Behavior of Metals Under Different Seasonal Conditions: Effects on the Quality of a Mexico–USA Border River

Spatial and seasonal mobilization trends of metals in surface water were evaluated in the US–Mexico San Pedro River (SPR). Water samples were collected at five sampling stations for the analysis of dissolved oxygen, pH, electric conductivity, sulfates, and metals (Cd, Cu, Fe, Mn, Pb, and Zn). Quality of the water was characterized through Ecological Criteria of Water Quality (ECWQ) established in Mexico and Water Quality Criteria (Environmental Protection Agency (EPA)). High total metal concentrations were detected as follows: Fe?>?Cu?>?Mn?>?Zn?>?Pb?>?Cd. Metal concentrations were slightly higher in dry season than in rainy season: Cd (below detection limit (BDL)–0.21 mg L^?1), Cu (BDL–13 mg L^?1), Fe (0.16–345 mg L^?1), Mn (0.12–52 mg L^?1), Pb (BDL–0.48 mg L^?1), and Zn (0.03–17.8 mg L^?1). Low pH and dissolved oxygen values as well as high sulfate content were detected in both seasons. High values of metals (Cd, Cu, Fe, Mn, Pb, Zn) were detected at station E1 representing pollution source, as well as at stations E2 (Cd, Cu, Fe, Mn), E3 (Fe, Mn, Pb), and E4 and E5 (Fe, Mn). Detected concentrations exceeded maximum permissible established in ECWQ and Water Quality Criteria (EPA). Efflorescence salts on sediments in the dry season could increase levels of metals in water column. This study provides valuable information on the potential mobility of metals in surface water of SPR located in an arid environment where transport processes are strongly linked to climate. The information derived from this study should help the regional and national authorities to address present environmental regulations.     

Trace Metals in the Water Columns of the Red Sea and the Gulf of Aqaba,Egypt

Seawater samples were collected from the northern Red Sea and the Gulf of Aqaba at different depths during February 1999 and analyzed for iron, zinc, manganese, nickel, copper, cadmium, cobalt and lead to determine the existing concentration of these metals, their distribution patterns and where contamination has occurred. The concentrations of Fe, Zn, Mn, Ni, Cu, Cd, Co, Pb were scatteredin the ranges: (0.56–4.44; mean 1.67±0.9 μg L^-1), (0.13–1.17; mean 0.24±0.12 μg L^-1), (0.06–0.21; mean 0.13±0.03 μg L^-1), (0.05–0.52; mean 0.16±0.06 μg L^-1), (0.07–0.29; mean 0.14±0.06 μg L^-1), (0.02–0.78; mean 0.49±0.14 μg L^-1), (0.06–0.29; mean 0.15±0.04 μg L^-1), and (0.02–0.68; mean 0.31±0.13 μg L^-1), respectively. The results revealed a small range of variation and regional irregularities. It also indicated significant higher concentrations for Fe, Cd and Pb compared to other metals. Compared to the northern Red Sea, significant higher concentrations for Ni and Cd are measured at the Gulf of Aqaba. Other metals, i.e. Fe, Zn, Mn, Cu, Co, and Pb are not significantly different in both areas indicating no distinct concentration gradients. Except for Pb, the distribution patterns indicated significantly lower concentrations at surface layer in both regions, then increasing to their maximum values at the sub-surface layers which followed by a decrease in deep water. The study indicated also that the mean concentrations of trace metals examined here are much lower than those reported for the Mediterranean Sea and typical of open ocean water.     

