Patterns of rhizosphere carbon flux in sugar maple (Acer saccharum) and yellow birch (Betula allegheniensis) saplings

Despite its importance in the terrestrial C cycle rhizosphere carbon flux (RCF) has rarely been measured for intact root–soil systems. We measured RCF for 8‐year‐old saplings of sugar maple (Acer saccharum) and yellow birch (Betula allegheniensis) collected from the Hubbard Brook Experimental Forest (HBEF), NH and transplanted into pots with native soil horizons intact. Five saplings of each species were pulse labeled with ¹³CO₂ at ambient CO₂ concentrations for 4–6 h, and the ¹³C label was chased through rhizosphere and bulk soil pools in organic and mineral horizons for 7 days. We hypothesized yellow birch roots would supply more labile C to the rhizosphere than sugar maple roots based on the presumed greater C requirements of ectomycorrhizal roots. We observed appearance of the label in rhizosphere soil of both species within the first 24 h, and a striking difference between species in the timing of ¹³C release to soil. In sugar maple, peak concentration of the label appeared 1 day after labeling and declined over time whereas in birch the label increased in concentration over the 7‐day chase period. The sum of root and rhizomicrobial respiration in the pots was 19% and 26% of total soil respiration in sugar maple and yellow birch, respectively. Our estimate of the total amount of RCF released by roots was 6.9–7.1% of assimilated C in sugar maple and 11.2–13.0% of assimilated C in yellow birch. These fluxes extrapolate to 55–57 and 90–104 g C m^?2 yr^?1 from sugar maple and yellow birch roots, respectively. These results suggest RCF from both arbuscular mycorrhizal and ectomycorrhizal roots represents a substantial flux of C to soil in northern hardwood forests with important implications for soil microbial activity, nutrient availability and C storage.     

CO2浓度升高对森林土壤微生物呼吸与根（际）呼吸的影响

 根呼吸与微生物呼吸的作用底物不同,二者对高浓度CO₂的响应机理及敏感程度亦不同。在大气CO₂浓度升高的背景下,精确区分根呼吸与微生物呼吸是构建森林生态系统碳循环模型和预测森林生态系统碳源/汇关系所必需的。根（际）呼吸与微生物呼吸对高浓度CO₂的响应呈增加、降低或无明显变化等不同趋势,根（际）呼吸变化主要与根生物量明显相关,细根的作用大于粗根;土壤微生物呼吸变化存在较大的不确定性,微生物量和微生物活性与土壤微生物呼吸相关或不相关。根系统对高浓度CO₂的响应会潜在地影响微生物的代谢底物,进而影响微生物呼吸强度。凡影响土壤总呼吸的生物与非生物因子都会直接或间接地影响根呼吸与土壤微生物呼吸。     

施肥对落叶松和水曲柳人工林土壤呼吸的影响

 以落叶松（Larix gmelinii）和水曲柳（Fraxinus mandshurica）人工林为研究对象,采用动态气室法（LI-6400-09叶室连接到LI-6400便携式CO₂/H₂O分析系统）对两种林分的土壤呼吸速率进行了观测,探讨了细根生物量、根中氮含量与土壤呼吸速率的关系,以及施肥对细根生物量、根中氮含量和土壤呼吸速率的影响。结果表明：1）施肥导致落叶松和水曲柳林分的活细根生物量降低18.4％和27.4％, 死细根生物量分别降低了34.8％和127.4 ％;2）施肥使落叶松和水曲柳林地土壤呼吸速率与对照相比分别减少了34.9％和25.8％;3 ）施肥对根中氮含量没有显著影响;4）落叶松和水曲柳林地的土壤呼吸与土壤温度表现出相同的季节变化,两种林分的土壤呼吸速率与地下5和10 cm处的温度表现出明显的指数关系 ,其相关性R²=0.93～0.98。土壤呼吸温度系数Q₁₀的范围在2.45～3.29。 施肥处理对Q₁₀没有产生影响,施肥处理导致细根生物量减少可能是引起林地土壤呼吸速率下降的主要原因。     

N fertilization affects on soil respiration, microbial biomass and root respiration in Larix gmelinii and Fraxinus mandshurica plantations in China

