Lyman break galaxies at z∼ 1 and the evolution of dust attenuation in star-forming galaxies with redshift     

D. Burgarella  E. Le Floc'h  T. T. Takeuchi  J. S. Huang  V. Buat  G. H. Rieke  K. D. Tyler 《Monthly notices of the Royal Astronomical Society》2007,380(3):986-998

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A submillimetre survey of the kinematics of the Perseus molecular cloud – I. Data     

Emily I. Curtis  John S. Richer  Jane V. Buckle 《Monthly notices of the Royal Astronomical Society》2010,401(1):455-472

We present submillimetre observations of the   J = 3 → 2  rotational transition of ¹²CO, ¹³CO and C¹⁸O across over 600 arcmin² of the Perseus molecular cloud, undertaken with the Heterodyne Array Receiver Programme (HARP), a new array spectrograph on the James Clerk Maxwell Telescope. The data encompass four regions of the cloud, containing the largest clusters of dust continuum condensations: NGC 1333, IC348, L1448 and L1455. A new procedure to remove striping artefacts from the raw HARP data is introduced. We compare the maps to those of the dust continuum emission mapped with the Submillimetre Common-User Bolometer Array (SCUBA; Hatchell et al.) and the positions of starless and protostellar cores (Hatchell et al.). No straightforward correlation is found between the masses of each region derived from the HARP CO and SCUBA data, underlining the care that must be exercised when comparing masses of the same object derived from different tracers. From the ¹³CO/C¹⁸O line ratio the relative abundance of the two species  ([¹³CO]/[C¹⁸O]∼ 7)  and their opacities (typically τ is 0.02–0.22 and 0.15–1.52 for the C¹⁸O and ¹³CO gas, respectively) are calculated. C¹⁸O is optically thin nearly everywhere, increasing in opacity towards star-forming cores but not beyond  τ₁₈∼ 0.9  . Assuming the ¹²CO gas is optically thick, we compute its excitation temperature, T _ex (around 8–30 K), which has little correlation with estimates of the dust temperature.  相似文献   

Biodegradation and environmental behavior of biodiesel mixtures in the sea: An initial study     

DeMello JA  Carmichael CA  Peacock EE  Nelson RK  Samuel Arey J  Reddy CM 《Marine pollution bulletin》2007,54(7):894-904

Biodiesel, a mixture of fatty acid methyl esters (FAMEs) derived from animal fats or vegetable oils, is rapidly moving towards the mainstream as an alternative source of energy. However, the behavior of biodiesel, or blends of biodiesel with fossil diesel, in the marine environment have yet to be fully understood. Hence, we performed a series of initial laboratory experiments and simple calculations to evaluate the microbial and environmental fate of FAMEs. Aerobic seawater microcosms spiked with biodiesel or mixtures of biodiesel and fossil diesel revealed that the FAMEs were degraded at roughly the same rate as n-alkanes, and more rapidly than other hydrocarbon components. The residues extracted from these different microcosms became indistinguishable within weeks. Preliminary results from physical-chemical calculations suggest that FAMEs in biodiesel mixtures will not affect the evaporation rates of spilled petroleum hydrocarbons but may stabilize oil droplets in the water column and thereby facilitate transport.  相似文献   

The Hubble Deep Field-North SCUBA Super-map – IV. Characterizing submillimetre galaxies using deep Spitzer imaging     

Alexandra Pope  Douglas Scott  Mark Dickinson  Ranga-Ram Chary  Glenn Morrison  Colin Borys  Anna Sajina  David M. Alexander  Emanuele Daddi †  David Frayer  Emily MacDonald  Daniel Stern 《Monthly notices of the Royal Astronomical Society》2006,370(3):1185-1207

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Decision-support Systems: Do they have a Future in Estuarine Management?     

