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In this study the rich variety of fossil microorganisms and other ultrastruchlres in the Messel oil shale is documented. The taphonomy of the micro- and the macro organisms is discussed and a basic model for microbial life in the Eocene Lake Messel is proposed. Documentation of the Messel microbiota was made using a scanning electron microscope fitted with an energy-dispersive X-ray analyzer, and a transmission electron microscope. The most common objects discovered were fossil bacteria in the form of cocci, coccobacilli, bacilli, curved rods and filaments, preserved as moulds, crusts, casts, encrusted casts and clay-coated casts. The main lithifying mineral is apatite, followed by siderite. The bacteria occur on fossil remains of macroorganisms. Sideritic bacteria are usually found on keratinous substrates, whereas apatitic bacteria occur preferentially on fish remains. Lithification of the bacteria was selective. It is suggested that the preserved bacteria were heterotrophic, Gram-positive anaerobes, which may have belonged to the group of clostridians.
The family Cimicidae consists of 6 subfamilies, 23 genera, and 91 species. Nineteen new species names, one new species, and one new genus have been proposed since the monograph by Usinger was published in 1966. A checklist includes the world cimicid fauna with sinonymy. A selected bibliography is concerned with cimicids as potential disease vectors; the bibliography is a comprehensive treatment of the cimicid literature of the Americas and islands of the Pacific, Atlantic and Indian Oceans.
Nine genera of phytoseiid mites with 22 species are described and illustrated on the basis of a survey of the literature, and by examination of material from orchards and their surroundings and of material from museum collections. Males, if available, are also described and figured. In addition to the species listed for the Netherlands, six species from around orchards in East Germany, Belgium and Poland were described briefly, and related species from other European countries (especially the British Isles and Germany) are noted. For each genus, a key to species (adult females) is given. For each species, a diagnosis is presented, and taxonomic problems are discussed for the following taxa: PhYloseius macropilis (Banks); Amblyseius reduclus Wainstein; A. cucumeris (Oudemans); A. masseei (Nesbitt); A. pOlentillae (Garman); A. rademacheri Dosse; A. isuki Chant. Keys are based on easily recognizable features and are aimed at "the interested non-taxonomist".
This paper aims to compile an exhaustive list of the behavioral patterns exhibited by the chimpanzees of the Mahale Mountains National Park, Tanzania. The compilation is based on the glossary compiled by Goodall (1989), but a substantial numbers of new terms have been added. Thus, we list 316 simple anatomical terms, 81 complex anatomical terms, 37 simple functional terms, and 81 complex functional terms, in addition to 116 synonyms. The behavioral patterns are divided into eight categories on the basis of degree of universality: (1) commonly seen in both Homo and two species of Pan, (1?) commonly seen in Homo and only one species of Pan, (2) patterns common to the genus Pan but not to Homo, (3) patterns common to the chimpanzee Pan troglodytes but not the bonobo Pan paniscus, (4) patterns common to eastern (P.t. schweinfurthii) and central (P.t. troglodytes) but not western (P.t. vents) chimpanzees, (5) patterns unique to the eastern chimpanzees, P.t. schweinfurthii, (6) patterns unique to the population of Mahale, (7) patterns unique to many individuals (at least most members of an age/sex class) of M group chimpanzees, (8) patterns limited to a single (idiosyncrasy) or a few individuals of M group. It is most likely that the behavior patterns of the last common ancestor of Homo and Pan are found in Categories 1 and I? and less likely in Categories 2 and 3. It is possible that behavior patterns belonging to Categories 5, 6 or 7 are cultures.
È stata effettuata una revisione sistematica sulle specie del genere Genista in Italia. L'indagine ha permesso di accertare la posizione tassonomica delle diverse entità che rappresentano il genere nel territorio italiano. In questa prima nota sono riferiti i risultati emersi dallo studio delle entità di sezioni a prevalente distribuzione in opposte zone del bacino del Mediterraneo e precisamente Erinacoides Spach del Mediterraneo occidentale ed Ephedrospartum Spach, Aureospartum sect. nova del Mediterraneo centrale. La sezione Erinacoides é rappresentata da G. salzmanii DC. in Sardegna e in Corsica, G. pichisermolliana sp. nov. in Sardegna, G. aspalathoides Lam. in Sicilia, Pantelleria, Africa settentrionale, G. desoleana Valso in Liguria, Toscana, Elba, Corsica e Sardegna, G. arbusensis Vals., G. sulcitana Valso e G. toluensis Valso in Sardegna. La sezione Aureospartum (sect. nova) comprende solo l'endemica sardo-sicula G. aetnensis (Raf.) DC. e l'Ephedrospartum racchiude G. ephedroides DC. presente in Sardegna, G. thyrrena Valso nell'arcipelago ponziano, G. gasparrini in Sicilia e G. cilentina Vals. in Campania e in Sicilia.
