Die Zytologie der bisexuellen und parthenogenetischen Fortpflanzung von Heteropeza pygmaea Winnertz,einer Gallmücke mit pädogenetischer Vermehrung

Heteropeza pygmaea (syn. Oligarces paradoxus) can reproduce as larvae by paedogenesis or as imagines (Fig. 1). The eggs of imagines may develop after fertilization or parthenogenetically. The fertilized eggs give rise to female larvae, which develop into mother-larvae with female offspring (Weibchenmütter). Only a few of the larvae which hatch from unfertilized eggs become motherlarvae with female offspring; the others die. Spermatogenesis is aberrant, as it is in all gall midges studied to date. The primary spermatocyte contains 53 or 63 chromosomes. The meiotic divisions give rise to two sperms each of which contains only 7 chromosomes (Figs. 5–11). The eggs of the imago are composed of the oocyte and the nurse-cell chamber. In addition to the oocyte nucleus and the nurse-cell nuclei there are three other nuclei in the eggs (Figs. 15–17). They are called small nuclei (kleine Kerne). In prometaphase stages of the first cleavage division it could be seen that these nuclei contain about 10 chromosomes. Therefore it is assumed that these nuclei originate from the soma of the mother-larva. The chromosome number of the primary oocyte is approximately 66. The oocyte completes two meiotic divisions. The reduced egg nucleus contains approximately 33 chromosomes. The polar body-nuclei degenerate during the first cleavage divisions. The fertilized egg contains 2–3 sperms. The primary cleavage nucleus is formed by the egg nucleus and usually all of the sperm nuclei and the small nuclei (Figs. 21–29). The most frequent chromosome numbers in the primary cleavage nuclei are about 77 and 67. The first and the second cleavage divisions are normal. A first elimination occurs in the 3rd, 4th, and 5th cleavage division (Fig. 30). All except 6 chromosomes are eliminated from the future somatic nuclei. Following a second elimination (Figs. 33, 34), the future somatic nuclei contain 5 chromosomes. No elimination occurs in the divisions of the germ line nucleus. In eggs which develop parthenogenetically the primary cleavage nucleus is formed by the egg nucleus and 2–3 small nuclei. It's chromosome number is therefore about 53 or 63. After two eliminations, which are similar to the ones which occur in fertilized eggs, the soma contains 5 chromosomes. The somatic nuclei of male larvae which arrise by paedogenesis contain 5 chromosomes; while the somatic nuclei of female larvae of paedogenetic origin contain 10 chromosomes. It was therefore assumed earlier that sex was determined by haploidy or diploidy. But the above results show that larvae from fertilized as well as from unfertilized eggs of imagines have 5 chromosomes in the soma, but are females, and the female paedogenetic offspring of larvae from unfertilized eggs have either 5 or 10 chromosomes in their somatic cells. Therefore sex determination is not by haploidy-diploidy but by some other, unknown, mechanism. The cytological events associated with paedogenetic, bisexual, and parthenogenetic reproduction in Heteropeza pygmaea are compared (Fig. 37). The occurrence and meaning of the small nuclei which are found in the eggs of most gall midges are discussed. It has been shown here that these nuclei function to restore the chromosome number in fertilized eggs; it is suggested that they function similarity in certain other gall midges. Consideration of the mode of restoration of the germ-line chromosome number leads to the conclusion that in Heteropeza few, if any, of the chromosomes are limited to the germ-line, i.e. can never occur in somatic cells (p. 124).     

The Karyotype of <Emphasis Type="Italic">Amoeba borokensis</Emphasis> from a “<Emphasis Type="Italic">proteus</Emphasis>-like” Amoeba Group (Amoebozoa: Euamoebida)

The karyotype of Amoeba borokensis was studied for the first time. At the metaphase of mitosis, this species has a haploid set of chromosomes (n = 27). This is exactly half of the diploid karyotype in Amoeba proteus (strain B). At first glance, it confirms the idea that has recently appeared that one species arises from another via multiple changes in chromosome number. However, comparative cytogenetic analysis revealed that four orthologous chromosomes from haploid sets of these two species were not distinguished by the pattern of DAPI-stained bands. It shows that the genetic distance between A. proteus and A. borokensis is higher than was believed earlier and these two species have diverged from each other. Analysis of data on the life cycles of A. proteus and A. borokensis shows that a kind of so-called “cyclic polyploidy” takes place in “proteus-like” amoebae. “Cyclic polyploidy” has recently been considered as an alternative to the sexual process for genetic recombination in agamic protists from different macrotaxons.     

