Relationships between soil microbial properties and aboveground stand characteristics of conifer forests in Oregon

Eight forest sites representing a large range of climate, vegetation, and productivity were sampled in a transect across Oregon to study the relationships between aboveground stand characteristics and soil microbial properties. These sites had a range in leaf area index of 0.6 to 16 m² m^–2 and net primary productivity of 0.3 to 14 Mg ha^–1 yr^–1.Measurements of soil and forest floor inorganic N concentrations and in situ net N mineralization, nitrification, denitrification, and soil respiration were made monthly for one year. Microbial biomass C and anaerobic N mineralization, an index of N availability, were also measured. Annual mean concentrations of NH ₄ ⁺ ranged from 37 to 96 mg N kg^–1 in the forest floor and from 1.7 to 10.7 mg N kg^–1 in the mineral soil. Concentrations of NO ₃ ^– were low ( < 1 mg N kg^–1) at all sites. Net N mineralization and nitrification, as measured by the buried bag technique, were low on most sites and denitrification was not detected at any site. Available N varied from 17 to 101 mg N kg^–1, microbial biomass C ranged from 190 to 1230 mg Ckg^–1, and soil respiration rates varied from 1.3 to 49 mg C kg^–1 day^–1 across these sites. Seasonal peaks in NH ₄ ⁺ concentrations and soil respiration rates were usually observed in the spring and fall.The soils data were positively correlated with several aboveground variables, including leaf area index and net primary productivity, and the near infrared-to-red reflectance ratio obtained from the airborne simulator of the Thematic Mapper satellite. The data suggest that close relationships between aboveground productivity and soil microbial processes exist in forests approaching semi-equilibrium conditions.Abbreviations IR infrared - LAI leaf area index - k _c proportion of microbial biomass C mineralized to CO₂ - NPP net primary productivity - TM Thematic Mapper     

Accumulation of organic matter along a pollution gradient: Application of odum's theory of ecosystem energetics

Forest soil biology in Scots pine forests of the Empetrum-Vaccinium type was studied around the industrialized city of Oulu, northern Finland since 1987. The forest sites lie along a sulphur and nitrogen concentration gradient in the mor humus ranging from 1.6 to 3.9 mg S g^–1 organic matter (OM) and from 14 to 23 mg N g^–1 OM. A number of biological parameters have earlier been found to vary along this gradient, thus indicating that the ecosystems are subjected to a pollution stress. Total microbial biomass and various activity parameters were studied in 1991. The different methods are discussed and the results interpreted within the light of Odum's theory of the energetic stabilization of ecosystems. Microbial biomass C determined by the fumigation-extraction (FE) technique varied from 5 to 10 mg g^–OM, N from 0.5 to 1.0 mg g^–1OM, and basal respiration rate from 0.040 to 0.097 mg CO₂ h^–1 g^–1OM. All decreased along the pollution gradient. Substrate induced respiration values (SIR) varied from 0.025 to 0.085 mg CO₂-C h^–1 g^–1dw. SIR correlated well with the biomass values determined by the FE technique. The lag time of the microbial community after glucose addition (varying from 13 to 22 h) was shortened and the specific respiration increment of the microbial community in response to glucose addition increased along the gradient. The metabolic quotient (respiration/biomass) of the microflora strongly depended on the technique and equation used in calculating the microbial biomass. The results show a reduced biomass, but a more intensive regeneration and intensified activity per biomass unit of microorganisms in polluted forest soil. This in turn denotes an alteration in the microbial community in favor of a higher proportion of r-strategists under the disturbed conditions. In contrast, K-strategists may be more dominant under less polluted conditions. This interpretation is presented with some reservations concerning methodology. There is a need for the calibration of each method for determining microbial biomass in different types of soil.     

The soil fauna of a beech forest on limestone: trophic structure and energy budget