The response of belowground biological processes to soil N availability in Larix gmelinii (larch) and Fraxinus mandshurica (ash) plantations was studied. Soil and root respiration were measured with Li-Cor 6400 and gas-phase O₂ electrodes, respectively. Compared with the control, N fertilization induced the decreases of fine root biomass by 52% and 25%, and soil respiration by 30% and 24% in larch and ash plantations, respectively. The average soil microbial biomass C and N were decreased by 29% and 42% under larch stand and 39% and 47% under ash stand, respectively. While the fine root tissue N concentration under fertilized plots was higher 26% and 12% than that under control plots, respectively, the average fine root respiration rates were increased by 10% and 13% in larch and ash stands under fertilized plot, respectively. Soil respiration rates showed significantly positive exponential relationships with soil temperature, and a seasonal dynamic. These findings suggest that N fertilization can suppress fine root biomass at five branch orders (<2 mm in diameter), soil respiration, and soil microbial biomass C and N, and alter soil microbial communities in L. gmelinii and F. mandshurica plantations.     

Arbuscular mycorrhizal colonization on carbon economy in perennial ryegrass: quantification by 13CO2/12CO2 steady-state labelling and gas exchange

Effects of the arbuscular mycorrhizal fungus (AMF) Glomus hoi on the carbon economy of perennial ryegrass (Lolium perenne) were investigated by comparing nonmycorrhizal and mycorrhizal plants of the same size, morphology and phosphorus status. Plants were grown in the presence of CO2 sources with different C isotope composition (delta13C -1 or -44). Relative respiration and gross photosynthesis rates, and belowground allocation of C assimilated during one light period ('new C'), as well as its contribution to respiration, were quantified by the concerted use of 13CO2/12CO2 steady-state labelling and 13CO2/12CO2 gas-exchange techniques. AMF (G. hoi) enhanced the relative respiration rate of the root + soil system by 16%, inducing an extra C flow amounting to 3% of daily gross photosynthesis. Total C flow into AMF growth and respiration was estimated at < 8% of daily gross photosynthesis. This was associated with a greater amount of new C allocated belowground and respired in mycorrhizal plants. AMF colonization affected the sources supplying belowground respiration, indicating a greater importance of plant C stores in supplying respiration and/or the participation of storage pools within fungal tissues. When ontogenetic and nutritional effects were accounted for, AMF increased belowground C costs, which were not compensated by increased photosynthesis rates. Therefore the instantaneous relative growth rate was lower in mycorrhizal plants.     

Rhizosphere bacterial community composition responds to arbuscular mycorrhiza, but not to reductions in microbial activity induced by foliar cutting

Differences in bacterial community composition (BCC) between bulk and rhizosphere soil and between rhizospheres of different plant species are assumed to be strongly governed by quantitative and qualitative rhizodeposit differences. However, data on the relationship between rhizodeposit amounts and BCC are lacking. Other soil microorganisms, e.g. arbuscular mycorrhizal fungi (AMF), may also influence BCC. We simulated foliar herbivory (cutting) to reduce belowground carbon allocation and rhizodeposition of pea plants grown either with or without AMF. This reduced soil respiration, rhizosphere microbial biomass and bacteriovorous protozoan abundance, whereas none of these were affected by AMF. After labelling plants with (13)CO(2), root and rhizosphere soil (13)C enrichment of cut plants were reduced to a higher extent (24-46%) than shoot (13)C enrichment (10-24%). AMF did not affect (13)C enrichment. Despite these clear indications of reduced rhizosphere carbon-input, denaturing gradient gel electrophoresis (DGGE) of 16S rRNA genes PCR-amplified targeting DNA and RNA from rhizosphere soil did not reveal any effects of cutting on banding patterns. In contrast, AMF induced consistent differences in both DNA- and RNA-based DGGE profiles. These results show that a reduction in rhizosphere microbial activity is not necessarily accompanied by changes in BCC, whereas AMF presence inhibits proliferation of some bacterial taxa while stimulating others.     

