Tracking the exposure of a pelagic seabird to marine plastic pollution.

We aimed to describe how debris originated from coastal cities and fisheries circulates and accumulates along the Argentine continental shelf and its potential interaction with southern giant petrels (SGP, Macronectes giganteus). We used tracking data of 31 SGPs (adults and juveniles) from Patagonian colonies. Lagrangian simulations of particles were released from coastal cities and fisheries. Oceanographic features together with plastic input generated a corridor of debris through the Argentine shelf with areas of high debris accumulation, exposing SGP to plastic consumption. During chick provisioning trips 93.9% of petrel's locations overlapped with areas of plastic accumulation. Although early developmental stages were more exposed to particles from cities, the exposure of petrels (all classes) to debris from fisheries was 10% higher than from cities. Measures to reduce debris from fisheries, would reduce plastic ingestion by giant petrels. Proper management of open sky dumpsters would reduce plastic consumption by chicks and juveniles.

How often should dead-reckoned animal movement paths be corrected for drift?

BACKGROUND: Understanding what animals do in time and space is important for a range of ecological questions, however accurate estimates of how animals use space is challenging. Within the use of animal-attached tags, radio telemetry (including the Global Positioning System, 'GPS') is typically used to verify an animal's location periodically. Straight lines are typically drawn between these 'Verified Positions' ('VPs') so the interpolation of space-use is limited by the temporal and spatial resolution of the system's measurement. As such, parameters such as route-taken and distance travelled can be poorly represented when using VP systems alone. Dead-reckoning has been suggested as a technique to improve the accuracy and resolution of reconstructed movement paths, whilst maximising battery life of VP systems. This typically involves deriving travel vectors from motion sensor systems and periodically correcting path dimensions for drift with simultaneously deployed VP systems. How often paths should be corrected for drift, however, has remained unclear. METHODS AND RESULTS: Here, we review the utility of dead-reckoning across four contrasting model species using different forms of locomotion (the African lion Panthera leo, the red-tailed tropicbird Phaethon rubricauda, the Magellanic penguin Spheniscus magellanicus, and the imperial cormorant Leucocarbo atriceps). Simulations were performed to examine the extent of dead-reckoning error, relative to VPs, as a function of Verified Position correction (VP correction) rate and the effect of this on estimates of distance moved. Dead-reckoning error was greatest for animals travelling within air and water. We demonstrate how sources of measurement error can arise within VP-corrected dead-reckoned tracks and propose advancements to this procedure to maximise dead-reckoning accuracy. CONCLUSIONS: We review the utility of VP-corrected dead-reckoning according to movement type and consider a range of ecological questions that would benefit from dead-reckoning, primarily concerning animal-barrier interactions and foraging strategies.

Nemertean Larval Dispersion Across Biogeographic Provinces of Southwest Atlantic.

The nemertean Malacobdella arrokeana is a commensal of the edible giant bivalve Panopea abbreviata; both species have a restricted geographic distribution, high specificity and populations settled along distinct biogeographic provinces. This supposes a high genetic structuring among populations and low intra-populational variability; nevertheless, a lack of genetic structure was detected previously between M. arrokeana populations from the Atlantic Northern Patagonia Gulfs System (NPGS) by means of mitochondrial and nuclear markers. Here, we present a model that explains this lack of genetic structure, integrating larval development and behavior, as well as bio-oceanographical model simulations. We observed in cultured larvae a maximum 30 days of planktonic life before settlement. Planuliform larval morphology and behavior of M. arrokeana suggested that the dispersion is more influenced by passive transport rather than active swimming. Modeling larvae as particles indicated that the limit of biogeographical provinces along the NPGS is not a barrier for dispersal, corroborating that larval dispersion is strictly related to season and to hydrodynamic diffusion patterns present in the area. These results explain the lack of genetic population structure recorded before in the NPGS. Our results provide novel baseline data regarding larval connectivity and oceanographic circulation patterns on the southwestern Atlantic. This information can be used as a reference for the implementation of management plans of invertebrate species with pelagic larvae to ensure the long-term viability of fishery resources shared by different government districts.