Summary The soil fauna of a mull beech forest on lime-stone in southern Lower Saxony (West Germany) was sampled quantitatively. Biomass estimates, trophic characteristics, and measurement and calculation of the energetic parameters of the constituent animal populations were used to construct an energy budget of the total heterotrophic subsystem of the forest. Mean annual zoomass amounted to about 15 g d wt m^–2; earthworms (about 10 g d wt m^–2) and other groups of the macrofauna were dominant. Protozoa constituted about 1.5 g d wt m^–2. Relative distribution of zoomass among the trophic categories was 50% macrosaprophages, 30% microsaprophages, 12% microphytophages, and 4% zoophages. Total annual consumption rate of the saprophagous and microphytophagous soil fauna (6328 and 4096 kJ m^–2 yr^–1, respectively) was of the same order of magnitude as annual litter fall (canopy leaves 6124 kJ m^–2 yr^–1, flowers and fruits 944 kJ m^–2 yr^–1, herbs 1839 kJ m^–2 yr^–1, fine woody material 870 kJ m^–2 yr^–1, tree roots 3404 kJ m^–2 yr^–1, without coarse woody litter). Primary decomposers (macrosaprophages) were the key group for litter comminution and translocation onto and into the soil, thus contributing to the high decomposition rate (k=0.8) for leaf litter. Consumption rates of the other trophic groups were (values as kJ m^–2 yr^–1): bacteriophages 2954, micromycophages 416, zoophages 153. Grazing pressure of macrophytophages (including rhizophages) was low. Faeces input from the canopy layer was not significant. Grazing pressure on soil microflora almost equalled microbial biomass; hence, a large fraction of microbial production is channelled into the animal component. Predator pressure on soil animals is high, as a comparison between consumption rates by zoophages and production by potential prey — mainly microsaprophages, microphytophages and zoophages — demonstrated. Soil animals contributed only about 11% to heterotrophic respiration. However, there is evidence that animals are important driving variables for matter and energy transfer: key processes are the transformation of dead organic material and grazing on the microflora. It is hypothesized that the soil macrosaprophages are donor-limited.     

Microbial biomass and nitrogen cycling responses to fertilization and litter removal in young northern hardwood forests

The influence of site fertility on soil microbial biomass and activity is not well understood but is likely to be complex because of interactions with plant responses to nutrient availability. We examined the effects of long-term (8 yr) fertilization and litter removal on forest floor microbial biomass and N and C transformations to test the hypothesis that higher soil resource availability stimulates microbial activity. Microbial biomass and respiration decreased by 20–30 % in response to fertilization. Microbial C averaged 3.8 mg C/g soil in fertilized, 5.8 mg C/g in control, and 5.5 mg C/g in litter removal plots. Microbial respiration was 200 µg CO₂-C g^–1 d^–1 in fertilized plots, compared to 270 µg CO₂-C g^–1 d^–1 in controls. Gross N mineralization and N immobilization did not differ among treatments, despite higher litter nutrient concentrations in fertilized plots and the removal of substantial quantities of C and N in litter removal plots. Net N mineralization was significantly reduced by fertilization. Gross nitrification and NO₃ ^– immobilization both were increased by fertilization. Nitrate thus became a more important part of microbial N cycling in fertilized plots even though NH₄ ⁺ availability was not stimulated by fertilization.Soil microorganisms did not mineralize more C or N in response to fertilization and higher litter quality; instead, results suggest a difference in the physiological status of microbial biomass in fertilized plots that influenced N transformations. Respiration quotients (qCO₂, respiration per unit biomass) were higher in fertilized plots (56 µg CO₂-C mg C^–1 d^–1) than control (48 µg CO₂-C mg C^–1 d ^–1) or litter removal (45 µg CO₂-C mg C^–1 d^–1), corresponding to higher microbial growth efficiency, higher proportions of gross mineralization immobilized, and lower net N mineralization in fertilized plots. While microbial biomass is an important labile nutrient pool, patterns of microbial growth and turnover were distinct from this pool and were more important to microbial function in nitrogen cycling.     

Soil respiration within riparian buffers and adjacent crop fields

We quantified rates of soil respiration among sites within an agricultural landscape in central Iowa, USA. The study was conducted in riparian cool-season grass buffers, in re-established multispecies (switchgrass + poplar) riparian buffers and in adjacent crop (maize and soybean) fields. The objectives were to determine the variability in soil respiration among buffer types and crop fields within a riparian landscape, and to identify those factors correlating with the observed differences. Soil respiration was measured approximately monthly over a two-year period using the soda-lime technique. Mean daily soil respiration across all treatments ranged from 0.14 to 8.3 g C m^–2 d^–1. There were no significant differences between cool-season grass buffers and re-established forest buffers, but respiration rates beneath switchgrass were significantly lower than those beneath cool-season grass. Soil respiration was significantly greater in both buffer systems than in the cropped fields. Seasonal changes in soil respiration were strongly related to temperature changes. Over all sites, soil temperature and soil moisture together accounted for 69% of the seasonal variability in soil respiration. Annual soil respiration rates correlated strongly with soil organic carbon (R = 0.75, P < 0.001) and fine root (<2 mm) biomass (R = 0.85, P < 0.001). Annual soil respiration rates averaged 1140 g C m^–2 for poplar, 1185 g C m^–2 for cool-season grass, 1020 g C m^–2 for switchgrass, 750 g C m^–2 for soybean and 740 g C m^–2 for corn. Overall, vegetated buffers had significantly higher soil respiration rates than did adjacent crop fields, indicating greater soil biological activity within the buffers.     

