Chloride cycling in two forested lake watersheds in the west-central adirondack mountains,New York,U.S.A.

The chemistry of precipitation, throughfall, soil water, ground water, and surface water was evaluated in two forested lake-watersheds over a 4-yr period to assess factors controlling Cl^? cycling. Results indicate that Cl^? cycling in these watersheds is more complex than the generally held view of the rapid transport of atmospherically derived Cl^? through the excosystem. The annual throughfall Cl^? flux for individual species in the northern hardwood forest was 2 to 5 times that of precipitation (56 eq ha^?1), whereas the Na⁺ throughfall flux, in general, was similar to the precipitation flux. Concentrations of soil-water Cl^? sampled from ceramic tension lysimeters at 20 cm below land surface generally exceeded the Na⁺ concentrations and averaged 31 μeq L^?1, the highest of any waters sampled in the watersheds, except throughfall under red spruce which averaged 34 μeq L^?1. Chloride was concentrated prior to storms and mobilized rapidly during storms as suggested by increases in streamwater Cl^? concentrations with increasing flow. Major sources of Cl^? in both watersheds are the forest floor and hornblende weathering in the soils and till. In the Panther Lake watershed, which contains mainly thick deposits of till (>3 m), hornblende weathering results in a net Cl^? flux 3 times greater than that in the Woods Lake watershed, which contains mainly thin deposits of till. The estimated accumulation rate of Cl^? in the biomass of the two watersheds was comparable to the precipitation Cl^? flux.     

Acidity status of surface waters in Massachusetts

The Massachusetts Acid Rain Monitoring project surveyed 80.5% of the state's 5294 named water bodies between 1983 and 1985. PH and acid neutralizing capacity (ANC) were measured monthly the first 14 mo and semi-annually afterwards. Sample collection and analysis were performed by volunteers. The majority of surface waters in Massachusetts were found to be sensitive to possible long term acidification, with 63% exhibiting ANC less than 200 μeq L^?1 and 22% with ANC less than 40 μeq L^?1. Seasonal patterns in ANC were observed, the median ANC being 384 μeq L^?1 in summer/fall and 134 μeq L^?1 in winter/spring. Geographical differences were also found across the state: the streams and lakes with lowest pH and ANC were located in the southeastern and north-central parts of the state, while the most alkaline surface waters were found in the western-most part of the state, which is the only area of the state with significant limestone deposits.     

Chemistry differences in two streams entering an acidic lake in the Adirondack Mountains,New York (U.S.A.)

Solution chemistry was measured in two major inlets, lake water column, lake outlet, and soils of the South Lake watershed in the Adirondack Mountains, New York. The east inlet had greater concentrations of H⁺, sulfate-S, and Al and smaller concentrations of base cations and silica than the west inlet (70, 116, 25, 90, 64 and 4, 99, 8, 228, 148 μeq L^?1 of H⁺ and sulfate-S, μmol L^?1 Al, μeq L^?1 total base cations and μmol L^?1 silica in east and west inlets, respectively). Concentrations of base cations in C horizon soil solutions (157 μeq L^?1 total base cations) were smaller and greater than west and east inlets, respectively. This suggests that water flowing into the west inlet contacted deeper mineral layers, whereas water reaching the east inlet did not. Lake and lake outlet concentrations were also intermediate between the two inlets, and the lake was acidic (pH 4.9 to 5.1) with relatively high total monomeric Al concentrations (8 to 9 μmol Al L^?1). The east inlet also had greater DOC concentrations than the west (0.38 and 0.24 μmol C L^?1, respectively), again indicating that soil solutions entering the east inlet passed through the forest floor but had more limited contact with deeper mineral layers in comparison with the west inlet. Differences between the streams are hypothesized to be related to contact of percolating solutions with mineral soil horizons and underlying glacial till, which provides neutralization of acidic solutions and releases base cations. This work indicates that processes controlling surface water acidification can be spatially quite variable over a small watershed.     

