In 1990–1991 the LITHOPROBE project completed 450 km of seismic reflection profiles across the late Archaean crust of the southwestern Superior province. The results define a broad three-fold division of crust: upper crust in the Abitibi greenstone belt is non-reflective and is a 6–8 km veneer of volcanic and plutonic supracrustal rocks, whereas, in the sediment-gneiss dominated Pontiac subprovince, upper crust comprises shallow northwest-dipping turbidite sequences; mid-crust, in both the Abitibi and the Pontiac subprovinces, is interpreted as imbricate sequences of metasedimentary and metaplutonic rocks; lower crust in both subprovinces has a horizontal layer parallel strycture which may represent interleaved mafic-intermediate gneisses. The seismic signature of the northern Abitibi greenstone belt may be represented in an exposed 25 km crustal section in the Kapuskasing stuctural zone.
Preliminary tectonic models based on the seismic data are consistent with a plate-tectonic scenario involving oblique subduction and imbrication of sedimentary, plutonic and volcanic sequences. The northern Abitibi supracrustal sequences either represent an allochthon, or overlie an allochthonous underthrust metasedimentary and plutonic sequence which may be equivalent to a metasedimentary subprovince such as the Pontiac or Quetico.
Seismic velocities have yet to be defined. However, crustal thicknesses are relatively constant at 35–40 km. The thinnest crust is adjacent to the Grenville Front where Moho is very well defined. 相似文献
Abstract Fossil pinnipeds in the extinct otariid subfamily Allodesminae are large, relatively highly evolved marine carnivores that became abundant and diverse in Middle Miocene time and were restricted to the North Pacific Ocean. Their record extends from early Middle Miocene through Late Miocene, with records from California, Oregon, Washington, Baja California and Japan. Allodesmines are characterized by extreme sexual dimorphism, a large orbit, retracted orbital margin of the zygomatic arch, a deeply mortised jugal-squamosal junction, wide palate, bulbous cheek tooth crowns, nearly flat tympanic bulla with wrinkled ventral surface, a large tympanohyal fossa, large ear ossicles and deep mandible. Eleven allodesmine species are known (eight of which are named), in at least four genera, and most belong to the typical genus Allodesmus Kellogg, 1922. The earliest and most generalized allodesmine known is from the early Middle Miocene (ca 16 Ma) Astoria Formation in coastal Oregon. The last known records are from Late Miocene rocks (ca 10 Ma) in California and Washington. New taxa proposed here are: the genus Brachyallodesmus Barnes and Hirota, to contain Allodesmus packardi Barnes, 1972; the genus Megagomphos Hirota and Barnes, to contain Allodesmus sinanoensis (Nagao, 1941); the species Allodesmus sadoensis Hirota, (Middle Miocene, Japan); the species Allodesmus megallos Hirota (Middle Miocene, Japan); and the species Allodesmus gracilis Barnes (Middle Miocene, California). Additionally, the genus Atopotarus Downs, 1956, and the species Allodesmus kelloggi Mitchell, 1966, are resurrected. Allodesmines were apparently a rapidly evolving group, and most appear to have been adapted to roles later filled by otariine, dusignathine and imagotariine otariids, and the Phocidae (true seals). They became extinct in Late Miocene time and left no living descendants. Although some of their characters evolved convergently with various living species of the pinniped family Phocidae, Allodesminae are an otariid group and not part of the evolutionary history of Phocidae. 相似文献
Abstract The fossil pinniped record of the North Pacific Ocean includes both Phocidae and Otariidae ( sensu lato ), extends from the Late Oligocene to the Late Pleistocene, is taxonomically diverse, and is constantly becoming more complete owing to additional important discoveries. The earliest and most diverse fossil pinnipeds in the North Pacific are otariids, the phocids not appearing until the latest Pliocene. The theoretical center of otariid pinniped evolutionary history has been considered by some to be in the eastern North Pacific. New materials from the western North Pacific, however, including representatives of the subfamilies Enaliarctinae, Imagotariinae, Odobeninae and Otariinae, indicate that pinniped evolutionary patterns were basin-wide phenomena, and that a more complete record undoubtedly would reveal numerous trans-Pacific distributions. This would be expected considering the distributions of living species. The paucity of fossil Phocidae and their absence from pre-Pliocene deposits are consistent with theories that the family primarily evolved outside the North Pacific. 相似文献
