Belowground net primary productivity and biomass allocation of a grassland in Inner Mongolia is affected by grazing intensity

The root system of permanent grasslands is of outstanding importance for resource acquisition. Particularly under semi-arid conditions, the acquisition of water and nutrients is highly variable during the vegetation growth period and between years. Additionally, grazing is repeatedly disturbing the functional equilibrium between the root system and the transpiring leaf canopy. However, very few data is available considering grazing effects on belowground net primary productivity (BNPP) and root-shoot dry mass allocation in natural grassland systems. We hypothesise that grazing significantly reduces BNPP due to carbon reallocation to shoot growth. Root biomass and BNPP were estimated by soil coring in 2004, 2005 and 2006 and from ingrowth cores in 2005 and 2006 at one site which has been protected from grazing since 1979 (UG79), at one winter grazing (WG), and one heavily grazed (HG) site. BNPP was estimated from the summation of significant increments of total and live root biomass and from accumulated root biomass of ingrowth cores. Belowground biomass varied from 1,490–2,670 g m^?2 and was significantly lower under heavy grazing than at site UG79. Root turnover varied from 0.23 to 0.33 year^?1 and was not significantly different between sites. Heavy grazing significantly decreased live root biomass and BNPP compared to site UG79. Taking BNPP estimates from live root biomass dynamics and ingrowth cores as the most reliable values, the portion of dry mass allocated belowground relative to total net primary productivity (BNPP/NPP) varied between 0.50–0.66 and was reduced under heavy grazing in 2005, but not in 2006. The positive correlation between cumulative root length density of ingrowth cores and leaf dry matter suggests that the ingrowth core method is suitable for studying BNPP in this semi-arid steppe system. Grazing effects on BNPP and BNPP/NPP should be considered in regional carbon models and estimates of belowground nutrient cycling.     

Leaf litterfall, fine-root production, and decomposition in shrublands with different canopy structure induced by grazing in the Patagonian Monte, Argentina

Selective sheep grazing in the Patagonian Monte induces the reduction of total and perennial grass cover, species replacement within life forms, and the increase in dominance of long-lived evergreen woody plants with slow growth rates and high concentration of secondary compounds in leaves. We hypothesized that these changes in the canopy structure induced by sheep grazing will affect the mass, chemistry and decomposability of leaf litter and fine roots. We selected two sites in the Patagonian Monte, representative of ungrazed and grazed vegetation states. At each site, we assessed canopy structure (total cover and absolute and relative grass and shrub cover), monthly leaf litterfall, and fine-root biomass and production in the upper soil (15 cm). We also estimated the rates of mass, C, soluble phenolics, lignin and N decay in litterbags containing both leaf litter and fine roots of each site under field conditions during two consecutive years. The ungrazed site exhibited higher total plant cover, absolute and relative grass- and shrub-cover than the grazed one. Leaf litterfall was lower at the grazed site than at the ungrazed site. Fine-root production did not vary between sites. Leaf litter and fine root tissues had higher concentration of secondary compounds at the grazed than at the ungrazed site. However, fine roots showed lower mass and C decay than leaf litter, attributable to the predominant secondary compound (lignin and soluble phenolics, respectively). Leaf litter decomposed slower but released more N during decay at the ungrazed than at the grazed site, probably due to its low concentration of secondary compounds. We concluded that changes in canopy structure induced by grazing disturbance such as those explored in our study could reduce leaf litterfall mass and increase the concentration of secondary compounds of both leaf litter and fine roots leading to slow N release to soil during decay.     