Contribution of micro-organisms to the carbon dynamics in black spruce (Picea mariana) forest soil in Canada

In order to clarify the role of micro-organisms in the carbon cycle of the boreal forest ecosystem, the vertical distribution of soil carbon, soil microbial biomass and respiratory activity was studied in a black spruce forest near Candle Lake in Saskatchewan, Canada. The total amount of carbon contained in moss and soil layers (to the depth of 50cm beneath the mineral soil surface) was 7.2kgm^–2, about 47% of which was in the L and FH horizons of the soil. Soil microbial biomass per dry weight of soil was largest in the L horizon, while the biomass per ground area was largest in the FH horizon. Soil respiration rate, measured using a portable infrared gas analyzer, was highest in the FH horizon, exceeding 50% of the total soil respiration. Low but significant CO₂ emission was detected even in deeper soil horizon (E horizon). We also examined the respiration rate of cut roots and the effect of root excision on respiration. The contribution of root respiration to total soil respiration, calculated from root biomass and respiration rate of cut roots, was about 54%. The amount of carbon evolved through microbial respiration during the snow-free season (June–October) was estimated as 221gCm^–2. Micro-organisms in the L horizon showed high respiratory activity as compared with those in deeper soil horizons.     

川西亚高山森林土壤呼吸和微生物生物量碳氮对施氮的响应

随着全球大气氮沉降的明显增加,将有可能显著影响我国西部地区受氮限制的亚高山森林生态系统。土壤微生物是生态系统的重要组成部分,是土壤物质循环和能量流动的重要参与者。由于生态系统类型、土壤养分、氮沉降背景值等的差异,土壤呼吸和土壤生物量碳氮对施氮的响应存在许多不确定性。而施氮会不会促进亚高山森林生态系统中土壤呼吸和微生物对土壤碳氮的固定?基于此假设,选择了川西60年生的四川红杉(Larix mastersiana)亚高山针叶林为研究对象,通过4个水平的土壤施氮控制试验(CK:0 g m~(-2) a~(-1)、N1:2 g m~(-2)a~(-1)、N2:5 g m~(-2) a~(-1)、N3:10 g m~(-2)a~(-1)),监测了土壤呼吸及土壤微生物生物量碳氮在一个生长季的动态情况。结果表明:施氮对土壤呼吸各指标和土壤微生物碳氮都有极显著的影响,施氮能促进土壤全呼吸、自养呼吸、异养呼吸通量和土壤微生物生物量碳氮的增长,施氮使土壤呼吸通量提高了11%—15%,土壤微生物量碳提高了5%—9%,土壤微生物量氮提高了23%—34%。在中氮水平下(5 g m~(-2) a~(-1))对土壤呼吸的促进最显著。相关分析发现,土壤呼吸与微生物生物量碳氮和微生物代谢商极呈显著正相关,微生物量碳氮与土壤温度呈极显著的正相关,与土壤湿度呈极显著负相关。通过一般线性回归拟合土壤呼吸速率与土壤10 cm温湿度的关系,发现土壤呼吸速率与土壤温度呈极显著的正相关,与土壤湿度极显著负相关(P0.001),中氮水平下土壤温度敏感性系数Q_(10)值(7.10)明显高于对照(4.26)。     

模拟氮沉降和降雨对华西雨屏区常绿阔叶林土壤呼吸的影响

从2013年12月至2014年11月,通过野外原位试验,对华西雨屏区常绿阔叶林进行了模拟氮沉降和降雨试验,采用LI-8100土壤碳通量分析系统(LI-COR Inc.,USA)测定了对照(CK)、氮沉降(N)、减雨(R)、增雨(W)、氮沉降+减雨(NR)、氮沉降+增雨(NW)6个处理水平的土壤呼吸速率,并通过回归方程分析了温度和湿度与土壤呼吸速率间的关系。结果表明:(1)氮沉降和增雨抑制了常绿阔叶林土壤呼吸速率,减雨促进了常绿阔叶林土壤呼吸速率。(2)减雨使华西雨屏区常绿阔叶林土壤呼吸年通量增加了258 g/m~2,而模拟氮沉降和增雨使华西雨屏区常绿阔叶林土壤呼吸年通量分别减少了321g/m~2和406g/m~2。(3)减雨增加了土壤呼吸的温度敏感性,模拟氮沉降和增雨降低了土壤呼吸的温度敏感性。(4)模拟温度和湿度与土壤呼吸速率间回归方程分析表明,土壤水分对土壤呼吸速率的影响较小。(5)模拟氮沉降和增雨处理减少土壤微生物生物量碳、氮的含量,减雨处理增加了土壤微生物生物量碳、氮的含量。(6)模拟氮沉降和降雨对华西雨屏区土壤CO_2释放的影响未表现出明显的交互作用。     

