A comparison of chromosomal and allozymal variation across a narrow hybrid zone in the grasshopper Caledia captiva

A hybrid zone between the Moreton and Torresian taxa of the grasshopper Caledia captiva in S.E. Queensland has been characterised in terms of allozyme and chromosome variation within the same individuals. — On chromosomal criteria (pericentric rearrangements), the zone is asymmetrical with evidence of high levels of introgression of Torresian chromosomes into the Moreton taxon. This is apparent from the analysis of two independent transects across the hybrid zone. Major changes in chromosomal frequency occur over distances of less than 0.5 km. and the level of introgression differs between the two transects, with much higher levels in the northern Moreton populations, characterised by an acrocentric X-chromosome, when compared with the southern metacentric-X Moreton populations. Chromosome analysis of samples taken from the same transect over two years has revealed no major changes in the structure of the zone. Moreover, a Moreton population located only 0.5 km. from the null point was found to be stable over 6 generations with evidence for a new balanced genome having originated following the differential incorportation of Torresian chromosomes. — Contrary to the chromosomal situation, the same hybrid zone was found to be symmetrical with respect to allozyme variation with evidence of movement of diagnostic alleles in both directions across the zone. The alleles are independent and not tightly linked to any of the pericentric rearrangements. Thus these 5 alleles are acting as markers of the background genome and reveal the relatively free movement of genes which are located outside the pericentric rearrangements. — It is proposed that the hybrid zone in Caledia captiva is unstable and is moving slowly in a westerly direction into the Torresian territory. This is due to the ability of the Moreton taxon to incorporate more readily into its genome those Torresian chromosomes or chromosome segments which increase the fitness of the Moreton taxon. On chromosomal criteria, the Torresian taxon does not share the same capacity. — It is suggested that, so long as the two taxa retain their ability to hybridise with subsequent asymmetrical introgression, the zone will continue to move westwards and eventually lead to the selective incorporation of the Torresian genome into the Moreton taxon. This will result in a polymorphic situation with clinal variation in chromosomal frequencies. The structure of the zone is dependent upon a fine balance between genomic reorganisation in recombinant genotypes and the relative dispersal capacities of the two hybridising taxa.     

ASSOCIATION BETWEEN LATITUDINAL VARIATION FOR EMBRYONIC DEVELOPMENT TIME AND CHROMOSOME STRUCTURE IN THE GRASSHOPPER CALEDIA CAPTIVA (ORTHOPTERA: ACRIDIDAE)

From southeastern Queensland to southern Victoria, over a transect of 11° latitude, the Moreton taxon of the Australian grasshopper Caledia captiva exhibits a cline in chromosome structure that involves change from a metacentric to an acrocentric genome. In this study, we show that embryonic development time covaries with chromosome structure along the transect. Both development time and chromosome short arm length exhibit an overall negative correlation with latitude, but with maxima just south of the northern limit of the taxon's distribution. Selection for such a pattern appears to arise from changes in voltinism along the cline in season length that exists along the transect. Populations with the highest temperature thresholds for avoidance of embryonic diapause also have the slowest development time and probably represent the northern extreme of a primarily univoltine life cycle. North of this region bivoltinism increases in frequency and, as expected from a split of the season length, development time decreases. Maximum chromosome short arm length occurs in the vicinity of the northern univoltine populations, rather than at the limit of distribution where bivoltinism prevails. We conclude that variation in chromosome structure could be contributing to the heritable variation for development time that forms the basis for adaptive change in this trait. These results provide justification for investigating causal relationships between chromosome structure and development time, with an ultimate aim of understanding the adaptive significance of chromosomal variation in C. captiva.     

The spatial distribution of chromosomes in metaphase neuroblast cells from subspecific F1 hybrids of the grasshopper Caledia captiva