Grazing and Ecosystem Carbon Storage in the North American Great Plains

Isotopic signatures of ¹³C were used to quantify the relative contributions of C₃ and C₄ plants to whole-ecosystem C storage (soil+plant) in grazed and ungrazed sites at three distinct locations (short-, mid- and tallgrass communities) along an east–west environmental gradient in the North American Great Plains. Functional group composition of plant communities, the source and magnitude of carbon inputs, and total ecosystem carbon storage displayed inconsistent responses to long-term livestock grazing along this gradient. C₄ plants [primarily Bouteloua gracilis (H.B.K.) Lag ex Steud.] dominated the long-term grazed site in the shortgrass community, whereas the ungrazed site was co-dominated by C₃ and C₄ species; functional group composition did not differ between grazed and ungrazed sites in the mid- and tallgrass communities. Above-ground biomass was lower, but the relative proportion of fine root biomass was greater, in grazed compared to ungrazed sites at all three locations. The grazed site of the shortgrass community had 24% more whole-ecosystem carbon storage compared to the ungrazed site (4022 vs. 3236 g C m⁻²). In contrast, grazed sites at the mid- and tallgrass communities had slightly lower (8%) whole-ecosystem carbon storage compared to ungrazed sites (midgrass: 7970 vs. 8683 g C m⁻²; tallgrass: 8273 vs. 8997 g C m⁻²). Differential responses between the shortgrass and the mid- and tallgrass communities with respect to grazing and whole-ecosystem carbon storage are likely a result of: (1) maintenance of larger soil organic carbon (SOC) pools in the mid- and tallgrass communities (7476–8280 g C m⁻²) than the shortgrass community (2517–3307 g C m⁻²) that could potentially buffer ecosystem carbon fluxes, (2) lower root carbon/soil carbon ratios in the mid- and tallgrass communities (0.06–0.10) compared to the shortgrass community (0.20–0.27) suggesting that variation in root organic matter inputs would have relatively smaller effects on the size of the SOC pool, and (3) the absence of grazing-induced variation in the relative proportion of C₃ and C₄ functional groups in the mid- and tallgrass communities. We hypothesize that the magnitude and proportion of fine root mass within the upper soil profile is a principal driver mediating the effect of community composition on the biogeochemistry of these grassland ecosystems.     

Effect of grazing on carbon stocks and assimilate partitioning in a Tibetan montane pasture revealed by 13CO2 pulse labeling

Since the late 1950s, governmental rangeland policies have changed the grazing management on the Tibetan Plateau (TP). Increasing grazing pressure and, since the 1980s, the privatization and fencing of pastures near villages has led to land degradation, whereas remote pastures have recovered from stronger overgrazing. To clarify the effect of moderate grazing on the carbon (C) cycle of the TP, we investigated differences in below‐ground C stocks and C allocation using in situ ¹³CO₂ pulse labeling of (i) a montane Kobresia winter pasture of yaks, with moderate grazing regime and (ii) a 7‐year‐old grazing exclosure plot, both in 3440 m asl. Twenty‐seven days after the labeling, ¹³C incorporated into shoots did not differ between the grazed (43% of recovered ¹³C) and ungrazed (38%) plots. In the grazed plots, however, less C was lost by shoot respiration (17% vs. 42%), and more was translocated below‐ground (40% vs. 20%). Within the below‐ground pools, <2% of ¹³C was incorporated into living root tissue of both land use types. In the grazed plots about twice the amount of ¹³C remained in soil (18%) and was mineralized to CO₂ (20%) as compared to the ungrazed plots (soil 10%; CO₂ 9%). Despite the higher contribution of root‐derived C to CO₂ efflux, total CO₂ efflux did not differ between the two land use types. C stocks in the soil layers 0–5 and 5–15 cm under grazed grassland were significantly larger than in the ungrazed grassland. However, C stocks below 15 cm were not affected after 7 years without grazing. We conclude that the larger below‐ground C allocation of plants, the larger amount of recently assimilated C remaining in the soil, and less soil organic matter‐derived CO₂ efflux create a positive effect of moderate grazing on soil C input and C sequestration.     