On the prediction of acid precipitation events and their effects on fishes

It is possible to predict acid rain events and melts of acid snow some 12 to 24 hr in advance, including estimation of the magnitude and duration of such events. This is sufficient notice to permit monitoring of stream chemistry and fish plasma and muscle ions before acid stress, and to continue this monitoring throughout and after specific events. Such a program has been in place for 2 yr in waters tributary to the Milford Bay Trout Hatchery, Ontario. During one snow melt in February 1984 surface waters showed a decline to pH 4 and associated negative ANC. Rainbow trout held in such water lost plasma Na and Cl rapidly and died within 28 hr. The hatchery water supply, consisting of a mixture of spring and surface water, showed a decline in alkalinity from 300 to 30 μeq.L^?1, and a pH change from 6.6 to 5.4, during snow melt. Total A1 concentration increased from 42 to 222 μg.L^?1 during snow melt with the “reactive” component increasing from 17 to 112 μg.L^?1. Rainbow trout held in this water did not show physiological stress. More rapid run-off of melt water could be expected to exhaust all of the alkalinity in the hatchery water supply permitting the pH to decline and A1 concentration to rise to levels lethal to the hatchery stock of rainbow trout.     

Response to a smelter closure in Cascade mountain lakes

A statistically significant decrease in sulfate was observed in high elevation Cascade lakes during 1983 through 1988. The total decrease averaged 2.2 μeq L^?1 in two slow-flush lakes and 4.2 μeq L^?1 in three fast-flush lakes for 1983–1985 vs 1986–1988, respectively. Coincident with these changes in sulfate concentrations were a sharp decrease of SO₂ emissions from the ASARCO smelter (100 km SE of the lakes), from 87 to 70 kt yr^?1 during 1983–1984 to 12 in 1985, the year of its closure, and a gradual change in SO₂ emissions from Mt. St. Helens, from 39 to 27 during 1983–1984 to 5 in 1988. The sharpest decreases occurred in non-marine sulfate in fast-flush lakes from 1984 to 1985 (about 2 μeq L^?1) and in slow-flush lakes from 1985 to 1986 (1 μeq L^?1, which point to the ASARCO closure as the sole cause. However, some of the more gradual decline in non-marine sulfate observed during 1983 through the 1988 sampling periods may have been due to a slow washout of sulfate enriched ash from the 1980 Mt. St. Helens' eruption. Sulfate concentrations in precipitation also declined significantly by about 2 μeq L^?1, but changes in volume-weighted sulfate content were not significant. Lake alkalinity did not show a consistent increase in response to decreased sulfate. This was probably due to either watershed neutralization of acidic deposition or the greater variability in alkalinity measurements caused by small changes in acidic deposition making it difficult to detect changes.     

Long-Term Annual and Seasonal Patterns of Acidic Deposition and Stream Water Quality in a Great Smoky Mountains High-Elevation Watershed

The recovery potential of stream acidification from years of acidic deposition is dependent on biogeochemical processes and varies among different acid-sensitive regions. Studies that investigate long-term trends and seasonal variability of stream chemistry in the context of atmospheric deposition and watershed setting provide crucial assessments on governing biogeochemical processes. In this study, water chemistries were investigated in Noland Divide watershed (NDW), a high-elevation watershed in the Great Smoky Mountains National Park (GRSM) of the southern Appalachian region. Monitoring data from 1991 to 2007 for deposition and stream water chemistries were statistically analyzed for long-term trends and seasonal patterns by using Seasonal Kendall Tau tests. Precipitation declined over this study period, where throughfall (TF) declined significantly by 5.76?cm?year^?1. Precipitation patterns play a key role in the fate and transport of acid pollutants. On a monthly volume-weighted basis, pH of TF and wet deposition, and stream water did not significantly change over time remaining around 4.3, 4.7, and 5.8, respectively. Per NDW area, TF SO₄ ^2- flux declined 356.16?eq?year^?1 and SO₄ ^2- concentrations did not change significantly over time. Stream SO₄ ^2- remained about 30???eq L^?1 exhibiting no long-term trends or seasonal patterns. SO₄ ^2- retention was generally greater during drier months. TF monthly volume-weighted NH₄ ⁺ and NO₃ ^- concentrations significantly increased by 0.80???eq L^?1?year^?1 and 1.24???eq L^?1?year^?1, respectively. TF NH₄ ⁺ fluxes increased by 95.76?eq?year^?1. Most of NH₄ ⁺ was retained in the watershed, and NO₃ ^- retention was much lower than NH₄ ⁺. Stream monthly volume-weighted NO₃ ^- concentrations and fluxes significantly declined by 0.56???eq L^?1?year^?1 and 139.56?eq?year^?1, respectively. Overall, in NDW, inorganic nitrogen was exported before 1999 and retained since then, presumably from forest regrowth after Frazer fir die-off in the 1970s from balsam wooly adelgid infestation. Stream export of NO₃ ^- was greater during winter than summer months. During the period from 1999 to 2007, stream base cations did not exhibit significant changes, apparently regulated by soil supply. Statistical models predicting stream pH, ANC, SO₄ ^2-, and NO₃ ^- concentrations were largely correlated with stream discharge and number of dry days between precipitation events and SO₄ ^2- deposition. Dependent on precipitation, governing biogeochemical processes in NDW appear to be SO₄ ^2- adsorption, nitrification, and NO₃ ^- forest uptake. This study provided essential information to aid the GRSM management for developing predictive models of the future water quality and potential impacts from climate change.     

