The dynamics of recovery and growth: how defoliation affects stored resources

Growth rate varies widely among species and the trade-off between growth rate and storage or maintenance traits is a principal axis of variation between species. Many plant species have substantial root stores, but very little is known about how growth rate modifies responses of these stores to defoliation and other stresses. Species with different growth rates are predicted to respond in distinct ways, because of variation in the pre-defoliation allocation to storage. Here, we quantified the dynamics of stored carbohydrates in seven species with varying growth rate, following defoliation in a pot experiment. For faster growing species, there was significant reduction in carbohydrate concentration following defoliation, followed by relatively fast recovery, whereas for slower growing species, carbohydrate concentration levels remained relatively invariant across treatments. Results for total carbohydrates mirrored those for concentration, but were not as significant. Our findings were consistent with the idea that faster growing species respond more rapidly than slower growers to defoliation, through changes in carbohydrate pool concentrations. Growth rate as an indicator of life-history and ecological strategy may therefore be key to understanding post-defoliation recovery and storage strategies.     

Responses of photosynthesis,leaf conductance and growth to different salinities in three coastal dune plants

The effects of soil-water salinity on growth and photosynthesis of three coastal dune plants were examined by salt-treatment in order to clarify the causal relationship between salinity and plant distribution in a dune habitat. Plants were cultivated hydroponically at three salinity levels: 0, 10 and 100 mM NaCl. With the 100 mM salt treatment,Calystegia soldanella (C₃ species) had the highest relative growth rate (RGR) (0.085 g g⁻¹ d⁻¹), followed byCarex kobomugi (C₃) (0.066), andIschaemum anthephoroides (C₄) (0.060). This order coincides with the distribution pattern of the three species on coastal dunes;Calystegia soldanella is generally distributed in more seaward areas whereasI. anthephoroides occurs further inland. The order of RGR was determined exclusively by leaf area ratio (LAR) among the three species. Due to its C₄ pathway,I. anthephoroides had higher net photosynthetic rate (Pn) and net assimilation rate (NAR) than the two C₃ plants at all NaCl concentrations, despite its low RGR. This apparent discrepancy is explainable by differences of LAR among the three species; LAR ofI. anthephoroides was lowest, and about half that ofCalystegia soldanella. These results suggest that LAR is one of the main determinants of salt tolerance based on RGR, whereas Pn or NAR may not be significant. This article is dedicated to Professor Hideo Iwaki, University of Tsukuba, in appreciation of the sincere encouragement he has given to the authors.     

Nutrition and growth of coniferous seedlings at varied relative nitrogen addition rate

The growth of two provenances of Pinus sylvestris L. were compared with two provenances of Picea abies (L.) Karst. and with Pinus contorta Dougl. when grown in solution cultures with low nutrient concentrations. Nitrogen was added at different exponentially increasing rates, and the other nutrients were added at a rate high enough to ensure free access of them to the seedlings. During an initial period of the culture (a lag phase), when the internal nutrient status was changing from optimum to the level of the treatment, deficiency symptoms appeared. The needles yellowed and the root/shoot ratio increased. The initial phase was followed by a period of exponential growth and steady-state nutrition. The needles turned green again, and the root/shoot ratio stabilized at a level characteristic of the treatment. These patterns were the same as previously reported for other tree species. The relative growth rate during exponential growth was numerically closely equal to the relative nitrogen addition rate. The maximum relative growth rates were about 6 to 7.5% dry weight increase day^-1. This is a much lower maximum than for broad-leaved species (about 20 to 30% day^-1) under similar growth conditions. The internal nitrogen concentrations of the seedlings and the relative growth rates were stable during the exponential period. Close linear relationships were found between these parameters and the relative addition rate up to maximum growth. During steady state the relative growth rates of the different plant parts were equal. However, there were large differences between genotypes in absolute root growth rate at the same seedling size because of differences in root/shoot ratio. Lodgepole pine had the highest root growth rate, whereas that of Norway spruce, especially the southern provenance, was remarkably low. Yet, Norway spruce had a high ability to utilize available nutrients. In treatments with free nutrient access, growth allocation to the shoot had a high priority in all genotypes, but there was still a marked tendency for luxury uptake of nutrients. Nitrogen productivity (growth rate per unit of nitrogen) was lower than in broadleaved species and highest in lodgepole pine. The relevance of the dynamic factors, i.e. maximum relative growth rate, nutrient uptake rate, nitrogen productivity, growth allocation and root growth rate, are discussed with regard to conifer characteristics and selection value.     