Fine‐root exploitation strategies differ in tropical old growth and logged‐over forests in Ghana

Understanding the changes in root exploitation strategies during post‐logging recovery is important for predicting forest productivity and carbon dynamics in tropical forests. We sampled fine (diameter < 2 mm) roots using the soil core method to quantify fine‐root biomass and architectural and morphological traits to determine root exploitation strategies in an old growth forest and in a 54‐yr‐old logged‐over forest influenced by similar parent material and climate. Seven root traits were considered: four associated with resource exploitation potential or an ‘extensive’ strategy (fine‐root biomass, length, surface area, and volume), and three traits which reflect exploitation efficiency or an ‘intensive’ strategy (specific root area, specific root length, and root tissue density). We found that total fine‐root biomass, length, surface area, volume, and fine‐root tissue density were higher in the logged‐over forest, whereas the old growth forest had higher total specific root length and specific root surface area than the logged‐over forest. The results suggest different root exploitation strategies between the forests. Plants in the old growth forest invest root biomass more efficiently to maximize soil volume explored, whereas plants in the logged‐over forest increase the spatial distribution of roots resulting in the expansion of the rhizosphere.     

Root distribution,standing crop biomass and belowground productivity in a semidesert in México

In a semidesert community in México (Zapotitlán de las Salinas, Puebla) the vertical distribution of roots and root biomass was estimated at 0–100 cm depth on two sampling dates, November 1995 (wet season) and January 1998 (dry season). Root productivity at 7 to 14.5 cm depth was estimated with the in-growth core technique every two months from March 1996 to February 1998. The relationship between environmental factors and seasonal root productivity was analyzed. Finally, we tested the effect of an irrigation equivalent to 20 mm of rain on root production. Seventy four percent of the total number of roots were found at 0-40 cm depth. Very fine roots (<1 mm diameter) were found throughout the soil profile (0-100 cm). In contrast, fine roots (1-3 mm diameter) were found only from 0–90 cm depth, and coarse roots (>3 mm diameter) from 0–60 cm depth. The root biomass was 971.5 g m^–2 (S.D. = 557.39), the very fine and fine roots representing 62.9% of the total. Total root productivity, as estimated with the ingrowth core technique, was 0.031 Mg ha^–1 over the dry season and 0.315 Mg ha^–1 over the wet season. Only very fine roots were obtained at all sampling dates. Rainfall was significantly correlated with very fine root production. The difference between fine root production in non-watered (0.054 g m^–2) and watered (0.429 g m^–2) treatments was significant. The last value was the same as that predicted for a rain of 20 mm, according to the exponential model describing the relation between the production of very fine roots and rainfall at the site.     

中亚热带杉木人工林细根生物量空间变异与取样数量估算

林木细根生物量具有一定的空间异质性,因此采用合理的细根取样策略对精确估算细根生物量十分重要。通过在福建省三明杉木人工林林内采用土钻法随机选取100个取样点,分析不同细根类型(杉木、林下植被、总细根)生物量的空间变异特征,并对细根生物量所需的取样数量进行估计。结果表明:不同细根类型单位面积生物量随径级(0—1、1—2 mm)及土层深度的增加变异增大,所需的取样数量也相应增加。Shapiro-Wilk检验表明,仅0—2 mm杉木细根和总细根单位面积生物量符合正态分布,其余各个细根类型不同径级不同土层单位面积生物量均不符合正态分布,均呈明显的右偏分布。蒙特卡罗统计模拟分析表明:在置信水平为95%、精度为80%的条件下,直径为0—1 mm、1—2 mm和0—2 mm的细根,杉木采集95、96、32个样品可以满足测定单位面积生物量的需要,林下植被分别采集98、98、63个样品可以满足测定单位面积生物量的需要,而总细根分别采集93、93、18个样品可以满足测定单位面积生物量的需要。     

Biomass and distribution of fine and coarse roots from blue oak (Quercus douglasii) trees in the northern Sierra Nevada foothills of California

