R.Paul Evans’s research while affiliated with Brigham Young University and other places

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Publications (76)


Map of ranges of cutthroat trout subspecies, lineages, and forms used in this study. “Free United States SVG Map” used with permission from simplemaps.com. Ranges adapted from literature, as well as www.nativetroutflyfishing.com.
Comparison of trees generated by Robert Behnke (2002; left) and Shiozawa et al. (2018; right). Only subspecies, lineages, and forms used in this project are included. Colorado (blue) is Colorado River blue lineage and Colorado (green) is Colorado River green lineage.
BUSCO gene percentages for each specimen.
Concatenated‐ and coalescent‐based species trees using three filtering schemes. Support values represented are bootstrap values and local posterior probabilities for each branch for the concatenated and coalescent trees, respectively.
Using de novo transcriptomes to decipher the relationships in cutthroat trout subspecies (Oncorhynchus clarkii)
  • Article
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July 2024

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312 Reads

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4 Citations

Andrea L. Kokkonen

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R. Paul Evans

For almost 200 years, the taxonomy of cutthroat trout (Oncorhynchus clarkii), a salmonid native to Western North America, has been in flux as ichthyologists and fisheries biologists have tried to describe the diversity within these fishes. Starting in the 1950s, Robert Behnke reexamined the cutthroat trout and identified 14 subspecies based on morphological traits, Pleistocene events, and modern geographic ranges. His designations became instrumental in recognizing and preserving the remaining diversity of cutthroat trout. Over time, molecular techniques (i.e. karyotypes, allozymes, mitochondrial DNA, SNPs, and microsatellite arrays) have largely reinforced Behnke's phylogenies, but have also revealed that some relationships are consistently weakly supported. To further resolve these relationships, we generated de novo transcriptomes for nine cutthroat subspecies, as well as a Bear River Bonneville form and two Colorado River lineages (blue and green). We present phylogenies of these subspecies generated from multiple sets of orthologous genes extracted from our transcriptomes. We confirm many of the relationships identified in previous morphological and molecular studies, as well as discuss the importance of significant differences apparent in our phylogenies from these studies within a geological perspective. Specific findings include three distinct clades: (1) Bear River Bonneville form and Yellowstone cutthroat trout; (2) Bonneville cutthroat trout (n = 2); and (3) Greenback and Rio Grande cutthroat trout. We also identify potential gene transfer between Bonneville cutthroat trout and a population of Colorado River green lineage cutthroat trout. Using these findings, it appears that additional groups warrant species‐level consideration if other recent species elevations are retained.

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Heterochronic shift in gene expression leads to ontogenetic morphological divergence between two closely related polyploid species

March 2024

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66 Reads

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1 Citation

iScience

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R. Paul Evans

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[...]

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Heterochrony—alteration to the rate or timing of development—is an important mechanism of trait differentiation associated with speciation. Heterochrony may explain the morphological divergence between two polyploid species, June sucker (Chasmistes liorus) and Utah sucker (Catostomus ardens). The larvae of both species have terminal mouths; however, as adults, June sucker and Utah sucker develop subterminal and ventral mouths, respectively. We document a difference in the timing of shape development and a corresponding change in the timing of gene expression, suggesting the distinctive mouth morphology in June suckers may result from paedomorphosis. Specifically, adult June suckers exhibit an intermediate mouth morphology between the larval (terminal) and ancestral (ventral) states. Endemic and sympatric Chasmistes/Catostomus pairs in two other lakes also are morphologically divergent, but genetically similar. These species pairs could have resulted from the differential expression of genes and corresponding divergence in trait development. Paedomorphosis may lead to adaptive diversification in Catostomids.


