CYTOGENETIC STUDIES IN CLARKIA,SECTION PRIMIGENIA. II. A CYTOLOGICAL SURVEY OF CLARKIA ARCUATA AND CLARKIA LASSENENSIS

Clarkia arcuata and C. lassenensis are the 2 members of the subsection Flexicaules. Although closely related morphologically, they show very different patterns of chromosomal variability in nature. About 25% of the plants grown from wild seed of C. arcuata, a predominantly cross-pollinating species, were heterozygous for 1 or 2 translocations; such heterozygotes were found in 5 of the 9 populations sampled. An analysis of the chromosome pairing in intraspecific crosses indicated that at least 5 different translocations giving a ring of 4 with the “standard” strain, 2 giving a ring of 6, and 2 giving a ring of 8 are present in nature. No arrangement was found with widespread distribution, and it is impossible to say at present what might be the primitive arrangement of this species. One population was found to contain an inversion, a rearrangement which is very rare in Clarkia at the intraspecific level. In C. lassenensis, a predominantly self-pollinating species, only 6% (3 plants) of a sample of 53 were translocation heterozygotes, and these heterozygotes were found in only 2 of 13 populations. Intraspecific crosses indicated that one chromosome arrangement, the “standard,” was present throughout the species range.     

CHROMOSOMAL DIFFERENTIATION IN CLARKIA DUDLEYANA

Snow , Richard . (U. California, Davis.) Chromosomal differentiation in Clarkia dudleyana. Amer. Jour. Bot. 47 (4) : 302—309. Illus. 1960.—Clarkia dudleyana (n=9) is a common, colonial annual of the early-summer California flora. Of 275 individuals, derived from 9 natural populations and their garden-grown representatives, 17.1% were heterozygous for reciprocal translocations. Supernumerary chromosomes were also found in about 2% of the plants examined. The translocation heterozygotes are not distributed regularly over the species range but are concentrated near the geographical center of distribution. Most of the populations contained none or only a few heterozygotes, but in one colony 69% of 42 plants sampled were heterozygous. Judging from the meiotic metaphase associations observed, at least 5 different chromosome arrangements are present at this locality. Hybrids between colonies have invariably been translocation heterozygotes, the largest association found in such hybrids being a chain of all 18 chromosomes (a potential ring of 18). No correlation is evident between geographical separation and degree of cytological differentiation. Heterozygotes with smaller rings of 4 or 6 chromosomes, whether from natural populations or resulting from interpopulation hybridization, are highly fertile owing to the regular alternate disjunction of the chromosomes of the rings. In the larger rings of 12 to 18 chromosomes, derived from interpopulation crosses, segregation is much more irregular and leads to high sterility. It is possible that at least in some localities the heterozygotes enjoy a selective advantage over their homozygous sibs. It is also postulated that homozygosity for a particular chromosome arrangement may be selectively favored in a certain habitat, as a result of a position effect attendant upon placing formerly non-linked genes in the same linkage group through reciprocal translocation. The high degree of chromosomal differentiation between some populations of this species suggests that the complex heterozygotes of Oenothera have arisen as a result of hybridization of cytologically differentiated races.     

CYTOGENETIC STUDIES IN CLARKIA,SECTION PRIMIGENIA. IV. A CYTOLOGICAL SURVEY OF CLARKIA GRACILIS

Clarkia gracilis (2n = 28) is an allotetraploid which combines genomes from two subsections of section Primigenia. Natural populations consist of plants homozygous for a single chromosome arrangement, which may differ from the arrangements in other populations by one or more reciprocal translocations. One arrangement, the “standard,” was widespread. Cytological observations on plants derived from crosses between populations of C. gracilis, and on triploid plants derived from crosses with C. amoena subsp. huntiana, one of the parents of the tetraploid, were used to determine the end arrangements present. Ten arrangements were identified, and it was found that the standard amoena subgenome of C. gracilis is identical in end arrangement to the previously defined standard arrangement of the diploid C. amoena. Hence a race of C. amoena with this arrangement was involved in the hybridization which gave rise to C. gracilis. Evidence was found that other arrangements of C. amoena have probably been introduced into C. gracilis by subsequent introgressive hybridization. Cytological differences, coupled with differences in morphology, ecology, and distribution indicate that C. gracilis should be subdivided into four subspecies instead of the three presently recognized.     