P. D. Jones  A. O. Tyler  A. W. Wither 《Estuarine, Coastal and Shelf Science》2002,55(6):993

Estuaries are highly complex ecosystems. Consequently they present daunting challenges to planners and regulators responsible for devising ‘ sustainable development ’ strategies or for taking rapid decisions with respect to ‘ crisis management ’. Over the lifetime of the Estuarine and Coastal Sciences Association, there have been significant developments in both the range and sophistication of the tools available to assist with these tasks. Indeed, managers are now faced with a confusing plethora of possibilities that may, or may not, help in achieving the optimum solution to a given problem.Typical problems confronting managers and the systems available to resolve the issues are considered. By way of illustration, we present some examples based on our experience over the last 25 years in the Mersey Estuary (which has seen dramatic improvements in water quality and a number of major proposed developments), from the Ribble Estuary and from along the north-west coast of the U.K.  相似文献   

汶川地震断裂作用研究新认识   总被引：2，自引：0，他引：2  

王焕  李海兵  司家亮  孙知明  付小方  刘栋梁  裴军令  李成龙  张佳佳  宋圣荣  郭力伟  MORI James  薛莲  BRODSKY E. Emily  云锟  龚正 《地球学报》2015,36(3):257-269

2008年汶川地震后,人们不得不思考问题是:大地震是如何发生的?下一次大地震什么时候发生?也就是涉及地质学家和地球物理学家一直未解决的科学问题:断层是如何破裂的?震后断裂是如何愈合的?我们试图通过对汶川地震断裂带结构、断裂摩擦行为和断裂愈合过程的研究来回答这些问题。本文将介绍通过对地表露头和汶川地震断裂科学钻探一号孔(WFSD)岩心中汶川地震主滑移带的详细研究,以及钻孔中长期温度监测来分析有关汶川地震断裂动态弱化和摩擦行为,并结合钻孔中长期水文监测计算所得断裂带渗透率变化,分析震后断裂愈合过程,进而探讨和认识汶川地震断裂作用所涉及的上述问题。经过详细研究,确定了汶川地震断裂带(映秀—北川断裂带)宽105~240 m、具有五个不同断裂岩组合的内部结构,是一条经常发生大地震、具多种弱化机制的断裂带;发现了汶川地震不仅具有同震石墨化作用,而且测量到目前世界上最低的动态摩擦系数(≤0.02),同时首次记录到大地震后断裂快速愈合信息。这些研究结果不仅直接回答了一直困扰在地震地质和地震物理学领域几十年的关键问题,而且对完善地震断裂理论和认识汶川地震机制具有极其重要的意义,为防震减灾提供了理论依据。  相似文献   

Do we know each other? Bilateral ties and the location of clean development mechanism projects     

Nives Dolšak  Emily Bowerman Crandall 《Climatic change》2013,118(3-4):521-536

This paper examines how bilateral ties between developed (home) countries and developing (host) countries influence the location of Clean Development Mechanism projects (CDMs). With the home-host country pair as the unit of analysis (2,058 country-pairs), we employ a logistic regression model to analyze decisions of home countries in selecting the location for their CDMs. We are most interested in examining how home countries’ familiarity with the host country influences CDM location decisions. The familiarity factors are: (1) colonial history; (2) bilateral trade; and (3) bilateral aid. Using a binary logistical model, we find that that bilateral familiarity factors strongly influence CDM location decisions. Further, with respect to host country characteristics, we find that total carbon dioxide emissions and UNFCCC specific domestic institutions influence CDM location decisions, but not general investment institutions or high carbon intensity of host country economies.  相似文献   

Developing country perspectives on ‘mitigation actions’, ‘NAMAs’, and ‘LCDS’     

Emily Tyler  Anya Boyd  Kim Coetzee  Marta Torres Gunfaus  Harald Winkler 《Climate Policy》2013,13(6):770-776

The MAPS programme, which seeks to deepen mitigation ambition in developing countries, is engaged in exploring the concepts of Nationally Appropriate Mitigation Actions (NAMAs) and Low Carbon Development Strategies (LCDS) from a developing country perspective. Here, climate mitigation practitioners in six developing countries were surveyed for their understanding of these concepts (anonymous, personal communications with climate mitigation practitioners in Argentina, Brazil, Chile, Colombia, India, and South Africa). It is found that there is much scope for clarity and conceptual elaboration in this policy space. NAMAs are largely interpreted as mitigation activities packaged for submission to the United Nations Framework Convention on Climate Change (UNFCCC) registry, but are not held to constitute the full set of mitigation activity in a developing country. New terminology may be needed to describe this broader set. A tighter interpretation of LCDS to distinguish between a strategic or coordinating policy action may be useful. Other themes arising include the way ‘national appropriateness’ is reflected in the concepts, and the role of international policy in deepening mitigation action in developing countries.  相似文献   