Phylogenetic tree inferred by maximum likelihood using W-IQ-Tree from 27 Sebastes mitogenomes. Sebastiscus tertius (MT117231) was used as an outgroup but is not displayed. Ultrafast bootstrap values >95 are not shown. “Sebastes norvegicus” by Jan Fekian is licensed under CC BY-SA 4.0/Silhouette of original.
Complete mitochondrial genomes of two rockfish: Sebastes maliger and Sebastes norvegicus (Scorpaenidae, Scorpaeniformes)

September 2022

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76 Reads

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3 Citations

We report the complete mitochondrial genomes of two rockfish: Sebastes maliger and Sebastes norvegicus. The mitogenomes consist of 13 protein-coding regions, 22 tRNAs, two rRNAs, and one control region. Sebastes mitogenome control regions are highly variable due to the presence of repeat sequences. The mitogenomes for S. maliger and S. norvegicus are 16,403 and 16,401 bp, respectively. Using these two mitogenomes and 25 additional Sebastes mitogenomes from GenBank, we examine the phylogenetic relationships in Sebastes. Sebastes maliger is sister to a clade including S. rubrivinctus, S. nigrocinctus, S. umbrosus, and S. oculatus, while S. norvegicus is sister to S. fasciatus.


Phylogenetic tree inferred by maximum likelihood using IQ-Tree from 33 Catostomidae mitogenomes, representing 16 species. Cobitis striata (AB054125), Cyprinus carpio (MK088487) and Gyrinocheilus aymonieri (AB242164) were used as outgroups but are not displayed. Bootstrap values >95 are not shown. Reproduction of June sucker and Utah sucker silhouettes was done with permission from © Joseph R. Tomelleri.
Complete mitochondrial genomes of June sucker and Utah sucker (Chasmistes liorus and Catostomus ardens)

March 2022

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44 Reads

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1 Citation

The relationship between June sucker (Chasmistes liorus, Jordan, 1878) and Utah sucker (Catostomus ardens, Jordan & Gilbert, 1881) has been a matter of controversy since the mid 1900s. Chasmistes liorus is endemic to Utah Lake, UT and has a subterminal mouth adapted for pelagic feeding. Catostomus ardens is widely distributed throughout the Bonneville Basin and Upper Snake River Basin and has a ventral mouth adapted for benthic feeding. Chasmistes has been recognized as a separate ancient genus. Despite being morphologically distinct, no study has successfully identified residual genetic markers that separate these species. Of these studies, several have used a subset of mitochondrial genes, but no study has analyzed the complete mitochondrial genomes (mitogenomes) of these suckers (Pisces: Catostomidae). To further explore the genetic relationships between these species, we report the complete mitogenomes of Chasmistes liorus and Catostomus ardens. DNA was sequenced using an Illumina HiSeq 2500 system and mitogenomes were assembled and annotated using Geneious v. 2021.2 and MitoAnnotator, respectively. The mitogenomes of Chasmistes liorus and Catostomus ardens are both 16,623 bp and are ∼0.072% divergent. We examine the phylogenetic relationship between Chasmistes liorus and Catostomus ardens using 33 mitogenomes, representing 16 species, from Catostomidae. Our data suggest that Chasmistes liorus is sister to Catostomus ardens. Additional samples from multiple localities and/or cohorts of these species will allow us to better resolve the complicated phylogenetic relationships between these species.


Geographic variation, isolation, and evolution of cutthroat trout with comments on future directions for management and research

September 2018

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2,033 Reads

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7 Citations

We review the history of cutthroat trout phylogenetic research using various molecular techniques, and present a well-resolved phylogeny based on mitochondrial DNA sequence data (approximately half of the mitochondrial genome) along with molecular clock estimates of divergence times of major evolutionary cutthroat trout lineages based on standard mitochondrial DNA mutation rates and fossil calibrations.