The spatial distribution of chromosomes has been analysed in radial metaphase neuroblast cells in F₁ hybrid embryos generated by crossing individuals of the Moreton and Torresian (TT) chromosomal taxa of the grasshopper Caledia captiva. The Moreton individuals were of two kinds depending on whether they carried an acrocentric X (MAX) or a metacentric X (MMX). No significant associations were detected between any pair of homologous chromosomes in either male or female (MAX x TT) and (MMX x TT) F₁ hybrids. This result was supported by data which showed that the mean separation between homologues is greater, although not significantly so, than the mean separation between non-homologous chromosomes within the two Moreton genomes. Indeed, in a number of cases, genome separation was clearly observed in radial metaphase preparations from these F₁ hybrids. By comparison the analysis of pairwise associations between non-homologous chromosomes within the MMX and MAX Moreton genomes revealed a number of significant associations and dissociations which strongly suggests that at least some chromosomes in these genomes are organised non-randomly at metaphase. Of particular interest was the highly significant X-5 association in the MMX genome since in a previous study X-5 rearrangements were found to occur repeatedly among different backcross progeny involving Moreton x Torresian F₁ hybrids. Additionally a comparison of the organisation of chromosomes in the MAX and MMX genomes, which differ primarily by the type of X chromosome, revealed that in a number of cases pairs of chromosomes are arranged very differently with respect to each other. The distribution of chromosomes on the hollow spindle was also analysed to investigate whether a specific spatial ordering of chromosomes exists within these Moreton genomes based on the association of pairs of short arms and pairs of long arms of most similar length (the Bennett model). The twelve chromosomes in both genomes were uniquely ordered in a single chain. However, because of computing limitations, only the ordered arrangement of chromosomes 1–10 was investigated. An analysis of 48 cells in the MMX and 38 cells in the MAX genomes showed that the predicted order in the ten chromosome sub-set in each genome did not rank in the top 20% of the 181,440 possible orders. This suggests that, although there is a good evidence that some non-homologous chromosomes may be associated non-randomly at metaphase in these genomes, they do not appear to show a specific, ordered arrangement as predicted by the Bennett model. The significance of the observed non-random organisation of chromosomes in the MMX and MAX genomes is discussed in relation to the generation of novel chromosome rearrangements in Moreton x Torresian F₁ hybrids and the evolution of the Moreton and Torresian genomes.     

The chromosomal component of reproductive isolation in the grasshopper Caledia captiva

An analysis of the relative viabilities of recombinant and nonrecombinant chromosomes among the surviving embryos from back-crosses involving the Moreton (M) and Torresian (T) taxa has revealed that these embryos do not contain a representative sample of gametes derived from the F₁ hybrid parent. The significant deviations in the hybrid gametic population arise entirely from intrachromosomal effects with no evidence of any between-chromosome interactions. This is interpreted as clear evidence to show that recombinational repatterning within heterozygous bivalents in the F₁ parent is a significant factor in inducing the observed deviant segregation ratios. Furthermore, by using a population which is chromosomally equivalent to the Torresian but genically similar to the Moreton, it has been shown that over 46% of the F₂ embryonic breakdown arises solely from the effects of chromosomal heterozygosity upon recombination repatterning among (Moreton × Torresian) F₁ hybrids. From these data it is proposed that each chromosome is internally coadapted in the sense that it contains balanced blocks of cis-acting acting loci which can be disrupted by recombinational change. Disruption of the linear association of the genes on structurally different chromosomes by recombination repatterning results in novel intrachromosomal associations which may be functionally inadequate and so lead to arrested embryonic development. It is speculated that an important factor in arresting development may involve interactions between the novel recombinant chromosomes of the gamete and maternal factors laid down in the egg during oogenesis which are responsible for the sequential activation of the genomes of the progeny during development. Thus coadaptation is interpreted in terms of the functional intergration of a chromosome with the products of the genome of the previous generation. The assessment of the relative viabilities of recombinant and nonrecombinant chromosomes has shown that the Torresian nonrecombinant chromosomes possess the highest viabilities in the sequence T^N>M^NT^R = M^R where N and R represent nonrecombinant and recombinant classes. This sequence is relevant to the structure of the hybrid zone between the Torresian and Moreton taxa and explains both its asymmetry and the basis of the observed introgression of Torresian chromosomes into the Moreton taxon and the absence of the reverse movement.     

