Carbon storage in forest soil of Finland. 1. Effect of thermoclimate

A total of 30 coniferous forest sites representing two productivityclasses, forest types, were investigated on a temperature gradient(effective temperature sum using +5^°C threshold 800–1300degree-days and annual mean temperature –0.6–+3.9^°C) inFinland for studying the effect of thermoclimate on the soil C storage.Other soil forming factors were standardized within the forest types sothat the variation in the soil C density could be related to temperature.According to the applied regression model, the C density of the 0–1 mmineral soil layer increased 0.266 kg m^–2 for every 100 degree-dayincrease in the temperature sum, and the layer contained 57% and28% more C under the warmest conditions of the gradient comparedto the coolest in the less and more productive forest type, respectively.Accordingly, this soil layer was estimated to contain 23 more C ina new equilibrium with a 4^°C higher annual meantemperature in Finland. The C density of the organic layer was notassociated with temperature. Both soil layers contained more C at thesites of the more productive forest type, and the forest type explained36% and 70% of the variation in the C density of the organic and 0–1m layers, respectively. Within the forest types, the temperature sumaccounted for 33–41% of the variation in the 0–1 m layer. Theseresults suggest that site productivity is a cause for the large variation inthe soil C density within the boreal zone, and relating the soil C densityto site productivity and temperature would help to estimate the soil Creserves more accurately in the boreal zone.     

青藏高原高寒草地3米深度土壤无机碳库及分布特征

准确评估土壤无机碳库的大小及其分布特征有助于全面理解陆地生态系统碳循环与气候变暖之间的反馈关系.然而, 由于深层土壤剖面信息匮乏, 使得目前学术界对深层土壤无机碳库的了解十分有限.该研究基于342个3 m深度和177个50 cm深度的土壤剖面信息, 采用克里格插值方法估算了青藏高原高寒草地不同深度的土壤无机碳库大小, 并在此基础上分析了该地区土壤无机碳密度的分布特征.结果显示, 青藏高原高寒草地0-50 cm,0-1 m,0-2 m和0-3 m深度的土壤无机碳库大小分别为8.26,17.82,36.33和54.29 Pg C, 对应的土壤无机碳密度分别为7.22,15.58,31.76和47.46 kg C·m^-2.研究区土壤无机碳密度总体呈现由东南向西北增加的趋势; 高寒草原土壤的无机碳密度显著大于高寒草甸的无机碳密度.整体上, 不同深度的高寒草原无机碳库约占整个研究区无机碳库的63%-66%.此外, 深层土壤中储存了大量无机碳, 1 m以下土壤无机碳库是1 m以内无机碳库的2倍.两种草地类型土壤无机碳的垂直分布存在差异: 对高寒草原而言, 0-50 cm土壤无机碳所占的比例最大; 但对高寒草甸而言, 在100-150 cm深度土壤无机碳出现富集.这些结果表明青藏高原深层土壤是一个重要的无机碳库, 需在未来碳循环研究中予以重视.     

Soil inorganic carbon stock in alpine grasslands on the Qinghai-Xizang Plateau: An updated evaluation using deep cores

Aims To estimate the size and spatial patterns of 3-m-deep soil inorganic carbon (SIC) stock across alpine grasslands on the Qinghai-Xizang Plateau.Methods We conducted a comprehensive investigation and collected soil samples from 342 3-m-deep cores and 177 50-cm-deep pits across the study area. Using Kriging interpolation, we interpolated site-level observations to the regional level. The distribution of SIC density was then overlaid with the regional vegetation map at a scale of 1:1000000 to calculate SIC stock of the alpine steppe and alpine meadow. Kruskal-Wallis tests were further conducted to examine the differences of SIC density between the two grassland types and among soil depths with 50 cm-depth intervals.Important findings The total SIC stock at depths of 50 cm, 1 m, 2 m and 3 m were estimated at 8.26, 17.82, 36.33 and 54.29 Pg C, with SIC density being 7.22, 15.58, 31.76 and 47.46 kg C·m^-2, respectively. SIC density exhibited large spatial variability, with an increasing trend from the southeastern to the northwestern plateau. Much larger SIC stock was observed in the alpine steppe than alpine meadow, with the former accounting for 63%-66% of the total stock at depths of 50 cm, 1 m, 2 m and 3 m. A large amount of SIC stock was found in deep soils (1-3 m), amounting to approximately 2 times as much carbon stored in the top 1-m-deep soil layer. The vertical distributions of SIC density differed between the two grassland types. The highest proportions of SIC occurred in the upper 50 cm layer for the alpine steppe while the highest proportions occurred in 100-150 cm layer for the alpine meadow. These results highlight that a large amount of SIC is stored in deep soil layers, which should be considered in evaluating terrestrial carbon balance under global change scenario.     