This research adds to the limited data on coarse and fine root biomass for blue oak (Quercus douglasii Hook and Arn.), a California deciduous oak species found extensively throughout the interior foothills surrounding the Central Valley. Root systems of six blue oak trees were analyzed using three methods — backhoe excavation, quantitative pits, and soil cores. Coarse root biomass ranged from 7 to 177 kg per tree. Rooting depth for the main root system ranged from 0.5 to 1.5 m, with an average of 70% of excavated root biomass located above 0.5 m. Of the total biomass in excavated central root systems, primary roots (including burls) accounted for 56% and large lateral roots (> 20 mm diameter) accounted for 36%. Data from cores indicated that most biomass outside of the root crown was located in fine roots and that fine root biomass decreased with depth. At surface depths (0–20 cm), small-fine (< 0.5 mm diameter) roots accounted for 71%, large-fine (0.5–2.0 mm) for 25%, and coarse (> 2 mm) for 4% of total root biomass collected with cores. Mean fine root biomass density in the top 50 cm was 0.43 kg m⁻³. Fine root biomass did not change with increasing distance from the trees (up to approximately 5 m). Thus, fine roots were not concentrated under the tree canopies. Our results emphasize the importance of the smallest size class of roots (<0.5 mm), which had both higher N concentration and, in the area outside the central root system, greater biomass than large fine (0.5–2.0 mm) or coarse (> 2.0 mm) roots. This revised version was published online in June 2006 with corrections to the Cover Date.     

Vegetation Composition Determines Microbial Activities in a Boreal Forest Soil

Abstract Forest soil ecology was studied in Fennoscandinavian dry Scots pine forests grazed by reindeer to varying extents (ungrazed, lichen-dominated-sites; grazed sites; and bryophyte-dominated sites). We hypothesized that the productivity parameters of the site (i.e., tree growth and soil nutrient concentrations), the vegetation composition, and the microbial activities are directly correlated. Since the productivity of the lichen-dominated ecosystem is low, microbial activities are assumed to be naturally low. Grazing was expected to decrease both the amount of Scots pine fine roots and the soil microbial activities. Several variables on the characteristics of the soil microbial community, Scots pine fine roots, soil nutrients, and tree growth were studied in relation to vegetation composition by using non-metric multidimensional scaling (NMDS). Basal respiration (Bas), metabolic quotient of the microbial community (qCO2), and pine fine root parameters increased toward the ungrazed, nutrient-poor, lichen-dominated sites, which were grouped at one end of the first axis in the NMDS ordination. Soil nutrient and tree growth parameters and thickness of the humus layer increased toward bryophyte-dominated sites, which were grouped at the other end of the first axis in the ordination. The grazed sites fell between them. These were characterized by lower Bas and qCO2 values and longer lag, compared to ungrazed lichen- or bryophyte-dominated sites, probably due to decreased carbon input and microclimatic change (the soil without lichen carpet is exposed to direct sunlight and wind). Microbial biomass (Cmic), fungal biomass (ergosterol concentration), and the specific growth rate (μCO2) were not related to vegetation ordination. The high fine root production is the most plausible explanation for the high microbial activities at nutrient-poor, lichen-dominated sites, which produce qualitatively poor and slowly decomposing litter, as fine roots secrete considerable amounts of organic substances. At bryophyte-dominated sites, the higher soil nutrient concentrations and the higher production of easily decomposable substrates are likely to maintain the microbial activities.     

Grazing enhances belowground carbon allocation,microbial biomass,and soil carbon in a subtropical grassland

Despite the large contribution of rangeland and pasture to global soil organic carbon (SOC) stocks, there is considerable uncertainty about the impact of large herbivore grazing on SOC, especially for understudied subtropical grazing lands. It is well known that root system inputs are the source of most grassland SOC, but the impact of grazing on partitioning of carbon allocation to root tissue production compared to fine root exudation is unclear. Given that different forms of root C have differing implications for SOC synthesis and decomposition, this represents a significant gap in knowledge. Root exudates should contribute to SOC primarily after microbial assimilation, and thus promote microbial contributions to SOC based on stabilization of microbial necromass, whereas root litter deposition contributes directly as plant‐derived SOC following microbial decomposition. Here, we used in situ isotope pulse‐chase methodology paired with plant and soil sampling to link plant carbon allocation patterns with SOC pools in replicated long‐term grazing exclosures in subtropical pasture in Florida, USA. We quantified allocation of carbon to root tissue and measured root exudation across grazed and ungrazed plots and quantified lignin phenols to assess the relative contribution of microbial vs. plant products to total SOC. We found that grazing exclusion was associated with dramatically less overall belowground allocation, with lower root biomass, fine root exudates, and microbial biomass. Concurrently, grazed pasture contained greater total SOC, and a larger fraction of SOC that originated from plant tissue deposition, suggesting that higher root litter deposition under grazing promotes greater SOC. We conclude that grazing effects on SOC depend on root system biomass, a pattern that may generalize to other C4‐dominated grasslands, especially in the subtropics. Improved understanding of ecological factors underlying root system biomass may be the key to forecasting SOC and optimizing grazing management to enhance SOC accumulation.     

