河套盆地周缘泉水化学组分对2015年4月15日阿左旗MS5.8地震的响应*

根据河套盆地周缘断裂带泉水的氢、氧同位素组成和水化学组分,讨论了该区地下水的化学类型、成因及其与地震活动的关系。于2014年9月下旬和2015年4月15日M_S5.8阿左旗地震震后在河套盆地周缘的乌拉山断裂带、色尔腾断裂带、狼山断裂带以及桌子山断裂带采集了17个泉水和井水样品,测得水样的TDS分布在143.8~42 553.0mg/L范围内,δD和δ¹⁸O值分别在-83.6‰~66.56‰和-11.16‰~8.2‰的范围内,来源为大气降水。根据舒卡列夫分类法,震前水样可划分为13种水化学类型,震后西山咀、圐圙朴隆等5个点采样点泉水的水化学类型发生变化。其中,乌拉山断裂带的水样以HCO₃-Ca型低矿化度地表水为主;色尔腾断裂带、狼山断裂带泉水受白垩系含水层影响,矿化度较高,富含HCO^-₃及SO^2-₄;桌子山一带受煤矿开采影响,水样以富SO^2-₄和Cl^-的高矿化度水为特征。地震前后TDS、阴、阳离子以及γNa/γCl、γ(SO₄+Cl)/γHCO₃、γHCO₃/γCl等毫克当量比值能够较好地反映地震。2015年4月15日阿左旗M_S5.8地震后,呼鲁斯太、迪延阿贵庙及八一井的水化学组成变化较大,对地震响应较为敏感。呼鲁斯太地区泉水的TDS稍有降低,但HCO^-₃在阴离子中所占比例有所增加,表明震后该地区含水层的泉水与较低矿化度的含碳酸盐岩含水层水发生了混合;八一井的TDS值有所增加,γNa/γCl比值有所降低,表明深部高矿化度水的混入;迪延阿贵庙水样的TDS稍有下降,但NaCl的相对含量较震前有所升高,表明有低矿化度NaCl水的混入。本工作不仅确定了该区水文地球化学背景,而且对地震监测和预测具有一定参考价值。     

Dispersion of naturally occurring ions in groundwater from various rock types in a portion of the San Pedro river basin, Arizona

The groundwater in an alluvial basin in southern Arizona was analyzed for concentrations of Ca⁺⁺, Mg⁺⁺, Na⁺, and Cl⁻, ions.

The variety of rock types in the area, plus the undisturbed state of the groundwater basin, make comparative rock mineralization-groundwater ionization interpretations possible. Ionic dispersion in groundwater eminating from source areas composed of differing rock types is plotted as isogram maps. These isolated areas of differing mineral composition each exhibit a unique ionic contribution to groundwater. The ion concentrations in groundwater were then used as naturally occurring tracers to determine source areas of recharge and to delineate subsurface barriers to the normal basin flow net. Ion dispersion plots reveal the carbonates of the Dragoon Mountains to be a major contributor of Ca⁺⁺ and Mg⁺⁺ to the deep alluvial portion of the basin. Cl⁻ dispersion patterns show the granitic intrusives of the Tombstone Hills produce a barrier effect in the normal flow pattern of the basin as well as being a contributor of Cl⁻ to groundwater.     

Distribution, source and evolution of nitrate in a glacial till of southern Alberta, Canada

This paper addresses the distribution, origin and controls upon nitrate in a 30-km² area of the Interior Great Plains Region of southern Alberta, Canada. High concentrations of nitrate (> 100 mg l⁻¹ NO⁻₃-N) occurred in several isolated enclaves below the water table in brown weathered till. Nitrate concentrations of over 300 mg l⁻¹-N were encountered in groundwater samples collected from these enclaves. Low nitrate concentrations (< 1.1 mg l⁻¹ NO⁻₃-N) were also encountered in the weathered till upgradient and downgradient of the nitrate enclaves. Groundwater samples collected from the underlying grey nonweathered till and bedrock had NO⁻₃-N concentrations of < 1.1 mg l⁻¹.

Through the application of geochemical (NO⁻₃-N and NH⁺₄-N) studies, environmental isotope studies (tritium), microbial analyses (nitrifiers) and laboratory experiments, it was shown that the high nitrates found in the weathered till are the result of the oxidation of ammonium present within the tills. It is postulated that this oxidation occurred during the Holocene epoch when water tables were much lower than present-day levels (5–18 m, and 2 m below ground, respectively).