Trends in Dissolved Gaseous Mercury in the Tahquamenon River Watershed and Nearshore Waters of Whitefish Bay in the Michigan Upper Peninsula

A field study was conducted in June of 1998 to characterize the dynamics of dissolved gaseous mercury (DGM) in the TahquamenonRiver watershed and nearshore waters of Whitefish Bay in the Upper Michigan Peninsula. We found that over a transect acrossthe watershed, DGM levels increased generally from a creek (mean = ～12 pg L^-1), passing through the watershed, to the nearshore surface waters of the bay (mean = ～29 pg L^-1). DGM levels in nearshore surface waters of the bayranged from ～15 to ～50 pg L^-1 and peaked generally around noontime, exhibiting diurnal trends. A significant DGM decline from ～32 pg L^-1 in the early morning to ～15 pg L^-1 during the day was observed in these surface waters following passage of a coldfront, probably caused by wind-induced mixing and decrease insolar radiation associated with the frontal passage.     

Boron content in freshwaters of Northern Italy

The B concentration was determined in bulk deposition and in surface freshwaters (lakes and rivers) of the river Po watershed in Northern Italy. The curcumin photometric method was used to determine B content for all analyses. The B concentrations were under detection limits (0.06 mg B L^?1) in bulk deposition and below 0.09 mg B L^?1 in lake waters. Approximately 65 % of river samples measured had B concentrations close to natural background levels for natural waters (0.1 mg B L^?1). There was a strong correlation (r < 0.85) between B concentration and those of both total dissolved P and anionic detergents. The elevated B concentrations may be related to anthropogenic sources.     

Acid-base chemistry of high-elevation streams in the great smoky mountains

Longitudinal and temporal variations in water chemistry were measured in several low-order, high-elevation streams in the Great Smoky Mountains to evaluate the processes responsible for the acid-base chemistry. The streams ranged in average base flow ANC from ?30 to 28 μeq L^?1 and in pH from 4.54 to 6.40. Low-ANC streams had lower base cation concentrations and higher acid anion concentrations than did the high-ANC streams. NO₃ ^? and SO₄ ^2? were the dominant acid anions. NO₃ ^? was derived from a combination of high leaching of nitrogen from old-growth forests and from high rates of atmospheric deposition. Streamwater SO₄ ^2? was attributed to atmospheric deposition and an internal bedrock source of sulfur (pyrite). Although dissolved Al concentrations increased with decreasing pH in the study streams, the concentrations of inorganic monomeric Al did not follow the pattern expected from equilibrium with aluminum trihydroxide or aluminum silicate phases. During storm events, pH and ANC declined by as much as 0.5 units and 15 μeq L^?1, respectively, at the downstream sites. The causes of the episodic acidification were increases in SO₄ ^2? and DOC.     

Airborne transport of sulphur: Impacts on chemical composition of rivers on north shore of the St. Lawrence River (Québec)

The St. Lawrence North Shore region (Québec) is subject to acid precipitation entailing sulphate deposition (17 to 22 kg SO₄ ^2? ha^?1 yr^?1) which poses a threat to sensitive aquatic ecosystems. Physicochemical surveys conducted in 1982–1983 revealed the extreme sensitivity of the region owing to weak mineralization of the waters (mean alkalinity of 55 μeq L^?1 and conductivity of 17 μS cm^?1). Calculation of the annual loads of S discharged from 21 rivers throughout the region shows atmospheric deposition as the principal source of sulphate. A decreasing west-east gradient in the concentration is interpreted in terms of the impact of long-range airborne transport, although certain local sources of S emission are not to be overlooked. Analysis of the seasonal variation in the sulphate load balance, conducted in a small drainage basin (40 km²), revealed that the sulphate anion plays a part in lowering the water pH in spring. The spring pH depression is apparently intensified by an additional input of sulphate stemming from the release of this element subsequent to accumulation in the drainage basin during summer and fall. Organic acids play a measurable role in the chemical equilibrium of surface waters in the region, particularly in the eastern sector where there is less S fallout. Low pH levels in this sector (5.5 to 6.0) point to some degree of organic acidification.     