Measuring Fine Root Turnover in Forest Ecosystems

Development of direct and indirect methods for measuring root turnover and the status of knowledge on fine root turnover in forest ecosystems are discussed. While soil and ingrowth cores give estimates of standing root biomass and relative growth, respectively, minirhizotrons provide estimates of median root longevity (turnover time) i.e., the time by which 50% of the roots are dead. Advanced minirhizotron and carbon tracer studies combined with demographic statistical methods and new models hold the promise of improving our fundamental understanding of the factors controlling root turnover. Using minirhizotron data, fine root turnover (y⁻¹) can be estimated in two ways: as the ratio of annual root length production to average live root length observed and as the inverse of median root longevity. Fine root production and mortality can be estimated by combining data from minirhizotrons and soil cores, provided that these data are based on roots of the same diameter class (e.g., < 1 mm in diameter) and changes in the same time steps. Fluxes of carbon and nutrients via fine root mortality can then be estimated by multiplying the amount of carbon and nutrients in fine root biomass by fine root turnover. It is suggested that the minirhizotron method is suitable for estimating median fine root longevity. In comparison to the minirhizotron method, the radio carbon technique favor larger fine roots that are less dynamics. We need to reconcile and improve both methods to develop a more complete understanding of root turnover.     

Biomass, morphology and nutrient contents of fine roots in four Norway spruce stands

Fine root systems may respond to soil chemical conditions, but contrasting results have been obtained from field studies in non-manipulated forests with distinct soil chemical properties. We investigated biomass, necromass, live/dead ratios, morphology and nutrient concentrations of fine roots (<2 mm) in four mature Norway spruce (Picea abies [L.] Karst.) stands of south-east Germany, encompassing variations in soil chemical properties and climate. All stands were established on acidic soils (pH (CaCl₂) range 2.8–3.8 in the humus layer), two of the four stands had molar ratios in soil solution below 1 and one of the four stands had received a liming treatment 22 years before the study. Soil cores down to 40 cm mineral soil depth were taken in autumn and separated into four fractions: humus layer, 0–10 cm, 10–20 cm and 20–40 cm. We found no indications of negative effects of N availability on fine root properties despite large variations in inorganic N seepage fluxes (4–34 kg N ha⁻¹ yr⁻¹), suggesting that the variation in N deposition between 17 and 26 kg N ha⁻¹ yr⁻¹ does not affect the fine root system of Norway spruce. Fine root biomass was largest in the humus layer and increased with the amount of organic matter stored in the humus layer, indicating that the vertical pattern of fine roots is largely affected by the thickness of this horizon. Only two stands showed significant differences in fine root biomass of the mineral soil which can be explained by differences in soil chemical conditions. The stand with the lowest total biomass had the lowest Ca/Al ratio of 0.1 in seepage, however, Al, Ca, Mg and K concentrations of fine roots were not different among the stands. The Ca/Al ratio in seepage might be a less reliable stress parameter because another stand also had Ca/Al ratios in seepage far below the critical value of 1.0 without any signs of fine root damages. Large differences in the live/dead ratio were positively correlated with the Mn concentration of live fine roots from the mineral soil. This relationship was attributed to faster decay of dead fine roots because Mn is known as an essential element of lignin degrading enzymes. It is questionable if the live/dead ratio can be used as a vitality parameter of fine roots since both longevity of fine roots and decay of root litter may affect this parameter. Morphological properties were different in the humus layer of one stand that was limed in 1983, indicating that a single lime dose of 3–4 Mg ha⁻¹ has a long-lasting effect on fine root architecture of Norway spruce. Almost no differences were found in morphological properties in the mineral soil among the stands, but vertical patterns were apparently different. Two stands with high base saturation in the subsoil showed a vertical decrease in specific root length and specific root tip density whereas the other two stands showed an opposite pattern or no effect. Our results suggest that proliferation of fine roots increased with decreasing base saturation in the subsoil of Norway spruce stands.     