Changes in soil carbon with stand age – an evaluation of a modelling method with empirical data

Forest soils store a substantial amount of carbon, often more than the forest vegetation does. Estimates of the amount of soil carbon, and in particular estimates of changes in these amounts are still inaccurate. Measuring soil carbon is laborious, and measurements taken at a few statistically unrepresentative sites are difficult to scale to larger areas. We combined a simple dynamic model of soil carbon with litter production estimated on the basis of stand parameters, models of tree allometry and biomass turnover rates of different biomass components. This integrated method was used to simulate soil carbon as forest stands develop. The results were compared with measurements of soil carbon from 64 forest sites in southern Finland. Measured carbon stocks in the organic soil layer increased by an average of 4.7±1.4 g m^?2 a^?1 with increasing stand age and no significant changes were measured in the amount of carbon in mineral soil. Our integrated method indicated that soil carbon stocks declined to a minimum 20 years after clear‐cutting and the subsequent increase in the soil carbon stock (F/H ? 1 m) was 5.8±1.0 g m^?2 a^?1 averaged over the period to next harvesting (～125 years). Simulated soil carbon accumulation slowed down considerably in stands older than 50 years. The carbon stock measured (F/H ? 1 m) for the study area averaged 6.8±2.5 kg m^?2. The simulated carbon stock in soil was 7.0±0.6 kg m^?2 on average. These tests of the validity of the integrated model suggest that this method is suitable for estimating the amount of carbon in soil and its changes on regional scales.     

Quantifying the effects of switchgrass (Panicum virgatum) on deep organic C stocks using natural abundance 14C in three marginal soils

Perennial bioenergy crops have been shown to increase soil organic carbon (SOC) stocks, potentially offsetting anthropogenic C emissions. The effects of perennial bioenergy crops on SOC are typically assessed at shallow depths (<30 cm), but the deep root systems of these crops may also have substantial effects on SOC stocks at greater depths. We hypothesized that deep (>30 cm) SOC stocks would be greater under bioenergy crops relative to stocks under shallow‐rooted conventional crop cover. To test this, we sampled soils to between 1‐ and 3‐m depth at three sites in Oklahoma with 10‐ to 20‐year‐old switchgrass (Panicum virgatum) stands, and collected paired samples from nearby fields cultivated with shallow rooted annual crops. We measured root biomass, total organic C, ¹⁴C, ¹³C, and other soil properties in three replicate soil cores in each field and used a mixing model to estimate the proportion of recently fixed C under switchgrass based on ¹⁴C. The subsoil C stock under switchgrass (defined over 500–1500 kg/m² equivalent soil mass, approximately 30–100 cm depth) exceeded the subsoil stock in neighboring fields by 1.5 kg C/m² at a sandy loam site, 0.6 kg C/m² at a site with loam soils, and showed no significant difference at a third site with clay soils. Using the mixing model, we estimated that additional SOC introduced after switchgrass cultivation comprised 31% of the subsoil C stock at the sandy loam site, 22% at the loam site, and 0% at the clay site. These results suggest that switchgrass can contribute significantly to subsoil organic C—but also indicated that this effect varies across sites. Our analysis shows that agricultural strategies that emphasize deep‐rooted grass cultivars can increase soil C relative to conventional crops while expanding energy biomass production on marginal lands.     

