Changes in Cu, Ni, and Zn availability following simulated conversion of biosolids-amended forest soils back to agricultural use

Soil Research ◽  
2010 ◽  
Vol 48 (3) ◽  
pp. 286 ◽  
Author(s):  
R. G. McLaren ◽  
A. Black ◽  
L. M. Clucas

In this study we examined the bioavailability and chemistry of Cu, Ni, and Zn in metal-spiked, biosolids-amended forest (Pinus radiata) soils that had undergone a simulated conversion back to agricultural use. Mixing of the biosolids-treated forest litter into the underlying mineral soil resulted in high concentrations of each metal in easily extractable and soil solution forms. There was also very little change in these concentrations during a subsequent 2-year incubation period of the samples. Chemical speciation of the soil solutions using WHAM 6 showed that Cu was dominated by organic complexes, whereas most Ni and Zn was present as Ni2+ and Zn2+, with generally <5% of these elements present as organic complexes. Addition of lime to the soils substantially decreased both readily extractable and soil solution metal concentrations. However, even in their unlimed state, although plant metal concentrations were increased by the original biosolids treatments, there were no adverse effects due to the metals on plant growth as determined in a wheat germination and seedling growth test. In this study, the DGT technique showed considerable promise for assessing metal availability to plants. However, the study suggests that conversion of biosolids-treated forest soils back for agricultural use is unlikely to result in any substantial problems related to the metal loadings built up in the forest litter layer.

CATENA ◽  
2021 ◽  
Vol 200 ◽  
pp. 105175
Author(s):  
Guia Cecchini ◽  
Anna Andreetta ◽  
Aldo Marchetto ◽  
Stefano Carnicelli

2013 ◽  
Vol 10 (3) ◽  
pp. 1365-1377 ◽  
Author(s):  
M. O. Rappe-George ◽  
A. I. Gärdenäs ◽  
D. B. Kleja

Abstract. Addition of mineral nitrogen (N) can alter the concentration and quality of dissolved organic matter (DOM) in forest soils. The aim of this study was to assess the effect of long-term mineral N addition on soil solution concentration of dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) in Stråsan experimental forest (Norway spruce) in central Sweden. N was added yearly at two levels of intensity and duration: the N1 treatment represented a lower intensity but a longer duration (43 yr) of N addition than the shorter N2 treatment (24 yr). N additions were terminated in the N2 treatment in 1991. The N treatments began in 1967 when the spruce stands were 9 yr old. Soil solution in the forest floor O, and soil mineral B, horizons were sampled during the growing seasons of 1995 and 2009. Tension and non-tension lysimeters were installed in the O horizon (n = 6), and tension lysimeters were installed in the underlying B horizon (n = 4): soil solution was sampled at two-week intervals. Although tree growth and O horizon carbon (C) and N stock increased in treatments N1 and N2, the concentration of DOC in O horizon leachates was similar in both N treatments and control. This suggests an inhibitory direct effect of N addition on O horizon DOC. Elevated DON and nitrate in O horizon leachates in the ongoing N1 treatment indicated a move towards N saturation. In B horizon leachates, the N1 treatment approximately doubled leachate concentrations of DOC and DON. DON returned to control levels, but DOC remained elevated in B horizon leachates in N2 plots nineteen years after termination of N addition. We propose three possible explanations for the increased DOC in mineral soil: (i) the result of decomposition of a larger amount of root litter, either directly producing DOC or (ii) indirectly via priming of old SOM, and/or (iii) a suppression of extracellular oxidative enzymes.


2018 ◽  
Vol 22 (8) ◽  
pp. 4455-4472 ◽  
Author(s):  
Katheryn Burd ◽  
Suzanne E. Tank ◽  
Nicole Dion ◽  
William L. Quinton ◽  
Christopher Spence ◽  
...  

Abstract. Boreal peatlands are major catchment sources of dissolved organic carbon (DOC) and nutrients and thus strongly regulate the landscape carbon balance, aquatic food webs, and downstream water quality. Climate change is likely to influence catchment solute yield directly through climatic controls on run-off generation, but also indirectly through altered disturbance regimes. In this study we monitored water chemistry from early spring until fall at the outlets of a 321 km2 catchment that burned 3 years prior to the study and a 134 km2 undisturbed catchment. Both catchments were located in the discontinuous permafrost zone of boreal western Canada and had  ∼  60 % peatland cover. The two catchments had strong similarities in the timing of DOC and nutrient yields, but a few differences were consistent with anticipated effects of wildfire based on peatland porewater analysis. The 4-week spring period, particularly the rising limb of the spring freshet, was crucial for accurate characterization of the seasonal solute yield from both catchments. The spring period was responsible for  ∼  65 % of the seasonal DOC and nitrogen and for  ∼  85 % of the phosphorous yield. The rising limb of the spring freshet was associated with high phosphorous concentrations and DOC of distinctly high aromaticity and molecular weight. Shifts in stream DOC concentrations and aromaticity outside the early spring period were consistent with shifts in relative streamflow contribution from precipitation-like water in the spring to mineral soil groundwater in the summer, with consistent relative contributions from organic soil porewater. Radiocarbon content (14C) of DOC at the outlets was modern throughout May to September (fraction modern carbon, fM: 0.99–1.05) but likely reflected a mix of aged DOC, e.g. porewater DOC from permafrost (fM: 0.65–0.85) and non-permafrost peatlands (fM: 0.95–1.00), with modern bomb-influenced DOC, e.g. DOC leached from forest litter (fM: 1.05–1.10). The burned catchment had significantly increased total phosphorous (TP) yield and also had greater DOC yield during summer which was characterized by a greater contribution from aged DOC. Overall, however, our results suggest that DOC composition and yield from peatland-rich catchments in the discontinuous permafrost region likely is more sensitive to climate change through impacts on run-off generation rather than through altered fire regimes.