Production and turnover rates of shallow fine roots in rangelands of the Patagonian Monte, Argentina

Selective sheep grazing in arid rangelands induces a decrease in total cover and grass cover and an increase in the dominance of shrubs. Both life forms differ in aboveground and belowground traits. We hypothesized that grazing disturbance leads to the replacement of grass by shrub fine roots in the upper soil, and this is reflected in changes in the seasonal dynamics of shallow fine roots at the community level. In two sites representative of non-grazed and grazed vegetation states in the Patagonian Monte, we assessed the canopy structure, and the fine root biomass, N concentration, production, and turnover during two consecutive years. The non-grazed site exhibited higher total, grass, and shrub cover than the grazed site. The grazed site had larger or equal fine root biomass than the non-grazed site except for late spring of the second year. This could be associated with the ability of shrubs to develop dimorphic-root systems occupying the soil freed by grasses at the grazed site, and with the larger contribution of grass than shrub fine roots in relation to an extraordinary precipitation event at the non-grazed site. This was consistent with the N concentration in fine roots. Fine root production was positively correlated to temperature at the grazed site and with precipitation at the non-grazed site. Fine root turnover did not differ between sites. Our results indicate that grazing leads to a shifting in the seasonality and main climatic controls of fine root production, while fine root turnover is mostly affected by changes in soil water conditions.     

Evaluating minirhizotron estimates of fine root longevity and production in the forest floor of a temperate broadleaf forest

The minirhizotron technique (MR) for in situ measurement of fine root dynamics offers the opportunity to obtain accurate and unbiased estimates of root production in perennial vegetation only if MR tubes do not affect the longevity of fine roots. Assuming fine root biomass is near steady-state, fine root production (g m^–2 yr^–1) can be estimated as the ratio of fine root biomass (g m^–2) to median fine root longevity (yr). This study evaluates the critical question of whether MR access tubes affect the longevity of fine roots, by comparing fine root survivorship obtained using MR with those from a non-intrusive in situ screen method in the forest floor horizons of a northern hardwood forest in New Hampshire, USA. Fine root survivorship was measured in 380 root screens during 1993–1997 and in six horizontal minirhizotron tubes during 1996–1997. No statistically significant difference was found between estimates of survivorship of fine roots (<1 mm dia.) at this site from MR versus from in situ screens, suggesting that MR tubes do not substantially affect fine root longevity in the forest floor of this northern hardwood forest and providing greater confidence in measurements of fine root production using the MR technique. Furthermore, the methodology for estimating fine root production from MR longevity data was evaluated by comparison of fine root longevity and production estimates made using single vs. multiple root cohorts, and using root-number, root-length, and root-mass weighted methods. Our results indicate that fine root-length longevity estimates based on multiple root cohorts throughout the year can be used to approximate fine root biomass production. Using this method, we estimated fine root longevity and production in the forest floor at this site to be 314 days (or 0.86 yr) and 303 g m^–2 yr^–1, respectively. Fine root production in this northern hardwood forest is approximately equivalent to standing biomass and was previously underestimated by root in-growth cores. We conclude that the use of MR to estimate fine root longevity and production as outlined here may result in improved estimates of fine root production in perennial vegetation.     

