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Rat eradication has become a common conservation intervention in island ecosystems and its effectiveness in protecting native vertebrates is increasingly well documented. Yet, the impacts of rat eradication on plant communities remain poorly understood. Here we compare native and non-native tree and palm seedling abundance before and after eradication of invasive rats (Rattus Rattus) from Palmyra Atoll, Line Islands, Central Pacific Ocean. Overall, seedling recruitment increased for five of the six native trees species examined. While pre-eradication monitoring found no seedlings of Pisonia grandis, a dominant tree species that is important throughout the Pacific region, post-eradication monitoring documented a notable recruitment event immediately following eradication, with up to 688 individual P. grandis seedlings per 100m2 recorded one month post-eradication. Two other locally rare native trees with no observed recruitment in pre-eradication surveys had recruitment post-rat eradication. However, we also found, by five years post-eradication, a 13-fold increase in recruitment of the naturalized and range-expanding coconut palm Cocos nucifera. Our results emphasize the strong effects that a rat eradication can have on tree recruitment with expected long-term effects on canopy composition. Rat eradication released nonnative C. nucifera, likely with long-term implications for community composition, potentially necessitating future management interventions. Eradication, nevertheless, greatly benefited recruitment of native tree species. If this pattern persists over time, we expect long-term benefits for flora and fauna dependent on these native species.

Between 1892 and 1930, 58 percent (30 taxa) of Hawaiian endemic forest birds either were greatly reduced or became extinct. The order in which the islands experienced major declines ofseveral forest birds is Oahu (ca. 1873-1887), Hawaii (1892-1900), Mo10kai (1893-1907), Maui (18941901), Kauai (after 1900), and Lanai (1926-1932). Loss of habitat, reduced food supply, introduced avian diseases, as well as predation by man, feral cats, mongooses, and Norway rats (Rattus norvegicus) all appear to have reduced some species ofbirds, but none ofthese factors adequately explains the accelerated rates ofdecline offorest birds that occurred after 1892. Although it has been assumed that roofrats (Rattus rattus) reached Hawaii with the first European ships at the end of the 18th century, there is circumstantial evidence, independent of the bird decline data, that indicates that this rat did not arrive until after 1840, probably between 1870 and 1880. The hypothesis is advanced that after its establishment on Oahu in the 1870s, R. rattus spread to the remaining large islands in the group, resulting in a stepwise accelerated decline offorest birds on each island in turn. Hawaii thus parallels some other Pacific islands where major reductions of birds have followed the establishment of R. rattus. The need for precautions to prevent rats from reaching rat-free islands in the Hawaiian group is emphasized.