Changes in the mode of Southern Ocean circulation over the last glacial cycle revealed by foraminiferal stable isotopic variability

Benthic foraminiferal oxygen and carbon isotopic records from Southern Ocean sediment cores show that during the last glacial period, the South Atlantic sector of the deep Southern Ocean filled to roughly 2500 m with water uniformly low in δ¹³C, resulting in the appearance of a strong mid-depth nutricline similar to those observed in glacial northern oceans. Concomitantly, deep water isotopic gradients developed between the Pacific and Atlantic sectors of the Southern Ocean; the δ¹³C of benthic foraminifera in Pacific sediments remained significantly higher than those in the Atlantic during the glacial episode. These two observations help to define the extent of what has become known as the ‘Southern Ocean low δ¹³C problem’. One explanation for this glacial distribution of δ¹³C calls upon surface productivity overprints or changes in the microhabitat of benthic foraminifera to lower glacial age δ¹³C values. We show here, however, that glacial-interglacial δ¹³C shifts are similarly large everywhere in the deep South Atlantic, regardless of productivity regime or sedimentary environment. Furthermore, the degree of isotopic decoupling between the Atlantic and Pacific basins is proportional to the magnitude of δ¹³C change in the Atlantic on all time scales. Thus, we conclude that the profoundly altered distribution of δ¹³C in the glacial Southern Ocean is most likely the result of deep ocean circulation changes. While the characteristics of the Southern Ocean δ¹³C records clearly point to reduced North Atlantic Deep Water input during glacial periods, the basinal differences suggest that the mode of Southern Ocean deep water formation must have been altered as well.     

Oxidation and emission of methane in a monomictic lake (Rotsee, Switzerland)

The build-up of methane in the hypolimnion of the eutrophic Lake Rotsee (Lucerne, Switzerland) was monitored over a full year. Sources and sinks of methane in the water column were characterized by measuring concentrations and carbon isotopic composition. In fall, high methane concentrations (up to 1 mM) were measured in the anoxic water layer. In the oxic layer, methane concentrations were much lower and the isotopic composition shifted towards heavy carbon isotopes. Methane oxidation rates peaked at the interface between oxic and anoxic water layers at around 8–10 m depth. The electron balance between the oxidants oxygen, sulphate, and nitrate, and the reductants methane, sulphide and ammonium, matched very well in the chemocline during the stratified season. The profile of carbon isotopic composition of methane showed strong indications for methane oxidation at the chemocline (including the oxycline). Aerobic methane oxidizing bacteria were detected at the interface using fluorescence in situ hybridization. Sequencing the responsible organisms from DGGE bands revealed that aerobic methanotrophs type I closely related to Methylomonas were present. Sulphate consumption occurred at the sediment surface and, only towards the end of the stagnation period, matched with a zone of methane consumption. In any case, the flux of sulphate below the chemocline was not sufficient to oxidize all the methane and other oxidants like nitrate, iron or manganese are necessary for the observed methane oxidation. Although most of the methane was oxidized either aerobically or anaerobically, Lake Rotsee was still a source of methane to the atmosphere with emission rates between 0.2 mg CH₄ m^?2 day^?1 in February and 7 mg CH₄ m^?2 day^?1 in November.     

Neodymium isotopic variations in seawater

New data for the direct measurement of the isotopic composition of neodymium in Atlantic Ocean seawater are compared with previous measurements of Pacific Ocean seawater and ferromanganese sediments from major ocean basins. Data for Atlantic seawater are in excellent agreement with Nd isotopic measurements made on Atlantic ferromanganese sediments and are distinctly different from the observed compositions of Pacific samples. These results clearly demonstrate the existence of distinctive differences in the isotopic composition of Nd in the waters of the major ocean basins and are characteristic of the ocean basin sampled. The average ε_Nd(0) values for the major oceans as determined by data from seawater and ferromanganese sediments are as follows: Atlantic Ocean,ε_Nd(0) ? ?12 ± 2; Indian Ocean,ε_Nd(0) ? ?8 ± 2; Pacific Ocean,ε_Nd(0) ? ?3 ± 2. These values are considerably less than ε_Nd(0) value sources with oceanic mantle affinities indicating that the REE in the oceans are dominated by continental sources. The difference in the absolute abundance of¹⁴³Nd between the Pacific and Atlantic Oceans corresponds to ～10⁶ atoms¹⁴³Nd per gram of seawater. The correspondence between the¹⁴³Nd/¹⁴⁴Nd in seawater and in the associated sediments suggests the possible application of this approach to paleo-oceanography.Distinctive differences in ε_Nd(0) values are observed in the Atlantic Ocean between deep-ocean water associated with North Atlantic Deep Water and near-surface water. This suggests that North Atlantic Deep Water may be relatively well mixed with respect to Nd isotopic composition whereas near-surface water may be quite heterogeneous, reflecting different sources for surface waters relative to deep water. This suggests that it may be possible to distinguish the sources of water masses within an ocean basin on the basis of Nd isotopic composition.The Nd isotopic variations in seawater are used to relate the residence time of Nd and mixing rates between the oceans.     