短期施氮肥降低杉木幼林土壤的根系和微生物呼吸

土壤呼吸是陆地生态系统碳循环的重要过程。在人工林生态系统中, 施肥不仅能提高人工林的生产力和固碳能力, 而且还会对土壤呼吸产生影响。为阐明施氮肥对人工林土壤总呼吸、根系和微生物呼吸的影响, 在中亚热带地区的湖南会同, 以5年生杉木(Cunninghamia lanceolata)幼林为研究对象, 施氮肥1年后, 利用LI-8100对土壤呼吸进行为期12个月的野外原位定点观测。结果发现: 施氮肥使土壤总呼吸、根系呼吸和微生物呼吸分别降低了22.7%、19.6%和23.5%; 土壤呼吸的温度敏感性(Q₁₀)为1.81-2.04, 施肥使土壤微生物呼吸的Q₁₀值从对照的2.04降低为1.84, 但土壤总呼吸的Q₁₀值没有发生显著变化; 施肥没有改变土壤呼吸的季节变化, 在双因素模型中, 土壤温度和含水量可以解释土壤呼吸季节变化的69.9%-79.7%。研究表明施氮肥能降低中亚热带地区杉木人工林土壤有机碳分解对温度升高的响应, 在全球变暖背景下有利于增加土壤有机碳储量。     

Liming and nitrogen fertilization affects phosphatase activities, microbial biomass and mycorrhizal colonisation in upland grassland

We have studied the effects of factorial combinations of lime and N additions on soil microbial biomass, respiration rates and phosphatase activity of an upland grassland. We also used an Agrostis capillaris seedling bioassay to assess the effect of the treatments on the activity of arbuscular-mycorrhizal (AM) fungi and root surface phosphatase enzymes and the concentrations of N and P in the bioassay plant shoots. In the F and H horizons, soil microbial biomass carbon (C^mic) decreased in response to the liming, while addition of lime and N together reduced basal respiration rates. In the Ah horizon, C^mic was unaffected by the treatments but basal respiration rates decreased in the plots receiving nitrogen. Soil phosphatase activity decreased only in the Ah horizon in plots receiving lime, either in combination with N or alone. The mass of root fwt. colonized by AM fungi increased in response to the treatments in the order nitrogenR²=28.7%, P=0.004). The results demonstrate the sensitivity of both free-living heterotrophic microorganisms and symbiotic mycorrhizal fungi to short-term (2 years) applications of lime and N to long-term upland grassland, particularly in relation to the key P cycling activities undertaken by these organisms.     

Short-term nitrogen fertilization decreased root and microbial respiration in a young Cunninghamia lanceolata plantation

Aims As the primary pathway for CO₂ emission from terrestrial ecosystems to the atmosphere, soil respiration is estimated to be 80 Pg C·a^-1 to 100 Pg C·a^-1, equivalent to 10 fold of fossil fuel emissions. As an important management practice in plantation forests, fertilization does not only increase primary production but also affects soil respiration. To investigate how nitrogen (N) fertilization affects total soil, root and microbial respiration, a N fertilization experiment was conducted in a five-year-old Cunninghamia lanceolata plantation in Huitong, Hunan Province, located in the subtropical region. MethodsOne year after fertilization, soil respiration was monitored monthly by LI-8100 from July 2013 to June 2014. Soil temperature and water content (0-5 cm soil depth) were also measured simultaneously. Available soil nutrients, fine root biomass and microbial communities were analyzed in June 2013. Important findings Total soil, root and microbial respiration rates were 22.7%, 19.6%, and 23.5% lower in the fertilized plots than in the unfertilized plots, respectively. The temperature sensitivity (Q₁₀) of soil respiration ranged from 1.81 to 2.04, and the Q₁₀ value of microbial respiration decreased from 2.04 in the unfertilized plots to 1.84 in the fertilized plots. However, neither the Q₁₀ value nor the patterns of total soil respiration were affected by N fertilization. In the two-factor model, soil temperature and moisture accounted for 69.9%-79.7% of the seasonal variations in soil respiration. These results suggest that N fertilization reduces the response of soil organic carbon decomposition to temperature change and may contribute to the increase of soil carbon storage under global warming in subtropical plantations.     

