Trace metals in the forest floor at saddleback mountain,maine in relation to aspect,elevation, and cover type

The objectives of this study were to obtain information about trace metal levels in a montane ecosystem in western Maine, and to compare these results to levels of trace metals reported in the literature for other areas of New England. Forest floor samples were collected at Saddleback Mountain, Maine from sites along two elevational transects on the western and eastern slopes. Five sites were located on the western slope, each in a different vegetation zone, and three sites were selected on the eastern slope, each corresponding in elevation and vegetation type as closely as possible to three of the western sites. Forest floor samples were collected as 15 x 15 cm blocks to the surface of the underlying mineral soil and sectioned into 2 cm depth increments. Zinc and Cr concentrations in the forest floor were significantly greater on the western slope (118 and 3.7 mg kg^?1, respectively), whereas Pb concentration was greater on the eastern slope (80 mg kg^?1) Cadmium, Cr, Cu, Ni, V, and Zn contents were significantly greater on the western slope (45, 83, 79, 143, and 1432 mg in ^?2, respectively). Copper, Ni, Cd, and Zn concentrations and contents in the forest floor decreased with increasing elevation, and no trends of increasing trace metal contents with increasing elevation were evident. Trace metal concentrations and contents were always lower in the deepest increment of the forest floor as compared to the surface increment (except for Cr), but concentration and content trends with depth varied. Chromium tended to increase with depth where a depth trend was evident. Overall, forest floor trace metal levels were strongly related to forest stand type and forest floor properties.     

Zinc Cu,Ni and Cd in the forest floor in the Northeastern United States

A regional study was conducted to assess current levels of trace metals in the forest floor, and to establish a baseline for future studies of metal accumulation. Quantitative forest floor samples collected from 78 sites in 9 states in the northeastern United States in 1978 and 1980 were analyzed for Zn, Cu, Ni, and Cd. Mean amounts present in the forest floor were 9.8 ± 1.9 (standard error of the mean), 1.7 ± 0.2, 0.86 ± 0.08, and 0.13 ± 0.01 kg ha^?1, for Zn, Cu, Ni, and Cd, respectively. Mean concentrations were 133 ± 25, 19.5 ± 1.6, 11 ± 0.8, and 1.7 ± 0.1 mg kg^?1, respectively. Differences in metal and organic matter concentrations and amounts among forest types were attributed to geographic location of specific forest types rather than to direct biotic influence. No element was strongly correlated with elevation for the entire sample area. Regional patterns of elemental amounts showed that trace metal levels are slightly higher in the southern part than in the northern part of the study region. Regional variation of Zn, Cu, Ni, and Cd in the forest floor was not indicative of atmospheric deposition except near point sources of pollution.     

Trace metal content of the forest floor in the green mountains of Vermont: Spatial and temporal patterns

The organic horizons of forest soils in eleven stands along an elevational gradient on Camels Hump Mountain, Vermont, were analyzed for Pb, Cu, Zn, Ni, Cd, organic matter and organic C. Lead concentration and amount increased with elevation. Vertical profiles of forest floor in the boreal forest showed that highest concentrations for most metals occurred in the upper F horizon. Comparison with 1966 and 1977 samples from the same stands showed that concentrations of Pb, Cu, and Zn and percent organic matter increased by as much as 148% in the intervening 14 yr. Estimates of 1966 amounts of Pb, Cu, and Zn indicated that increases in trace metal amounts over the 14 yr period are consistent with annual deposition rates reported in the literature.     

Flüssebilanzen und aktuelle Änderungsraten der Schwermetall-Vorräte in Wald-Ökosystemen des Soiling

Flux balances and current rates of change of heavy metal stores in forest ecosystems of the Soiling The inventory of the heavy metals Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb is calculated for a beech and a spruce forest ecosystem in the Soiling mountains on the basis of measured concentrations in the vegetation and soil compartments and their dry mass per hectare. The inventory is compared with measured heavy metal fluxes coupled with precipitation above and below the canopy, with seepage water fluxes below the rooting zone (50 cm depth), with litterfall, and with the current increment to biomass. The ratios between heavy metal stores in the forest floor layers (table 3) and the annual flux with litterfall (table 4) show decreasing tendency for liberation of the elements by decomposition of organic matter (OM) in the following order: Mn>OM>Ni>Cd>Cu>Cr ≈? Zn>Co ≈? Fe ≈? Pb Manganese is set free faster than total organic matter. The flux balances for the total ecosystems (table 4) show input > output in the case of Cr, Fe, Cu, Cd, and Pb; input ≈? output for Ni and Zn; input < output for Mn and Co. Heavy metal stores in mineral soil are decreasing by percolation losses and increment to biomass (mainly wood) in the case of all elements investigated, except Zn (under beech), Cd and Pb (table 4). The concentrations of Cu and Pb in the forest floor layers have reached levels at which deleterious effects on microorganisms and litter decomposition are to be expected.     