Through the use of Eh measurements, the enumeration of denitrifying bacteria and laboratory experiments, the potential for denitrification was shown to exist below the present-day water table in the weathered till as well as in the nonweathered till and bedrock. Isotopic data showed that less denitrification may be occurring within the nitrate enclaves than in adjacent downgradient areas.     

Open-system degassing of sulfur from Krakatau 1883 magma

We present the first sulfur and oxygen isotopic data for tephra from the catastrophic 1883 eruption of Krakatau. Sulfur isotopic ratios in unaltered Krakatau tephra erupted August 26–27, 1883 are markedly enriched in ³⁴S relative to mantle sulfur. High δ³⁴S values of +6.3 to +16.4‰ can best be explained by open-system or multi-stage degassing of SO₂ from the oxidized rhyodacitic and gray dacitic magmas with ³⁴S enrichment of SO²⁻₄ remaining in the melt. Lower whole-rock δ³⁴S values of +2.6‰ and +4.0‰ in two oxidized gray dacitic samples indicate more primitive subarc mantle sulfur in the 1883 magma chamber. Initial δ³⁴S of the rhyodacitic magma was probably in the +1.5‰ to +4.0‰ range and similar to δ³⁴S values measured in arc volcanic rocks from the Mariana Arc.     

Causes of acidity in the River Lillån in the coastal zone of central northern Sweden

Factors controlling acidity were studied in the acidic River Lillån in the coastal zone of central northern Sweden. The stream drains the hilly wave-washed terrain and the sediment-covered coastal plain which are the dominating types of landscape in the region. A synoptic study of 38 small streams, representing both types of landscape was also made. Acidity in all streams is caused by organic acids in combination with catchment sources of sulfate. The most acidic streams occur in the hilly terrain because of a high terrestrial export of organic acids and low buffering capacity. Acidic episodes during snowmelt were associated with strongly decreased base cation concentrations, decreased SO²⁻₄ and slightly increased organic acids concentrations. Frequently occurring acid episodes caused by rainstorms and associated outwash of organic acids from forest soils are typical for events in late summer and autumn. It is suggested that, in all essential aspects, the acidity in surface waters in this part of Sweden is of natural origin.     

Formation of a salt plume in the Coastal Plain aquifer of Israel: the Be''er Toviyya region

The formation and development of a salt plume (salinity up to 800 mg Cl 1⁻¹) in the inner part of the Coastal Plain aquifer of Israel is analyzed. Massive groundwater exploitation during the 1950s caused a large drop in the water level and formation of a hydrologic depression in the Be'er Toviyya-Kefar Warburg area. The depression reached a maximal depth during the late 1960s; thereafter a reduction in the rate of pumpage led to restoration of water levels and shallowing of the depression, until its complete disappearance towards the end of the 1980s. A spot of high salinity first appeared in 1956, following a deep drawdown in the water levels. This saline plume has been continuously expanding with increasing salinity concentrations (200–800 mg Cl 1⁻¹) in its center. The average rate of radial expansion was about 50 m year⁻¹. The expansion and salinization did not cease as the depression disappeared. Rather, equalization of water levels in wells situated within the plume area with those of situated along its margins resulted in the salinization of the latter within a period of 1 year.

Mass balances for water and chloride contents were made for the period 1967–1990. Taking into consideration the storage change, pumpage, natural replenishment and artificial recharge, the lateral inflow to the depression is estimated as 60 × 10⁶ m³. Upon addition of the chloride balance, and taking into consideration the chloride concentrations of the surrounding fresh water and the apparent possible end-member of the saline source (based on geochemical considerations), the saline inflow is estimated as (40–60) × 10⁶ m³. These estimates indicate that a large amount of saline water penetrated into the aquifer, of about half of the natural replenishment of the study area, with an estimated salinity of 1900–2700 mg Cl 1⁻¹.