Decline of arbuscular mycorrhizal fungi in northern hardwood forests exposed to chronic nitrogen additions

Arbuscular mycorrhizal (AM) fungi are important below-ground carbon (C) sinks that can be sensitive to increased nitrogen (N) availability. The abundance of AM fungi (AMF) was estimated in maple (Acer spp.) fine roots following more than a decade of experimental additions of N designed to simulate chronic atmospheric N deposition. Abundance of AMF was measured by staining and ocular estimation, as well as by analyzing for the AMF indicator fatty acid 16:1omega5c in phospholipid (biomass indicator) and neutral lipid (lipid storage indicator) fractions. Arbuscular mycorrhizal fungal biomass, storage structures and lipid storage declined in response to N addition measured by both methods. This pattern was found when AM response was characterized as colonization intensity, on an areal basis and in proportion to maple above-ground biomass. The phospholipid fraction of the fatty acid 16:1omega5c was positively correlated with total AMF colonization and the neutral lipid fraction with vesicle colonization. Decreased AMF abundance with simulated N deposition suggests reduced C allocation to these fungi or a direct soil N-mediated decline. The fatty acid (phospholipid and neutral lipid fractions) 16:1omega5c was found to be a good indicator for AMF active biomass and stored energy, respectively.     

Periodic carbon flushing to roots of Quercus rubra saplings affects soil respiration and rhizosphere microbial biomass

Patterns of root/shoot carbon allocation within plants have been studied at length. The extent, however, to which patterns of carbon allocation from shoots to roots affect the timing and quantity of organic carbon release from roots to soil is not known. We employed a novel approach to study how natural short-term variation in the allocation of carbon to roots may affect rhizosphere soil biology. Taking advantage of the semi-determinate phenology of young northern red oak (Quercus rubra L.), we examined how pulsed delivery of carbon from shoots to roots affected dynamics of soil respiration as well as microbial biomass and net nitrogen mineralization in the rhizosphere. Young Q. rubra exhibit (1) clear switches in the amount of carbon allocated below-ground that are non-destructively detected simply by observing pulsed shoot growth above-ground, and (2) multiple switches in internal carbon allocation during a single growing season, ensuring our ability to detect short-term effects of plant carbon allocation on rhizosphere biology separate from longer-term seasonal effects. In both potted oaks and oaks rooted in soil, soil respiration varied inversely with shoot flush stage through several oak shoot flushes. In addition, upon destructive harvest of potted oaks, microbial biomass in the rhizosphere of saplings with actively flushing shoots was lower than microbial biomass in the rhizosphere of saplings with shoots that were not flushing. Given that plants have evolved with their roots in contact with soil microbes, known species-specific carbon allocation patterns within plants may provide insight into interactions among roots, symbionts, and free-living microbes in the dynamic soil arena.     

Nitrogen supply affects arbuscular mycorrhizal colonization of Artemisia vulgaris in a phosphate-polluted field site

Root colonization by arbuscular mycorrhizal fungi (AMF) was investigated in industrially polluted grassland characterized by exceptionally high phosphorus levels (up to 120 g kg(-1) soil). Along a pollution-induced nitrogen gradient, soil and tissue element concentrations of Artemisia vulgaris plants and their mycorrhizal status were determined. Additionally, we compared mycorrhization rates and above-ground biomass of A. vulgaris at N-fertilized and control plots in the N-poor area. Despite high soil and tissue P concentrations, plants from N-deficient plots, which were characterized by low tissue N concentrations and N : P ratios, were strongly colonized by AMF, whereas at a plot with comparable P levels, but higher soil and plant N concentrations and N : P ratios, mycorrhization rates were significantly lower. Correlation analyses revealed a negative relationship between percentage root colonization of A. vulgaris by AMF and both tissue N concentration and N : P ratio. Accordingly, in the fertilization experiment, control plants had higher mycorrhization rates than N-fertilized plants, whereas the species attained higher biomass at N-fertilized plots. The results suggest that N deficiency stimulates root colonization by AMF in this extraordinarily P-rich field site.     

