes or nonparasitic (i.e., do not feed at all) following metamorphosis. Parasitic lampreys feed for several months to several years (either in their natal stream or after migrating to larger fresh or marine water bodies) before embarking on a nontrophic upstream migration, sexual maturation, and spawning (followed by death); nonparasitic lampreys eliminate the pa
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