Morphological and chromosomal variation of the Dryopteris varia (L.) Kuntze complex (Dryopteridaceae) in Korea

The Dryopteris varia complex is highly variable in morphology, resulting in taxonomic confusion in delimiting taxon boundaries and determining relationships. We have examined the variation in morphology, chromosome number and mode of reproduction of the Korean members of the D. varia complex to clarify their taxonomic identities. Landmark analysis of the leaf blades and pinnae and the principal components analysis of 31 morphological characters revealed seven entities within the D. varia complex in Korea; these comprise D. varia s. str., D. pacifica, D. sacrosancta, D. bissetiana, D. saxifraga, D. saxifragivaria, and the Suak population which is considered to be a new taxon. Mitotic chromosome counts and examination of reproduction modes indicated that D. bissetiana in Korea appears to be agamosporous with diploid (2n = 82) or triploid (2n = 123) chromosome numbers. However, D. saxifraga is sexual diploid or agamosporous triploid, and the other taxa are agamosporous triploid. Dryopteris bissetiana, D. saxifraga and D. saxifragivaria are similar in major morphological characteristics, but show differences in attachment and shape of rachis scales. The results also suggest that agamosporous triploid D. saxifragivaria was probably derived from hybridization between sexual diploid D. saxifraga and D. bissetiana.     

Cytotaxonomic study of genusHymenasplenium (Aspleniaceae) in Xishuangbanna, Southwestern China

The gametic chromosome numbers of sevenHymenasplenium (Aspleniaceae) species from Xishuangbanna, Yunnan Prov., China, were investigated. All the examined individuals ofH. obscurum, H. cheilosorum andH. latipinnum were sexual diploids with n=39 chromosomes. Intraspecific cytological variation was found inH. excisum, which has a sexual diploid (n=39) and a tetraploid (n=78). Only a triploid apogamous cytotype (n=ca.117) was found inH. laterepens. Hymenasplenium apogamum showed the most complicated intraspecific variation and included a sexual diploid (n=39), a sexual tetraploid (n=78) and an apogamous triploid (n=ca.117). This work reports for the first time the sexual diploids ofH. cheilosorum andH. apogamum, which are only apogamous elsewhere in east Asia, Himalayas and Indochina. These results may indicate that this area is one of the diversity centers ofHymenasplenium. Most of the above species have chromosome numbers based on x=39. In contrast,H. costarisorum contains a sexual diploid (n=36) and a sexual tetraploid (n=72), indicating that its basic number is x=36.     

Cytological and Reproductive Studies of Japanese Diplazium (Woodsiaceae; Pteridophyta). II. Polyploidy and Hybridity in the Species Group with Summer-Green Bi- to Tripinnate Leaves

Diplazium with summer-green bi- to tripinnate leaves. Diplazium mesosorum and D. sibiricum var. sibiricum are sexual diploids (2n=82; n=41ll); D. chinense and D. squamigerum are sexual tetraploids (2n=164; n=82ll); and D. sibiricum var. glabrum is a sterile triploid (2n=123; meiosis irregular). Diplazium nipponicum includes both sterile triploid and sexual tetraploid populations. The triploid is larger in relation to several morphological characteristics and occurs in more southern regions than the tetraploid. Allozyme analysis suggests that the triploid is a hybrid of recurrent origin between the tetraploid and an unknown diploid. Diplazium × bittyuense is a sterile tetraploid, and the mitotic chromosome number, meiotic chromosome behavior, and allozyme analysis confirm the working hypothesis that it is a hybrid between D. nipponicum and D. chinense. Apomicts are not found within Diplazium with summer-green bi- to tripinnate leaves, and the taxonomic complexity can be attributed to polyploidy and natural hybridization. Received 3 March 2000/ Accepted in revised form 19 April 2000     

Adventitious buds ofdryopteris sparsa complex (dryopteridaceae): Developmental anatomy and systematic implication

Adventitious buds of theDryopteris sparsa complex were examined anatomically and taxonomically. While no buds are found inD. hayatae andD. sparsa, they occur inD. sabaei, D. yakusilvicola, and in putative hybrids of which one parent seems to beD. sabaei. The buds function as a means of vegetative reproduction in the species and hybrids. The buds arise as a pair on stipes of abortive leaves without lamina. InD. sabaei the youngest bud primordium observed consists of a small group of surface and subsurface meristematic cells surrounded by differentiated tissue cells, and the meristematic cells appear to be quiescent. As the bud primordia develop, the inner and then outer parenchymatous cells below the meristematic cells divide each into several small cells, among which the procambial strands are later differentiated to connect the bud primordium to the vascular strand of the leaf. The meristematic cells also undergo cell divisions, and the bud primordium becomes larger. A shoot organization of the bud primordium is later established. The bud-bearing, uniquely abortive leaves and delayed development of the buds support the taxonomic relationship of agamosporousD. yakusilvicola having been derived from hybridization betweenD. sabaei andD. sparsa.     

