In this study, we sampled aquatic snails for the presence of hairworm cysts from 46 streams in Payne County, Oklahoma. Gordiid cysts were found at 70 % (32/46) of sites examined. Based on cyst morphology, we were able to identify three morphological types of gordiid cysts, including Paragordius, Gordius, and Chordodes/Neochordodes. Using our gordiid cyst presence data in conjunction with environmental variables, we developed an ecological niche model using Maxent to identify areas suitable for snail infections with gordiids. The model successfully predicted all presence localities of gordiid cysts in snails over a geographic area of 1,810 km 2 . We used this information, along with arthropod host infections and crowdsourcing, citizen scientists sampling for adult free-living worms during peak emergent times in areas predicted suitable by the model, to document Paragordius varius, Chordodes morgani, and a new species of gordiid (Gordius n. sp.). To our knowledge, this is the first ecological niche model attempted on such a narrow geographic scale (county level) that recovered known locations successfully. We provide new scanning electron micrographs and molecular data for these species. Our field data and ecological niche model clearly indicate that gordiid cysts are easy to detect in the environment and together these sampling techniques can be useful in discovering new species of gordiids, even in relatively well sampled areas for these cryptic parasites.
Increased nutritional demands for endurance exercise of dogs are typically met through increased amounts of their current food. As a result, protein intake is also increased, and excessive nitrogen may affect the dog’s water balance. Sixteen unconditioned Alaskan sled dogs underwent a 6-week exercise training protocol, wherein 8 dogs were fed increasing amounts of their normal kibble to maintain body weight, while the other 8 were fed the same amount of kibble, with increasing calorie needs met by equal amounts of sugar and oil. The diets resulted in similar calorie intakes (181.3±20.0 and 205.7±36.3 kcal/kg0.75, for the control and low protein dogs respectively) but control dogs had higher protein intakes (32.2±0.0 and 19.4±2.4% of metabolic energy intake). After 6 weeks of training the dogs completed a 5 day exercise test in which they travelled 24 km per day, where total energy expenditure was determined using doubly-labelled water technique. Dogs expended an average of 1,491±264 kcal/day (145±25 kcal/kg0.75/day), with no difference between the dietary treatments and no negative performance indicators. Following the exercise test the dogs underwent a 24 hour dehydration test (water withheld) followed by an 8 hour rehydration test (with ad libitum water intake recorded) where total body water was determined using deuterium oxide. Blood and urinary samples were also collected. Following exercise conditioning, control dogs had higher serum urea nitrogen than low protein dogs, and this as well as albumin decreased further during the 5 day exercise test. Low-protein dogs had lower overall total body water and higher fractional excretion of Na+, suggesting some renal adaptation. These findings suggest that reduced protein intake did not negatively affect athletic performance, though some facets of body chemistry were altered.
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