It is suggested that the salt plume was formed as a result of a drop in water level combined with a flow of underlying saline water bodies from deeper strata. The chemical composition of the groundwater points to the existence of two saline water bodies of Ca-chloride composition and a marine Br/Cl ratio: (1) saline water with low Na/Cl (0.6), So₄/Cl, and B/Cl ratio; (2) saline water with higher Na/Cl (> 0.6), So₄/Cl, and B/Cl ratios. These chemical compositions resemble Ca-chloride saline waters found in other locations in the Coastal Plain aquifer and in underlying formations. The saline water bodies may occur in either pockets at the bottom of the aquifer or lumachelle and sandstone layers of high hydraulic conductivity in underlying sediments.     

Influence of artificial groundwater lakes on the abundance and activity of bacteria in adjacent subsurface systems

Bacterial abundances and activity, estimated by 4′,6-diamidino-2-phenylindole staining (DAPI) and the reduction of 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyl tetrazolium chloride (INT), were investigated in two oligotrophic artificial groundwater lakes and the surrounding aquifers. To evaluate the effect of lake water on groundwater downstream, samples were taken from wells at different distances from the lakes, and the total number of bacteria and the number of active bacteria in these samples were compared with samples collected upstream. In addition, sterilized sandy sediments were exposed in groundwater wells to measure the number and activity of bacteria attached to particles. At one of the study sites, where the lake sediments were disturbed by dredging, total bacterial abundance and the number of respiring bacteria in the groundwater aquifer was clearly influenced by the lake water. The average bacterial abundances decreased from 2.6 ± 1.9 × 10⁵ cells ml⁻¹ in the well closest to the lake (S2) to 2.9 ± 3.8 × 10⁴ cells ml⁻¹ in the most distant one (S4), which was equivalent to cell numbers in the upstream well. The number of respiring bacteria showed a similar tendency with 1.3 ± 2.7 × 10⁴ active cells ml⁻¹ in S2 and 1.9 ± 1.5 × 10³ active cells ml⁻¹ in S4. At the second study site, which was not influenced by dredging, bacteria in the downstream wells seemed not to be affected by the lake water. The number and activity of bacteria, which colonized exposed sediments, were not significantly different in the upstream and downstream wells, indicating a minor influence of lake water on this habitat. Our results suggest that gravel-pit lakes may influence the free living bacterial assemblages in nearshore groundwater systems, but do not visibly affect numbers and activity of bacteria attached to the surface of aquifer sediments.     

On the strength of electric currents and zonal magnetic fields at the top of the Earth''s core: Methodology and preliminary estimates

A new method is described for estimating: (a) the meridional electric current density, j_θ, (b) the vertical growth rate of the zonal magnetic field, ∂B_φ/∂r, or its scale-height, B_φ/∂B_φ/∂r) and (c) the vertical growth rate of the vertical current density, ∂j_r/∂r, at a few isolated points on the top surface of the Earth's core from observations of the internal geomagnetic field at the Earth's surface. The theoretical technique rests on combining unaccelerated, gravitationally-driven Boussinesq fluid dynamics of the core with frozen-flux electromagnetism, the mantle being treated as a spherically symmetric insulator.

Insertion into this theory of main field models for epochs 1965, 1975 leads to preliminary values for these quantities of magnitude: (a) j_θ 1 A/m², (b) ∂B_φ/∂r 10⁻⁶ T/m or B_φ/(∂B_φ/∂r) 10 m, (c) ∂j_r/∂r 10⁻⁶ A/m³. Some geophysical implications of these estimates are discussed.     

Water flow path interactions with soil hydraulic properties in till soil at Gårdsjön, Sweden

In 1989, in a hydrological research programme within a deacidification project in the Gårdsjön area in southwest Sweden, flow paths and residence times of soil water and groundwater in microcatchments were examined to support the interpretation of the hydrochemical changes. Saturated hydraulic conductivity and soil water retention were analysed on more than 100 cylinder samples. The catchments have shallow sandy-silty till soil with a mean depth in the main catchment of 43 cm. Porosity of the mineral soil in the main catchment was high and ranged from 38 to 85%. The samples from the B-horizon had generally higher porosity. Porosity and the content of organic matter were correlated. The soil water retention was relatively high at all tensions, likely owing to the high content of organic matter. Dissolved organic substances were most probably transported from the shallow soil on the steep sides of the catchment down to the valley where it precipitated. The high porosities could be a consequence of long-term weathering, provided that the organic substances present have increased the leaching of the weathering products. Measured values of saturated hydraulic conductivity were close to log-normally distributed with a mean for all samples of 3 × 10⁻⁵ m s⁻¹. There was a significant increase in conductivity toward the ground surface with the mean conductivity of the samples in the uppermost 10 cm of the mineral soil of 4 × 10⁻⁵ m s⁻¹, which was about 13 times higher than the conductivity of 3 × 10⁻⁶ m s⁻¹ at 1 m depth. From the relationship between runoff at the catchment outlet and groundwater levels, the conductivity was estimated to be 15–200 times higher in the upper soil layer than in the deeper ones. In one profile, 44–64% of the yearly lateral flow was estimated to occur above 30 cm depth. The conductivity was correlated with the content of drainable water, which indicated the importance of the largest pores for the saturated hydraulic conductivity.     