Annual and seasonal changes in fine root biomass of a Quercus ilex L. forest

The biomass, production and mortality of fine roots (roots with diameter <2.5 mm) were studied in a typical Mediterranean holm oak (Quercus ilex L.) forest in NE Spain using the minirhizotron methodology. A total of 1212 roots were monitored between June of 1994 and March of 1997. Mean annual fine root biomass in the holm oak forest of Prades was 71±8 g m^–2 yr^–1. Mean annual production for the period analysed was 260+11 g m^–2 yr^–1. Mortality was similar to production, with a mean value of 253±3 g m^–2 yr^–1. Seasonal fine root biomass presented a cyclic behaviour, with higher values in autumn and winter and lower in spring and summer. Production was highest in winter, and mortality in spring. In summer, production and mortality values were the lowest for the year. Production values in autumn and spring were very similar. The vertical distribution of fine root biomass decreased with increasing depth except for the top 10–20 cm, where values were lower than immediately below. Production and mortality values were similar between 10 and 50 cm depth. In the 0–10 cm and the 50–60 cm depth intervals, both production and mortality were lower.     

Belowground drought response of European beech: fine root biomass and carbon partitioning in 14 mature stands across a precipitation gradient

How tree root systems will respond to increased drought stress, as predicted for parts of Central Europe, is not well understood. According to the optimal partitioning theory, plants should enhance root growth relative to aboveground growth in order to reduce water limitations. We tested this prediction in a transect study with 14 mature forest stands of European beech (Fagus sylvatica L.) by analysing the response of the fine root system to a large decrease in annual precipitation (970–520 mm yr⁻¹). In 3 years with contrasting precipitation regimes, we investigated leaf area and leaf biomass, fine root biomass and necromass (organic layer and mineral soil to 40 cm) and fine root productivity (ingrowth core approach), and analysed the dependence on precipitation, temperature, soil nutrient availability and stand structure. In contrast to the optimal partitioning theory, fine root biomass decreased by about a third from stands with >950 mm yr⁻¹ to those with <550 mm yr⁻¹, while leaf biomass remained constant, resulting in a significant decrease, and not an increase, in the fine root/leaf biomass ratio towards drier sites. Average fine root diameter decreased towards the drier stands, thereby partly compensating for the loss in root biomass and surface area. Both δ¹³C‐signature of fine root mass and the ingrowth core data indicated a higher fine root turnover in the drier stands. Principal components analyses (PCA) and regression analyses revealed a positive influence of precipitation on the profile total of fine root biomass in the 14 stands and a negative one of temperature and plant‐available soil phosphorus. We hypothesize that summer droughts lead to increased fine root mortality, thereby reducing root biomass, but they also stimulate compensatory fine root production in the drier stands. We conclude that the optimal partitioning theory fails to explain the observed decrease in the fine root/leaf biomass ratio, but is supported by the data if carbon allocation to roots is considered, which would account for enhanced root turnover in drier environments.     

Growth and carbon stock change in eucalypt woodlands in northeast Australia: ecological and greenhouse sink implications

Data from 57 permanent monitoring sites are used to document the growth in woody vegetation and estimate the carbon sink in 27 M ha of eucalypt woodlands (savannas), contained within c. 60 M ha of grazed woodlands in Queensland (northeast Australia). The study sites are shown to be representative of the environment and structure of the eucalypt woodlands in the defined study area. Mean basal area increment for all live woody plants in 30 long‐term sites, with an average initial basal area of 11.86 ± 1.38 (SE) m² ha^?1, was 1.06 m² ha^?1 over a mean 14 years timeframe. The majority of the measurement period, commencing between 1982 and 1988, was characterized by below‐average rainfall. The increase in live tree basal area was due primarily to growth of existing trees (3.12 m² ha^?1) rather than establishment of new plants (0.25 m² ha^?1) and was partly offset by death (2.31 m² ha^?1). A simple but robust relationship between stand basal area and stand biomass of all woody species was developed for the eucalypt dominant woodlands. Analysis of above‐ground carbon stocks in live and standing dead woody plants gave a mean net above‐ground annual carbon increment for all 57 sites of 0.53 t C ha^?1 y^?1, similar to values estimated elsewhere in world savannas. Published root : shoot ratios were used to infer C flux in woody root systems on these sites. This results in an estimated sink in above‐ and below‐ground biomass of 18 Mt C y^?1 over the eucalypt woodlands studied, and potentially up to 35 Mt C y^?1 if extended to all grazed woodlands in Queensland. It is suggested that introduction of livestock grazing and altered fire regimes have triggered the change in tree‐grass dominance in these woodlands. Thus, change in carbon stocks in the grazed woodlands of Queensland is identified as an important component of human‐induced greenhouse gas flux in Australia, equivalent in magnitude to c. 25% of the most recently published (1999) total estimated national net emissions. The latter inventory takes into account emissions from land clearing, but does not include the sink identified in the present study. This sequestration also represents a small but significant contribution to the global terrestrial carbon sink.     