Soil carbon stock and its changes in northern China's grasslands from 1980s to 2000s

Climate warming is likely to accelerate the decomposition of soil organic carbon (SOC) which may lead to an increase of carbon release from soils, and thus provide a positive feedback to climate change. However, SOC dynamics in grassland ecosystems over the past two decades remains controversial. In this study, we estimated the magnitude of SOC stock in northern China's grasslands using 981 soil profiles surveyed from 327 sites across the northern part of the country during 2001–2005. We also examined the changes of SOC stock by comparing current measurements with historical records of 275 soil profiles derived from China's National Soil Inventory during the 1980s. Our results showed that, SOC stock in the upper 30 cm in northern China's grasslands was estimated to be 10.5 Pg C (1 Pg=10¹⁵ g), with an average density (carbon stock per area) of 5.3 kg C m^?2. SOC density (SOCD) did not show significant association with mean annual temperature, but was positively correlated with mean annual precipitation. SOCD increased with soil moisture and reached a plateau when soil moisture was above 30%. Site‐level comparison indicated that grassland SOC stock did not change significantly over the past two decades, with a change of 0.08 kg C m^?2, ranging from ?0.30 to 0.46 kg C m^?2 at 95% confidence interval. Transect‐scale comparison confirmed that grassland SOC stock remained relatively constant from 1980s to 2000s, suggesting that soils in northern China's grasslands have been carbon neutral over the last 20 years.     

Changes in carbon storage in temperate humic loamy soils after forest clearing and continuous corn cropping in France

Soil samples from forest and agricultural sites in three areas of southwest France were collected to determine the effect of forest conversion to continuous intensive corn cropping with no organic matter management on soil organic carbon (C) content. Soils were humic loamy soils and site characteristics that may affect soil C were as uniform as possible (slope, elevation, texture, soil type, vegetation). Three areas were selected, with adjacent sites of various ages of cultivation (3 to 35 yr), and paired control forest sites. The ploughed horizon (0-Dt cm) and the Dt-50 cm layer were collected at each agricultural site. In forest sites, each 10 cm layer was collected systematically down to 1 meter depth. Carbon concentrations were converted to total content to a given depth as the product of concentration, depth of sample and bulk density, and expressed in units of kg m^-2. For each site and each sampled layer, the mineral mass of soil was calculated, in order to base comparisons on the same soil mass rather than the same depth. The pattern of C accumulation in forest soils showed an exponential decrease with depth. Results suggested that soil organic carbon declined rapidly during the first years of cultivation, and at a slower rate thereafter. This pattern of decrease can be fitted by a bi-exponential model assuming that initial soil organic carbon can be separated into two parts, a very labile pool reduced during the first rapid decline and more refractory fractions oxidizing at a slower rate. Sampling to shallow depths (0-Dt cm) resulted in over-estimation of the rate of carbon release in proportion to the initial amount of C, and in under-estimation of the total loss of C with age. The results for the 0–50 cm horizon indicated that losses of total carbon average about 50% in these soils, ranging in initial carbon content from 19 to 32.5 kg m^-2. Carbon release to the atmosphere averaged 0.8 kg m^-2 yr^-1 to 50 cm depth during the first 10 years of cultivation. The results demonstrate that temperate soils may also be an important source of atmospheric carbon, when they are initially high in carbon content and then cultivated intensively with no organic matter management.     

