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1 Five temperate floras were studied to assess to what extent seed size correlations with other plant attributes are consistent across floras. The floras were from three continents: Australia (semiarid woodlands of western New South Wales, arid woodlands of Central Australia, and the Sydney region), North America (Indiana Dunes) and Europe (Sheffield region, UK). The plant attributes used were growth form, plant height, perenniality and dispersal mode. We used general linear models to consider not only the primary correlations between seed size and each other attribute, but also the overlap patterns among correlations to determine if each correlation could be interpreted as a secondary effect via a third variable. 2 Plant height and growth form were consistently correlated with the largest proportion of log seed mass variation (up to 37% in Central Australia). Although there was strong overlap in the amount of log seed mass variation explained by the two attributes (6-22%), each could explain small but significant variation after the other in all floras. The strong association between growth form/plant height and seed size was found not only among unassisted and wind-adapted species, but also among species dispersed by other means. 3 In all floras, dispersal mode was also able to account for significant variation in log seed mass independently of growth form and plant height. The association between plant perenniality and seed size could be explained as a secondary correlation of growth form and plant height with both seed size and perenniality. 4 There were significant differences in log seed mass among the five floras. However, seed size ranged over at least five orders of magnitude in each flora. Differences between floras could account for relatively little (4%) of the variation in seed size between species, compared to the attributes growth form (20%), plant height (20%) and dispersal mode (29%), despite the quite different soils and climates of the five floras. This suggests that seed size is more strongly associated with other plant attributes than with the environmental conditions for establishment. It appears that within any one community, plants have found a diversity of possible solutions to the problems of seedling establishment, resulting in a wide range of log seed mass.

Summary1. We provide a brief overview of progress in our understanding of introduced plant species. 2. Three main conclusions emerge from our review: (i) Many lines of research, including the search for traits that make species good invaders, or that make ecosystems susceptible to invasion, are yielding idiosyncratic results. To move forward, we advocate a more synthetic approach that incorporates a range of different types of information about the introduced species and the communities and habitats they are invading. (ii) Given the growing evidence for the adaptive capacity of both introduced species and recipient communities, we need to consider the implications of the long-term presence of introduced species in our ecosystems. (iii) Several foundational ideas in invasion biology have become widely accepted without appropriate testing, or despite equivocal evidence from empirical tests. One such idea is the suggestion that disturbance facilitates invasion. 3. We use data from 200 sites around the world to provide a broad test of the hypothesis that invasions are better predicted by a change in disturbance regime than by disturbance per se. Neither disturbance nor change in disturbance regime explained more than 7% of the variation in the % of cover or species richness contributed by introduced species. However, change in disturbance regime was a significantly better predictor than was disturbance per se, explaining approximately twice as much variation as did disturbance. 2012, 100, 116-127 doi: 10.1111/j.1365-2745.2011.01915.x 4. Synthesis. Disturbance is a weak predictor of invasion. To increase predictive power, we need to consider multiple variables (both intrinsic and extrinsic to the site) simultaneously. Variables that describe the changes sites have undergone may be particularly informative. Journal of Ecology

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Summary• It has long been believed that plant species from the tropics have higher levels of traits associated with resistance to herbivores than do species from higher latitudes. A meta-analysis recently showed that the published literature does not support this theory. However, the idea has never been tested using data gathered with consistent methods from a wide range of latitudes.• We quantified the relationship between latitude and a broad range of chemical and physical traits across 301 species from 75 sites world-wide.• Six putative resistance traits, including tannins, the concentration of lipids (an indicator of oils, waxes and resins), and leaf toughness were greater in highlatitude species. Six traits, including cyanide production and the presence of spines, were unrelated to latitude. Only ash content (an indicator of inorganic substances such as calcium oxalates and phytoliths) and the properties of species with delayed greening were higher in the tropics.• Our results do not support the hypothesis that tropical plants have higher levels of resistance traits than do plants from higher latitudes. If anything, plants have higher resistance toward the poles. The greater resistance traits of high-latitude species might be explained by the greater cost of losing a given amount of leaf tissue in low-productivity environments.

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SummaryMost plant species have a range of traits that deter herbivores. However, understanding of how different defences are related to one another is surprisingly weak. Many authors argue that defence traits trade off against one another, while others argue that they form coordinated defence syndromes.We collected a dataset of unprecedented taxonomic and geographic scope (261 species spanning 80 families, from 75 sites across the globe) to investigate relationships among four chemical and six physical defences.Five of the 45 pairwise correlations between defence traits were significant and three of these were tradeoffs. The relationship between species' overall chemical and physical defence levels was marginally nonsignificant (P = 0.08), and remained nonsignificant after accounting for phylogeny, growth form and abundance. Neither categorical principal component analysis (PCA) nor hierarchical cluster analysis supported the idea that species displayed defence syndromes.Our results do not support arguments for tradeoffs or for coordinated defence syndromes. Rather, plants display a range of combinations of defence traits. We suggest this lack of consistent defence syndromes may be adaptive, resulting from selective pressure to deploy a different combination of defences to coexisting species.

Abstract. Harsh conditions in arid and semi‐arid environments make seedling establishment rare. Plant recruitment in arid environments often occurs only in years with above average rainfall or in safe sites under the canopy of nurse plants that provide shelter from high temperatures and low moisture. Associations of establishing seedlings with adult plants are referred to as nurse‐protégé interactions and are thought to be commensalisms in which seedlings benefit from the micro‐environment created by adult plants with no effect for the latter. This phenomenon is thought to be more frequent in harsh than in mild environments and appears to occur frequently in deserts and arid and semi‐arid biomes. Here, we investigate whether nurse‐protégé interactions are more common in arid environments by searching the published literature from the previous 92 years using the terms nurse plants, protégé plants, facilitation, nucleation and facultative mutualism. We then quantitatively compared these reports from arid zones to other environments. A total of 296 papers were found which referred to nurse‐protégé interactions. More than half (158) focused on arid and semi‐arid zones. This information was also used to explore hypotheses of potential causative forces that might have selected for such interactions in the arid zones such as seed trapping, nutrient, moisture, protection from browsing or trampling and support availability. Because of the large number of different nurse species (147, from 98 genera and 40 families) and protégé species (429, from 273 genera and 84 families), described across a diversity of environments, we suggest that there may be more than one causative factor selecting for nurse‐protégé interactions in arid and semi‐arid environments.