Nitrogen mineralization,nitrification and denitrification in upland and wetland ecosystems

Summary Nitrogen mineralization, nitrification, denitrification, and microbial biomass were evaluated in four representative ecosystems in east-central Minnesota. The study ecosystems included: old field, swamp forest, savanna, and upland pin oak forest. Due to a high regional water table and permeable soils, the upland and wetland ecosystems were separated by relatively short distances (2 to 5 m). Two randomly selected sites within each ecosystem were sampled for an entire growing season. Soil samples were collected at 5-week intervals to determine rates of N cycling processes and changes in microbial biomass. Mean daily N mineralization rates during five-week in situ soil incubations were significantly different among sampling dates and ecosystems. The highest annual rates were measured in the upland pin oak ecosystem (8.6 g N m^–2 yr^–1), and the lowest rates in the swamp forest (1.5 g N m^–2 yr^–1); nitrification followed an identical pattern. Denitrification was relatively high in the swamp forest during early spring (8040 g N₂O–N m^–2 d^–1) and late autumn (2525 g N₂O–N m^–2 d^–1); nitrification occurred at rates sufficient to sustain these losses. In the well-drained uplands, rates of denitrification were generally lower and equivalent to rates of atmospheric N inputs. Microbial C and N were consistently higher in the swamp forest than in the other ecosystems; both were positively correlated with average daily rates of N mineralization. In the subtle landscape of east-central Minnesota, rates of N cycling can differ by an order of magnitude across relatively short distances.     

Forest soil respiration across three climatically distinct chronosequences in Oregon

To assess the relative influence of edaphoclimatic gradients and stand replacing disturbance on the soil respiration of Oregon forests, we measured annual soil respiration at 36 independent forest plots arranged as three replicates of four age classes in each of three climatically distinct forest types. Annual soil respiration for the year 2001 was computed by combining periodic chamber measurements with continuous soil temperature measurements, which were used along with site-specific temperature response curves to interpolate daily soil respiration between dates of direct measurement. Results indicate significant forest type, age, and type × age interaction effects on annual soil respiration. Average annual soil respiration was 1100–1600, 1500–2100, and 500–900 g C m⁻² yr⁻¹ for mesic spruce, montane Douglas-fir, and semi-arid pine forests respectively. Age related trends in annual soil respiration varied between forest types. The variation in annual soil respiration attributable to the climatic differences between forest types was 48%(CV). Once weighted by the age class distribution for each forest type, the variation in annual soil respiration attributable to stand replacing disturbance was 15%(CV). Sensitivity analysis suggests that the regional variation in annual soil respiration is most dependent on summer base rates (i.e. soil respiration normalized to a common temperature) and much less dependent on the site-specific temperature response curves (to which annual rates are relatively insensitive) and soil degree-days (which vary only 10% among plots).     

Interactive Effects of Nitrogen and Phosphorus on Soil Microbial Communities in a Tropical Forest

Elevated nitrogen (N) deposition in humid tropical regions may exacerbate phosphorus (P) deficiency in forests on highly weathered soils. However, it is not clear how P availability affects soil microbes and soil carbon (C), or how P processes interact with N deposition in tropical forests. We examined the effects of N and P additions on soil microbes and soil C pools in a N-saturated old-growth tropical forest in southern China to test the hypotheses that (1) N and P addition will have opposing effects on soil microbial biomass and activity, (2) N and P addition will alter the composition of the microbial community, (3) the addition of N and P will have interactive effects on soil microbes and (4) addition-mediated changes in microbial communities would feed back on soil C pools. Phospholipid fatty acid (PLFA) analysis was used to quantify the soil microbial community following four treatments: Control, N addition (15 g N m⁻² yr⁻¹), P addition (15 g P m⁻² yr⁻¹), and N&P addition (15 g N m⁻² yr⁻¹ plus 15 g P m⁻² yr⁻¹). These were applied from 2007 to 2011. Whereas additions of P increased soil microbial biomass, additions of N reduced soil microbial biomass. These effects, however, were transient, disappearing over longer periods. Moreover, N additions significantly increased relative abundance of fungal PLFAs and P additions significantly increased relative abundance of arbuscular mycorrhizal (AM) fungi PLFAs. Nitrogen addition had a negative effect on light fraction C, but no effect on heavy fraction C and total soil C. In contrast, P addition significantly decreased both light fraction C and total soil C. However, there were no interactions between N addition and P addition on soil microbes. Our results suggest that these nutrients are not co-limiting, and that P rather than N is limiting in this tropical forest.     

