The geographical distribution of Polycelis (Polycelis) sapporo and Seidlia schmidti in the Far East

Polycelis (Polycelis) sapporo (Ijima et Kaburaki, 1916) is a non-stenothermal species, common in Hokkaidô (including all of the adjacent islands), Northern Japan, except in the alpine region. It is also distributed in Aomori Prefecture in the northernmost part of Honshû. To the south, its range is bounded by a line from the base of the Tsugaru Peninsula, over Mt. Iwaki, Mt. Shirakami, Mt. Tashiro, Lake Towada, Mt. Hakkôda, the Natsudomari Peninsula, to the west of Mutsu and Ôhata in the Shimokita Peninsula. In Russia, the species is recorded only from the southern part of Sakhalin. Seidlia schmidti (Zabusov, 1916) is a stenothermal species found in cold-water biotops. It occurs in the North and East of Hokkaidô including the Shiretoko Peninsula and Rishiri Island. In Russia, the species is recorded from the southern part of Sakhalin, Primorskiy, Habarovsk including the base of the Chukotskiy Peninsula, and the Kamchatka Peninsula (and Bering Island).     

Geographical distribution of Phagocata vivida in the Far East

Phagocata vivida (Ijima et Kaburaki, 1916) is common in cold-water habitats in mountainous and hilly regions in Japan; in Northern Japan it occurs in lowland areas. Comparative studies of the material from South Korea and Primorskiy in Northeast Siberia, Russia, show that Ph. vivida is distributed widely in these geographic areas. Phagocata miyadii Okugawa, 1939, reported from North Korea and Northeastern China is a synonym of Ph vivida. Geographical distribution of this species in the Japanese Islands now becomes very clear. Judging by its geographical and vertical distributions, the species probably is a preglacial faunal element that entered Japan by the northern route to Old Honshû Island along the coast of the Old Sea of Japan.     

Studies on the speciation of the European freshwater planarians Polycelis nigra and Polycelis tenuis based on the analysis of enzyme variation by means of iso-electric focusing

Polycelis nigra Ehrenberg and Polycelis tenuis Ijima differ morphologically and karyologically. No difference, however, was found in the isozyme pattern of malate dehydrogenase and tetrazolium oxidase, indicating a close relationship. Most sibling species differ at half of the loci.It could be deduced that the reproductive behaviour of a single population of Polycelis nigra in a Dutch pond was not panmictic. Two genetically different strains retained their identities during two years of observation. If pseudogamy occurs in this diploid planarian, the presence of heterozygous specimens indicates the absence of a true meiosis.The iso-electrofocusing technique by which these population-genetical studies were carried out, also lends itself to a comparison of overall protein banding patterns. The membrane proteins especially are conservative. The sodium dodecyl sulphate extracted proteins of Polycelis nigra-tenuis, Planaria torva and Phagocata vitta were very similar, while their water soluble proteins were not. This technique may be of great help in taxonomic studies of the higher taxa.     

Karyology of four land-planarian species of the genus Bipalium from Japan

We have employed a new scale for characterizing chromosomal forms in the karyotypes of four species of Bipalium from five localities in Japan. Specimens of Bipalium nobile Kawakatsu et Makino, 1982, from Yokohama had a diploid chromosome number of 2x = 10 (2m + 2sm + 2sm + st & sm + 2sm); specimens of the same species from Toyonaka had this number as well but with slightly different chromosomal form (2m + 2sm + sm & st + 2st + m & sm). An undescribed species from Sanjô, Bipalium sp. 2, with two dorsal stripes and a yellow head crescent, had 2x = 10 (2m + 2sm + 2sm + 2sm + 2m); and another undescribed species from Chichijima Island, Bipalium sp. 3, with five dorsal stripes, had 2x = 10 (2m + 2sm + 2sm + 2sm + 2m). A non-sexual bipaliid tentatively identified as Bipalium kewense Moseley, 1878, from Chichijima Island had 2x = 18 (2m + 2m + 2m + 2sm + 2st + 2sm + 2sm + 2sm + 2sm).     