Defoliation increases carbon limitation in ectomycorrhizal symbiosis of <Emphasis Type="Italic">Betula pubescens</Emphasis>

Boreal forest trees are highly dependent on root-colonizing mycorrhizal fungi. Since the maintenance of mycorrhizal symbiosis implies a significant carbon cost for the host plant, the loss of photosynthetic leaf area due to herbivory is expected to reduce the host investment in mycorrhizae. We tested this hypothesis in a common garden experiment by exposing ectomycorrhizal white birch (Betula pubescens Ehrh.) seedlings to simulated insect defoliation of 50 or 100% intensity during either the previous or the current summer or repeatedly during both seasons before harvest. The shoot and root growth of the seedlings were distinctly reduced by both 100% defoliation and repeated 50% defoliation, and they were more strongly affected by previous-year than current-year defoliation. The root to shoot ratio significantly decreased after 100% defoliation, indicating reduced proportional allocation to the roots. Ergosterol concentration (i.e. fungal biomass) in the fine roots decreased by 100% defoliation conducted either in the year of harvest or in both years. No such decrease occurred following the 100% defoliation conducted in the previous year, indicating the importance of current photosynthates for fungal symbionts. The trend was similar in the colonization percentage of thick-mantled mycorrhizae in the roots, the most marked decline occurring in the repeatedly defoliated seedlings. The present results thus support the prediction that the plant investment in ectomycorrhizae may decline as a response to foliage loss. Moreover, the colonization percentage of thick-mantled mycorrhizae correlated positively with the ratio of leaf to heterotrophic plant biomass in the defoliated birch seedlings, but not in the control ones. This tends to indicate a stronger carbon limitation of ectomycorrhizal colonization in defoliated seedlings.     

Biomass and compositional responses of ectomycorrhizal fungal hyphae to elevated CO2 and nitrogen fertilization

The extramatrical mycelia (EMM) of ectomycorrhizal fungi make up a large proportion of the microbial diversity and biomass in temperate forest soils. Thus, their response to elevated CO(2) can have large effects on plant nutrient acquisition and carbon movement through forests. Here, the effects of CO(2) and nitrogen (N) fertilization on EMM biomass and community structure in Pinus taeda forest plots were examined using sand-filled mesh bags buried in the field, the contents of which were analyzed by phospholipid fatty acid (PLFA) and DNA sequencing. A total of 2138 sequences comprising 295 taxa were recovered; most (83.5%) were from ectomycorrhizal fungal taxa. No biomass increase was detected in elevated CO(2) plots relative to control plots, but individual taxa responded to both CO(2) and N fertilization, four of the six most abundant taxa were less frequent in N-fertilized plots. Thelephoroid and athelioid taxa were both frequent and abundant as EMM, and thelephoroid richness was extremely high. Russula and Cortinariaceae taxa were less abundant and boletoid taxa were more abundant as EMM relative to ectomycorrhizas. The EMM community, sampled across seasons and years, was dynamic with a high degree of interspecific variation in response to CO(2) enrichment and N fertilization.     

小兴安岭阔叶红松林不同演替系列森林细根生物量的研究

以小兴安岭地区阔叶红松林旱生演替系列的蒙古栎次生林和蒙古栎红松林、中生演替系列的枫桦次生林和枫桦红松林、湿生演替系列的白桦次生林和云冷杉红松林这6种林型为研究对象,采用土钻取样法对不同演替系列细根生物量的空间变化、垂直分布规律及其影响因子进行系统地研究。结果表明：（1）3种演替系列总细根生物量存在显著差异（P<0.05）。中生演替系列生物量最高,平均达8.56 t·hm^-2,其次是旱生演替系列8.18 t·hm^-2,湿生演替系列生物量最低,为5.79 t·hm^-2;（2）对于不同演替系列细根生物量垂直变化,在阔叶红松林的正向演替过程中,森林细根生物量逐渐增加,且随着土层的增加而降低,拟合效果均达显著水平（P<0.05）,中根和粗根的垂直分布差异较大;（3）在小兴安岭地区,6块林地不同径级细根生物量与土壤有机C和全N、土壤容重、土壤含水率呈显著负相关（P>0.05）,而土壤pH值与细根生物量呈显著正相关性（P>0.05）。     