Land-use change effects on soil C and N transformations in soils of high N status: comparisons under indigenous forest, pasture and pine plantation

Globally, land-use change is occurring rapidly, and impacts on biogeochemical cycling may be influenced by previous land uses. We examined differences in soil C and N cycling during long-term laboratory incubations for the following land-use sequence: indigenous forest (soil age = 1800 yr); 70-year-old pasture planted after forest clearance; 22-year-old pine (Pinus radiata) planted into pasture. No N fertilizer had been applied but the pasture contained N-fixing legumes. The sites were adjacent and received 3–6 kg ha^–1 yr^–1volcanic N in rain; NO₃ ^–-N leaching losses to streamwater were 5–21 kg ha^–1 yr^–1, and followed the order forest < pasture = pine. Soil C concentration in 0–10 cm mineral soil followed the order: pasture > pine = forest, and total N: pasture > pine > forest. Nitrogen mineralization followed the order: pasture > pine > forest for mineral soil, and was weakly related to C mineralization. Based on radiocarbon data, the indigenous forest 0–10 cm soil contained more pre-bomb C than the other soils, partly as a result of microbial processing of recent C in the surface litter layer. Heterotrophic activity appeared to be somewhat N limited in the indigenous forest soil, and gross nitrification was delayed. In contrast, the pasture soil was rich in labile N arising from N fixation by clover, and net nitrification occurred readily. Gross N cycling rates in the pine mineral soil (per unit N) were similar to those under pasture, reflecting the legacy of N inputs by the previous pasture. Change in land use from indigenous forest to pasture and pine resulted in increased gross nitrification, net nitrification and thence leaching of NO₃ ^–-N.     

Soil carbon cycling in a temperate forest: radiocarbon-based estimates of residence times, sequestration rates and partitioning of fluxes

Temperate forests of North America are thought to besignificant sinks of atmospheric CO₂. Wedeveloped a below-ground carbon (C) budget forwell-drained soils in Harvard Forest Massachusetts, anecosystem that is storing C. Measurements of carbonand radiocarbon (¹⁴C) inventory were used todetermine the turnover time and maximum rate ofCO₂ production from heterotrophic respiration ofthree fractions of soil organic matter (SOM):recognizable litter fragments (L), humified lowdensity material (H), and high density ormineral-associated organic matter (M). Turnover timesin all fractions increased with soil depth and were2–5 years for recognizable leaf litter, 5–10 years forroot litter, 40–100+ years for low density humifiedmaterial and >100 years for carbon associated withminerals. These turnover times represent the timecarbon resides in the plant + soil system, and mayunderestimate actual decomposition rates if carbonresides for several years in living root, plant orwoody material.Soil respiration was partitioned into two componentsusing ¹⁴C: recent photosynthate which ismetabolized by roots and microorganisms within a yearof initial fixation (Recent-C), and C that is respiredduring microbial decomposition of SOM that resides inthe soil for several years or longer (Reservoir-C).For the whole soil, we calculate that decomposition ofReservoir-C contributes approximately 41% of thetotal annual soil respiration. Of this 41%,recognizable leaf or root detritus accounts for 80%of the flux, and 20% is from the more humifiedfractions that dominate the soil carbon stocks.Measurements of CO₂ and ¹⁴CO₂ in thesoil atmosphere and in total soil respiration werecombined with surface CO₂ fluxes and a soil gasdiffusion model to determine the flux and isotopicsignature of C produced as a function of soil depth. 63% of soil respiration takes place in the top 15 cmof the soil (O + A + Ap horizons). The average residencetime of Reservoir-C in the plant + soil system is8±1 years and the average age of carbon in totalsoil respiration (Recent-C + Reservoir-C) is 4±1years.The O and A horizons have accumulated 4.4 kgC m^–2above the plow layer since abandonment by settlers inthe late-1800's. C pools contributing the most to soilrespiration have short enough turnover times that theyare likely in steady state. However, most C is storedas humified organic matter within both the O and Ahorizons and has turnover times from 40 to 100+ yearsrespectively. These reservoirs continue to accumulatecarbon at a combined rate of 10–30 gC m^{minus 2}yr^–1. This rate of accumulation is only 5–15% of the total ecosystem C sink measured in this stand using eddy covariance methods.     