Present state of oil pollution in the northern Indian Ocean

A consolidated picture of oil pollution for the northern Indian Ocean is presented. Oil slicks were sighted on 5582 observations, about 83.5% of the total observations of 6689. The range of concentrations, of the floating tar balls, is 0–6.0 mg/m² in the Arabian Sea. Similarly, the oil tanker route in the Bay of Bengal has the range of 0–69.75 mg/m². North of this route, the Bay of Bengal is comparatively free from this floating tar. Mean concentrations of dissolved and dispersed hydrocarbons for 0–20 m are 32.5 and 24.1 μg kg^?1, respectively, in the Arabian Sea and the Bay of Bengal.     

Pb–Nd isotopic constraints on sedimentary input into the Lesser Antilles arc system

The Lesser Antilles arc is a particularly interesting island arc because it is presently very active, it is located perpendicular to the South American continent and its chemical and isotopic compositions display a strong north–south gradient. While the presence in the south of a thick pile of sedimentary material coming from the old South American continent has long been suspected to explain the geochemical gradient, previous studies failed to demonstrate unambiguously a direct link between the arc lava compositions and the subducted sediment compositions.Here, we present new Nd, Sm, Th, U and Pb concentrations and Nd–Pb isotopic data for over 60 sediments from three sites located in the fore arc region of the Lesser Antilles arc. New data for DSDP Site 543 drill core located east of Dominica Island complement the data published by White et al. [White, W.M., Dupré, B. and Vidal, P., 1985. Isotope and trace element geochemistry of sediments from the Barbados Ridge–Demerara Plain region, Atlantic Ocean. Geochimica et Cosmochimica Acta, 49: 1875–1886.] and confirm their relatively uniform isotopic compositions (i.e., ²⁰⁶Pb/²⁰⁴Pb between 19.13 and 19.53). In contrast, data obtained on DSDP Site 144 located further south, on the edge of the South American Rise and on sediments from Barbados Island are much more variable (²⁰⁶Pb/²⁰⁴Pb ranges from 18.81 to 27.69). The very radiogenic Pb isotopic compositions are found in a 60 m thick black shale unit, which has no age equivalent in the Site 543 drill core. We interpret the peculiar composition of the southern sediments as being due to two factors, (a) the proximity of the South American craton, which contributes coarse grain old detrital material that does not travel far from the continental shelf, and (b) the presence of older sediments including the thick black shale unit formed during Oceanic Anoxic events 2 and 3.The north–south isotopic change known along the Lesser Antilles arc can be explained by the observed geographical changes in the composition of the subducted sediments. About 1% contamination of the mantle wedge by Site 543 sediments explains the composition of the northern islands while up to 10% sediments like those of Site 144 is required in the source of the southern island lavas. The presence of black shales in the subducted pile provides a satisfactory explanation for the very low Δ8/4 values that characterize the Lesser Antilles arc.     

