From moonlight to movement and synchronized randomness: Fourier and wavelet analyses of animal location time series data. (41/77)

High-resolution animal location data are increasingly available, requiring analytical approaches and statistical tools that can accommodate the temporal structure and transient dynamics (non-stationarity) inherent in natural systems. Traditional analyses often assume uncorrelated or weakly correlated temporal structure in the velocity (net displacement) time series constructed using sequential location data. We propose that frequency and time-frequency domain methods, embodied by Fourier and wavelet transforms, can serve as useful probes in early investigations of animal movement data, stimulating new ecological insight and questions. We introduce a novel movement model with time-varying parameters to study these methods in an animal movement context. Simulation studies show that the spectral signature given by these methods provides a useful approach for statistically detecting and characterizing temporal dependency in animal movement data. In addition, our simulations provide a connection between the spectral signatures observed in empirical data with null hypotheses about expected animal activity. Our analyses also show that there is not a specific one-to-one relationship between the spectral signatures and behavior type and that departures from the anticipated signatures are also informative. Box plots of net displacement arranged by time of day and conditioned on common spectral properties can help interpret the spectral signatures of empirical data. The first case study is based on the movement trajectory of a lion (Panthera leo) that shows several characteristic daily activity sequences, including an active-rest cycle that is correlated with moonlight brightness. A second example based on six pairs of African buffalo (Syncerus caffer) illustrates the use of wavelet coherency to show that their movements synchronize when they are within approximately 1 km of each other, even when individual movement was best described as an uncorrelated random walk, providing an important spatial baseline of movement synchrony and suggesting that local behavioral cues play a strong role in driving movement patterns. We conclude with a discussion about the role these methods may have in guiding appropriately flexible probabilistic models connecting movement with biotic and abiotic covariates.  (+info)

Suitability of electronic mini-boluses for the early identification of goat kids and effects on growth performance and development of the reticulorumen. (42/77)

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Neoplasia and granulomas surrounding microchip transponders in Damaraland mole rats (Cryptomys damarensis). (43/77)

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Microchip-associated sarcoma in a shrew (Suncus murinus). (44/77)

A 16-mo-old female house musk shrew (Suncus murinus) with a 1-wk history of a rapidly growing subcutaneous mass in the interscapsular region was euthanized and submitted for necropsy. Macroscopic examination identified an irregular, well-demarcated, solid, tan-white subcutaneous mass. A small cavity containing a microchip device was present at the center of the mass. In addition, massive splenomegaly was evident grossly. Histologically, the subcutaneous mass comprised spindle cells arranged in a storiform pattern of interweaving bundles, consistent with a high-grade soft tissue sarcoma with multifocal necrosis. Immunohistochemical investigation suggested that the neoplastic cells were positive for neuron-specific enolase and (rarely) alpha-smooth muscle actin and negative for cytokeratin, desmin, S100, and vimentin. In light of the mesenchymal histopathologic phenotype and the lack of specific immunoreactivity pattern, the mass was considered to be most consistent with a poorly differentiated sarcoma. To our knowledge, this is the first report of a microchip-associated soft tissue sarcoma in a shrew.  (+info)

A system for implanting laboratory mice with light-activated microtransponders. (45/77)

The mouse is the most commonly used laboratory animal, accounting for up to 80% of all mammals used in research studies. Because rodents generally are group-housed, an efficient system of uniquely identifying individual animals for use in research studies, breeding, and proper colony management is required. Several temporary and permanent methods (for example, ear punching and toe clipping) are available for labeling research mice and other small animals, each with advantages and disadvantages. This report describes a new radiofrequency identification tagging method that uses 500-mum, light-activated microtransponders implanted subcutaneously into the ear or tail of mice. The preferred location for implanting is in the side of the tail, because implantation at this site was simple to perform and was associated with shorter implantation times (average, 53 versus 325 s) and a higher success rate (98% versus 50%) compared with the ear. The main benefits of using light-activated microtransponders over other identification methods, including other radiofrequency identification tags, is their small size, which minimizes stress to the animals during implantation and low cost due to their one-piece (monolithic) design. In addition, the implantation procedure uses a custom-designed 21-gauge needle injector and does not require anesthetization of the mice. We conclude that this method allows improved identification and management of laboratory mice.  (+info)

Retinal image recognition for verifying the identity of fattening and replacement lambs. (46/77)

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Genotyping errors in a calibrated DNA register: implications for identification of individuals. (47/77)

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Validation of a system for monitoring feeding behavior in beef cattle. (48/77)

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