Performance and allocation patterns of the perennial herb,Plantago lanceolata,in response to simulated herbivory and elevated CO2 environments

Summary We tested the prediction that plants grown in elevated CO₂ environments are better able to compensate for biomass lost to herbivory than plants grown in ambient CO₂ environments. The herbaceous perennial Plantago lanceolata (Plantaginaceae) was grown in either near ambient (380 ppm) or enriched (700 ppm) CO₂ atmospheres, and then after 4 weeks, plants experienced either 1) no defoliation; 2) every fourth leaf removed by cutting; or 3) every other leaf removed by cutting. Plants were harvested at week 13 (9 weeks after simulated herbivory treatments). Vegetative and reproductive weights were compared, and seeds were counted, weighed, and germinated to assess viability.Plants grown in enriched CO₂ environments had significantly greater shoot weights, leaf areas, and root weights, yet had significantly lower reproductive weights (i.e. stalks + spikes + seeds) and produced fewer seeds, than plants grown in ambient CO₂ environments. Relative biomass allocation patterns further illustrated differences in plants grown in ambient CO₂ environments. Relative biomass allocation patterns further illustrated differences in plant responses to enriched CO₂ atmospheres: enriched CO₂-grown plants only allocated 10% of their carbon resources to reproduction whereas ambient CO₂-grown plants allocated over 20%. Effects of simulated herbivory on plant performance were much less dramatic than those induced by enriched CO₂ atmospheres. Leaf area removal did not reduce shoot weights or reproductive weights of plants in either CO₂ treatment relative to control plants. However, plants from both CO₂ treatments experienced reductions in root weights with leaf area removal, indicating that plants compensated for lost above-ground tissues, and maintained comparable levels of reproductive output and seed viability, at the expense of root growth.     

Plant biomass partitioning and chemical defense: Response to defoliation and nitrate limitation

Summary Plant growth and allocation to root, shoot and carbon-based leaf chemical defense were measured in response to defoliation and nitrate limitation inHeterotheca subaxillaris. Field and greenhouse experiments demonstrated that, following defoliation, increased allocation to the shoot results in an equal root/shoot ratio between moderately defoliated (9% shoot mass removed) and non-defoliated plants. High defoliation (28% shoot mass or >25% leaf area removed) resulted in greater proportional shoot growth, reducing the root/shot ratio relative to moderate or non-defoliated plants. However, this latter effect was dependent on nutritional status. Despite the change in distribution of biomass, defoliation and nitrate limitation slowed the growth and development ofH. subaxillaris. Chronic defoliation decreased the growth of nitrate-rich plants more than that of nitrate-limited plants. The concentration of leaf mono- and sesqui-terpenes increased with nitrate-limitation and increasing defoliation. Nutrient stress resulting from reduced allocation to root growth with defoliation may explain the greater allocation to carbon-based leaf defenses, as well as the defoliation-related greater growth reduction of nitrate-rich plants.     

Growth and biomass allocation of shrub and grass seedlings in response to predicted changes in precipitation seasonality

Anthropogenic emissions contribute to an annual 0.5% increase in atmospheric CO₂. As global CO₂ levels increase, regional precipitation patterns will likely be altered. Our primary objective was to determine whether a reduction in summer precipitation or an increase in winter/spring precipitation, predicted by global climate change models, will favor the establishment of C₄ grasses or C₃ shrubs in southern savannas. Our secondary objective was to determine how defoliation and microsite light availability interact with altered precipitation regimes to influence grass and shrub seedling growth and biomass allocation patterns. Seedlings of 3 shrub species (Prosopis glandulosa var. glandulosa, Acacia berlandieri, and A. greggii var. wrightii) and 3 grass species (Aristida purpurea var. wrightii, Setaria texana, and Stipa leucotricha) were watered based on probable changes in precipitation in a CO₂ enriched atmosphere (0.6, 0.8, and 1.0 current ambient summer precipitation and 1.0, 1.15, and 1.30 current winter/spring precipitation). Seedlings were defoliated at 3 levels (non-defoliated, single defoliation, and repeated defoliation) within 2 levels of microsite light availability (100 and 50% ambient). Defoliation significantly reduced total shrub and grass seedling biomass. Reducing light availability decreased shrub seedling root:shoot ratio, but total biomass was not significantly affected. Grass seedling biomass and root:shoot ratio decreased when light availability was reduced. Changing the seasonality of precipitation by reducing summer rainfall or increasing winter/spring rainfall did not significantly influence growth or biomass allocation of grass and shrub seedlings in a semiarid savanna. Microsite variations in defoliation intensity and light availability influence seedling growth and biomass allocation more than changing seasonality of precipitation. Shrub and grass seedling establishment and growth on semiarid rangelands are already limited by summer precipitation, so a further reduction as proposed by climate change models will have a limited impact on seedling dynamics.     

