A CYTOGENETIC ANALYSIS OF CERTAIN POLYPLOIDS IN GRINDELIA (COMPOSITAE)

Two diploid taxa, Grindelia procera and G. camporum, and 3 tetraploid ones, G. camporum, G. hirsutula, and G. stricta, have been studied to ascertain their interrelationships. Meiosis in diploid parental strains was regular, the common chromosome configuration being 5 rod bivalents and 1 ring bivalent. The average chiasmata frequency per chromosome was 0.60. Pollen fertility was about 90% in all strains examined. Diploid interspecific hybrids had normal meiosis with an average chiasmata frequency of 0.56 per chromosome. No heterozygosity for inversions or interchanges was detected, and pollen fertility was above 85%. Meiosis in parental tetraploid strains was characterized by the presence of quadrivalents in addition to a complementary number of bivalents. The average chiasmata frequency per chromosome was 0.59 and pollen fertility was generally about 80%. Tetraploid interspecific hybrids also had quadrivalents, normal meiosis, and high pollen fertility. Close genetic relationships between the diploids and between the tetraploids are indicated, and geographical, ecological, and seasonal barriers to gene exchange exist. Attempts to obtain hybrids between diploids and tetraploids were successful in a few cases. The hybrids were tetraploid and had normal meiosis and fertility similar to parental and F₁ tetraploids. Their origin was by the union of unreduced gametes of the diploid female parent and normal pollen from the tetraploid parent. On the basis of chromosome homology, normal meiosis, plus high fertility exhibited in the diploid, tetraploid, and diploid X tetraploid interspecific hybrids, these species of Grindelia are considered to be a part of an autopolyploid complex. Gene exchange between diploids and diploids, tetraploids and tetraploids, and diploids and tetraploids is possible. Tetraploid G. camporum may have originated by hybridization between G. procera and diploid G. camporum with subsequent doubling of chromosomes and selection for the combined characteristics of the diploids.     

AUTOPOLYPLOIDY IN HEUCHERA MICRANTHA (SAXIFRAGACEAE)

Heuchera micrantha (Saxifragaceae) is a morphologically variable species comprising five varieties: diversifolia, erubescens, hartwegii, micrantha, and pacifica. Both diploids (2n = 14) and tetraploids (2n = 28) occur within the species. The tetraploid cytotype occupies the central portion of the geographic range of the species, whereas diploids occur primarily in the southern and northern portions of the range. Both diploids and tetraploids have been detected within vars. diversifolia, pacifica, and hartwegii. All counts for vars. erubescens and micrantha are diploid and tetraploid, respectively. Several lines of evidence suggest that tetraploid H. micrantha is of autopolyploid origin. The species is distinct morphologically and is also well separated geographically from other closely related species in subsection Micranthae. The two cytotypes are karyologically identical, possess nearly the same suite of allozymes, and have a very high genetic identity (Ī = 0.971). Significantly, an earlier study documented tetrasomic inheritance in the tetraploid cytotype. Following theoretical expectations, the mean number of alleles per locus, proportion of loci that are polymorphic, and observed heterozygosity are significantly higher for the autotetraploid than for the diploid. The occurrence of both cytotypes in three of the varieties suggests that autopolyploidy may have occurred several times independently in H. micrantha. This was further substantiated by discriminant analysis using morphological characters, which provided evidence for a minimum of two separate origins for the autopolyploid cytotype.     

CHROMOSOME RACES IN CLAYTONIA LANCEOLATA (PORTULACACEAE)

Chromosome numbers of n = 8, 12, and 16 were determined for 11 populations of Claytonia lanceolata occurring in the southwestern Rocky Mountains of Utah. No evidence of the wide infra-populational variation of chromosome numbers known in the related eastern species, C. virginica, was observed. The chromosome numbers in C. lanceolata probably evolved from a base number of x = 8. Diploids(n = 8) apparently produced tetraploids (n = 16) of putative autoploid origin. Pairing relationships, including the presence of univalents, bivalents, and trivalents, suggest the chromosome numbers of n = 12 are triploids derived from natural hybridization between diploids and tetraploids. Higher chromosome numbers previously reported in C. lanceolata from Colorado, and presumably based on x = 12, can be explained by subsequent polyploid increases in the triploids. The diploid and tetraploid populations analyzed in this study occupy different ecological habitats. The diploids occur at lower elevations along the foothills, whereas the tetraploids are restricted to higher montane and sub-alpine elevations. The triploids were discovered at intermediate elevations.     

