Consequences of regime shifts for marine food webs

Climate-mediated ecological regime shifts can re-structure entire ecosystems from primary producers to top predators. As a consequence, major trophodynamic pathways change with the altered mix of dominating species. Four cases of ecosystem regime shifts forced by climate variability are presented (North Sea, central Baltic Sea, central North Pacific and Humboldt Current ecosystems) and the effect on food chains is elucidated. Different types of trophodynamic control mechanisms set in motion through the impact of climate variability and the potential impact of regime shifts on biogeochemical cycles are discussed.     

Detritus fuels ecosystem metabolism but not metazoan food webs in San Francisco estuary's freshwater delta

Detritus from terrestrial ecosystems is the major source of organic matter in many streams, rivers, and estuaries, yet the role of detritus in supporting pelagic food webs is debated. We examined the importance of detritus to secondary productivity in the Sacramento and San Joaquin River Delta (California, United States), a large complex of tidal freshwater habitats. The Delta ecosystem has low primary productivity but large detrital inputs, so we hypothesized that de tritus is the primary energy source fueling production in pelagic food webs. We assessed the sources, quantity, composition, and bioavailability of organic matter among a diversity of habitats (e.g., marsh sloughs, floodplains, tidal lakes, and deep river channels) over two years to test this hypothesis. Our results support the emerging principle that detritus dominates riverine and estuarine organic matter supply and supports the majority of ecosystem metabolism. Yet in contrast to prevailing ideas, we found that detritus was weakly coupled to the Delta's pelagic food web. Results from independent approaches showed that phytoplankton production was the dominant source of organic matter for the Delta's pelagic food web, even though primary production accounts for a small fraction of the Delta's organic matter supply. If these results are general, they suggest that the value of organic matter to higher trophic levels, including species targeted by programs of ecosystem restoration, is a function of phytoplankton production.     

Microphytobenthos: The ecological role of the “secret garden” of unvegetated,shallow-water marine habitats. II. role in sediment stability and shallow-water food webs

The microphytobenthos form an important component of all shallow-water ecosystems where enough light reaches the sediment surface to support appreciable primary production. Although less conspicuous than macroalgae or vascular plants, the microphytobenthos can contribute significantly to primary production and can modify habitat characteristics. The microphytobenthos alter sediment properties (e.g., erodibility) both directly, in the extreme forming a mat or scum on the sediment surface, and indirectly by modifying the activities of benthic infauna (e.g., pelletization, burrowing, tube building, and sediment tracking). Carbon dioxide fixed by the microphytobenthos supports higher, grazing trophic levels. These include deposit-feeding and suspension-feeding macrofauna as well as meiofauna and microfauna. Quantitative relations between the feeding and growth rates of macrofauna and the abundance of microphytobenthos and suspended organic matter (i.e., functional responses) are reviewed. Given the current state of knowledge of the direct and indirect interactions involving trophic dynamics, sediment properties, and benthic microalgae, we argue for reductionist studies of particular interactions as distinct entities. This is a prerequisite for the emergence of a comprehensive picture of unvegetated ecosystems and the ability to predict their responses to man’s activities. *** DIRECT SUPPORT *** A01BY074 00005     

离散单元法同拉格朗日元法及其在岩土力学中的应用

离散单元法是一种适合于节理岩体的数值分析方法，拉格朗日元法则特点适用于解决大变形的问题。本文叙述了离散单元法和拉格朗日元法的基本原理以及有关参数的选择问题。文中还举出两种方法在岩土力学中的应用范围。     

硫化物矿物的主微(痕)量元素分析进展

金属或半金属元素(Fe、Mo、As、Cu、Co、Ni、Zn、Pb等)、贵金属元素(Au、Ag)和铂族元素(PGE)、稀有分散元素(Re、Ga、In等)以高浓度富集或微量赋存于硫化物矿物中,常形成具有工业意义和经济价值的大型矿床,对研究矿床成因、经济地质、环境地球化学具有重要意义。因此,对硫化物组成的精确分析是了解上述方向的重要途径。硫化物矿物的主微(痕)量元素的快速、精确定量分析一直以来备受关注,本文就近几十年来对硫化物矿物的定量分析进展作了详细介绍,重点评述了电子探针(EPMA)、X射线荧光光谱(XRF)、电感耦合等离子体质谱(ICP-MS和LA-ICPMS)和电感耦合等离子体发射光谱(ICP-AES)在硫化物矿物主微(痕)量分析中的应用。     