Effects of Elevated CO2 and Defoliation on Compensatory Growth and Photosynthesis of Seedlings in a Tropical Tree,Copaifera aromatica1

After defoliation by herbivores, some plants exhibit enhanced rates of photosynthesis and growth that enable them to compensate for lost tissue, thus maintaining their fitness relative to competing, undefoliated plants. Our aim was to determine whether compensatory photosynthesis and growth would be altered by increasing concentrations of atmospheric CO₂. Defoliation of developing leaflets on seedlings of a tropical tree, Copaifera aromatica, caused increases in photosynthesis under ambient CO₂, but not under elevated CO₂. An enhancement in the development of buds in the leaf axils followed defoliation at ambient levels of CO₂. In contrast, under elevated CO₂, enhanced development of buds occurred in undefoliated plants with no further enhancement in bud development due to exposure to elevated CO₂. Growth of leaf area after defoliation was increased, particularly under elevated CO₂. Despite this increase, defoliated plants grown under elevated CO₂ were further from compensating for tissue lost during defoliation after 5¹/₂ weeks than those grown under ambient CO₂ concentrations.     

Acorn mass and seedling growth in Quercus rubra in response to elevated CO2

Abstract. In order to explore whether seed size affects plant response to elevated CO₂, plants grown from red oak (Quercus rubra L.) acorns were studied for differences in their first year response to CO₂ concentrations of 350 and 700 μl/l. Overall, at final harvest, total biomass of plants grown in elevated CO₂ were 47 % larger than that of plants grown in ambient CO₂. There were significant interactions between CO₂ treatments and initial acorn mass for total biomass, as well as for root, leaf, and stem biomass. Although total biomass increased with increasing initial acorn mass for both high and ambient CO₂ plants, high CO₂ plants exhibited a greater increase than ambient CO₂ plants, as indicated by a steeper slope in high CO₂ plants. However, CO₂ levels did not affect biomass partitioning traits, such as root/shoot ratio, leaf, stem, and root weight ratios, and leaf area ratio. These results suggest that variation in seed size or initial plant size can cause intraspecific variation in response to elevated CO₂.     

Elevated CO2 affects the interactions between aphid pests and host plant flowering

1 Broad beans (Vicia faba L.) were grown at either ambient (350 μL/L) or elevated (700 μL/L) CO₂. Elevated CO₂ increased shoot weight by 14% and root weight by 24% compared to ambient, but did not affect flowering. 2 A single pea aphid (Acyrthosiphon pisum (Harris)) and its progeny decreased shoot and root weights by 20 and 24%, respectively, at ambient CO₂ after 20 days, but did not affect flower number. At elevated CO₂A. pisum decreased shoot and root weights by 27 and 34% and flower number decreased by 73%. 3 A single glasshouse and potato aphid (Aulacorthum solani (Kaltenbach)) and its progeny had no effect on the growth of bean plants after 20 days at ambient CO₂. At elevated CO₂, A. solani decreased shoot and root weights by 20 and 18%, and flower number by 60%. 4 The large reduction in flowering caused by aphids at elevated CO₂ suggests a change in resource allocation within the plants to compensate for aphid infestation. 5 Aphid density was unaffected by elevated CO₂, although there were significant effects of CO₂ on the resulting population structure of both A. pisum and A solani. We suggest that at elevated CO₂, aphids appear not to achieve their maximum reproductive potential and their populations are limited by the lower carrying capacity of their host plants.     

