Oxygen consumption in the epilimnia and hypolimnia of two eutrophic,warm‐monomictic lakes     

S. F. Mitchell  Carolyn W. Burns 《新西兰海洋与淡水研究杂志》2013,47(3):427-441

Oxygen consumption was estimated for two eutrophic New Zealand lakes using a simple 2‐layer model, from estimates of net changes in oxygen, phytoplankton photosynthesis, inflow and outflow, diffusion, eddy diffusion, and changes in the depth of the thermocline. Of the total oxygen consumption, 75–85% occurred in the epilimnia. Epilimetic oxygen consumption per m³ and per m² in Lake Johnson were higher than in Lake Hayes, reflecting known differences in the trophic status of the lakes, but estimates for the hypolimnia of the two lakes were similar. Daily hypolimnetic areal deficits were sensitive to both the depths and time intervals chosen.

In the epilimnia, monthly oxygen production by photosynthesis averaged 1.1 and 1.8 times the initial oxygen content in Lakes Hayes and Johnson respectively. Diffusion appeared to be of similar magnitude to photosynthesis in the isothermal period, but was less important during stratification. Losses to the hypolimnia by eddy diffusion were less than 10% of photosynthesis. Photosynthesis in the hypolimnia contributed 30–40% of the oxygen consumed there and eddy diffusion supplied a further 20%.

In Lake Johnson a 3–5 m stratum of water in the metalimnion became anoxic for 2–3 months each summer while there were still up to 5.2 g.rer³ of oxygen remaining in the hypolimnion. Metalimnetic anoxia is attributed largely to oxygen consumption in situ, resulting from the highly eutrophic state of the lake and intense thermal stratification. Zooplankton respiration accounted for less than 10% of the maximum net decline in metalimnetic oxygen in 1970–71, but was more important in the other 2 years.

Changes in the oxygen content of the hypolimnion indicate that Lake Hayes has become more eutrophic since 1954–55. In Lake Johnson low oxygen concentrations at the autumn overturn (<5 g.m^‐3) represent a threat to the trout population.  相似文献   

Paleoclimatic implications of the spatial patterns of modern and LGM European land-snail shell δO     

Natalie M. Kehrwald  William D. McCoy  Stephen J. Burns 《Quaternary Research》2010,74(1):166-6869

The oxygen isotopic composition of land-snail shells may provide insight into the source region and trajectory of precipitation. Last glacial maximum (LGM) gastropod shells were sampled from loess from Belgium to Serbia and modern land-snail shells both record δ¹⁸O values between 0‰ and − 5‰. There are significant differences in mean fossil shell δ¹⁸O between sites but not among genera at a single location. Therefore, we group δ¹⁸O values from different genera together to map the spatial distribution of δ¹⁸O in shell carbonate. Shell δ¹⁸O values reflect the spatial variation in the isotopic composition of precipitation and incorporate the snails' preferential sampling of precipitation during the warm season. Modern shell δ¹⁸O decreases in Europe along a N-S gradient from the North Sea inland toward the Alps. Modern observed data of isotopes in precipitation (GNIP) demonstrate a similar trend for low-altitude sites. LGM shell δ¹⁸O data show a different gradient with δ¹⁸O declining toward the ENE, implying a mid-Atlantic source due to increased sea ice and a possible southern displacement of the westerly jet stream. Balkan LGM samples show the influence of a Mediterranean source, with δ¹⁸O values decreasing northward.  相似文献   

Evaluation of High-Frequency Mean Streamwater Transit-Time Estimates Using Groundwater Age and Dissolved Silica Concentrations in a Small Forested Watershed     

Norman E. Peters  Douglas A. Burns  Brent T. Aulenbach 《Aquatic Geochemistry》2014,20(2-3):183-202