Egg maturation and parthenogenetic recovery of diploidy in the scorpion Liocheles australasiae (Fabricius) (Scorpions, ischnuridae)

In the scorpion Liocheles australasiae, egg maturation and parthenogenetic recoveries of chromosome number and nuclear DNA content were examined by histological, karyological observations and quantitative measurements of DNA. The primary oocyte becomes mature through two successive maturation divisions. The first maturation division takes place in the primary oocyte to produce a secondary oocyte and a first polar body. The second maturation division soon occurs in the secondary oocyte, in which the nucleus is divided into a mature egg nucleus and a second polar body nucleus, not followed by cytoplasmic fission. The first polar body, in one case, was successively divided into two second polar bodies; in the other case it was not divided. In either case, these polar bodies remained attached to the early embryo. The fate of these polar bodies during further embryogenesis were studied. In the karyological analysis, the chromosome number was divided into two groups, one from 27-32, the other was 54-64. The former was presumably the metaphase chromosome number at the meiotic division; the latter was presumably the metaphase chromosome number at the mitotic division. DNA content in the diploid nucleus of the primary oocyte, doubled before the maturation divisions, was reduced through the maturation divisions by one-half in the nuclei of the secondary oocyte and the first polar body and by one-fourth in the nuclei of the egg and the second polar bodies. The first reduction of DNA content corresponded to halving the number of the chromosomes in the first maturation division and the second to the nuclear division in the secondary oocyte. These reductions represent a common process of egg maturation, except the final production of the mature egg with two haploid nuclei, an egg nucleus, and a second polar body nucleus. These two nuclei, which were formed apart in the mature egg, drew near to fuse into a zygote nucleus. The chromosome number and nuclear DNA content were doubled in the zygote and each blastomere in embryos, supporting the hypothesis that the egg nucleus fuses with the second polar body nucleus and this conjugation initiates subsequent embryonic development.     

Genetic structure of diploid-polyploid complex of spined loach genus <Emphasis Type="Italic">Cobitis</Emphasis> (<Emphasis Type="Italic">Cypriniformes,Cobitidae</Emphasis>) in the Lower Danube

The extremely high diversity of spined loach biotypes in the Lower Danube has been detected by biochemical genetic investigation and cytometric analysis of 358 specimens collected in the riverbed and shallow channels. Along with two diploid species (C. elongatoides and C. “tanaitica”), six hybrid forms were revealed, namely, diploid C. elongatoides-“tanaitica”; triploid C. 2 elongatoides-“tanaitica,” C. elongatoides-2 “tanaitica,” and C. 2 elongatoides-species-1; and tetraploid C. 3 elongatoides-“tanaitica” and C. elongatoides-species-2-2 “tanaitica.” In addition, specimens with recombinant genotypes were also found. In spite of the apomictic mode of reproduction, the polyploids did not possess clonal structure, but according to the level of polymorphism and the genotype distribution, they were isomorphous to parental diploid species. Thus, in contrast to the polyploidy in Cobitids of the Dnieper, which have appeared in the basin due to the expansion, the polyploids of the Lower Danube are autochthonous and were derived by crossing with local diploid species. The process is apparently proceeds without any limitations.     

Behaviour and transmission of supernumerary chromosomes in diploid <Emphasis Type="Italic">Dactylis glomerata</Emphasis>

The somatic stability and the mode of transmission of B chromosomes were studied in diploid Orchard Grass: Dactylis glomerata L. ssp. judaica Steb. et Zoh. Somatic mosaics (different numbers of B's in different tillers) were detected in 4 out of 17 plants. Examination of the first and the second divisions of the male gametophyte revealed non-disjunction and preferential migration of the B's to the generative nucleus. Progeny from eight different cross-combinations were examined. The results obtained corroborate the direct evidence on accumulation of B's in the pollen grains, but the transmission patterns observed are too complex to be explained by this mechanism only.     