Restoring the capacity of spent mushroom compost to treat coal mine drainage by reducing the inflow rate: A microcosm experiment

Four volumes of spent mushroom compost were exposed to synthetic coal mine drainage (pH 3.5, 48 mg L^?1 Fe, 22 mg L^?1 Mn) under oxidizing conditions (Eh 300 to 400 mV) at a relatively high rate of flow. After 15 days, the compost lost its ability to elevate pH, to lower the redox potential, to lower outlet iron concentrations, and to lower manganese concentrations, with larger volumes retaining more Fe and H⁺, but less Mn. Estimated retention maxima per liter of spent mushroom compost were 281 μeq H⁺, 5.56 g Fe, and 0.15 g Mn. These values are similar to those reported elsewhere for peat. The ‘saturated’ compost was then mixed and exposed to mine water in order to eliminate ‘dead zones’ in the compost. Subsequently, the compost was re-exposed to synthetic mine water (pH 4.0, 60 mg L^?1 Fe, O mg L^?1 Mn) under a much lower flow rate and less oxidizing regime for a period of 114 days. Under the low flow regime, iron was first exported from the compost as reducing conditions were established, and then retained on a stable basis. In addition, Eh was lowered and pH was elevated by the compost. On a net basis, the capacity of the compost to retain iron was increased and apparently stable under the decreased flow conditions.     

Fish species distribution and water chemistry in Nova Scotia lakes

During the summers of 1981-1984, 19,714 fish (23 species) were netted in 234 Nova Scotian lakes. Surface and mid-depth water samples were also analyzed for major ions, metals, and DOC. Lakewater pH varied from 4.4 to 7.7, including eight lakes which produced no fish in standard 23-hr net sets. Fish data were partitioned into 6 pH groupings for analysis. Stepwise multiple regressions of fish species vs. H+, S0₄,A1, Fe, and Mn showed little predictive power. Productive lakes ranged up to 530 μg L^?1 Al, 1680 pg L^?1 Fe, and 836 μg L^?1 Mn. Apart from pH, fish distribution and abundance showed no significant relationships with water chemistry data. We note, however, that the more acidic lakes had fewer species of fish.     

EFFECT OF LANTHANUM ON RICE PRODUCTION,NUTRIENT UPTAKE,AND DISTRIBUTION

ABSTRACT

Split root solution culture experiments were conducted to study the effects of the rare earth element lanthanum (La) on rice (Oryza sativa) growth, nutrient uptake and distribution. Results showed that low concentrations of La could promote rice growth including yield (0.05 mg L^?1 to 1.5 mg L^?1), dry root weight (0.05 mg L^?1 to 0.75 mg L^?1) and grain numbers (0.05 mg L^?1 to 6 mg L^?1). High concentrations depressed grain formation (9 mg L^?1 to 30 mg L^?1) and root elongation (1.5 mg L^?1 to 30 mg L^?1). No significant influence on straw dry weight was found over the whole concentration range except for the 0.05 mg L^?1 treatment. In the pot and field experiments, the addition of La had no significant influence on rice growth.Lanthanum had variable influence on nutrient uptake in different parts of rice. Low concentrations (0.05 mg L^?1 to 0.75 mg L^?1) increased the root copper (Cu), iron (Fe), and magnesium (Mg), and grain Cu, calcium (Ca), phosphorus (P), manganese (Mn), and Mg uptake. High concentrations (9 to 30 mg L^?1) decreased the grain Ca, zinc (Zn), P, Mn, Fe and Mg, and straw Ca, Mn, and Mg uptake. With increasing La concentration, root Zn, P, Mn, Cu, and Ca concentrations increased, and grain Ca and Fe, and straw Mn, Mg, and Ca concentrations decreased. Possible reasons are discussed for the differences between the effects of La in nutrient solutions and in pot and field experiments.     

Chemical effects of spring and summer alum additions to a small,Northwestern Ontario Lake

Aluminum was added as aluminum sulfate (alum) to Lake 114, a small, shallow lake of the Experimental Lakes Area, northwestern Ontario, in spring and summer point-source additions. Aluminum and H⁺ gradients were established during the additions, with high Al and low pH (about 1000 μg L^?1 Al, pH 4.7) near the alum sources, and background conditions (< 50 μg L^?1 Al, pH 5.7) further from the sources. Approximately 80% of the added Al was lost from the water column in two weeks. Phosphorus concentrations remained unchanged during the additions, whereas lake alkalinity decreased and sulfate increased close to the sources. Dissolved organic carbon (DOC) concentrations decreased slightly (from 540 μM L^?1 to about 500 μM L^?1) near the alum source during the summer addition.     