Enriched atmospheric CO2 and defoliation: effects on tree chemistry and insect performance

We examined the effects of CO₂ and defoliation on tree chemistry and performance of the forest tent caterpillar, Malacosoma disstria. Quaking aspen (Populus tremuloides) and sugar maple (Acer saccharum) trees were grown in open-top chambers under ambient or elevated concentrations of CO₂. During the second year of growth, half of the trees were exposed to free-feeding forest tent caterpillars, while the remaining trees served as nondefoliated controls. Foliage was collected weekly for phytochemical analysis. Insect performance was evaluated on foliage from each of the treatments. At the sampling date coincident with insect bioassays, levels of foliar nitrogen and starch were lower and higher, respectively, in high CO₂ foliage, and this trend persisted throughout the study. CO₂-mediated increases in secondary compounds were observed for condensed tannins in aspen and gallotannins in maple. Defoliation reduced levels of water and nitrogen in aspen but had no effect on primary metabolites in maple. Similarly, defoliation induced accumulations of secondary compounds in aspen but not in maple. Larvae fed foliage from the enriched CO₂ or defoliated treatments exhibited reduced growth and food processing efficiencies, relative to larvae on ambient CO₂ or nondefoliated diets, but the patterns were host species-specific. Overall, CO₂ and defoliation appeared to exert independent effects on foliar chemistry and forest tent caterpillar performance.     

Biomass allocation in old-field annual species grown in elevated CO2 environments: no evidence for optimal partitioning

Increased atmospheric carbon dioxide supply is predicted to alter plant growth and biomass allocation patterns. It is not clear whether changes in biomass allocation reflect optimal partitioning or whether they are a direct effect of increased growth rates. Plasticity in growth and biomass allocation patterns was investigated at two concentrations of CO₂ ([CO₂]) and at limiting and nonlimiting nutrient levels for four fast‐ growing old‐field annual species. Abutilon theophrasti, Amaranthus retroflexus, Chenopodium album, and Polygonum pensylvanicum were grown from seed in controlled growth chamber conditions at current (350 μmol mol^?1, ambient) and future‐ predicted (700 μmol mol^?1, elevated) CO₂ levels. Frequent harvests were used to determine growth and biomass allocation responses of these plants throughout vegetative development. Under nonlimiting nutrient conditions, whole plant growth was increased greatly under elevated [CO₂] for three C3 species and moderately increased for a C4 species (Amaranthus). No significant increases in whole plant growth were observed under limiting nutrient conditions. Plants grown in elevated [CO₂] had lower or unchanged root:shoot ratios, contrary to what would be expected by optimal partitioning theory. These differences disappeared when allometric plots of the same data were analysed, indicating that CO₂‐induced differences in root:shoot allocation were a consequence of accelerated growth and development rates. Allocation to leaf area was unaffected by atmospheric [CO₂] for these species. The general lack of biomass allocation responses to [CO₂] availability is in stark contrast with known responses of these species to light and nutrient gradients. We conclude that biomass allocation responses to elevated atmospheric [CO₂] are not consistent with optimal partitioning predictions.     

Enriched rhizosphere CO2 concentrations can ameliorate the influence of salinity on hydroponically grown tomato plants

Our previous work indicated that salinity caused a shift in the predominant site of nitrate reduction and assimilation from the shoot to the root in tomato plants. In the present work we tested whether an enhanced supply of dissolved inorganic carbon (DIC, CO₂+ HCO₃) to the root solution could increase anaplerotic provision of carbon compounds for the increased nitrogen assimilation in the root of salinity-stressed Lycopersicon esculentum (L.) Mill. cv. F144. The seedlings were grown in hydroponic culture with 0 or 100mM NaCl and aeration of the root solution with either ambient or CO₂-enriched air (5000 μmol mol^?1). The salinity-treated plants accumulated more dry weight and higher total N when the roots were supplied with CO₂-enriched aeration than when aerated with ambient air. Plants grown with salinity and enriched DIC also had higher rates of NO^?₃ uptake and translocated more NO^?₃ and reduced N in the xylem sap than did equivalent plants grown with ambient DIC. Incorporation of DIC was measured by supplying a 1 -h pulse of H¹⁴CO^?₃ to the roots followed by extraction with 80% ethanol. Enriched DIC increased root incorporation of DIC 10-fold in both salinized and non-salinized plants. In salinity-stressed plants, the products of dissolved inorganic ¹⁴C were preferentially diverted into amino acid synthesis to a greater extent than in non-salinized plants in which label was accumulated in organic acids. It was concluded that enriched DIC can increase the supply of N and anaplerotic carbon for amino acid synthesis in roots of salinized plants. Thus enriched DIC could relieve the limitation of carbon supply for ammonium assimilation and thus ameliorate the influence of salinity on NO^?₃ uptake and assimilation as well as on plant growth.     