1. The migration of the spotted mackerel, Pneumatophorus tapeinacephalus distributing in the coastal sea of Japan was investigated in relation to the geographical distribution of the fishing grounds, seasonal change of fishing condition. sea conditions and fork length. Secondarily, some anatomical and histological observations were carried out on spotted mackerels caught in the coastal sea area around Kagoshima and its vicinity to clarify the sex differentiation and the seasonal cycle of the gonads. 2. Spotted mackerels are distributed throughout a wide sea area stretching from north of Formosa to the south of Japan Sea. including the Pacific coastal sea from Kyushu to Chiba Prefecture. The northern limit of the distribution area is assumed to be the sea areas off San-in and Chosi. 3. The schools of adult fish make a feeding migration to the circumference of Saishu Island and to the sea area off Ashizuri cape in summer. and these schools make a spawning migration toward the sea area around the Osumi Islands and the southern area of the East China Sea in winter. 4. In winter some schools of adult fish remain living in the sea area south of the Izu Islands. These schools belong to a group isolated incompletely from that of the East China Sea. as some of them are those which came from the East China Sea. 5. The larvae grow while they are being brought by the sea current or tide current. When they have reached 50~60mm. in total length. they aggregate in schools and approach the coast. In spring they swim in the coastal nursery grounds. 6. From summer to autumn, the schools of the young fish make a feeding migration to the sea off San-in and to the eastern coastal sea of Chiba Prefecture. In winter. they make a seasonal migration to the coastal sea of South Kyushu, the East China Sea and the southern sea area of the Izu Islands. 7. The range of vertical distribution of the larvae is supposed to be the layer from the surface to 40m. in depth. The vertical distribution of the adult fish is chiefly in the layer, 40-70m. in depth, during the period from late autumn to early spring. It becomes shallower in late spring and summer, the depth being about 20-40m. 8. The ranges of water temperature and salinity in the sea where the adult fish schools are distributed are 17.0-26.0°C and 34.0~34.8%0. respectively. 9. The spawning takes place during the period from the end of January to June in the southern part of the East China Sea and the sea areas around the Osumi Islands, off Ashizuri Cape and around the Izu Islands. These spawning grounds are sea areas where a comparatively rapid current is running towards a land shelf. 10. The ranges of the optimum water temperatures and salinities for the spawning are assumed to be 17-23°C and 34.0-34.8 0/00, respectively. 11. The primordial germ cells seem to migrate to the gonad by amoeboid movement from other places than the gonad. 12. The early indifferent gonad is very slender and suspended with a mesogonium, in the coelom. It is composed of peritoneal epithelium, stroma cells and primordial germ cells. 13. The formation of the gonocoel begins as a longitudinal depression on the surface of the gonad, facing the mesentery. This depression takes place in the gonad of the fish, about 60mm. in fork length, prior to the sex differentiation. 14. The sex differentiation occurs directly without a phase of a juvenile hermaphrodite. 15. The gonad in which the gonocoel is greatly enlarged becomes an ovary, while that in which the gonocoel is left narrow becomes a testis. 16. In the early ovary the layer containing oogonia is surrounded with stroma cells. The surface of the ovary is covered with cuboidal epithelium. 17. In the ovary of the fish, 100-130mm. in fork length, the wall of the ovocoel forms small protuberances, which become the lobes of the ovary. The oocytes are situated in these lobes. The yolk formation begins in the oocytes, 15.....,20.a in diameter, 18. The maturing process of eggs is clasified into the following 7 stages; the chromatin nucleolus, the peripheral nucleolus, the yolk vesicle, the early yolk globule, the late yolk globule, the migrating nucleus and the matured stage. Ovarian eggs at the migrating nucleus stage and the matured stage are observed in the fish, more than 300mm. in fork length. 19. The surface of the early testis is covered with peritoneal epithelium. The interior is filled up with the multiplied stroma cells and the spermatogonia scattered among them. In the testis of a somewhat later stage, a lot of branches are stretched out of the testocoel. Some of the spermatogonia are arranged directly beneath the peritoneal epithelium and the others are buried deep in the testis. The testis lacks a layer of stroma cells under the peritoneal epithelium. 20. In the testis of young male fish the spermatogonia increase in number and surround the small branches of testocoel; they form seminiferous tubules. The testocoel and its large branches become the rete apparatus constructed of collecting ducts. The maturation division appears in the testes of the fish more than 280mm. in fork length. 21. The sex ratio of the young fish is approximately 1 : 1. The ratio between the gonad length and the fork length shows an exponential increase. The gonads of adult fish are enlarged about 9-13 % of the original length during the spawning season. 22. During the months from July to November the oocytes in the ovaries of adult female :fish are at the chromatin nucleolus stage and the peripheral nucleolus stage. During the same season there are only spermatogonia in the testes of adult male fish. The gonads of adult fish begin to increase in size in December and become the largest in March and April. The increase in size of the ovary is chiefly due to the enlargement of ova on account of yolk deposition. The increase in size of the testis is due to accumulation of spermatozoa. 23. A few oogonia can be seen m the ovanes of adult female fish during and immediately after spawning. Numerous spermatogonia appear along the inner walls of the seminiferous tubules late in the spawning season.
Die Pilzgattung Hygrocybe wird taxonomisch besprochen, wobei die bisherige Sektion Oreocybe Boertmann (subgenus Cuphophyllus) den Status einer eigenen Untergattung erhält. Ein Bestimmungsschlüssel zur Gattung wird vorgelegt, wobei Gruppen sehr ähnlicher Arten, die früher teilweise nicht getrennt wurden, im Hauptschlüssel zu Aggregaten zusammen gefaßt wurden. Diese Aggregate werden getrennt aufgeschlüsselt. 50 europäische Arten der Gattung Hygrocybe werden schließlich hinsichtlich ihrer Morphologie, Taxonomie, Ökologie und Verbreitung vorgestellt.