Die Zytologie der Bastarde aus der Kreuzung parthenogenetischer Weibchen von Solenobia triquetrella F. R. mit Männchen der bisexuellen Rasse

Crossing of the diploid parthenogenetic form with bisexual Solenobia triquetrella males results in normal sexes in F₁ and F₂. Therefore, oogenesis and spermatogenesis of the hybrids are expected to be normal. This is the case. If diploid or tetraploid parthenogenetic females are crossed, relatively often gynanders are observed in F₁. Their appearance is explained by the assumption that in the antagonism between the zygotic nucleus (?Befruchtungskern“) and the nucleus resulting from the fusion of the second polar nucleus with the inner daughter nucleus of the first polar nucleus (?Richtungskopulationskern“ [R.K.K.]) in gynanders neither the zygotic nucleus (as during bisexual propagation) nor the R.K.K. (as during parthenogenesis) dominates and suppresses the other nucleus. In the X0 type the reduced chromosome number in the tetraploid egg is 61, in the XY type 62. The sperm nucleus carries a set of 31 Chromosomes. Therefore, the intersexual F₁ hybrid should be triploid and should have 92 or 93 chromosomes respectively. It is shown that this is indeed the case. No elimination of single chromosomes has been observed, which clearly disproves the attempt to explain the complicated mosaic of the intersexes by the assumption that the 3A∶2X ratio changes during development. In all cases tested chromosome conjugation must have been complete, since in metaphase I the egg always shows 31 trivalents. (Spermatogenesis will be described in Mitteilung II.) Each autosomal trivalent consists of 3 homologous chromosomes, 2 of which are derived from the mother and the third from the sperm. During the reductional division the two maternally derived homologues seem always to go to opposite poles, while the paternal chromosome migrates to either one; therefore the daughter in the XY type must have a distribution of, for example, 42∶51=93, in the X0 type of, for example, 45∶47=92. It is proved that this is the case. The second maturation division in the egg is normal. All chromosomes are divided equationally; thus the mature egg nucleus contains a variable number of chromosomes. Further propagation of predominantly female intersexes is possible by parthenogenesis. Since during parthenogenesis the organism is derived from the R.K.K. the triploid chromosome number remains unchanged as is demonstrated. The parthenogenetic propagation of F₁ eggs thus must lead to the same result as in F₁. It is made highly probable that this is the case.     

Intraspecific divergence in wheats of the Emmer group using in situ hybridization with the Spelt-1 family of tandem repeats

Fluorescence in situ hybridization (FISH) was used to study the distribution of Spelt-1 repetitive DNA sequences on chromosomes of 37 accessions representing eight polyploidy wheat species of the Emmer evolutionary lineage: Triticum dicoccoides Körn, T. dicoccum (Schrank) Schuebel, T. durum Desf., T. polonicum L., T. carthlicum Nevski, T. aethiopicum Jakubz., T. aestivum L., and T. spelta L. Substantial polymorphism in the number, distribution, and the sizes of the Spelt-1 loci was revealed. On the chromosomes of the accessions examined, Spelt-1 tandem repeats were found in seven different positions (per haploid chromosome set). These were “potential hybridization sites”, including the subtelomeric regions of either short or long arms of chromosomes 2A and 6B, the short arm of chromosome 1B, and the long arms of chromosomes 2B and 3B. However, in individual genotypes, only from one to three Spelt-1 loci were revealed. Furthermore, no hybridization with Spelt-1 probe was detected on chromosomes from 12 accessions. Thus, the total number of Spelt-1 sites in karyotypes varied from zero to three, with the average number of 1.16. This was substantially lower than in the species of the Timopheevi section and diploid Aegilops speltoides Tausch, a putative donor of the B genome. The decrease of the content of Spelt-1 sequences in the genomes of the Emmer group wheats in comparison with the species of the Timopheevii group and diploid Ae. speltoides was assumed to result from the repetitive sequences reorganization during polyploidization and the repeat elimination during wheat evolution.     