Karyotaxonomical analysis in the genusAngelica (Umbelliferae)

Morphometric karyotype characters were studied in 25Angelica spp. (Umbelliferae, Apioideae) and in one species of the related genusTommasinia. For three species the chromosome numbers are new. In our study the majority of the species investigated are diploids with 2n = 22, some are tetraploids with 2n = 44 (for these tetraploids also diploid cytotypes are reported in the literature). Among the diploid species,A. miqueliana has a distinct karyotype consisting of submetacentric and acrocentric chromosomes only, the remaining diploids with 2n = 22 as well as tetraploids with 2n = 44 have rather symmetrical karyotypes, consisting of metacentric and submetacentric chromosomes. The very different chromosome number 2n = 28 has been found inA. gmelinii. Its karyotype includes two distinct groups of chromosomes: 8 pairs of rather large metacentrics and submetacentrics and 6 pairs of very short and asymmetrical chromosomes. Chromosome numbers and structures appear to be useful in the taxonomy of some intrageneric taxa inAngelica.     

Genetic variation in sympatric populations of diploid and polyploid brine shrimp (Artemia parthenogenetica)

We examined genetic variation in sympatric diploid and polyploid brine shrimp Artemia parthenogenetica from each of three populations (China, Italy and Spain). Italian and Spanish tetraploids are closely related (I=0.964). Diploids and tetraploids within each of the two European populations are also closely related (mean I=0.905). Most alleles found in diploids also exist in sympatric polyploids. In contrast, the asexual Artemia (2N, 4N and 5N) in our study share few alleles with their close sexual relative, A. tunisiana (mean I=0.002). These results, as well as the work of other authors, strongly suggest that at least the tetraploid Artemia in our study have an autopolyploid origin.Clonal diversity of polyploid Artemia can be very high at least in some population. Both diploids and polyploids had low clonal diversities in the populations dominated by polyploids and high clonal diversities in the population dominated by diploids.The most common genotypes of sympatric diploid and polyploid Artemia frequently differed. Some alleles occurred only in diploids, while others were restricted to polyploids. These results suggest that polyploidy in Artemia has led to genetic divergence from diploid progenitors, and that ploidy-level variation must also be considered in developing an understanding of spatial and temporal allozyme polymorphism in asexual populations.     

TRITICUM URARTU AND GENOME EVOLUTION IN THE TETRAPLOID WHEATS

The A genome of the tetraploid wheats (AABB, 2n = 28) shows 5-6 bivalents in crosses with Triticum boeoticum (2n = 14) and various Aegilops diploids (2n = 14). The B genome has never been similarly identified with any species, and is commonly thought to have been modified at the tetraploid level. Triticum boeoticum was presumably accepted as the A-genome donor because of its morphological similarity to the wild tetraploids and because it was formerly the only known wild diploid wheat. The B donor has been thought to be Ae. speltoides or another species of the Sitopsis section of Aegilops, but these diploids show pairing affinity with A rather than B. More recently, another diploid wheat, T. urartu, was found to be sympatric with T. boeoticum throughout the natural range of the tetraploids. The synthetic boeoticum-urartu amphiploid was virtually identical morphologically with the wild tetraploid wheats, whereas various boeoticum-Sitopsis amphiploids were markedly different. But the urartu genome, like those of T. boeoticum and Sitopsis, paired with A and not with B. However, cytological evidence also shows (1) that the genomes of any plausible parental combination pair with one another, (2) that the A and B genomes of the tetraploid wheats pair with one another in the absence of the gene Ph, and (3) that homoeologous chromosomes of the tetraploids have differentiated further, presumably as a result of diploidization. Consequently, chromosome pairing at Meiosis I can be expected to give ambiguous evidence regarding the identity of the tetraploid genomes with their parental prototypes. A hypothesis regarding the expected pairing affinities between tetraploid homoeologues that have differentiated from closely related parental chromosomes is advanced to explain the anomalous pairing behavior of the A and B genomes. Triticum boeoticum and T. urartu are inferred to be the parents of the tetraploid wheats.     