Heavy metal contamination of soils in Northern Slovakia

Environmental damages like forest decline in Northern Slovakia could be a result of long-distance transport of pollutants with the dominating north-west winds. On 10 sites, primarily in the northbound upper slopes of west-east oriented mountain ranges in Northern Slovakia, the extent of the heavy metal contamination in soils along a north-south transect was examined. Oi, Oe, Oa, A, and B horizons were sampled and the total concentrations of Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn were determined. The ranges of heavy metal concentrations in the forest floor were higher than reported for comparable samples from Bavarian soils except for Zn (Cd: 0.65–1.77; Cr: 12–40; Cu: 19–41; Ni: 8–24; Pb: 70–187; Zn: 31–92 mg kg^?1), in the mineral soil the concentrations were lower. The depth distribution of the metal concentrations indicated a contamination with Cd, Cr, Cu, Ni, Pb, and Zn. The concentration differences between forest floor and mineral soil tended to be higher at the northern than at the southern sites for Cu, Ni, Pb, and Zn, indicating a long-distance transport from the north. Correlation and principal component analyses of the total metal concentrations revealed three groups: Cu, Pb, and Zn inputs mainly seemed to result from long-distance transport from the north, Cr and Ni inputs additionally from local sources. Cd probably had its origin mainly in local sources. This result was further confirmed by the grouping of the sites when clustered.     

Accumulation of,and interactions between,calcium and heavy metals in wood and bark of Picea abies

Spreading of wood ashes from the pulp and paper industry will change the content and proportions of calcium (Ca), copper (Cu), cadmium (Cd), and zinc (Zn) in forest soils and thus also in the forest trees. The accumulation and distributions of, and interaction between, Ca and heavy metals in wood and bark of two‐year‐old Norway spruce (Picea abies [L.] Karst.) were investigated in this study. The treatment was carried out for 3 months in nutrient solutions, and there was a low or a high addition of Ca, Cd, Cu or Zn. The metal accumulation in, and distribution between, the bark, the wood formed during the treatment period (new wood), and the wood formed before the treatment period (old wood) was analyzed with AAS. The contents of the metals in the stems (i.e., bark, new wood, old wood) increased with elevated addition of the metal in question, also at the low addition of Ca, Cu, and Zn. Interactions between Ca and the heavy metals were found. Elevated Ca additions decreased the Cd content of the bark and the Zn content of the old wood, and tended to decrease the Cu content of the bark and the Cd content of the old wood. The Ca content decreased in both, wood and bark after Cu addition and the high Cd addition. Thus, even small changes in metal availability and proportions in forest soil, such as after spreading of wood ashes in the forest, will be reflected in the content of the metals in the wood and bark of forest trees.     

Atmospheric bulk deposition of trace metals to the Seine river Basin, France: concentrations, sources and evolution from 1988 to 2001 in Paris

Concentrations of Cd, Cu, Ni, Pb and Zn were determined in bulk atmospheric deposition collected at five stations in the Seine River basin (France), to evaluate sources and fluxes of atmospheric trace metals. Bulk deposition (wet + dry) was sampled weekly from March 2001 to February 2002 for 4 sites and from March to December 2001 for the last one. The concentrations of the elements in bulk deposition (dissolved + particulate form) followed the order: Zn > Pb > Cu > Ni > Cd. Concentrations of Zn, Pb and Ni were highly correlated with one another, suggesting a common source, related to the combustion of coal and heavy fuel. Metal concentrations in bulk deposition did not exhibit a high degree of temporal variability over the annual cycle and were not obviously related to meteorological parameters (rainfall, wind). Estimates of the total annual direct atmospheric deposition of metals to the Seine Estuary ranged from 16 kg yr^{? 1} for Cd to 5600 kg yr^{? 1} for Zn. Loadings of Cd, Cu and Ni from direct atmospheric inputs were less than 1% of those contributed by the Seine River and loadings of Pb and Zn represented 1.27% and 1.56% of the Seine contribution. Direct atmospheric inputs are negligible compared to fluvial inputs, but the indirect atmospheric deposition to the estuary was not estimated. Based on these results, trace metal concentrations in Paris have decreased by a factor of 4.6 for Zn and by a factor of 50 for Ni from 1988 to 2001. Of particular interest is the continued decrease in bulk deposition of Pb during this period, underlining the impact of policy initiatives concerning the reduction of lead on emissions in France.     

