9 research outputs found

    A comparison of coyote ecology after 25 years: 1978 versus 2003

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    Most ecological studies of coyotes are of short duration and studies are generally never repeated, thus the opportunity to compare changes in coyote (Canis latrans Say, 1823) ecology over time is rare. We compared coyote home ranges, activity patterns, age, and diet at the Welder Wildlife Refuge in south Texas between 1978-1979 and 2003-2004 (25 years later). The Minta index of overlap between 1978 and 2003 home ranges was 51.7 ± 7.0 (n = 7), much greater than the Minta index value based on randomized tests (28.7 ± 8.6), indicating similar spatial patterns between time periods. The Minta index was 12.3 ± 6.2 (n = 7) for core areas, whereas the Minta index value based on randomized tests was 4.0 ± 3.0. Although overall diets were similar between 1978 and 2003, we detected some differences in prey species consumed. Activity patterns were similar between the two study periods, with peaks in movement occurring around sunrise and sunset. There was no difference in the mean age between the two populations (P = 0.44, n = 68, t [66] = 2.00). Our findings suggest that population features, such as home-range position and age structure, are similar between extended time periods, while individual-level patterns, such as the prey species consumed and distribution of locations within a home range, are dynamic and may reflect changes in the local environment

    A comparison of coyote ecology after 25 years: 1978 versus 2003

    Get PDF
    Most ecological studies of coyotes are of short duration and studies are generally never repeated, thus the opportunity to compare changes in coyote (Canis latrans Say, 1823) ecology over time is rare. We compared coyote home ranges, activity patterns, age, and diet at the Welder Wildlife Refuge in south Texas between 1978-1979 and 2003-2004 (25 years later). The Minta index of overlap between 1978 and 2003 home ranges was 51.7 ± 7.0 (n = 7), much greater than the Minta index value based on randomized tests (28.7 ± 8.6), indicating similar spatial patterns between time periods. The Minta index was 12.3 ± 6.2 (n = 7) for core areas, whereas the Minta index value based on randomized tests was 4.0 ± 3.0. Although overall diets were similar between 1978 and 2003, we detected some differences in prey species consumed. Activity patterns were similar between the two study periods, with peaks in movement occurring around sunrise and sunset. There was no difference in the mean age between the two populations (P = 0.44, n = 68, t [66] = 2.00). Our findings suggest that population features, such as home-range position and age structure, are similar between extended time periods, while individual-level patterns, such as the prey species consumed and distribution of locations within a home range, are dynamic and may reflect changes in the local environment

    Effectiveness of Twenty, Twenty-Five Diazacholesterol, Avian Gonadotropin-Releasing Hormone, and Chicken Riboflavin Carrier Protein for Inhibiting Reproduction in Coturnix Quail

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    Contraception may provide a useful nonlethal management tool when it is desirable to reduce populations of birds. We tested the efficacy of 20,25 diazacholesterol, and immunization with avian gonadotropin-releasing hormone (AGnRH-I) and chicken riboflavin carrier protein (cRCP) as contraceptives and investigated their modes of action in Coturnix quail (Coturnix coturnix japonica). Females that were paired with males treated with 20,25 diazacholesterol produced lower percentages of eggs that were fertile and hatched. Females treated with 20,25 diazacholesterol and paired with control males laid fewer eggs, and lower percentages of their eggs were fertile and hatched. Treatment with 20,25 diazacholesterol reduced testosterone levels in males and progesterone levels in females. Nonesterified cholesterol levels were reduced, whereas desmosterol levels increased in birds treated with 20,25 diazacholesterol. Treatment with AGnRH-I and cRCP immunocontraceptive vaccines did not decrease average egg production and hatchability or hormone levels, but this failure might have been due to the vaccination protocol. If registered, wildlife managers may be able to use 20,25 diazacholesterol when other methods, such as lethal control, are undesirable for reducing damage caused by specific breeding behaviors such as the building of nests

    Estimating brown hyaena occupancyusing baited camera traps

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    Conservation and management of brown hyaenas (Hyaena brunnea) is hampered by a lack ofinformation on abundance and distribution, which is difficult and labour-intensive to obtain.However, occupancy surveys offer a potentially efficient and robust means of assessingbrown hyaena populations. We evaluate the efficacy of camera trapping for estimatingbrown hyaena occupancy, and the effect of environmental variables and lures on detectionprobability. We estimated population density in Pilanesberg National Park, South Africa, at2.8/100 km2, occupancy at 1.0 and model-averaged detection probability at 0.1. Using a fishlure increased detection probability to 0.2 and significantly increased encounter rates. Wealso found that brown hyaenas are more likely to be detected in areas of scrub or woodlandrather than grassland. Our results suggest that 13 camera sites would be needed to achievean occupancy estimate with S.E. of 0.05, and a minimum of 16–34 sampling occasions (withand without the fish lure) should be used in comparable study areas. We conclude thatcamera trapping is a viable method of estimating brown hyaena occupancy at local andlandscape scales and capture–recapture analysis is also possible at a local scale
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