Isozymes of Eleusine (Gramineae) and the origin of finger millet

The predominantly African grass genus Eleusine comprises nine species, including diploids and tetraploids based on n = 8, 9, and 10. Among the polyploids are the important crop finger millet, Eleusine coracana subsp. coracana, and its putative wild ancestor, E. coracana subsp. africana. Eleusine coracana is believed to be an allotetraploid derived by hybridization between E. indica and an unknown diploid. To evaluate this hypothesis, 16 isozyme loci coding nine enzymes were compared among seven of the nine Eleusine species (E. intermedia and E. semisterilis were unavailable). Genetic variability differed substantially among diploid species, ranging from P = 0.563, A = 1.6, H = 0.208 in E. indica to P = 0.188, A = 1.2, H = 0.042 in E. jaegeri. The diploids tended to be genetically distinct, with values of Rogers' Similarity ranging from S = 0.294 (E. jaegeri/floccifolia) to S = 0.794 (E. indica/tristachya). Both subspecies of the tetraploid E. coracana exhibited fixed heterozygosity at several loci, verifying their hypothesized allotetraploid status. Both tetraploids also possessed E. indica marker alleles at all loci, corroborating ancestry by this taxon. Genotypes of the non-indica ancestor, inferred separately for each tetraploid, differed substantially from all candidate diploids and also from each other. These data indicate that 1) none of the candidate diploids investigated is likely to have been the non-indica ancestor of E. coracana, and 2) the non-indica ancestor of the wild tetraploid may differ from that of the crop. The latter conclusion is inconsistent with the complete chromosomal homology exhibited between the two tetraploid subspecies, indicating the need for additional evidence bearing on their relationships.     

Habitat differentiation, hybridization and gene flow patterns in mixed populations of diploid and autotetraploid Dactylorhiza maculata s.l. (Orchidaceae)

Detailed ecological, morphological and molecular analyses were performed in mixed populations of diploid and autotetraploid Dactylorhiza maculata s.l. in Scandinavia. Comparisons were made with pure populations of either diploid ssp. fuchsii or tetraploid ssp. maculata. It was shown that mixed populations are the result of secondary contact between ssp. fuchsii and ssp. maculata. No patterns of recent and local autopolyploidization were found. Morphology and nuclear DNA markers (internal transcribed spacers of nuclear ribosomal DNA) showed that diploids and tetraploids from mixed populations have similar levels of differentiation to diploids and tetraploids from pure populations. Vegetation analyses, as well as analyses of environmental variables, revealed that diploid and tetraploid individuals in mixed populations are ecologically well differentiated on a microhabitat level. Diploids and tetraploids in pure populations have wider ecological amplitudes than they do in mixed populations. Triploid hybrids grew in intermediate microhabitats between diploids and tetraploids in the mixed populations. Plastid DNA markers indicated that both diploids and tetraploids may act as the maternal parent. Based on morphology and nuclear markers triploids are more similar to tetraploids than to diploids. There were indications of introgressive gene flow between ploidy levels. Plastid markers indicated that gene flow from diploid to tetraploid level is most common, but nuclear markers suggested that gene flow in opposite direction also may occur. Similar patterns of differentiation and gene flow appeared in localities that represented contrasting biogeographic regions. Disturbance and topography may explain why hybridization was slightly more common and the differentiation patterns somewhat less clear in the Scandinavian mountains than in the coastal lowland. An erratum to this article can be found at     

Morphological and cytological studies of colchicine-induced tetraploids inTorenia fournieri lind