Cytogenetic studies inClarkia,section primigenia. III. Cytogenetics of monosomics inClarkia amoena

Naturally occurring monosomic plants, with 13 instead of the usual 14 somatic chromosomes, have been found in several populations ofClarkia amoena subsp.huntiana (Onagraceae). These plants show no obvious phenotypic differences from their 14 chromosome sibs. Three types of meiotic pairing were found amongst 7 monosomic strains: 4 bivalents+chain of 4+univalent, 3 bivalents+chain of 4+chain of 3, and 2 bivalents+one heteromorphic rod bivalent+ring of 4+chain of 3. All are basically translocation heterozygotes of a peculiar kind composed of two genomes, one with 6, the other with 7 chromosomes. Both genomes can be transmitted through pollen and eggs, but because of the nature of the meiotic divisions, gametes with 6 chromosomes are in functional excess. Self-pollination of 5 of the monosomic strains does not give 12 chromosome nullisomic progeny. The nullisomics produced by the other 2 strains are weaker and later flowering than their 13 or 14 chromosome sibs, and are partially or completely sterile. The 6 chromosome genomes are hence usually inviable when homozygous. Crosses of the monosomics to a standard cytological strain, and intercrosses between monosomic strains, have allowed analysis of the end arrangements of chromosomes. Six different 7-chromosome genomes and 3 different 6-chromosome genomes have been identified. The translocation scheme proposed to account for the origin of the 6-chromosome genomes involves partition of most of the genetic material of one chromosome amongst two others plus the loss of a small centromere-bearing chromosome. This loss accounts for the lethality of the 6-genomes when homozygous. The fact that vigorous, healthy nullisomics are formed whenever two monosomics of different geographical origin are crossed indicates that the 3 monosomic genomes have had an independent origin, since they obviously complement one another's genetic deficiencies. The hybrid nullisomics are fairly fertile, and if formed in nature might serve as the starting point for a new race or species with a reduced basic chromosome number.     

STABILITY OF A CHROMOSOMAL HYBRID ZONE IN THE CLARKIA NITENS AND CLARKIA SPECIOSA SSP. POLYANTHA COMPLEX (ONAGRACEAE)

Clarkia nitens and Clarkia speciosa polyantha (Onagraceae) are distinct chromosomal taxa differing by at least six reciprocal translocations. Where the taxa have come into contact, a chromosome boundary zone exists characterized by high levels of translocation heterozygosity due to at least 12 new chromosome arrangements which have evolved there. Previous studies have shown that these boundary arrangements are distributed such that they provide for full interfertility between adjacent populations. It was hypothesized that the geographic distributions of each of these arrangements will remain generally stable due largely to the very adverse effect that major changes would have on fertility. Evidence is presented here that over a ten year period the frequencies and geographic distributions of the chromosome arrangements within this boundary region have remained stable. The frequencies of the various chromosomal configurations (nine pairs, ring of four, two rings of four, ring of six, ring of four + ring of six, and ring of eight) from surveys in 1968 and 1978 have been analyzed statistically. In general, the analysis indicates that there have been no detectable changes over the 10-yr period.     

TRIVALENT FORMATION IN MULTIPLE TRISOMICS OF CLARKIA UNGUICULATA

Vasek, F. C. (U. California, Riverside.) Trivalent formation in multiple trisomics of Clarkia unguiculata. Amer. Jour. Bot. 50(3): 244–247. 1963.—A series of multiple trisomics, ranging from 2n + 1 to 2m + 7, was scored for univalents and trivalents at first metaphase. The mean number of trivalents per cell per extra chromosome was 0.43, 0.46, 0.46, 0.56, 0.54, 0.55 and 0.59 for plants with 1, 2, 3, 4, 5, 6 and 7 extra chromosomes respectively. These trivalent frequencies are interpreted to fall into 2 classes, indicating that the cytological differences between triploids and single trisomies may be based on a threshold effect. The results are compared with available data from other genera, and it is suggested that the observed increase in trivalent formation per extra chromosome may be associated with an increase in chiasma frequency.     