Chemical composition of hoarfrost,rime and snow during a winter inversion in Utah,U.S.A.

We present data on the chemical composition of hoarfrost, rime, and snow grains that accumulated during an eighteen-day long temperature inversion event in Salt Lake City, Utah in December 1985 and January 1986. Chemical analyses show that the precipitation formed during this inversion event was acidic (as low as pH 3.85) and had nitrate and sulfate contents up to 1680 and 1290 μeq · L^?1, respectively. Ammonia, nitrate, and sulfate deposition of 361, 615, and 792 μeq · m^?2, respectively, occurred in a six-day period due to the accumulation of snow grains during this inversion.     

Adirondack headwater lake chemistry relationships with watershed characteristics

The Adirondack Region of New York State has been identified as having surface waters sensitive to acidic deposition and as receiving large annual inputs of acidic deposition. The large amount of data available for this region makes a quantitative study of the region possible. Compiled from a variety of sources, the Adirondack Watershed Data Base (AWDB) contains information on lake chemistry; lake elevation, area, and volume; and associated watershed data, such as size, slope, aspect, elevation, vegetation and wetland types, beaver activity, fire and logging history, and soils data. Bivariate and multivariate procedures were used to examine relationships between watershed attributes and lake chemistry. Because the variables in the data base are being refined and modified, the current relationships should be considered preliminary. Preliminary results indicate that wet deposition, lake elevation, and forest cover are the principal variables that are associated with variance in the data for lake pH and acid neutralizing capacity (ANC) in the Adirondacks. For headwater lakes in the Adirondacks, we estimate approximately 50% have a total ANC ≤ 40 μeq L^?1 and 40% have a pH ≤ 5.5.     

The consequences of liming a highly acidified catchment in central Scotland

Research during the mid 1980s identified acidified, forested catchments in central Scotland whose hydrochemistry was not capable of supporting native fish populations. Calcium concentrations were around 20 μeq l^?1, less than the suggested critical value of 50 μeq l^?1, with hydrogen concentrations around 70 μeq l^?1, greater than the critical value of about 30 μeq l^?1. Limestone was applied by aerial application to the source areas of selected streams in 1990 with around 5% (15 ha) of the total catchment area of 270 ha treated at 10 tonnes ha^?1. Stream monitoring, carried out over the period 1989–1995, showed an immediate response to liming followed by a progressive decline. Calcium values were elevated to >150 μeq l^?1 and hydrogen concentrations reduced to 20 μeq l^?1, reverting in time towards pre-liming values. Although salmonid survival was improved during low flow conditions in summer, only a few fry survived to the autumn as acid episodes increased, and these were subsequently lost from the system during the winter period. Budget calculations indicated losses of around 30% of the applied calcium during the first four years. Studies on the vegetation and soils revealed a greater than expected penetration of calcium to depth (10–20 cm) in the soil profile. Results suggest that source area liming at this rate has had minimal effects on the vegetation and by increasing the proportion of the catchment limed to 15% could have a much greater success in reducing the frequency of biologically damaging episodes.     

Acid pulses from snowmelt at acidic cone pond,New Hampshire

A study was undertaken to examine whether ‘acid pulses’ from snowmelt created permanent changes in a pond's chemistry. Water samples were collected from clearwater acidic Cone Pond in the White Mountain National Forest, New Hampshire. The pond, inlet, and outlet were intensively sampled throughout winter and early spring 1983–84. Thaws brought more H⁺ into upper waters of the pond, but most was gone within a week. In contrast, SO₄ ^2? and Al showed dilution with increased streamflow into the pond, and NO₃ ^? was only detected in ice, slush, and surface waters. Bottom waters were anoxic throughout the winter and had pH 6.0 compared to 4.7 for most of the water column. Alkalinity at the bottom rose from 0 in November 1983 to 190 μeq L^?1 in April 1984. Between November and April the pond gained Al but lost SO₄ ^2? and H⁺. Most of the Al gain came after ice-out when loading through the inlet increased, but during the final snowmelt a temporary increase in Al concentration was also seen throughout the water column.     