The heterochromatin of grasshoppers from the Caledia captiva species complex

C-band variation between the Caledia taxa is extensive with numerous large interstitial and telomeric blocks of heterochromatin being present in the South-east Australian and Moreton taxa while the Torresian types possess small centromeric or telomeric C-bands. In situ hybridization using ³H-cRNA from a 168 bp (base pairs) highly repeated sequence, originally isolated from the South-east Australian taxon, defined further variation between the C. captiva taxa. This sequence family is present in each of the interstitial and telomeric constitutive heterochromatic blocks in the South-east Australian and Moreton taxa. However, it is represented in only a fraction of the heterochromatic regions, defined by C-banding, within the three Torresian types. A second, unrelated 144 bp sequence family, originally isolated from the Daintree taxon, is restricted to the procentric blocks of heterochromatin of chromosomes 2–7, 9 and 10 in the Daintree taxon. This sequence is A-T rich and possesses a region of dyad symmetry. Quantitative measurements for the two sequence families revealed a wide range of copy numbers between the C. captiva taxa. The 168 bp family has approximately 150,000, 35,000 and 4,000 copies, respectively, in the South-east Australian/ Moreton, Torresian and Daintree genomes. There are 2,000,000 and 100,000 copies of the 144 bp sequence in the Daintree and Papuan Torresian taxa, respectively. The distributional, quantitative and sequence characteristics of these repeat families imply that past amplification or introgression has played a major role in the evolution of these sequences. There is an overall negative correlation between the quantity of the 168 bp sequence and the levels of reproductive isolation and genie divergence between the various taxa. It is possible that some of the reduction in the viability of the hybrid individuals is due to the quantitative changes in these sequences. Moreover, the quantitative and qualitative characteristics of highly repeated DNA families may play a role in the modulation of such essential cellular functions as cell cycle duration, nuclear organization and gene expression.     

Biased gene conversion and asymmetrical introgression between subspecies

Data from chromosomal in situ hybridization and restriction fragment length polymorphism (RFLP) of ribosomal DNA (rDNA) obtained from the same individuals of two subspecies of the Australian grasshopper Caledia captiva, suggest the occurrence of biased exchange of DNA sequences in hybrid individuals. Thus, there are a disproportionate number of Torresian individuals that possess Moreton ribosomal RNA gene sequences. This bias correlates with the previously described pattern of asymmetrical introgression of Moreton rDNA into Torresian populations. The present findings demonstrate the potential effect of biased gene conversion on the frequencies of introduced gene variants.     

THE EFFECT OF A PARTIAL BARRIER ON THE MOVEMENT OF A HYBRID ZONE

Computer simulations of clines (Brues, 1972; Endler, 1977) as well as theoretical arguments (Nagylaki, 1975), have shown that steps in gene frequencies will be pulled to partial barriers (areas of reduced gene flow) if they form within approximately a cline width of the partial barrier. The behavior of a hybrid zone between two chromosomal taxa (“Moreton” and “Torresian”) of the acridine grasshopper Caledia captiva in southeast Queensland has been analyzed and found to comform qualitatively with a model of altered gene flow patterns. Clines in four enzyme systems were analyzed for 1983 and 1986 along a transect across the hybrid zone. The clines have shifted towards an area of regenerating forest, while homozygote frequencies have increased at this point. This forest barrier has broken the continuity of the spatial distribution of C. captiva, forming population islands in part of the hybrid zone, and thus reducing the amount of gene flow. The distance between the barrier and the original cline is approximately of the order of a cline width, so that they would be expected to interact. Historical information suggests that the secondary contact between the “Moreton” and “Torresian” taxa occurred very recently (1844–1940), due to the intensive land-clearing activities during the European settlement.     

Karyotypes of two rare rodents, Hapalomys delacouri and Typhlomys cinereus (Mammalia, Rodentia), from Vietnam

Karyotypes of Hapalomys delacouri (Rodentia, Muridae) and Typhlomys cinereus (Rodentia, Platacanthomyidae) from Vietnam are described for the first time. The diploid karyotype of Hapalomys delacouri is 38 (NFa=48), consisting of six pairs of bi-armed and 12 pairs of acrocentric autosomes decreasing in size; plus a large metacentric X chromosome and Y chromosome, also metacentric, that is equal in size to the largest pair of acrocentric autosomes. The newly described karyotype differs significantly from that reported for Hapalomys delacouri from northern Thailand. The latter record very likely represents a different species of Hapalomys, possibly the taxon Hapalomys pasquieri described from north-central Laos.The diploid karyotype of Typhlomys cinereus is 38 (NF=48), consisting of five pairs of meta- to submetacentric and 14 pairs of acrocentric chromosomes varying in size from large to small; sex chromosomes were not defined.     

The polytene chromosomes of Nilodorum biroi (Kieffer) (Diptera: Chironomidae)

The polytene chromosomes of the salivary glands of Nilodorum biroi (Kieffer) comprise three long metacentric or submetacentric chromosomes. It is considered that this is a derived condition from a diploid number of 8, by the tandem fusion of a small acrocentric element (C) to a metacentric chromosome (AB). A standard chromosome map for the genus is provided and the chromosomal polymorphism of Indian and Australian populations is described.     

