10 resultados para miyako


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A marine geophysical survey was carried out, on the RN Science 1 of the Institute of Oceanography, Chinese Academy of Sciences (IOCAS), in 2000, at the Miyako Section of Okinawa Trough. Here we present seismic and acoustic evidence of a gas seep on the sea floor on the western part of the Okinawa Through, near the lower slope of the East China Sea Slope and discuss the possibility of related formation of gas hydrate. A gas column reflection was observed in echo-sounder data above a section where the sea floor reflector was missing, on both the echo-sounder and the seismic data for line H14. The seismic data also show an acoustic curtain reflection and a turbidity reflection at this section. These anomalies are the evidence of the existence of a gas seep, which occupies an area 2.2 km in diameter. Based on the acoustic curtain on line H14, we believe that the amount of gas contained in the sediments below the gas seep is larger than 1 % by volume of sediment. Tectonically, the gas seep developed in a small basin controlled by basement uplift in the north, south and east. The thickness of the sediment layer can be greater than 3.5 km. A mud diapir structure was found in layer D beneath the gas seep. Over-pressure may occur due to the large sediment thickness and also the tectonic basement uplift in the north, south, and east. The mud diapir could be the preferential pathway for methane-rich fluids. The acoustic curtain may indicate that free gas related to the gas seep can be formed on the sea floor. We also note that the layer above the acoustic curtain on profile H14 may contain gas hydrate.

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Coral reefs are characterized by enormous carbonate production of the organisms. It is known that rapid calcification is linked to photosynthesis under control of the carbonate equilibrium in seawater. We have established a model simulating the coexisting states of photosynthesis and calcification in order to examine the effects of photosynthesis and calcification on the carbonate system in seawater. Supposing that the rates of photosynthesis and calcification are proportional to concentrations of their inorganic carbon source, the model calculations indicate that three kinds of unique interactions of the organic and inorganic carbon productions are expected. These are photosynthetic enhancement of calcification, calcification which benefits photosynthesis and carbonate dissolution induced by respiration. The first effect appears when the photosynthetic rate is more than approximately 1.2 larger than that of calcification. This effect is caused by the increase of CO3 content and carbonate saturation degree in seawater. If photosynthesis use molecular carbon dioxide, the second effect occurs when the calcification rate is more than approximately 1.6 times larger than that of photosynthesis. Time series model experiments indicate that photosynthesis and calcification potentially enhance each other and that organic and inorganic carbon is produced more efficiently in the coexisting system than in the isolated reactions. These coexisting effects on production enhancement of photosynthesis and calcification are expected to appear not only in the internal pool of organisms but also in a reef environment which is isolated from the outer ocean during low tide. According to the measurements on the fringing type Shiraho Reef in the Ryukyu Islands, the diurnal change of water properties (pH, total alkalinity, total carbon dioxide and carbonate saturation degree) were conspicuous. This environment offers an appropriate condition for the appearance of these coexisting effects. The photosynthetic enhancement of calcification and the respiratory inducement of decalcification were observed during day-time and night-time slack-water periods, respectively. These coexisting effects, especially the photosynthetic enhancement of calcification, appear to play important roles for fluorishing coral reef communities.

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2nd copy in case with Miyako meisho zue, 1786.

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Mode of access: Internet.

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Wydział Neofilologii: Katedra Orientalistyki

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本文通过5’-RACE和3’-RACE方法克隆了西双版纳地区的卵黄萤Luciola ovalis和端黑萤Luciola terminalis两种荧光素酶基因。两个荧光素酶基因被连接到pET-15b载体上并在BL21(DE3)菌株中表达。L. ovalis荧光素酶基因的开放阅读框有1635个碱基,编码一个544个氨基酸的蛋白。L. terminalis荧光素酶基因有一个1647bp的开放阅读框,编码一个548个氨基酸的蛋白。它们的氨基酸序列和北美萤火虫(Photinus pyralis)的氨基酸序列分别有65.3%和65.9%的相似性,而彼此之间又有73.5%的相似性。两种在大肠杆菌中表达的荧光素酶均有很高的活性,它们的最大发光波长分别是566 nm和563 nm。同时表达的四种荧光素酶(L. ovalis、L. terminalis、Hotaria parvula和Pyrocoelia miyako)在不同pH下活性变化很大,四种荧光素酶在pH 6.5-7.5之间有比较高的活性,其中L. ovalis和P. miyako两种荧光素酶在pH 7.0时活性最高,而另两种在pH 7.5时活性最高。当pH大于8.0时,这四种荧光素酶的活性都散失很快,可见它们对pH变化非常敏感。序列分析和结构模拟发现,荧光素酶活性位点周围有六个非常保守的结构域,这六个保守区域包含了大多数在催化发光反应中与底物荧光素和ATP结合的氨基酸。L. terminalis萤火虫荧光素酶的三级结构与L. cruciata荧光素酶晶体结构非常相似,而L. ovalis荧光素酶的三级结构在AMP结合位点附近有两个偏离的环。