Trace elements in surface soils from the mineralized area of Madison County, Missouri, U.S.A.

Duplicate, bulked surface soil samples, from sites 10m apart, were collected at 97 locations 1000 m apart on a regular grid measuring 8x11 km. Data were obtained for Ag, Ba, Be, Cd, Co, Cr, Cu, Li, Mn, Ni, Pb, V and Zn. One field sample was a good predictor of its nearby duplicate for Co, Cu, Ni and Pb, satisfactory for Ba, Be, Cr, Mn and Zn, but poorer for Cr, Li and V. Maps of the variation in precision of the field samples did not reveal any association between abandoned mine sites and high variability. The median coefficient of variation for trace elements in the field duplicates was between 8 and 19.5%. The duplicated field data were averaged to yield a mean soil metal concentration at each sample location. Concentrations of Ba, Be, Cr, Li, Sr and V were comparable with other published values for similar soils in Missouri. Concentrations of Co, Cu, Mn, Ni, Pb and Zn were higher which was explained by pollution from mining activities. A graphical technique was used to calculate background levels for metals in the second group. Samples of forest litter were collected at 12 locations: Ag, Ba, Cd, Mn, Sr and Zn concentrations were higher in the litter whereas Li and V concentrations were higher in the subjacent mineral soil. Computer isoline maps of the distribution of elements revealed an association between areas of high soil Cu, Co, Ni, Pb and Zn and abandoned mines or mineralized rocks.     

Carbon stock and deposition in phytomass of the Russian forests

Russian forests occupy an area of 771 Mha with a wood volume of 81.6 × 10⁹ m³. In this paper we estimate the carbon (C) storage and annual C deposition in living vegetation for stands of different age groups according to information in the Russian National Forest Inventory (NFI). Conversion of root C storage into phytomass was based on phytomass/storage ratios calculated from data from 1900 test areas in the different forest regions of Russia. We developed these conversion ratios for different phytomass fractions, namely: stems, branches, roots and foliage, for different forest forming species. Of the total forest area (771 Mha), C storage in the living phytomass is 35.07 Pg C. Total annual C deposition in forest vegetation is estimated at 213.2 Tg C. We considered the role of the main forest forming species in the C cycle of the forest vegetation taking into account the actual structure of the Russian forests.     

Anomalous contents of heavy metals in soils and vegetation of a mine area in S.W. Sardinia,Italy

Samples of soils and vegetation from the mining area of South-West Sardinia (Italy) were analyzed for Pb, Zn, Cd, and Cu content. The area (more than 100 km²) is inhabited by many thousands of people; land utilization includes mainly grapes on some small plains and permanent sheep pasture on the hills. The levels of Pb, Zn, and Cd were found to be exceptionally high in most samples. Lead concentration was up to 71000 μg g^?1 in the soils and 4000 jig g^?1 in vegetation; Cd concentration was found up to 665 μg g^?1 in soils and 26.5 μg g^?1 in vegetation. The heavy metal content of some soil samples was highly variable. Data show that Pb is easily absorbed by plant roots and translocated to foliage. In spite of the high heavy metal level, no signs of toxicity were apparent in vegetation.     