A description of Echinorhynchus baeri Kostylew, 1928 (Acanthocephala: Echinorhynchidae) from Salmo trutta in Turkey, with notes on synonymy, geographical origins, geological history, molecular profile, and X-ray microanalysis

December 2016

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384 Reads

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9 Citations

Parasite

A population of Echinorhynchus baeri Kostylew, 1928 with 18-24 rows of 8-10 proboscis hooks each and long fusiform eggs measuring 95-110 × 18-22 μm collected from Salmo trutta (Salmonidae) in a branch of the Murat River in Turkey is described and specimens are designated as neotype. Specimens of two similar populations of E. baeri (E. baeri Kostylew, 1928 and E. sevani Dinnik, 1932) were previously described from Salmo ischchan in Lake Sevan, Armenia. Waters of Lake Sevan and the Murat River were previously joined during the Middle Miocene-Pliocene. The two populations from Lake Sevan and ours from Turkey had identical morphology and size eggs. The proboscis armature and eggs, among other features of our Turkish specimens, proved intermediate between E. baeri and E. sevani, thus eliminating the significance of the described differences between these two species and confirming their synonymy with priority to Echinorhynchus baeri (junior synonym: Echinorhynchus sevani Dinnik, 1932). Echinorhynchus baeri is apparently a highly variable species. The two descriptions from Lake Sevan did not include features or illustrations of females, except for references to trunk and egg size but the eggs were illustrated. Complete morphometric comparisons are made and females of the Turkish material are described for the first time. DNA sequencing (mitochondrial cytochrome oxidase subunit I gene; nuclear 18S rRNA gene) results from two available E. baeri individuals were equivocal. New features to the Acanthocephala include the presence of rootless uncalcified apical proboscis hooks studied with X-ray microanalysis. © O.M. Amin et al., published by EDP Sciences, 2016.


Fig. 25. Phylogeny generated using 18S rDNAsequence data. Numbers at internal nodes are maximum likelihood support values. Family status within Archiacanthocephala is identified on the right.  
Figs. 1-6. Sexually mature specimens of Moniliformis saudi sp. n. from the desert hedgehog, Paraechinus aethiopicus (Ehrenberg) in Saudi Arabia. Fig. 1. An egg with concentric shells and smooth surface. Fig. 2. Holotype male. Note the number and location of giant nuclei in the body wall, the near contiguous, post-equatorial ovoid testes, and extent and location of pseudosegmentation. Figs. 3, 4. Ventral hooks nos. 1, 2, 4, 8 (Fig. 3) and smaller dorsal hooks (Fig. 4) of the same specimen in Figs. 1, 2. Fig. 5. The short and robust reproductive system of the allotype female. Fig. 6. The anterior end of the same specimen showing the size proportion of the proboscis and the receptacle, the anterior trunk festoons, and the nucleated cells at the posterior end of the receptacle.
Figs. 19-24. SEM micrographs and stained whole mounts and sections of adults of Moniliformis saudi sp. n. from the desert hedgehog, Paraechinus aethiopicus (Ehrenberg), in Saudi Arabia. Fig. 19. An ovarian ball; note the filaments. Fig. 20. A cluster of eggs showing their shape and smooth surface. Fig. 21. The posterior part of a male specimen showing the cement glands and Saefftigen's pouch overlapping the cement gland and common sperm ducts. Fig. 22. A section of the anterior end of a specimen showing the oblique muscular bands enveloping the proboscis receptacle and two adjacent darker lemnisci on both sides. Figs. 23, 24. Internal appearance of pseudosegmentation in the posterior and anterior trunk of two separate specimens, respectively.
Figs. 26-33. Histopathology of specimens of Moniliformis saudi sp. n. in the intestine of Paraechinus aethiopicus (Ehrenberg). Fig. 26. Normal host intestinal tissue showing vascular mucosa with well-developed columnar epithelial cells (arrows) lining the villi and including goblet cells. Fig. 27. A specimen invading the host mucosa compressing the villi and causing necrosis of epithelial lining and hemorrhaging. Fig. 28. The worm penetrating host mucosa with the hook (arrow) around proboscis resulting in blood loss (lower right) due to damaged capillaries. Fig. 29. An acanthocephalan compressing and penetrating the villi of the host mucosa causing necrotic tissue and hemorrhaging surrounding the worm. Fig. 30. The acanthocephalan has extended into the lower reaches of the mucosa with subsequent hemorrhaging of capillary beds and tissue necrosis. Fig. 31. Higher magnification of Fig. 30. Worm penetrating the intestinal mucosa damaging villi and causing blood loss and necrosis. Fig. 32. The damaged mucosa created by the invading worm causing extensive necrosis and hemorrhaging. Note remnants of connective tissue from the intestinal villi. Fig. 33. Compression on the host villi within the intestinal mucosa due to the presence of a worm. Note extensive hemorrhaging on the left side of the invading specimen. Abbreviations: H-hemorrhaging; MU-mucosa; N-necrosis; P-proboscis; V-villi; W-worm.
Morphological and molecular descriptions of Moniliformis saudi sp. n. (Acanthocephala: Moniliformidae) from the desert hedgehog, Paraechinus aethiopicus (Ehrenberg) in Saudi Arabia, with a key to species and notes on histopathology