TRISOMIC TRANSMISSION IN CLARKIA UNGUICULATA

Vasek , F. C. (U. California, Riverside.) Trisomic transmission in Clarkia unguiculata. Amer. Jour. Bot. 48(9): 829–833. 1961.—Seven primary trisomic plants derived from a triploid-diploid cross were self-pollinated. The 7 progenies included diploids and trisomics, the latter varying in frequency from 16 to 30%. In addition, 2 of the progenies included tetrasomic plants. Crosses were made between diploids and either trisomics or tetrasomics. The extra chromosome of 1 progeny was readily transmitted through the pollen of trisomic and tetrasomic plants. When a trisomic of the same progeny was used as a seed parent, only diploids and tetrasomics were found among the offspring, indicating a duplication of the extra chromosome. The extra chromosomes of other progenies were not transmitted through either pollen or eggs in controlled diploid-trisomic crosses but trisomics of these progenies were recovered after self-pollination. It is suggested that differential pollen-tube growth precluded transmission to diploid-trisomic hybrids and that under conditions of reduced pollen competition the extra chromosome normally would be transmitted through pollen. The extra chromosomes generally occur as univalents at metaphase and are ordinarily included in telophase nuclei.     

PHENOTYPIC VARIATION IN TRISOMICS OF CLARKIA UNGUICULATA

Vasek , F. C. (U. California, Riverside.) Phenotypic variation in trisomics of Clarkia unguiculata. Amer. Jour. Bot. 50(4): 308–314. 1963.—Progenies of 3n × 2n crosses included, in addition to diploids, plants trisomic for 1, 2, 3, 4, 5, 6 or 7 chromosomes. Means and variances were calculated for 15 phenotypic traits, including 3 width/length ratios, in one set of progenies, and for 10 of the traits, including 2 of the ratios, in another set of progenies. In 25 trait comparisons, including 15 different traits, the means for each chromosome number class were heterogeneous in 11 comparisons, which included 8 different traits. Single trisomics differed significantly from diploids in 5 comparisons (4 different traits). Despite these significant differences the variation followed no particular pattern except that sepal length increased and pollen fertility decreased with chromosome number, and trisomics, as a group, sometimes differed from diploids with regard to the width/length ratio of leaves or petals. The variances were heterogeneous in 5 comparisons (4 different traits). Sepal length and pollen fertility were the only traits for which single trisomics were more variable than diploids and for which the entire population was more variable than diploids. In addition, in 4 progenies of self-pollinated trisomics, diploids and trisomics (which within each progeny were trisomic for the same Chromosome) differed significantly in mean value in only 3 traits (out of 60 trait comparisons). Variances were significantly different in 6 comparisons (4 different traits) but, surprisingly, diploids were more variable than trisomics in 3 of these 6 comparisons. Except for sepal length, pollen fertility and some width/length ratios, a wide variety and number of extra chromosomes rarely had a significant effect on the mean or variability of various phenotypic traits, and single specific extra chromosomes had very little effect except sometimes on pollen fertility or an occasional ratio. A large amount of variation, probably caused by the environment and the general genetic background, may obscure possible specific trisomic phenotypes. Morphological identification of specific trisomics is considered impractical in this species.     

Genetic mapping of cytological and isozyme markers on chromosomes 1R, 3R, 4R and 6R of rye

Cytogenetic maps involving chromosomes 1R, 3R, 4R and 6R have been developed from the analysis of offspring of crosses between multiple heterozygous rye plants. The maps include isozyme loci GpiR1, Mdh-R1 and Pgd2 (located in chromosome 1R), Mdh-R2 (located in chromosome 3R), Pgm-R1 (located in chromosome 4R) and Aco-R1 (located in chromosome 6R). Various telomeric and interstitial C-bands of these four chromosomes, the centromere split of chromosome 3R, and translocation TR01 were used as cytological markers. By means of electron microscope analysis of spread pachytene synaptonemal complexes, the breakpoint of TR01 was physically mapped in chromosome arms 4RS and 6RL. From the linkage data, conclusions were derived concerning the cytological locations of the isozyme loci and the physical extent of the evolutive translocations involving chromosome arm 6RL.     

