Polyunsaturated fatty acids in a lacustrine sediment as a possible indicator of paleoclimate     

Kimitaka Kawamura  Ryoshi Ishiwatari 《Geochimica et cosmochimica acta》1981,45(2):149-155

Polyunsaturated fatty acids (C_18:2 and C_18:3ω3 were analyzed in the upper 20m layer of a 200 m long sediment core taken from Lake Biwa. Concentration maxima occur in layers at depths of 0.2, 1–5, 11–12, and 16m. The vertical changes in the $\text{(C}{}_{\mathrm{18:2}}\text{C(C}{}_{\mathrm{18:0}}$ ratio appear to correlate with paleoclimatic condition suggested from palynological evidence. On the basis of $\text{C}{}_{\mathrm{18:2}}\text{C}{}_{\mathrm{18:0}}$ ratios, it was suggested that it has been colder at 200, 1000–4000, 15,000 and 20,000 yr BP than at other times.  相似文献   

Algal lipids as a possible contributor to the polymethylene chains in kerogen     

Ryoshi Ishiwatari  Tsutomu Machihara 《Geochimica et cosmochimica acta》1982,46(8):1459-1464

Lipid fraction and cell-wall materials have been separated from three types of algae (blue green, Microcystis sp.; green, Scenedesmus sp. and diatomaceous Diatoma sp.) and their KMnO₄ oxidation products (aliphatic $\text{α,ω-C}{}_2\text{-C}{}_{12}$ dicarboxylic acids; aliphatic normal C₁₄–C₂₄ monocarboxylic acids; benzoic acid and C₁₈ isoprenoidal ketone) examined by gas chromatography and gas chromatographymass spectrometry. The results suggest that the lipid material could make a greater contribution to polymethylene chains in kerogen than the cell-wall material, when the kerogens are mainly derived from algal components.  相似文献   

Generation of unsaturated and aromatic hydrocarbons by thermal alteration of young kerogen     

Ryoshi Ishiwatari  Kazuo Fukushima 《Geochimica et cosmochimica acta》1979,43(8):1343-1349

Monounsaturated, monoaromatic and polyaromatic hydrocarbons generated by artificial thermal alteration of young marine (Tanner basin, offshore California) kerogen were studied by computerized GC-MS. Their relative amounts changed with temperature (150–410°C) and time (5–120 hr) of heating as follows: Monounsaturates → Monoaromatics → Polyaromatics. Distribution of alkyl homologs of phenanthrene also changed with increasing degree of thermal alteration. These results are in agreement with those observed for crude oils and shales.  相似文献   

Early stage incorporation of biolipids into kerogen in a lacustrine sediment: Evidence from alkaline potassium permanganate oxidation of sedimentary lipids and humic matter     

Ryoshi Ishiwatari  Tsutomu Machihara 《Organic Geochemistry》1983,4(3-4)

Lipids, fulvic acid, humic acid and kerogen were isolated from a lacustrine sediment in which the organic matter is probably derived predominantly from phytoplankton (Lake Haruna, Japan). An alkaline KMnO₄ oxidation study of the organic matter showed that distributions of polymethylene chain lengths in the lipids, humic acid and kerogen fractions are almost the same. The polymethylene chains in the sediment are dominant in the kerogen, lipids and humic acid, their relative abundance estimated by the oxidation being: kerogen (42% of the total amounts of polymethylene chains estimated) > lipids (38%) > humic acid (19%) > fulvic acid (1%). It was concluded that algal lipids may have been incorporated into the kerogen and humic acid fractions after the death of the algae and during, after, their deposition.  相似文献   

Fatty acid geochemistry of a 200 m sediment core from Lake Biwa,Japan. Early diagenesis and paleoenvironmental information     

Kimitaka Kawamura  Ryoshi Ishiwatari 《Geochimica et cosmochimica acta》1984,48(2):251-266

Fatty acids (FAs), β- and ω-hydroxy acids, α,ω-dicarboxylic acids and n-alkanes were studied in a 200 m sediment core taken from Lake Biwa, Japan. FAs showed bimodal distribution with peaks at C₁₆ and C₂₂-C₂₈. Their distribution patterns clearly changed with depth from lower molecular weight (C₁₂-C₁₉) predominance to higher molecular weight (C₂₀-C₃₂) predominance in the upper 20 m interval. Analyses of related compounds (β- and ω-hydroxy acids and α, ω-dicarboxylic acids) suggest that β- and ω-oxidative degradation of C₁₂-C₁₉ FAs has occurred in the sediments.The ratio of bound C₁₂-C₁₉ to unbound FAs increases with depth in the upper 0–1 m sediments, suggesting that unbound FAs are more labile. However, the ratio varies significantly in deeper sections and may be associated with water temperature.In the sediments deeper than 20 m in depth, C₁₂-C₁₉ FAs gradually decrease. On the other hand, higher molecular weight FAs (HFAs: C₂₀-C₃₂), which were probably derived from terrestrial plants, increase in concentration from 20 m to 100 m, suddenly decrease at 100 m and show progressively lower concentration in deeper sediments. These fluctuations are interpreted in relation to paleolimnological changes of the lake and the drainage basin. ω-Hydroxy C₂₀-C₃₀ acids and C₂₀-C₃₀α, ω-dicarboxylic acids show a distribution pattern similar to HFAs. Branched chain FAs, ω-hydroxy acids and C₉-C₁₉α,ω-dicarboxylic acids show a major peak around 3–15 m in depth. This peak is probably caused by increased bacterial activity in the water column and surface sediments in the past, which may be associated with an increase in primary production of the lake.  相似文献   