REE diffusion in calcite

Chemical diffusion of four rare-earth elements (La, Nd, Dy and Yb) has been measured in natural calcite under anhydrous conditions, using rare-earth carbonate powders as the source of diffusants. Experiments were run in sealed silica capsules along with finely ground calcite to ensure stability of the single-crystal samples during diffusion anneals. Rutherford backscattering spectroscopy (RBS) was used to measure diffusion profiles. The following Arrhenius relations were obtained over the temperature range 600–850°C: D_La =2.6×10⁻¹⁴ exp(−147±14 kJ mol⁻¹/RT) m² s⁻¹, D_Nd =2.4×10⁻¹⁴ exp(−150±13 kJ mol⁻¹/RT) m² s⁻¹, D_Dy =2.9×10⁻¹⁴ exp(−145±25 kJ mol⁻¹/RT) m² s⁻¹, D_Yb =3.9×10⁻¹² exp(−186±23 kJ mol⁻¹/RT) m² s⁻¹. In contrast to previous findings for refractory silicates (e.g. zircon), differences in transport rates among the REE are not pronounced over the range of temperature conditions investigated in this study. Diffusion of the REE is significantly slower than diffusion of the divalent cations Sr and Pb and slower than transport of Ca and C at temperatures above 650°C. Fine-scale zoning and isotopic and REE chemical signatures may be retained in calcites under many conditions if diffusion is the dominant process affecting alteration.     

Origin of the high variability of water mineral content in the bedrock aquifers of Southern Madagascar

This study assesses the causes of the high spatial variability of the mineral content of groundwater in crystalline bedrock of Southern Madagascar. Although many kilometres from the coast and at a mean altitude of 400 m a.s.l, wells drilled in this area produce water with electrical conductivities in the range of 300–30,000 μS cm⁻¹ with a high spatial variability. Chemical and isotopic data are used to identify the processes involved in the groundwater mineralization. It is shown that the chemical composition of the groundwater in this region has its origin in (i) normal silicate and carbonate weathering reactions and (ii) input of marine salts, probably via rainfall recharge, modified by evapo-concentrative processes probably including precipitation and re-dissolution of secondary evaporites in the unsaturated zone. To obtain a better understanding of the spatial salinity distribution, well parameters such as yields, weathered zone thickness, weathered materials and morphological positions (upper slope, mid-slope, lower slope or valley bottom) are scrutinized.

A correlation was found between high salinity and low flow, shallow groundwater environments (flat hill tops, valley bottoms, weakly developed and clayey weathered zones) and between low salinity and high flow environments (granular, well-developed weathered zones and situation on valley slopes).     

