Carboxylate-releasing cluster roots of Proteaceae play a key role in acquiring phosphorus (P) from ancient nutrient-impoverished soils in Australia. However, cluster roots are also found in Proteaceae on young, P-rich soils in Chile where they allow P acquisition from soils that strongly sorb P. Unlike Proteaceae in Australia that tend to proficiently remobilize P from senescent leaves, Chilean Proteaceae produce leaf litter rich in P. Consequently, they may act as ecosystem engineers, providing P for plants without specialized roots to access sorbed P. We propose a similar ecosystem-engineering role for species that release large amounts of carboxylates in other relatively young, strongly P-sorbing substrates, e.g. young acidic volcanic deposits and calcareous dunes. Many of these species also fix atmospheric nitrogen and release nutrient-rich litter, but their role as ecosystem engineers is commonly ascribed only to their diazotrophic nature. We propose that the P-mobilizing capacity of Proteaceae on young soils, which contain an abundance of P, but where P is poorly available, in combination with inefficient nutrient remobilization from senescing leaves allows these species to function as ecosystem engineers. We suggest that diazotrophic species that colonize young soils with strong P-sorption potential should be considered for their positive effect on P availability, as well as their widely accepted role in nitrogen fixation. Their P-mobilizing activity possibly also enhances their nitrogen-fixing capacity. These diazotrophic species may therefore facilitate the establishment and growth of species with less-efficient P-uptake strategies on more-developed soils with low P availability through similar mechanisms. We argue that the significance of cluster roots and high carboxylate exudation in the development of young ecosystems is probably far more important than has been envisaged thus far.

Arabidopsis thaliana (L.) Heynh. has been described as a freezing-tolerant species based on freezing-resistance assays. Nonetheless, this type of experiment does not discriminate between freezing-tolerance and freezing-avoidance mechanisms. The purpose of this paper was to determine which of these two freezing-resistance mechanisms is responsible for freezing resistance in A. thaliana. This was achieved by comparing the thermal properties (ice-nucleation temperature and the freezing temperature) of leaves and the lethal temperature to 10, 50 and 90% of the plants (LT₁₀, LT₅₀, and LT₉₀, respectively). Two wild-type genotypes were used (Columbia and Ler) and their mutants (esk-1 and frs-1, respectively), which differ in their freezing resistance. This study's results indicated that the mutant esk-1, described as a freezing-tolerant species showed freezing tolerance only after a cold-acclimation period. The mutant frs-1, described as freezing sensitive, presented freezing avoidance. Both wild genotypes presented LT₅₀ similar to or higher than the ice-nucleation temperature. Thus, the main freezing-resistance mechanism for A. thaliana is avoidance of freezing by supercooling. No injury of the photosynthetic apparatus was shown by measuring the maximal photochemical efficiency (F_v/F_m) and pigments (chlorophyll and carotenoid) during cold acclimation in all genotypes. During cold acclimation, Columbia and esk-1 increased total soluble carbohydrates in leaves. esk-1 was the only genotype that presented freezing tolerance after cold acclimation. This feature could be related to an increase in sugar accumulation in the apoplast.

Colobanthus quitensis is one of only two vascular plant species that occur in the Antarctic islands. We evaluated morphological and physiological traits and survival after freezing in individuals of C. quitensis collected in two populations: one from the Andes of central Chile and the other from the maritime Antarctic. We addressed whether these populations are ecotypes in terms of shoot morphology and physiology, and cold resistance. We also evaluated genetic differentiation at the internal transcribed spacer (ITS) regions. Under controlled growing conditions, Andean plants had longer and narrower leaves and longer peduncles. However, shoot biomass was similar in both populations. There was a 1.17% sequence divergence of ITS regions between populations. Survival to freezing at temperatures from 0° to −16°C was not different in nonacclimated plants. After cold-acclimation at 4°C, freezing tolerance was greater in Antarctic plants. Both Andean and Antarctic plants increased soluble sugars with inc...

Summary: Proteaceae species in south‐western Australia thrive on phosphorus‐impoverished soils, employing a phosphorus‐mining strategy involving carboxylate‐releasing cluster roots. Some develop symptoms of phosphorus toxicity at slightly elevated soil phosphorus concentrations, due to their low capacity to down‐regulate phosphorus uptake. In contrast, Proteaceae species in Chile, e.g.Embothrium coccineumJ.R. Forst. & G. Forst., occur on volcanic soils, which contain high levels of total phosphorus, but phosphorus availability is low. We hypothesised that the functioning of cluster roots ofE. coccineumdiffers from that of south‐western Australian Proteaceae species, in accordance with the difference in soil phosphorus status. With more phosphorus to be gained from the soil with high levels of total phosphorus, we expect less investment in biomass and more release of carboxylates. Furthermore, we hypothesised thatE. coccineumregulates its phosphorus‐uptake capacity, avoiding phosphorus toxicity when grown at elevated phosphorus levels. To test these hypotheses,E. coccineumseedlings were grown at a range of phosphorus supplies in nutrient solution. We show thatE. coccineumallocated at least five times less biomass to cluster roots that released at least nine times more carboxylates per unit cluster root weight compared with south‐western Australian species (e.g.Banksia,Hakea). The highest phosphorus supply caused a growth inhibition and high leaf phosphorus concentration, without symptoms of phosphorus toxicity. We accept our hypotheses on the functioning of cluster roots and the high capacity to reduce the net phosphorus uptake in plants grown at a high‐phosphorus supply. This novel combination of traits indicates divergent functioning of Proteaceae species from southern South America, exposed to frequent phosphorus input due to volcanic activity, in contrast with the functioning of south‐western Australian Proteaceae species that thrive on severely phosphorus‐impoverished soils. These traits could explain the functioning ofE. coccineumon soils that are rich in total phosphorus, but with a low concentration of available phosphorus.