Many previous investigations of mean streamwater transit times (MTT) have been limited by an inability to quantify the MTT dynamics. Here, we draw on (1) a linear relation (r ² = 0.97) between groundwater ³H/³He ages and dissolved silica (Si) concentrations, combined with (2) predicted streamwater Si concentrations from a multiple-regression relation (R ² = 0.87) to estimate MTT at 5-min intervals for a 23-year time series of streamflow [water year (WY) 1986 through 2008] at the Panola Mountain Research Watershed, Georgia. The time-based average MTT derived from the 5-min data was ~8.4 ± 2.9 years and the volume-weighted (VW) MTT was ~4.7 years for the study period, reflecting the importance of younger runoff water during high flow. The 5-min MTTs are normally distributed and ranged from 0 to 15 years. Monthly VW MTTs averaged 7.0 ± 3.3 years and ranged from 4 to 6 years during winter and 8–10 years during summer. The annual VW MTTs averaged 5.6 ± 2.0 years and ranged from ~5 years during wet years (2003 and 2005) to >10 years during dry years (2002 and 2008). Stormflows are composed of much younger water than baseflows, and although stormflow only occurs ~17 % of the time, this runoff fraction contributed 39 % of the runoff during the 23-year study period. Combining the 23-year VW MTT (including stormflow) with the annual average baseflow for the period (~212 mm) indicates that active groundwater storage is ~1,000 mm. However, the groundwater storage ranged from 1,040 to 1,950 mm using WY baseflow and WY VW MTT. The approach described herein may be applicable to other watersheds underlain by granitoid bedrock, where weathering is the dominant control on Si concentrations in soils, groundwater, and streamwater.  相似文献   

Observations on the crystal structures of lueshite     

Roger H. Mitchell  Peter C. Burns  Kevin S. Knight  Christopher J. Howard  Anton R. Chakhmouradian 《Physics and Chemistry of Minerals》2014,41(6):393-401

Laboratory powder XRD patterns of the perovskite-group mineral lueshite from the type locality (Lueshe, Kivu, DRC) and pure NaNbO₃ demonstrate that lueshite does not adopt the same space group (Pbma; #57) as the synthetic compound. The crystal structures of lueshite (2 samples) from Lueshe, Mont Saint-Hilaire (Quebec, Canada) and Sallanlatvi (Kola, Russia) have been determined by single-crystal CCD X-ray diffraction. These room temperature X-ray data for all single-crystal samples can be satisfactorily refined in the orthorhombic space group Pbnm (#62). Cell dimensions, atomic coordinates of the atoms, bond lengths and octahedron tilt angles are given for four crystals. Conventional neutron diffraction patterns for Lueshe lueshite recorded over the temperature range 11–1,000 K confirm that lueshite does not adopt space group Pbma within these temperatures. Neutron diffraction indicates no phase changes on cooling from room temperature to 11 K. None of these neutron diffraction data give satisfactorily refinements but suggest that this is the space group Pbnm. Time-of-flight neutron diffraction patterns for Lueshe lueshite recorded from room temperature to 700 °C demonstrate phase transitions above 550 °C from Cmcm through P4/mbm to \(Pm\overline{3} m\) above 650 °C. Cell dimensions and atomic coordinates of the atoms are given for the three high-temperature phases. The room temperature to 400 °C structures cannot be satisfactorily resolved, and it is suggested that the lueshite at room temperature consists of domains of pinned metastable phases with orthorhombic and/or monoclinic structures. However, the sequence of high-temperature phase transitions observed is similar to those determined for synthetic NaTaO₃, suggesting that the equilibrated room temperature structure of lueshite is orthorhombic Pbnm.  相似文献   

Evaluating the efficacy of technical measures: a case study of selection device legislation in the UK Crangon crangon (brown shrimp) fishery     

Catchpole  Tom L.; Revill  Andrew S.; Innes  James; Pascoe  Sean 《ICES Journal of Marine Science》2008,65(2):267-275

  相似文献   

Late glacial and Holocene vegetation history at Governor Bog,King Valley,western Tasmania,Australia     