The present paper concerns a morphological and cytological comparison between the naturally occurring diploid and the colchicine induced tetraploid ofTorenia fournieri Lind.Treatment of growing points of young seedlings with 0.20% aqueous colchicine for 10 hours on two successive days was most effective in inducing tetraploidy. The induced tetraploids showed the usual gigas characters associated with autotetraploidy. There was a significant reduction in pollen fertility and seed setting of tetraploids as compared to their diploid progenitors.The chromosome numbers of the diploids and the induced tetraploids were determined as n=9 and n=18, respectively. The diploids showed normal meiosis whereas tetraploids were characterized by a high frequency of unequal distribution of chromosomes at anaphase. The induced tetraploids possessed larger flowers. The variability in flower size of the tetraploids offers a good scope for evolving a better horticultural variety of this species.     

The effect of B chromosomes on homoeologous pairing in species hybrids

The effect of B chromosomes on chromosome pairing at meiosis was investigated in the species hybrid Lolium temulentum x L. perenne at both the diploid and tetraploid level. The presence of B chromosomes drastically reduced association of homoeologous chromosomes in both the diploids and tetraploids. This was evident from the high frequency of univalents recorded in PMC's of diploid hybrids with B's and from the predominantly bivalent association of homologous chromosomes in tetraploids of this type. In the absence of B's homoeologous pairing was extensive giving a high frequency of bivalents in the diploids and multivalents as well as bivalents and univalents in the tetraploids.     

Relationships among genetic distance,forage yield and heterozygosity in isogenic diploid and tetraploid alfalfa populations

Isogenic diploid and tetraploid alfalfa (Medicago sativa L.) was studied with molecular markers to help understand why diploid performance and breeding behavior does not always predict that of tetraploids. In a previous study of partially heterozygous alfalfa genotypes, we detected a low correlation between yields of isogenic diploid (2x) and tetraploid (4x) single-cross progenies, and genetic distances were more highly correlated with yields of tetraploids than diploids. These differences may be related to the level of RFLP heterozygosity expected among progenies derived from heterozygous parents at the two ploidy levels. The objectives of this study were to determine the relationships among genetic distance, forage yield and heterozygosity in isogenic 2 x and 4 x alfalfa populations. Four diploid genotypes were chromosome doubled to produce corresponding isogenic autotetraploids, and these genotypes were mated in 4 × 4 diallels to produce 6 single-cross families at each ploidy level for field evaluation. Allele compositions of parents were determined at 33 RFLP loci by monitoring segregation of homologous restriction fragments among individuals within progenies, and these were used to estimate RFLP heterozygosity levels for all single-cross progenies at both ploidy levels. RFLP heterozygosity rankings were identical between progenies of isogenic diploid and tetraploid parents; but significant associations (P < 0.05) between estimated heterozygosity levels and forage yield were detected only at the tetraploid level. Since tetraploid families were nearly 25% more heterozygous than the corresponding diploid families, inconsistencies in the association between molecular marker diversity and forage yields of isogenic 2 x and 4 x single crosses may be due to recessive alleles that are expressed in diploids but masked in tetraploids. The gene action involved in heterosis may be the same at both ploidy levels; however, tetraploids benefit from greater complementary gene interactions than are possible for equivalent diploids. Present address: AgResearch Grasslands, New Zealand Pastoral Agriculture Research Institute, Palmerston North, New Zealand     

Genome size and polyploidy variation in the tropical hardwood genusTerminalia (Combretaceae)

Chromosome complements and 2C DNA amounts of six species ofTerminalia have been studied.Terminalia oliveri, T. myriocarpa andT. arjuna are diploid (2n = 24),T. chebula andT. bellirica are tetraploid (2n = 48),T. muelleri shows a triploid number (2n = 36). Two well demarcated groups of species are recognizable on the basis of chromosome length and 2C DNA values which range from 3.60 pg (T. oliveri) to 12.80 pg (T. bellirica) showing a 3.5-fold difference. Differences of DNA per basic genome or per chromosome are greatest (1.97-fold) betweenT. oliveri andT. arjuna. Two species groups (1)T. oliveri andT. chebula, and (2)T. myriocarpa, T. arjuna, T. muelleri, T. bellirica, therefore are well differentiated by DNA per basic genome, irrespective of polyploidy. The mean values of the two groups are 1.81 pg and 3.34 pg, respectively, showing a 1.84-fold difference. Within diploids and tetraploids there is 1.97-fold and 1.76-fold variation, respectively.     