Oxygen-isotope ratios in metamorphic eclogites

Rocks having O¹⁸-values less than those of normal basalts (5 to 7 permil) are very rare. However, anomalously low -values are common in European B-type eclogites, including those from N. W. Spain (1.5 to 5.6 permil), W. France, S. Germany, and W. Norway. Since isotopic exchange with sediments during metamorphism would have increased their -values, we tentatively conclude that the isotopically light eclogites descended from basaltic rocks which interacted with light meteoric waters at high temperatures, as did the Tertiary igneous rocks of W. Scotland. Isotopically heavy eclogites from S. Germany (8.6 to 10.5 permil) are isotopically similar to calc-silicate rocks from N. W. Spain and are possibly derived from dolomitic pelites.Coexisting quartz and rutile effectively fractionate the isotopes of oxygen and thereby constitute a potentially useful geothermometer. The average quartz-rutile fractionation in B-type eclogites is 6.5 permil.Lamont-Doherty Geological Observatory of Columbia University Contrib. No. 1559.     

Aggregation of aquatic humic substances

Humic substances (HS) were isolated from Penwhirn Reservoir (PR) and Esthwaite Water (EW) and their removal from solution by centrifugation was studied as a function of pH, humic concentration and molecular weight, and CaCl₂ concentration. Large amounts (up to 50%) of PR HS could be removed but only small amounts (? 3%) of EW HS. At pH ? 5 removal of PR HS by Ca²⁺ can be explained satisfactorily in terms of decreases in humic solubilities induced by complexation with the cation. However, removal induced by protonation of the PR HS is unusual in that it decreases with increasing humic concentration.The results suggest that PR HS comprise a range of molecules differing in solubility, with the high-molecular-weight (40,000) components being the least soluble. The EW HS consist of molecules of weight-average molecular weight 5000 and resemble similarly sized PR HS in that they remain unaggregated in solution even when highly complexed with Ca²⁺.     

Calcium isotope ratios in animal and human bone

Calcium isotopes in tissues are thought to be influenced by an individual’s diet, reflecting parameters such as trophic level and dairy consumption, but this has not been carefully assessed. We report the calcium isotope ratios (δ^44/42Ca) of modern and archaeological animal and human bone (n = 216). Modern sheep raised at the same location show 0.14 ± 0.08‰ higher δ^44/42Ca in females than in males, which we attribute to lactation by the ewes. In the archaeological bone samples the calcium isotope ratios of the herbivorous fauna vary by location. At a single site, the archaeological fauna do not show a trophic level effect. Humans have lower δ^44/42Ca than the mean site fauna by 0.22 ± 0.22‰, and the humans have a greater δ^44/42Ca range than the animals. No effect of sex or age on the calcium isotope ratios was found, and intra-individual skeletal δ^44/42Ca variability is negligible. We rule out dairy consumption as the main cause of the lower human δ^44/42Ca, based on results from sites pre-dating animal domestication and dairy availability, and suggest instead that individual physiology and calcium intake may be important in determining bone calcium isotope ratios.     

Ferric-ferrous ratios,H2O contents and D/H ratios of phlogopite and biotite from lavas of different tectonic regimes