Organochlorine insecticide residues in the rain water in Delhi,India

Rain water samples were regularly collected from three sites, namely, Netaji Nagar, Moti Nagar and Town Hall within the Delhi city area from July, 1980 to June, 1982. The pesticide residues were adsorbed on polyurethane foam coated with 0.5 % DC-200 and subsequently extracted and analyzed for DDT, HCH and their metabolites/isomers. The concentration of total DDT ranged from 0.22 to 108 μg L^?1 with a mean value of 12.5 μg L^?1. The samples of rain water contained varying levels of 4,4-DDT, 2,4-DDT, 4,4-DDE, and 4,4-DDD. The 4,4-DDT, 4,4-DDE and 2,4-DDT were the main components of total DDT. The range of HCH residues in rain water was from 0.08 to 43 μg L^?1 with a mean of 5.3 μg L^?1. The residues of HCH consisted mainly of α- and γ-isomers with traces of β and δ-isomers. The α- and γ-isomers accounted for 76 and 24% of total HCH, respectively. The concentrations of DDT and HCH in rain water were generally less than 10 μg L^?1 and exceeded 10 in only 4 and 3 cases, respectively. The residues of these insecticides were generally higher during October to December. Residues of DDT were higher at Moti Nagar which is near a DDT factory. Residues of HCH were maximum at Town Hall, a commercial area of the city.     

Chronic effects of low ph and elevated aluminum on survival,maturation, spawning and embryo-larval development of the fathead minnow in soft water

Fathead minnows (Pimephales promelas) were exposed to a range of pH and A1 concentrations in soft water (8 mg Ca L^?1) to determine effect levels at various life stages. The tested pH levels ranged from 8.0 through 5.2 and inorganic monomeric Al from 15 through 60 μg L^?1. Reproductive processes including spawning, embryogenesis and early larval survival were more sensitive to acid stress than were juvenile growth and survival. Juvenile survival was significantly reduced at pH 5.2 + 60 μg Al L^?1 (P <0.05). Spawning success was reduced at pH 6.0 and 5.5 (P <0.10) and failed completely at pH 5.2, regardless of Al concentration. An apparant beneficial effect of added Al was observed during spawning at pH 7.5 + 35 μg Al L^?1, but this effect was not significantly greater than at pH 7.5 + 15 μg Al L^?1. A significant (P <0.05) decrease in larval survival occurred at pH 6.0 + 15 μg Al L^?1 and lower compared to the survival at pH 7.5 + 15 μg Al L^?1. Aluminum at 30 μg L^?1 provided protection resulting in short term increased embryo-larval survival at pH 5.5. The effect of parental exposure on progeny survival was assessed by an interchange of embryos from the spawning treatment to all tested exposure conditions. When reared at pH 8.0 + 15 μg Al L^?1 through 6.0 + 15 μg Al L^?1 or at pH 5.5 + 30 μg Al L^?1, parental exposure did not significantly influence progeny survival. However, survival was significantly reduced among progeny from brood fish reared at pH 5.5 + 15 μg Al L^?1 as compared to those spawned at pH 6.0 + 15 μg Al L^?1 and above, or at pH 5.5 + 30 μg Al L^?1 (P <0.05). Juvenile or 14 d larval growth effects were not detected under any exposure condition (P >0.05). Ultimately, fathead minnow young-of-the-year recruitment and production potential can be expected to diminish when environmental pH falls to 6.0, and to fail completely at 5.5 and lower.     

