Who goes first? Condition and danger dependent pioneering in a group-living bark beetle (Dendroctonus ponderosae)

Among group-living organisms, some individuals initiate groups by being the first to attack a prey item or the first to colonize a new settlement site. In the group-living mountain pine beetle (Dendroctonus ponderosae), first attackers (known as pioneers) on live trees suffer higher mortality due to tree defenses than do beetles that join aggregations. This study examined factors that affect an individual’s propensity to initiate an aggregation. When placed on an unoccupied tree, the probability of successfully entering the tree was positively correlated with body condition (residual of mass versus length regression). However, beetles in better condition took longer to initiate tunnel construction than those in poorer condition, suggesting that pioneering is a “desperation” strategy used when low energy reserves preclude further dispersal or when potential trees are rare. These contrasting patterns suggest pioneering is a nonlinear behavioral response, such that beetles with the smallest energy reserves and beetles with the greatest energy reserves both avoid pioneering. We further found that pioneering was more likely when the environment favored success, such as in smaller diameter trees (which may have weaker defenses) and earlier in the season (when the probability of recruiting conspecifics is higher). Our results suggest that pioneers incorporate both internal and external variables in their decision to attack an uncolonized tree.     

Correlates of group size in a cooperatively breeding cichlid fish (Neolamprologus pulcher)

Neolamprologus pulcher, a cooperatively breeding cichlid fish from Lake Tanganyika, lives in permanent social groups comprising one breeding pair and helpers of both sexes. Variation in group size (1-14 helpers) provides an opportunity to investigate factors that affect how many helpers remain in a group and in turn how group size affects reproductive success. This field study showed that larger groups live in larger territories with more shelter. Group size was more strongly correlated with territory quality than with breeder size. Experimental enhancement of territory quality did not affect group size but group size decreased when territory quality was reduced. Breeders living in a large group benefit because such individuals feed more often and have lower workloads and greater reproductive success. Helpers in larger groups also fed more frequently but did not have lower workloads. This is one of the first experimental studies to examine the factors influencing group size in cooperative breeders.     

Corridor Length and Patch Colonization by a Butterfly, Junonia coenia

Abstract: Corridors have been proposed to reduce isolation and increase population persistence in fragmented landscapes, yet little research has evaluated the types of landscapes in which corridors will be most effective. I tested the hypothesis that corridors increase patch colonization by a butterfly, Junonia coenia , regardless of the butterfly's initial distance from a patch. I chose J. coenia because it has been shown to move between patches preferentially through corridors. Individuals were released 16–192 m away from open experimental patches into adjacent open corridors or forest. Neither corridors nor distance had a significant effect on patch colonization, but there was a significant interaction between the presence or absence of corridors and distance. At small distances (16–64 m), J. coenia was more likely to colonize open patches when released within forest than within open corridors, most likely because J. coenia used corridors as habitat. Nevertheless, patch colonization by butterflies released within forest decreased rapidly as distance from patches increased, as predicted by a null model of random movement. Colonization did not change with distance in the corridor, and at long distances (128–192 m), butterflies released in corridors were twice as likely to colonize open patches as those released in forest. These results suggest that one critical factor, interpatch distance, may determine the relative effectiveness of corridors and other landscape configurations, such as stepping stones, in reducing isolation in fragmented landscapes. When distances between patches are short compared to an animal's movement ability, a stepping stone approach may most effectively promote dispersal. Alternatively, the conservation value of corridors is highest relative to other habitat configurations when longer distances separate patches in fragmented landscapes.     

Is it possible to mitigate greenhouse gas emissions in pastoral ecosystems of the tropics?

Climate change science has been discussed and synthesized by the world's best minds at unprecedented scales. Now that the Kyoto Protocol may become a reality, it is time to be realistic about the likelihood of success of mitigation activities. Pastoral lands in the tropics hold tremendous sequestration potential but also strong challenges to potential mitigation efforts. Here we present new analyses of the global distribution of pastoral systems in the tropics and the changes they will likely undergo in the next 50 years. We then briefly summarize current mitigation options for these lands. We then conclude by attempting a pragmatic look at the realities of mitigation. Mitigation activities have the greatest chance of success if they build on traditional pastoral institutions and knowledge (excellent communication, strong understanding of ecosystem goods and services) and provide pastoral people with food security benefits at the same time.     