Abstract The Cetacea are the most diverse and highly aquatically adapted group of mammals. Their fossil record extends back at least to the Middle Eocene ( ca 50 Ma), and they will possibly be found earlier, judging by the relatively highly evolved nature of the earliest known whales. The most likely terrestrial ancestors of whales are the mesonychids, primitive hoofed mammals with omnivorous diets. Recently discovered archaeocetes with large, mesonychid-like heads and dentitions and functional hind limbs reconfirm earlier ideas about the mesonychid origin of cetaceans and the amphibious nature of the earliest transitional forms. Fossil cetaceans are relatively abundant and diverse thoughout the world, and are now known from every continent, including Antarctica. Odontocetes evolved echolocation to locate food. Mysticetes developed bulk feeding adaptations. Both undoubtedly evolved from archaeocetes, and the monophyly of Cetacea is the most parsimonious present hypothesis. Chromosomal and molecular evidence has taken an increasingly important role in determining cetacean relationships, but fossils and classical comparative morphological studies remain a necessary and pivotal source of information about cetacean phylogeny. 相似文献
Abstract Fossil whales in the very rare, primitive, extinct cetacean family Aetiocetidae are small, relict, toothed mysticetes that persisted into Late Oligocene time after more highly derived baleen-bearing mysticetes had already evolved. No known aetiocetid could be ancestral to baleen-bearing mysticetes, but aetiocetid morphology is in many ways intermediate between archaeocetes and baleen-bearing mysticetes, demonstrating the probable transitional steps passed through in the evolution of baleen-bearing mysticetes. Their discovery indicates that mysticetes evolved from Archaeocetes, and supports theories of the monophyly of Cetacea. Late Oligocene aetiocetids have been found on both sides of the North Pacific Ocean: on Vancouver Island, British Columbia, Canada; in Oregon and Washington, USA; in Baja California Sur, México; and the islands of Kyushu and Hokkaido, Japan. The most primitive North American aetiocetid, Chonecetus sookensis Russell, 1968, is from the early Late Oligocene Hesquiat Formation on Vancouver Island, British Columbia, Canada. A more derived, Late Oligocene species, Chonecetus goedertorum Barnes and Furusawa, new species, from the Late Oligocene Pysht Formation, Olympic Peninsula, Washington, has the primitive placental mammalian tooth count of 11/11. The type genus of the family, Aetiocetus Emlong, 1966, has as its type species, A. cotylalveus Emlong, 1966, known only from the Late Oligocene Yaquina Formation on the coast of Oregon. It has 11 upper teeth on each side of the rostrum. A more derived species, Aetiocetus weltoni Barnes and Kimura, new species, from a higher stratigraphic level in the Yaquina Formation, has a more posteriorly positioned cranial vertex and a tooth count of 11/12. We describe four new species of aetiocetids in three genera from the Late Oligocene Morawan Formation near Ashoro, Hokkaido, Japan. The most primitive, Ashorocetus eguchii Barnes and Kimura, new genus and species, has a primitive stage of cranial telescoping, and is closely related to Chonecetus Russell, 1968. Another, Morawanocetus yabukii Kimura and Barnes, new genus and species, in some ways intermediate between Chonecetus and Aetiocetus, has a suite of unique derived characters, including a much foreshortened brain case. The third, Aetiocetus tomitai Kimura and Barnes, new species, is the most primitive species of Aetiocetus yet discovered. The fourth, Aetiocetus polydentatus Sawamura, new species, the most derived species of Aetiocetus known, has a highly telescoped cranium, homodonty, polydonty and a dental count of 13–14/14–15. The fossil record now indicates considerable diversity in the family, with several different contemporaneous lineages in three new subfamilies: Chonecetinae, Morawanocetinae and Aetiocetinae. Aetiocetids are not known outside the North Pacific. Many Recent mysticetes are essentially cosmopolitan, and aetiocetids might have also been relatively widely dispersed. We suspect that with time their remains will be found around other ocean basins also. If so, then they may be potentially useful in trans-oceanic geological correlations. 相似文献