Taxonomy and geographical distribution of Dugesia japonica and D. ryukyuensis in the Far East

Dugesia japonica Ichikawa et Kawakatsu, 1964, is a common and polymorphic species of freshwater planarian distributed widely in the Far East. In 1976 the geographic populations were separated into 2 subspecies (D.j.japonica and D.j. ryukyuensis). The taxonomy of this species is reconsidered once again from the morphological, anatomical, histological, and karyological viewpoints. From the result of these studies, D.j. ryukyuensis is elevated to the rank of species: D. ryukyuensis Kawakatsu, 1976. D. japonica (n = 8, 2x = 16, 3x = 24) differs from D. ryukyuensis (n = 7, 2x = 14, 3x = 21) in having an asymmetrical penis papilla without a well-developed valve surrounding its basal part, and a well-developed vagina (distribution: the Japanese Islands, Taiwan, the Korean Peninsula, China, and Primorskiy, Northeast Siberia, in Russia). D. ryukyuensis is characterized by an asymmetrical penis papilla with a well-developed valve surrounding its basal part, and a less-developed vagina (distribution: the Southwest Islands of Japan).     

Distribution,abundance, and size of rhabdoids in Dugesia polychroa. (Turbellaria: Tricladida)

The ontogenetic changes in the distribution, abundance, and size of rhabdoids were examined in an undisturbed laboratory population of Dugesia polychroa. Irrespective of triclad age, rhabdoids in the epidermis and parenchyma were more abundant on the dorsal than the ventral side of the body. No significant differences were found in the abundance of epidermal or parenchymal rhabdoids among the anterior, medial, and posterior regions of the body. Rhabdoid number and size changed significantly with triclad age, with a marked depression coinciding with the onset of cocoon production. Rhabdoid discharge was correlated with physical and/or physiological disturbance and occurred in the absence of any overt environmental disturbance. Simple allometric relationships were observed between rhabdoid size and number on one hand and body plan area on the other. Different allometric trends were observed from field-collected individuals compared to the undisturbed laboratory population. The potential function of rhabdoids in the Tricladida is discussed in light of these findings.     

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.     

Further survey of chromosomal polymorphisms in the freshwater planarian Polycelis auriculata

Although the chromosomal number of Polycelis (Seidlia) auriculata Ijima et Kaburaki is basically 2n = 6, this species shows remarkable chromosomal polymorphisms in different populations. Among worms collected at 30 stations in the central part of Japan's Main Island and in Hokkaido, we found five new karyotypes, considered to be variations of tetraploidy and diploidy: 4n?fis¹. + 1 = 3SM + 2A + 3T₁ + 2T₂ + 4M = 14, 4n?fis².(B) = 2SM + 2A + 4T₁ + 2T₂ + 4M + (0?2B) = 14 –16, 4n?fis². + 1 = 2SM + 2A + 4T₁ + 2T₂+5M= 15, 4n?fis².?2 = 2SM + 2A + 4T₁ + 4M = 12, and 2nM- = 2SM + 2A = 4 (where SM = submetacentric; A = acrocentric; T₁ and T₂ = telocentric; M = metacentric; B = B-chromosome; fis¹. and fis². = occurrence of one or two centric fissions, respectively; and M- = deletion of a metacentric chromosome). These karyotypes exist singly in one individual or as various mixoploids within the same individual. No individual having only karyotype 2nM- has yet been found. This brings the total number of known karyotypes in P. auriculata to 17; these can be arranged in an order that we believe reflects their evolution.     

Variation in karyotypes of Dugesia japonica japonica (Turbellaria) from Ôsaka Prefecture,Central Japan

An analysis of the karyotypes of Dugesia japonica japonica Ichikawa et Kawakatsu, 1964, from 30 localities of seven river systems in Ôsaka Prefecture, Central Japan, revealed a total of 26 karyotypes of which 12 are new-found varieties. More than two karyotypes were found in many localities. The mixoaneuploidic triploid karyotype showed the widest distribution (21 localities), orthoploidic diploid karyotype and orthoploidic mixoploid of diploid and triploid karyotype were next (13 localities, respectively), and other karyotypes (triploidic aneuploid, orthoploidic triploid and mixoploid of triploid & tetraploid) were also found. Some correlation of karyotype with elevation was also detected.     

The karyotypes of Dugesia species from Spain (Turbellaria,Tricladida)

Some species of Planarians, new to Spain, are recorded. Dugesia polychroa, D. sicula, D. iberica and D. gonocephala s. 1. have been investigated karyologically. The former possesses a diploid complement characteristic of the biotype A (2n = 8); the second is diploid with 2n = 18; diploidy and triploidy were found in sexual populations of D. iberica with n = 8. Triploidy occurred in all the asexual strains of the D. gonocephala group with a basic number of either 8 or 9. In this latter case B-chromosomes were occasionally found.     