April 2016

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835 Reads

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35 Citations

Folia Parasitologica

A new acanthocepohalan species, Moniliformis saudi sp. n. is described from the desert hedgehog, Paraechinus aethiopicus (Ehrenberg), in central Saudi Arabia. Fourteen other valid species of Moniliformis Travassos, 1915 are recognised. The new species of Moniliformis is distinguished by having a small proboscis (315-520 µm long and 130-208 µm wide) with two apical pores, 14 rows of 8 hooks each and small hooks, thre largest being 25-31 µm long anteriorly. Distinguishing features are incorporated in a dichotomous key to the species of Moniliformis. The description is augmented by scanning electron microscopical (SEM) observation and DNA analysis of nuclear (18S rRNA) and mitochondrial (cytochrome oxidase subunit 1; cox1) gene sequences. Attached worms cause extensive damage to the immediate area of attachment in the host intestine. This includes tissue necrosis and blood loss due to damage to capillary beds. Worms also obstruct essential absorbing surfaces.


Morphological and molecular description of Tenuisentis niloticus (Meyer, 1932) (Acanthocephala: Tenuisentidae) from Heterotis niloticus (Cuvier) (Actinopterygii: Arapaimidae), in Burkina Faso, with emendation of the family diagnosis and notes on new features, cryptic genetic diversity and histopathology

February 2016

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574 Reads

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12 Citations

Systematic Parasitology

Specimens described as Rhadinorhynchus niloticus Meyer, 1932 (Rhadinorhynchidae) from two male specimens collected from Heterotis niloticus (Cuvier) in the Egyptian Nile were later redescribed in the genus Tenuisentis Van Cleave, 1936 (Tenuisentidae) based on 12 specimens collected from the same host species in the White Nile. That redescription basically distinguished the two genera based on five traits but did not actually provide a formal description. His account left out information about cerebral ganglion, lemnisci, some reproductive structures, eggs, proboscis hook dissymmetry and roots, size of trunk and a few other structures. We provide (i) the first complete description of this species enhanced by SEM, molecular, and histo-pathological studies; (ii) expand the existing descriptions; (iii) correct questionable accounts advanced by Van Cleave on the cement gland and the hypodermal giant nuclei; and (iv) add descriptions of new features such as the para-receptacle structure which we also report from Paratenuisentis Bullock & Samuel, 1975, the only other genus in Tenuisentidae Van Cleave, 1936. The subsequent description of a few more specimens from the same host collected in Mali was more informative yet incomplete and at variance with our specimens from Burkina Faso. Genetic divergence and phylogenetic analyses of mitochondrial (cytochrome oxidase c subunit I; COI) and nuclear (18S ribosomal RNA) gene relationships uncovered a cryptic species complex containing two lineages. Based on our studies, the family diagnosis is emended. The acanthocephalan causes damage to the host intestine as depicted in histopathological sections. The invading worm can extend from the mucosal layer to the muscularis externa of the host with subsequent tissue necrosis, villi compression, haemorrhaging and blood loss.


