Variability of mitochondrial DNA cytochrome <Emphasis Type="Italic">b</Emphasis> gene in the red vole <Emphasis Type="Italic">Clethrionomys rutilus</Emphasis> Pallas, 1779, population in the flood-plain middle stream of the Kolyma River

The intrapopulation variability of a cytochrome b gene fragment and the corresponding amino acid sequence was studied in the red vole Clethrionomys rutilus Pallas, 1779 from the flood-plain of the Kolyma River. Wide polymorphic variability of these properties was observed. Differences in the cytochrome b gene sequence were determined between the red voles of the studied population and the species collected in neighborhoods of Novosibirsk and Omsk. The revealed results point to the urgency of the cytochrome b gene nucleotide sequence and the variants of the respective amino acid sequence as genetic markers of originality of different red vole populations.     

Identifying Fishes through DNA Barcodes and Microarrays

Background

International fish trade reached an import value of 62.8 billion Euro in 2006, of which 44.6% are covered by the European Union. Species identification is a key problem throughout the life cycle of fishes: from eggs and larvae to adults in fisheries research and control, as well as processed fish products in consumer protection.

Methodology/Principal Findings

This study aims to evaluate the applicability of the three mitochondrial genes 16S rRNA (16S), cytochrome b (cyt b), and cytochrome oxidase subunit I (COI) for the identification of 50 European marine fish species by combining techniques of “DNA barcoding” and microarrays. In a DNA barcoding approach, neighbour Joining (NJ) phylogenetic trees of 369 16S, 212 cyt b, and 447 COI sequences indicated that cyt b and COI are suitable for unambiguous identification, whereas 16S failed to discriminate closely related flatfish and gurnard species. In course of probe design for DNA microarray development, each of the markers yielded a high number of potentially species-specific probes in silico, although many of them were rejected based on microarray hybridisation experiments. None of the markers provided probes to discriminate the sibling flatfish and gurnard species. However, since 16S-probes were less negatively influenced by the “position of label” effect and showed the lowest rejection rate and the highest mean signal intensity, 16S is more suitable for DNA microarray probe design than cty b and COI. The large portion of rejected COI-probes after hybridisation experiments (>90%) renders the DNA barcoding marker as rather unsuitable for this high-throughput technology.

Conclusions/Significance

Based on these data, a DNA microarray containing 64 functional oligonucleotide probes for the identification of 30 out of the 50 fish species investigated was developed. It represents the next step towards an automated and easy-to-handle method to identify fish, ichthyoplankton, and fish products.     

Genetic linkage maps of barfin flounder (<Emphasis Type="Italic">Verasper moseri</Emphasis>) and spotted halibut (<Emphasis Type="Italic">Verasper variegatus</Emphasis>) based on AFLP and microsatellite markers

Barfin flounder (Verasper moseri) and spotted halibut (Verasper variegatus) are two economically important marine fish species for aquaculture in China, Korea and Japan. Construction of genetic linkage maps is an interesting issue for molecular marker-assisted selection (MAS) and for better understanding the genome structure. In the present study, we constructed genetic linkage maps for both fish species using AFLP and microsatellite markers based on an interspecific F₁ hybrid family (female V. moseri and male V. variegatus). The female genetic map comprised 98 markers (58 AFLP markers and 40 microsatellite markers), distributing in 27 linkage groups, and spanning 637 cM with an average resolution of 8.9 cM. Whereas the male genetic map consisted of 86 markers (48 AFLP and 38 microsatellite markers) in 24 linkage groups, covering a length of 625 cM with an average marker spacing of 10 cM. The expected genome length was 1,128 cM in female and 1,115 cM in male, and the estimated coverage of genome was 56% for both genetic maps. Moreover, five microsatellite markers were observed to be common to both genetic maps. This is the first time to report the genetic linkage maps of V. moseri and V. variegatus that could serve as the basis for genetic improvement and selective breeding, candidate genes cloning, and genome structure research.     

Some aspects of biology and aquaculture potentials of <Emphasis Type="Italic">Tilapia guineensis</Emphasis> (dumeril) in Nigeria

The paper emphasizes on the several attempts made to raise the brackish water tilapia species, Tilapia guineensis both on an experimental and production basis by researchers and fish farmers in Nigeria. Besides, the aquaculture potentials of Tilapia guineensis have been reported by several authors. However, problems exist which are not found with the culture of other tilapia species. Even under most favourable conditions (e.g. the monosex culture of Tilapia guineensis), a poor growth rate and a mediocre feed conversion do not presage profitable aquaculture exploitation. The present review therefore throws light on areas of further research to enhance the growth performance of Tilapia guineensis with emphasis on fish larvae nutrition and first feeding (development of bio-encapsulated feed for larval fish based on nutritionally enriched nematodes and Calanoid copepods), digestibibilty of the feed ingredients, elucidation of the dietary protein requirements, improved culture technique through the use of the Recirculating Aquaculture Systems and the adoption of the most recent technology (The YY Male technology) that produces Genetically Male Tilapia through genetic manipulation. Specific recommended areas for further research are also proffered.     

