A 50-year record of nitrate concentrations in the Slapton Ley Catchment,Devon, United Kingdom

Slapton Ley, a coastal lake, is the largest natural body of fresh water in south-west England. There was concern in the 1960s that the lake was becoming increasingly eutrophic. To quantify inputs of water, sediment and nutrients into the lake, Slapton Ley Field Centre initiated a programme of weekly water quality sampling in September 1970. Of all the chemical properties which have been measured over the decades, the nitrate record has been the subject of more research than any other. The weekly monitoring has been supplemented by research projects aimed at understanding aspects of processes and patterns of nitrate delivery to the stream network. Three aspects of the nitrate record are reviewed: short-term process dynamics; the annual cycle of influent streams and the lake itself; and long-term trends. In the first two decades of monitoring, there was increasing concern about a trend of rising nitrate concentrations, an issue in most lowland rivers in the United Kingdom at the time. In the 1990s, nitrate concentrations levelled off and then have fallen steadily in recent years. In relation to eutrophication, there are clear signs of improvement in the influent streams, but concerns remain about water quality in the lake itself.     

Arsenic removal from aqueous solutions by mixed magnetite–maghemite nanoparticles

In this study, magnetite–maghemite nanoparticles were used to treat arsenic-contaminated water. X-ray photoelectron spectroscopy (XPS) studies showed the presence of arsenic on the surface of magnetite–maghemite nanoparticles. Theoretical multiplet analysis of the magnetite–maghemite mixture (Fe₃O₄-γFe₂O₃) reported 30.8% of maghemite and 69.2% of magnetite. The results show that redox reaction occurred on magnetite–maghemite mixture surface when arsenic was introduced. The study showed that, apart from pH, the removal of arsenic from contaminated water also depends on contact time and initial concentration of arsenic. Equilibrium was achieved in 3 h in the case of 2 mg/L of As(V) and As(III) concentrations at pH 6.5. The results further suggest that arsenic adsorption involved the formation of weak arsenic-iron oxide complexes at the magnetite–maghemite surface. In groundwater, arsenic adsorption capacity of magnetite–maghemite nanoparticles at room temperature, calculated from the Langmuir isotherm, was 80 μmol/g and Gibbs free energy (∆G⁰, kJ/mol) for arsenic removal was −35 kJ/mol, indicating the spontaneous nature of adsorption on magnetite–maghemite nanoparticles.     

Can biomass burning produce a globally significant carbon-isotope excursion in the sedimentary record?

Negative carbon-isotope excursions have been comprehensively studied in the stratigraphic record but the discussion of causal mechanisms has largely overlooked the potential role of biomass burning. The carbon-isotopic ratios (δ¹³C) of vegetation, soil organic matter and peat are significantly lower than atmospheric carbon dioxide (CO₂), and thereby provide a source of low ¹³C CO₂ when combusted. In this study, the potential role of biomass burning to generate negative carbon isotope excursions associated with greenhouse climates is modeled. Results indicate that major peat combustion sustained for 1000 yr increases atmospheric CO₂ from 2.5× present atmospheric levels (PAL) to 4.6× PAL, and yields a pronounced negative δ¹³C excursion in the atmosphere ( 2.4‰), vegetation ( 2.4‰) and the surface ocean ( 1.2‰), but not for the deep ocean ( 0.9‰). Release of CO₂ initiates a short-term warming of the atmosphere (up to 14.4 °C, with a duration of 1628 yr), which is consistent with the magnitude and length of an observed Toarcian excursion event. These results indicate that peat combustion is a plausible mechanism for driving negative δ¹³C excursions in the rock record, even during times of elevated pCO₂.     

An autochthonous geological model for the eastern Andes of Ecuador

We describe a traverse across the Cordillera Real and sub-Andean Zone of Ecuador, poorly known areas with very little detailed mapping and very little age control. The spine of the Cordillera comprises deeply eroded Triassic and Jurassic plutons, the roots of a major arc, emplaced into probable Palaeozoic pelites and metamorphosed volcanic rocks. The W flank comprises a Jurassic (?) submarine basaltic–andesitic volcanic sequence, which grades up into mixed Jurassic/Cretaceous volcanic and sedimentary rocks of the Inter-Andean Valley. The sub-Andean Zone, on the E flank of the Cordillera, comprises a newly recognized Cretaceous basin of cleaved mudrocks, quartz arenites and limestones. East of the syndepositional Cosanga Fault, the Cretaceous basin thins into a condensed sequence that is indistinguishable from the rocks of the adjacent hydrocarbon-bearing Oriente Basin. The principal penetrative deformation of the Cordillera Real was probably latest Cretaceous/Palaeocene. It telescoped the magmatic belts, but shortening was largely partitioned into the pelites between plutons. The plutons suffered inhomogenous deformation; some portions completely escaped tectonism. The pelites conserve two foliations. The earliest comprises slaty cleavage formed under low- or sub-greenschist conditions. The later is a strong schistosity defined by new mica growth. It largely transposed and obliterated the first. Both foliations may have developed during a single progressive deformation. We find inappropriate recent terrane models for the Cordillera Real and sub-Andean Zone of Ecuador. Instead we find remarkable similarities from one side of the Cordillera to the other, including a common structural history. In place of sutures, we find mostly intrusive contacts between major plutons and pelites. Triassic to Cretaceous events occurred on the autochthonous western edge of the Archaean Guyana Shield. The latest Cretaceous–Paleocene deformation is interpreted as the progressive collision of an oceanic terrane(s) with the South American continent. Young fault movements have subsequently juxtaposed different structural levels through the Cordillera Real orogen.     