Relationships and origins of the Dryopteris varia (L.) Kuntze species complex (Dryopteridaceae) in Korea inferred from nuclear and chloroplast DNA sequences

The Dryopteris varia species complex belongs to D. subg. Erythrovariae sect. Variae and includes eight closely related, controversial species. In Korea, six species belong to the complex; D. varia s. str., Dryopteris pacifica, Dryopteris sacrosancta, Dryopteris bissetiana, Dryopteris saxifraga, and Dryopteris saxifragivaria. The morphology of these species is highly variable due to the frequent occurrence of agamospory, hybridization, and/or polyploidization. We analyzed sequences of the nDNA pgiC and cpDNA rbcL, trnL–trnF IGS and atpF–atpH IGS regions from all six of these species to elucidate their relationships and origins, and to investigate the parentage of the putative hybrid taxon, D. saxifragivaria. Fourteen nDNA pgiC haplotypes and five cpDNA haplotypes were obtained from accessions of the D. varia complex in Korea. In particular, all accessions examined appear to have multiple pgiC haplotypes. Maximum parsimony and Bayesian inference analyses of the nDNA and cpDNA sequence data show that the agamosporous triploids D. sacrosancta and D. pacifica are of allopolyploid origin involving interspecific hybridization. The results also indicate that agamosporous triploid individuals of D. saxifragivaria in Korea were derived from hybridization between sexual diploid individuals of D. saxifraga (maternal) and agamosporous diploid individuals of D. bissetiana (paternal). In addition, our results strongly suggest that the agamosporous triploid D. varia s. str. is probably of autopolyploid origin, and cytoplasmic gene flow has occurred from D. sacrosancta to Dryopteris chinensis of D. subg. Dryopteris.     

Genotypic variation in progeny of the agamic grass complexPennisetum sectionBrevivalvula in West Africa

The genotypic variation of 1180 progeny from 118 genitors belonging to five taxa ofPennisetum sect.Brevivalvula has been estimated by isoenzyme electrophoresis with observations on five enzymatic systems, in order to compare the type of reproduction in polyploid and diploid taxa. A total of 112 different isozyme genotypes has been found, over all taxa. Genotypic variation was found among all progeny of the diploid populations ofP. polystachion andP. subangustum, as a consequence of their sexual reproduction system. At the polyploid level the type of reproduction appears to be predominantly agamic, but genotypic variation in the progeny was not rare: five tetraploid and one hexaploidP. pedicellatum, one pentaploid and one hexaploidP. polystachion and one hexaploidP. hordeoides, in a total of 90 genitors. Genetic relationships have been observed between the diploid sexualP. polystachion andP. subangustum, and, to a lesser extent, with the tetraploids of the same taxa as well. TetraploidP. polystachion andP. pedicellatum share genotypes with most other chromosomal taxa.     

Clonal diversity in the agamospermous polyploids ofTaraxacum hondoense in northern Honshu,Japan

Chromosome numbers and allozyme variations were surveyed in 74 polyploid populations ofTaraxacum hondoense, in northern Honshu, Japan. Most of the populations (94.4%) consisted of triploid (2n=24), indicating the predominance of this ploidy level. Approximately 42.6% were found to contain tetraploid (2n=32), and a few plants were pentaploid (2n=40). Electrophoretic analysis at6 Pgdh-1 revealed twelve phenotypes with four alleles (including one putative null allele). The triploids showed excessive heterozygosity (82.4%) and all of the tetraploids and pentaploids were heterozygote. Phenotype IV was the most frequent and widely distributed in northern Honshu. Forty five percent of the populations were found to contain multiple phenotypes at 6Pgdh-1. A total of 21 clones were distinguished using three polymorphic loci (6Pgdh-1, Got andMdh), and a considerable amount of clonal diversity was detected both within and among polyploid populations ofT. hondoense. Factors causing multiclonality in agamospermous polyploids are discussed.     