Infection with the parasitic angiosperm Striga hermonthica influences the response of the C3 cereal Oryza sativa to elevated CO2

Upland rice (Oryza sativa L.) was grown at both ambient (350 μmol mol^?1) and elevated (700 μmol mol^?1) CO₂ in either the presence or absence of the root hemi‐parasitic angiosperm Striga hermonthica (Del) Benth. Elevated CO₂ alleviated the impact of the parasite on host growth: biomass of infected rice grown at ambient CO₂ was 35% that of uninfected, control plants, while at elevated CO₂, biomass of infected plants was 73% that of controls. This amelioration occurred despite the fact that O. sativa grown at elevated CO₂ supported both greater numbers and a higher biomass of parasites per host than plants grown at ambient CO₂. The impact of infection on host leaf area, leaf mass, root mass and reproductive tissue mass was significantly lower in plants grown at elevated as compared with ambient CO₂. There were significant CO₂ and Striga effects on photosynthetic metabolism and instantaneous water‐use efficiency of O. sativa. The response of photosynthesis to internal [CO₂] (A/C_i curves) indicated that, at 45 days after sowing (DAS), prior to emergence of the parasites, uninfected plants grown at elevated CO₂ had significantly lower CO₂ saturated rates of photosynthesis, carboxylation efficiencies and ribulose‐1,5‐bisphosphate carboxylase/oxygenase (Rubisco; EC 4.1.1.39) contents than uninfected, ambient CO₂‐grown O. sativa. In contrast, infection with S. hermonthica prevented down‐regulation of photosynthesis in O. sativa grown at elevated CO₂, but had no impact on photosynthesis of hosts grown at ambient CO₂. At 76 DAS (after parasites had emerged), however, infected plants grown at both elevated and ambient CO₂ had lower carboxylation efficiencies and Rubisco contents than uninfected O. sativa grown at ambient CO₂. The reductions in carboxylation efficiency (and Rubisco content) were accompanied by similar reductions in nitrogen concentration of O. sativa leaves, both before and after parasite emergence. There were no significant CO₂ or infection effects on the concentrations of soluble sugars in leaves of O. sativa, but starch concentration was significantly lower in infected plants at both CO₂ concentrations. These results demonstrate that elevated CO₂ concentrations can alleviate the impact of infection with Striga on the growth of C₃ hosts such as rice and also that infection can delay the onset of photosynthetic down‐regulation in rice grown at elevated CO₂.     

Effect of CO2 enrichment and elevated temperature on methane emissions from rice, Oryza sativa

Methane emissions from rice grown within Temperature Gradient Greenhouse Tunnels under doubled CO₂ concentrations were 10–45 times less than emissions from control plants grown under ambient CO₂. For two cultivars of rice (cvs. Lemont and IR-72), methane emissions increased with a temperature increase of 2°, from outdoor ambient temperatures to the first cell of the ambient CO₂ tunnel (ambient temperature + 2 °C). Within both tunnels and for both cultivars methane emissions decreased with further temperature increases (from 2° to 5 °C above ambient). Carbon dioxide enrichment stimulated both above- and below-ground production. Our original hypothesis was that increased CO₂ would stimulate plant productivity and therefore stimulate methane emission, since direct linkages between these parameters have been observed. We hypothesize that CO₂ enrichment led to the attenuation of methane production due to increased delivery of oxygen to the rhizosphere because of increased root biomass and porosity. The increased root biomass due to elevated CO₂ may have more effectively aerated the soil, suppressing methane production. However, this study may be unique because the low organic content (< 1%) of the sandy soils in which the rice was grown created very little oxygen demand.     

Effects of long-term exposure to elevated CO2 and N fertilization on the development of photosynthetic capacity and biomass accumulation in Quercus suber L.