Attenuation of nitrate in aquitard sediments of southern Ontario

To examine nitrate persistence, detailed geochemical profiling, using core-squeezed water and piezometer samples, was carried out at five sites in southern Ontario where groundwater is moving downward in silt-rich aquitard sediments at rates of 16 to more than 20 cm year⁻¹. Elevated levels of NO₃⁻-N (5–50 mg 1⁻¹) that occur in the shallow groundwater as a result of agricultural activity, were found to be consistently attenuated, generally to very low levels (< 0.05 mg 1⁻¹-N), at the ‘redoxcline’, the horizon marking the boundary between the surficial weathered (brown) sediments and the underlying unweathered (grey) sediments. Tritium dating suggests that groundwater at the redoxcline depths (3–5 m) was recharged between 1970 and 1980, thus the N03 depletion appears to result from biodegradation reactions since no major landuse changes have occurred during this period. The close association of the nitrate depletion zones with the redoxcline, where, in particular, sediment sulphur contents increase abruptly, and where also porewater SO₄²⁻ levels increase, suggests that the dominant attenuation reaction is autotrophic denitrification using reduced sulphur compounds present in the unweathered sediment as the electron donor. Mass balance calculations suggest that the increase in the downward rate of migration of the redoxcline, owing to added sulphur consumption from NO₃⁻ contamination, is only about 1 mm year⁻¹ at these sites. Review of the literature indicates that most silt- and clay-rich sediments have S contents in the same range, or higher, than those investigated here, thus, in most cases where aquifers are overlain by several metres or more of unweathered confining sediments, it is likely that a high degree of protection is afforded from surficial NO₃⁻ contamination.     

Intensifying groundwater acidification at Birkenes, southern Norway

Groundwater chemical data from Birkenes, southern Norway, collected during the period October 1980 to November 1993, reveal intensifying acidification in the 1990s, as evidenced by decreases in pH, acid-neutralising capacity and alkalinity, and increases in hardness/alkalinity ratio, ‘acidification’, nitrate, non-marine sulphate (SO₄^*), non-marine hardness (Ca^* + Mg^*) and dissolved aluminium. The whole monitoring period is characterised by slopes of four or more on a plot of (Ca^* + Mg^*) vs. alkalinity.

Owing to its proximity to the sea, the Birkenes catchment receives seasalt-influenced precipitation, which results in episodic, natural acidification of the groundwater via cation exchange of marine Na⁺ with soil-bound H⁺ and/or Al³⁺. However, it is uncertain whether all of the recent groundwater acidification can be attributed to intensifying seasalt deposition alone: the steep slopes on the (Ca^* + Mg^*) vs. alkalinity plot and the increase in groundwater SO₄^* suggest that strong acids, of possible anthropogenic origin, may be involved. Additionally, seasalt deposition appears not to have increased during the 1990s: Cl⁻ content in precipitation has not increased significantly and river water pH has not decreased significantly over the period 1990–1993. The suggestion is made that the observed intensification in groundwater acidification at Birkenes partly results from the exhaustion or weakening of an acid buffering system caused by soil acidification, under persisting, even if abating, anthropogenic acid loading.     

The Effect of Copper on the Settlement Success of Larvae from the Scleractinian Coral Acropora tenuis

This study examined the effect of copper on the settlement success of planula larvae of the reef-building coral Acropora tenuis during 1994 and 1996 at Magnetic Island, Great Barrier Reef. Copper concentrations of 2, 10, 20 μg l⁻¹ did not inhibit larval settlement after 48-h exposure. However, copper concentrations of 42 μg l⁻¹ and 81 μg l⁻¹ significantly reduced settlement success of A. tenuis larvae after 48-h exposure compared with controls using normal seawater. At 200 μg l⁻¹ copper, all larvae died. EC₅₀ values for the effect of copper on A. tenuis larval settlement were calculated from the 1996 results using measured copper concentrations. The 48-h EC₅₀ was 35 μg l⁻¹ with an upper and lower 95% confidence limit of 37 μg l⁻¹ and 32 μg l⁻¹, respectively. The 48-h NOEC value for both experiments was 20 μg l⁻¹ copper. These experiments provide some of the first data on sub-lethal effects of trace metals on tropical marine organisms, and demonstrate that relatively low copper concentrations impair or inhibit settlement of coral larvae.     

Steady state analysis of unsaturated flow above a shallow water-table aquifer drained by ditches