Arsenic Concentrations in Groundwater,Soils, and Irrigated Rice in Southwestern Bangladesh

Arsenic (As) poisoning of groundwater in Bangladesh has become a major environmental and health issue. The extensive use of groundwater in irrigation of rice has resulted in elevated As in soils and crops. A study was undertaken to determine As concentrations in groundwater, soils, and crops in 16 districts of southwestern Bangladesh. Groundwater samples were collected from shallow-tube and hand-tube wells (STW and HTW) used for irrigation and drinking water. Soil and rice plants were sampled from the command area of the tube wells. Arsenic concentrations were determined using an atomic absorption spectrometer equipped with flow injection hydride generator. Groundwater samples contained <10 to 552 μg As L^?1. Arsenic concentrations in 59% of STW samples exceeded 50 μg As L^?1, the national standard for As in drinking water. Unlike groundwater, most of the surface water samples contained <10 μg As L^?1. Concentrations of As in the soils from the command area of the tube wells ranged from 4.5 to 68 mg kg^?1. More than 85% of the soils contained <20 mg As kg^?1. The mean As concentration in the rice grain samples was 0.23 mg kg^?1, which is much less than the maximum food hygiene standard. A positive relationship was observed between groundwater and soil As, implying that soil As level increases as a result of irrigation with contaminated water. However, irrigation water As did not show any relation with rice grain As. The findings suggest that surface water bodies are a safe source of irrigation water in the As-contaminated areas.     

Aluminum retention in a man-made Sphagnum wetland

Runoff from a highway interchange in western Maryland had Al concentrations averaging about 50 mg L^?1, with a maximum of 206 mg L^?1. As an alternative to expensive chemical treatment of this Al-rich water, in August 1984, the drainage was diverted through a 500 m² man-made wetland, constructed from organic peat. For a 10 week period, Al concentrations in water leaving the wetland averaged 1.5 mg L^?1. as compared to Al concentrations at the two major inflows to the wetland of 35.3 and 6.6 mg L^?1. However, effective treatment of the drainage by the wetland was not observed over the entire 27 mo sampling period. Peat chemical analysis indicated that over the 27 mo, total Al concentration in the peat increased from 2375 μg g^?1 to 13 634 μg g^?1. Of this increase 5.5 % was contributed by exchangeable Al, 4.3% by adsorbed Al, 39.8% by organically bound Al, 33.1% by oxide bound Al, and 17.2% by precipitated and residual Al. Changes in Fe, Mn, Ca, Mg, K, and Na chemistry in the peat associated with Al retention are discussed.     

Natural Mercury Levels in Geological Enriched and Geological Active Areas: Case Study of Katun River and Lake Teletskoye,Altai (Siberia)

Natural geological Hg deposits control the Hg levels inthe upper Katun river. Very high levels of total Hg areobserved in the watercolumn (up to 20 ng L^-1) and thesediments (up to 244 μg g^-1) close to the depositarea, but almost normal levels (1.8 ng L^-1 in the watercolumn and 0.14 μg g^-1 in the sediments) are reached60 km downstream of that zone. In general, low dissolvedmethylmercury (MMHg) concentrations were found (0.04–0.05 ngL^-1) due to unfavourable methylation conditions. The MMHgconcentrations in the sediments vary from 23.3 ng g^-1, inthe vicinity of the geological Hg deposits, to 0.17 ng g^-1 60 km downstream.Total Hg levels in Lake Teletskoye (a geological activearea) are slightly increased (1.1–1.8 ng L^-1) compared toLake Baikal and fairly constant alover the Lake, suggestingmultiple sources. High mercury concentrations in springs andsoils coincide with high radon concentrations in the samecompartments as well as high soil exhalation fluxes. Theseresults in combination with the fact that Lake Teletskoye islocated in an active fault zone suggest that the Rn and Hgsources may be fault aligned spring waters and deep seatedgases escaping through open cracks. Methylmercuryconcentrations in the Lake (0.03–0.1 ng L^-1) werecomparable to the concentrations found in Katun river butrelative to the total Hg burden this means a higher percentage.     