Effects of liming on nutrient limitation of epilithic algae in an acid lake

The processes of lake acidification and lake restoration frequently involve major changes in DIC and DIN, both of which may potentially limit algal growth. We evaluate nutrient limitation of benthic algal biomass and species abundances during summers 1987 and 1989, before and after the liming of Lake Earnest (NE Pennsylvania) in November 1988. Limestone addition caused immediate increases in pH from 4.7 to 7.2. Alkalinity was ?34 μeq L^?1 in summer 1987, but rose to 620 μeq L^?1 in summer 1989, whereas DIN declined from 10.7 μmol L^?1 to 1.1 μmol L^?1 The algae were sampled after 45 to 46 d from clay flower pot substrates diffusing combinations of N, P and C. Algal biomass was strongly C-limited in 1987, but NP-limited in 1989. Mougeotia sp., which comprised >99% of total algal biovolume prior to liming, declined to < 1% of the community on control substrates, while Oedogonium sp. increased to 43% of total biovolume in 1989. The stimulation of chlorophyll-a accrual with C-enrichment during 1987 was consistent with the later increase in chlorophyll-a on control substrates following liming. Species enhanced by the diffused nutrients, however, generally differed from those which dominated the natural community.     

Primary production in a eutrophic acid lake

Total P concentrations, chlorophyll concentrations, and phytoplankton production were investigated bi-weekly in Tibbs Run Lake, Monongalia County, West Virginia, from March 1977 to March 1978. Mean H⁺ concentration in the lake was 25.1 μeq 1^?1 (pH 4.6). The acidic condition of the lake is attributed to inputs of acid via precipitation (mean H⁺ concentration of the bulk precipitation was 79 μeq 1^?1, pH 4.1), and the low buffering capacity of the watershed (bedrock composition of sandstone). Effect of the watershed is shown by the net retention of imput of P (ca. 26%) and H⁺ (ca. 68%). Total P loading to the lake was 0.495 g P m^?2 yr^?1. The single inflow accounted for 95% of the total loading while bulk precipitation accounted for the remainder. Mean summer chlorophyll concentration was 22.2 mg m^?2. Phytoplankton production expressed volumetrically as aP-vol-x value was 9.78 mg C m^?3 h^?1. Regression analysis indicated that H⁺ do not affect chlorophyll concentrations or phytoplankton production but rather that P limits algal biomass. Trophic status of Tibbs Run Lake based on a P budget model, chlorophyll concentration, and volumetric production all indicate that the lake is meso-eutrophic.     

Formiate and acetate in wet deposition at Pallanza (NW Italy) in relation to major ion concentrations

Weekly samples of wet deposition were collected at Pallanza (NW Italy) from January 1987 to December 1988. Their chemistry is characterized by high mineral acidity, with a median pH value of 4.26; only in 2 out of 62 samples was pH higher than 6.0. Sulphate, nitrate and ammonium are the main ions. Formiate and acetate showed a volume weighted average of 7 and 4 μeq L^?1, respectively; the values for the dissociated forms are 5 and 1 μeq L^?1, respectively. The contribution of formiate and acetate (dissociated form) to the total ionic concentration is about 2%, while the contribution to free hydrogenion is about 13%, mainly deriving from formic acid. Seasonal variations in concentration and the relationships between organic acid and other ions indicate that the photolysis of isoprenoid compounds released into the atmosphere from vegetation is a significant source for formic acid. In the case of acetic acid there is a contribution from anthropogenic emissions, more marked during the winter period.     

