Vibrio Clade 3.0: New Vibrionaceae Evolutionary Units Using Genome-Based Approach

2021 ◽  
Vol 79 (1) ◽  
Author(s):  
Chunqi Jiang ◽  
Mami Tanaka ◽  
Sayo Nishikawa ◽  
Sayaka Mino ◽  
Jesús L. Romalde ◽  
...  
Keyword(s):  
1990 ◽  
Vol 5 ◽  
pp. 13-30 ◽  
Author(s):  
D. A. Springer ◽  
A. I. Miller

The way we view species distribution patterns, particularly at the level commonly referred to as the “community”, has changed over the past 70 years in biology and, subsequently, in paleontology. Because the degree to which species associations can be interpreted as ecological and evolutionary units depends ultimately on recognition and interpretation of faunal spatial variability, we need to understand the nature of this variability at all levels of resolution before we can adequately address questions of “community” structure and dynamics. While it is possible to recognize spatial variability at several levels, from the distributions of individuals within a species to the overall pattern created by the global biota, we must ask whether these patterns really comprise a hierarchy with natural discontinuities (Fig. 1), or whether it is more realistic to view them as a continuous variability spectrum.


2015 ◽  
Vol 17 (2) ◽  
pp. 455-471 ◽  
Author(s):  
Luke B. Klicka ◽  
Barbara E. Kus ◽  
Pascal O. Title ◽  
Kevin J. Burns

2020 ◽  
Vol 49 (6) ◽  
pp. 659-667
Author(s):  
Franziska Trede ◽  
Anna Lemkul ◽  
Anagaw Atickem ◽  
Jacinta C. Beehner ◽  
Thore J. Bergman ◽  
...  

2014 ◽  
Vol 23 (9) ◽  
pp. 1220-1234 ◽  
Author(s):  
Jimin Pei ◽  
Wenlin Li ◽  
Lisa N. Kinch ◽  
Nick V. Grishin

2014 ◽  
Vol 9 (1) ◽  
pp. 104-113 ◽  
Author(s):  
Christoph Schubart ◽  
Bianca Aichinger

AbstractBristle crabs of the genus Pilumnus (Brachyura: Heterotremata: Pilumnidae) are common inhabitants of European waters. They are easily identifiable as a genus, but with the exception of P. inermis, intrageneric classification turns out to be quite complex. There is no general agreement on the number and distinction of species. Therefore, this genus is well-suited for comparative molecular studies. Specimens of the Pilumnus hirtellus complex, here defined as including Pilumnus hirtellus, P. villosissimus, P. spinifer, P. aestuarii, and an undescribed species, were gathered from throughout the Mediterranean Sea and the eastern Atlantic Ocean. DNA sequence data were obtained from the barcoding region of the cytochrome oxidase 1 mitochondrial gene and used for reconstruction of a phylogenetic tree and a haplotype network. The morphology of the gastric ossicles was compared in the search of separating characters. Our results give evidence for five genetic clusters within the P. hirtellus complex. There is negligible geographic variation within these clusters. Unambiguous mtDNA sequences within morphologically variable local populations argue against possible hybridization. The here encountered evolutionary units are relatively young and possibly allow to study ongoing processes of morphological, genetic, and ecological differentiation, leading to speciation and radiations in the coastal marine environment.


<em>Abstract</em>.—Lahontan Cutthroat Trout (LCT) <em>Oncorhynchus clarkii henshawi </em>and Paiute Cutthroat Trout (PCT) <em>O. c. selernis </em>are found in the Lahontan hydrographic basin of northern Nevada, northeastern California, and southeastern Oregon and together form the Lahontan Basin evolutionary lineage of Cutthroat Trout <em>O. clarkii</em>. The Alvord Cutthroat Trout <em>O. c. </em>ssp. native to the Alvord Lake subbasin in the northwestern Lahontan Basin was also part of this lineage but went extinct due to Rainbow Trout <em>O. mykiss </em>introgression in the mid-20th century. Both LCT and PCT are federally listed as threatened under the U.S. Endangered Species Act. Given its historic distribution in a single small stream and both phenotypic and genetic distinctiveness, PCT is currently recognized as a separate evolutionarily significant unit (ESU). For LCT, three ESUs are identified based upon meristic, morphological, ecological, and genetic data. These putative LCT ESUs separate lacustrine forms in the western Lahontan Basin (Truckee, Carson, and Walker River basins) from largely fluvial forms in the eastern Lahontan Basin (Humboldt and Reese River basins) and northwestern Lahontan Basin (Quinn River, Coyote Lake, and Summit Lake basins). The more recent recognition of a much longer evolutionary history of Cutthroat Trout and several influential genetic papers identifying previously unrecognized diversity within Cutthroat Trout have prompted a need to re-evaluate the overall taxonomy of this species. Here, we review earlier literature and draw on new information from recent studies to delineate uniquely identifiable evolutionary units within the Lahontan Basin lineage of Cutthroat Trout. Though in several cases various anthropogenic and natural influences have made definitive conclusions difficult, based on this collective information and the goal of conserving potentially important genetic, evolutionary, and life history diversity, we propose recognition of six uniquely identifiable evolutionary units within the Lahontan Cutthroat Trout lineage: (1) Paiute Cutthroat Trout—upper East Carson River; (2) western Lahontan Basin—Truckee, Walker, and Carson rivers together with Summit Lake; (3) northwestern Lahontan Basin—Quinn River; (4) eastern Lahontan Basin—Humboldt and Reese rivers; (5) Lake Alvord basin—Virgin-Thousand and Trout Creek drainages; and (6) Coyote Lake basin—Willow and Whitehorse rivers.


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