The effects of long‐term (4 year) CO₂ enrichment (70 Pa versus 35 Pa) and nitrogen nutrition (8 mm versus 1 mm NO₃^–) on biomass accumulation and the development of photosynthetic capacity in leaves of cork oak (Quercus suber L., a Mediterranean evergreen tree) were studied. The evolution of photosynthetic parameters with leaf development was estimated by fitting the biochemical model of Farquhar et al. (Planta 149, 78–90, 1980) with modifications by Sharkey (Botanical Review 78, 71–75, 1985) to A–C_i response curves. CO₂ enrichment had a small reduction effect on the development of the maximum CO₂ fixation capacity by Rubisco (V_Cmax), and no effect over maximum electron transport capacity (J_max), day‐time respiration (R_d) and Triose‐P utilization (TPU). However, there was a statistically significant effect of N fertilization and the interaction CO₂ × N over the evolution of V_Cmax, J_max and TPU. Relative stomatal limitation (estimated from A–C_i curves) was higher (+20%) for plants grown under ambient CO₂ than for plants grown under elevated CO₂. There was a significant effect of CO₂ and N fertilization over total biomass accumulation as well as leaf area. Plants grown at elevated CO₂ had 27% more biomass than plants grown at ambient CO₂ when given high N. However, for plants grown under low N there was no significant effect of CO₂ enrichment on biomass accumulation. Plants grown under low N also had significantly higher root : shoot ratios whereas there were no differences between CO₂ treatments. The larger biomass accumulation of Q. suber under elevated CO₂ is attributable to a higher availability of CO₂ coupled to a larger leaf area, with no significant decrease in photosynthetic capacity under CO₂ enrichment and elevated N fertilization. For low N fertilization, the effects of CO₂ enrichment over leaf area and biomass accumulation are lost, suggesting that in native ecosystems with low N availability, the effects of CO₂ enrichment may be insignificant.     

Elevated CO2 changes the interactions between nematode and tomato genotypes differing in the JA pathway

Interactions between the root‐knot nematode Meloidogyne incognita and three isogenic tomato (Lycopersicon esculentum) genotypes were examined when plants were grown under ambient (370 ppm) and elevated (750 ppm) CO₂. We tested the hypothesis that, defence‐recessive genotypes tend to allocate ‘extra’ carbon (relative to nitrogen) to growth under elevated CO₂, whereas defence‐dominated genotypes allocate extra carbon to defence, and thereby increases the defence against nematodes. For all three genotypes, elevated CO₂ increased height, biomass, and root and leaf total non‐structural carbohydrates (TNC):N ratio, and decreased amino acids and proteins in leaves. The activity of anti‐oxidant enzymes (superoxide dismutase and catalase) was enhanced by nematode infection in defence‐recessive genotypes. Furthermore, elevated CO₂ and nematode infection did not qualitatively change the volatile organic compounds (VOC) emitted from plants. Elevated CO₂ increased the VOC emission rate only for defence‐dominated genotypes that were not infected with nematodes. Elevated CO₂ increased the number of nematode‐induced galls on defence‐dominated genotypes but not on wild‐types or defence‐recessive genotypes roots. Our results suggest that CO₂ enrichment may not only increase plant C : N ratio but can disrupt the allocation of plant resources between growth and defence in some genetically modified plants and thereby reduce their resistance to nematodes.     

Effects of atmospheric CO2 enrichment and root restriction on leaf gas exchange and growth of banana (Musa)

The effects of atmospheric CO₂ enrichment and root restriction on photosynthetic characteristics and growth of banana (Musa sp. AAA cv. Gros Michel) plants were investigated. Plants were grown aeroponically in root chambers in controlled environment glasshouse rooms at CO₂ concentrations of 350 or 1 000 μmol CO₂ mol^-1. At each CO₂ concentration, plants were grown in large (2001) root chambers that did not restrict root growth or in small (20 1) root chambers that restricted root growth. Plants grown at 350 μmol CO₂ mol^-1 generally had a higher carboxylation efficiency than plants grown at 1 000 μmol CO₂ mol^-1 although actual net CO₂ assimilation (A) was higher at the higher ambient CO₂ concentration due to increased intercellular CO₂ concentrations (C_i resulting from CO₂ enrichment. Thus, plants grown at 1 000 μmol CO₂ mol^-1 accumulated more leaf area and dry weight than plants grown at 350 μmol CO₂ mol^-1. Plants grown in the large root chambers were more photosynthetically efficient than plants grown in the small root chambers. At 350 μmol CO₂ mol^-1, leaf area and dry weights of plant organs were generally greater for plants in the large root chambers compared to those in the small root chambers. Atmospheric CO₂ enrichment may have compensated for the effects of root restriction on plant growth since at 1 000 μmol CO₂ mol^-1 there was generally no effect of root chamber size on plant dry weight.     