Growth temperature influences the underlying components of relative growth rate: an investigation using inherently fast- and slow-growing plant species

We examined the effect of growth temperature on the underlying components of growth in a range of inherently fast‐ and slow‐growing plant species. Plants were grown hydroponically at constant 18, 23 and 28 °C. Growth analysis was conducted on 16 contrasting plant species, with whole plant gas exchange being performed on six of the 16 species. Inter‐specific variations in specific leaf area (SLA) were important in determining variations in relative growth rate (RGR) amongst the species at 23 and 28 °C but were not related to variations in RGR at 18 °C. When grown at 18 °C, net assimilation rate (NAR) became more important than SLA for explaining variations in RGR. Variations in whole shoot photosynthesis and carbon concentration could not explain the importance of NAR in determining RGR at the lower temperatures. Rather, variations in the degree to which whole plant respiration per unit leaf area acclimated to the different growth temperatures were responsible. Plants grown at 28 °C used a greater proportion of their daily fixed carbon in respiration than did the 18 and 23 °C‐grown plants. It is concluded that the relative importance of the underlying components of growth are influenced by growth temperature, and the degree of acclimation of respiration is of central importance to the greater role played by NAR in determining variations in RGR at declining growth temperatures.     

Modelling the relative growth rate as a function of plant nitrogen concentration

The relationship between the relative growth rate (RGR) and the nitrogen concentration of the whole plant (PNC) was analyzed by using experimentally determined relations (1) between the PNC and the fraction of dry matter (LWR) and nitrogen in leaves, (2) between the specific leaf area (SLA) and the leaf nitrogen concentration (LNC) and (3) between the net assimilation rate (NAR) and the LNC on an area basis. A strong dependence of RGR on nitrogen concentration resulted from the increase in NAR, LWR and SLA with increasing PNC. A curvilinear relationship between RGR and PNC gave an optimum curve for nitrogen productivity against PNC.     

The effect of potassium on growth of Carex species from swamp habitats varying from oligotrophic to eutrophic and comparison of physiological reactions of Carex species to P stress and K stress

In a growth experiment at potassium levels varying between 0.001 m M and 3.0 m M potassium, relative growth rate (RGR) and other growth parameters were determined in Carex species: C. rostrata Stokes, C. limosa L., C. lasiocarpa Ehrh., C. diandra Schrank and C. acutiformis Ehrh., listed in order of increasing nutrient availability of their habitats. Carex species of nutrient poor sites did grow faster at low potassium concentration than species from nutrient rich habitats. The RGR of C. limosa was not affected by the K concentration, even at the lowest potassium concentration (0.001) m M ) used. At high potassium availability Carex species from nutrient-rich sites responded with greatly increased RGR, whereas the Carex from nutrient-poor sites absorbed potassium in excess of immediate growth requirements: luxury consumption. A comparison is made of the physiology of the Carex species as affected by stress and abundance of phosphate and potassium.     