Sediment trace metal contamination in the Ivory Coast,West Africa

To help expand our global perspective on trace metal contamination, concentrations of Cu, Fe, Hg, Mn, Ni, Pb, and Zn were determined for sediments from the Ebrie Lagoon in the Ivory Coast, a developing West African nation. Excess loading of several metals, especially Hg, Pb, and Zn was found at several sites. The maximum concentration of Hg measured in sediments from the Ebrie Lagoon (2250 ng g^?1) is about 30 times greater than natural levels. Similarly, Pb and Zn concentrations for the Ivorian lagoonal sediments are as high as 250 and 560 μg g^?1, respectively, showing sizeable anthropogenic inputs. Trace metal sources to the Ebrie Lagoon include untreated sewage and industrial wastes.     

Impact of Acid Mine Drainage (AMD) on Water Quality, Stream Sediments and Periphytic Diatom Communities in the Surrounding Streams of Aljustrel Mining Area (Portugal)

Aljustrel mining area is located in the Iberian Pyrite Belt, one of the greatest concentrations of massive sulphide deposits that extends from Lousal (Portugal) to Aznalcóllar (Spain). The surrounding streams, Roxo, Água Azeda and Água Forte, are influenced by the erosion of the tailing deposits and the input of acid mine drainage (AMD) from the abandoned Aljustrel pyrite mines, recently reopened in 2007. The purpose of this study was to understand how these adverse conditions influenced the stream sediments, water quality and periphytic diatom communities and establish the pre-restoration local conditions to judge the success of rehabilitation program now under way. For stream sediments, the highest metal concentration samples were found at sites F, G and H. Arsenic, Cu, Fe, Pb and Sb detected concentrations, generally exceeded the probable effect concentration values reaching level 4: the highest toxicity level. In surficial water samples of AMD affected sites (F, G and H), low pH values (1.5 to 3.5) and high metal concentrations of As (6,837 μg L^?1), Cd (455 μg L^?1), Cu (68,795 μg L^?1), Fe (1,262,000 μg L^?1), Mn (19,451 μg L^?1), Pb (136 μg L^?1), and Zn (264,377 μg L^?1) were found. In these sites, the diversity index (H′) for diatoms was low (0.6 to 2.8) and the dominant taxa were Eunotia exigua (site F, 33.5%) and Pinnularia acoricola (abundances in sites: F, 86.8%; G, 88.5%; and H, 91.1%). In opposition, in less AMD impacted, H′ was high (1.5 to 4.6) and low metal concentrations and high pH were found. Achnanthidium minutissimum was the dominant taxon in (abundances in sites: A, 76.1% and B, 24.39%). Canonical correspondence analysis showed that spatial variation due to mine influence was more important than seasonal variation, which did not show any pattern.     

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.     

In Situ partitioning and biomagnification of mercury in industrially polluted Husainsagar Lake,Hyderabad, India

The distribution of Hg in water, sediment, plankton and fish along with the in situ biomagnification of the metal in Husainsagar Lake, India were measured. The concentration of Hg in the water was 10 μg L^?1 and exceeded the water quality criteria standards. Sediments of the lake at different sites had Hg concentrations several thousand fold more than that of the overlying water column and showed relationship with the water content of the wet sediment. Sediments in the lake acted as a `sink' for the metal. The concentrations of Hg increased from nanoplankton → phytoplankton -> zooplankton. Fish, an end organism in the food chain, had Hg concentrations higher than that of nanoplankton and lower than those of phytoplankton and zooplankton. This trend did not illustrate the expected pattern of food chain enrichment in the classical sense as noted for chlorinated hydrocarbons (DDT).     