Peter I Øy is located in the Bellinghausen Sea, 400 km NE of Thurston Island, West Antarctica. It is a Pleistocene volcanic island situated adjacent to a former tranform fault on the continental rise of the presently passive margin between the Pacific and Antarctica. New K-Ar age determinations ranging from 0.1 to 0.35 Ma show that the volcanism responsible for this island took place at the same time as post-subduction, rift-related volcanism occurred in the nearby Marie Byrd Land and the Antarctic Peninsula. The rocks of the island are alkalic basalt and hawaiite, benmoreite and trachyte. The basic tocks typically contain phenocrysts of olivine (Fo61–84), diopsidic augite, and plagioclase (ca. An60). Small xenoliths are present and consist of mantle-type spinel lherzolite, cumulate clinopyroxenite and gabbro and felsic inclusions that consist of medium-grained strained quartz, plagioclase, and abundant colorless glass. Chemically, the basic rocks are characterized by rather high MgO (7.8–10.2 wt.%) and TiO2 (3.1–3.7 wt.%) and relatively low CaO (8.4–9.5 wt.%) contents. They have steep REE patterns, [(La/Yb)N = 20] with HREE only 5 x chrondrite. Y and Sc are almost constant at relatively low levels. Compatible trace elements such as Ni and Cr show considerable variation (190–300 and 150–470 ppm, respectively.), whereas V shows only little variation. Sr and Nd isotope ratios vary slightly with 87Sr/86Sr averaging 0.70388 and 143Nd/144Nd 0.512782, both typical for ocean island volcanism. Lead isotope ratios are consistently high in basalts; 206Pb/204Pb = 19.194, 207Pb/204Pb = 15.728 and 208Pb/204Pb = 39.290, whereas benmoreïte is somewhat less radiogenic. Oxygen isotope analyses average δ18O = +6.0‰. Incompatible trace elements vary by a factor of 1.5–2.0 within the range of the basic rocks. It is proposed that the incompatible trace-element variations represent different degrees (<10%) of partial melting, and that these melts were later modified by minor (<15‰) olivine and spinel fractionation. The very small variation in Y (and Sc) and the very fractionated REE pattern indicate that the source had an Y- and HREE-rich residual phase, most probably garnet. Furthermore, it is suggested that the source was slightly hydrous and that melting took place at 18–20 kbar. Trachyte was derived by multiphase fractionation of ne-normative basalts, and benmoreite from hy-normative parental liquids. The rocks of Peter I Øy are generally of the same type and age as those outcropping in extensional regimes on the nearby continent, and therefore, these occurrences may be related to each other in some way. However, the Peter I Øy rocks are considerably more radiogenic in strontium and less radiogenic in neodymium than the rocks of the Antarctic Peninsula and Marie Byrd Land. Possible explanations are that Peter I Øy represent asthenospheric hot spot activity, or transtensional rifting as subduction ceased. 相似文献
The relationship between the sill of the variogram and the sample variance is explored. The common practice of using the sample variance as an estimate of the variogram sill is questioned, and a conceptual framework for determining the appropriateness of this heuristic is constructed. 相似文献
Prior to the penetration of the European capitalist economy into central and northern Australia, the Aboriginal mode of production was one of hunting and gathering. Spiritual, economic and social relationships betwen people and land produced a spatial distribution of small bands of people living on their traditional lands. To the incoming white settlers the low population density and type of land use appeared uneconomic. This observation was used as ideological justification for the expropriation and development of the land for commercial pastoralism. This paper discusses the articulation of the Aboriginal and European modes of production in the East Kimberley region of northwest Australia. It argues that the introduced capitalist economy virtually destroyed the Aboriginal means of subsistence, incorporating Aborigines into the new mode of production within various subordinate roles. The exploitation of Aborigines, formerly as labour and now predominantely as consumers, is fundamental to the maintenance of the capitalist mode of production in pastoral areas. The spatial effects of the dominant mode of production have been to centralise Aborigines in locations suited to the various phases of development of the European economy, undermining the traditional Aboriginal social-spatial structure. The centralisation of the Aboriginal population also enhances the opportunities for the further development of the mining industry, which is in direct competition with Aboriginal interests in land. Aboriginal resistance to these spatial tendencies is intense in many quarters, but efforts to return to living on traditional lands and to develop alternative ways of living are hampered by the dominant mode of production. 相似文献
This short note presents a method for efficiently updating ordinary kriging estimates and variances when one or more additional samples are incorporated into the kriging system. First, the foundation linear algebra result is presented. Then the update equations are derived. Finally, an illustrative application of updating is briefly discussed. 相似文献