A common response to low phosphorus availability is increased relative biomass allocation to roots. The resulting increase in root:shoot ratio presumably enhances phosphorus acquisition, but may also reduce growth rates by diverting carbon to the production of heterotrophic rather than photosynthetic tissues. To assess the importance of increased carbon allocation to roots for the adaptation of plants to low P availability, carbon budgets were constructed for four common bean genotypes with contrasting adaptation to low phosphorus availability in the field ("phosphorus efficiency"). Solid-phase-buffered silica sand provided low (1 microM), medium (10 microM), and high (30 microM) phosphorus availability. Compared to the high phosphorus treatment, plant growth was reduced by 20% by medium phosphorus availability and by more than 90% by low phosphorus availability. Low phosphorus plants utilized a significantly larger fraction of their daytime net carbon assimilation on root respiration (c. 40%) compared to medium and high phosphorus plants (c. 20%). No significant difference was found among genotypes in this respect. Genotypes also had similar rates of P absorption per unit root weight and plant growth per unit of P absorbed. However, P-efficient genotypes allocated a larger fraction of their biomass to root growth, especially under low P conditions. Efficient genotypes had lower rates of root respiration than inefficient genotypes, which enabled them to maintain greater root biomass allocation than inefficient genotypes without increasing overall root carbon costs.

The role of interspecific interactions among herbivorous insects is considered to be limited, especially in specialist communities. In the current study we report on exploitative interspecific interaction between two closely related phloem—feeding species of gall—forming aphids (Homoptera; Pemphigidae; Fordinae), mediated by the supply of photoassimilates from the host plant. Geoica sp. forms a spherical gall on the leaflet midrib of Pistacia palaestina (Anacardiaceae), while Forda formicaria forms crescent—shaped galls on the leaflet margin of the same host plant. Using 14C labeling, we were able to trace the food supply (assimilated carbohydrates) from the leaves to galls of each species. We found that Geoica galls are strong sinks. These galls divert the normal phloem transport of the plant and reduce the amount of assimilates imported by F. formicaria, especially when they are located on the same leaflet. By the end of the season Geoica caused death of 84% of F. formicaria galls that were located on the same leaflet, and reduced reproductive success in the surviving galls by 20%. This is because the presence of Geoica causes early senescence (but not abscission) of the leaflet it is on (whether or not F. formicaria is present). The interaction is asymmetrical: F. formicaria did not affect reproductive output of Geoica nor did it cause visible damage to the leaflets. To our knowledge, this it the first demonstration of exploitation competition for plant assimilates between two insect—induced sinks. This exploitative competition, mediated by manipulation of plant phloem transport, stands in contrast to the absence of interference competition for galling sites between the two aphid species. Although their spatial distributions partly overlapped, the niche breadth of each species (measured from gall positions on leaves along the shoot axis) was not affected by the presence of the other. Moreover, when both species were located on the same leaf, they formed galls independently on the same or different leaflets, and there was no indication of interference competition over galling sites.

Photosynthetic rates of seagrasses have until recently been measured a s gas exchange of chamber-enclosed leaves mainly in the laboratory, and in situ measurements under natural conditions are scarce. In this work we explore the possibility of rneasunng such rates by pulse amplitude modulated (PAM) fluorometry, using a newly developed underwater device. This was done by first comparing photosynthetic O2 evolution (net photosynthesis corrected for dark respiration) with rates of electron transport (ETR) derived from fluorescen.ce measurements of the effective quantum yield of photosystem I1 multiplied with the estlnlated photon flux of photosynthetic active radiation absorbed by this photosystem. In the field, ETRs were then measured both as rapid light curves (RLCs) and by in situ point measurements under ambient light during the day. Photosynthetic O2 volution showed a linear relationship with ETR within a range of irradiances for the Mediterranean seagrass Cymodocea nodosa, while the tropical Halophila stipulacea and a temperate intertidal population of Zostera marina exhibited decreasing O2 evolution rates relative to ETRs at high lrradiances. These differences are likely due to photorespiration, w h~c h is absent in C. nodosa. The molar ratio between photosynthetic O2 evolution and ETR within the range of their linear relationship was found to be 0.3 for C. nodosa, which is close to the theoretical stoichiometric ratio of 0.25, but was higher and lower for 2. manna and H. stjpulacea, respectively. Point measurements of ETR in the field showed good agreements wlth rates derived from RLCs for H. stipulacea and Z. marina, but values varied greatly between replicate measurements for C. nodosa a t high irradiances. It is speculated that this variation was partly due to lightflecks caused by waves in the shallow water where these measurements were done. In all, this work shows that PAM fluorometry can efficiently yield photosynthetic rates for seagrasses in the laboratory, without the typical lag experienced by O2 electrodes, a s well a s in situ under natural conditions which are not disturbed by enclosures.

Recruiting wild halophytes with economic potential was suggested several decades ago as a way to reduce the damage caused by salinization of soil and water. A range of cultivation systems for the utilization of halophytes have been developed, for the production of biofuel, purification of saline effluent in constructed wetlands, landscaping, cultivation of gourmet vegetables, and more. This review critically analyses past and present halophyte-based production systems in the context of genetics, physiology, agrotechnical issues and product value. There are still difficulties that need to be overcome, such as direct germination in saline conditions or genotype selection. However, more and more research is being directed not only towards determining salt tolerance of halophytes, but also to the improvement of agricultural traits for long-term progress.

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The contribution of each of the salt‐transporting processes to the NaCl balance of the leaves of the salt‐recreting mangrove Avicennia marina (Forssk.) Vierh. was quantitatively investigated. Transpiration rates, xylem sap concentration, leaf salt content, recretion rates and rates of salt retranslocation out of the leaves were continuously monitored during three day periods and the salt fluxes in and out of the leaves were calculated. The results indicated that salt filtration by the roots is by far the most important salt‐rejecting mechanism, preventing some 80% of the salt which is carried towards the root surface by the transpiration stream, from entering the shoot. Out of the remaining quantity of salts which enter the root xylem and reach the leaves, only 40% is removed by the salt‐recreting glands.

Knowledge of belowground structures and processes is essential for understanding and predicting ecosystem functioning, and consequently in the development of adaptive strategies to safeguard production from trees and woody plants into the future. In the past, research has mainly been concentrated on growth models for the prediction of agronomic or forest production. Newly emerging scientific challenges, e.g. climate change and sustainable development, call for new integrated predictive methods where root systems development will become a key element for understanding global biological systems. The types of input data available from the various branches of woody root research, including biomass allocation, architecture, biomechanics, water and nutrient supply, are discussed with a view to the possibility of incorporating them into a more generic developmental model. We discuss here the main focus of root system modelling to date, including a description of simple allometric biomass models, and biomechanical stress models, and then build in complexity through static growth models towards architecture models. The next progressive and logical step in developing an inclusive developmental model that integrates these modelling approaches is discussed.

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