稻米和土壤微量元素的空间变异

Consumption of rice is the main source of micronutrients to human in Asia. A paddy field with unknown anthropogenic contamination in Deqing County, Zhejiang Province, China was selected to characterize the spatial variability and distribution of micronutrients in rice grain and soil. A total of 96 paired soil and rice grain samples were collected at harvest. The micronutrients in the soil samples were extracted by diethylenetriamine pentaacetic acid (DTPA). The mean micronutrient concentrations in rice grain were 3.85 μg Cu g-1, 11.6 μg Fe g-1, 39.7 μg Mn g-1, and 26.0 μg Zn g-1. The mean concentrations were 2.54 μg g-1 for DTPA-Cu, 133.5 μg g-1 for DTPA-Fe, 30.6 μg g-1 for DTPA-Mn, and 0.84 μg g-1 for DTPA-Zn. Semivariograms showed that measured micronutrients in rice grain were moderately dependent, with a range distance of about 110 m. The concentrations of the DTPA-extractable micronutrients all displayed strong spatial dependency, with a range distance of about 60 m. There was some resemblance of spatial structure between soil pH and the grain Cu, Fe, Mn, and Zn. By analogy, similar spatial variation was observed between soil organic matter (SOM) and DTPA-extractable micronutrients in the soil. Kriging estimated maps of the attributes showed the spatial distributions of the variables in the field, which is beneficial for better understanding the spatial variation of micronutrients and for potentially refining agricultural management practices at a field scale.     

Modelization of the mercury fluxes at the air-sea interface

Aqueous and atmospheric Hg° concentrations for remote marine areas such as the equatorial Pacific Ocean and for coastal seas such as the North Sea and the Scheldt Estuary are discussed. Biological processes seem to be at the origin of the supersaturated Hg° concentrations in the water. On the other hand, transfer velocities across the air-sea interface were calculated with a classical shear turbulence model and with a wave breaking model. With these data, Hg° fluxes from the sea to the atmosphere were calculated: in the Pacific Ocean they range from 0.43 to 6.5 μg g Hg.m^?2. yr^?1 at a wind speed of 2.8 m.s^?1 and from 10.3 to 156 μg Hg.m^?2 yr^?1 at a wind speed of 54 m.s^?1, but they are still higher when wave breaking is considered (from 11 to 168 μg Hg.m^?2.yr^?1). These transfer fluxes are an order of magnitude higher in the Scheldt Estuary.     

Crop Residue Effects on Total and Dissolved Losses of Fe,Mn, Cu,and Zn by Runoff

Runoff may cause losses of micronutrients from soils. This can result in environmental problems such as contaminant transfers to water or a decrease in soil fertility. Appropriate soil management may reduce these micronutrient losses. This study examined the effect of applying crop residues to the soil surface on iron (Fe), manganese (Mn), copper (Cu), and zinc (Zn) losses by runoff. Runoff and sediment yield were measured on 1-m² plots using a rainfall simulator with constant 65 mm h^?1 intensity. Eight successive rainfall applications were performed at 65 mm each. Corn (Zea mays L.) straw was applied to plots at rates ranging from 0 to 8 t ha^?1. Both total and dissolved concentrations of the micronutrients studied were decreased by corn straw applications. After 520 mm cumulative rainfall, total soil losses ranged from 150 to 15354 kg ha^?1 depending on the amount of corn straw applied. Total micronutrient concentrations in runoff were as follows: Fe from 14.98 to 611.12 mg L^?1, Mn from 0.03 to 0.61 mg L^?1, Cu from 0.10 to 1.43 mg L^?1, and Zn from 0.21 to 5.45 mg L^?1. The relative contribution of the dissolved fraction to the total micronutrient content loss was low, but varied depending on the nutrient, being less than 1 percent for Fe and Mn and almost 10 percent for Zn. Total and dissolved concentrations in runoff of the studied elements decreased exponentially as the rate of applied corn straw increased. In conclusion, the addition of corn straw to soil reduced micronutrient losses.