Metal Pools, Fluxes, and Budgets in an Acidified Forested Catchment on the Precambrian Shield, Central Ontario, Canada

Atmospheric emissions of metals have decreased in North America; yet, metals remain an environmental concern due to their environmental persistence and toxicity to biota. In this study, pools and mass budgets were calculated for 15 metals in an acidified forested catchment in Central Ontario. Metals that were enriched in bulk deposition over background average values (As, Cd, Pb, Zn) were generally enriched in the forest floor and upper lake sediment. While the metal pool in vegetation is small compared with the soil pool, internal cycling of metals via litterfall is comparable to atmospheric deposition, soil water, and stream fluxes. Partitioning coefficients calculated from metal concentrations in soil water and bulk soil suggest that Cd, Mn, Ni, and Zn are the most mobile. The mineral soil and lake sediments were sinks for most metals, while the wetland was a source of metals during the study year, which was a drought year. Overall, lithogenic metals (Al, Ba, Co, Fe, Mn, Rb, Sr, Zn) primarily from a weathering source generally exhibited net export from the catchment, while metals contained in atmospheric pollution (As, Cd, Cr, Cu, Ni, Pb, V) exhibited net retention. Despite the acidified nature of the catchment, it functions to retain many pollutant metals.     

The Impact of Wood Ash and Green Liquor Dregs Application on Ca, Cu, Zn and Cd Contents in Bark and Wood of Norway Spruce

To counteract nutrient depletion and acidification of forest soils, recycling of waste products from the forest industry has been suggested. Spreading of these waste products will probably change the concentration and availability of Ca and heavy metals in forest soils and thereby the contents of these metals in trees. This field study aimed at examining the influence of pellets of wood ash (ash) or a mixture of wood ash and green liquor dregs (ash+GLD) on the contents of Ca, Cd, Cu and Zn in wood and bark of Norway spruce [Picea abies (L.) Karst.]. The waste products were spread in an amount of 3000 kg ha^?1 in 1996 at a felling site in Sweden and in 1999 and 2002 young spruce trees, planted in 1995, were collected and wood and bark were analysed for Ca, Cd, Cu and Zn with AAS. Changes in the metal content of wood and bark of young spruce trees were found 3 and 6 years after spreading pellets of ash or ash+GLD compared with the control. The effect of the treatments on the metal contents of bark and wood differed and was larger after 3 years than after 6 years. Treatment with ash+GLD tended to have less effect on the metal contents of bark and wood than treatment with only ash. An increase in the contents of Cu and Zn in bark or wood, compared with the control, was only found for the ash treatment and only 3 years after application. Both the ash and ash+GLD treatment decreased the Cd content of the wood and/or bark after 3 years, and after 6 years it still was, or tended to be, lower than the control.     

Trace element release from forest floor can be monitored by ion exchange resin tubes

Risk assessment of heavy metal input into forest ecosystems requires information about metal fluxes from the forest floor (organic layer) into the mineral soil. Common methods for the monitoring of element fluxes are generally time‐consuming and expensive. Additionally, the reliability of the results is in part contested especially for trace elements, showing very low concentrations which are sometimes even below analytical detection limit. We used ion exchange resin tubes installed below the forest floor to determine heavy metal and As fluxes at 25 forest monitoring sites in Germany. Chloride tracer experiments and the comparison of our data with throughfall and lysimeter data, determined within the Level II monitoring network, proved the accuracy of our method. Mean trace element fluxes based on the resin method were 50 g As ha^–1 yr^–1, 2 g Cd ha^–1 yr^–1, 168 g Cu ha^–1 yr^–1, 176 g Ni ha^–1 yr^–1, and 186 g Pb ha^–1 yr^–1.The results show that the organic layer may change into a source of heavy metals after emission has decreased.     

Levels and Bioaccessibilities of Metals in Dusts from an Arid Environment

The elemental composition and bioaccessibility of trace metals have been determined in a variety of geosolids (soils, road dusts and house dusts) from an arid, coastal region (Dhahran, Saudi Arabia). Concentrations of many elements reflected those of the local geology, ascertained by analysis of desert sand. Several trace metals (e.g. Cu, Sb, Zn, Pb, Tl and Sn) were moderately enriched in both road and house dusts, reflecting external and internal (household) anthropogenic sources. For a given trace metal, bioaccessibilities, assessed using a physiologically based extraction test, were broadly similar across the range of geosolids. Median values for a simulated gastric phase ranged from less than 10% (Ba, Cu, Cr, Ni and V) to more than 50% (As, Cd, Sb, Sn and Tl), and for a subsequently simulated intestinal phase from less than 15% (Ba, Cr, Cu, Ni, V and Zn) to more than 50% (As, Cd, Sb, Tl and U). Results suggest that the levels and bioaccessibilities of trace metals in dusts from arid environments are controlled by the dilution of anthropogenic particulates by variable (but significant) proportions of fine, baseline sand.     