Soil seed banks of woodland, heathland, grassland, mire and montane communities, Cairngorm Mountains, Scotland

The size and species composition of soil seed banks were assessed at 111 altitudinally diverse sites in the Cairngorm Mountains. Mean densities of germinable seeds varied from 83 000 m^–2 in Scots pine (Pinus sylvestris L.) woodland at 230–490 m to 200 m^–2 in moss (Racomitrium lanuginosum (Hedw.) Brid.) heath at 1000–1120 m. Seed banks were dominated by Calluna vulgaris (L.) Hull, not only wherever it was prominent in the vegetation, but also at some sites with less than 5% cover of parent plants in the ground vegetation. Many species conspicuous in the vegetation were under-represented in or absent from the seed bank and surface vegetation generally was more species rich than was the underlying seed bank, especially in high montane communities. Multiple regression was used to examine the relationship between the density of buried Calluna seeds and the abundance of parent plants in the vegetation, site altitude and the organic matter content of the soil. The model fitted to woodland communities accounted for 95% of the variation in seed density. The heathland model was less predictive but still explained 52% of the variation in seed bank size. In mire communities there was no relationship, collective or individual, between buried seed density and the measured environmental variables, possibly due to variations in the duration and frequency of waterlogging at these sites. The potential role of seed banks for initiating the recolonisation of disturbed ground is discussed. Densities of buried seeds at most Calluna-dominant sites were probably sufficient to generate successful recolonisation but the prospects for recovery were poor at other sites, particularly in graminaceous communities at 800 m or higher.     

Organic matter accumulation following fires in a moorland soil chronosequence

Severe fires in 1957 and 1976 removed the vegetation and soil organic matter from the litter layers and organic horizons of soils at two adjacent moorland sites leaving exposed the uppermost mineral horizon of the soil. In the period since, plant recolonization and soil organic matter reaccumulation have occurred to give a chronosequence. Assuming no major changes in the carbon and nitrogen content of the unburned soil since 1957, the rates of accumulation of soil C and N were estimated to be 0.035 kg C m^–2 y^–1 and 0.001 kg N m^–2 y^–1 over the first 19 years, and 0.50 kg C m^–2 y^–1 and 0.023 kg N m^–2 y^–1 over the period from 19 to 38 years after burning. Solid-state ¹³C NMR (cross-polarization, magic angle spinning ¹³C nuclear magnetic resonance spectroscopy) showed that the ratio of alkyl- and methyl-C-to-O-alkyl-C increased with stage of decomposition and in the unburned soil with decreasing particle-size. For the organic matter that had reaccumulated in the 1957-burned soil, the alkyl-C-to-O-alkyl-C ratio of the > 2000 μm and 2000–250 μm particle-size fractions were greater than those of the corresponding size fractions from the unburned soil, indicating that the reaccumulated soil organic matter was subject to decomposition but limited fragmentation or comminution.     

Effect of soil compaction on root growth and uptake of phosphorus

Summary Zea mays L. andLolium rigidum Gaud. were grown for 18 and 33 days respectively in pots containing three layers of soil each weighing 1 kg. The top and bottom layers were 100 mm deep and they had a bulk density of 1200 kg m^–3, while the central layer of soil was compacted to one of 12 bulk densities between 1200 and 1750 kg m^–3. The soil was labelled with³²P and³³P so that the contribution of the different layers of soil to the phosphorus content of the plant tops could be determined. Soil water potential was maintained between –20 and –100 kPa.Total dry weight of the plant tops and total root length were slightly affected by compaction of the soil, but root distribution was greatly altered. Compaction decreased root length in the compacted soil but increased root length in the overlying soil. Where bulk density was 1550 kg m^–3, root length in the compacted soil was about 0.5 of the maximum. At that density, the penetrometer resistance of the soil was 1.25 and 5.0 MPa and air porosity was 0.05 and 0.14 at water potentials of –20 and –100 kPa respectively, and daytime oxygen concentrations in the soil atmosphere at time of harvest were about 0.1 m³m^–3. Roots failed to grow completely through the compacted layer of soil at bulk densities 1550 kg m^–3. No differences were detected in the abilities of the two species to penetrate compacted soil.Ryegrass absorbed about twice as much phosphorus from uncompacted soil per unit length of root as did maize. Uptake of phosphorus from each layer of soil was related to the length of root in that layer, but differences in uptake between layers existed. Phosphorus uptake per unit length of root was higher from compacted than from uncompacted soil, particularly in the case of ryegrass at bulk densities of 1300–1500 kg m^–3.     