Climate oscillations, glacial refugia, and dispersal ability: Factors influencing the genetic structure of the least salmonfly, Pteronarcella badia (Plecoptera), in Western North America

December 2015

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379 Reads

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22 Citations

BMC Evolutionary Biology

Background: Phylogeographic studies of aquatic insects provide valuable insights into mechanisms that shape the genetic structure of communities, yet studies that include broad geographic areas are uncommon for this group. We conducted a broad scale phylogeographic analysis of the least salmonfly Pteronarcella badia (Plecoptera) across western North America. We tested hypotheses related to mode of dispersal and the influence of historic climate oscillations on population genetic structure. In order to generate a larger mitochondrial data set, we used 454 sequencing to reconstruct the complete mitochondrial genome in the early stages of the project. Results: Our analysis revealed high levels of population structure with several deeply divergent clades present across the sample area. Evidence from five mitochondrial genes and one nuclear locus identified a potentially cryptic lineage in the Pacific Northwest. Gene flow estimates and geographic clade distributions suggest that overland flight during the winged adult stage is an important dispersal mechanism for this taxon. We found evidence of multiple glacial refugia across the species distribution and signs of secondary contact within and among major clades. Conclusions: This study provides a basis for future studies of aquatic insect phylogeography at the inter-basin scale in western North America. Our findings add to an understanding of the role of historical climate isolations in shaping assemblages of aquatic insects in this region. We identified several geographic areas that may have historical importance for other aquatic organisms with similar distributions and dispersal strategies as P. badia. This work adds to the ever-growing list of studies that highlight the potential of next-generation DNA sequencing in a phylogenetic context to improve molecular data sets from understudied groups.


Fig 1.  Distribution map for R. solitarius.
A) Map showing the locations of eight relict dace populations that were included in this study. The natural species range of the relict dace is contained within the four valleys that are labeled. A colored circle represents each sampling locality, and the color of each circle varies so that subsequent figures can be interpreted more easily. Colors for each population are as follows: Big Spring (red), Twin Springs (pink), Franklin River (light blue), Ruby Lake National Wildlife Refuge Pond #246 (dark blue), Quilici Spring (dark green), Odgers Creek (light green), Steptoe Ranch (yellow), and McGill/Dairy Springs (orange). B) The location of the study area in western North America. C) Pluvial drainage systems that existed in the study area during the Pleistocene Epoch. Relict dace currently reside in spring systems that are considered to be remnants of these pluvial drainages.
Table 1.  AMOVA Results.
Populations were categorized as either Ruby/Butte or Goshute/Steptoe in accordance with phylogenetic placement in one of two clades. Within population variation explains the majority of the molecular variation observed within these samples of relict dace.
Fig 2.  Relict dace phylogeny.
Phylogeny based on concatenated mtDNA sequences. Maximum likelihood bootstraps and Bayesian posterior probabilities are listed above each node that they support (in that order). Divergence time estimates are marked with red arrows, and 95% credible intervals for each estimate are listed in brackets below the mean value.
Fig 3.  Relict dace mtDNA haplotype network.
Haplotype network showing the intraspecific genetic diversity of relict dace populations throughout the species’ native range. Circles represent unique haplotypes, and the size of the circle represents the number of individuals that carry that haplotype. Hash marks between haplotypes represent base changes. Colors represent sampling localities.
Pluvial Drainage Patterns and Holocene Desiccation Influenced the Genetic Architecture of Relict Dace, Relictus solitarius (Teleostei: Cyprinidae)

September 2015

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137 Reads

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8 Citations

Changing drainage patterns have played a significant role in the evolution of western North American aquatic taxa. Relict dace, Relictus solitarius, is a Great Basin endemic cyprinid with a native range that is restricted to four valleys in eastern Nevada. Relictus solitarius now occupies spring systems that are the remnants of Pleistocene-era pluvial lakes, although it may have occurred in the area for much longer. Here we use mitochondrial DNA sequence data to assess range-wide genetic diversity of R. solitarius, and to estimate divergence times to determine whether pluvial drainages played an important role in shaping intraspecific genetic diversity. Genetic diversification within R. solitarius began during the early to mid-Pleistocene, separating populations within two sets of valleys (Butte/Ruby and Goshute/Steptoe). Additional diversification in each of the two sets of valleys occurred more recently, in the mid-to late-Pleistocene. Holocene desiccation has further isolated populations , and each population sampled contains unique mtDNA haplotypes. Pluvial drainage patterns did contribute to the genetic structure observed within R. solitarius, but most of the intraspecific diversification does not appear to be associated with the Last Glacial Maximum. Holocene desiccation has also contributed to the observed genetic structure. The relict dace populations we sampled are all unique, and we recommend that future management efforts should strive to preserve as much of the genetic diversity as possible.