Cadmium,zinc, copper,and barium in foraminifera tests

The concentrations of cadmium, zinc, copper and barium have been determined on 2-mg samples of single-species foraminifera populations. Cleaning techniques were tested using North Atlantic core tops, and followed by a detailed downcore study for the last 30,000 years in South Atlantic core V22-174. Raw foram tests cleaned by crushing followed by ultrasonic removal of fine-grained material, and dissolved in a pH 5.5 acetate buffer, contain appreciable amounts of trace elements associated with ferromanganese and alumino-silicate contaminants. A reductive/complexing cleaning treatment reduces ferromanganese contamination by 1–2 orders of magnitude. Acetate buffers at pH 5.5 complex iron and raise the solubility of ferromanganese oxides; these buffers are unsuitable for separating carbonate lattice-bound trace elements from the fraction associated with ferromanganese phases. Improved mechanical and ultrasonic reductive cleaning combined with a mild dissolution in distilled water under 1 atm.P_CO2 reduces contaminant levels another order of magnitude. The Cd and Zn concentrations (order 10^?8 mole Cd/mole Ca and 10^?5 mole Zn/mole Ca) of species with low surface area show an increase with decreasing isotopic temperatures. This increase is consistent with the increasing concentrations of these metals from low values in surface waters to higher values at depth. The variance of Cd and Zn over the last 30,000 years in the central South Atlantic is consistent with the probable variability of the dissolved trace elements at the calcification levels of the species analyzed. Cu and Ba are irreproducible and probably sensitive to residual contaminant phases. The trace element content of the tests differs from levels observed in a recent coprecipitation study. Foraminifera may be a significant vector in zinc cycling in the ocean.     

全球海洋碳循环模式MOM4_L40对碳和营养物自然分布的模拟

本文介绍了国家气候中心发展的一个全球海洋碳循环环流模式,并分析评估了该模式的基本性能.该模式是在美国地球物理流体动力学实验室(GFDL,Geophysical Fluid Dynamics Laboratory)的全球海洋环流模式MOM4(Modular Ocean Model Version 4)基础上发展的一个垂直方向40层、包含生物地球化学过程的全球三维海洋碳循环环流模式,简称为MOM4_L40(Modular Ocean Model Version 4 With 40Levels).该模式在气候场强迫下长期积分1000年,结果分析表明,与观测相比,模式较好地模拟了海洋温度、盐度、总二氧化碳、总碱、总磷酸盐的表面和垂直分布特征.模拟的海洋总二氧化碳分布与观测基本相符,表层为低值区,其下为高值区,高值区域位于10°S—60°N之间,但2000m以上模拟值较观测偏小,2000m以下模拟值较观测偏大.总体来说,MOM4_L40模式是一个可信赖的海洋碳循环过程模拟研究工具.     

Aerosol deposition velocities on the Pacific and Atlantic oceans calculated from7Be measurements

The concentrations of⁷Be have been measured in Pacific and Atlantic ocean water for the past several years to determine the deposition velocity of aerosol particles on the ocean surface.⁷Be is produced at a relatively constant rate in the atmosphere by spallation reactions of cosmic rays with atmospheric nitrogen and oxygen. Immediately after its formation⁷Be becomes attached to aerosol particles, and therefore can serve as tracers of the subsequent behavior of these particles. Isopleths of⁷Be surface water concentrations,⁷Be inventory in the ocean, and deposition velocity have been prepared for the Pacific Ocean from 30°S to 60°N and for the Atlantic Ocean from 10°N to 55°N. The concentrations, inventories and deposition velocities tended to be higher in regions where precipitation was high, and generally increased with latitude. The average flux of⁷Be across the ocean surface was calculated to be 0.027 atoms cm^?2 s^?1 which is probably not significantly greater than the worldwide average⁷Be flux across land and ocean surfaces of 0.022 atoms cm^?2 s^?1 calculated by Lal and Peters. The average deposition velocity was calculated to be 0.80 cm s^?1. This value may be 10–50% too low, since it was calculated using atmospheric⁷Be concentrations which were measured at continental stations. Measurements of atmospheric⁷Be concentrations at ocean stations suggest that the concentrations at the continental stations averaged 10–50% higher than the concentrations over the ocean.     

Identification of recycled continental material in the mantle from Sr,Nd and Pb isotope investigations

Pb, Nd and Sr isotope compositions of oceanic basalts have been used to identify recycled components of continent derivation in the mantle. The isotopic compositions of Sr, Nd and Pb, together with U, Pb, Sm, Nd, Rb, and Sr abundances have been determined for back-arc basalt glasses from the Scotia Sea and Parece Vela and West Philippine Basins, in addition to basalts from South Sandwich Islands, Ascension, St. Helena and Tristan da Cunha. Comparisons made between the isotopic compositions of South Sandwich Islands basalts and Atlantic MORB glasses permit the identification of recycled components of continent derivation in the source of the island arc basalts. Recycled Sr of continent derivation is also recognisable in back-arc basalt glasses from the Scotia Sea and Parece Vela and West Philippine Basins. However, contemporary reinjection of material with the isotopic structures similar to those identified as a component of island arc and back-arc regions cannot be the sole or dominant influence on the fine structure observed in MORB glasses from the Atlantic Ocean, nor the isotopic compositions of Tristan da Cunha, St. Helena and Ascension basalts. Recycled materials are likely to have been responsible for the generation of these heterogeneities only if they have been stored in the mantle for periods of time exceeding 10⁹ years.     