Impacts of Reservoir Creation on the Biogeochemical Cycling of Methyl Mercury and Total Mercury in Boreal Upland Forests

The FLooded Upland Dynamics Experiment (FLUDEX) at the Experimental Lakes Area (ELA) in northwest Ontario was designed to test the hypothesis that methylmercury (MeHg) production in reservoirs is related to the amount, and subsequent decomposition, of flooded organic matter. Three upland forest sites that varied in the amounts of organic carbon stored in vegetation and soils (Low C, 30,870 kg C ha⁻¹; Medium C, 34,930 kg C ha⁻¹; and High C, 45,860 kg C ha⁻¹) were flooded annually from May to September with low-organic carbon, low-MeHg water pumped from a nearby lake. Within five weeks of flooding, MeHg concentrations in the reservoir outflows exceeded those in reservoir inflows and remained elevated for the duration of the experiment, peaking at 1.60 ng L⁻¹ in the Medium C reservoir. We estimated the net production of MeHg in each reservoir by calculating annual changes in pools of MeHg stored in flooded soils, periphyton, zooplankton, and fish. Overall, there was an initial pulse of MeHg production (range = 120–1590 ng m⁻² day⁻¹) in all FLUDEX reservoirs that lasted for 2 years, after which time net demethylation (range = 360–1230 ng MeHg degraded m⁻² day⁻¹) began to reduce the pools of MeHg in the reservoirs, but not back to levels found prior to flooding. Rates of MeHg production were generally related to the total amount of organic carbon flooded to create the reservoirs. Large increases in MeHg stores in soils compared to those in water and biota indicate that flooded soils were the main sites of MeHg production. This study should assist hydroelectric utilities and government agencies in making informed decisions about selecting sites for future reservoir development to reduce MeHg contamination of the reservoir fisheries.     

Digital Mapping of Soil Organic Carbon Contents and Stocks in Denmark

Estimation of carbon contents and stocks are important for carbon sequestration, greenhouse gas emissions and national carbon balance inventories. For Denmark, we modeled the vertical distribution of soil organic carbon (SOC) and bulk density, and mapped its spatial distribution at five standard soil depth intervals (0−5, 5−15, 15−30, 30−60 and 60−100 cm) using 18 environmental variables as predictors. SOC distribution was influenced by precipitation, land use, soil type, wetland, elevation, wetness index, and multi-resolution index of valley bottom flatness. The highest average SOC content of 20 g kg⁻¹ was reported for 0−5 cm soil, whereas there was on average 2.2 g SOC kg⁻¹ at 60−100 cm depth. For SOC and bulk density prediction precision decreased with soil depth, and a standard error of 2.8 g kg⁻¹ was found at 60−100 cm soil depth. Average SOC stock for 0−30 cm was 72 t ha⁻¹ and in the top 1 m there was 120 t SOC ha⁻¹. In total, the soils stored approximately 570 Tg C within the top 1 m. The soils under agriculture had the highest amount of carbon (444 Tg) followed by forest and semi-natural vegetation that contributed 11% of the total SOC stock. More than 60% of the total SOC stock was present in Podzols and Luvisols. Compared to previous estimates, our approach is more reliable as we adopted a robust quantification technique and mapped the spatial distribution of SOC stock and prediction uncertainty. The estimation was validated using common statistical indices and the data and high-resolution maps could be used for future soil carbon assessment and inventories.     