Giemsa C-banding in Gibasis (Commelinaceae)

Extensive C-band polymorphism has been found within and between diploid (2n=10) and tetraploid (2n=20) populations of Gibasis karwinskyana and Gibasis consobrina from Mexico. In G. karwinskyana, where the polymorphism is most pronounced, diploids and tetraploids share a similar banding pattern when collected from the same area. The banding pattern of G. consobrina shows less variation, and is most like that of G. karwinskyana collected closest to it. These findings have led to reconsideration of the relationships within and between populations of these two species.     

THE EFFECT OF INBREEDING IN DIPLOID AND TETRAPLOID POPULATIONS OF EPILOBIUM ANGUSTIFOLIUM (ONAGRACEAE): IMPLICATIONS FOR THE GENETIC BASIS OF INBREEDING DEPRESSION

The partial dominance model for the evolution of inbreeding depression predicts that tetraploids should exhibit less inbreeding depression than their diploid progenitors. We tested this prediction by comparing the magnitude of inbreeding depression in tetraploid and diploid populations of the herbaceous perennial Epilobium angustifolium (Onagraceae). Inbreeding depression was estimated in the greenhouse for three tetraploid and two diploid populations at four life stages. The mating system of a tetraploid population was estimated and compared to a previous estimate for diploids. Tetraploids showed less inbreeding depression than diploids at all life history stages, and these differences were significant for seed-set and cumulative fitness, but not for germination, survival, or plant dry mass at nine weeks. This result suggests that the genetic basis of inbreeding depression may differ among life stages. The primary selfing rate of the tetraploid population was r = 0.43, which is nearly identical to that of a diploid population (r = 0.45), indicating that differences in inbreeding depression between diploids and tetraploids are probably not due to differences in the mating system. Cumulative inbreeding depression, calculated from the four life history stages, was significantly higher for diploids () than for tetraploids (), supporting the partial dominance model of inbreeding depression.     

Isozyme diversity in sour,sweet, and ground cherry

Thirty-six sour (Prunus cerasus L.), sweet (P. avium L.), and ground cherry (P. fruticosa Pall.) selections were evaluated for seven enzyme systems and principal coordinate analysis was used to examine isozyme divergence among these cherry species. The enzyme systems studied were phosphoglucose isomerase (PGI), isocitrate dehydrogenase (IDH), phosphoglucomutase (PGM), 6-phosphogluconate dehydrogenase (6-PGD), leucine aminopeptidase (LAP), shikimate dehydrogenase (SKDH), and malate dehydrogenase (MDH). The first principal coordinate, which accounted for 41% of the total variation, separated the diploid sweet cherry selections from the sour, ground, and sour x ground cherry tetraploids. An additional 86 selections were evaluated for up to six of the enzyme systems to determine the polymorphisms at the enzyme loci and the level of heterozygosity between the diploid sweet cherry and the tetraploid species and interspecific hybrids. 6-PGD was the most polymorphic enzyme exhibiting 16 patterns. The tetraploid cherry species were more heterozygous than the diploid sweet cherry with an average heterozygosity of 78% compared to 19% for the diploids.     

Integrated taxonomy of the <Emphasis Type="Italic">Asplenium normale</Emphasis> complex (Aspleniaceae) in China and adjacent areas