An emission pathway for stabilization at 6?Wm?2 radiative forcing   总被引：1，自引：0，他引：1  

Toshihiko Masui  Kenichi Matsumoto  Yasuaki Hijioka  Tsuguki Kinoshita  Toru Nozawa  Sawako Ishiwatari  Etsushi Kato  P. R. Shukla  Yoshiki Yamagata  Mikiko Kainuma 《Climatic change》2011,109(1-2):59-76

Representative Concentration Pathway 6.0 (RCP6) is a pathway that describes trends in long-term, global emissions of greenhouse gases (GHGs), short-lived species, and land-use/land-cover change leading to a stabilisation of radiative forcing at 6.0 Watts per square meter (Wm^?2) in the year 2100 without exceeding that value in prior years. Simulated with the Asia-Pacific Integrated Model (AIM), GHG emissions of RCP6 peak around 2060 and then decline through the rest of the century. The energy intensity improvement rates changes from 0.9% per year to 1.5% per year around 2060. Emissions are assumed to be reduced cost-effectively in any period through a global market for emissions permits. The exchange of CO₂ between the atmosphere and terrestrial ecosystem through photosynthesis and respiration are estimated with the ecosystem model. The regional emissions, except CO₂ and N₂O, are downscaled to facilitate transfer to climate models.  相似文献   

Ophiolitic Complex of the Matachingai River on Eastern Chukotka: Fragment of Lithosphere in Mesozoic Back-Arc Basin     

G. V. Ledneva  B. A. Bazylev  A. V. Moiseev  S. D. Sokolov  A. Ishiwatari  D. V. Kuzmin  B. V. Belyatsky 《Geotectonics》2018,52(4):447-467

The Matachingai River basin is known among the few ophiolitic complexes on eastern Chukotka as the southern boundary of the Chukotka Fold System (in terms of tectonics, the Chukotka microcontinent or a fragment of the Arctic Alaska–Chukotka microplate). This complex comprises tectonic blocks of residual spinel harzburgite with dunite bodies and pyroxenite, olivine gabbro, and leucogabbro veins; blocks of hornblende gabbro, diorite, and plagiogranite; and Upper Jurassic–Lower Cretaceous basaltic–cherty and cherty–carbonate rocks. The geological relationships of rocks within tectonic blocks, the compositions of primary minerals, the bulk geochemistry of rocks, as well as the strontium, neodymium, and lead isotopic compositions, make it possible to consider individual tectonic blocks of the complex as fragments of a disintegrated oceanic-type lithosphere that formed in a back-arc spreading center. The melts, crystallization products of which are represented by hornblende gabbro of blocks, olivine gabbro of veins, and basalts, separated from geochemically and isotopically heterogeneous mantle. Blocks composed of rocks with various modal composition are likely relicts of an oceanic lithosphere of different segments of a back-arc basin. The studied complex may be a lithosphere of one of the Middle–Late Jurassic back-arc basins. Fragments of these basins are retained in ophiolitic complexes on Great Lyakhovsky Island of the New Siberian Islands Archipelago, western Chukotka, and the Brooks Range in Alaska.  相似文献   

Relict chromian spinels in Tulu Dimtu serpentinites and listvenite,Western Ethiopia: implications for the timing of listvenite formation     

Ayano Sofiya  Akira Ishiwatari  Naoto Hirano  Tatsuki Tsujimori 《International Geology Review》2017,59(13):1621-1631