Root to shoot ratio of crops as influenced by CO2

Crops of tomorrow are likely to grow under higher levels of atmospheric CO₂. Fundamental crop growth processes will be affected and chief among these is carbon allocation. The root to shoot ratio (R:S, defined as dry weight of root biomass divided by dry weight of shoot biomass) depends upon the partitioning of photosynthate which may be influenced by environmental stimuli. Exposure of plant canopies to high CO₂ concentration often stimulates the growth of both shoot and root, but the question remains whether elevated atmospheric CO₂ concentration will affect roots and shoots of crop plants proportionally. Since elevated CO₂ can induce changes in plant structure and function, there may be differences in allocation between root and shoot, at least under some conditions. The effect of elevated atmospheric CO₂ on carbon allocation has yet to be fully elucidated, especially in the context of changing resource availability. Herein we review root to shoot allocation as affected by increased concentrations of atmospheric CO₂ and provide recommendations for further research. Review of the available literature shows substantial variation in R:S response for crop plants. In many cases (59.5%) R:S increased, in a very few (3.0%) remained unchanged, and in others (37.5%) decreased. The explanation for these differences probably resides in crop type, resource supply, and other experimental factors. Efforts to understand allocation under CO₂ enrichment will add substantially to the global change response data base.Abbreviations R:S root to shoot ratio, dry weight basis     

Elevated atmospheric CO2 alters microbial population structure in a pasture ecosystem

An increase in concentration of atmospheric CO₂ is one major factor influencing global climate change. Among the consequences of such an increase is the stimulation of plant growth and productivity. Below‐ground microbial processes are also likely to be affected indirectly by rising atmospheric CO₂ levels, through increased root growth and rhizodeposition rates. Because changes in microbial community composition might have an impact on symbiotic interactions with plants, the response of root nodule symbionts to elevated atmospheric CO₂ was investigated. In this study we determined the genetic structure of 120 Rhizobium leguminosarum bv. trifolii isolates from white clover plants exposed to ambient (350 μmol mol^?1) or elevated (600 μmol mol^?1) atmospheric CO₂ concentrations in the Swiss FACE (Free‐Air‐Carbon‐Dioxide‐Enrichment) facility. Polymerase Chain Reaction (PCR) fingerprinting of genomic DNA showed that the isolates from plants grown under elevated CO₂ were genetically different from those isolates obtained from plants grown under ambient conditions. Moreover, there was a 17% increase in nodule occupancy under conditions of elevated atmospheric CO₂ when strains of R. leguminosarum bv. trifolii isolated from plots exposed to CO₂ enrichment were evaluated for their ability to compete for nodulation with those strains isolated from ambient conditions. These results indicate that a shift in the community composition of R. leguminosarum bv. trifolii occurred as a result of an increased atmospheric CO₂ concentration, and that elevated atmospheric CO₂ affects the competitive ability of root nodule symbionts, most likely leading to a selection of these particular strains to nodulate white clover.     

An oxygen-mediated positive feedback between elevated carbon dioxide and soil organic matter decomposition in a simulated anaerobic wetland

We examined the effects of elevated atmospheric CO₂ on soil carbon decomposition in an experimental anaerobic wetland system. Pots containing either bare C₄‐derived soil or the C₃ sedge Scirpus olneyi planted in C₄‐derived soil were incubated in greenhouse chambers at either ambient or twice‐ambient atmospheric CO₂. We measured CO₂ flux from each pot, quantified soil organic matter (SOM) mineralization using δ¹³C, and determined root and shoot biomass. SOM mineralization increased in response to elevated CO₂ by 83–218% (P<0.0001). In addition, soil redox potential was significantly and positively correlated with root biomass (P= 0.003). Our results (1) show that there is a positive feedback between elevated atmospheric CO₂ concentrations and wetland SOM decomposition and (2) suggest that this process is mediated by the release of oxygen from the roots of wetland plants. Because this feedback may occur in any wetland system, including peatlands, these results suggest a limitation on the size of the carbon sink presented by anaerobic wetland soils in a future elevated‐CO₂ atmosphere.     