The one-dimensional pressure head profile above a fixed water-table was studied for different steady infiltration rates. As shown in previous studies, when the infiltration rate (q_in) is less than the soil saturated hydraulic conductivity (Ks), this profile can be divided into two parts: (1) from the water-table surface (z₀) to an elevation z_γ, the pressure head varies from 0 to a value h_γ such as K(h_γ)=−q_in; (2) above the elevation z_γ the pressure head is constant and equal to h_γ. Above the water-table the zone where the pressure head is variable has been called ‘transition zone’. Its height is shown to be highly variable and to depend on soil properties as well as on the infiltration rate. This transition zone is not the ‘capillary fringe’ as defined by Gillham (Gillham R.W., 1984. The capillary fringe and its effect on water-table response. J. Hydrol. 67, 307–324). Numerical experiments performed with HYDRUS-2D^® for the case of a water-table drained by parallel ditches have shown that the height of the transition zone is similar in the one-dimensional profile and in the two-dimensional system as long as the local slope of the water-table is small. This result is important since in a two-dimensional system, the transition zone is the place where all the horizontal component of the unsaturated flow occurs. The ratio of the horizontal component of the unsaturated flow vs the total horizontal flow in both the unsaturated and saturated zones has been computed. For a given soil, this ratio decreases as the infiltration rate increases; for a given infiltration rate, the soil with the thinnest transition zone transfers the largest amount of water above the water-table.     

The impact of freshwater and wastewater irrigation on the chemistry of shallow groundwater: a case study from the Israeli Coastal Aquifer

Differences in the impact of irrigation with freshwater versus wastewater on the underlying shallow groundwater quality were investigated in the Coastal Aquifer of Israel. Seven research boreholes were drilled to the top-most 3–5 m of the saturated zone (the water table region-WTR) in the agricultural fields. The unsaturated zone and the WTR below the irrigated fields consist mainly of clayey sands, while the main aquifer comprises mainly of calcareous sandstones and sands. We show that the salinity and composition of the groundwater at the WTR are highly variable over a distance of less than 1 km and are controlled by the irrigating water and the processes in the overlying unsaturated zone. Tritium data in this groundwater (4.6 tritium units (TU)) support that these water are modern recharge. The water at the WTR is more saline and has a different chemical composition relative to the overlying irrigation water. High SAR values (sodium adsorption ratio) in wastewater irrigation lead to absorption of Na⁺ onto the clay and release of Ca²⁺ into the recharging water, resulting in low Na/Cl (0.4 compared to 1.2 in the wastewater) and high Ca/Cl ratios. In contrast, in the freshwater-irrigated field the irrigation water pumped from the aquifer (Na/Cl=0.9; SAR=0.6) is modified into Na-rich groundwater (Na/Cl=2.0) due to reverse base-exchange reactions. The high NO₃ concentration (>100 mg/l) in the WTR below both fields is derived from the agricultural activities. In the freshwater field, the source of NO₃ is fertilizer leachates, whereas in the wastewater field, where less fertilizers are applied, nitrate is probably derived from nitrification of the NH₄ in the wastewater. Some of the original inorganic nitrogen in the wastewater is consumed by the agricultural plants, resulting in a lower inorganic-N/Cl ratio in the WTR as compared to that in the wastewater. This study demonstrates the important role of the composition of irrigation water, combined with lithology and land use, in determining the quality of the water that recharge the aquifer below agricultural fields.     

Magnetic domain observations of nucleation processes in natural pyrrhotite and titanomagnetite

Magnetic domain patterns have been observed on particles of natural pyrrhotite and titanomagnetite undergoing hysteresis. These observations indicate that hysteresis properties are governed by two distinct mechanisms: (1) wall-pinning and (2) nucleation of reverse domains. Particles which are dominated by wall-pinning spontaneously nucleate reverse domains in saturation remanence (J_rs). The coercivity of such grains is determined by the presence of potential wells encountered by the wall in its traverse across the grain. However, many pseudosingle-domain particles (PSD) between 5 and 30 μm in diameter do not nucleate reverse domains in J_rs, but remain as saturated single-domains. These particles require a reverse field H_n to nucleate domain walls. When H_n is sufficiently large, the nucleating field controls magnetization reversal by driving the wall across the particle in a single Barkhausen jump, and the muscopic coercivity is nucleation-dominated.

The proportion P (w=0) of particles of a given size d which fail to nucleate walls in J_rs is found to be given by A exp(−Bd^1/2), where A and B are experimentally determined constants. The nucleation field H_n in pyrrhotite is observed to increase with decreasing grain size, exceeding 500 Oe in 5 μm particles.

The difficulty with which reverse domains are nucleated subsequent to saturation may thus provide a mechanism for achieving the high values of J_rs/J_s and coercive force observed in fine, pseudosingle-domain particles.     