Production and export of dissolved C in arctic tundra mesocosms: the roles of vegetation and water flow

To better understand carbon (C) cycling in arctic tundra we measureddissolved C production and export rates in mesocosms of three tundra vegetationtypes: tussock, inter-tussock and wet sedge. Three flushing frequencies wereused to simulate storm events and determine potential mass export of dissolved Cunder increased soil water flow scenarios. Dissolved C production and exportrates differed between vegetation types (inter-tussock < tussock < wetsedge). In the absence of flushing, dissolved organic C (DOC) dominatedproduction in tussock and inter-tussock soils but was consumed in wet sedgesoils (8.3, 32.7, and –0.4 g C g soil^–1day^–1). Soil water dissolved C concentrations declined over time when flushedat high and medium frequencies but were variable at low flushing frequency.Total yield of dissolved C and DOC increased with increased flushing frequency.The ratio of DOC to dissolved inorganic C exported dropped with increasedflushing under tussock but not inter-tussock or wet sedge vegetation. Massexport per liter of water added declined as flushing frequency increased intussock and inter-tussock mesocosms. Export and production of dissolved C werestrongly correlated with above ground biomass, but not with photosynthetic ratesor below ground biomass. DOC quality was examined by measuring production ofToolik Lake bacteria fed mesocosm soil water. When normalized for DOCconcentration, wet sedge soil water supported significantly higher bacterialproduction. Our results indicate that arctic tundra soils have high potentialsfor dissolved C export, that water flow and vegetation type mainly controldissolved C export, and that responses of aquatic microbes to terrestrial inputsdepend on the vegetation type in the watershed.     

Land use induced changes of organic carbon storage in soils of China

Using the data compiled from China's second national soil survey and an improved method of soil carbon bulk density, we have estimated the changes of soil organic carbon due to land use, and compared the spatial distribution and storage of soil organic carbon (SOC) in cultivated soils and noncultivated soils in China. The results reveal that ～ 57% of the cultivated soil subgroups ( ～ 31% of the total soil surface) have experienced a significant carbon loss, ranging from 40% to 10% relative to their noncultivated counterparts. The most significant carbon loss is observed for the non‐irrigated soils (dry farmland) within a semiarid/semihumid belt from northeastern to southwestern China, with the maximum loss occurring in northeast China. On the contrary, SOC has increased in the paddy and irrigated soils in northwest China. No significant change is observed for forest soils in southern China, grassland and desert soils in northwest China, as well as irrigated soils in eastern China. The SOC storage and density under noncultivated conditions in China are estimated to ～ 77.4 Pg (10¹⁵ g) and ～ 8.8 kg C m^?2, respectively, compared to a SOC storage of ～ 70.3 Pg and an average SOC density of ～ 8.0 kg C m^?2 under the present‐day conditions. This suggests a loss of ～ 7.1 Pg SOC and a decrease of ～ 0.8 kg C m^?2 SOC density due to increasing human activities, in which the loss in organic horizons has contributed to ～ 77%. This total loss of SOC in China induced by land use represents ～ 9.5% of the world's SOC decrease. This amount is equivalent to ～ 3.5 ppmv of the atmospheric CO₂ increase. Since ～ 78% of the currently cultivated soils in China have been degraded to a low/medium productivities and are responsible for most of the SOC loss, an improved land management, such as the development of irrigated and paddy land uses, would have a considerable potential in restoring the SOC storage. Assuming a restoration of ～ 50% of the lost SOC during the next 20–50 years, the soils in China would absorb ～ 3.5 Pg of carbon from the atmosphere.     

Ecosystem carbon stocks and their changes in China’s grasslands

The knowledge of carbon (C) stock and its dynamics is crucial for understanding the role of grassland ecosystems in China’s terrestrial C cycle. To date, a comprehensive assessment on C balance in China’s grasslands is still lacking. By reviewing published literature, this study aims to evaluate ecosystem C stocks (both vegetation biomass and soil organic C) and their changes in China’s grasslands. Our results are summarized as follows: (1) biomass C density (C stock per area) of China’s grasslands differed greatly among previous studies, ranging from 215.8 to 348.1 g C m⁻² with an average of 300.2 g C m⁻². Likewise, soil C density also varied greatly between 8.5 and 15.1 kg C m⁻². In total, ecosystem C stock in China’s grasslands was estimated at 29.1 Pg C. (2) Both the magnitude and direction of ecosystem C changes in China’s grasslands differed greatly among previous studies. According to recent reports, neither biomass nor soil C stock in China’s grasslands showed a significant change during the past 20 years, indicating that grassland ecosystems are C neutral. (3) Spatial patterns and temporal dynamics of grassland biomass were closely correlated with precipitation, while changes in soil C stocks exhibited close associations with soil moisture and soil texture. Human activities, such as livestock grazing and fencing could also affect ecosystem C dynamics in China’s grasslands.     