Defoliation reduces soil biota – and modifies stimulating effects of elevated CO2

To understand the responses to external disturbance such as defoliation and possible feedback mechanisms at global change in terrestrial ecosystems, it is necessary to examine the extent and nature of effects on aboveground–belowground interactions. We studied a temperate heathland system subjected to experimental climate and atmospheric factors based on prognoses for year 2075 and further exposed to defoliation. By defoliating plants, we were able to study how global change modifies the interactions of the plant–soil system. Shoot production, root biomass, microbial biomass, and nematode abundance were assessed in the rhizosphere of manually defoliated patches of Deschampsia flexuosa in June in a full‐factorial FACE experiment with the treatments: increased atmospheric CO₂, increased nighttime temperatures, summer droughts, and all of their combinations. We found a negative effect of defoliation on microbial biomass that was not apparently affected by global change. The negative effect of defoliation cascades through to soil nematodes as dependent on CO₂ and drought. At ambient CO₂, drought and defoliation each reduced nematodes. In contrast, at elevated CO₂, a combination of drought and defoliation was needed to reduce nematodes. We found positive effects of CO₂ on root density and microbial biomass. Defoliation affected soil biota negatively, whereas elevated CO₂ stimulated the plant–soil system. This effect seen in June is contrasted by the effects seen in September at the same site. Late season defoliation increased activity and biomass of soil biota and more so at elevated CO₂. Based on soil biota responses, plants defoliated in active growth therefore conserve resources, whereas defoliation after termination of growth results in release of resources. This result challenges the idea that plants via exudation of organic carbon stimulate their rhizosphere biota when in apparent need of nutrients for growth.     

Effects of defoliation and atmospheric CO2 depletion on nitrate acquisition,and exudation of organic compounds by roots of Festuca rubra

The aim of this study was to investigate the physiological basis of increased root exudation from Festuca rubra, in response to defoliation. The hypothesis, that assimilate supply to roots is a key determinant of the response of root exudation to defoliation was tested by imposing CO₂-deplete (< 50 mol mol^–1) atmospheres to F. rubra. This was done as a non-destructive means of preventing supply of new assimilate to roots of intact and defoliated plants. F. rubra was grown in axenic sand systems, with defoliation and CO₂-depletion treatments applied to plants at 14 and 35 days after planting. Root exudation and NO₃ ^– uptake were quantified throughout, and post-treatment uptake and allocation of N were determined from the distribution of ¹⁵N label, supplied as ¹⁵NO₃ ^–. Defoliation of F. rubra resulted in significantly (P <0.01) increased root exudation, CO₂-depletion did not result in increased exudation from plants of either age. When treatments were applied to F. rubra after 14 days, defoliation and CO₂-depletion each reduced NO₃ ^– uptake significantly (P <0.05). However, in older plants, uptake of NO₃ ^– was less sensitive to defoliation and CO₂-depletion. The results indicate that increased root exudation following defoliation is not related directly to reduced assimilate supply to roots. This was evident from the lack of effect of CO₂-depletion on root exudation, and the absence of correlation between root-C efflux and the rate of NO₃ ^– uptake. The physiological basis of increased exudation following defoliation remains uncertain, but may be dependent on physical damage, either directly or as a consequence of systemic responses to wounding.     

Changes in needle quality and larch bud moth performance in response to CO2 enrichment and defoliation of treeline larches

Abstract. 1. It is hypothesised that the larch bud moth cycle is controlled by host‐tree foliage quality. In a Free Air CO₂ Enrichment (FACE) experiment at the Swiss alpine treeline (2180 m a.s.l.), the effects of elevated CO₂ and previous year defoliation on needle quality of larch and the performance of the larch bud moth were investigated. 2. Starch and lignin concentrations increased and water content decreased in elevated CO₂‐grown needles compared with ambient CO₂ concentration. Defoliation resulted in reduced N, water, starch, and sugar concentrations in needles of the next year generation. No interactions between elevated CO₂ and defoliation on needle quality were observed. 3. Needle quality changes due to needle maturation over the course of the experiment, however, were much larger than the effects of elevated CO₂ and defoliation. For example, N concentration was on average 38% lower and lignin concentration 55% higher at the end of the experiment (early July 2003) than at the beginning (mid June 2003). 4. On non‐defoliated trees, larch bud moth larvae grew somewhat more slowly under elevated CO₂ compared with ambient CO₂ concentration. If, however, trees had been defoliated, this response was reversed, with a faster growth of larch bud moth on high CO₂‐exposed trees than on control trees. Pupal weight was not affected by either CO₂ treatment or defoliation. 5. These results suggest that the larch bud moth has to cope with large changes in food quality due to needle maturation during its development, and that additional CO₂‐ and defoliation‐induced alterations in needle chemistry have comparatively minor influences on larch bud moth performance at the treeline.