 Complete chemical analyses, including ferric and ferrous iron, H₂O contents and δD values for 16 phlogopite and biotite and 2 hornblende separates are presented. Samples were obtained from volcanic rocks from four localities: (1) phlogopite phenocrysts from minette lavas from the western Mexico continental arc, (2) biotite and hornblende phenocrysts from andesite lavas from Mono Basin, California, (3) phlogopite and biotite from clinopyroxenite nodules entrained in potassic lavas from the East African Rift, Uganda, and (4) phlogopite phenocrysts from a wyomingite lava in the Leucite Hills, Wyoming. The Fe₂O₃ contents in the micas range from 0.8 to 10.5 wt%, corresponding to 0.09 to 1.15 Fe³⁺ per formula unit (pfu). Water contents vary from 1.6 to 3.0 wt%, corresponding to 1.58 to 3.04 OH pfu, significantly less than would be expected for a site fully occupied by hydroxyl. Cation- and anion-based normalization procedures provide accurate mineral formulae with respect to most cations and anions, but are unable to generate accurate estimates of Fe³⁺/Fe^T, and overestimate OH at the expense of O on the hydroxyl site. These inaccuracies are present despite acceptable adjusted totals and stoichiometric calculated site occupancies. The phlogopite and biotite phenocrysts in arc-related lavas from western Mexico and eastern California have the highest Fe³⁺/Fe^T ratios (56–87%), reflecting high magmatic oxygen fugacities (ΔNNO = +2 to +5), in contrast to those from Uganda (25–40%) and the Leucite Hills (23%). There is no correlation between the OH content and the Fe³⁺/Fe^T ratio in the micas. Values of KMg/Fe²⁺D (± 2σ errors) were calculated for three phlogopite-olivine pairs (0.12 ± 0.12, 0.26 ± 0.14, 0.09 ± 0.12), two biotite-hornblende pairs (0.73 ± 0.08 and 1.22 ± 0.10) and a single phlogopite-augite pair (1.15 ± 0.12). Values of KF/OHD for two biotite and hornblende pairs could not be determined without significant error because of the extremely low F contents (< 0.2 wt%) of the four phases. The δD values obtained in this study encompass a large range (−137 to −43‰). The phlogopite and biotite separates from Uganda have δD values of −70 to −49‰, which overlap those believed to represent “primary” mantle. There is a larger range in δD values (−137 to −43‰) for phlogopite phenocrysts from western Mexico minette lavas, although their range in δ¹⁸O values (5.2–6.2‰) is consistent with “normal” mantle. It is unlikely, therefore, that the variable δD values reflect heterogeneity in the mantle source region of the minette magmas. Nor can the extremely low δD values reflect degassing of H₂ or H₂O since almost 100% loss of dissolved water in the magma is required, an unrealistic scenario given the stability of the hydrous phenocrysts. The very low δD values of the Mascota minette phlogopites require that the hydrogen be introduced from an external source (e.g., meteoric water). Whatever the process responsible for the observed hydrogen isotope composition, it had no effect on the δ¹⁸O value, f _{O 2}, a _{H 2O} or bulk composition of the host magmas. Received: 5 January 1995 / Accepted: 19 March 1996     

Sulfur isotope ratios of Icelandic rocks

Sulfur isotope ratios have been determined in 27 selected volcanic rocks from Iceland together with their whole rock chemistry. The ³⁴S of analyzed basalts ranges from –2.0 to +0.4 with an average value of –0.8 Tholeiitic and alkaline rocks exhibit little difference in ³⁴S values but the intermediate and acid rocks analyzed have higher ³⁴S values up to +4.2 It is suggested that the overall variation in sulfur isotope composition of the basalts is caused by degassing. The small range of the ³⁴S values and its similarity to other oceanic and continental basalts, suggest that the depleted mantle is homogeneous in its sulfur isotope composition. The ³⁴S of the depleted mantle is estimated to be within the range for undegassed oceanic basalts, –0.5 to +1.0     

Molecular size of aquatic humic substances

Aquatic humic substances, which account for 30 to 50% of the organic carbon in water, are a principal component of aquatic organic matter. The molecular size of aquatic humic substances, determined by small-angle X-ray scattering, varies from 4.7 to 33 Å in their radius of gyration, corresponding to a molecular weight range of 500 to greater than 10,000. The aquatic fulvic acid fraction contains substances with molecular weights ranging from 500 to 2000 and is monodisperse, whereas the aquatic humic acid fraction contains substances with molecular weights ranging from 1000 to greater than 10,000 and is generally polydisperse.     

Bacteriogenic sulfur isotopic ratios in geology

Stable sulfur isotopes may aid in distinguishing sulfides of a magmatic hydrothermal origin from sulfides containing biogenic sulfur. For those sulfide ore depositis that are intimately associated with the intrusive body from which it is inferred their ore solutions were derived, the variation in S³⁴ values is generally less than ± 5 permil. Biogenic sulfides, on the other hand, exhibit a broad spread in S³⁴ values that is rately less than a few permil. The reason for this is that the sulfur produced, as hydrogen sulfide by anaerobic bacteria, is isotopically fractionated by variable amounts resulting in a relatively broad spread in S³⁴ values.Raw culture experiments have illustrated the isotopic effects resulting from reduction of sulfate to hydrogen sulfate by sulfate reducing bacteria. The characteristics of enrichment of S³² to a highly variable extent in hydrogen sulfide is verified by these experiments.In addition, a series of closed system raw culture experiments resulted in fractionation factors between 1.043 to 1.062 which are similar to variations in S³⁴ between juxtaposed sulfides in nature produced by bacteriogenic processes.Speech delivered on October 1, 1965, on the occasion of the colloquy concerning Sulphurisotopes organized by the Deutsche Forschungsgemeinschaft at Bad Sooden-Allendorf.     