Dynamic identification of moisture sources in the Orinoco basin in equatorial South America

Abstract

The main areas of net moisture uptake are examined in air masses over the Orinoco River basin, located in equatorial South America, north of the Amazon basin. Although the Orinoco River has the third largest average annual discharge in the world (with 5.4 × 10¹¹ m³ year^?1 draining into the Atlantic Ocean), the sources of moisture that feed it have not previously been studied in any detail. The results are presented from analyses of back-tracking of all the air masses over the Orinoco basin over a period of five years (2000–2004) using the diagnostic Lagrangian tool FLEXPART. The input data for the model were obtained from the European Centre for Medium-range Weather Forecasts (ECMWF). Air transported into the Orinoco basin experiences a large uptake of water over the tropical North Atlantic within the three days prior to its arrival over the basin. The Tropical South Atlantic and the eastern coast of the Pacific become significant moisture sources for about 5–10 days before arriving over the Orinoco basin. Contrary to what might be expected, large areas of the Amazon basin, along with the Gulf of Mexico, do not provide significant moisture to the study area. Interestingly, over these zones the air experiences net moisture loss. Preliminary analysis of the processes that occur leads to the conclusion that most of the water observed over the Orinoco basin derives from advective fluxes into the area, while recycling of moisture is negligible.     

Global distribution of gaseous mercury in the troposphere

Atmospheric mercury concentrations were measured during a nautical expedition on the Atlantic Ocean between Hamburg (54°N, 10°E) and Santo Domingo (20°N, 67°W). In addition, samples were taken during flights on a commerical aircraft in the upper and middle troposphere between 60°N and 55°S, mostly over the Pacific Ocean. The data obtained in the lower troposphere over the Northern Atlantic show considerable variation in the Hg concentrations, with values ranging between 1 and 11 ng/m³; the average concentration was found to be 2.8 ng/m³. The upper tropospheric data show an interhemispheric difference with average values of 1.45 ng/m³ and 1.08 ng/m³ in the Northern and Southern Hemisphere, respectively. This suggests that mercury production occurs predominantly over the continents both by natural and anthropogenic processes. The mercury content in aerosols was found to be 0.3 ng/m³, or one-tenth of the atmospheric concentration. The data indicate a mean residence time of mercury in the atmosphere of a few months to one year.     

Oscillating glacial northern and southern deep water formation from combined neodymium and carbon isotopes

While ocean circulation is driven by the formation of deep water in the North Atlantic and the Circum-Antarctic, the role of southern-sourced deep water formation in climate change is poorly understood. Here we address the balance of northern- and southern-sourced waters in the South Atlantic through the last glacial period using neodymium isotope ratios of authigenic ferromanganese oxides in thirteen deep sea cores from throughout the South Atlantic. The data indicate that northern-sourced water did not reach the Southern Ocean during the late glacial, and was replaced by southern-derived intermediate and deep waters. The high-resolution neodymium isotope record (~ 300 yr sample spacing) from two spliced deep Cape Basin sites indicates that over the last glacial period northern-sourced water mass export to the Southern Ocean was stronger during the major Greenland millennial warming intervals (and Southern Hemisphere cool periods), and particularly during the major interstadials 8, 12, and 14. Northern-sourced water mass export was weaker during Greenland stadials and reached minima during Heinrich Events. The benthic foraminiferal carbon isotopes in the same Cape Basin core reflect a partial control by Southern Hemisphere climate changes and indicate that deep water formation and ventilation occurred in the Southern Ocean during major Greenland cooling intervals (stadials). Together, neodymium isotopes and benthic carbon isotopes provide new information about water mass sourcing and circulation in deep Southern Ocean waters during rapid glacial climate changes. Combining carbon and neodymium isotopes can be used to monitor the relative proportion of northern- and southern-sourced waters in the Cape Basin to gain insight into the processes which control the carbon isotopic composition of deep waters. In this study we show that deep water formation and circulation was more important than biological productivity and nutrient regeneration changes for controlling the carbon isotope chemistry of Antarctic Bottom Water during millennial-scale glacial climate cycles. This observation also lends support to the hypothesis that ocean circulation is linked to interhemispheric climate changes on short timescales, and that ventilation in the glacial ocean rapidly switched between the northern and Southern Hemisphere on millennial timescales.     