2002 ◽  
Vol 11 (4) ◽  
pp. 285-300 ◽  
Author(s):  
V. MÄNTYLAHTI ◽  
P. LAAKSO

Increasing concentrations of arsenic and heavy metals in agricultural soils are becoming a growing problem in industrialized countries. These harmful elements represent the basis of a range of problems in the food chain, and are a potential hazard for animal and human health. It is therefore important to gauge their absolute and relative concentrations in soils that are used for crop production. In this study the arsenic and heavy metal concentrations in 274 mineral soil samples and 38 organogenic soil samples taken from South Savo province in 2000 were determined using the aqua regia extraction technique. The soil samples were collected from 23 farms.The elements analyzed were arsenic, cadmium, chromium, copper, mercury, nickel, lead and zinc. The median concentrations in the mineral soils were:As 2.90 mg kg –1, Cd 0.084 mg kg –1, Cr 17.0 mg kg –1, Cu 13.0 mg kg –1, Hg 0.060 mg kg –1, Ni 5.4 mg kg –1, Pb 7.7 mg kg –1, Zn 36.5 mg kg –1. The corresponding values in the organogenic soils were:As 2.80 mg kg –1, Cd 0.265 mg kg –1, Cr 15.0 mg kg –1, Cu 29.0 mg kg –1, Hg 0.200 mg kg –1, Ni 5.9 mg kg –1, Pb 11.0 mg kg –1, Zn 25.5 mg kg –1. The results indicated that cadmium and mercury concentrations in the mineral and organogenic soils differed. Some of the arsenic, cadmium and mercury concentrations exceeded the normative values but did not exceed limit values. Most of the agricultural fields in South Savo province contained only small amounts of arsenic and heavy metals and could be classified as “Clean Soil”. A draft for the target values of arsenic and heavy metal concentrations in “Clean Soil” is presented.;


2019 ◽  
Vol 34 ◽  
pp. 41-66 ◽  
Author(s):  
Raffaella Balestrini ◽  
Carlo Andrea Delconte ◽  
Andrea Buffagni ◽  
Alessio Fumagalli ◽  
Michele Freppaz ◽  
...  

A number of studies have reported decreasing trends of acidifying and N deposition inputs to forest areas throughout Europe and the USA in recent decades. There is a need to assess the responses of the ecosystem to declining atmospheric pollution by monitoring the variations of chemical species in the various compartments of the forest ecosystem on a long temporal scale. In this study, we report on patterns and trends in throughfall deposition concentrations of inorganic N, dissolved organic N (DON) and C (DOC) over a 20-year (1995–2015) period in the LTER site -Val Masino (1190 m a.s.l.), a spruce forest, in the Central Italian Alps. The same chemical species were studied in the litter floor leachates and mineral soil solution, at three different depths (15, 40 and 70 cm), over a 10-year period (2005–2015). Inorganic N concentration was drastically reduced as throughfall and litter floor leachates percolated through the topsoil, where the measured mean values (2 µeq L-1) were much lower than the critical limits established for coniferous stands (14 µeq L-1). The seasonal temperature dependence of throughfall DOC and DON concentration suggests that the microbial community living on the needles was the main source of dissolved organic matter. Most of DOC and DON infiltrating from the litter floor were retained in the mineral soil. The rainfall amount was the only climatic factor exerting a control on DOC and N compounds in throughfall and forest floor leachates over a decadal period. Concentration of SO4 and NO3 declined by 50% and 26% respectively in throughfall deposition. Trends of NO3 and SO4 in forest floor leachates and mineral soil solution mirrored declining depositions. No trends in both DON and DOC concentration and in DOC/DON ratio in soil solutions were observed. These outcomes suggest that the declining NO3 and SO4 atmospheric inputs did not influence the dynamic of DON and DOC in the Val Masino forest. The results of this study are particularly relevant, as they are based on a comprehensive survey of all the main compartments of the forest ecosystem. Moreover, this kind of long-term research has rarely been carried out in the Alpine region.


2001 ◽  
Vol 1 ◽  
pp. 457-466 ◽  
Author(s):  
E. Ring ◽  
L. Hogbom ◽  
H.A. Nohrstedt

Biofuels, such as brash from forest fellings, have been proposed as an alternative energy source. Brash removal may affect the sustainability of forest production, e.g., through a change in the availability of cations and N in the soil. We report initial effects of brash removal on inorganic N content in humus and mineral soil, soil-solution chemistry, and field-layer biomass after clear felling an N-fertilisation experiment in central Sweden. The experiment comprised six different fertiliser levels, ranging from 0 to 600 kg N ha�1. Urea was given every 5th year during 1967 to 1982 to replicated plots, giving total doses of 0 to 2400 kg N ha�1. Clear felling took place in 1995, 13 years after the last fertilisation. The removal of brash decreased the NO3� content in the humus layer after clear felling. A decrease in the NO3� concentration of the soil solution was indicated during most of the study period as well. No effect of the previous N fertilisation was found in the humus layer, but in the mineral soil there was an increase in NO3� content for the highest N dose after clear felling (p = 0.06). The soil-solution chemistry and the field-layer biomass showed an irregular pattern with no consistent effects of brash removal or previous fertilisation.


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