Strontium-calcium ratios in Cenozoic planktonic foraminifera

The $\text{Sr}\text{Ca}$ ratio and other parameters have been measured in fossil planktonic foraminifera from the Atlantic and Pacific Ocean basins in order to evaluate the $\text{Sr}\text{Ca}$ ratio of seawater during the last 75 million years. Results on well-preserved samples indicate that the ratio has increased to its present value by 10–15% during the Cenozoic, and that minima occurred between 55-45 Ma and 10-5 Ma, when the ratio was 15–25% less than at present. The long-term increase may reflect either decreasing deposition of aragonite with a high $\text{Sr}\text{Ca}$ ratio in shallow seas, or decreasing seafloor spreading rates and consequently decreasing hydrothermal supply of Ca during the Cenozoic. Other geologic evidence suggests that the Eocene minimum (near 50 Ma) may have resulted from increased aragonite sedimentation, while the Late Miocene minimum (between 10-5 Ma) may have been caused by an increased rate of seawater-basalt exchange when seafloor spreading rates increased on the East Pacific Rise near 10 Ma.     

Spiral galaxies with non-typical mass-to-light ratios

Total mass-to-light ratio M/L _B for S0 — Irr galaxies, whereM is the dynamical mass within the optical radius R ₂₅ (corresponding to 25 ^m /sq. arcsec in the B band), increases systematically with (B-V)₀ color, but slower than that is predicted by stellar population evolution models without dark halo. It shows that the mean ratio between dark halo and stellar masses is higher for more “blue“ galaxies. However some galaxies don’t follow this general trend. The properties of galaxies with extremely high and extremely low values of M/L _B ratios are compared, and different factors, accounting for the extremes, are analyzed. The conclusion is that in some cases too high or too low M/L _B ratios are associated with observational errors, in other cases—with non-typical dark halo mass fraction, and in some cases — with peculiarities of disc stellar population. Particularly, discs of some galaxies with low M/L _B ratios turn out to be unusually “light” for their luminosity and colors, which indicates a substantial deficit of low mass stars as the most probable cause of low M/L _B .     

Hydrogen and oxygen isotope ratios in nodular and bedded cherts

Hydrogen and oxygen isotopic compositions of cherts (δD for hydroxyl hydrogen in the chert, δ¹⁸O for the total oxygen) have been determined for a suite of samples from the central and western United States. When plotted on a δD-δ¹⁸O diagram, Phanerozoic cherts define domains parallel to the meteoric water line which are different for different periods of geologic time. The elongation parallel to the meteoric water line suggests that meteoric waters were involved in the formation of many cherts.The existence of different chert δ-values for different geologic times indicates that once the granular microcrystalline quartz of cherts crystallizes its isotopic composition is preserved with time. An explanation for the change with time of the isotopic composition of cherts involving large changes with time in the isotopic composition of ocean water is unlikely since δ¹⁸O of the ocean would have had to decrease by about 3‰between Carboniferous and Triassic time and then increase about 5%.` from Triassic to Cretaceous time. Such isotopic changes cannot be accounted for by extensive glaciation, sedimentation of hydrous minerals, or input of water from the mantle into the oceans.The variation with time of the chert δ-values can be satisfactorily explained in terms of past climatic temperature fluctuations if the chert-water isotope fractionation with temperature is approximated by 1000 lnα = 3.09 × 10⁶T^?2 – 3.29. Crystallization temperatures so inferred suggest that the average climatic temperatures for the central and western U.S. decreased from about 34 to 20°C through the Paleozoic, increased to 35–40°C in the Triassic, and then decreased through the Mesozoic to Tertiary values of about 17°C. A few data for the Precambrian suggest the possibility that Earth surface temperatures may have reached about 52°C at 1.3 b.y. and about 70°C at 3 b.y.     

边界元法(续)

二、积分方程的数值解积分方程(16)一般来说是不能得到解析解的,因此必须求助于数值方法,如象有限元法那样。但这里仅对区域表面进行离散化,而不必对整个物体这样做。