The central-marginal model is widely accepted in chromosomally polymorphic species of Drosophila. In fact, geographically and ecologically central populations of Drosophila show higher levels of polymorphism for paracentric inversions, whereas marginal populations tend to be monomorphic. This fact has been variously explained. Chromosomal polymorphisms in grasshoppers have also been attributed to show such geographical structuring, as in the case of the South-American grasshopper Dichroplus pratensis Bruner (Orthoptera: Acrididae). However, in three other cases involving Acrididae – Leptysma argentina Bruner, Trimerotropis pallidipennis (Burmeister) and Cornops aquaticum (Bruner), it is clear that chromosomal polymorphisms (sometimes with a wide extension over the Argentine area) do not conform to this pattern, and show instead clear correlations with environmental variables, especially minimum temperature, showing low or null frequencies of the rearrangements at one extreme of the environmental gradient and with high or fixed frequencies at the other. Furthermore, this correlation with temperature might also be true in the case of D. pratensis. These aforementioned examples emphasise the dangers of over-generalization when discussing chromosomal polymorphisms, and suggests that such polymorphisms should be considered very much in a case-specific manner in terms of the particular genetic system under study., Pablo C. Colombo., and Obsahuje seznam literatury
C. aquaticum (Acrididae: Leptysminae) inhabits water-hyacinths in the Neotropical region. The blue-flowered water-hyacinth, Eichhornia crassipes, has been introduced elsewhere without its natural enemies and has become a weed; recently C. aquaticum was considered as a possible biological control agent. In this work, six populations were sampled and cytologically studied. C. aquaticum has 2n = 23 chromosomes in males and 24 in females, with an X0/XX sex determination system. All chromosomes are acro-telocentric and the basic karyotype includes three Robertsonian (Rb) translocations between pairs 1/6, 2/5, and 3/4. These polymorphisms are restricted to the lower course of the Paraná river, between Rosario and Buenos Aires. Fusion frequencies increase southwards, thus showing a geographical cline. The polymorphisms mostly accord with Hardy-Weinberg and gametic phase equilibria. The rearrangements cause a drastic chiasma repatterning in the fusion bivalents (or trivalents) which reduces the proximal chiasma frequency. Recombination is also reduced due to the loss of independent segregation. A recombination index that takes into account both these factors correlates negatively with the number of pairs of chromosomes affected by fusions among populations, which does not accord with the "central-marginal" pattern.
The New World grasshopper Cornops aquaticum (Leptysminae: Acrididae) shows a geographical pattern for three Robertsonian polymorphisms in its southernmost area of distribution in Argentina and Uruguay. The frequency and distribution of chiasmata were analysed in five Argentinian populations. This study reveals a strong redistribution of chiasmata in fusion carriers, with a reduction in proximal and increase of distal chiasma frequency in fusion bivalents and trivalents, when all three karyotypes were compared. However, when only fusion bivalents and trivalents were compared, chiasma frequency was significantly higher in the former than in the latter. This higher chiasma frequency in fusion bivalents is due to an increase in proximal chiasma frequency. It is argued that the reduction in proximal chiasma frequency (relative to unfused bivalents) in fusion bivalents may be due to interference across the centromere. Proximal chiasma reduction in trivalents may be attributed either to a physical effect of structural heterozygosity or to an adaptation to the polymorphic condition. Therefore the differences in the distribution of chiasmata in trivalents and Robertsonian bivalents have different causes.
The grasshopper Dichroplus pratensis Bruner is polymorphic and polytypic for a complex Robertsonian system. In this species, centric fusions induce changes in number and position of chiasmata, and thus potentially affect intrachromosomal genetic recombination and genetic variability. Males and females, from 23 populations covering most of the geographic range of the species and spanning 22 degrees of latitude, were studied. We analyzed chiasma frequency in relation to variability in six exomorphological characters. The chromosomal polymorphisms of D. pratensis are widely geographically distributed, and show a central-marginal pattern, in which the central populations (those occupying the ecologically optimal habitats) have high mean frequencies of different fusions per individual (F) of up to F = 3.00 and total chiasma frequencies as low as XT = 8.98 per cell, while those near the margins of the distribution (central Patagonia and the Andes) have very low levels of chromosomal polymorphisms [down to F = 0.00 in most geographically marginal locations), monomorphic karyotypes and high chiasma frequencies (XT = 11.66, in the southernmost (Rada Tilly, 45°57´S) and XT = 12.01 in the northernmost population (Volcán, 23°55´S)]. Increasing chiasma frequencies towards the margins of the range are positively and significantly correlated with increasing levels of morphological variability. The decrease in fusion polymorphism and the consequent increase in genetic recombination (both inter- and intrachromosomal) in the marginal areas, is a result of natural selection favouring higher levels of variability, which could be adaptive in ecologically harsher and changing environments.