Much ado about nothings: using zero similarity points in distance-decay curves

Distance decay is used to describe the (usually exponential) decay in ecological similarity of assemblages between two sites as a function of their distance apart along an environmental gradient. Exponential distance-decay curves are routinely fitted by calculating the ecological similarity between each pair of sites, and fitting a linear regression to the points on a scatter plot of log-similarity vs. distance (x-axis). However, pairs of sites where the assemblages have no species in common pose a problem, because the similarity is zero, and the log transformation cannot be applied. Common fixes to this problem (i.e., either removing or transforming the zero values) are shown to have undesirable consequences and to give widely disparate estimates. A new method is presented as a special case of a generalized dissimilarity model. It is fitted very quickly and easily using existing software, and it does not require removal or transformation of the zero similarity points. Its simplicity makes it convenient for use in conjunction with the resampling methods that are routinely employed to test hypotheses, to obtain standard errors of estimated parameters, or to compare distance-decay curves. A word of caution about standard application of the bootstrap is noted, and modified bootstrap and jackknife alternatives are demonstrated.     

Patterns of egg yolk antioxidant co-variation in an avian brood parasite–host system

Despite their importance to offspring fitness outcomes, there has been little previous work on egg-mediated maternal effects in avian brood parasites which lay their eggs in the nests of other species. Here, we examine patterns of egg yolk antioxidant deposition in an avian host (red-winged blackbird, Agelaius phoeniceus) and their brood parasite (brown-headed cowbird, Molothrus ater). Cowbird nestlings compete directly for food with host blackbird chicks and succeed, despite hatching from a smaller egg, by begging more intensely and growing as or more rapidly than their hosts. Dietary-derived antioxidants, such as carotenoids and vitamins E and A, deposited in egg yolk, may enhance growth rate and reduce oxidative stress, and therefore provide a potential mechanism by which female cowbirds could enhance the competitiveness of their young in host nests. However, provision of antioxidants to eggs is costly so we predicted that female cowbirds should adjust the amount of antioxidants in response to variation in host quality. We found that whilst red-winged blackbird clutches parasitised by cowbirds did not differ in the pattern of antioxidant deposition compared to non-parasitised clutches, levels of vitamin E deposited in cowbird eggs were closely matched to that of the individual host clutch in which cowbirds laid their egg. This supports the prediction that female cowbirds adjust the antioxidant concentration of their eggs to increase the likely competitiveness of their offspring in the host nest into which they are laid and may help explain the success of cowbirds in competing with larger host young.     

Lessons in Ecosystem Management from Management of Threatened and Pest Loranthaceous Mistletoes in New Zealand and Australia

Loranthaceous mistletoes are interesting because of their complex dependence on suitable host trees and avian dispersers and because of their patchy distribution at the landscape level. Although their over- and under-abundance in Australia and New Zealand have been widely documented, little attention has been given to the need for an ecosystem approach to their management. Although the current status of mistletoes is very different in Australia and New Zealand, some of the causal factors and the long-term effects of changes in mistletoe abundance are similar in the two countries. We suggest that mistletoe abundance in pre-European landscapes was dependent on a series of evolutionary and environmental filters relating to host specificity, pollination, dispersal, infection, environmental habitat quality, predation, and disturbance. European settlement modified these filters in a number of ways, resulting in either increases or decreases in mistletoe abundance. The three broad groups of changes that have occurred with European settlement involve fragmentation, predation, and altered disturbance regimes. Although managers have usually addressed mistletoe over- or under-abundance with short-term solutions (e.g., pruning infected trees), we suggest that management must address the underlying causes of the problems involving mistletoes. This requires an ecosystem approach to management that addresses both the direct and indirect causes of the current status of mistletoes.