Cd, Ni, Pb, and Zn Concentrations in Forest Vegetation and Soils in Maine

Bioaccumulation of trace metals in plant tissues can present a health risk to wildlife, and potentially to humans. The Passamaquoddy tribe in Maine was concerned about health risks of cadmium (Cd) because of a health advisory for moose liver and kidney consumption due to high Cd levels. This study found relatively low to moderate concentrations of Cd, nickel (Ni), lead (Pb), and zinc (Zn) concentrations in four common terrestrial moose browse species, associated forest soils, and two species of aquatic vegetation on Passamaquoddy tribal land in eastern Maine. Terrestrial plant tissue concentrations ranged from 0.1 to 1.97, 0.65 to 7.08, 0.29 to 2.0, and 42 to 431 mg kg^?1 for Cd, Ni, Pb and Zn, respectively. Deciduous species, particularly aspen and birch, may be a more significant source of Cd and Zn to wildlife compared to coniferous or aquatic species. Aquatic plant tissue concentrations ranged from 0.11 to 0.14, 0.46 to 1.01, 0.8 to 0.9, and 22 to 41 mg kg^?1 for Cd, Ni, Pb and Zn, respectively. Total O horizon concentration means for coniferous and deciduous were 0.50 and 1.00, 4.27 and 4.11, 55 and 21, and 55 and 167 mg kg^?1 for Cd, Ni, Pb and Zn, respectively. The study provides baseline vegetation and soil trace metal concentrations for a remote region in Maine impacted by non-point sources.     

Efficient Purification of Heavy-Metal-Contaminated Water by Microalgae-Activated Pine Bark

Batch experiments were performed to study metal sorption by pine bark and algae-treated bark. The biosorption of copper (Cu), lead (Pb), zinc (Zn), cadmium (Cd), cobalt (Co), and nickel (Ni) in synthetic multimetal aqueous solutions was studied as a function of metal content in solution, and amount and size of bark particles used for sorption. Influence of water hardness (Ca²⁺ only was tested) on the metal sorption process was also evaluated. Metal uptake from solutions with high heavy metal content (i.e. 10× the limit for leachate from landfills) was found to be independent of Ca²⁺ concentration. At low metal content in solution (i.e. 1× the limit for leachate from landfills), uptake of Cu, Zn, Ni, and Cd decreased with increasing Ca²⁺ content in water. Microalgae-treated bark was found to increase the metal sorption efficiency. Air-drying of bark-entrapped algae was shown to be the best method for sorbent drying. In general, the green algae, Chlorella sp. and Pseudokirchneriella subcapitata showed the best results in metal uptake. Sorption of Co, Zn, Ni, and Cd from solution with high levels of both heavy metals and calcium increased by almost 50% with algae treatment of bark was applied. At low levels of metals and calcium content, 100% uptake of Cu and Pb in water was observed. Uptake of other metals from solution with low metal and Ca content was relatively high (50–60%). Low pH (pH 3.0) had no influence on metal sorption from solutions with high metal content. For solutions with low metal content a decrease of metal uptake by 10–15% was observed for all the metals but Pb. Thus, the treatment of bark with microalgae was successful and influenced positively the uptake capacity of the bark.     

植被恢复模式对土壤重金属质量分数和土壤酶活性的影响——以山东省淄博市四宝山破坏山体为例

矿产资源开采造成了严重的重金属污染,为选择合理植被恢复模式以修复土壤重金属污染,以淄博市四宝山破坏山体不同植被恢复模式为对象,测定土壤有机质、全氮、碱解氮、有效磷、速效钾质量分数,pH值等主要化学性质,土壤多酚氧化酶、过氧化氢酶、过氧化物酶、脲酶活性和Cu、Zn、Cd等7种重金属质量分数,分析不同植被恢复模式对土壤重金属质量分数及土壤酶活性的影响.结果表明:1)实验区土壤中重金属Zn轻度污染,Cu和Cd重度污染,其他重金属均不构成污染;2)各人工植被恢复模式土壤重金属质量分数均低于灌草丛的,其中黑松林对土壤Cu、Cd的修复效果最好,侧柏林对土壤Zn的修复效果最好;3)土壤重金属全量在垂直分布上规律复杂,有效量均表现为下层高于上层,土壤有效Cu、有效Zn、有效Cd下层比上层依次高9.24％～18.94％、0.97％～20.09％和5.48％～35.51％;4)在影响土壤酶活性的各种因素中,破坏山体土壤重金属有效量与土壤化学性质的影响最为明显,处于同等重要的地位.本研究发现,Cu、Zn、Cd均对4种土壤酶活性表现出了抑制作用,建议用土壤多酚氧化酶、过氧化氢酶、脲酶活性作为破坏山体土壤重金属Cu污染的评价指标.     