Below-ground respiratory responses of sugar maple and red maple saplings to atmospheric CO2 enrichment and elevated air temperature

The research described in this paper represents a part of a much broader research project with the general objective of describing the effects of elevated [CO2] and temperature on tree growth, physiological processes, and ecosystem-level processes. The specific objective of this research was to examine the below-ground respiratory responses of sugar maple (Acer saccharum Marsh.) and red maple (Acer rubrum L.) seedlings to elevated atmospheric [CO2] and temperature. Red maple and sugar maple seedlings were planted in the ground in each of 12 open-top chambers and exposed from 1994 through 1997 to ambient air or air enriched with 30 Pa CO2,< in combination with ambient or elevated (+4 °C) air temperatures. Carbon dioxide efflux was measured around the base of the seedlings and from root-exclusion zones at intervals during 1995 and 1996 and early 1997. The CO2 efflux rates averaged 0.4 μmol CO2 m-2 s-1 in the root-exclusion zones and 0.75 μmol CO2 m-2 s-1 around the base of the seedlings. Mineral soil respiration in root-exclusion zones averaged 12% higher in the high temperature treatments than at ambient temperature, but was not affected by CO2 treatments. The fraction of total efflux attributable to root + rhizosphere respiration ranged from 14 to 61% in measurements made around red maple plants, and from 35 to 62% around sugar maple plants. Root respiration rates ranged from 0 to 0.94 μmol CO2 s-1 m-2 of soil surface in red maple and from 0 to 1.02 in sugar maple. In both 1995 and 1996 root respiration rates of red maple were highest in high-CO2 treatments and lowest in high temperature treatments. Specific red maple root respiration rates of excised roots from near the soil surface in 1996 were also highest under CO2 enrichment and lowest in high temperature treatments. In sugar maple the highest rates of CO2 efflux were from around the base of plants exposed to both high temperature and high-CO2, even though specific respiration rates were< lowest for this species under the high temperature and CO2 enrichment regime. In both species, patterns of response to treatments were similar in root respiration and root mass, indicating that the root respiration responses were due in part to differences in root mass. The results underscore the need for separating the processes occurring in the roots from those in the forest floor and mineral soil in order to increase our understanding of the effects of global climate change on carbon sequestration and cycling in the below-ground systems of forests.     

Elevated CO2, rhizosphere processes,and soil organic matter decomposition

The rhizosphere is one of the key fine-scale components of C cycles. This study was undertaken to improve understanding of the potential effects of atmospheric CO2 increase on rhizosphere processes. Using C isotope techniques, we found that elevated atmospheric CO2 significantly increased wheat plant growth, dry mass accumulation, rhizosphere respiration, and soluble C concentrations in the rhizosphere. When plants were grown under elevated CO2 concentration, soluble C concentration in the rhizosphere increased by approximately 60%. The degree of elevated CO2 enhancement on rhizosphere respiration was much higher than on root biomass. Averaged between the two nitrogen treatments and compared with the ambient CO2 treatment, wheat rhizosphere respiration rate increased 60% and root biomass only increased 26% under the elevated CO2 treatment. These results indicated that elevated atmospheric CO2 in a wheat-soil system significantly increased substrate input to the rhizosphere due to both increased root growth and increased root activities per unit of roots. Nitrogen treatments changed the effect of elevated CO2 on soil organic matter decomposition. Elevated CO2 increased soil organic matter decomposition (22%) in the nitrogen-added treatment but decreased soil organic matter decomposition (18%) without nitrogen addition. Soil nitrogen status was therefore found to be important in determining the directions of the effect of elevated CO2 on soil organic matter decomposition.     