Contrasting the geochemistry of aluminum among peatlands

Aluminum concentrations were measured in surface waters, pore waters and surface peats of 15 wetlands in south-central Ontario. Wetlands were grouped floristically and chemically as mineralpoor, moderately-poor or mineral-rich fen. Mineral-poor fens were dominated bySphagnum, were low in alkalinity (0.31μeq L^?1) and pH (4.5–6.3). Moderately-poor fens had a mixture of vegetation (Sphagnum, sedges and grasses), mid-alkalinity (23–91μeq L^?1) and pH (5.8–6.4). Mineral-rich fens were dominated by sedges and grasses, had high alkalinity (104–181μeq L^?1) and circumneutral pH (6.2–6.3). Surface water Al concentrations were less in mineral-poor versus moderately-poor and mineral-rich fens (F=32.0; P<0.05). Pore water Al concentrations were lower in 4 of 5 mineral versus the mineral-rich fens (F=92.15; P<0.05). In all but two cases pore water Al (all species <0.2μm) were greater within the fen peats versus the overlying surface waters suggesting that peats could act as a source of Al to the overlying waters. In all wetlands, 70 and 30% of peat Al was recovered by a hydroxylamine hydrochloride/acetic extract (primarily inroganic) and an ammonium hydroxide extract (primarily organic), respectively. Differences in “extractable” Al recovered by the two reagents (i.e., inorganic+organic Al) among the 15 wetlands were independent of wetland type. Distribution coefficients, k _d , were different among the 3 types of wetlands (F=25.0; P<0.05) with theSphagnum dominated mineral-poor fens containing higher values versus the sedge and grass dominated mineral-rich fens. Lower surface and pore water concentrations of Al in mineralpoor versus mineral-rich fens may in part be a result of differences in the degree of minerotrophic influences between the two types of peatlands. As well, the greater binding capacity ofSphagnum peat as indicated by higher k _d 's in the mineral-poor fens, may have contributed to the observed lower pore water and surface water Al concentrations in mineral-poor versus mineral-rich fens. It has been postulated that anthropogenic acidification of peatlands will accelerate the transformation of a mineral-rich fen to that of a mineral-poor fen and ultimately to bog. Changes in Al geochemistry that may ensue as this transition occurs include decreases in pore and surface water Al concentrations with concurrent increases in peat bound Al.     

Behavior of Iodine in a Forest Plot,an Upland Field and a Paddy Field in the Upland Area of Tsukuba,Japan. Iodine Concentration in Precipitation,Irrigation Water,Ponding Water and Soil Water to a Depth of 2.5 m

In the course of a series of studies conducted to investigate the long-term behavior of ¹²⁹I (which has a half-life of 16 million years) in the environment, the concentration of stable iodine (¹²⁷I) in precipitation, irrigation water and soil water to a depth of 2.5 m in a forest plot, an upland field and a paddy field in the upland area of Tsukuba, Japan, was determined. In the forest plot, the mean iodine concentrations in soil water at all the depths ranged from 0.13 to 0.21 μg L^?1, about one-tenth of the values recorded in precipitation (weighted mean 2.1 μg L^?1). This finding suggests that the major part of iodine in precipitation was sorbed onto the surface soil horizon under oxidative conditions. In the upland field, the mean iodine concentration in soil water was 2.2 μg L^?1 at a depth of 0.2 m and it decreased to 0.34–0.44 μg L^?1 at a depth of 0.5 m or more; these concentrations were about one-fifth of that in precipitation. This suggested that the major part of the iodine derived from precipitation was sorbed onto the subsurface soil horizon (at depths between 0.2 and 0.5 m). In the paddy field, during the non-irrigation period, the mean iodine concentrations in soil water at all the depths ranged from 1.8 to 4.8 μg L^?1, almost the same values as those recorded in precipitation. During the irrigation period, the mean iodine concentrations at depths of 0.2 and 0.5 m were 18.8 and 16.7 μg L^?1, values higher than the 10.9 μg L^?1 value recorded in irrigation water and the 11.8 μg L^?1 value recorded in ponding water. However, at a depth of 1.0 m or more, the mean iodine concentrations in soil water rapidly decreased from 7.3 to 1.8 μg L^?1. These data suggested that a significant amount of iodine flowed out from the paddy field by surface runoff and a considerable amount of iodine that leached to a depth of 0.5 m was retained onto the mildly oxidative soil horizon (2Bw) that lay at depths between 0.5 and 1.0 m. At a depth of 2.5 m in the paddy field, the mean iodine concentration in soil water decreased to 1.8 μg L^?1, but this level was much higher than those in the forest plot and upland field at the same depth, which suggested that a significant amount of iodine had leached into the groundwater-bearing layer. There was a negative correlation (r=-0.889) between the E_h of soil and the iodine concentration in soil water (0.2 m depth) of the paddy field. Particularly, when the E_h of soil fell below approximately 150 mV, the iodine concentration rapidly increased to above 10μg L^?1. As for the chemical forms of iodine in precipitation, irrigation water, ponding water and soil water during the winter irrigation period in the paddy field with oxidative conditions, 58–82% of iodine consisted of IO^? ₃ and 17–42% of iodine consisted of I^?. In the soil water during the summer irrigation period in the paddy field under reductive conditions, 52–58% of iodine consisted of I^?, and 42–47% consisted of IO^? ₃.