Editorial Type:
Article Category: Research Article
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Online Publication Date: 01 Jul 2015

Lack of Hybridization between Naturally Sympatric Populations of Red and Blacktail Shiner (Cyprinella lutrensis and C. venusta) in Texas, but Evidence of Introgression among Three Lineages of the C. lutrensis Species Group

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Page Range: 272 – 280
DOI: 10.1643/CG-14-046
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Hybridization is more common in actinopterygian fishes than any other group of vertebrates. This is especially true for members of the family Cyprinidae; for example, Hubbs found 68 different combinations of inter-generic and intra-generic hybridization among cyprinids collected east of the continental divide. Hybridization between two cyprinid species, the red shiner and the blacktail shiner (Cyprinella lutrensis and C. venusta), has been described in detail in Georgia where C. lutrensis is an introduced species. However, hybridization has not been thoroughly assessed where the two species are naturally sympatric. Our specific objectives were to determine the extent of ongoing hybridization between the two species using nuclear markers and morphometrics and to determine the extent of historical introgression using mitochondrial DNA (mtDNA). We collected 100 individuals from four different locations along the Bosque River and an additional 100 individuals from four locations along the Paluxy River. We used amplified fragment length polymorphism (AFLP) to verify species identification and determine hybrid status of each individual. A total of 56 AFLP fragments were scored, with 82.14% (47 fragments) being polymorphic (95% criterion). Based on these nuclear markers, we only identified two hybrids out of the 200 specimens analyzed; one from the Bosque River, Texas and one from the Paluxy River, Texas. There were no instances of introgression of mitochondrial DNA (mtDNA) from one species into the nuclear background of the other species. We did, however, discover the sympatric occurrence of three mtDNA lineages of C. lutrensis within a single nuclear gene pool; there was only one mtDNA lineage of C. venusta. Overall body shape was assessed using a truss network and was found to be statistically different with red shiner having the shorter and deeper body. The minimal amount of hybridization inferred from AFLP data, in combination with the absence of mtDNA introgression and limited morphological overlap, indicates that pre- or postzygotic isolating mechanisms effectively minimize genetic exchange between naturally sympatric populations of C. lutrensis and C. venusta within these two river systems.

Copyright: © 2015 by the American Society of Ichthyologists and Herpetologists
Fig. 1.
Fig. 1.

Map depicting locations of the eight collecting sites on the Bosque and Paluxy rivers.


Fig. 2.
Fig. 2.

Location of anatomical landmarks (closed circles) and corresponding distances (dashed lines) used to quantify overall body morphology (A). Map of morphometric distances used to create truss network obtained from digitized anatomical landmarks (B).


Fig. 3.
Fig. 3.

Admixture proportions (qi) from STRUCTURE indicating membership of individual specimens of C. lutrensis and C. venusta from the (A) Bosque and (B) Paluxy rivers. Individuals with low q-values are C. venusta. Bars indicate 90% credible regions. Individuals with C. lutrensis cyt b haplotypes are indicated with filled circles whereas those with C. venusta haplotypes are indicated with open circles.


Fig. 4.
Fig. 4.

Principal coordinate plot based on AFLPs of C. lutrensis (open symbols) and C. venusta (closed symbols) from the Bosque (squares) and Paluxy (circles) rivers showing distinct genetic differences between species. Individuals identified as hybrids are identified with stars.


Fig. 5.
Fig. 5.

Maximum likelihood tree of cyt b haplotypes of C. lutrensis and C. venusta from the Bosque and Paluxy rivers along with reference specimens of other species within these species groups. Only individuals representative of unique haplotypes are shown. Bootstrap values for major clades are indicated. Reference specimens are indicated by the first three letters of the specific epithet (ven  =  C. venusta, gar  =  C. garmani, lut  =  C. lutrensis, lep  =  C. lepida, sua  =  C. suavis, pro  =  C. proserpina, lab  =  C. labrosa) followed by the cyt b designations (in brackets) given in Schönhuth and Mayden (2010). Cyprinella proserpina and C. labrosa are outgroups.


Received: 17 Mar 2014
Accepted: 01 Dec 2014
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