Plant allometry, leaf nitrogen and phosphorus stoichiometry, and interspecific trends in annual growth rates

• Background Life forms as diverse as unicellular algae,zooplankton, vascular plants, and mammals appear to obey quarter-powerscaling rules. Among the most famous of these rules is Kleiber's(i.e. basal metabolic rates scale as the three-quarters powerof body mass), which has a botanical analogue (i.e. annual plantgrowth rates scale as the three-quarters power of total bodymass). Numerous theories have tried to explain why these rulesexist, but each has been heavily criticized either on conceptualor empirical grounds. • N,P-Stoichiometry Recent models predicting growth rateson the basis of how total cell, tissue, or organism nitrogenand phosphorus are allocated, respectively, to protein and rRNAcontents may provide the answer, particularly in light of theobservation that annual plant growth rates scale linearly withrespect to standing leaf mass and that total leaf mass scalesisometrically with respect to nitrogen but as the three-quarterspower of leaf phosphorus. For example, when these relationshipsare juxtaposed with other allometric trends, a simple N,P-stoichiometricmodel successfully predicts the relative growth rates of 131diverse C₃ and C₄ species. • Conclusions The melding of allometric and N,P-stoichiometrictheoretical insights provides a robust modelling approach thatconceptually links the subcellular ‘machinery’ ofprotein/ribosomal metabolism to observed growth rates of uni-and multicellular organisms. Because the operation of this ‘machinery’is basic to the biology of all life forms, its allometry mayprovide a mechanistic explanation for the apparent ubiquityof quarter-power scaling rules.     

The effect of an elevated atmospheric CO2 concentration on growth, photosynthesis and respiration of Plantago major

The effect of an elevated atmospheric CO₂ concentration on growth, photosynthesis and root respiration of Plantago major L. ssp. major L. was investigated. Plants were grown in a nutrient solution in growth chambers at 350 and 700 μl I⁻¹ CO₂ during 7 weeks. The total dry weight of the Co₂-enriched plants at the end of this period was 50% higher than that of control plants. However, the relative growth rate (RGR) was stimulated only during the first half of the growing period. The transient nature of the stimulation of the RGR was not likely to be due to end-product inhibition of photosynthesis. It is suggested that in P. major , a rosette plant, self-shading causes a decline in photosynthesis and results in an increase in the shoot: root ratio and a decrease in RGR. CO₂-enriched plants grow faster and cosequently suffer more from self-shading. Corrected for this ontogenetic drift, high CO₂ concentrations stimulated the RGR of P. major throughout the entire experiment.     

Supplemental manganese improves the relative growth, net assimilation and photosynthetic rates of salt-stressed barley

Previous results in our laboratory indicated that a reduced Mn concentration in the leaves of barley was highly correlated with the reduced relative growth and net assimilation rates of salt-stressed plants. If Mn deficiency limits the growth of salt-stressed barley, then increasing leaf Mn concentrations should increase growth. In the present study, the effect of supplemental Mn on the growth of salt-stressed barley ( Hordeum vulgare L. cv. CM 72) was tested to determine if a salinity-induced Mn deficiency was limiting growth. Plants were salinized with 125 mol m⁻³ NaCl and 9.6 mol m⁻³ CaCl₂. Supplemental Mn was applied in 2 ways: 1) by increasing the Mn concentration in the solution culture and 2) by spraying Mn solutions directly onto the leaves. Growth was markedly inhibited at this salinity level. Dry matter production was increased 100% in salt-stressed plants treated with supplemental Mn to about 32% of the level of nonsalinized controls. The optimum solution culture concentration was 2.0 mmol m⁻³, and the optimum concentration applied to the leaves was 5.0 mol m⁻³. Supplemental Mn did not affect the growth of control plants. Further experiments showed that supplemental Mn increased Mn concentrations and uptake to the shoot. Supplemental Mn increased the relative growth rate of salt-stressed plants and this increase was attributed to an increase in the net assimilation rate; there were no significant effects on the leaf area ratio. Supplemental Mn also increased the net photosynthetic rate of salt-stressed plants. The data support the hypothesis that salinity induced a Mn deficiency in the shoot, which partially reduced photosynthetic rates and growth.     