Vocal Diversity and Taxonomy of Nomascus in Cambodia

It is usually thought that Nomascus gabriellae is the only Nomascus sp. in Cambodia. We studied vocal diversity among different wild populations of Nomascus in Cambodia to assess their taxonomic relationships and to examine whether their vocal patterns correspond to forms previously described for Nomascus leucogenys siki and Nomascus gabriellae. We tape-recorded crested gibbon songs in southern Mondulkiri Province, in central Rattanakiri Province, and in 2 different districts of the Virachey National Park in northern Rattanakiri. We also tape-recorded typical songs of Nomascus leucogenys siki near the type locality of the taxon in the Bach Ma National Park in central Vietnam. We analyzed 40 song bouts from different gibbon groups, including 151 phrases of 33 females and 235 phrases of 39 males. Discriminant analyses revealed marked separation of the most southern songs (Mondulkiri) from those of all other localities. Vocal differences among the 3 gibbon populations in northeast Cambodia (Rattanakiri) are less pronounced; they do not differ more among each other than each of them differs from the northernmost sample from Bach Ma (Vietnam). Vocal characteristics of the study populations revealed no cline, and populations do not differ significantly in vocal variability. We conclude that Cambodian crested gibbons represent 2 distinct taxa: Those from southern Mondulkiri are Nomascus gabriellae, those from northeast Cambodia (Rattanakiri) closely correspond to the sample from Bach Ma (Vietnam) and, together with the latter, represent a different taxon. We provisionally assign them to Nomascus leucogenys siki because of the close geographic distance between Bach Ma and the type locality of the taxon. We postulate that a taxonal boundary exists between southern Mondulkiri and central Rattanakiri and discuss the possible factors that may have acted as distribution barriers.     

Comparative cytogenetics of the African elephant (Loxodonta africana) and Asiatic elephant (Elephas maximus)

G- and C-banded karyotypes of the two extant species of the mammalian order Proboscidea are presented for the first time. Chromosome complements were 2n = 56 in both Loxodonta africana and Elephas maximus. Comparisons between the species demonstrated a high level of chromosome band homology, with 26 conserved autosomal pairs. The normal diploid karyotype of L. africana had 25 acrocentric/telocentric and two metacentric/submetacentric autosomal pairs. E. maximus differed by having one less acrocentric and one additional submetacentric pair due to either a heterochromatic arm addition or deletion involving autosomal pair 27. Several acrocentric autosomes of L. africana exhibited small short arms that were absent in homologous chromosomes of E. maximus. The X chromosomes in both species were large submetacentric elements and were homologous. However, the small acrocentric Y chromosomes differed; in E. maximus it was slightly larger and had more distinct G-bands than its counterpart in L. africana. Extant Elephantidae appear to be relatively conservative in their rates of chromosomal change compared to some other mammalian families. The high-quality banded karyotypes presented here should prove useful as references in future chromosome analyses of elephant populations and in comparative cytogenetic studies with other ungulate orders.     

Karyotypic diversity in polyploid gibel carp,Carassius auratus gibelio Bloch

Polyploid gibel carp, Carassius auratus gibelio, is an excellent model system for evolutionary genetics owing to its specific genetic background and reproductive modes. Comparative karyotype studies were performed in three cultured clones, one artificially manipulated group, and one mated group between two clones. Both the clones A and P had 156 chromosomes in their karyotypes, with 36 metacentric, 54 submetacentric, 36 subtelocentric, 24 acrocentric, and six small chromosomes. The karyotype of clone D contained 162 chromosomes, with 42 metacentric, 54 submetacentric, 36 subtelocentric, 24 acrocentric, and six small chromosomes. All the three clones had six small chromosomes in common. Group G, being originated from the clone D by artificial manipulation, showed supernumerary microchromosomes or chromosomal fragments, in addition to the normal chromosome complement that was identical to the clone D. The offspring from mating between clones D and A had 159 chromosomes. Comparing with the clone A, the DA offspring showed three extra metacentric chromosomes. In addition, variable RAPD fingerprint patterns and unusual SCAR marker inheritance were, respectively, detected among individuals of artificial group G and in the mated DA offspring. Both the chromosome and molecular findings suggest that genome reshuffling might have occurred by manipulation or mating of the clones.     