Very fine roots respond to soil depth: biomass allocation,morphology, and physiology in a broad-leaved temperate forest

Very fine roots (<0.5 mm in diameter) of forest trees may serve as better indicators of root function than the traditional category of <2 mm, but how these roots will exhibit the plasticity of species-specific traits in response to heterogeneous soil nutrients is unknown. Here, we examined the vertical distribution of biomass and morphological and physiological traits of fine roots across three narrow diameter classes (<0.5, 0.5–1.0, and 1.0–2.0 mm) of Quercus serrata and Ilex pedunculosa at five soil depths down to 50 cm in a broad-leaved temperate forest. In both species, biomass and the allocation of very fine roots were higher in the surface soil but lower below 10-cm soil depth compared to values for larger roots (0.5–2.0 mm). When we applied these diameter classes, only very fine roots of Q. serrata exhibited significant changes in specific root length (SRL; m g⁻¹) and root nitrogen (N) concentrations with soil depth, whereas the N concentrations only changed significantly in I. pedunculosa. The SRL and root N concentrations of larger roots in the two species did not significantly differ among soil depths. Thus, very fine roots may exhibit species-specific traits and change their potential for nutrient and water uptake in response to soil depth by plasticity in root biomass, the length, and the N in response to available resources.     

Root distribution of a Mediterranean shrubland in Portugal

The distribution of roots of an Erica (Erica scoparia and Erica lusitanica) dominated Mediterranean maquis was studied using three different approaches: root counts on trench walls (down to 120 cm), estimation of the maximum rooting depth using an allometric relationship and estimation of fine root biomass and fine root length using soil cores (down to 100 cm). Roots were classified according to diameter (fine, 1.0 mm; small, 1.1–5.0 mm; medium, 5.1–10.0 mm; coarse, >10.0 mm) and species (Erica sp., Pteridium aquilinum, Rubus ulmifolius and Ulex jussiaei). The depth corresponding to 50% of all roots (D ₅₀) was determined by fitting a new model to the cumulative root distribution. Fine roots represented 96% of root counts. Root counts of Erica represented 59%, Ulex 34%, Rubus 6% and Pteridium 1%. Overall root counts showed a D ₅₀ of 26 cm. D ₅₀ was higher for Ulex (40 cm) and Erica (22 cm), than for Pteridium (9 cm) and Rubus (3 cm). D ₅₀ for fine roots was 27 cm, for small roots 11 cm, for medium roots 6 cm and for coarse roots 4 cm. The estimated average maximum rooting depth of the 28 deepest Erica roots was 222 cm. The deepest Erica root was estimated to reach 329 cm. A total of 82% of roots growing deeper than 125 cm were not reaching more than 175 cm. The overall fine root length density ranged from 4.6 cm/cm³ at 10 cm to 0.8 cm/cm³ at 80 cm. The overall fine root biomass ranged from 7.7 mg/cm³ at 10 cm to 0.6 mg/cm³ at 40 cm. D ₅₀ for root biomass was 12 cm and D ₅₀ for root length was 14 cm. Fine root biomass was estimated as 1.6 kg/m² and the respective root length as 18.7 km/m².