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Dispositif de suivi de l'abondance et de l'impact du cerf - Fiche finale de capitalisation - PROTEGE
SPREP Publications, Biodiversity Conservation, BRB
Available Online

PROE / SPREP

2025
Des dispositifs innovants de suivi ont été développés afin de mesurer l’impact du Cerf Rusa sur le sous-bois de forêts humides de Nouvelle Calédonie et évaluer l’abondance de cette espèce envahissante, dans trois zones prioritaires du territoire. L’élaboration de ces dispositifs poursuit des objectifs complémentaires aux actions de régulation professionnelle mises en œuvre dans le cadre de PROTEGE. Le suivi vise notamment à réaliser un état initial et à évaluer les bénéfices des opérations de régulation, grâce à des outils adaptés à des zones d’intervention difficiles d’accès et caractérisées par une biodiversité exceptionnelle, plus de 80% des espèces végétales des forêts humides d’altitude étant endémiques à la Nouvelle-Calédonie. Un travail initial de sectorisation a permis mieux de caractériser les enjeux, les pressions sur l’environnement ainsi que le contexte socio-économique afin de délimiter les zones d’intervention prioritaires. Pour la première fois en Nouvelle-Calédonie, un protocole standardisé de mesure de l’impact des cerfs a été élaboré. Il s’appuie sur plusieurs indicateurs et prend en compte les spécificités des espèces végétales concernées et des contraintes associées à sa mise en œuvre. En complément, PROTEGE a permis d’élaborer une méthodeinnovante d’évaluation de l’abondance des cerfs, reposant sur l’utilisation d’un drone équipé de capteur thermique pour l’enregistrement de vidéos nocturnes. Un algorithme développé spécifiquement a par ailleurs vocation à réaliser automatiquement les détections à partir de ces vidéos, facilitant considérablement le traitement des données. La mise en œuvre de ce protocole pour la prospection de 4 700 hectares a révélé des densités de populations et des concentrations de hardes localement très élevées, atteignant par endroits des niveaux parmi les plus élevés enregistrés à l’échelle mondiale. Ces résultats fournissent des informations précieuses pour le ciblage de futures interventions et le suivi de leurs bénéfices. FICHE FINALE DE CAPITALISATION DU PROJET PROTEGE, financé par l'Union Européenne.
Seasonal variation in movements and survival of invasive Pacific rats on sub-tropical Henderson Island: implications for eradication.
Biodiversity Conservation, BRB
Available Online

Bond, A.L.

,

Churchyard, T.

,

Donaldson, A.

,

Duffield, N.

,

Havery, S.

,

Kelly, J.

,

Lavers, J.L.

,

McClelland, J.T.W.

,

Oppel, S.

,

Proud, T.

,

Russell, J.C.

2019
Invasive rodents are successful colonists of many ecosystems around the world, and can have very flexible foraging behaviours that lead to differences in spatial ranges and seasonal demography among individuals and islands. Understanding such spatial and temporal information is critical to plan rodent eradication operations, and a detailed examination of an island’s rat population can expand our knowledge about possible variation in behaviour and demography of invasive rats in general. Here we investigated the movements and survival of Pacific rats (Rattus exulans) over five months on sub-tropical Henderson Island in the South Pacific Ocean four years after a failed eradication operation. We estimated movement distances, home range sizes and monthly survival using a spatially-explicit Cormack-Jolly-Seber model and examined how movement and survival varied over time. We captured and marked 810 rats and found a median maximum distance between capture locations of 39 ± 25 m (0–107 m) in a coastal coconut grove and 61 ± 127 m (0–1,023 m) on the inland coral plateau. Estimated home range radii of Pacific rats on the coral plateau varied between ‘territorial’ (median: 134 m; 95% credible interval 106–165 m) and ‘roaming’ rats (median: 778 m; 290–1,633 m). The proportion of rats belonging to the ‘roaming’ movement type varied from 1% in early June to 23% in October. There was no evidence to suggest that rats on Henderson in 2015 had home ranges that would limit their ability to encounter bait, making it unlikely that limited movement contributed to the eradication failure if the pattern we found in 2015 is consistent across years. We found a temporal pattern in monthly survival probability, with monthly survival probabilities of 0.352 (0.081–0.737) in late July and 0.950 (0.846–0.987) in late August. If seasonal variation in survival probability is indicative of resource limitations and consistent across years, an eradication operation in late July would likely have the greatest probability of success.
Recovery of introduced Pacific rats following a failed eradication attempt on subtropical Henderson Island, South Pacific Ocean
Biodiversity Conservation, BRB
Available Online

Bond, A.L.

,

Churchyard, T.

,

Cuthbert, R.J.

,

Duffi eld, N.

,

Havery, S.

,

Kelly, J.

,

Lavers, J.L.

,

McClelland, G.T.W.

,

Oppel S.

,

Proud, T.

,

Torr, N.

,

Vickery, J.A.

2019
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.