Features of the embryonic development of <Emphasis Type="Italic">Dienia ophrydis</Emphasis> (Orchidaceae)

A new Dienia type of the embryogenesis of orchid plants differing from the Liparis type, earlier observed for the tribe Malaxideae, has been described in Dienia ophrydis (J. Köenig) Seidenf. (Orchidaceae). The Dienia-type embryogenesis is characterized by the following features: (1) development of a single-celled suspensor formed by a cb-derivative, (2) linear arrangement of embryo cells at the tetrad stage, (3) atypical origin of some tiers, and (4) no divisions of the ci and cb cells. A hypothesis about the convergent similarity between the Dienia and Caryophyllaceae types of embryogenesis has been proposed. A number of embryo sac and embryo structures typical for D. ophrydis, including “petassum,” “fitting,” and “suspensor mantle,” have been first described. A “petassum” represents the remains of cell walls of the pollen tube and probably the filamentous apparatus of synergids sealing the micropyle side of a fertilized embryo sac. The sole suspensor cell has a special appendix (“fitting”), which connects it to the embryo. The suspensor and the fitting are surrounded by a special envelope (“suspensor mantle”), which does not cover the basal cell of the embryo (ci).     

Weitere Untersuchungen über Chromosomenverhältnisse und DNS-Gehalt bei Anuren (Amphibia)

The karyotypes of the toad Bufo marinus L. (2n=22) and the frogs Limnodynastes tasmaniensis Gthr. (2n=24), Rana temporaria L., R. esculenta L. (both 2n=26) and R. arvalis Nills. (2n=24) were analysed in colchicine treated leukocyte and spermatogonial metaphases and/or embryonic and larval mitoses. The DNA content of Feulgen stained erythrocyte nuclei was measured microspectrophotometrically. Heteromorphic sex chromosomes are absent in all species. L. tasmaniensis has the lowest DNA content among these species. The south American toad B. marinus shows a karyotype similar to the other known toad species and contains the same amount of DNA as the European species B. calamita with the lowest DNA amount among the European toads. In southern German populations of R. temporaria besides animals with the “standard”-karyotype (2n=26) individuals with 1 or 2, in rare cases with 3 or 4 supernumerary chromosomes have been found. The supernumeraries are heterochromatic and smaller than the smallest chromosome of the “standard”-karyotype. If only 1 or 2 supernumerary chromosomes are present, they seem to show normal mendelian inheritance as a rule. The observation of a few tadpoles with intraindividual different numbers of supernumeraries points to the occurrence of unequal distribution of these chromosomes in individuals containing a higher number of supernumerary chromosomes. The karyotype of R. esculenta is very similar to the “standard”-karyotype of R. temporaria, but the chromosomes of R. esculenta are somewhat longer than those of R. temporaria. R. esculenta contains about 54% more DNA than R. temporaria in the erythrocyte nuclei, so that it must be assumed that all chromosomes of R. esculenta contain more DNA than their homologues in R. temporaria. R. arvalis possesses about 28% more DNA than R. temporaria. It is supposed that these interspecific differences in DNA content of the Rana species — as observed earlier in Bufo species — are not a consequence of differential polyteny but are caused during evolutionary processes by local increase in DNA in the chromosomes of R. esculenta and R. arvalis.     

Cytologie de la Pseudogamie chez Luffia lapidella Goeze (Lepidoptera Psychidae)

Summary The bisexual species Luffia lapidella has a pseudogamic (or gynogenetic) form, which is thelytokous and very similar to the parthenogenetic L. ferchaultella, but its egg needs the stimulation of the sperm.The inseminated egg restores its diploid chromosomal number in performing the same kind of restitutional first meiotic division as ferchaultella does. The second division, although already diploid, is normal and is followed by the formation of two nuclei, one of them degenerating as a polar body. The sperm starts developing as in the normal egg, but by metaphase II, it stops growing to a pronucleus and remains as a contracted and pycnotic body. Although attracted by the central female nucleus, it does not fuse with it. The male centriole behaves normally, it possibly plays a role in the first cleavage mitosis. The egg divides diploid and without any paternal chromosomes.

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Travail subventionné par le Fonds National Suisse de la Recherche Scientifique.     

On oviposition in weevils of the genus <Emphasis Type="Italic">Larinus</Emphasis> Dej. (Coleoptera,Curculionidae)

The following actions performed by females of several Larinus Dej. species during egg laying are described: search of an appropriate place on the plant, making the hole for the egg, oviposition proper, and sealing the hole. The hole preparation takes the longest time and the greatest effort. Only one individual usually completes development in one flower head. Females of Larinus vulpes Ol. prefer larger flower heads for oviposition and occasionally lay eggs into stems. The ability of females to distinguish the flower heads with already laid eggs is discussed. Species of Larinus may be divided into two groups with “early” and “late” oviposition. The evolution of egg laying in the genus Larinus is discussed.     