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Polyandry is an important component of both sexual selection and kin structuring within cooperatively breeding species. A female may have multiple partners within a single reproductive attempt (simultaneous polyandry) or across multiple broods within and/or across years (sequential polyandry). Both types of polyandry confer a range of costs and benefits to individuals and alter the genetic structure of social groups over time. To date, many molecular studies of cooperative breeders have examined the evolution of cooperative breeding in relation to simultaneous polyandry. However, cooperatively breeding vertebrates are iteroparous, and thus sequential polyandry is also likely, but more rarely considered in this context. We examined sequential polyandry in a cooperatively breeding bird that has a low level of within-brood polyandry. Over a 5-year period (2006–2010), we monitored individual mating relationships using molecular markers in a population of individually marked apostlebirds (Struthidea cinerea). Divorce occurred between reproductive seasons in 17 % (8/48) of pairs and appeared to be female-driven. The level of sequential polyandry was also driven by the disappearance of males after breeding, and over 90 % of females, for whom we had suitable data, bred with multiple males over the period of study. This sequential polyandry significantly altered the relatedness of group members to the offspring in the nest. However, in about half of the cases, the second male was related (first- or second-order relative) to the first male of a sequentially polyandrous female and this alleviated the reduction in relatedness caused by polyandry. Our findings suggest that even in species with high within-brood parentage certainty, helper-offspring relatedness values can quickly erode through sequential polyandry.

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We have cloned two gibberellin (GA) 3β-hydroxylase genes, OsGA3ox1 and OsGA3ox2, from rice by screening a genomic library with a DNA fragment obtained by PCR using degenerate primers. We have used full-scan GC-MS and Kovats retention indices to show function for the two encoded recombinant fusion proteins. Both proteins show 3β-hydroxylase activity for the steps GA20 to GA1, GA5 to GA3, GA44 to GA38, and GA9 to GA4. In addition, indirect evidence suggests that the OsGA3ox1 protein also has 2,3-desaturase activity, which catalyzes the steps GA9 to 2,3-dehydro-GA9 and GA20 to GA5 (2,3-dehydro GA20), and 2β-hydroxylase activity, which catalyzes the steps GA1 to GA8 and GA4 to GA34. Molecular and linkage analysis maps the OsGA3ox1 gene to the distal end of the short arm of chromosome 5; the OsGA3ox2 gene maps to the distal end of the short arm of chromosome 1 that corresponds to the D18 locus. The association of the OsGA3ox2 gene with the d18 locus is confirmed by sequence and complementation analysis of three d18 alleles. Complementation of the d18-AD allele with the OxGA3ox2 gene results in transgenic plants with a normal phenotype. Although both genes show transient expression, the highest level for OsGA3ox1 is from unopened flower. The highest level for OsGA3ox2 is from elongating leaves.

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[1] Kyōwarabe, Atooi, Tsuginefu -- [2] Dekisai Kyō miyage, Horik awa no mizu, Kyō uchimairi, Miyako kagetsu meisho -- [3] Rakuyō meishoshū, Keishi junranshū, Kinki rekiranki -- [4] Fusō keikashi, Meisho miyakodori, Kyō machikagami -- [5] Kyō suzume, Ymashiro meiseki junkōshi, Keijō shōran, Miyako meishoguruma -- [6-7] Yamashiro meishōshi -- [8] Kyōhabutae, Kyōhabutae oridome, Yamashiro meisho jisha monogatari, Rakuyō jūnisha reigenki -- [9-13] Kyōtobō mokushi -- [14] Miyako meisho zue, Miyako meisho zue shūi -- [15] Yōshū fushi, Hinami kiji -- [16] Sakuin.