普通小麦栽培品种丰抗13的4B—1D染色体易位的鉴定

通过细胞学观察,在普通小麦栽培品种“丰抗13”和“京红1号”的杂交后代中,发现有多价体出现,这就表明有染色体易位发生。为进一步弄清究竟是哪条染色体发生了易位,我们采用单体测交方法,观察鉴定所有各单体系F_1的花粉母细胞第一次减数分裂中期Ⅰ(以下简称PMCs中Ⅰ)染色体构型。从鉴定结果发现,凡2n=42的F_1 PMCs中Ⅰ出现19~Ⅱ 1~Ⅳ,而2n=41的F_1PMCs中Ⅰ的染色体构型不同,单体与易位有关的两个单体系4B和1D F_1 PMCs中的Ⅰ构型中有部分呈现为19个二价体加1个三价体,即19~Ⅱ 1~Ⅲ,没有单价体,而其余各单体系F_1 PMCs中Ⅰ构型则表现为18个二价体,1个四价体和1个单价体,即18~Ⅱ 1~Ⅰ 1~Ⅳ。因此,可以肯定“丰抗13”存在1个染色体易位,其有关染色体就是4B和1D。     

Primary trisomics obtained from autotriploid by diploid reciprocal crosses in cucumber

To promote cytogenetical studies on cucumber (Cucumis sativus L., 2n = 2x = 14), the reciprocal crosses were made between autotriploid and diploid for selecting the primary trisomics. Meanwhile, chromosome behavior during meiosis in autotriploid cucumber was investigated to look for cytological evidences for origin of primary trisomics. Many viable F₁ seeds were obtained from reciprocal crosses between autotriploid and diploid. The number of chromosomes of 56 surviving progenies varied from 14 to 28, with plants having 2n = 15 occurring at the highest frequency (51.8%). Primary trisomics were firstly obtained in this study. Four types of primary trisomics were isolated and they could be distinguished from each other, as well as diploid. Variable chromosome configurations, e.g. univalent, bivalents and trivalents were observed in many pollen mother cells of the autotriploid at metaphase I. Binomial chromosome distribution was observed at anaphase I and frequency of 8/13 was 6.25%. The meiosis of autotriploid, especially the class of gametes with eight chromosomes, gave the cytological evidence of producing 2x + 1 type gamete and could be induced into primary trisomic plants from progeny of autotriploid–diploid crosses. These studies have established a ground work for selecting a series of primary trisomics, and further using them for associating linkage groups with specific chromosomes in cucumber.     

Redundant segments inZea mays detected by translocations of monoploid origin

Twenty-two independently occurring spontaneous reciprocal translocations were isolated from monoploid X diploid crosses in maize and their breakpoints were determined. As 12 of the translocations involved the same two chromosomes and had breakpoints at approximately the same positions (6L. 2–3, 7L. 2–3) and two other translocations appeared to be identical with breakpoints at 2L. 9, 6L. 4, 14 of the 22 translocations probably arose by crossing over within duplicate segments of nonhomologous chromosomes. Thus, at least part of the bivalents seen at diakinesis and chromatid bridges seen at anaphase I in monoploid plants appear to be generated by recombination between redundant chromosome segments. The other eight translocations each occurred once. Because our evidence indicates that recombination between nonhomologous illegitimately synapsed chromosome segments does not occur in maize, these were probably also produced by recombination between redundant segments. If one assumes that their breakpoints also mark regions of interchromosomal redundancy, other conclusions can be reached: A) corn does not contain detectable homoeologous chromosomes, thus it is precently a true diploid, and B) as exchanges giving rise to translocations did not occur in the centromeres or proximal heterochromatin, these regions either do not possess redundancy or are rarely involved in chiasma formation. Furthermore, the duplicated segments in the genome giving rise to translocations in haploid microsporocytes probably have the same serial order with respect to the centromere.This work was partially supported by U.S. Atomic Energy Commission Contract AT(11-1)-2121.     

A CYTOGENETIC STUDY OF CLARKIA UNGUICULATA II. SUPERNUMERARY CHROMOSOMES

Mooring , John S. (Washington State U., Pullman.) A cytogenetic study of Clarkia unguiculata. II. Supernumerary chromosomes. Amer. Jour. Bot. 47(10): 847–854. Illus. 1960.—Supernumerary chromosomes morphologically comparable to those of the basic complement occur in high frequency in wild populations of this onagraceous annual plant. This paper evaluates the role that these supernumerary chromosomes play in the population dynamics of this species. The results of crossing plants with various numbers of supernumeraries showed that these chromosomes often increased in number in the seed parent. Examination of microsporocytes showed that almost 30% of the 491 plants determined had 1 or more supernumerary chromosomes. Studies of natural populations revealed that the frequency of individuals with supernumeraries varied from 0 to 79% in different populations, and also that in 1 population their frequency varied significantly in different years. It is concluded that supernumerary chromosomes in this species are adaptive under at least certain conditions. It is speculated that they are components of polygenic systems which increase tolerance to environmental extremes.     