Phylogeographic structure in the threatened Yarra pygmy perch <Emphasis Type="Italic">Nannoperca obscura</Emphasis> (Teleostei: Percichthyidae) has major implications for declining populations

Molecular genetic information should be a pre-requisite when evaluating conservation priorities in highly structured species such as freshwater fishes. Nuclear (allozyme) and mitochondrial (cytochrome b) markers were used to investigate phylogeographic structure in the Yarra pygmy perch Nannoperca obscura (Klunzinger), a threatened freshwater fish endemic to mainland south-eastern Australia. Complementary patterns of strong, geographically defined sub-structure were observed including a major east–west divergence (at the Glenelg River), four diagnosable lineages, and statistically-significant differences between most populations. Accordingly, four Evolutionarily Significant Units (ESUs) are defined and multiple, drainage-scale Management Units (MUs) suggested. Since Nannoperca obscura is a relatively poor disperser with no apparent gene flow between most populations, any regional extirpation would see the irreversible loss of genetic diversity. This is problematic, as several populations, most notably a recently discovered ESU in the Murray-Darling Basin, are feared extirpated through a combination of anthropogenic threats and severe drought. The potential loss of unique evolutionarily components within N. obscura soon after their discovery highlights with some urgency, the need to define and protect conservation units in highly modified freshwater habitats.     

DNA分子标记技术及其在水产动物遗传上的应用研究

随着DNA分子标记技术的发展,其在动物遗传上发挥了重大作用,使用DNA分子标记可以观察到整个基因组的遗传多样性。目前,在水产养殖种类中使用的遗传标记主要包括线粒体DNA、RFLP、RAPD、AFLP、微卫星、SNP和EST标记。DNA分子标记的应用使得人们对水产养殖动物的遗传多样性、近亲繁殖、种类和品系鉴定以及遗传连锁图谱建立的研究都取得了很大进展,也加快了数量性状位点(QTL)基因的鉴定作为分子标记辅助选择(MAS)的研究。将这些标记技术在水产动物上的应用进行了论述,以及如何从人类基因组工程和斑马鱼这种模式鱼的研究中得到启发,更好的应用于水产动物基因组学和遗传学研究做一讨论。     

Barcoding,molecular taxonomy,and exploration of the diversity of shrews (Soricomorpha: Soricidae) on Mount Nimba (Guinea)

We tested the efficiency of cytochrome oxidase I (COI)‐barcoding as a taxonomic tool to discriminate and identify sympatric shrew species on Mount Nimba (Guinea). We identified 148 specimens at the species level using morphological characters and comparison with type specimens, including several taxa from Mount Nimba. We identified ten morphospecies and tested aspects of genetic diversity and monophyly using genetic data from three mitochondrial (16S, cytochrome b, and COI) and one nuclear marker (the breast cancer gene, BRCA). Nine morphospecies were validated under the phylogenetic and genetic species concepts, including the recently diverged species Crocidura buettikoferi, Crocidura theresae, and Crocidura grandiceps. Under the same concepts, our analyses revealed the presence of two cryptic species amongst animals identified as Crocidura muricauda. We then tested the efficiency of barcoding thanks to commonly used phenetic methods, with the 148 specimens representing 11 potentially valid species based on morphological and molecular data. We show that COI‐barcoding is a powerful tool for shrew identification and can be used for taxonomic surveys. The comparison of genetic divergence values shows the presence of a barcoding gap (i.e. difference between the highest intraspecific and the lowest interspecific genetic divergence values). Given that only a few COI sequences are available for Afrotropical shrews, our work is an important step forward toward their enrichment. We also tested the efficiency of the three other sequenced markers and found that cytochrome b is as efficient as COI for barcoding shrews. © 2012 The Linnean Society of London, Zoological Journal of the Linnean Society, 2012, 166 , 672–687.     

Microsatellite DNA markers for parental assignment in hybrid striped bass (Morone saxatilis × Morone chrysops)

Development of nine polymorphic microsatellites from a genomic library of hybrid striped bass (female Morone chrysops × male Morone saxatilus) DNA is described. Breeding of hybrid striped bass for aquaculture is based largely on breeding wild fish. Molecular markers such as microsatellites will be useful tools for developing broodstock, estimating heritability for production traits, and selective breeding via marker‐assisted selection. The nine polymorphic microsatellites include six dinucleotide and three complex repeat motifs. The number of alleles detected among a sample of 10 individuals of each species was relatively low. All polymerase chain reaction primer pairs also amplified products in the sea bass Dicentrarchus labrax.     