Variability of T Tauri-like stars in NGC 2264

The variability of the T Tauri-like stars in NGC 2264 in U, B, V, R and I colours has been studied. It is found that the range of variability in amplitude in I is less than in U, B and V. A method of determining relative opacities at these wavelengths from the variability in different colours of these dust embedded stars is also described.     

Decomposition of Structural Amplitude Effect and AVO Attributes: Application to a Gas-water Contact

—?The structural amplitude effect, associated with focusing and defocusing due to the reflector curvature, importantly contributes to reflection seismic amplitudes. This paper develops a conciliatory approach for estimating the structural amplitude effect and the attributes of amplitude variation versus offset (AVO). The AVO attributes are extracted from raw amplitudes, in which the structural effect is taken into account explicitly based on a structural model reconstructed from travel-time inversion. One of the goals is to conduct the AVO analysis not just locally (per CDP) but also horizontally to see the global variation along the reflection. The lateral variations of AVO attributes are decomposed by the Chebyshev expansion. The method is demonstrated with an example of weak shallow gas-water contact appearing on a 2-D seismic profile of a site survey in the North Sea.     

Effect of increased nitrogen fixation on stratospheric ozone

Nitrogen compounds are produced by biological reactions and by industrial processes from the abundant nitrogen gas (N₂) in the atmosphere. The formation of compounds from atmospheric nitrogen is called fixation. In nature, nitrogen compounds undergo many conversions, but under aerobic conditions, characterized by the presence of oxygen, they tend to be converted to the nitrate (NO ₃ ^- ) form. Under anaerobic conditions, characterized by the absence of oxygen, the nitrate is denitrified, and the nitrogen contained therein is converted into nitrogen gas (N₂) and nitrous oxide (N₂O), which escape into the atmosphere. The nitrous oxide diffuses into the stratosphere, where it decomposes to yield nitrogen gas and small amounts of nitric oxide (NO) and nitrogen dioxide (NO₂), which react with ozone (O₃) to convert it to oxygen (O₂). The ozone in the stratosphere is produced by the reaction of light with oxygen and is destroyed primarily by reactions with the nitrogen oxides.As long as the production and destruction are equal, the ozone in the stratosphere is maintained at a constant concentration. Increased nitrogen fixation will lead to increased denitrification, increased amount of nitrous oxide moving into the stratosphere, and a reduction in ozone concentration.Ozone in the stratosphere attenuates the ultraviolet light received from the sun. As the ozone concentration decreases, more ultraviolet light will reach the surface of the earth. The fear is that this additional radiation will have detrimental effects on living organisms and possibly on the climate.Because the global use of fixed nitrogen in fertilizers has increased greatly in recent years and in 1974 amounted to almost 40 million metric tons, the eventual generation of nitrous oxide from the fertilizer nitrogen after application to the soil has been cited as a potential environmental hazard. In response to this concern, this document estimates nitrogen fixation, nitrous oxide production, and ozone reduction based on two methods of calculation and on various increases in nitrogen fixation. Uncertainties and information gaps in the nitrogen cycle are pointed out.This document does not review either the projected biological effects of ozone depletion or the stratospheric chemistry of ozone. These topics are dealt with at length in other studies.World fixation of nitrogen in 1974, expressed in millions of metric tons per year (MT/yr), was estimated to be as follows.Most of the estimates given are based on inadequate data; consequently, actual amounts may be significantly different from those shown. The study of nitrogen fixed in the oceans has not progressed far enough to permit reliable estimates. However, estimates of the amount of nitrogen fixed for fertilizer and other industrial uses in 1974 are considered reliable. The trend of industrial fixation of nitrogen offers some indication of the trend in total amount of nitrogen fixed. It is estimated that 174 MT of nitrogen were fixed by all processes in 1950. Total fixation in 1850 could have been 150 MT of nitrogen.Nitrous oxide-nitrogen production on land is estimated as 5 to 10 MT/yr; published estimates of production in the ocean, however, range from less than 1 to 100 MT/yr. The higher value was based on reported supersaturation of ocean waters with nitrous oxide.Two methods of estimating the decrease in ozone concentration in the stratosphere were used. Method I is based on nitrogen fixation. It involves the assumptions that the relative increase in production of nitrous oxide is proportional to the relative increase in total nitrogen fixation and that sufficient time has elapsed for the rate of denitrification to come to equilibrium with fixation; i.e., the lag time between increased fixation and increased denitrification has passed. This method, using fixation estimated for 1950 as a base, suggests that the reduction in ozone would be 5.8 and 11.5% as a consequence of increased fixation of 50 and 100 MT of nitrogen per year, respectively.Method II is based on nitrous oxide evolution. It involves the assumption that the global rate of production of nitrous oxide is 100 MT/yr (based on supersaturation of this gas in the ocean and on changes in measured concentrations of nitrous oxide in the atmosphere). Method II leads to estimates of ozone reduction much lower than those from Method I. For example, on the assumption that global production of nitrous oxide-nitrogen is 100 MT/yr and that 5% of the nitrogen denitrified is released as nitrous oxide, the estimated ozone reduction is 1% with an increase of 100 MT/yr in nitrogen fixation. This method is forced to assume an unknown source of nitrous oxide in the ocean and an unknown sink for nitrous oxide in the troposphere.There are great uncertainties in many of the estimates that have been made for nitrogen fixation and for nitrous oxide production, and there are many information gaps that need to be filled before the question of the effects of increased nitrogen fixation on the ozone layer can be answered. Perhaps the biggest information needs are in the areas of nitrogen transformations and the quantities of nitrous oxide produced in the ocean. Other needs deal with the complexities of the nitrogen cycle on land. The lag time between fixation by various processes and denitrification must be known as a basis for estimating how soon predicted effects based on equilibrium conditions can be expected. Concentrations of nitrous oxide and their fluctuations in the troposphere (lower atmosphere) need to be monitored to provide an index to variations and increases in production. Improved models are needed to relate the ozone concentration in the stratosphere to nitrogen fixation and nitrous oxide production on earth.In spite of the uncertainties in the predictions of the effects of increased fixation of nitrogen on stratospheric ozone, the potential hazard is sufficiently serious that, in addition to research on the various phases of the global nitrogen cycle that impinge upon the nitrous oxide-ozone question, research on the efficiency of use of all fixed forms of nitrogen should be worthwhile. Editor's Note: Although the data for sources, sinks, reservoirs, and rate processes in this article are undergoing rapid revision presently, it, nonetheless, is one of the clearest statements of the physics, chemistry, and biology of the fertilizer/ozone problem available to date.This report was developed by eleven scientists (see Appendix 1 for names and affiliations) representing the subject matter areas of atmospheric chemistry, chemical engineering, environmental science and chemistry, microbiology, oceanography, plant genetics, soil biochemistry, soil physics, and soil chemistry. This task force of scientists chaired by Parker F. Pratt, met under the auspices of the Council for Agricultural Science and Technology (CAST), whose headquarters office is at the Department of Agronomy, Iowa State University, Ames, Iowa 50011, U.S.A. The task force met in Denver, Colorado from October 23 to 25, 1975, to prepare a first draft of the report. The chairman then prepared a revised version and returned it to members of the task force for review and comment. A second revision was then prepared and returned for further comment. Finally, the report was edited and reproduced for transmittal through the U.S. Congressional Committees concerned with the matter of ozone depletion. It was originally issued as a CAST Report Number 53, January, 1976, but had not been formally published heretofore.     