Human and ecological risks of metals in soils under different land-use types in an urban environment of Bangladesh

Trace metal contamination in soil is of great concern owing to its long persistence in the environment and toxicity to humans and other organisms.Concentrations of six potentially toxic trace metals,Cr,Ni,Cu,As,Cd,and Pb,in urban soils were measured in Dhaka City,Bangladesh.Soils from different land-use types,namely,agricultural field,park,playground,petrol station,metal workshop,brick field,burning sites,disposal sites of household waste,garment waste,electronic waste,and tannery wast,and construction waste demolishing sites,were investigated.The concentration ranges of Cr,Ni,Cu,As,Pb,and Cd in soils were 2.4–1258,8.3–1044,9.7–823,8.7–277,1.8–80,and 13–842 mg kg^-1,respectively.The concentrations of metals were subsequently used to establish hazard quotients(HQs)for the adult population.The metal HQs decreased in the order of As>Cr>Pb>Cd>Ni>Cu.Ingestion was the most vital exposure pathway of studied metals from soils followed by dermal contact and inhalation.The range of pollution load index(PLI)was 0.96–17,indicating severe contamination of soil by trace metals.Considering the comprehensive potential ecological risk(PER),soils from all land-use types showed considerable to very high ecological risks.The findings of this study revealed that in the urban area studied,soils of some land-use types were severely contaminated with trace metals.Thus,it is suggested that more attention should be paid to the potential health risks to the local inhabitants and ecological risk to the surrounding ecosystems.     

Fluxes of Cu,Zn, Pb,Cd, Cr,and Ni in temperate forest ecosystems

The literature on the fluxes of six heavy metals in temperate forest ecosystems is reviewed. Special attention is given to wet and dry deposition and internal flux, to metal budgets for ecosystems and soils, to concentrations in aqueous compartments of the ecosystem and to speciation in soil solutions. Metal fluxes are discussed in relation to pollution load, soil type, tree species and land use. The mobility of Cu and Pb is strongly dependent on the solubility of organic matter. These metals are commonly accumulated in forest soils. Zinc, Cd and Ni are greatly influenced by soil acidity and are often lost in considerable amounts from acidified soils. Chromium is often at balance in forest ecosystems. Implications for metal solubility and budgets in forest soils are discussed in connection with an increase in soil acidification.     

Trace elements in the hydrologic cycle of a tolerant hardwood forest ecosystem

The concentrations and annual fluxes of Fe, Al, Mn, Cu and Pb were measured during 1983 in bulk precipitation, throughfall, stem-flow, forest floor percolate, mineral soil solution below the root zone and streamflow in a maple-birch stand on an acid podzolic soil at the Turkey Lakes Watershed (TLW), Ontario. Inputs of metals to TLW in precipitation were small in comparison with those in the eastern United States and Europe. Considerable loss of Mn and Cu from the vegetation during both the growing and the dormant (leafless) periods was observed and presumed to be due to leaching. The enrichment in soil solution of all metals examined, in relation to throughfall, was greatest for Al (7X) and least for Cu (1.2X). Aluminum was mobilized in both the forest floor and the mineral soil, the latter possibly in association with SO₄ ^2?. Copper was solubilized in the lower forest floor or the mineral soil. Surface soil contents of Al and Cu were reduced by Al and, to a lesser extent, Cu leaching beyond the effective rooting zone. Iron, Mn and Pb were mobilized largely in the F horizon of the forest floor, most likely by organic acids. Leaching of Fe, Mn and Pb was reduced by metal accumulation in vegetation, the lower forest floor, or mineral soil within the effective rooting zone of the vegetation. Most (80 to 99%) of the metals leached from the rooting zone were retained in the watershed and did, not appear in streamwater.