A new method for non-destructive measurement of biomass, growth rates, vertical biomass distribution and dry matter content based on digital image analysis

BACKGROUND AND AIMS: Biomass is an important trait in functional ecology and growth analysis. The typical methods for measuring biomass are destructive. Thus, they do not allow the development of individual plants to be followed and they require many individuals to be cultivated for repeated measurements. Non-destructive methods do not have these limitations. Here, a non-destructive method based on digital image analysis is presented, addressing not only above-ground fresh biomass (FBM) and oven-dried biomass (DBM), but also vertical biomass distribution as well as dry matter content (DMC) and growth rates. METHODS: Scaled digital images of the plants silhouettes were taken for 582 individuals of 27 grass species (Poaceae). Above-ground biomass and DMC were measured using destructive methods. With image analysis software Zeiss KS 300, the projected area and the proportion of greenish pixels were calculated, and generalized linear models (GLMs) were developed with destructively measured parameters as dependent variables and parameters derived from image analysis as independent variables. A bootstrap analysis was performed to assess the number of individuals required for re-calibration of the models. KEY RESULTS: The results of the developed models showed no systematic errors compared with traditionally measured values and explained most of their variance (R(2) > or = 0.85 for all models). The presented models can be directly applied to herbaceous grasses without further calibration. Applying the models to other growth forms might require a re-calibration which can be based on only 10-20 individuals for FBM or DMC and on 40-50 individuals for DBM. CONCLUSIONS: The methods presented are time and cost effective compared with traditional methods, especially if development or growth rates are to be measured repeatedly. Hence, they offer an alternative way of determining biomass, especially as they are non-destructive and address not only FBM and DBM, but also vertical biomass distribution and DMC.     

Strategies of leaf expansion in Ficus carica under semiarid conditions

Leaf area expansion, thickness and inclination, gas exchange parameters and relative chlorophyll content were analysed in field‐grown fig (Ficus carica L.) leaves over time, from emergence until after full leaf expansion (FLE). Ficus carica leaves showed a subtle change in shape during the early stages of development, and FLE was reached within ca. 30 days after emergence. Changes in leaf thickness and inclination after FLE demonstrated good adaptation to environmental conditions during summer in areas with a Mediterranean climate. Changes in gas exchange parameters and relative chlorophyll content showed that F. carica is a delayed‐greening species, reaching maximum values 20 days after FLE. Correlation analysis of datasets collected during leaf expansion, confirmed dependence among structural and functional traits in F. carica. Pn was directly correlated with stomatal conductance (Gs), transpiration (E), leaf area (LA) and relative chlorophyll content up to FLE. The effect of pruning on leaf expansion, a cultural technique commonly applied in this fruit tree, was also evaluated. Although leaf development in pruned branches gave a significantly higher relative leaf area growth rate (RGR_l) and higher LA than non‐pruned branches, no significant differences were found in other morphological and physiological traits, indicating no pruning effect on leaf development. All studied morphological and physiological characteristics indicate that F. carica is well adapted to semiarid conditions. The delayed greening strategy of this species is discussed.     

Theory for growth of plants derived from the nitrogen productivity concept

A theory is developed on the assumption that growth of plants is determined by the current amount of nitrogen in the plants. The nitrogen-growth relation is formalized in the nitrogen productivity concept (amount of biomass produced per amount of nitrogen in the biomass and per unit of time), which is essentially a constant for a given species under fixed environmental conditions. A number of results follow for increases in whole plant biomass: (A) The relative growth rate is a linear function of the internal nitrogen concentration. (B) The maximal relative growth rate uniquely determines the scaling of the time axis. (C) Exponential growth is consistent only with stable internal nitrogen concentration. Dose-response curves expressed in reduced variables (the ratio between a variable and the same variable for a plant growing under optimal conditions) are universal, so that all species and all environmental conditions yield the same curve. This is confirmed by experimental data. The shape (linear, exponential, etc.) of the nitrogen uptake curve is the only parameter differentiating these universal curves. The Mitscherlich curve or variations of it can be fitted very closely to the derived dose-response curves, except under exponential growth. A conclusion drawn from the analysis is that the results of nutrition experiments cannot be properly interpreted unless the variation with time of the amount of nitrogen in the plant is known. The theory can be extended to more complex situations, for example, time-varying environmental conditions.     