The origin of a Robertsonian chromosomal translocation in house mice inferred from linked microsatellite markers

The western European house mouse, Mus domesticus, includes many distinct Robertsonian (Rb) chromosomal races. Two competing hypotheses may explain the distribution of Rb translocations found in different populations: they may have arisen independently multiple times, or they may have arisen once and been spread through long-distance dispersal. We investigated the origin of the Rb 5.15 translocation using six microsatellite loci linked to the centromeres of chromosomes 5 and 15 in 84 individuals from three Rb populations and four neighboring standard-karyotype populations. Microsatellite variation on the 5.15 metacentric chromosomes was significantly reduced relative to the amount of variation found on acrocentric chromosomes 5 and 15, suggesting that linked microsatellite loci can track specific mutational events. Phylogenetic analyses resulted in trees which are consistent with multiple origins of the 5.15 metacentric chromosomes found in the three Rb populations. These results suggest that cytologically indistinguishable mutations have arisen independently in natural populations of house mice.     

Chromosome number and ploidy-level in a Dutch population ofCrenobia alpina Dana (Planaria)

A Dutch population ofCrenobia alpina was found to have a chromosome number of 2n=42. One pair of large chromosomes is acrocentric and probably shows a secondary constriction; one small pair is acrocentric as well. All other chromosomes are metacentric or sub-metacentric; it has not been possible to discriminate with certainty between them. According to the hypothesis ofDahm (1958) populations with, 2n=42 are autohexaploid, the basic genome consisting of seven chromosomes. On basis of the karyotype it was concluded that the Dutch population described here, is not autohexaploid but functionally diploid, perhaps allohexaploid.     

The pattern of phylogenomic evolution of the Canidae

Canidae species fall into two categories with respect to their chromosome composition: those with high numbered largely acrocentric karyotypes and others with a low numbered principally metacentric karyotype. Those species with low numbered metacentric karyotypes are derived from multiple independent fusions of chromosome segments found as acrocentric chromosomes in the high numbered species. Extensive chromosome homology is apparent among acrocentric chromosome arms within Canidae species; however, little chromosome arm homology exists between Canidae species and those from other Carnivore families. Here we use Zoo-FISH (fluorescent in situ hybridization, also called chromosomal painting) probes from flow-sorted chromosomes of the Japanese raccoon dog (Nyctereutes procyonoides) to examine two phylogenetically divergent canids, the arctic fox (Alopex lagopus) and the crab-eating fox (Cerdocyon thous). The results affirm intra-canid chromosome homologies, also implicated by G-banding. In addition, painting probes from domestic cat (Felis catus), representative of the ancestral carnivore karyotype (ACK), and giant panda (Ailuropoda melanoleuca) were used to define primitive homologous segments apparent between canids and other carnivore families. Canid chromosomes seem unique among carnivores in that many canid chromosome arms are mosaics of two to four homology segments of the ACK chromosome arms. The mosaic pattern apparently preceded the divergence of modern canid species since conserved homology segments among different canid species are common, even though those segments are rearranged relative to the ancestral carnivore genome arrangement. The results indicate an ancestral episode of extensive centric fission leading to an ancestral canid genome organization that was subsequently reorganized by multiple chromosome fusion events in some but not all Canidae lineages.     

Physical mapping of the 5S ribosomal RNA genes in Arabidopsis thaliana by multi-color fluorescence in situ hybridization with cosmid clones

The 5S ribosomal RNA genes were mapped to mitotic chromosomes of Arabidopsis thaliana by fluorescence in situ hybridization (FISH). In the ecotype Landsberg erecta, hybridization signals appeared on three pairs of chromosomes, two of which were metacentric and the other acrocentric. Hybridization signals on one pair of metacentric chromosomes were much stronger than those on the acrocentric and the other pair of metacentric chromosomes, probably reflecting the number of copies of the genes on the chromosomes. Other ecotypes, Columbia and Wassilewskija, had similar chromosomal distribution of the genes, but the hybridization signals on one pair of metacentric chromosomes were very weak, and detectable only in chromosomes prepared from young flower buds. The chromosomes and arms carrying the 5S rDNA were identified by multi-color FISH with cosmid clones and a centromeric 180 bp repeat as co-probes. The metacentric chromosome 5 and its L arm carries the largest cluster of the genes, and the short arm of acrocentric chromosome 4 carries a small cluster in all three ecotypes. Chromosome 3 had another small cluster of 5S rRNA genes on its L arm. Chromosomes 1 and 2 had no 5S rDNA cluster, but they are morphologically distinguishable; chromosome 1 is metacentric and 2 acrocentric. Using the 5S rDNA as a probe, therefore, all chromosomes of A. thaliana could be identified by FISH. Chromosome 1 is large and metacentric; chromosome 2 is acrocentric carrying 18S-5.8S-25S rDNA clusters on its short arm; chromosome 3 is metacentric carrying a small cluster of 5S rDNA genes on its L arm; chromosome 4 is acrocentric carrying both 18S-5.8S-25S and 5S rDNAs on its short (L) arm; and chromosome 5 is metacentric carrying a large cluster of 5S rDNA on its L arm.     