Modification of the deep salinity-maximum in the Southern Ocean by circulation in the Antarctic Circumpolar Current and the Weddell Gyre

The evolution of the deep salinity-maximum associated with the Lower Circumpolar Deep Water (LCDW) is assessed using a set of 37 hydrographic sections collected over a 20-year period in the Southern Ocean as part of the WOCE/CLIVAR programme. A circumpolar decrease in the value of the salinity-maximum is observed eastwards from the North Atlantic Deep Water (NADW) in the Atlantic sector of the Southern Ocean through the Indian and Pacific sectors to Drake Passage. Isopycnal mixing processes are limited by circumpolar fronts, and in the Atlantic sector, this acts to limit the direct poleward propagation of the salinity signal. Limited entrainment occurs into the Weddell Gyre, with LCDW entering primarily through the eddy-dominated eastern limb. A vertical mixing coefficient, κ_V of (2.86 ± 1.06) × 10^?4 m² s^?1 and an isopycnal mixing coefficient, κ_I of (8.97 ± 1.67) × 10² m² s^?1 are calculated for the eastern Indian and Pacific sectors of the Antarctic Circumpolar Current (ACC). A κ_V of (2.39 ± 2.83) × 10^?5 m² s^?1, an order of magnitude smaller, and a κ_I of (2.47 ± 0.63) × 10² m² s^?1, three times smaller, are calculated for the southern and eastern Weddell Gyre reflecting a more turbulent regime in the ACC and a less turbulent regime in the Weddell Gyre. In agreement with other studies, we conclude that the ACC acts as a barrier to direct meridional transport and mixing in the Atlantic sector evidenced by the eastward propagation of the deep salinity-maximum signal, insulating the Weddell Gyre from short-term changes in NADW characteristics.     

Beryllium‐7 wet deposition variation with storm height,synoptic classification,and tree canopy state in the mid‐Atlantic USA

Short‐lived fallout isotopes, such as beryllium‐7 (⁷Be), are increasingly used as erosion and sediment tracers in watersheds. ⁷Be is produced in the atmosphere and delivered to the Earth's surface primarily in precipitation. However, relatively little has been published about the variation in ⁷Be wet deposition caused by storm type and vegetation cover. Our analysis of precipitation, throughfall, and sediments in two forested, headwater catchments in the mid‐Atlantic USA indicates significant variation in isotope deposition with storm type and storm height. Individual summer convective thunderstorms were associated with ⁷Be activity concentrations up to 5.0 Bq l^?1 in precipitation and 4.7 Bq l^?1 in throughfall, while single‐event wet depositional fluxes reached 168 Bq m^?2 in precipitation and 103 Bq m^?2 in throughfall. Storms originating from the continental USA were associated with lower ⁷Be activity concentrations and single‐event wet depositional fluxes for precipitation (0.7–1.2 Bq l^?1 and 15.8–65.0 Bq m^?2) and throughfall (0.1–0.3 Bq l^?1 and 13.5–98.9 Bq m^?2). Tropical systems had relatively low activity concentrations, 0.2–0.5 Bq l^?1 in precipitation and 0.2–1.0 Bq l^?1 in throughfall, but relatively high single‐event depositional fluxes due to large rainfall volumes, 32.8–67.6 Bq m^?2 in precipitation and 25.7–134 Bq m^?2 in throughfall. The largest sources of ⁷Be depositional variation were attributed to storm characteristics including precipitation amount and maximum storm height. ⁷Be activity associated with fluvial suspended sediments also exhibited the highest concentration and variability in summer (175–1450 Bq kg^?1). We conclude the dominant source of variation on event‐level ⁷Be deposition is storm type. Our results illustrate the complex relationships between ⁷Be deposition in precipitation and throughfall and demonstrate event‐scale relationships between the ⁷Be in precipitation and on suspended sediment. Copyright © 2015 John Wiley & Sons, Ltd.     