Taxonomic studies on marine triclads (Turbellaria,Tricladida, Maricola)

The genus Procerodes forms a heterogeneous assemblage of taxa. Although it is premature to attempt phylogenetic weighting of the characters, the genus contains three well delimited subgroups, one with a subantarctic, panaustral distribution, one world-wide in distribution, and one occurring principally in the northern hemisphere. Outside of these subgroups, species in this genus are problematic since a number of their features also occurs in other procerodids. All recognized groups exhibit a wide distributional range. Many of the world-wide taxonomic relations lie on the species level and some at the level of genera. Poor dispersal capacity of extant species of Procerodes suggests that the biogeographic patterns may be very old.     

Chromosomes of Temnocephala minor,an ectosymbiotic turbellarian on Australian crayfish found in Kagoshima Prefecture,with karyological notes on exotic turbellarians found in Japan

Records of exotic turbellarian species found in Japan are reviewed from taxonomic and karyological viewpoints. Temnocephala minor Haswell, 1888, an ectocommensal on a freshwater crayfish of Australia, was found from culture ponds of Cherax tenuimanus (introduced from W. Australia) in Kagoshima Prefecture. T. minor had the chromosome number of 2x = 18 (2sm + 2m + 2m + 2sm + 2m + 2m + 2m + 2sm + 2m). The following 3 species of exotic freshwater triclads were recorded from tanks and ponds used for tropical fish culture: Dugesia austroasiatica Kawakatsu, 1985 (2x = 16), Dugesia tigrina (Girard, 1850) (2x = 16) and Rhodax? sp. (3x = 24; 3x = 24 &; 3x + 1LB + 1SB = 25 + 1SB). The following 3 species of exotic terrestrial triclads were recorded: Bipalium nobile Kawakatsu et Makino, 1982 (2x = 10), Bipalium kewense Moseley, 1878 (2x = 18), and Platydemus manokwari de Beauchamp, 1962 (n = 6, 2x = 12). An extensive occurrence of P. manokwari in the Southwest Islands of Japan may be due to an unexpected introduction of the animal in very recent years.     

Karyological and taxonomic studies of Dugesia japonica Ichikawa et Kawakatsu in the Far East

A review of previous studies on the taxonomy, karyology and chorology of a polymorphic species Dugesia japonica from the Far East is presented. Two subspecies are now known: D. j. japonica (n = 8, 2x = 16, 3x = 24) and D. j. ryukyuensis (n = 7, 2x = 14, 3x = 21). An attempt has also been made to determine the definition of the B-chromosome as LB and SB and the variation of the karyotypes of both subspecies is described. Every known karyotype of D. japonica is classified into six groups (see Table 2). D. japonica from many localities has a diploid karyotype (2x), a triploid karyotype (3x) and an orthoploidic mixoploid karyotype of 2x & 3x. The origin and the karyological significance of these karyotypes are discussed.     

Ploidy, geographical distribution and morphological differentiation of Parasenecio auriculata (Senecioneae; Asteraceae) in Japan

Parasenecio auriculata is a woodland perennial herb widely distributed in Northeastern Asia, constituted by a poorly understood polyploidy with a diploid (2n=2x=60) and a tetraploid (2n=4x=120). In this study, for a better understanding of the polyploidal evolution, cytogeography and morphological variation were analyzed in Japanese P. auriculata, including two varieties; var. bulbifera endemic to central Hokkaido and var. kamtschatica widely distributed in northern Honshu and Hokkaido. The occurrence of two polyploidal levels was reconfirmed. While var. bulbifera is predominantly tetraploid, var. kamtschatica is comprised of diploid and tetraploid. Morphological variation among 22 quantitative characteristics is continuous and not distinctive among cytotypes or varieties, but plant size tended to be larger in the order, diploid of var. kamtschatica, var. bulbifera, and tetraploid of var. kamtschatica. The cytotype distribution showed a conspicuous geographical pattern. Besides var. bulbifera endemic to the central Hokkaido, the diploid of var. kamtschatica is mainly found in Southern Hokkaido, and the tetraploid has a disjunct distribution in eastern and northern Hokkaido and northern Honshu. Such a geographical pattern is possibly attributable to the differentiation of climatic preference among cytotypes and varieties, and may have been established in association with the climatic cline along the Japanese archipelago.     

Karyological and taxonomic studies of Dugesia japonica from the Southwest Islands of Japan-II

The karyotypes of Dugesia japonica from the southern part of the Southwest Islands of Japan (the Nansei Shotô) include diploidy, triploidy, mixoploidy, and mixoaneuploidy. Animals having karyotypes based on n = 8 were found on Okinawa Island, Ishigaki Island, Iriomote Island, and Yonaguni Island, while animals having karyotypes based on n = 7 were found on Okinawa Island, Miyako Island, and Ishigaki Island. Toward the northern end of this island chain, at Tanegashima Island, Yakushima Island, and Amami-Ôshima Island, karyotypes based on n = 8 occurred; and on one of these, Tanegashima Island, n = 7 also occurred. Our data provide further support of the karyotypical distinction between the two subspecies of D. japonica: D. j. japonica has karyotypes based on n = 8 and D. j. ryukyuensis has karyotypes based on n = 7. Taking into consideration the geological history of the Southwest Islands and the ties of their faunas to those of adjacent areas, we can explain the current geographical distribution of the two subspecies in these islands as the result of two separate invasions by D. japonica, one in the Miocene and one after the early Quaternary.     