A review of chromosomal variation in Dugesia japonica and D. ryukyuensis in the Far East

The chromosome numbers of Dugesia japonica Ichikawa et Kawakatsu, 1964, are n = 8, 2x = 16 and 3x = 24; those of Dugesia ryukyuensis Kawakatsu, 1976, are n = 7, 2x = 14 and 3x = 21. The karyotypes of both species include diploid, triploid and mixoploid; aneuploidic and mixoaneuploidic karyotypes may occur. In 785 specimens studied of D. japonica, the occurrence rates of specimens having each karyotype are substantially the same (29–37%). Diploid sexual specimens represented nearly 10% of the total and virtually no triploid or mixoploid sexual specimens were found. The diploid karyotype can be inherited by both sexual and asexual reproduction; the triploid and mixoploid karyotypes will be inherited only by asexual reproduction. In 51 specimens studied of D. ryukyuensis, the different karyotypes are diploid (ca 39%), triploid (ca 57%) and mixoploid (ca 4%). Diploid sexual specimens represented nearly 25% of the total; sexual specimens with tripooidic karyotypes made up nearly 27%. The diploid, triploid and mixoploid karyotypes were also found in juveniles hatched from cocoons. The diploid karytyype is inherited by both sexual and asexual reproductions; the other karyotypes may be inherited by parthenogenesis or self-fertilization (including pseudogamy) and asexual reproduction.     

Electrophoretic identification of polyploidCamellia japonica (Theaceae) cultivars and evidence for their sexual origin

Electrophoretic examination of allozymes from 189Camellia japonica cultivars revealed some banding patterns not explainable by codominant diploid genetics. At several loci encoding dimeric enzymes, 5 and 6 banded patterns were observed in 7 cultivars. These patterns are interpreted as resulting from triploidy or aneuploidy, where three variant alleles code for products which are electrophoretically distinguishable and associate to form three homodimers and three heterodimers. The presence of allozyme multiplicity in these clones suggests a sexual rather than a somatic mode of triploid origin.     

Variability of microsatellites BM224 and Bcal7 in populations of green toads (Bufo viridis complex) differing by nuclear DNA content and ploidy

The variability of microsatellites BM224 and Bcal7 was studied for the first time in three species of the diploid-polyploid complex of Bufo viridis (B. viridis, B. oblongus, and B. pewzowi). The locus Bcal7 was established to be monomorphic in all samples studied. In microsatellite BM224, three allele variants were found. Among tetraploid toads, the western Asiatic species B. oblongus was characterized by one allele only, the eastern B. pewzowi, by the two other alleles. A similar distribution was also revealed in triploid individuals on the borders of range between tetraploid and diploid species. Among the diploid species B. viridis samples, all three allele variants of microsatellite BM224 were observed. Their distribution in the area proved to be geographically determined. In diploid toads, a similarity was revealed between the distribution of microsatellite BM224 alleles and variability of the nuclear DNA content.     

Polyploidy and aneuploidy inOphrys,Orchis, andAnacamptis (Orchidaceae)

Studies on chromosome numbers and karyotypes in Orchid taxa from Apulia (Italy) revealed triploid complements inOphrys tenthredinifera andOrchis italica. InO. tenthredinifera there is no significant difference between the diploid and the triploid karyotypes. The tetraploid cytotype ofAnacamptis pyramidalis forms 36 bivalents during metaphase I in embryo sac mother cells. Aneuploidy was noticed inOphrys bertolonii ×O. tarentina with chromosome numbers n = 19 and 2n = 38. There were diploid (2n = 2x = 36), tetraploid (2n = 4x = 72), hexaploid (2n = 6x = 108) and octoploid (2n = 8x = 144) cells in the ovary wall of the diploid hybridOphrys apulica ×O. bombyliflora. Evolutionary trends inOphrys andOrchis chromosomes are discussed.     

Chromosomal C-band variation inAllium schœnoprasum (Liliaceae) in eastern North America

Variation in C-banding was studied in seven populations ofAllium schnoprasum from eastern N. America, including populations referable to var.sibiricum, var.laurentianum, and ± intermediate. 23 bands were recognized on five pairs of chromosomes, and were treated as 23 loci. No banding site was monomorphic throughout the plants studied. The level of polymorphism per population was >60%, and the average heterozygosity values varied from 0.21 to 0.27. The various banding patterns of chromosomes were shown to depend on the random combination of individual bands. Nei's genetic distances between populations varied from 0 to 0.070 (mean: 0.033). The matrix of genetic distances was analysed by non-metric multidimensional scaling, and the results showed a significant relationship between longitude and population scores on the ordination. The chromosomal data did not clearly discriminate between the two native varieties ofA. schnoprasum, but were interpreted as a longitudinal cline. It is suggested that studies of C-banding variation in vascular plants should focus on individual banding sites, rather than on whole chromosome banding patterns.     