华西雨屏区苦竹林土壤呼吸对模拟氮沉降的响应

2007年11月至2008年11月, 对华西雨屏区苦竹(Pleioblastus amarus)人工林进行了模拟氮沉降试验, 氮沉降水平分别为对照(CK, 0 g N·m^-2·a^-1)、低氮(5 g N·m^-2·a^-1)、中氮(15 g N·m^-2·a^-1)和高氮(30 g N·m^-2·a^-1)。每月下旬, 采用红外CO₂分析法测定土壤呼吸速率, 并定量地对各处理施氮(NH₄NO₃)。结果表明: 2008年试验地氮沉降量为8.241 g·m^-2, 超出该地区氮沉降临界负荷。在生长季节, 苦竹林根呼吸占总土壤呼吸的60%左右。模拟氮沉降促进了苦竹林土壤呼吸速率, 使苦竹林土壤每年向大气释放的CO₂增加了9.4%~28.6%。在大时间尺度上(如1 a), 土壤呼吸主要受温度的影响。2008年6~10月, 土壤呼吸速率24 h平均值均表现为: 对照<低氮<中氮<高氮。氮沉降处理1 a后, 土壤微生物呼吸速率和土壤微生物生物量碳、氮增加, 并且均与氮沉降量具有相同趋势。各处理土壤呼吸速率与10 cm土壤温度、月平均气温呈极显著指数正相关关系, 利用温度单因素模型可以解释土壤呼吸速率的大部分。模拟氮沉降使得土壤呼吸Q₁₀值增大, 表明氮沉降可能增强了土壤呼吸的温度敏感性。在氮沉降持续增加和全球气候变暖的背景下, 氮沉降和温度的共同作用可能使得苦竹林向大气中排放的CO₂增加。     

Production,Respiration, and Overall Carbon Balance in an Old-growth <Emphasis Type="Italic">Pseudotsuga</Emphasis>-<Emphasis Type="Italic">Tsuga</Emphasis> Forest Ecosystem

Ground-based measurements of stores, growth, mortality, litterfall, respiration, and decomposition were conducted in an old-growth forest at Wind River Experimental Forest, Washington, USA. These measurements were used to estimate gross primary production (GPP) and net primary production (NPP); autotrophic respiration (R_a) and heterotrophic (R_h) respiration; and net ecosystem production (NEP). Monte Carlo methods were used to calculate uncertainty (expressed as ± 2 standard deviations of 200–400 calculations). Live carbon (C) stores were 39,800 g C m^–2 (34,800–44,800 g C m^–2). The store of C in detritus and mineral soil was 22,092 g C m^–2 (20,600–23,600 g C m^–2), and the total C stores were 61,899 g C m^–2 (56,600–67,700 g C m^–2). Total NPP was 597 g C m^–2 y^–1 (453 to 741 g C m^–2 y^–1). R_a was 1309 g C m^–2 y^–1 (845–1773 g C m^–2 y^–1), indicating a GPP of 1906 g C m^–2 y^–1 (1444–2368 g C m^–2 y^–1). R_h, including the respiration of heart rots in tree boles, was 577 g C m^–2 y^–1 (479–675 g C m^–2 y^–1). Long-term NEP was estimated to be +20 g C m^–2 y^–1 (–116 to +156 g C m^–2 y^–1), indicating this stand might be a small sink. These estimates contrast with the larger sink estimated at the same site using eddy-flux methods. Several hypotheses to explain this discrepancy were explored, including (a) undetected biomass increases, (b) underestimates of NPP, (c) unmeasured losses, and (d) a temporal mismatch between the two sets of measurements. The last hypothesis appears the most likely.     

Association of Microbial Community Composition and Activity with Lead, Chromium, and Hydrocarbon Contamination

Microbial community composition and activity were characterized in soil contaminated with lead (Pb), chromium (Cr), and hydrocarbons. Contaminant levels were very heterogeneous and ranged from 50 to 16,700 mg of total petroleum hydrocarbons (TPH) kg of soil⁻¹, 3 to 3,300 mg of total Cr kg of soil⁻¹, and 1 to 17,100 mg of Pb kg of soil⁻¹. Microbial community compositions were estimated from the patterns of phospholipid fatty acids (PLFA); these were considerably different among the 14 soil samples. Statistical analyses suggested that the variation in PLFA was more correlated with soil hydrocarbons than with the levels of Cr and Pb. The metal sensitivity of the microbial community was determined by extracting bacteria from soil and measuring [³H]leucine incorporation as a function of metal concentration. Six soil samples collected in the spring of 1999 had IC₅₀ values (the heavy metal concentrations giving 50% reduction of microbial activity) of approximately 2.5 mM for CrO₄²⁻ and 0.01 mM for Pb²⁺. Much higher levels of Pb were required to inhibit [¹⁴C]glucose mineralization directly in soils. In microcosm experiments with these samples, microbial biomass and the ratio of microbial biomass to soil organic C were not correlated with the concentrations of hydrocarbons and heavy metals. However, microbial C respiration in samples with a higher level of hydrocarbons differed from the other soils no matter whether complex organic C (alfalfa) was added or not. The ratios of microbial C respiration to microbial biomass differed significantly among the soil samples (P < 0.05) and were relatively high in soils contaminated with hydrocarbons or heavy metals. Our results suggest that the soil microbial community was predominantly affected by hydrocarbons.     