Denitrification in the top and sub soil of grassland on peat soils

Denitrification is an important process in the nitrogen (N) balance of intensively managed grassland, especially on poorly drained peat soils. Aim of this study was to quantify the N loss through denitrification in the top and sub soil of grassland on peat soils. Sampling took place at 2 sites with both control (0 N) and N fertilised (+ N) treatments. Main difference between the sites was the ground water level. Denitrification was measured on a weekly basis for 2 years with a soil core incubation technique using acetylene (C₂H₂) inhibition. Soil cores were taken from the top soil (0–20 cm depth) and the sub soil (20–40 cm depth) and incubated in containers for 24 hours. The denitrification rate was calculated from the nitrous oxide production between 4 and 24 hours of incubation. Denitrification capacities of the soils and the soil layers were also determined.The top soil was the major layer for denitrification with losses ranging from 9 to 26 kg N ha^–1 yr^–1 from the O N treatment. Losses from the top soil of the + N treatment ranged from 13 to 49 kg N ha^–1 yr^–1. The sub soil contributed, on average, 20% of the total denitrification losses from the 0–40 layer. Losses from the 0–40 cm layer were 2 times higher on the + N treatment than on the O N treatment and totalled up to 70 kg N ha^–1 yr^–1. Significant correlation coefficients were found between denitrification activity on the one hand, and ground water level, water filled pore space and nitrate content on the other, in the top soil but not in the sub soil. The denitrification capacity experiment showed that the availability of easily decomposable organic carbon was an important limiting factor for the denitrification activity in the sub soil of these peat soils.     

Productivity and water relations of burnt and long-unburnt semi-arid shrubland in Western Australia

This study provides a comparison between vegetation of relatively recent and long-unburnt shrubland in terms of structural and functional groups, annual net primary productivity and water relations. Adjacent areas of vegetation long-unburnt or burnt 5 years previously were compared within a remnant block of Acacia–Allocasuarina–Melaleuca arid shrubland at Kalannie, south west Western Australia. Species were classified according to growth and life form, fire response, phenology and rooting morphology and densities, mean plant above-ground dry weights and shoot:root dry mass ratios of each assessed. Species compositions, seedling densities and absence of recruitment in the long-unburnt area suggested marked dependence on fire in maintenance of biodiversity. Comparisons of above-ground standing dry biomass and annual net primary productivity of total (above-ground plus below-ground) dry matter showed the 4.09 kg m^–2 biomass of long-unburnt vegetation to be increasing at 0.52 kg m^–2 year^–1 versus 0.45 and 0.18 kg m^–2 year^–1 for vegetation of the burnt area. Water relations of soils indicated consistently wetter profiles in burnt than long-unburnt areas and no deep drainage during the year of study. Lower water stress of key species in burnt than long-unburnt areas were indicated by less negative pre-dawn water potentials and higher stomatal conductance during the year of study and more negative carbon-isotope composition (¹³C) in wood laid down over the past 5 years. Budgets for water use were estimated for both sites and compared with annual net primary productivities. Data suggested much greater transpiration loss per unit dry matter gain by the rapidly growing plants at the burnt site (437 ml H₂O g^–1 DM) than by the plants of the long-unburnt community (92 ml H₂O g^–1 DM). Results are discussed in relation to composition and functioning of other Western Australian ecosystems. It is clear that time since fire affects productivity and water-use of vegetation of semi-arid shrublands and is therefore an important consideration for management and protection of remnant vegetation.     

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.     