Influence of genotype and geography on shell shape and morphometric trait variation among North Atlantic blue mussel (Mytilus spp.) populations

The influence of geography and genotype on shell shape (outline) and trait (morphometric) variation among North Atlantic blue mussels and their hybrids has been examined. Shape differences among reference taxa (Mytilus trossulus, Mytilus edulis and Mytilus galloprovincialis) were consistent with an association between taxon‐specific genes and shape genes. Newfoundland M. edulis × M. trossulus populations and northern Quebec M. trossulus populations exhibited an uncoupling of taxon‐specific genes from shape genes, whereas Nova Scotia M. trossulus populations and SW England M. edulis × M. galloprovincialis populations exhibited an association between taxon‐specific genes and shape genes. We found no evidence of a geographic effect (NE versus NW Atlantic) for shape variation, indicating that the genotype effect is stronger than any geographic effect at macrogeographic scales. Pronounced differences were observed in trait variability consistent with an association between taxon‐specific genes and trait genes in European populations, and trait divergence of New York M. edulis from all European mussels. Trait variability in mussels from Newfoundland, Nova Scotia and northern Quebec indicated an uncoupling of taxon genes from trait genes, whereas trait variability in SW England M. edulis × M. galloprovincialis populations was consistent with background genotype, indicating a strong association between taxon genes and trait genes. A pronounced macrogeographic split (NE versus NW Atlantic) regardless of taxonomy was observed, indicating that geography exerts a greater influence than genotype on trait variation at the macrogeographic scale. This is consistent with pronounced within‐taxon genetic divergence, indicative of different selection regimes or more likely of different evolutionary histories of mussels on either side of the North Atlantic. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 96 , 875–897.     

Meiotic drive favors Robertsonian metacentric chromosomes in the common shrew (Sorex araneus, Insectivora, mammalia)

Meiotic drive has attracted much interest because it concerns the robustness of Mendelian segregation and its genetic and evolutionary stability. We studied chromosomal meiotic drive in the common shrew (Sorex araneus, Insectivora, Mammalia), which exhibits one of the most remarkable chromosomal polymorphisms within mammalian species. The open question of the evolutionary success of metacentric chromosomes (Robertsonian fusions) versus acrocentrics in the common shrew prompted us to test whether a segregation distortion in favor of metacentrics is present in female and/or male meiosis. Performing crosses under controlled laboratory conditions with animals from natural populations, we found a clear trend toward a segregation distortion in favor of metacentrics during male meiosis, two chromosome combinations (gm and jl) being significantly preferred over their acrocentric homologs. Apart for one Robertsonian fusion (hi), this trend was absent in female meiosis. We propose a model based on recombination events between twin acrocentrics to explain the difference in transmission ratios of the same metacentric in different sexes and unequal drive of particular metacentrics in the same sex. Pooled data for female and male meiosis revealed a trend toward stronger segregation distortion for larger metacentrics. This is partially in agreement with the frequency of metacentrics occurring in natural populations of a chromosome race showing a high degree of chromosomal polymorphism.     

中国西南地区鹿药属4种15居群核型研究

对产于中国西南部的鹿药属（Maianthemum）4种植物进行了细胞学研究,包括染色体数目,多倍化,非整倍性和随体染色体,以及核型不对称性和核型进化。结果表明：1）除了在云南丽江采集的Maianthemum tatsienensis染色体数目为2n=72之外,其余的居群全为2n=36;2）核型在居群间存在变异,特别是在具中部染色体和近中部染色体的数目以及随体染色体的数目和位置上。此外,M．nanchuanense和M．szechuanicum的核型是首次报道,B染色体也是首次在该属中发现。我们推测鹿药属的进化方式包括频繁的染色体畸变以及不同水平上的多倍化,而中国西南部是该属的分化中心。