The role of <Emphasis Type="Italic">Calamagrostis</Emphasis> communities in preventing soil acidification and base cation losses in a deforested mountain area affected by acid deposition

The effects of grass growth and N deposition on the leaching of nutrients from forest soil were studied in a lysimeter experiment performed in the Moravian-Silesian Beskydy Mts. (the Czech Republic). It was assumed that the grass sward formed on sites deforested due to forest decline would improve the soil environment. Lysimeters with growing acidophilous grasses (Calamagrostis arundinacea and C. villosa), common on clear-cut areas, and with unplanted bare forest soil were installed in the deforested area affected by air pollution. Wet bulk deposition of sulphur in SO₄^2– corresponded to 21.6–40.1 kg ha^–1 and nitrogen in NH₄⁺ and NO₃^– to 8.9–17.4 kg N ha^–1, with a rain water pH of 4.39–4.59 and conductivity of 18.6–36.4 S cm^–1 during the growing seasons 1997–1999. In addition, the lysimeters were treated with 50 kg N ha^–1 yr^–1 as ammonium nitrate during the 3 years of the experiment. Rapid growth of planted grasses resulted in a very fast formation of both above- and below-ground biomass and a large accumulation of nitrogen in the tissue of growing grasses. The greatest differences in N accumulation in aboveground biomass were observed at the end of the third growing season; in C. villosa and C. arundinacea, respectively, 2.66 and 3.44 g N m^–2 after addition of nitrogen and 1.34 and 2.39 g N m^–2 in control. Greater amounts of nitrogen were assessed in below-ground plant parts (9.93–12.97 g N m^–2 in C. villosa and 4.29–4.39 g N m^–2 in C. arundinacea). During the second and third year of experiment, the following effects were the most pronounced: the presence of growing grasses resulted in a decrease of both the acidity and conductivity of lysimetric water and in a lower amount of leached nitrogen, especially of nitrates. Leaching of base cations (Ca²⁺ and Mg²⁺) was two to three times lower than from bare soil without grasses. An excess of labile Al³⁺ was substantially eliminated in treatments with grasses. Enhanced N input increased significantly the acidity and losses of nutrients only in unplanted lysimeters. The leaching of N from treatments with grasses (3.9–5.6 kg N ha^–1) was 31–46% of the amount of N in wet deposition. However, the amount of leached N (4.2–6.0 kg N ha^–1) after N application was only 7.1–8.9% of total N input. After a short three year period, the features of soil with planted grasses indicated a slight improvement: higher pH values and Ca²⁺ and Mg²⁺ contents. The ability of these grass stands to reduce the excess nitrogen in soil is the principal mechanism modifying the negative impact on sites deforested by acid depositions. Thus it is suggested that grass sward formation partly eliminates negative processes associated with soil acidification and has a positive effect on the reduction of nutrient losses from the soil.     

Patterns of restoration of soil physciochemical properties and microbial biomass in different landslide sites in the sal forest ecosystem of Nepal Himalaya

The pattern of natural restoration in soil components and processes was documented in five landslide-damaged (1–58-year-old) sites in the moist tropical sal (Shorea robusta) forest ecosystem of Nepal Himalaya. Comparisons were made with an undisturbed forest site in the same region. Concentrations of soil organic C, total N, total P and extractable nutrients (Ca, Mg and K) increased with the age of sites. The 58-year-old site showed concentrations of soil organic C, total N and total P that were 75–89% of concentrations in the undisturbed sal forest. The soil microbial biomass, the active fraction of soil organic matter, showed similar seasonal variations at all sites. The amount of mean microbial biomass (expressed as C, N and P contents) increased 4–5 times at the 58-year-old site relative to the 1-year-old site, and the bulk increase occurred within the initial 15 year. The increase in the C/N ratio of soil microbial biomass with age (9.4–11.6 years) reflected change in its composition. Although the net N-mineralization rate increased consistently until 58 years of age, the proportion of nitrification rate relative to ammonification rate distinctly decreased beyond 40 years. On the other hand, the soil available-N (both NO₃⁻ and NH₄⁺) concentrations increased from 1 to 40 year and then declined; with age the proportion of NH₄⁺ increased, however. Rates of restoration in soil properties were faster in the early successional stages (1–15 year) than late stages. Among different soil properties the restoration of soil microbial biomass (C and N) was faster than soil organic C and total N. Best fit power function models showed that the estimated times for the 58-year-old site to reach the level of the undisturbed, mature sal forest would be about 30–35 year for microbial biomass (C and N) and about 100–150 year for organic C and total N. Higher accumulation of soil microbial biomass and high N-mineralization rate at late successional stages indicated the re-establishment of enriched soil and restitution of nutrient cycling during the course of ecosystem restoration.     

