Resource manipulation reveals interactive phenotype-dependent foraging in free-ranging lizards.

Recent evidence suggests that individuals differ in foraging tactics and this variation is often linked to an individual's behavioural type (BT). Yet, while foraging typically comprises a series of search and handling steps, empirical investigations have rarely considered BT-dependent effects across multiple stages of the foraging process, particularly in natural settings. In our long-term sleepy lizard (Tiliqua rugosa) study system, individuals exhibit behavioural consistency in boldness (measured as an individual's willingness to approach a novel food item in the presence of a threat) and aggressiveness (measured as an individual's response to an 'attack' by a conspecific dummy). These BTs are only weakly correlated and have previously been shown to have interactive effects on lizard space use and movement, suggesting that they could also affect lizard foraging performance, particularly in their search behaviour for food. To investigate how lizards' BTs affect their foraging process in the wild, we supplemented food in 123 patches across a 120-ha study site with three food abundance treatments (high, low and no-food controls). Patches were replenished twice a week over the species' entire spring activity season and feeding behaviours were quantified with camera traps at these patches. We tracked lizards using GPS to determine their home range (HR) size and repeatedly assayed their aggressiveness and boldness in designated assays. We hypothesised that bolder lizards would be more efficient foragers while aggressive ones would be less attentive to the quality of foraging patches. We found an interactive BT effect on overall foraging performance. Individuals that were both bold and aggressive ate the highest number of food items from the foraging array. Further dissection of the foraging process showed that aggressive lizards in general ate the fewest food items in part because they visited foraging patches less regularly, and because they discriminated less between high and low-quality patches when revisiting them. Bolder lizards, in contrast, ate more tomatoes because they visited foraging patches more regularly, and ate a higher proportion of the available tomatoes at patches during visits. Our study demonstrates that BTs can interact to affect different search and handling components of the foraging process, leading to within-population variation in foraging success. Given that individual differences in foraging and movement will influence social and ecological interactions, our results highlight the potential role of BT's in shaping individual fitness strategies and population dynamics.

Vessel diameter and related hydraulic traits of 31 Eucalyptus species arrayed along a gradient of water availability.

We present two comprehensive data sets that describe xylem vessel diameters and related sapwood traits for species of Eucalyptus from arid and semi-arid woodlands and forests in Australia. Between 2009 and 2014, sapwood of mature trees was sampled in south-western, south-eastern and eastern Australia. One additional species was sampled from tropical north-western Australia. The first data set describes samples collected from the basal stem section (130 cm above ground) of three individuals of 31 species of which eight species were replicated at sites that differed in climatic conditions. The second data set describes vessel characteristics of three trees from each of 10 species that were sampled at 8 m below the tree apex. The sampled trees of these 10 species are also part of the first data set. In total, we report diameters (D) for over 25 100 vessels, from 494 digital images taken from 117 trees. We also report vessel frequencies, void-to-wood ratios, sapwood densities and hydraulically weighted vessel diameters (Dh). Supporting data of the first data set include tree diameter at breast height (130 cm above ground), tree height, sample locations, and summary climate data. In this data set, diameter of individual vessels ranges from 10 to over 300 µm, and vessel frequency from 360 to 9070 vessels cm-2 . Wood density ranges from 0.47 to 0.96 g cm-3 . Void-to-wood ratio ranges from 6% to 27% and Dh ranges from 46 to 236 µm. Mean annual rainfall (P) at sample sites ranges from 246 to 2274 mm and FAO56 reference evaporation (E) from 777 to 2110 mm. The aridity index (E/P) ranges from 0.15 to 2.93 (dimensionless). Tree diameters range from 9 to 90 cm and tree heights range from 6 to 70 m. D and Dh in the second data set range from 11 to 271 and 68 to 205 µm, respectively. These datasets will make a valuable contribution to future continental-scale and global-scale studies of the relationship between xylem hydraulic architecture and climate. The data sets are unique in the sense that they are phylogenetically constrained, allowing in-depth assessment of plasticity of hydraulic attributes within a single tree genus.

Climate determines vascular traits in the ecologically diverse genus Eucalyptus.

Current theory presumes that natural selection on vascular traits is controlled by a trade-off between efficiency and safety of hydraulic architecture. Hence, traits linked to efficiency, such as vessel diameter, should show biogeographic patterns; but critical tests of these predictions are rare, largely owing to confounding effects of environment, tree size and phylogeny. Using wood sampled from a phylogenetically constrained set of 28 Eucalyptus species, collected from a wide gradient of aridity across Australia, we show that hydraulic architecture reflects adaptive radiation of this genus in response to variation in climate. With increasing aridity, vessel diameters narrow, their frequency increases with a distribution that becomes gradually positively skewed and sapwood density increases while the theoretical hydraulic conductivity declines. Differences in these hydraulic traits appear largely genotypic in origin rather than environmentally plastic. Data reported here reflect long-term adaptation of hydraulic architecture to water availability. Rapidly changing climates, on the other hand, present significant challenges to the ability of eucalypts to adapt their vasculature.