Interactions among plants,bacteria, and fungi reduce extracellular enzyme activities under long‐term N fertilization

Atmospheric nitrogen (N) deposition has enhanced soil carbon (C) stocks in temperate forests. Most research has posited that these soil C gains are driven primarily by shifts in fungal community composition with elevated N leading to declines in lignin degrading Basidiomycetes. Recent research, however, suggests that plants and soil microbes are dynamically intertwined, whereby plants send C subsidies to rhizosphere microbes to enhance enzyme production and the mobilization of N. Thus, under elevated N, trees may reduce belowground C allocation leading to cascading impacts on the ability of microbes to degrade soil organic matter through a shift in microbial species and/or a change in plant–microbe interactions. The objective of this study was to determine the extent to which couplings among plant, fungal, and bacterial responses to N fertilization alter the activity of enzymes that are the primary agents of soil decomposition. We measured fungal and bacterial community composition, root–microbial interactions, and extracellular enzyme activity in the rhizosphere, bulk, and organic horizon of soils sampled from a long‐term (>25 years), whole‐watershed, N fertilization experiment at the Fernow Experimental Forest in West Virginia, USA. We observed significant declines in plant C investment to fine root biomass (24.7%), root morphology, and arbuscular mycorrhizal (AM) colonization (55.9%). Moreover, we found that declines in extracellular enzyme activity were significantly correlated with a shift in bacterial community composition, but not fungal community composition. This bacterial community shift was also correlated with reduced AM fungal colonization indicating that declines in plant investment belowground drive the response of bacterial community structure and function to N fertilization. Collectively, we find that enzyme activity responses to N fertilization are not solely driven by fungi, but instead reflect a whole ecosystem response, whereby declines in the strength of belowground C investment to gain N cascade through the soil environment.     

Increased litterfall in tropical forests boosts the transfer of soil CO2 to the atmosphere

Aboveground litter production in forests is likely to increase as a consequence of elevated atmospheric carbon dioxide (CO(2)) concentrations, rising temperatures, and shifting rainfall patterns. As litterfall represents a major flux of carbon from vegetation to soil, changes in litter inputs are likely to have wide-reaching consequences for soil carbon dynamics. Such disturbances to the carbon balance may be particularly important in the tropics because tropical forests store almost 30% of the global soil carbon, making them a critical component of the global carbon cycle; nevertheless, the effects of increasing aboveground litter production on belowground carbon dynamics are poorly understood. We used long-term, large-scale monthly litter removal and addition treatments in a lowland tropical forest to assess the consequences of increased litterfall on belowground CO(2) production. Over the second to the fifth year of treatments, litter addition increased soil respiration more than litter removal decreased it; soil respiration was on average 20% lower in the litter removal and 43% higher in the litter addition treatment compared to the controls but litter addition did not change microbial biomass. We predicted a 9% increase in soil respiration in the litter addition plots, based on the 20% decrease in the litter removal plots and an 11% reduction due to lower fine root biomass in the litter addition plots. The 43% measured increase in soil respiration was therefore 34% higher than predicted and it is possible that this 'extra' CO(2) was a result of priming effects, i.e. stimulation of the decomposition of older soil organic matter by the addition of fresh organic matter. Our results show that increases in aboveground litter production as a result of global change have the potential to cause considerable losses of soil carbon to the atmosphere in tropical forests.     

Partitioning of belowground C in young sugar maple forest

Background and aims

Trees allocate a high proportion of assimilated carbon belowground, but the partitioning of that C among ecosystem components is poorly understood thereby limiting our ability to predict responses of forest C dynamics to global change drivers.

Methods

We labeled sugar maple saplings in natural forest with a pulse of photosynthetic ¹³C in late summer and traced the pulse over the following 3 years. We quantified the fate of belowground carbon by measuring ¹³C enrichment of roots, rhizosphere soil, soil respiration, soil aggregates and microbial biomass.

Results

The pulse of ¹³C contributed strongly to root and rhizosphere respiration for over a year, and respiration comprised about 75 % of total belowground C allocation (TBCA) in the first year. We estimate that rhizosphere carbon flux (RCF) during the dormant season comprises at least 6 % of TBCA. After 3 years, 3.8 % of the C allocated belowground was recovered in soil organic matter, mostly in water-stable aggregates.

Conclusions

A pulse of carbon allocated belowground in temperate forest supplies root respiration, root growth and RCF throughout the following year and a small proportion becomes stabilized in soil aggregates.