Gamete composition and chromosome variation in pollen-derived plants from octoploid triticale x common wheat hybrids

Summary Anther culture of secondary octoploid triticale (AABBDDRR) and F₁ hybrids (AABBDDR) of octoploid triticale x common wheat crosses was carried out, and 96 pollen-derived plants were developed and studied cytologically. In addition to the 8 types of pollen-derived plants with the theoretically predicted chromosome number, plants with the chromosome constitutions of 2n = 38, 43, 45, 47, 74, and mixoploids were obtained. The haploids and the diploids had different distributions. The frequencies of plants with one and two (pairs of) rye chromosomes were extremely high, and anther culture may be an expeditious route for creating alien addition lines of distant hybrid F₁s. Chromosome aberrations, including deletions, inversions, translocations, as well as isochromosomes and ring chromosomes, were observed in some plants. Abnormal meioses, such as chromosome non-disjunction, were also found. The reasons for the chromosome aberrations are discussed.     

EVOLUTIONARY MODIFICATION IN CLARKIA I. SELECTION FOR HAIRLESSNESS

Plants of Clarkia unguiculata with moderate numbers of long hairs on the ovary and calyx were selected for relative “hairlessness” through 11 generations. Inbreeding depression, manifested as a high degree of sterility, necessitated co-selection for fertility. The proportion of fertile plants among families ranged from 0–50% in the 5th selected generation and increased to a range of 53–100% in the 10th selected generation. At the same time, the mean number of hairs on the ovary decreased from a range of 0.0–1.1 to a range of 0.0–0.2; and the mean number of hairs per sepal from 0.5–16.0 to 0.1–2.2. The percentage of plants per family with no hairs on the ovary and no hairs on the calyx increased from a range of 0–63 in the 5th selected generation to a range of 4–88 in the 10th selected generation. Nonselected progenies have long hairs on both ovary (mean 10–17) and sepals (mean 46–50) in all plants. The demonstrated response to selection has important implications regarding catastrophic selecion and the evolution of Clarkia species in marginal habitats.     

Characterization of ‘Sun II’ oat monosomics through C-banding and identification of eight new ‘Sun II’ monosomics

 Monosomics are a powerful tool for genetic mapping in allopolyploid plant species such as oat (Avena sativa L., 2n=6x=42). A C-banded karyotype of the oat cultivar Sun II was compared with previously described oat karyotypes and was used to identify the missing chromosome in each line of Sun II aneuploids. These included new aneuploids, isolated among derivatives of oat haploids obtained from Sun II oat×maize crosses, along with the original Sun II aneuploid set which had been obtained by cytological screening of a Sun II population for spontaneous aneuploids. Eight new Sun II monosomics were identified among the derivatives of haploids from the oat×maize crosses, to give a total of 18 unique Sun II monosomic/nullisomic lines. All seven C-genome chromosomes are represented by Sun II monosomics. Chromosomes 13, 14 and 17 are not represented by Sun II aneuploids but are found in the Kanota monosomic series. Therefore, monosomics of some form are now available for all 21 oat chromosomes. A reciprocal translocation involving chromosomes 3C and 14, found in a portion of the original set of Sun II monosomic lines, was also described. No new translocations were detected in the Sun II×maize crosses. Received: 11 December 1996 / Accepted: 15 July 1997     

Polyploid inter-specific hybrids in the genus Fragaria

Conclusion In conclusion we think it necessary to lay stress on the great faculty to form diploid gametes, and in result polyploid forms shown by allFragaria species, as has been noted by the majority of investigators having worked with these plants.In result of our investigations of diploid-hexaploid and octoploid-hexaploid hybrids, we have found 16 cases of doubling of the chromosome number in sexual cells of hybrids, and 5 cases of doubling in pure species. A cytological analysis of all F₂ hybrids at our disposal (the number of chromosomes has been counted in 14 plants out of 25), as well as of back crosses (the number of chromosomes has been counted in 2 plants out of 6), will doubtless considerably increase this number. The differences in the chromosome sets (7 chromosomes being a whole set) of the species used in crossing, evidently, greatly promotes the above mentioned phenomenon.Starting from experimental data, there may be two ways of explaining the origin of the polyploid series ofFragaria, with 14, 28, 42, 56 somatic chromosomes, found under natural conditions. The first way is that of hybridisation, as a source of origin of polyploid species, (with different chromosome sets) with subsequent doubling of the chromosome number, giving rise to allopolyploids. In regards to the second way, cross pollination is but an external stimulating influence, similar to a series of other factors disturbing the normal course of reduction division, and giving rise to autopolyploids (analogous to the origin of our tetraploid). It is evident, that high polyploid species of the strawberry have originated in the first way.With 1 plate     

