Aim We studied dynamics of four populations of New Zealand forest birds for 5–9 years after reintroduction to islands. We primarily aimed to predict whether these populations were viable, and what, if any, management was needed to maintain them. However, the small scale of these islands also provided an opportunity to study density‐dependent population growth over a short time frame. Location We studied New Zealand robin (toutouwai, Petroica australis) and stitchbird (hihi, Notiomystis cincta) populations reintroduced to Tiritiri Matangi, a 220‐ha offshore island near Auckland, and saddleback (tieke, Philesturnus carunculatus) and stitchbird populations reintroduced to Mokoia, a 135‐ha island in Lake Rotorua. These islands are free of mammalian predators, but have highly modified habitat following clearing and regeneration. Methods We closely monitored each population, individually marking all or most of the birds and in some cases experimentally manipulated population density or food supply. We used model selection procedures to understand factors affecting survival, fecundity and dispersal, and developed stochastic simulation models. Results The Tiritiri Matangi robin and Mokoia saddleback populations grew without management and appear to be viable. Both showed strong evidence of density‐dependent growth, with fecundity (saddlebacks) and juvenile survival (both populations) declining with increasing density. Neither stitchbird population appears viable without management and supplementation experiments showed reproduction and/or survival to be limited by food supply. The Tiritiri Matangi population appears viable as long as supplementary feeding continues. However, the Mokoia population has a high mortality rate regardless of supplementary feeding, resulting in tenuous viability even with intensive management. Mokoia stitchbirds suffer from infection by Aspergillus fumigatus, a pathogenic fungus that is prevalent in highly modified habitats and more abundant on Mokoia than Tiritiri Matangi. Main conclusions Some forest birds can thrive in regenerating forest on islands and strong evidence of density dependence can be detected in such populations in as little as 5 years. This allows density‐dependent models to be developed, providing guidance when island populations are harvested for further translocations. Other species are limited by food supply in regenerating environments, a problem potentially overcome by management. However, prevalence of A. fumigatus may render highly modified environments uninhabitable by some species regardless of management.
Summary 1.Reintroductions provide a good opportunity to study density-dependent population growth, as populations can be studied at a range of densities and the change in density is not confounded with environmental conditions. An understanding of density dependence is also necessary to predict dynamics of reintroduced populations under different management regimens, and assess the extent to which they can be harvested for further reintroductions. 2. We monitored a North Island saddleback ( Philesturnus rufusater ) population for 6 years after reintroduction to Mokoia, a 135 ha island in New Zealand that was made suitable for saddlebacks by eradicating introduced Norway rats ( Rattus norvegicus ). We modelled adult and juvenile survival using Program , and modelled numbers of young fledged per pair using Proc Mixed in SAS with individual female as a random factor. 3. Juvenile survival clearly declined as the population increased, and the decline was closely correlated with the number of breeding pairs. Reproduction also showed a clear decline that was explained by two factors: a difference in quality between territories occupied immediately after reintroduction and those occupied later, and an overall decline as the number of pairs increased. Reproduction was also strongly affected by age, and this needed to be accounted for when modelling density dependence. 4. A stochastic simulation model incorporating these dynamics closely predicted the observed population growth. The equilibrium population size was insensitive to density dependence in reproduction, but highly sensitive to density dependence in juvenile survival. 5. The model is being used to plan management strategies for potential reintroductions of saddlebacks to mainland areas with predator control. The species is currently confined to predator-free islands and one fenced mainland sanctuary.
Global patterns in diversity were estimated for cyanobacteria-dominated hypolithic communities that colonize ventral surfaces of quartz stones and are common in desert environments. A total of 64 hypolithic communities were recovered from deserts on every continent plus a tropical moisture sufficient location. Community diversity was estimated using a combined t-RFLP fingerprinting and high throughput sequencing approach. The t-RFLP analysis revealed desert communities were different from the single non-desert location. A striking pattern also emerged where Antarctic desert communities were clearly distinct from all other deserts. Some overlap in community similarity occurred for hot, cold and tundra deserts. A further observation was that the producer-consumer ratio displayed a significant negative correlation with growing season, such that shorter growing seasons supported communities with greater abundance of producers, and this pattern was independent of macroclimate. High-throughput sequencing of 16S rRNA and nifH genes from four representative samples validated the t-RFLP study and revealed patterns of taxonomic and putative diazotrophic diversity for desert communities from the Taklimakan Desert, Tibetan Plateau, Canadian Arctic and Antarctic. All communities were dominated by cyanobacteria and among these 21 taxa were potentially endemic to any given desert location. Some others occurred in all but the most extreme hot and polar deserts suggesting they were relatively less well adapted to environmental stress. The t-RFLP and sequencing data revealed the two most abundant cyanobacterial taxa were Phormidium in Antarctic and Tibetan deserts and Chroococcidiopsis in hot and cold deserts. The Arctic tundra displayed a more heterogenous cyanobacterial assemblage and this was attributed to the maritime-influenced sampling location. The most abundant heterotrophic taxa were ubiquitous among samples and belonged to the Acidobacteria, Actinobacteria, Bacteroidetes, and Proteobacteria. Sequencing using nitrogenase gene-specific primers revealed all putative diazotrophs were Proteobacteria of the orders Burkholderiales, Rhizobiales, and Rhodospirillales. We envisage cyanobacterial carbon input to the system is accompanied by nitrogen fixation largely from non-cyanobacterial taxa. Overall the results indicate desert hypoliths worldwide are dominated by cyanobacteria and that growing season is a useful predictor of their abundance. Differences in cyanobacterial taxa encountered may reflect their adaptation to different moisture availability regimes in polar and non-polar deserts.
The Hihi (Stitchbird, Notiomystis cincta) is an endemic New Zealand honeyeater that after European colonization survived on only one offshore island. Attempts to reintroduce Hihi to other islands have been unsuccessful, with populations slowly declining. The main hypothesis for these declines was an inadequate year‐round supply of carbohydrate food (nectar and fruit) due to human impacts on the forest habitat. When Hihi were reintroduced to Mokoia, another island with regenerating forest, we tested whether survival was limited by carbohydrate food in the year after release. We conducted an “on‐off” experiment in which ad libitum sugar water was available to birds for 2 out of every 4 weeks. We compared the masses of individual birds at the end of on and off periods to identify times when birds lost condition with no supplementary food and would be likely to starve. We also used mark‐recapture analysis of resighting data to test whether mortality rates were higher when supplementary food was unavailable. The only effect of the supplementary food was that Hihi spent less time foraging for nectar and fruit and more time foraging for invertebrates. There was no time of year when birds lost mass when the food was taken away, and survival rates were not significantly lower when supplementary food was absent. The low (38%) annual survival rate could not be accounted for by shortage of carbohydrate food, and population viability analysis suggests that the population is likely to slowly decline. Our experiment shows that declines of reintroduced Hihi populations may be unrelated to food supply and that alternative hypotheses should be developed and tested. Our results also show the importance of using experimental methods, when possible, to test hypotheses about factors thought to be limiting reintroduced populations.
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