Citations (17)


... Two studies investigated the effects of hatchery programs on diversity and fitness (Dayan et al., 2024) of natural populations, while multiple studies examined effects to diversity of altered habitats (Hugentobler et al., 2024;Moccetti et al., 2024) or harvest impacts (Miettinen et al., 2024). Two studies characterized variation at the genomic (Carbonneau et al., 2024) or transcriptomic (Kokkonen et al., 2024) level to assist with conservation of rare taxa and remote populations, while Thompson et al. (2024) Parentage analyses of returning adults indicated that the program provided a demographic boost in productivity in the 3 years evaluated (ranging from 6.0-48.6 times higher productivity), presumably due to limited spawning habitat and density dependence during incubation stages for fish in natural habitat. There was no statistical difference in adult run timing or size at age between hatchery reared versus wild fish, but hatchery-reared fish were younger as returning adults on average than wild fish. ...

Reference:

Advances in salmonid genetics—Insights from Coastwide and beyond
Using de novo transcriptomes to decipher the relationships in cutthroat trout subspecies (Oncorhynchus clarkii)

... For example, Malmstrøm et al. (2016) sequenced and assembled the complete nuclear genome of S. norvegicus and deposited SRA-archive (Sequence Read Archive) to GenBank. Later, Campbell et al. (2022) used this SRA-archive to assemble the complete mitochondrial genome of S. norvegicus. However, when analyzing species-specific mtDNA (D-loop) and nuclear DNA (RP2 S7) sequences from these genomes (data not shown), we found that the studied specimen actually belongs to another redfish species, S. viviparus. ...

Complete mitochondrial genomes of two rockfish: Sebastes maliger and Sebastes norvegicus (Scorpaenidae, Scorpaeniformes)

... For WCT, fitness consequences of hybridization are theoretically likely, and have been observed. Current best estimates suggest that WCT and Yellowstone Cutthroat Trout diverged from one another approximately 3 million years ago, while cutthroat trout (including WCT) and Rainbow Trout diverged around 10 million years ago (Shiozawa et al., 2018). During this time, the species have accumulated major structural genomic differences in terms of chromosome number and organization (e.g., Thorgaard et al., 2018). ...

Geographic variation, isolation, and evolution of cutthroat trout with comments on future directions for management and research

... Apparently, together with the brown trout, its parasite Echinorhynchus baeri Kostylev, 1928 (Acanthocephala) also crossed the area of the current watershed between the Caspian Sea and the Indian Ocean. E. baeri has been described as endemic to Lake Sevan (the Caspian Sea basin), but it has recently been discovered in the Euphrates River basin [169]. ...

A description of Echinorhynchus baeri Kostylew, 1928 (Acanthocephala: Echinorhynchidae) from Salmo trutta in Turkey, with notes on synonymy, geographical origins, geological history, molecular profile, and X-ray microanalysis

Parasite

... Distribution in Saudi Arabia: Figure 3 Previous records: Al Qaseem [13], Taif, 80 km W Al Juf, Jabrin, Hasa, 96 km N Qunfida, Buraidah, Rafha, Hail, Hofuf, Mecca bypass [3], Riyadh Province [14], Al Majma'h, Badaya, Buraidah, Ghamas, Mlida, Muznab, Riyadh, Shmasya, Um Sedra, Unizah [15], Al Adare, Al-Madinah Al-Munawwarah, Al-Ula, Khaybar, Sakaka [16], Turaif [17]. Unizah [18,19], Thumamah [20], Ara'r [21], Bsitah, Al Daba'ah [22]. ...

