No abstract

The Xishuangbanna tropical rainforest in Yunnan Province is the greatest biodiversity hotspot in China. However, the biodiversity of this region is under threat, making seed conservation through seed and/or germplasm banking particularly urgent and crucial. Seed desiccation sensitivity limits the possibility of seed banking of 47% of tropical rainforest species. Thus, knowing if a species has desiccation-sensitive seeds is an important first step in seed banking; however, often resources are limited, making it difficult to determine storage behaviour for all the species in a region. Prediction of seed sensitivity using the SCR-SM model based on seed-coat ratio (SCR) and seed dry mass (SM) might be an alternative for determining desiccation sensitivity of seeds of each species. Here, seed-desiccation sensitivity of 101 woody species from the Xishuangbanna tropical forest were analysed using this model, and physiological determinations were made for a total of 25 species. Seed storage behaviour for 59 species was used for model validation, and storage behaviour of 88% of these species was successfully predicted. Seed storage behaviour of 83% of the 59 species was successfully predicted using the 1000-seed weigth-moisture content (TSW-MC) criteria, which include seeds with 1000-seed weight >500 g and seed moisture content at shedding of 30 -70%. The two predictive methods were subsequently used to predict seed desiccation sensitivity for another 42 species from Xishuangbanna whose storage behaviour was uncertain. Our results indicated that~50% of the species in Xishuangbanna are likely to have desiccation-sensitive seeds.Journal compilation Ó CSIRO 2014 www.publish.csiro.au/journals/ajb PðD À SÞ ¼ e 3:269À9:974aþ2:156b 1 þ e 3:269À9:974aþ2:156b ;where a is SCR and b is log 10 (seed mass) in g. For estimation of P(D-S), seed mass should range between 0.01 mg and 24 g, and SCR between 0 and 1. When P(D-S) > 0.5, seeds are likely to be desiccation-sensitive, and when P(D-S) < 0.5 seeds are likely to be desiccation-tolerant. The TSW-MC criteria for identificationAccording to the TSW-MC criteria (Chin et al. 1984;Hong and Ellis 1996), seeds with a TSW of >500 g and MC of >30% are desiccation-sensitive. In our study, seed storage behaviour of 306 Australian Journal of Botany Q. Lan et al.

Foliar endophytic fungi (FEF) are diverse and ubiquitously associated with photosynthetic land plants. However, processes shaping FEF assemblages remain poorly understood. Previous studies have indicated that host identity and host habitat are contributing factors, but these factors are often difficult to disentangle. In this study, we studied FEF assemblages from plants grown in a botanical garden, enabling us to minimize the variation in abiotic environmental conditions and fungal dispersal capacity. FEF assemblages from 46 Ficus species were sequenced using next‐generation methods, and the results indicated that closely related host species had clearly differentiated FEF assemblages. Furthermore, host phylogenetic proximity was significantly correlated with the similarity of their FEF assemblages. In the canonical correspondence analysis, eleven leaf traits explained 32.9% of the total variation in FEF assemblages, whereas six traits (specific leaf area, leaf N content, leaf pH, toughness, latex alkaloid content, and latex volume per leaf area) were significant in the first two dimensions of ordination space. In the multiple regression on distance matrix analysis, 21.0% of the total variance in FEF assemblage was explained by both host phylogeny and leaf traits while phylogeny alone explained 7.9% of the variance. Thus, our findings suggest that both evolutionary and ecological processes are involved in shaping FEF assemblages.

Plant compensatory regrowth is an induced process that enhances plant tolerance to herbivory. Plant behavior against herbivores differs between species and depends on resource availability, thus making general predictions related to plant compensatory regrowth difficult. To understand how soil nutrients determine the degree of compensatory regrowth for different plant species, we selected saplings of three Ficus species and treated with herbivore insects and artificial injury in both glasshouse conditions and in the field at two soil nutrient levels. Compensatory regrowth was calculated by biomass, relative growth rate and photosynthetic characteristics. A similar pattern was found in both the glasshouse and in the field for species F. hispida, where overcompensatory regrowth was triggered only under fertile conditions, and full compensatory regrowth occurred under infertile conditions. For F. auriculata, overcompensatory regrowth was stimulated only under infertile conditions and full compensatory regrowth occurred under fertile conditions. Ficus racemosa displayed full compensatory regrowth in both soil nutrient levels, but without overcompensatory regrowth following any of the treatments. The three Ficus species differed in biomass allocation following herbivore damage and artificial injury. The root/shoot ratio of F. hispida decreased largely following herbivore damage and artificial injury, while the root/shoot ratio for F. auriculata increased against damage treatments. The increase of shoot and root size for F. hispida and F. auriculata, respectively, appeared to be caused by a significant increase in photosynthesis. The results indicated that shifts in biomass allocation and increased photosynthesis are two of the mechanisms underlying compensatory regrowth. Contrasting patterns among the three Ficus species suggest that further theoretical and empirical work is necessary to better understand the complexity of the plant responses to herbivore damage.