Allozyme Variation and Phylogenetic Relationships of Asian, North American, and European Populations of the Threespine Stickleback, Gasterosteus aculeatus

Copeia ◽  
1992 ◽  
Vol 1992 (2) ◽  
pp. 432 ◽  
Author(s):  
Thomas R. Haglund ◽  
Donald G. Buth ◽  
Robin Lawson
1991 ◽  
Vol 69 (10) ◽  
pp. 2261-2270 ◽  
Author(s):  
Laurie L. Consaul ◽  
Suzanne I. Warwick ◽  
John McNeill

The Polygonum lapathifolium complex consists of populations that are widely distributed in the Northern Hemisphere and that have been classified at different taxonomic levels. Allozyme data were used to test the current North American taxonomic status of members of the complex (including P. lapathifolium var. lapathifolium, P. lapathifolium var. salicifolium, and P. scabrum) and to verify diploidy in the P. lapathifolium complex and polyploid origins of the morphologically similar P. persicaria and P. pensylvanicum. Of the 15 enzyme systems surveyed in 50 populations of the complex, only 3 of the 23 loci (Acon, Lap, and Skdh) were polymorphic in the North American populations and a total of 6 loci in European populations. Fifteen multilocus genotypes were evident in the complex. Four genotypes (all with Lap-10.67 were exclusive to North American populations of P. lapathifolium, providing support for a North American element of the complex. Nine genotypes (all with Lap-10.63) were found in North American and European populations of P. scabrum, all European populations of the P. lapathifolium complex, and three populations of North American P. lapathifolium var. lapathifolium. Lap-10.67 was also found in the native tetraploid P. pensylvanicum, whereas Lap-10.63 was found in the introduced tetraploid P. persicaria. Genetic distances among populations did not support the current taxonomic divisions within the complex, nor did it support separate species status of P. scabrum. Allozyme data provided support for the allotetraploid origins of P. pensylvanicum and P. persicaria, with members of the P. lapathifolium complex as one of the parents of each. Key words: Polygonum lapathifolium, Polygonum scabrum, Polygonum pensylvanicum, Polygonum persicaria, allozymes.


1984 ◽  
Vol 62 (11) ◽  
pp. 2313-2316 ◽  
Author(s):  
Jocelyn Hudon ◽  
Helga Guderley

The genetic relationships between four species of sticklebacks, Gasterosteus aculeatus Linneaus form trachurus, Gasterosteus wheatlandi Putnam, Pungitius pungitius (Linneaus), and Apeltes quadracus (Mitchill) were estimated by a locus-by-locus analysis of interspecific allozyme variation as well as by a band-counting analysis of soluble proteins in muscle. The locus-by-locus data was analysed both by a qualitative cladistic analysis and by a quantitative phenetic analysis. Both the locus-by-locus analysis and the band-counting analysis generated phylogenies which concord with the previously established relationships among these species. Our analyses indicate that these species have diverged considerably with a genetic identity of only 0.37 between the two congeneric species.


Zoomorphology ◽  
2020 ◽  
Author(s):  
Harald Ahnelt ◽  
David Ramler ◽  
Maria Ø. Madsen ◽  
Lasse F. Jensen ◽  
Sonja Windhager

AbstractThe mechanosensory lateral line of fishes is a flow sensing system and supports a number of behaviors, e.g. prey detection, schooling or position holding in water currents. Differences in the neuromast pattern of this sensory system reflect adaptation to divergent ecological constraints. The threespine stickleback, Gasterosteus aculeatus, is known for its ecological plasticity resulting in three major ecotypes, a marine type, a migrating anadromous type and a resident freshwater type. We provide the first comparative study of the pattern of the head lateral line system of North Sea populations representing these three ecotypes including a brackish spawning population. We found no distinct difference in the pattern of the head lateral line system between the three ecotypes but significant differences in neuromast numbers. The anadromous and the brackish populations had distinctly less neuromasts than their freshwater and marine conspecifics. This difference in neuromast number between marine and anadromous threespine stickleback points to differences in swimming behavior. We also found sexual dimorphism in neuromast number with males having more neuromasts than females in the anadromous, brackish and the freshwater populations. But no such dimorphism occurred in the marine population. Our results suggest that the head lateral line of the three ecotypes is under divergent hydrodynamic constraints. Additionally, sexual dimorphism points to divergent niche partitioning of males and females in the anadromous and freshwater but not in the marine populations. Our findings imply careful sampling as an important prerequisite to discern especially between anadromous and marine threespine sticklebacks.


Author(s):  
L. Leveelahti ◽  
P. Leskinen ◽  
E.H. Leder ◽  
W. Waser ◽  
M. Nikinmaa

2004 ◽  
Vol 91 (6) ◽  
pp. 918-925 ◽  
Author(s):  
Ryan K. Oyama ◽  
David A. Baum

Genetics ◽  
2021 ◽  
Vol 217 (1) ◽  
Author(s):  
Juntao Hu ◽  
Sara J S Wuitchik ◽  
Tegan N Barry ◽  
Heather A Jamniczky ◽  
Sean M Rogers ◽  
...  

Abstract Epigenetic mechanisms underlying phenotypic change are hypothesized to contribute to population persistence and adaptation in the face of environmental change. To date, few studies have explored the heritability of intergenerationally stable methylation levels in natural populations, and little is known about the relative contribution of cis- and trans-regulatory changes to methylation variation. Here, we explore the heritability of DNA methylation, and conduct methylation quantitative trait loci (meQTLs) analysis to investigate the genetic architecture underlying methylation variation between marine and freshwater ecotypes of threespine stickleback (Gasterosteus aculeatus). We quantitatively measured genome-wide DNA methylation in fin tissue using reduced representation bisulfite sequencing of F1 and F2 crosses, and their marine and freshwater source populations. We identified cytosines (CpG sites) that exhibited stable methylation levels across generations. We found that additive genetic variance explained an average of 24–35% of the methylation variance, with a number of CpG sites possibly autonomous from genetic control. We also detected both cis- and trans-meQTLs, with only trans-meQTLs overlapping with previously identified genomic regions of high differentiation between marine and freshwater ecotypes. Finally, we identified the genetic architecture underlying two key CpG sites that were differentially methylated between ecotypes. These findings demonstrate a potential role for DNA methylation in facilitating adaptation to divergent environments and improve our understanding of the heritable basis of population epigenomic variation.


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