The seasonal variation of streamwater chemistry in three forested Mediterranean catchments

Streamwater chemistry is described for three streams draining undisturbed, evergreen broad-leaved forested catchments on phyllites in NE Spain: two streams with no or negligible flow in summer are located in the Prades massif, and one perennial stream is in the wetter Montseny mountains. Weekly data for a study period of 2–4 years are provided to (1) describe the seasonal variations in streamwater chemistry, (2) analyse the relationship between stream discharge and solute concentrations using a two-component mixing model and (3) search for patterns of temporal variation in stream solute concentrations after discounting the effects of discharge. At Prades, concentrations of all analysed ions, except NO⁻₃, showed marked seasonal variations in stream water, whereas at Montseny only ions related to mineral weathering (HCO⁻₃, Na⁺, Ca²⁺ and Mg²⁺) showed strong seasonality. Ion concentrations were more closely dependent on instantaneous discharge at Montseny than at Prades. The residuals of the relationship between solute concentrations and discharge retained a strong seasonality at Prades, but not at Montseny. These differences are related to the major hydrochemical processes that determine the streamwater chemistry at each site. The same processes are probably operative in the three catchments, but are of varying relative importance. At Montseny, the mixing of waters of different chemical composition seems to be the major process controlling streamwater chemistry, although the soilwater end-member composition predicted by the mixing model applied did not match the measured soilwater chemistry. In the drier Prades catchments, the two major hydrochemical processes determining the seasonal variation of streamwater chemistry are (1) the restart of flow after the summer drought, which flushes out the solutes accumulated during the dry period, and (2) the seasonal changes in groundwater chemistry that result from the interplay of water residence time, temperature and CO₂ partial pressure. In Mediterranean catchments with relatively high precipitation, such as Montseny, the seasonal variation in the streamwater chemistry is largely determined by the same processes as at humid-temperate sites, whereas in drier Mediterranean catchments, such as Prades, the major hydrochemical processes are clearly distinct.     

Towards a classification of organic enrichment in marine sediments based on biogeochemical indicators

A nomogram is developed to show that pH, redox potentials (Eh_NHE) and measures of dissolved sulfides (H₂S + HS⁻ + S²⁻)(total free S²⁻) can be used to classify organic enrichment impacts in marine sediments. The biogeochemical cycle of sulfur in marine sediments is described to show that changes in macrobenthic infauna community structure associated with high levels of organic matter supply result from stress due to oxygen deficiency (hypoxia and anoxia) and toxic effects of S²⁻. The changes reflect enhancement of microbial sulfate reduction under conditions of high organic matter sedimentation and the progressive formation of hypoxic–anoxic conditions measured by decreased Eh_NHE and increased concentrations of S²⁻. The nomogram provides a basis for classification of the oxic status of marine sediments based on changes in inter-related biological and biogeochemical variables along an organic enrichment gradient.     

A case study on fuel oil contamination in a mangrove swamp in Hong Kong

Mangroves commonly found along tropical and subtropical coastlines are susceptible to oil pollution. In December 2000, around 500 1 m tall Kandelia candel saplings at the age of 3–5 years old located at the foreshore region of Sheung Pak Nai swamp, Hong Kong SAR, were found to be damaged by oil pollution. More than 80% of the saplings were either dead or washed away and leaving less than 5% healthy saplings with dense green leaves. Elevated concentrations of light n-alkanes (ranging from n-C₁₄ to n-C₂₀), pristane and phytane were recorded in surface sediments collected in December 2000. The ratio between light and total n-alkanes was 0.4. The total petroleum hydrocarbons (60–80 μg g⁻¹ TPH) and unresolved complex mixtures (60–70 μg g⁻¹ UCM) were higher than the background values of other mangrove sediments in Hong Kong, which were 40 and 20 μg g⁻¹, respectively. In certain root zone sediments, TPH concentrations were above 1000 μg g⁻¹. These results suggest that surface sediments in Sheung Pak Nai were contaminated by petroleum oil, most likely by illegal discharge of fuel oil which occurred between 1998 and 2002. One year later, in December 2001, unhealthy saplings had recovered and re-grown. The concentrations of TPH and UCM in sediments declined to around 40 μg g⁻¹, pristane and phytane dropped by 80%, and the ratio of light to total n-alkanes was 0.15, suggesting that residual oil in sediments was weathered leading to a remarkable recovery of the unhealthy saplings.