Morphological and molecular descriptions of Moniliformis saudi sp. n. (Acanthocephala: Moniliformidae) from the desert hedgehog, Paraechinus aethiopicus (Ehrenberg) in Saudi Arabia, with a key to species and notes on histopathology

Folia Parasitologica

... A p-distance measure was employed to infer genetic distances between species. A Maximum Likelihood tree was generated with a rotiferan Brachionus plicatilis as an outgroup based on the sister taxa status of Rotifera and Acanthocephalan (Amin et al., 2016). Confidence levels at each node assessed by 10000 bootstrap replications. ...

Morphological and molecular description of Tenuisentis niloticus (Meyer, 1932) (Acanthocephala: Tenuisentidae) from Heterotis niloticus (Cuvier) (Actinopterygii: Arapaimidae), in Burkina Faso, with emendation of the family diagnosis and notes on new features, cryptic genetic diversity and histopathology

Systematic Parasitology

... Bae et al. 2004;James and Andrew 2006;Sheffield et al. 2008;Wei et al. 2010b;Huang et al. 2015;Sproul et al. 2015;Chen et al. 2016;Chen and Du 2017c;Wang et al. 2017aWang et al. , 2017b Cao et al. 2019b). In both species, ATP6, ATP8, COII, COIII, CYTB, ND2, ND4 and ND4L started with ATG (Met), while COI, ND3 and ND6 started with ATT (Ile) ( ...

Climate oscillations, glacial refugia, and dispersal ability: Factors influencing the genetic structure of the least salmonfly, Pteronarcella badia (Plecoptera), in Western North America

BMC Evolutionary Biology

... Geographic ranges of freshwater species contracted or fragmented during harsh climatic conditions of the Last Glacial Maximum (26,000-19,000 years ago) followed by demographic growth and range expansion as the climate warmed during the terminal Pleistocene and early Holocene (19,000-10,000 years ago; Berendzen et al. 2003;Faber et al. 2009;Kawamura et al. 2009;Bagley et al. 2013). Patterns of genetic variation in North American freshwater fishes were further shaped by rising sea levels at the end of the Pleistocene that isolated coastal river drainages (Bermingham and Avise 1986) and mid-Holocene (9000-5000 years ago) droughts (Douglas et al. 2003;Houston et al. 2015). The Alligator gar's shallow phylogeographic structure suggests that the three haplogroups diverged relatively recently and is likely a result of former isolation in separate refugia during the Last Glacial Maximum. ...

Pluvial Drainage Patterns and Holocene Desiccation Influenced the Genetic Architecture of Relict Dace, Relictus solitarius (Teleostei: Cyprinidae)

... This is a rough estimation based on the results of excavations of 370 graves conducted by the Russian mission; due to the fact that burials of the Byzantine period are hardly distinguished from Roman ones, the real percentage is probably higher. Similar observations are made for cemeteries at Fag el-Gamus ( Evans et al. 2015 The coffins had minimal carving decoration: there was a mask that had been made separately and attached with dowels to the front part of the cover. It was placed within a carved outline of the front strands of a tripartite wig. ...

Rethinking burial dates at a Graeco-Roman Cemetery: Fag el-Gamous, Fayoum, Egypt

Journal of Archaeological Science Reports

... Recently, another landscape genomics study reported high connectivity among two Sweltsa stonefly species across locations on both mainstem habitats and higher-elevation tributaries in a montane ecosystem, and that the small portion of variance in allele frequency was explained by climate-related variables indicating influence on adaptive genetic variation (Malison et al. 2022). Although stoneflies can be considered to have poor dispersal abilities, short-distance dispersal has also been previously reported for different species (Briers et al. 2002;Sproul et al. 2014). For instance, between-stream dispersal at small spatial scales (< 1 km) has been directly observed in markrecapture studies (Briers et al. 2004;MacNeale et al. 2005). ...

Comparative phylogeography of codistributed aquatic insects in western North America: Insights into dispersal and regional patterns of genetic structure
  • Citing Article
  • July 2014

Freshwater Biology