The origin of the North Indian sugarcanes

The “North Indian sugarcanes”, cultivated by Indian peasants during many centuries, have been studied morphologically very exactly byC. A. Barber from 1910 to 1920. They were named “Saccharum Barberi” byJeswiet. Barber distinguished four groups. In 1931 the present author found the following chromosome numbers in these groups: 2n=116 and 2n=82 in the Sunnabile group; 2n=82 in the Mungo group; 2n=124 and 2n=107 in the Nargori group and about 91 in the Saretha group. The first three groups are sterile, the last is fertile. It is shown that the North Indian sugarcanes are hybrids between ancient indigenous sugar canes with a basic number of 17 chromosomes, and forms ofS. spontaneum withn=40,n=48 andn=56 respectively. Differences in the numbers of chromosomes contributed by the mother type may in part have their origin in endo-duplication, as commonly observed inSaccharum hybrids. Details are presented in Table 2. The differences found between different forms of IndianS. spontaneum in respect to chromosome number, sugar content and mosaic resistance may be attributed to intercrossing with canes of the fertile Saretha group.     

Noncanonical meiosis in the nematode <Emphasis Type="Italic">Caenorhabditis elegans</Emphasis> as a model for studying the molecular bases of the homologous chromosome synapsis,crossing over,and segregation

The nematode C. elegans is a classic study object of developmental biology and genetics, which is particularly suitable for studying the molecular bases of meiosis. Developing meiocytes are located in the threadlike gonads of C. elegans in linear gradient order of the stages of meiosis, which facilitates studying the order of intracellular events during meiosis. C. elegans has polycentric chromosomes. This causes a special order of events during meiosis, and as a consequence, meiosis in C. elegance differs from canonical meiosis of most eukaryotes. In the meiotic prophase I, all chromosomes carry single protein “pairing centers.” They are responsible for joining homologous chromosomes in pairs. This initiates the formation of synaptonemal complexes (SCs). Programmed double-stranded DNA breaks appear after initiation of the SC assembly, and they give rise to meiotic recombination. The initiation of meiotic recombination after the chromosome pairing distinguishes the C. elegans meiotic pattern from those in the absolute majority of eukaryotes studied. C. elegans has strict crossing over interference, which allows for the formation of one chiasma per bivalent. In the late prophase I, the polycentric centromeres are remodeled, one of the chromosome ends acquires a cuplike kinetochore, and during two meiotic divisions, chromosomes behave as monocentric. The study of meiosis in C. elegans allows for separate investigation of synapsis and recombination of homologous chromosomes and provides material for studying the evolution of meiosis.     

Biotic Interactions between Two Species of Microalgae in Mixed Culture

Biotic interactions in a mixed culture of two microalgae species—Scenedesmus quadricauda (Turp.) Breb. and Monoraphidium arcuatum (Korsch.) Hind.—used in bioassay in monocultures as test objects were studied. The toxic effect of cell-free filtrates from different “age” monoculture (2, 7, 10, 15, 21, and 28 days) of S. quadricauda on the growth of the “young” test culture of M. arcuatum and, conversely, the toxic effect of cell-free filtrates from the different “age” (2, 7, 10, 15, 21, and 28 days) monoculture of M. arcuatum on the growth of the “young” test culture of S. quadricauda was evaluated. Simultaneously, the toxicity of their own filtrates of different “ages” was monitored by a test culture of each species. The interactions of the species in the mixed culture can be regarded as negative, as an antagonistic one, when both populations inhibit the growth of each other through metabolites and food resource competition, while the effect of S. quadricauda on M. arcuatum is much stronger. The main factor constraining the growth of monoculture S. quadricauda is the rapid depletion of the food resource from the medium and not the inhibition of growth by its own metabolites. The depletion of the food resources from the medium in monoculture of M. arcuatum occurs much later than in monoculture of S. quadricauda. Metabolites of S. quadricauda cause a strong inhibitory effect on the growth of M. arcuatum, and the metabolites of M. arcuatum cause a weak inhibitory effect on the growth of S. quadricauda. The filtrates of the “old” culture of S. quadricauda (21–28 days) cause the greatest inhibitory effect on cell division of M. arcuatum. The filtrates of the “old” culture of S. quadricauda (21–28 days) cause the greatest inhibitory effect on cell division of M. arcuatum. Comparative analysis of the cell number dynamics of two species, S. quadricauda and M. arcuatum, in mono- and two-species algal cultures, as well as experiments with filtrates of these monocultures, showed that the interaction of species can be explained by the food resource competition and allelopathic interaction (exometabolite effect).     