Serpentinites (massive and schistose) and listvenite occur as tectonic sheets and lenses within a calcareous metasedimentary mélange of the Tulu Dimtu, western Ethiopia. The massive serpentinite contains high-magnesian metamorphic olivine (forsterite [fo] ~96 mol%) and rare relict primary mantle olivine (Fo_90–93). Both massive and schistose serpentinites contain zoned chromian spinel; the cores with the ferritchromite rims preserve a pristine Cr/(Cr+Al) atomic ratio (Cr# = 0.79–0.87), suggesting a highly depleted residual mantle peridotite, likely formed in a suprasubduction zone setting. Listvenite associated with serpentinites of smaller ultramafic lenses also contain relict chromian spinel having identical Cr# to those observed in serpentinites. However, the relict chromian spinel in listvenite has significantly higher Mg/(Mg+Fe²⁺) atomic ratios. This suggests that a nearly complete metasomatic replacement of ultramafic rocks by magnesite, talc, and quartz to prevent Mg–Fe²⁺ redistribution between relict chromian spinel and the host, that is, listvenite formation, took place prior to re-equilibration between chromian spinel and the surrounding mafic minerals in serpentinites. Considering together with the regional geological context, low-temperature CO₂-rich hydrothermal fluids would have infiltrated into ultramafic rocks from host calcareous sedimentary rocks at a shallow level of accretionary prism before a continental collision to form the East African Orogen (EAO).  相似文献   

Glacial–interglacial productivity and environmental changes in Lake Biwa,Japan: A sediment core study of organic carbon,chlorins and biomarkers     

Ryoshi Ishiwatari  Koichi Negishi  Hiroyasu Yoshikawa  Shuichi Yamamoto 《Organic Geochemistry》2009,40(4):520-530

Temporal changes in paleoproductivity of Lake Biwa (Japan) over the past 32 kyr have been studied by analyzing bulk organic carbon and photosynthetic pigments (chlorins) in the BIW95-5 core. Primary productivity was estimated on the assumption of C/N_org values of 8 for autochthonous organic matter (OM) and 25 for allochthonous OM and using an equation developed for the marine environment. The estimate indicates that primary productivity ranges from 50 to 90 g C m^?2 yr^?1 in the Holocene, while it is ～60 g C m^?2 yr^?1 on average in the last glacial. Pheophytin a and pheophorbide a are the major chlorins. A downcore profile of chlorin concentration normalized to autochthonous organic carbon (OC) shows a decreasing trend. Chlorin productivity was corrected by removal of the effect of post-burial chlorin degradation. The temporal profile of chlorin productivity thereby obtained resembles that from autochthonous OC.The difference in primary productivity between the Holocene and the glacial for the lake is markedly smaller than that for Lake Baikal situated in the boreal zone. This difference between the two lakes is probably caused by the difference in their climatic conditions, such as temperature and precipitation. Precipitation at Lake Biwa is relatively large during the glacial and the Holocene because of the continuous influence of the East Asian monsoon. Lake Baikal precipitation is generally small as a result of control by the continental (Siberia) climate regime. In addition, a significant difference in productivity between the glacial and the Holocene for Lake Baikal may be essentially controlled by the hydrodynamic systems in the lake.Lake Biwa terrigenous OM input events occurred at least five times over the period 11–32 kyr BP, suggesting enhanced monsoon activity. Molecular examination of the layer with a large input of terrigenous OM during the Younger Dryas indicates that concentrations of terrigenous biomarkers such as n-C₂₇–C₃₁ alkanes, lignin phenols, cutin acids, ω-hydroxy acids and C₂₉ sterols are high, suggesting that soil OM with peat-like material entered the lake as a result of flooding. An enhanced sedimentation rate in the last 3000 years might have been partially caused by agricultural activity around the lake.  相似文献   

Phenols in hydrothermal petroleums and sediment bitumen from Guaymas Basin, Gulf of California     

Simoneit BR  Leif RN  Ishiwatari R 《Organic Geochemistry》1996,24(3):377-388

The aliphatic, aromatic and polar (NSO) fractions of seabed petroleums and sediment bitumen extracts from the Guaymas Basin hydrothermal system have been analyzed by gas chromatography and gas chromatography-mass spectrometry (free and silylated). The oils were collected from the interiors and exteriors of high temperature hydrothermal vents and represent hydrothermal pyrolyzates that have migrated to the seafloor by hydrothermal fluid circulation. The downcore sediments are representative of both thermally unaltered and thermally altered sediments. The survey has revealed the presence of oxygenated compounds in samples with a high degree of thermal maturity. Phenols are one class of oxygenated compounds found in these samples. A group of methyl-, dimethyl- and trimethyl-isoprenoidyl phenols (C27-C29) is present in all of the seabed NSO fractions, with the methyl- and dimethyl-isoprenoidyl phenols occurring as major components, and a trimethyl-isoprenoidyl phenol as a minor component. A homologous series of n-alkylphenols (C13-C33) has also been found in the seabed petroleums. These phenols are most likely derived from the hydrothermal alteration of sedimentary organic matter. The n-alkylphenols are probably synthesized under hydrothermal conditions, but the isoprenoidyl phenols are probably hydrothermal alteration products of natural product precursors. The suites of phenols do not appear to be useful tracers of high temperature hydrothermal processes.  相似文献