Chromosome banding in the genusPinus

Somatic chromosomes (2n=24) ofPinus luchuensis Mayr at metaphase were observed by fluorescent banding methods with chromomycin A₃ (CMA) and DAPI. CMA-bands appeared at the interstitial and/or proximal regions of nearly all chromosomes. DAPI-bands appeared at the interstitial and/or centromeric regions of nearly all chromosomes, and pairs of DAPI-dots appeared at the centromeric regions. Each homologous pair of chromosomes in the chromosome complement was identified by the CMA and DAPI fluorescent banding patterns. The interstitial CMA-bands were mostly localized at the secondary constrictions of the Feulgen-stained chromosomes. The fluorescent banding pattern ofP. luchuensis was very similar to that ofP. thunbergii, but was different from that ofP. densiflora.     

Cytological and Reproductive Studies on Japanese Diplazium (Woodsiaceae; Pteridophyta): Apomictic Reproduction in Diplazium with Evergreen Bi- to Tripinnate Leaves

Diplazium , including polymorphic terrestrial species with evergreen bi- to tripinnate leaves. Diplazium hachijoense, D. virescens var. virescens, var. conterminum, var. okinawaense, and two other unnamed varieties, D. kawakamii var. kawakamii, D. dilatatum var. heterolepia, D. taiwanense, D. × kawabatae (=D. dilatatum × taiwanense), D. × takii (=D. hachijoense × virescens var. virescens), and D.× nakamurae (= D. hachijoense × virescens var. conterminum) are apomictic triploids (2n=n=123). Diplazium amamianum and D. esculentum are sexual diploids (2n=82, n=41) and D. subtripinnatum is a sexual tetraploid (2n= 164, n=82). Diplazium dilatatum var. dilatatum includes both sexual diploid and apomictic triploid populations. Cultivated gametophytes of six triploid taxa produced sporophytes apogamously, confirming their apomictic reproduction. All three putative hybrids, D. × kawabatae, D. × takii, and D. × nakamurae, are triploid, apomictic, and fertile taxa, therefore they are not the result of hybridization between known pairs of Japanese Diplazium plants. Received 16 March 1999/ Accepted in revised form 30 September 1999     

The karyotypes ofMicroseris bigelovii,M. douglasii,andM. pygmaea (Asteraceae)

The karyotypes of the three annuals,Microseris bigelovii, M. douglasii andM. pygmaea, consist of 2n = 18, small, submetacentric chromosomes. Length, centromere position, C-banding pattern, silver staining of NOR's, and the use of base specific fluorochromes, allow the identification of four of the nine chromosome pairs. The banding pattern ofM. bigelovii andM. pygmaea is identical, but intraspecific differences are found between strains ofM. douglasii.     

Directional and Fluctuating Asymmetry in Sexual and Asexual Otiorhynchus alpicola Populations

This study concerns the contribution of directional asymmetry (DA) and fluctuating asymmetry (FA) as a characterization of variation in six sexual (diploid) and two asexual (triploid and tetraploid) populations of the weevil Otiorhynchus alpicola. It is shown that DA in sexual populations is about 1 % of the mean length of each of the seven bilateral traits and the average contribution of DA to trait variation is even lower in asexual populations (about 0.85 in triploids and 0.65 in tetraploids forms). The average contribution of FA to the total phenotypic variance is about 23 %, 12 % and 19 % in diploid, triploid and tetraploid populations, respectively. Since FA is generally regarded as a measure of developmental stability, our data indicate that triploid forms of O. alpicola are developmentally more stable than diploid and tetraploid forms. The relationship between the level of ploidy and FA is discussed.     

Cytotaxonomic study of ferns of Yunnan,southwestern China

A cytotaxonomic study was made of 90 fern species of Yunnan, southwestern China, based on collections from northwestern, central, and southwestern Yunnan and a few Cheng's collections. The results verified most of the formerly reported basic chromosome numbers of Chinese genera, and recorded for the first time the basic numbers ofGymnogrammitis andSorolepidium and Chinese members of several other genera. Cytotaxonomy of some problematical genera was discussed. Biogeographical relationships between Japanese, Chinese, and Himalayan ferns were compared with special reference to local cyto-reproductive variations inConiogramme, Deparia, Onychium, andPteris cretica. The present evidence indicates that most triploid species examined are agamosporous, as general in filicalean ferns, and also suggests the sexual 32-spored sporogenesis inHypodematium crenatum andSorolepidium graciale as in Lindsaeaceae.     