Seeding Dates and Cultivars Effects on Stink Bugs Population and Damage on Common Bean <Emphasis Type="Italic">Phaseolus vulgaris</Emphasis> L

Fields experiments were conducted during two growing seasons (2010–2011 and 2012–2013) at three seeding dates to identify stink bug (Hemiptera: Pentatomidae) species and to determine their seasonal population density fluctuation and damage caused to three common bean (Phaseolus vulgaris L.) cultivars “Ica Pijao,” “Cubacueto 25–9,” and “Chévere.” Stink bug species observed were Nezara viridula (L.), Piezodorus guildinii (Westwood), Chinavia rolstoni (Rolston), Chinavia marginatum (Palisot de Beauvois), and Euschistus sp. The most prevalent species was N. viridula in both seasons. The largest number of stink bugs was found in beans seeded at the first (mid September) and third (beginning of January) seeding dates. Population peaked at BBCH 75 with 1.75, 0.43, and 1.25 stink bugs/10 plants in 2010–2011 and with 2.67, 0.45, and 1.3 stink bugs/10 plants in 2012–2013 in the fields seeded the first, second, and third seeding dates, respectively. The lowest numbers of stink bugs were found in beans seeded at the second (mid November) seeding date. A significant negative correlation between relative humidity and number of stink bugs was found in 2010–2011, and a similar tendency was observed in 2012–2013. The highest seed and pod damage levels occurred in cv. “Chévere” and the lowest in cv. “ICA Pijao” during both seasons. Results suggest that cv. “ICA Pijao” and the second (mid November) seeding date is the best choice to reduce stink bug damage.     

Induced Bivalent Interlocking and the Course of Meiotic Chromosome Synapsis

WHEN chromosomes pair at meiosis the bivalents so formed do not normally interlock. Heat-treatments can, however, induce bivalent interlocking in the locust Locusta migratoria. Only the longest bivalents interlock and usually only two are found per cell; two “rod” bivalents, with single chiasmata, two “ring” bivalents, each with two or three chiasmata, or one “rod” and one “ring” bivalent (Fig. 1a, b and c). The nature of this interlocking and the metaphase orientational and congressional properties of interlocked bivalents are analysed in detail elsewhere¹.     

The ultrastructure of the zoospores of the parasitic dinoflagellate <Emphasis Type="Italic">Ichthyodinium chabelardi</Emphasis> Hollande et J. Cachon, 1952 (Alveolata: Dinoflagellata)

This is the first study on the ultrastructure of the zoospores of Ichthyodinium chabelardi, a parasitoid of the fish egg and early larval stages. The zoospores were characterized by the cell structure specific for dinoflagellates; particularly, cells contained large trichocysts and the “dinokaryon”-type nucleus. An unusual large electron-transparent zone was the only significant difference from the “classical” cell structure in Dinoflagellata. We did not find cell structures for the penetration to the host cell (microtubular basket, conoid, or secretory organelles such as rhoptries). The data on the fine structure of the zoospores of I. chabelardi agree with the results of molecular phylogeny; this allows us argue that excluding this species from Dinoflagellata and assigning it to Protalveolata was a mistake.     

Behavior of sex chromosomes at early meiosis stages in three wood mice species of the genus <Emphasis Type="Italic">Apodemus</Emphasis> (Rodentia,Muridae)

The prophase of the first meiotic division was studied in field mice of the species Apodemus (Sylvaemus) flavicollis, A. (S.) ponticus, and A. (S.) uralensis by light and electron microscopy. The karyotypes of three species were described on the base of electron microscopy of synaptonemal complexes in spermatocytes I. The axial elements of the sex chromosomes at early-middle pachytene synapse along the major portion of the Y axis; at late pachytene-early diplotene, the synapsis region shrinks; and at diakinesis-metaphase I, X and Y chromosomes associate end-to-end in all species studied. The behavior of sex chromosomes in the synapsis in the species studied was quite uniform. The results are discussed in the context of earlier data on the behavior of sex chromosomes in various rodent species in meiosis prophase I and their banding.