Comparison of the behavioural and acute toxicity of copper to sheepshead,Atlantic croaker and pinfish

Sheepshead (Archosargus probatocephalus), Atlantic croaker (Micropogon undulatus) and pinfish (Lagodon rhomboides) were each exposed to aqueous solutions of reagent grade cupric chloride in artificial seawater in four static bioassays. The 24, 48, 72 and 96-h TL_m were determined to be, respectively, 4.17, 3.02, 2.19 and 1.14 mg Cu²⁺·I^?1 for sheepshead, 9.15, 7.55, 7.20 and 5.66 mg Cu²⁺·I^?1 for croaker, and 7.33, 4.43, 4.14 and 2.75 mg Cu²⁺·I^?1 for pinfish. These results are compared with literature values of experimental concentrations of copper producing subtle behavioural changes in these species.     

Lead in corals: reconstruction of historical industrial fluxes to the surface ocean

Twentieth century environmental lead chronologies for the western North Atlantic, Pacific, and Indian Oceans have been reconstructed from annually-banded scleractinian corals. Measurements of lattice-bound Pb in sequential coral bands reveal temporal changes in surface water Pb concentrations and Pb isotopic distributions. Perturbations are observable in all specimens studied, attesting to global augmentation of environmental Pb by industrialization.In the western North Atlantic, Pb perturbations have occurred in direct response to the American industrial revolution and the subsequent introduction and phasing-out of alkyl Pb additives in gasoline. Surface ocean conditions near Bermuda may be reliably reconstructed from the coral data via a lead distribution coefficient of 2.3 for the species,Diploria strigosa. Based on²¹⁰Pb measurements, a similar distribution coefficient may be characteristic of corals in general. Surface Pb concentrations in the pre-industrial Sargasso Sea were about 15–20 pM. Concentrations rose to near 90 pM by 1923 as a result of metals manufacture and fossil fuel combustion. Beginning in the late 1940's, increased utilization of leaded gasoline eventually led to a peak concentration of 240 pM in 1971, representing an approximate 15-fold increase over background. Surface ocean concentrations are presently declining rapidly (128 pM in 1984) as a result of curtailed alkyl Pb usage. Lead isotopic shifts parallel the concentration record indicating that characteristic industrial and alkyl Pb source signatures have not changed appreciably in time. Industrial releases recorded in the Florida Keys reflect a weaker source and evidence of recirculated Pb (5–6 years old) from the North Atlantic subtropical gyre. An inferred background concentration of 38 pM suggests influence of shelf and/or resuspended inputs of Pb to these coastal waters.In remote areas of the South Pacific and Indian Oceans, industrial signals are fainter and the corals studied much younger than their Atlantic counterparts. Contemporary Pb concentrations implied by coral measurements (assumingK_D = 2.3) are 40–50 pM for surface waters near Tutuila and Galapagos in the South Pacific, and 25–29 pM near Mauritius in the Indian Ocean. A single coral band from Fiji (1920 ± 5yr) implies a pre-industrial surface water concentration of 16–19 pM Pb for the South Pacific. In view of reported surface water measurements and the North Atlantic coral data, the Pacific coral extrapolations may be slightly high. This could be a result of small variations inK_D among different coral genera, or incorporation of diagenetic Pb by corals sampled in coastal environments.     

High magnitude global seismicity and lateral velocity gradients

Summary A new significant correlation has been sought between high magnitude global seismicity and lateral surface wave velocity gradients. Rayleigh wave velocity divisioning of Eurasia, Africa, Pacific Ocean, Atlantic Ocean and Indian Ocean into regions of similar group velocity dispersion character of 30 sec period bySanto andSato [1]³) has been mainly used for calculating the gradients. It is quite striking to note that all earthquakes of magnitude 8.6 and above during 1897–1956 have occurred in regions having gradients of the order of 1.5·10^–3 sec^–1.Finally, some potential areas for high magnitude earthquake occurrences are predicted and the possible velocity gradients in regions, where division pattern is not yet investigated like South America and Australia, are also estimated.N.G.R.I. Contribution No. 70-170.     