Morphological and molecular genetic study of the Persian sturgeon <Emphasis Type="Italic">Acipenser persicus</Emphasis> Borodin (Acipenseridae) taxonomic status

Morphological and molecular genetic analyses of the Russian sturgeon sensu Berg (1934) were accomplished using the sample of individuals collected in the southern part of the Caspian Sea. The distribution of specimens in the space of principal components calculated using 28 morphometric characters demonstrates the absence of separate clusters. Frequency distributions of six studied meristic characters are unimodal and do not demonstrate the existence of morphologically distinguishable forms within the analyzed sample. The results of molecular genetic study, based on the cytochrome b polymorphism analysis of the same sample of fish, demonstrate its homogeneity. The joined results of morphological and molecular genetic analyses of the Russian sturgeon sensu Berg (1934) do not support the validity of the Persian sturgeon as a separate species Acipenser persicus. The text was submitted by the authors in English     

Phylogeny of Glaucosomatidae inferred from molecular evidence

Most species of glaucosomatids (Teleostei: Glaucosomatidae) are endemic to Australia, except Glaucosoma buergeri that is widely distributed from Australia to Japan. This study elucidated phylogenetic relationships among glaucosomatids based on the morphological characters of the saccular‐otolith sagitta, in addition to molecular evidence of mitochondrial 16S rDNA, cytochrome oxidase I (COI) and cytochrome b (cyt b) sequences, and nuclear rhodopsin sequences. The topologies of individuals' phylogenetic trees, based on 16S rDNA, COI and cyt b sequences, were statistically indistinguishable from one another, and were only slightly different from a tree based on rhodopsin sequences. These molecular tree topologies, however, differed from species relationships in morphology‐based phylogenetic hypothesis proposed in previous studies. Specimens of G. buergeri from Australia and Taiwan showed differences in the sagitta and molecular differentiation at the four genes, suggesting a possible speciation event. Both molecular and morphological evidences indicate that Glaucosoma magnificum is the plesiomorphic sister species of other glaucosomatid species. Glaucosoma hebraicum is the sister species of a clade composed of G. buergeri and Glaucosoma scapulare. Molecular and morphological evidences also support the species status of G. hebraicum.     

Isolation and characterization of polymorphic microsatellite markers in Pagellus bogaraveo,and cross‐species amplification in Sparus aurata and Dicentrarchus labrax

Several new fish species are currently being included in breeding programmes. However, as specific molecular markers have not yet been developed, this represents a commercial handicap with respect to traditional aquaculture species such as gilthead sea bream or Atlantic salmon. In the present study, 12 new microsatellite loci were developed for blackspot sea bream (Pagellus bogaraveo) that show high levels of polymorphism, especially useful in parentage assignment and individual identification. In addition, cross‐amplification was obtained for two important species for Spanish aquaculture, gilthead sea bream and sea bass.     

Polymorphic microsatellite loci optimised for studies on the convict cichlid fish (<Emphasis Type="Italic">Amatitlania siquia</Emphasis>)

The neotropical convict cichlid fish (Amatitlania siquia) is an important model species for the study of animal behaviour. It is therefore surprising that no genetic markers are available for this species. Here, we have optimised four polymorphic microsatellite loci for use with this fish, where each locus comprises between 9 and 28 alleles. We demonstrate how these markers can be used to genotype fry (young) and for the analyses of genetic structure and prevalence of interfamilial mixing within biparental broods of wild convict cichlids. These microsatellites will facilitate future research, hitherto not possible, on the molecular, behavioural and evolutionary ecology of the convict cichlid and possibly other closely related species.     

Molecular phylogeny and phylogeography of the Cuban cave-fishes of the genus Lucifuga: evidence for cryptic allopatric diversity

Underground environments are increasingly recognized as reservoirs of faunal diversity. Extreme environmental conditions and limited dispersal ability of underground organisms have been acknowledged as important factors promoting divergence between species and conspecific populations. However, in many instances, there is no correlation between genetic divergence and morphological differentiation. Lucifuga Poey is a stygobiotic fish genus that lives in Cuban and Bahamian caves. In Cuba, it offers a unique opportunity to study the influence of habitat fragmentation on the genetic divergence of stygobiotic species and populations. The genus includes four species and one morphological variant that have contrasting geographical distributions. In this study, we first performed a molecular phylogenetic analysis of the Lucifuga Cuban species using mitochondrial and nuclear markers. The mitochondrial phylogeny revealed three deeply divergent clades that were supported by nuclear and morphological characters. Within two of these main clades, we identified five lineages that are candidate cryptic species and a taxonomical synonymy between Lucifuga subterranea and Lucifuga teresinarum. Secondly, phylogeographic analysis using a fragment of the cytochrome b gene was performed for Lucifuga dentata, the most widely distributed species. We found strong geographical organization of the haplotype clades at different geographic scales that can be explained by episodes of dispersal and population expansion followed by population fragmentation and restricted gene flow. At a larger temporal scale, these processes could also explain the diversification and the distribution of the different species.     