Annual trace element cycles in calcite–aragonite speleothems: evidence of drought in the western Mediterranean 1200–1100 yr BP     

Emily A. McMillan  Ian J. Fairchild  Silvia Frisia  Andrea Borsato  Frank McDermott 《第四纪科学杂志》2005,20(5):423-433

Each of two calcitic stalagmites from Grotte de Clamouse, Herault, southern France, displays a discrete aragonite layer dated at around 1100 yr BP. The layer of fanning aragonite ray crystals is immediately preceded by calcite with Mg and Sr compositions that are uniquely high for the past 3 kyr. Trace element compositions close to the boundary between original aragonite and calcite are consistent with quasi‐equilibrium partitioning of trace elements between the phases. Study of modern dripwaters demonstrates that pronounced covariation of Mg/Ca and Sr/Ca ratios in dripwater occurs owing to large amounts of calcite precipitation upflow of the drips that fed the stalagmites. Trace element to Ca ratios are enhanced during seasonally dry periods. Ion microprobe data demonstrate a pronounced covariation of trace elements, including Mg and Sr in calcite, and Sr, U and Ba in aragonite. The mean peak spacing is close to the long‐term mean of annual growth rates determined by differences in U‐series ages and so the trace element peaks are interpreted as annual. The trace element chemistry of the stalagmites on annual to inter‐annual scales thus directly reflects the amounts of prior calcite precipitation, interpreted as an index of aridity. The longer‐term context is a multi‐decadal period of aridity (1200–1100 yr BP) possibly correlated with an analogous episode in Central America. The arid period culminated in the nucleation of aragonite, but within a decade was followed by a return to precursor conditions. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

Role of electrochemical reactions in pressure solution     

George W. Greene  Emily E. Meyer  Jacob N. Israelachvili 《Geochimica et cosmochimica acta》2009,73(10):2862-6892

Using a Surface Forces Apparatus we have measured changes in the electrical potential difference between quartz and mica surfaces that correlate with the changing quartz dissolution rate when surfaces are pressed together at relatively low pressures (2-3 atm) in aqueous electrolyte solutions of 30 mM CaCl₂ at 25 °C. No detectable dissolution or voltage potential difference is measured in symmetrical systems (e.g. mica-mica or quartz-quartz) or between dry surfaces subjected to similar pressures, indicating that the dissolution can not be attributed to a simple pressure effect, slow aging (creep), or plastic deformation of the quartz surface. In quartz-mica systems brought together under pressure or to close proximity in electrolyte solution, the onset of quartz dissolution is marked by a sudden, rapid decrease in the quartz thickness at initial rates in the range from 1 to 4 nm/min, which after several hours settles into a constant rate of approximately 0.01 nm/min (∼5 μm/yr). Concomitantly, the potential drops to a constant value once the dissolution rate has stabilized. The decrease in the decay rate is interpreted as being due to saturation of the confined aqueous film and/or to the buildup of a Stern layer on the quartz surface, and the constant rate as being due to the steady-state chemical dissolution and diffusion of the dissolving silica into the surrounding reservoir. The dissolution is ‘non-uniform’: the surfaces become rough as dissolution proceeds, with the appearance of pits in a manner analogous to corrosion. On occasions, the process of rapid dissolution followed by a gradual transition to steady dissolution repeats itself, suggesting that the pit structure and Stern layer are fragile and subject to collapse and/or expulsion from the gap. Preliminary experiments on the dissolution of multi-faceted milled quartz particles (∼1.0 μm diameter) compressed between two muscovite surfaces suggest an asymmetry in the dissolution rates at different crystallographic planes. The origin of the electrical potential is interpreted as arising from the overlapping of the electric double-layers of two dissimilar surfaces when they are forced into close proximity. This electrical potential difference, for as yet unknown reasons, appears to be the driving force for the dissolution, rather than pressure.  相似文献