Dissolved organic carbon export from a cutover and restored peatland

High demand for horticultural peat has increased peatland drainage and peat extraction in Canada. The hydrology and carbon cycling of these cutover peatlands is greatly altered, necessitating active restoration efforts to permit the regeneration of Sphagnum mosses and the re‐establishment of natural peatland function. The effect of peatland extraction and restoration on the export of dissolved organic carbon (DOC) was examined for three successive seasons (May to October, 1999 to 2001) at two different sites (cutover and restored) in eastern Québec. A shift towards higher DOC concentrations was observed following peatland extraction (maximum: 182·6 mg L^?1) and concentrations remained high post‐restoration (maximum: 191·0 mg L^?1). The cutover site exported more DOC than the restored site in all three study seasons. The highest exports occurred during the wettest year (1999), with cutover and restored site export of 10·3 and 4·8 g m^?2, respectively. In 2000, 8·5 g C m^?2 was released from the cutover site, while the restored site released less than half that amount (3·4 g C m^?2). In 2001, the restored site released about the same amount of DOC as in the previous year (3·5 g C m^?2), while the cutover site load dropped to 6·2 g C m^?2. Both sites were net exporters of DOC in all years. Copyright © 2007 John Wiley & Sons, Ltd.     

Orographic distillation and spatio‐temporal variations of stable isotopes in precipitation in the North Atlantic

Little is known about the spatial and temporal variability of the stable isotopic composition of precipitation in the North Atlantic and its relationship to the North Atlantic Oscillation (NAO) and anthropogenic climate change. The islands of the Azores archipelago are uniquely positioned in the middle of the North Atlantic Ocean to address this knowledge gap. A survey of spatial and temporal variability of the stable isotope composition of precipitation in Azores is discussed using newly presented analyses along with Global Network of Isotopes in Precipitation data. The collected precipitation samples yield a new local meteoric water line (δ²H = 7.1 * δ¹⁸O + 8.46) for the Azores region and the North Atlantic Ocean. The annual isotopic mean of precipitation shows a small range for the unweighted and precipitation mass‐weighted δ¹⁸O‐H₂O values. Results show an inverse relation between the monthly δ¹⁸O‐H₂O and the amount of precipitation, which increases in elevation and into the interior of the island. Higher amounts of precipitation (from convective storm systems) do not correspond to the most depleted values of stable isotopes in precipitation. Precipitation shows an orographic effect with depleted δ¹⁸O‐H₂O values related to the Rayleigh effect. Monthly δ¹⁸O‐H₂O values for individual precipitation sampling stations show little relationship to air temperature. Results show a local source of moisture during the summer with the characteristics of the first vapour condensate. The stable isotope composition of precipitation is strongly correlated to the NAO index, and δ¹⁸O‐H₂O values show a statistically significantly trend towards enrichment since 1962 coincident with the increased air temperature and relative humidity due to climate change. Results are in line with observations of increasing sea surface temperature and relative humidity.     

Terrestrial‐originated submarine groundwater discharge through deep multilayered aquifer systems beneath the seafloor

A large quantity of submarine groundwater discharge (SGD) of about 1000 m³ day^?1 m^?1 of the 600‐km‐long shoreline of South Atlantic Bight has been estimated by Moore (Global Biogeochemical Cycles, 2010b, 24, GB4005, doi: 10.1029/2009GB003747 ). However, there is great uncertainty in estimating the percentage of net, land‐originated groundwater recharge of SGD. Moreover, most previous studies considered the homogeneous case for the coastal superficial aquifers. Here, we investigated the terrestrial‐originated SGD through a multilayered submarine aquifer system, which comprises two confined aquifers and two semi‐permeable layers. The inland recharge includes a constant part representing the annual average and a periodical part representing its seasonal variation. An analytical solution was derived and used to analyse the distributions of the terrestrial‐originated SGD from the multilayered aquifers along the Winyah Bay transect, South Atlantic Bight. It is found that the width of the zone of SGD from the upper aquifer ranges from ~0.8 to ~8.0 km depending on the leakance of the seabed semi‐permeable layer. A head of the upper aquifer at a coastline 1.0 m higher than the mean sea level will cause a SGD of 1.82– 18.3 m³ day^?1 m^?1 from that aquifer as the seabed semi‐permeable layer's leakance varies from 0.001 to 0.1 day^?1, providing considerable possibility for considerable land‐originated SGD. Seasonal terrestrial‐originated SGD variations predicted by the analytical model provide consistent explanation of the seasonal variation of ²²⁶Ra observed by Moore (Journal of Geophysics, 2007, 112, C10013, doi: 10.1029/2007JC004199 ). The contribution of the lower aquifer to SGD is only 1.2–12% of that of the upper aquifer. Copyright © 2014 John Wiley & Sons, Ltd.