The nitrogen cycle in lodgepole pine forests,southeastern Wyoming

Storage and flux of nitrogen were studied in several contrasting lodgepole pine (Pinus contorta spp.latifolia) forests in southeastern Wyoming. The mineral soil contained most of the N in these ecosystems (range of 315–860 g · m^–2), with aboveground detritus (37.5–48.8g · m^–2) and living biomass (19.5–24.0 g · m^–2) storing much smaller amounts. About 60–70% of the total N in vegetation was aboveground, and N concentrations in plant tissues were unusually low (foliage = 0.7% N), as were N input via wet precipitation (0.25 g · m^–2 · yr^–1), and biological fixation of atmospheric N (<0.03 g · m^–2 · yr^–1, except locally in some stands at low elevations where symbiotic fixation by the leguminous herbLupinus argenteus probably exceeded 0.1 g · m^–2 · yr^–1).Because of low concentrations in litterfall and limited opportunity for leaching, N accumulated in decaying leaves for 6–7 yr following leaf fall. This process represented an annual flux of about 0.5g · m^–2 to the 01 horizon. Only 20% of this flux was provided by throughfall, with the remaining 0.4g · m^–2 · yr^–1 apparently added from layers below. Low mineralization and small amounts of N uptake from the 02 are likely because of minimal rooting in the forest floor (as defined herein) and negligible mineral N (< 0.05 mg · L^–1) in 02 leachate. A critical transport process was solubilization of organic N, mostly fulvic acids. Most of the organic N from the forest floor was retained within the major tree rooting zone (0–40 cm), and mineralization of soil organic N provided NH₄ for tree uptake. Nitrate was at trace levels in soil solutions, and a long lag in nitrification was always observed under disturbed conditions. Total root nitrogen uptake was calculated to be 1.25 gN · m^–2 · yr^–1 with estimated root turnover of 0.37-gN · m^–2 · yr^–1, and the soil horizons appeared to be nearly in balance with respect to N. The high demand for mineralized N and the precipitation of fulvic acid in the mineral soil resulted in minimal deep leaching in most stands (< 0.02 g · m^–2 · yr^–1). These forests provide an extreme example of nitrogen behavior in dry, infertile forests.     

Soil and total ecosystem respiration in agricultural fields: effect of soil and crop type

A study was made of the effect of soil and crop type on the soil and total ecosystem respiration rates in agricultural soils in southern Finland. The main interest was to compare the soil respiration rates in peat and two different mineral soils growing barley, grass and potato. Respiration measurements were conducted during the growing season with (1) a closed-dynamic ecosystem respiration chamber, in which combined plant and soil respiration was measured and (2) a closed-dynamic soil respiration chamber which measured only the soil and root-derived respiration. A semi-empirical model including separate functions for the soil and plant respiration components was used for the total ecosystem respiration (TER), and the resulting soil respiration parameters for different soil and crop types were compared. Both methods showed that the soil respiration in the peat soil was 2–3 times as high as that in the mineral soils, varying from 0.11 to 0.36 mg (CO₂) m^–2 s^–1 in the peat soil and from 0.02 to 0.17 mg (CO₂) m^–2 s^–1 in the mineral soils. The difference between the soil types was mainly attributed to the soil organic C content, which in the uppermost 20 cm of the peat soil was 24 kg m^–2, being about 4 times as high as that in the mineral soils. Depending on the measurement method, the soil respiration in the sandy soil was slightly higher than or similar to that in the clay soil. In each soil type, the soil respiration was highest on the grass plots. Higher soil respiration parameter values (R_s0, describing the soil respiration at a soil temperature of 10°C, and obtained by modelling) were found on the barley than on the potato plots. The difference was explained by the different cultivation history of the plots, as the potato plots had lain fallow during the preceding summer. The total ecosystem respiration followed the seasonal evolution in the leaf area and measured photosynthetic flux rates. The 2–3-fold peat soil respiration term as compared to mineral soil indicates that the cultivated peat soil ecosystem is a strong net CO₂ source.