The Asplenium normale D. Don complex comprises several taxa that are either diploid or tetraploid. The tetraploids are assumed to have originated from diploid ancestors by relatively recent autopolyploidization or allopolyploidization. Some of the diploids are readily recognized morphologically but most of the taxa have until now been placed into a single species. However, phylogenetic studies have challenged this treatment and emphasized the notion that the taxonomic treatment of this complex needs to be revised. An integrative taxonomic approach was employed to delimit species in the complex using cytological, morphological, and DNA sequence data. Initially, we employed a diploid first approach to establish a robust taxonomic framework. Special efforts were made to collect and identify the diploid progenitors of each polyploid lineage identified in the plastid DNA based phylogenetic hypothesis. A total of six distinct diploid species were identified. The distinctive nature of the six diploids is strongly supported by sequence differences in plastid DNA and nuclear loci, as well as by the results of morphometric analysis. Diagnostic morphological characters were identified to distinguish the six diploid species, resulting in their revised taxonomy, which includes two novel species, namely, Asplenium normaloides and A. guangdongense. Further studies to strengthen the taxonomic classification of all of the tetraploid taxa are warranted.     

Reproductive biology of the fernPhegopteris decursive-pinnata

Four diploid plants and four tetraploid plants ofPhegopteris decursive-pinnata were investigated for determination of the reproductive characteristics of their gametophytes and two major features were recognized. First, gametophytes of the diploids showed an ontogenetic sequence of gametangium formation which is unfavorable for intragametophytic selfing, whereas those of the tetraploids showed that favorable for intragametophytic selfing. Second, 41 to 72% of the isolated gametophytes of the diploids produced sporophytes in the intragmetophytic selfing tests, whereas all of the isolated gametrophytes of the tetraploids produced sporophytes in the tests. Based on these developmental and genetic features of gametophytes, the dissimilar mating systems of the diploids and the tetraploids of this species are discussed.     

Photosynthetic characteristics in <Emphasis Type="Italic">Oryza</Emphasis> species

Photosynthetic rate (P _N), SPAD value, specific leaf area (SLA), flag leaf area (FLA), and nitrogen content (LN) of genus Oryza were investigated and their correlation was analyzed to assess some of the main photosynthetic traits among different species in the genus Oryza. The results revealed wide variation in these traits. The species O. rufipogon and O. australiensis exhibited maximum photosynthetic rate. Comparison of different types of genomes (diploid: 2n=2x=24; tetraploid: 2n=4x=48) and growth habit (shade- or sun-grown) showed the species of diploid (with genome symbol EE; 2n=2x=24) genomes, with perennial and sun-grown species, had high apparent photosynthesis compared to others. The species with BB/BBCC, shade-grown and the tetraploids showed high SPAD value, and the flag leaf in sun-grown species and diploids were thicker (low SLA) compared with others. However, no significant difference could be noticed among the different types of genomes. Higher leaf area was noticed among the species of CC/CCDD genome, perennial shade-grown species and tetraploids than in others. The variety IR 36 exhibited highest leaf nitrogen concentration. Correlation analysis showed a strong relationship between P _N and leaf nitrogen concentration while no marked relationships were observed among other characteristics. It implies that the species with thick and small leaves with high nitrogen concentration and high photosynthesis evolved better than others. O. rufipogon, with the same genome as O. sativa, could be one of the wild rice resources for elite crop improvement.     

Influence of ploidy level on morphology,growth and drought susceptibility in <Emphasis Type="Italic">Spathiphyllum wallisii</Emphasis>

In this study, we analysed morphological, anatomical and physiological effects of polyploidisation in Spathiphyllum wallisii in order to evaluate possible interesting advantages of polyploids for ornamental breeding. Stomatal density was negatively correlated with increased ploidy level. Stomatal size increased in polyploids. Tetraploid Spathiphyllum plants had more ovate and thicker leaves. The inflorescence of tetraploids had a more ovate and thicker spathum, a more cylindrical spadix and a thicker but shorter flower stalk. Biomass production of the tetraploids was reduced, as expressed by lower total dry weights, and tetraploids produced fewer shoots and leaves compared with their diploid progenitors. Furthermore, tetraploid Spathiphyllum plants were more resistant to drought stress compared with diploid plants. After 15 days of drought stress, diploids showed symptoms of wilting, while the tetraploids showed almost no symptoms. Further, measurements of stomatal resistance, leaf water potential, relative water content and proline content indicated that the tetraploid genotypes were more resistant to drought stress compared with the diploids.