Eric A. Colhoun  Guus van de Geer  Sean J. Fitzsimons 《第四纪科学杂志》1991,6(1):55-66

  相似文献   

Solubility of plutonium(VI) carbonate in saline solutions     

Sean D. Reilly 《Geochimica et cosmochimica acta》2007,71(11):2672-2679

Among the plutonium oxidation states found to form in the environment, mobile plutonium(VI) can exist under oxidizing conditions and in waters with high chloride content due to radiolysis effects. We are investigating the solubility and speciation of plutonium(VI) carbonate under conditions relevant to natural waters and brines such as those found near some geologic radioactive waste repositories. The solid Pu(VI) phase PuO₂CO₃(s) was prepared and its solubility was measured in NaCl and NaClO₄ solutions in a CO₂ atmosphere as a function of pH and ionic strength (0.1-5.6 m). The concentration of soluble plutonium in solution was calculated from spectroscopic data and liquid scintillation counting. Spectroscopic measurements also revealed the plutonium oxidation state. The apparent solubility product of PuO₂CO₃(s) was determined at selected electrolyte concentrations to be, log K_s,0 = −13.95 ± 0.07 (0.1 m NaCl), log K_s,0 = −14.07 ± 0.13 (5.6 m NaCl), and log K_s,0 = −15.26 ± 0.11 (5.6 m NaClO₄). Specific ion interaction theory was used to calculate the solubility product at zero ionic strength, .  相似文献   

Rethinking big data in digital humanitarianism: practices,epistemologies, and social relations   总被引：1，自引：0，他引：1  

Ryan Burns 《GeoJournal》2015,80(4):477-490

  相似文献   

The High-Resolution Coronal Imager (Hi-C)     

Ken Kobayashi  Jonathan Cirtain  Amy R. Winebarger  Kelly Korreck  Leon Golub  Robert W. Walsh  Bart De Pontieu  Craig DeForest  Alan Title  Sergey Kuzin  Sabrina Savage  Dyana Beabout  Brent Beabout  William Podgorski  David Caldwell  Kenneth McCracken  Mark Ordway  Henry Bergner  Richard Gates  Sean McKillop  Peter Cheimets  Simon Platt  Nick Mitchell  David Windt 《Solar physics》2014,289(11):4393-4412

The High-Resolution Coronal Imager (Hi-C) was flown on a NASA sounding rocket on 11 July 2012. The goal of the Hi-C mission was to obtain high-resolution (≈?0.3?–?0.4′′), high-cadence (≈?5 seconds) images of a solar active region to investigate the dynamics of solar coronal structures at small spatial scales. The instrument consists of a normal-incidence telescope with the optics coated with multilayers to reflect a narrow wavelength range around 19.3 nm (including the Fe xii 19.5-nm spectral line) and a 4096×4096 camera with a plate scale of 0.1′′?pixel^?1. The target of the Hi-C rocket flight was Active Region 11520. Hi-C obtained 37 full-frame images and 86 partial-frame images during the rocket flight. Analysis of the Hi-C data indicates the corona is structured on scales smaller than currently resolved by existing satellite missions.  相似文献   

Response of surface water chemistry to reduced levels of acid precipitation: comparison of trends in two regions of New York,USA     

Douglas A. Burns  Michael R. McHale  Charles T. Driscoll  Karen M. Roy 《水文研究》2006,20(7):1611-1627

In light of recent reductions in sulphur (S) and nitrogen (N) emissions mandated by Title IV of the Clean Air Act Amendments of 1990, temporal trends and trend coherence in precipitation (1984–2001 and 1992–2001) and surface water chemistry (1992–2001) were determined in two of the most acid‐sensitive regions of North America, i.e. the Catskill and Adirondack Mountains of New York. Precipitation chemistry data from six sites located near these regions showed decreasing sulphate (SO₄^2?), nitrate (NO₃^?), and base cation (C_B) concentrations and increasing pH during 1984–2001, but few significant trends during 1992–2001. Data from five Catskill streams and 12 Adirondack lakes showed decreasing trends in SO₄^2? concentrations at all sites, and decreasing trends in NO₃^?, C_B, and H⁺ concentrations and increasing trends in dissolved organic carbon at most sites. In contrast, acid‐neutralizing capacity (ANC) increased significantly at only about half the Adirondack lakes and in one of the Catskill streams. Flow correction prior to trend analysis did not change any trend directions and had little effect on SO₄^2? trends, but it caused several significant non‐flow‐corrected trends in NO₃^? and ANC to become non‐significant, suggesting that trend results for flow‐sensitive constituents are affected by flow‐related climate variation. SO₄^2? concentrations showed high temporal coherence in precipitation, surface waters, and in precipitation–surface water comparisons, reflecting a strong link between S emissions, precipitation SO₄^2? concentrations, and the processes that affect S cycling within these regions. NO₃^? and H⁺ concentrations and ANC generally showed weak coherence, especially in surface waters and in precipitation–surface water comparisons, indicating that variation in local‐scale processes driven by factors such as climate are affecting trends in acid–base chemistry in these two regions. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献