Carbon dioxide efflux and pCO2 in soils of threeQuercus ilex montane forests

Soil CO₂ efflux and pCO₂ in the soil atmosphere were measured during one year at three montane sites of Mediterranean sclerophyllous forests in NE Spain. Two sites were located in the upper and lower slopes of a small catchment in the Prades mountains (mean precipitation 550 mm year^–1), and a third site was located on a lower slope in the Montseny mountains (mean precipitation 900 mm year^–1). The three sites were similar in bedrock and vegetation, but differed in soil characteristics and water availability. Seasonal variation of CO₂ efflux and soil pCO₂ were affected by soil temperature and, to a lesser extent, by soil moisture. Annual mean soil CO₂ efflux (considered as soil respiration) was similar at Montseny and at the comparably located site at Prades (83 ± 18 S.E. vs. 75 ± 9 mg CO₂ m^–2 hour^–1 , respectively), and was highest at the Prades upper slope site (122 ± 22 mg C0₂ m^–2 hour^–1 ). Despite those relatively similar CO₂ effluxes, mean soil pCO₂ was much higher at both Prades sites than at Montseny. Soil pCO₂ always increased with depth at Prades while maxima pCO₂ at Montseny were often at 20–30 cm depth. A model based on gas diffusion theory was able to explain why soil pCO₂ was much higher at Prades than at Montseny, and to reproduce the shape of the vertical profile of pCO₂ at the Prades soils. Nevertheless, the model failed to simulate the soil pCO₂ maximum found at 20–30 cm depth at the Montseny site. Model simulations using a time-variable CO₂ production rate suggested that pCO₂ maxima at intermediate depth could be the result of a transient situation instead of an equilibrium one.     

Ecosystem consequences of plant life form changes at three sites in the semiarid United States

Many semiarid rangelands have recently experienced changes in dominant plant life form. Both woody plant expansion into grasslands and the invasion of annual grasses into shrublands have potential influence on regional carbon cycling. Soil carbon content, chemistry, and distribution may change following shifts in dominant plant life form because plant life forms differ in litter chemistry and patterns of detrital input. This study assesses the amount, quality, and distribution of soil C below woody vegetation and grasses at three rangelands in Texas, New Mexico, and Utah. At each of these sites there has been a well-documented shift in dominant plant life form. In Texas and New Mexico, woody plants have increased in grasslands, while grasses have invaded into former shrublands in Utah. We measured total soil carbon, particulate organic matter (POM) C, and the carbon isotopic composition of soil carbon beneath woody plants and grasses at each of these three sites. At the La Copita Research Area in south-central Texas there was significantly more soil C found beneath Prosopis glandulosa, the dominant woody plant, than was found beneath grasses. Mean soil C content to 1 m was 7.2 kg C m^–2 beneath P. glandulosa and 6.0 kg C m^–2 beneath grasses. There was also significantly more POM C beneath P. glandulosa than beneath grasses. Stable carbon isotopic composition indicated that the expansion of P. glandulosa in savannas in Texas first influences carbon cycling in surface soils, then deep soil C, and finally throughout the soil profile. At the Sevilleta National Wildlife Refuge in central New Mexico, we found that there was significantly more soil C in the upper 10 cm of the soil profile beneath Larrea tridentata than was found beneath Bouteloua spp. Stable carbon isotopic composition indicated that the expansion of L. tridentata influenced C cycling throughout the soil profile. At Curlew Valley in northern Utah, we found no significant differences in total profile soil C beneath different plant life forms. However, there was significantly more soil C found at the soil surface beneath woody plants than was observed beneath annual grasses. There was significantly less POM C beneath annual grasses than was found beneath woody plants or perennial grasses. Based on stable carbon isotopic analyses, we concluded that the invasion of grasses into shrublands influenced only the upper 30 cm of the soil profile. We determined that following changes in plant life form dominance, the most consistent change in soil C was an alteration in content and distribution of POM C, a slowly cycling pool of soil C. While we failed to find a consistent change in total profile soil C with plant life form across our sites, the change in soil C chemistry may have important implications for long-term soil C storage in semiarid systems where there have been shifts in plant life form. Received: 30 March 1999 / Accepted: 11 August 1999