A comparative study of isoenzyme patterns ofHydrilla verticillata (L.f.) Royle in Japan

Isoenzyme patterns of 226 accessions ofHydrilla verticillata collected in Japan were compared. 17 and 23 electrophoretic phenotypes were identifiable in diploid and triploid accessions, respectively, in dioecious ones. To the contrary, monoecious plants showed no variation of banding patterns and were assumed to be rametes of the same clone. The cytological change from diploid to triploid was suggested to occur many times in dioecious plants.     

Cytological and Reproductive Studies of Japanese Diplazium (Woodsiaceae; Pteridophyta). III. The Cytological Complexity of Species Groups with Simply Pinnate to Bipinnatifid Leaves

Diplazium with simply pinnate or bipinnatifid leaves. Diplazium wichurae var. wichurae, D. wichurae var. amabile, D. okudairae, and D. pin-faense are sexual diploids (2n=82; n=41II); D.× kidoi and D. × okudairaeoides are sterile diploids (2n= 82; meiosis irregular); D. donianum var. donianum is an apomictic triploid (2n=123; n=123II); D. donianum var. aphanoneuron is a sterile triploid (2n=123; meiosis irregular); D. crassiusculum, D. cavalerianum, D. incomptum, D. longicarpum, and D. pullingeri are sexual tetraploids (2n= 164; n=82II); and D. lobatum is an apomictic tetraploid (2n=164; n=164II). This is the first report of the chromosome numbers of D. lobatum, D. crassiusculum, D. incomptum, D. longicarpum, D. pullingeri, and D. × okudairaeoides, as well as the mitotic chromosome numbers of D. wichurae var. amabile, D. okudairae, D. pinfaense, and D. ×kidoi. The mitotic chromosome number, meiotic behavior, sterility, and allozyme analysis confirm that D. × kidoi and D. × okudairaeoides are hybrids between D. pin-faense and D. wichurae var. wichurae and D. okudairae and D. wichurae var. wichurae, respectively. Diplazium with simply pinnate to bipinnatifid leaves displayed an extraordinary cytological and reproductive complexity: a polyploidal series with diploids to hexaploids, sexual and apomictic reproduction, and natural hybridization. Received 14 August 2001/ Accepted in revised form 1 October 2001     

Unreduced gametes in diploid Medicago and their importance in alfalfa breeding

Summary In the genus Medicago, it is known that 2n gametes have been important in the evolution and breeding of cultivated alfalfa, which is a natural polysomic polyploid (2n=4x=32), however little is known on the frequency of male and female 2n gametes in diploid relatives of alfalfa. To obtain data on the frequency of 2n gametes, more than 12,000 2x–4x and 4x–2x crosses were made in 1982 at Madison (USA). Diploid parents in crosses were from four populations of M. coerulea, two of M. falcata and one diploid population of cultivated M. sativa which was derived by haploidy. The tetraploid seed parent in the crosses was a male-sterile M. sativa clone and vigorous tetraploid M. sativa plants were used as pollen parents. Each of 274 diploid plants was utilized both as male and as female. Of the 548 cross combinations, 266 crosses produced variable quantities of seeds which were sown in 1983 in a greenhouse at Perugia (Italy); the plants were subsequently space transplanted in the field in 1984. The identification of ploidy level of these genotypes was made on the basis of morphological characters, plant fertility, pollen stainability and chromosome counts.Of the 515 plants analyzed, the majority behaved as normal tetraploids indicating that many diploid plants produced 2n gametes. Diplogynous and diplandrous gamete production was not correlated with each other, which indicated a different genetic control of 2n sporogenesis in the 2 sexes. Only 4 F₁ triploid plants confirmed the presence of a very effective triploid block in alfalfa. In consequence, bilateral sexual polyploidization is a more likely alternative for the origin of tetraploid alfalfa than triploid bridges. The present study showed that it is possible to efficiently identify genotypes able to produce high frequencies of 2n gametes within natural populations of diploids Medicago that are useful in alfalfa breeding.Part of this study was conducted at the Agronomy Department, University of Wisconsin, Madison, Wis, USA, while one of us (F. Veronesi) was in receipt of financial assistance provided by the National Research Council of Italy; part was conducted at Centro di Studio per il Miglioramento Genetico delie Piante Foraggere, C.N.R., Perugia, Italy. The paper was presented at the Eucarpia Fodder Crops Section Meeting, Svalöv, Sweden, 16–19th September 1985