The gekko Phyllodactylus marmoratus has at least three distinct chromosome races; 2n=39, 2n=26 ZZ/ZW and 2n=34. Specimens from these races are morphologically distinguishable, have a degree of habitat specialization and occur in a defined distribution. The 2n=36 race found in Eastern Australia is the presumed primordial type. The 2n=34 race occurs in Western Australia and is regarded as a fusion derivative. The 2n=36 ZZ/ZW race, which is only found on the Murray River system in Eastern Australia has a heteromorphic sex chromosome system present in the female. Giemsa banding suggests that this heteromorphism is the result of a pericentric inversion.
Comparative fluorescence studies on the chromosome of ten species of acridid grasshoppers, with varying amounts and locations of C-band positive heterochromatin, indicate that the only regions to fluoresce differentially are those that C-band. Within a given species there is a marked tendency for groups of chromosomes to accumulate heterochromatin with similar fluorescence behaviour at similar sites. This applies to all three major categories of heterochromatin - centric, interstitial and telomeric. Different sites within the same complement, however, tend to have different fluorescence properties. In particular, centric C-bands within a given species are regularly distinguishable in their behaviour from telomeric C-bands. Different species on the other hand, may show distinct forms of differential fluorescence at equilocal sites. These varying patterns of heterochromatin heterogeneity, both within and between species, indicate that whatever determines the differential response to fluorochromes has tended to operate both on an equilocal basis and in a concerted fashion. This is reinforced by the fact that structural rearrangements that lead to the relocation of centric C-bands, either within or between species, may also be accompanied by a change in fluorescence behaviour.
A karyotypic analysis of populations of the gekkos Gehyra variegata and G. punctata reveals three chromosome races in G. variegata (2n = 44; 2n = 40a; 2n = 40b), and three in G. punctata (2n = 44; 2n = 42; 2n = 38). The chromosome races have differentiated by a series of chromosome fusions. The ordered nature of these changes suggests that the phylogenetic relationships of the races cut across the current taxonomy, and it is argued that there is but one 2n = 44 race, occurring as a number of morphologically distinct populations, two of which were erroneously described as the separate Gehyra species. Isolated populations within a number of the chromosome races show pronounced morphological differences. It is believed that these gekkos are an ancient Australian group which differentiated chromosomally during a number of colonizing radiations. Since then, populations within each race have been isolated by geographic barriers and have speciated allopatrically. This suggests that the chromosome races are at least good species and may be of a higher taxon.
Five distinct classes of secondary constriction are found in the hylid frogs from the genera Litoria and Cyclorana, each of which is defined by its C-banding pattern and morphology (King, 1980, 1987). In-situ hybridization experiments utilizing 18S + 28S copy RNA probes derived from Xenopus and Drosophila rDNA templates, were made on nine species of frogs possessing the major constriction types. Types 1, 2, 4, and 5 are confirmed as being NORs. These results also indicate that type 1 and 2 constriction types are not differentially despiralized as previously suggested, but show absolute differences in the quantity of ribosomal DNA present. This variation took two forms, deletion polymorphism and amplification polymorphism. These differences were observed between homologues within cells and between cells within individuals. Animals possessing these 'despiralized' constrictions are therefore mosaics for both deletion and amplification polymorphisms. Polymorphism frequencies vary greatly between constriction types. Some specimens have a higher level of presence/absence heterozygosity, (L. moorei, type 2, L. nannotis type 5, L. raniformis (animal A, pair 8 type 2), than do others (L. peronii, L. rothii, L. caerulea). The above species also vary markedly in the degree and frequency of amplification of the NORs. The type 4 constrictions analysed (L. coplandi, L. lesueuri and C. novaehollandiae) have a particularly low frequency of presence/absence heterozygosity, and they have fewer size heteromorphisms between homologues. The type 3 ephemeral constrictions did not hybridize to cRNA probes at any stage. In all but one of the species studied, a single pair of chromosomes possessed an NOR. However, in L. raniformis these occurred on two pairs of chromosomes.(ABSTRACT TRUNCATED AT 250 WORDS)
Many theoretical papers investigating the relationship between chromosomal change and speciation are found to have been based on erroneous data. For rather than considering those negatively heterotic, or at least potentially negatively heterotic rearrangements which can have a possible role in speciation, these papers have included substantial amounts of information on rearrangements which are not implicated in this process. Common forms of chi'omosomal repatterning such as heterochromatic addition and polymorphism are in this category. Their inclusion in theoretical studies, often cited as supporting or opposing a chromosomal involvement in speciation, invalidates these findings. A new approach is suggested.
A chromosomal, analysis of the monitor Varanus acanthurus Boulenger has been made using G-and C--banding and silver-staining techniques. This species has two cytotypes, one of which has a pericentric-inversion polymorphism, whereas the other is chromosomally monomorphic. A ZZ,.' ZW sex-chromosome system is also present in both cytotypes of this species. The banding patterns of these mechanisms are described and their evolution is discussed.
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