Non-native invasive mammal species have caused major ecological change on many islands. To conserve native species diversity, invasive mammals have been eradicated from several islands not inhabited by humans. We reviewed the challenges associated with campaigns to eradicate invasive mammals from islands inhabited by humans and domestic animals. On these islands, detailed analyses of the social, cultural, and economic costs and benefits of eradication are required to increase the probability of local communities supporting the eradication campaign. The ecological benefits of eradication (e.g., improvement of endemic species' probability of survival) are difficult to trade-off against social and economic costs due to the lack of a common currency. Local communities may oppose an eradication campaign because of perceived health hazards, inconvenience, financial burdens, religious beliefs, or other cultural reasons. Besides these social challenges, the presence of humans and domestic animals also complicates eradication and biosecurity procedures (measures taken to reduce the probability of unwanted organisms colonizing an island to near zero). For example, houses, garbage-disposal areas, and livestock-feeding areas can provide refuges for certain mammals and therefore can decrease the probability of a successful eradication. Transport of humans and goods to an island increases the probability of inadvertent reintroduction of invasive mammals, and the establishment of permanent quarantine measures is required to minimize the probability of unwanted recolonization after eradication. We recommend a close collaboration between island communities, managers, and social scientists from the inception of an eradication campaign to increase the probability of achieving and maintaining an island permanently free of invasive mammals.
Rats continue to invade rat-free islands around the world, and it remains difficult to successfully intercept them before they establish populations. Successful biosecurity methods should intercept rats rapidly, before they can establish a population. Current island biosecurity practice employs techniques used for high-density rat eradication, assuming that they will be equally effective on low-density invaders. However, such approaches are often untested. Adult male Norway rats (Rattus norvegicus) were individually released onto forested rat-free islands in New Zealand to test methods of detecting and eliminating a single invader. Only half the rats released were caught within a two-week timeframe, although the mean time to interception was just under 14 days. Permanent island biosecurity surveillance systems performed better than contingency responses. Success rates were higher on islands where complete coverage could be obtained, although surveillance systems using multiple devices eventually detected most invading rats. For some rats a change of methods was necessary. Single invading rats left a rat-free island despite the presence of excessive natural food resources. With surveillance systems comprising an array of tested island biosecurity devices, and where necessary a contingency response using alternative methods, it should be possible to maintain islands as rat-free even when they have a high reinvasion rate.
Anthropogenic activity is now recognised as having profoundly and permanently altered the Earth system, suggesting we have entered a human-dominated geological epoch, the ‘Anthropocene’. To formally define the onset of the Anthropocene, a synchronous global signature within geological-forming materials is required. Here we report a series of precisely-dated tree-ring records from Campbell Island (Southern Ocean) that capture peak atmospheric radiocarbon (14C) resulting from Northern Hemisphere-dominated thermonuclear bomb tests during the 1950s and 1960s. The only alien tree on the island, a Sitka spruce (Picea sitchensis), allows us to seasonally-resolve Southern Hemisphere atmospheric 14C, demonstrating the ‘bomb peak’ in this remote and pristine location occurred in the last-quarter of 1965 (October-December), coincident with the broader changes associated with the post-World War II ‘Great Acceleration’ in industrial capacity and consumption. Our findings provide a precisely-resolved potential Global Stratotype Section and Point (GSSP) or ‘golden spike’, marking the onset of the Anthropocene Epoch.
Rifleman, or titipounamu Acanthisitta chloris, is New Zealand’s smallest endemic passerine. The species has a fragmented distribution and is threatened in the Rakiura region in the south of the South Island. The only known population of South Island rifleman A. c. chloris in the Rakiura region persisted on Codfish Island/Whenua Hou. To create a second population of rifleman in Rakiura, 30 caught from Codfish Island were reintroduced onto nearby Ulva Island in February 2003, the first translocation of rifleman. Survival and dispersal were monitored for 1 month post-release, and subsequently during the first and second breeding seasons. Mortality was greatest during holding and transfer, with low to moderate post-release mortality. All founding pairs bred in the first breeding season, and both founders and offspring bred in the second season. Dispersal across the island was greater for offspring. A simple deterministic matrix model indicated positive annual population growth (λ = 1.33), and low risk of short-term extinction. Holding/transfer techniques should be improved for future reintroductions, and longer-term monitoring should be undertaken for a more accurate assessment of vital rates. Based on the survival of founding birds, reproduction by the release generation and their offspring, and high probability of population persistence, the rifleman reintroduction was considered to be successful and a good model for future reintroductions of small passerine birds.
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