Inherent allocation patterns and potential growth rates of herbaceous climbing plants

We tested the hypothesis that herbaceous climbing plants, unlike non-climbing herbs, maximize height growth and leaf area, with minimal expenditure in support structures. The enhanced investment in leaf area was expected to result in high relative growth rates in terms of biomass increment. Four leguminous herbaceous climbers from nutrient-poor sites and four non-leguminous herbaceous climbers from nutrient-rich sites, were compared with non-climbing, self-supporting leguminous and non-leguminous herbaceous species from similar habitats. Plants were grown in hydroponic cultures in controlled environment chambers. All climbers had inherently taller shoots than self-supporting plants when compared at an equal amount of total plant dry weight, due to longer stems per unit of support biomass. In contrast to the hypothesis, the relative growth rates of all climbers were relatively low compared to the range found for self-supporting species. The biomass allocation patterns of the non-leguminous climbers were similar to those of the self-supporting species. Leguminous climbers allocated more biomass to support tissue and less biomass to leaves than non-climbers. As a result, height growth was even more emphasized in leguminous climbers than in non-leguminous climbers. Climbing legumes had high rates of net carbon gain, which partly compensated the lower relative leaf weight. We conclude that leguminous herbaceous climbers maximize height growth by a large investment in support biomass, enabling them to keep a large proportion of their leaves in the better illuminated environment at the top of the vegetation canopy.     

Relative growth rate, biomass allocation pattern and water use efficiency of three wheat cultivars during early ontogeny as dependent on water availability

We have investigated the water use efficiency of whole plants and selected leaves and allocation patterns of three wheat cultivars (Mexipak, Nesser and Katya) to explore how variation in these traits can contribute to the ability to grow in dry environments. The cultivars exhibited considerable differences in biomass allocation and water use efficiency. Cultivars with higher growth rates of roots and higher proportions of biomass in roots (Nesser and Katya) also had higher leaf growth rates, higher proportions of their biomass as leaves and higher leaf area ratios. These same cultivars had lower rates of transpiration per unit leaf area or unit root weight and higher biomass production per unit water use. They also had higher ratios of photosynthesis to transpiration, and lower ratios of intercellular to external CO₂ partial pressure. The latter resulted from large differences in stomatal conductance associated with relatively small differences in rates of photosynthesis. There was little variation between cultivars in response to drought, and differences in allocation pattern and plant water use efficiency between cultivars as found under well-watered conditions persisted under dry conditions. At the end of the non-watered treatment, relative growth rates and transpiration rates decreased to similar values for all cultivars. High ratios of photosynthesis to transpiration, and accordingly high biomass production per unit of transpiration, is regarded as a favourable trait for dry environments, since more efficient use of water postpones the decrease in plant water status.     

Plant growth analysis: towards a synthesis of the classical and the functional approach

A method of calculating relative growth rates (RGR) and net assimilation rates is presented. The method is based on the fitting of a polynomial through the relative growth rate values calculated by the 'classical' approach rather than through the In-transformed plant weights as in the 'functional' method. Additional ways of reducing the harvest-to-harvest variation characteristic of the classical approach are discussed. The main advantages of the present approach over the functional one are: (1) The degree of the polynomial can be increased (within certain limits) without inducing spurious fluctuations in RGR. Thus, quite complex trends in RGR can be described. (2) There is little interference between RGR values in different parts of the experiment. The main advantages over the classical approach are: (1) The erratic fluctuations in RGR are dampened. (2) As frequent small harvests are allowed, the workload at each harvest can be diminished and a more reliable impression of ontogenetic drift in RGR can be obtained. (3) RGR is described by a continuous function, thus facilitating further calculations and compilations.