Length–weight relationships of 16 fish species from the Tarim River,China

This paper reports the length–weight relationships of 16 fish species belonging to three families and ten genera from the Tarim River in China. Length–weight relationships for ten fish species were unknown to Fishbase, and new maximum lengths are given for six species. The r² values ranged from 0.972 to 0.995. Values of b varied from 2.79 to 3.49.     

Bioregion heterogeneity correlates with extensive mitochondrial DNA diversity in the Namaqua rock mouse, <Emphasis Type="Italic">Micaelamys namaquensis</Emphasis>(Rodentia: Muridae) from southern Africa - evidence for a species complex

Background  

Intraspecific variation within the diverse southern African murine rodents has not been extensively investigated, yet cryptic diversity is evident in several taxa studied to date. The Namaqua rock mouse, Micaelamys namaquensis Smith, 1834 is a widespread endemic murine rodent from the subregion. Currently, a single species with four subspecies is recognised, but in the past up to 16 subspecies were described. Thus, this species is a good candidate for the investigation of patterns and processes of diversification in a diverse but under-studied mammalian subfamily and geographic region. Here, we report genetic differentiation based on mitochondrial DNA (mtDNA) cytochrome b (cyt b) sequences among samples collected over an extensive coverage of the species' range.     

Length–weight and length–length relationships of fishes from the Ouémé River in Bénin (West Africa)

The relationships between total (TL) and standard (SL) lengths for 50 fish species and between TL and wet weight for 52 fish species caught in the Ouémé River are presented. Relationships between TL and SL are linear. Between TL and weight, the relationships are of the form TW = aTL^b. The b values range from 2.3307 to 3.5185. Student's t‐test revealed that 38.5% of the species have b values significantly different from 3.     

Identification, phylogenetic relationships and a new maximum size of two rudd populations (Scardinius, Cyprinidae) from the Adriatic Sea drainage, Croatia

In order to determine an unknown fish population from the Vrana Lake, mitochondrial cytochrome b gene and non-coding nuclear region Cyfun P were investigated. Stabile population of Bulldog rudd, Scardinius dergle Heckel & Kner, the endemic Croatian freshwater fish in the Krka River, was genetically characterized with the same markers in order to compare it with the material from the Vrana Lake. Genetic markers were sequenced and aligned with the similar ones obtained from the GenBank in order to determine taxonomic and phylogenetic position of these two species. A significant discrepancy between nuclear genetic markers of our specimens and the sequence from the GenBank was found. Phylogenetic analysis suggested that the specimens from the Vrana Lake belong to the species S. hesperidicus. Morphometric characteristics, the maximum length and body mass showed new maximum values for both S. dergle and S. hesperidicus.     

Validation of microsatellite multiplexes for parentage analysis and species discrimination in two hybridizing species of coral reef fish (Plectropomus spp., Serranidae)

Microsatellites are often considered ideal markers to investigate ecological processes in animal populations. They are regularly used as genetic barcodes to identify species, individuals, and infer familial relationships. However, such applications are highly sensitive the number and diversity of microsatellite markers, which are also prone to error. Here, we propose a novel framework to assess the suitability of microsatellite datasets for parentage analysis and species discrimination in two closely related species of coral reef fish, Plectropomus leopardus and P. maculatus (Serranidae). Coral trout are important fisheries species throughout the Indo‐Pacific region and have been shown to hybridize in parts of the Great Barrier Reef, Australia. We first describe the development of 25 microsatellite loci and their integration to three multiplex PCRs that co‐amplify in both species. Using simulations, we demonstrate that the complete suite of markers provides appropriate power to discriminate between species, detect hybrid individuals, and resolve parent–offspring relationships in natural populations, with over 99.6% accuracy in parent–offspring assignments. The markers were also tested on seven additional species within the Plectropomus genus with polymorphism in 28–96% of loci. The multiplex PCRs developed here provide a reliable and cost‐effective strategy to investigate evolutionary and ecological dynamics and will be broadly applicable in studies of wild populations and aquaculture brood stocks for these closely related fish species.