The Biology of Allium monanthum (Liliaceae) I. Polyploid Complex and Variations in Karyotype

Abstract Plants of Allium monanthum Maxim., whose gender expression are usually dioecious, but rarely hermaphrodite or gynomonoecious, proved to constitute a polyploid complex, consisting of diploid, triploid, and tetraploid individuals. The basic chromosome complement of this species consists of seven metacentric or submetacentric chromosomes and one acrocentric, the latter possessing a satellite on the short arm. Thus, the karyotype formula is expressed as 7V+11 (x=8). The diploid plants (2n = 16) were confined to central Honshu, Japan. Typical female plants possessed the standard karyotype, whereas male plants were heterozygous for two kinds of translocations. The 3x plants (2n=24) are somewhat widely distributed in the areas from the Kanto to Hokuriku district in Honshu. All female triploid plants possessed the standard karyotype. The geographical distribution of 4x plants (2n=32) which express mostly a female phenotype occurred nearly throughout the whole areas investigated; they are geographically isolated from the 2x plants. A majority of 4x plants had the standard karyotype. The remaining tetraploids were of the aberrant type, 4x/51, which has five acrocentric chromosomes, and two aneuploids 4x+1 and 4x-1. Both 3x and 4x forms seem to be of autopolyploid origin. Three kinds of aberrant nucleolar chromosomes with an extra satellite or an inseried secondary constriction were found in the heterozygotes for translocations of 2x plants and also in some plants of the 3x form. These aberrant plants usually form their own homogeneous populations, but were somewhat scattered throughout the range in their distribution. Thus, these individuals are considered to have perpetuated these types of chromosome aberrations which originated in the remote past.     

Trisomics and aneuploids of ryegrass

Summary Primary trisomics (2 n + 1 = 15), double trisomics (2 n + 1 + 1 = 16) and aneuploids with 24 to 30 chromosomes, as well as a diploid and tetraploids, were found in the progeny of a hypertriploid (2 n = 22) plant of perennial ryegrass, Lolium perenne L. Trisomics and double trisomics differed in their mean chromosome association, chiasma number and spike morphology. A few aneuploids and tetraploids had reciprocal translocations. The diploid, primary trisomics and tetraploids were more fertile than the double trisomics and aneuploids. Most trisomics and aneuploids were probably produced through female transmission. One double trisomic had a high univalent number, a low chiasma number and loose chromosome coiling. Both the extra chromosomes carried secondary constrictions. The gene for desynapsis might be located on one of these chromosomes.     

Construction of synteny groups of Brassica alboglabra by RAPD markers and detection of chromosome aberrations and distorted transmission under the genetic background of B. campestris

Interspecific hybrids were produced by crosses between the inbred lines of B. campestris and B. alboglabra, and were backcrossed twice to B. campestris. Genetical constitutions of the BC₂ plants were analyzed by RAPD (random amplified polymorphic DNA), flow cytometry and cytological observations. By using 140 arbitrary primers, a total of 137 polymorphic bands were obtained and 125 were found to be specific to B. alboglabra. Based on the presence and absence of the specific RAPD markers of B. alboglabra, 13 synteny groups were constructed. The number of markers in each synteny group was found to be different and varied from 2 to 28. This reflects the difference in the degree of genetic variability among the B. alboglabra chromosomes from those of B. campestris. Losses or gains of RAPD markers were observed frequently in most of the synteny groups, which indicated the occurrence of chromosome translocations and/or deletions in the chromosomes of B. alboglabra. In a population of 40 BC₂ plants, chromosome transmission rates were analyzed by using the RAPD markers in each synteny group. Most of the chromosomes of the synteny groups were transmitted with rates of 0.37–0.68. An extremely high transmission rate, 0.98, was however observed in one of the synteny groups. Inheritance data of the synteny groups revealed relationships among themselves. The plants lacking the RAPD markers of two synteny groups tended to lose others belonging to the rest of the synteny groups, indicating the effects of these groups on the transmission of B. alboglabra chromosomes to the B. campestris background. Received: 26 February 1999 / Accepted: 30 December 1999