Geographical distribution and cytological variation ofLemna paucicostata Hegelm. in Japan

More than 100 strains ofLemna paucicostata Hegelm. collected from various localities in Japan were classified into 4 types according to the criterion of Yukawa and Takimoto (1976). N-1 type strains are widely distributed in Hokkaido, Honshu, Shikoku and Kyushu, N-2 type strains only in the area on the Japan Sea side of north Japan, K type strain only at the campus of Kyoto University, and S type strains in southern Japan. Numbers of chromosomes in somatic cells of N-1, N-2, K and S type strains were 2n=66–84, 40, 50 and 40, respectively. In N-2 and S type strains, all chromosomes (20 bivalent chromosomes) were lined up on the equatorial plate at metaphase of the first meiotic division (MI). However, in N-1 type strains, several chromosomes, and in the K type strain, more chromosomes were away from the equatorial plate at MI. Pollen fertility was 60–70%, higher than 90%, 0% and higher than 90%, in N-1, N-2, K and S type strains, respectively.     

New records of the carabidicolous Laboulbeniales (Ascomycetes) of Japan (II)

Six carabidicolous species of Laboulbeniales are reported as new for the Japanese mycoflora. They areLaboulbenia finitima, L. separata, L. borneensis, L. manubriolata, Dimeromyces caribaeus, andDixomyces ornatus. In Japan, the former three species are parasitic onMochtherus luctuosus and the latter three species onPerigona nigriceps. Laboulbenia finitima occurs on the left legs (tarsi and tibiae);L. separata on the left elytral margin:L. borneensis on the pronotum;L. manubriolata on the pronotum and elytra;Dimeromyces caribaeus on the right inferior posterior surface of the prothorax (pronotal hypomeron); andDixomyces ornatus on the outer margin of the right elytron. Comments and photographs are given for each fungus.     

Studies on the speciation of Japanese freshwater planarian Polycelis auriculata based on the analysis of its karyotypes and constitutive proteins

Various kinds of chromosomal polymorphisms or karyotypic variations are found in the Japanese freshwater planarian Polycelis auriculata. Within this species, there are found worms whose chromosome numbers are 2n = 6, 10, 11, 12 and others, and 3x = 6 and 9. There are some which have cells with triploidy and tetraploidy complements (3x = 6 & 4x = 8), and others which have cells with triploidy and hexaploidy complements (3x = 6 & 6x = 12). These worms with such varied karyotypes are usually found in separate habitats, though occasionally they occur together. Electrophoretic analysis of the proteins extracted from the karyotipically different worms which belong to three different local populations shows some dissimilarity in the constitutive proteins according to their karyotypic differences. The results obtained suggest that this species is still in the process of speciation or chromosomal evolution.     

Materials for the fungus flora of Japan (53)

Two interesting ascomycetes are described as new to Japan:Ascotricha amesii (Xylariaceae), isolated from garden soil in Osaka; andAuxarthron reticulatum, isolated from forest soil in Tokyo. ADicyma anamorph is associated with the former species. (52): Tubaki, K., Tokumasu, S. and Konno, M., Nippon Kingakukai Kaiho38: 249–250. 1997.     

An electron-microscopic study of syncytium formation during early embryonic development of the freshwater planarian Bdellocephala brunnea

To substantiate the assumption that the egg cell and blastomeres in planarian embryos influence surrounding yolk cells to form a syncytium, embryos at 1- to 8-cell stages were examined by electron microscopy. Within special areas of the endoplasmic reticulum both in the egg cell and in the blastomeres, a large number of vacuoles of various sizes formed and then disappeared at least four times over the period from egg-laying through the 8-cell stage as if their contents were being secreted. These activities diminished markedly at the 8-cell stage. Yolk cells surrounding the egg cell and blastomeres were aggregated in close contact with one another in a small clump shortly after egg-laying, and then, late in the 4-cell stage, became fused, forming a syncytium. The correlation between release of vacuoles by the egg cell and blastomeres and the formation of a syncytium by the yolk cells indicate that the cell fusion could be induced by a factor contained in the vacuoles.