Two mycotrophic species (Lactuca sativa and Abutilon theophrasti) and one nonmycotrophic species (Beta vulgaris) were grown in a P-deficient soil, and the effects of mycorrhizal inoculation on three variables that determine growth rate were assessed for each. The phosphorus-use efficiency (PUE, dW/dP) is the ratio of d. wt increase to P content increase. Plant P is the amount of P (the limiting resource) controlled by the plant, which can be allocated to various purposes. The phosphorus efficiency index (PEI, dP/Pdt) is the efficiency with which plant P is used to acquire P from the soil. Inoculated and control plants of a given species initially contained the same amount of P because all plants were grown from seed. Mycorrhizal colonization significantly increased the PEI of Lactuca and Abutilon (by 23 and 32%, respectively). As expected, mycorrhizal inoculation did not significantly increase the PEI of Beta. As a result, mycorrhizal inoculation significantly increased the P content of Lactuca and Abutilon, but not Beta. Mycorrhizal colonization decreased the PUE of lettuce, but did not significantly affect that of Abutilon or Beta. Mycorrhizal inoculation therefore slightly increased the growth rate of Lactuca, greatly increased the growth rate of Abutilon, and ultimately had no significant effect on the growth rate of Beta.

Relationships between nitrogen (N) content and growth are routinely measured in plants. This study determined the effects of N on the separate morphological and physiological components of plant growth, to assess how N-limited growth is effected through these components. Lettuce (Lactuca sativa) plants were grown hydroponically under contrasting N-supply regimes, with the external N supply either maintained continuously throughout the period of study, or withdrawn for up to 14 d. Richards' growth functions, selected using an objective curve-fitting technique, accounted for 99.0 and 99.1% of the variation in plant dry weight for control and N-limited plants respectively. Sublinear relationships occurred between N and relative growth rates under restricted N-supply conditions, consistent with previous observations. There were effects of treatment on morphological and physiological components of growth. Leaf weight ratio increased over time in control plants and decreased in N- limited plants. Shoot:root ratio followed a similar pattern. On a whole-plant basis, assimilation of carbon decreased in N-limited plants, a response paralleled by differences in stomatal conductance between treatments. Changes in C assimilation, expressed as a function of stomatal conductance to water vapour, suggest that the effects of N limitation on growth did not result directly from a lack of photosynthetic enzymes. Relationships between plant N content and components of growth will depend on the availability of different N pools for remobilization and use within the plant.

Most recent reviews of plant salinity response have included the concept of a nutritional disturbance as one likely mechanism by which shoot growth might be inhibited. None the less, few studies of dicotyledonous plants have presented data on nutrient transport into the most intensively growing shoot tissues. In this paper net nutrient deposition was followed for 3 d in 8 sequential, growing leaves of Lactuca sativa, which were grown either in conditions of moderate salinization, or in a growth-stimulating concentration of NaCl. The nutrient deposition was studied from 0.7 to 3.7 d following completion of stepwise salinization. This deposition was followed in immature leaves, which had attained only 1–2% of ultimate leaf mass by the completion of the study. In such young leaves development is still dominated by cell division. The transport of Ca2+ specifically to the youngest leaves was reduced by more than twice as much as was K+ transport. Transport of the other major divalent cationic nutrient, Mg2+, was not decreased for these leaves. The factors of increase for Na+ and Cl− after 3.7 d after completion of salinization averaged 152 and 62% over control levels for the three youngest leaves (for Na+ and Cl−, respectively). Though significant, these increases were only 27 and 14% as great as increases in three leaf sets of more developed growing leaves. Decreases in net K+ deposition and leaf K+ concentration were not greater for the youngest than they were for the oldest leaves. Net S deposition was reduced 44% more in younger than older growing leaves, but for most leaves not beyond the level expected due to reduced sink strength. The reduction in net P deposition also seemed more related to reduced sink strength, but was reduced to approx. 50% in both younger and more developed growing leaves. While Fe concentration was not reduced by salinization at any developmental stage, Zn2+ net transport and Zn concentration were both reduced in the two youngest leaves (57 and 70%, respectively). Given the moderate treatment imposed (Na:Ca ratio of 22) the results suggest that Ca2+ transport to the youngest leaves is probably highly sensitive to salinization of the root medium and is perhaps a key physiological response in the inhibition of leaf growth.