Two-layer rotating hydraulics: Strangulation,remote and virtual controls

The hydraulics of two-layer, rotating channel flow is examined in the limit where the channel width is large compared to the internal Rossby radius of deformation, but small compared to the external deformation radius. In this limit the baroclinic flow is contained in boundary layers along each side wall, while the barotropic flow is distributed over the width of the channel. Width variations along the channel cause the strength of the barotropic flow to vary and the barotropic variations influence the baroclinic boundary layers in two independent ways. The dual nature of this forcing gives rise to a new type of critical condition which we refer to as a remote control. Virtual and narrows controls also arise. Steady solutions can be obtained by solving a pair of simple quadratic equations and examples are given showing various combinations of controls.Woods Hole Oceanographic Institution Contribution No. 7252.     

Flow of winter-transformed Pacific water into the Western Arctic

The dynamics of the flow of dense water through Barrow Canyon is investigated using data from a hydrographic survey in summer 2002. The focus is on the winter-transformed Bering water—the highest volumetric mode of winter water in the Chukchi Sea—which drains northward through the canyon in spring and summer. The transport of this water mass during the time of the survey was 0.2–0.3 Sv. As the layer flowed from the head of the canyon to the mouth, it sank, decelerated, and stretched. Strong cyclonic relative vorticity was generated on the seaward side of the jet, which compensated for the stretching. This adjustment was incomplete, however, in that it did not extend across the entire current, possibly because of internal mixing due to shear instabilities. The resulting vorticity structure of the flow at the canyon mouth was conducive for baroclinic instability and eddy formation. Multiple eddies of winter-transformed Bering water were observed along the Chukchi–Beaufort shelfbreak. Those to the west of Barrow Canyon were in the process of being spawned by the eastward-flowing shelfbreak current emanating from Herald Canyon, while the single eddy observed to the east originated from the Barrow Canyon outflow. It is argued that such an eddy formation is a major source of the ubiquitous cold-core anti-cyclones observed historically throughout the Canada Basin. Implications for the ventilation of the upper halocline of the Western Arctic are discussed.