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Rodent eradications are a useful tool for the restoration of native biodiversity on islands, but occasionally these operations incur non-target mortality. Changes in cereal bait colour could potentially mitigate these impacts but must not compromise the eradication operation. Changing bait colour may reduce mortality of Henderson crakes (Zapornia atra), an endemic globally threatened flightless bird on Henderson Island, Pitcairn Islands, South Pacific Ocean. Crakes had high non-target mortality in a failed 2011 rat eradication operation and consumed fewer blue than green cereal pellets. We examined which cereal bait properties influenced its acceptance by captive Pacific rats (Rattus exulans) on Henderson Island. We held 82 Pacific rats from Henderson Island in captivity and provided them with non-toxic cereal bait pellets of varying properties (blue or green, moist or dry). We estimated the proportion of rats consuming bait using logistic generalised linear mixed models. We found no effect of sex, females’ reproductive status, bait colour or bait moisture on rats’ willingness to consume baits. Rats’ bait consumption was unaffected by cereal bait properties (colour or moisture). The use of blue bait is unlikely to affect future eradication operational success but may reduce non-target mortality of Henderson crakes. Timing cereal bait distribution in relation to precipitation may also reduce crake mortality without compromising palatability to rats.

Rodent eradications in tropical environments are often more challenging and less successful than those in temperate environments. Reduced seasonality and the lack of a defined annual resource pulse influence rodent population dynamics differently than the well-defined annual cycles on temperate islands, so an understanding of rodent ecology and population dynamics is important to maximise the chances of eradication success in the tropics. Here, we report on the recovery of a Pacific rat (Rattus exulans) population on Henderson Island, South Pacific Ocean, following a failed eradication operation in 2011. We assessed changes in the rat population using capture rates from snap-trapping and investigated seasonality by using capture rates from live-trapping. Following the failed eradication operation in 2011, rat populations increased rapidly with annual per capita growth rates, r, of 0.48–5.95, increasing from 60–80 individuals to two-thirds of the pre-eradication abundance within two years, before decreasing (r = -0.25 – -0.20), presumably as the population fluctuated around its carrying capacity. The long-term changes in rat abundance may, however, be confounded by short-term fluctuations: four years after the eradication attempt we observed significant variation in rat trapping rates among months on the plateau, ranging from 36.6 rats per 100 corrected trap-nights in mid-June to 12.6 in late August. Based on mark-recapture, we also estimated rat density fluctuations in the embayment forest between 20.4 and 42.9 rats ha-1 within one month in 2015, and a much lower rat density on the coral plateau fluctuating between 0.76 and 6.08 rats ha-1 in the span of two months. The causes for the short-term density fluctuations are poorly understood, but as eradication operations on tropical and subtropical islands become more frequent, it will be increasingly important to understand the behaviour and ecology of the invasive species targeted to identify times that maximise eradication success.

1. Anthropogenic disturbances particularly affect biodiversity in sensitive freshwater ecosystems by causing species loss. Thus, measuring the response of species to multiple disturbances is a key issue for conservation and environmental management. 2. As it is not practical to assess the response of every species in a community, we compared the performance of trait and taxonomic-based groupings of species for their abilities to predict species loss in a threatened freshwater fish assemblage. Specifically, we examined responses of a Fijian freshwater fish assemblage to deforestation, placement of anthropogenic barriers (overhanging culverts) and the presence of introduced cichlids. 3. Species grouped by traits showed more consistent responses to disturbances than taxonomic groups. In particular, species belonging to trait groups that were estuary associated favoured medium-to-hard substrate, while feeding specialists were highly likely to be absent in catchments with high deforestation and overhanging culverts. The presence of introduced cichlids (Oreochromis mossambicus and O. niloticus) had a smaller effect than deforestation and barriers, but was negatively associated with species richness of diadromous species with climbing ability and positively associated with presences of some piscivores. The trait groups also revealed that detritivores, species favouring soft substrate, and those with a broad dietary range were less sensitive to anthropogenic disturbances. 4. Our study indicates that using traits to predict species loss from disturbed environments can aid in detecting the responses of rare species to disturbance. In addition, we provided a method to estimate the consistency of species’ responses to disturbance. This study may ultimately help managers identify the most effective actions for conserving sensitive species that are seldom recorded in surveys.

ABSTRACT: Coastal fish populations are typically threatened by multiple human activities, including fishing pressure and run-off of terrestrial pollution. Linking multiple threats to their impacts on fish populations is challenging because the threats may influence a species directly, or indirectly, via its habitats and its interactions with other species. Here we examine spatial variation in abundance of coral reef fish across gradients of fishing pressure and turbidity in Fiji. We explicitly account for multiple pathways of influence to test the alternative hypotheses that (1) habitat moderates predation by providing shelter, so habitat loss only affects prey fish populations if there are abundant predators, (2) habitat change co-drives biomass of both prey and predator functional groups. We examined responses of 7 fish functional groups and found that habitat change co-drives both predator and prey responses to turbidity. Abundances of all functional groups were associated with changes in habitat cover; however, the responses of their habitats to turbidity were mixed. Planktivore and piscivore abundance were lower in areas of high turbidity, because cover of their preferred habitats was lower. Invertivore, browser and grazer abundance did not change strongly over the turbidity gradient, because different components of their habitats exhibited both increases and decreases with turbidity. The effects of turbidity on fish populations were minor in areas where fish populations were already depleted by fishing. These findings suggest that terrestrial run-off modifies the composition of reef fish communities indirectly by affecting the benthic habitats that reef fish use.

Coastal ecosystems can be degraded by poor water quality. Tracing the causes of poor water quality back to land-use change is necessary to target catchment management for coastal zone management. However, existing models for tracing the sources of pollution require extensive data-sets which are not available for many of the world’s coral reef regions that may have severe water quality issues. Here we develop a hierarchical Bayesian model that uses freely available satellite data to infer the connection between land-uses in catchments and water clarity in coastal oceans. We apply the model to estimate the influence of land-use change on water clarity in Fiji. We tested the model’s predictions against underwater surveys, finding that predictions of poor water quality are consistent with observations of high siltation and low coverage of sediment-sensitive coral genera. The model thus provides a means to link land-use change to declines in coastal water quality