Habitat use and subspecific status of Merlins, Falco columbarius , wintering in central Utah

Most ornithological literature for Utah reports the status of the Merlin ( Falco columbarius ) as rare or scarce. Only the most recently published checklists (Behle and Perry 1975, Behle et al. 1985) record it as uncommon. Likewise, a 1998 printed checklist (Utah Ornithological Society 1998) list it as uncommon. Also misrepresented in the literature are the status and distribution of the 3 rather distinct subspecies, each of which occupies dissimilar habitats during the breeding season. We made random observations of Merlins in northern Utah beginning in the 1950s and then studied them continuously between 1992 and 1997 in Utah County, Utah. During the 1992-1997 period, we were able to clearly allocate 95 males and 76 females to subspecies, including within our count 58 falcons trapped (some fitted with radio telemetry). The winter habitat in which they occurred was categorized as either urban (mainly dense residential area) or rural (agricultural lands, dairy farms, or scattered homes). There was a statistically significant ( X 2 F. c. columbarius frequenting urban areas 68% of the time, and prairie parkland-breeding F. c. richardsonii frequenting rural habitats 78% of the time.     

Use of interstate highway overpasses and billboards for nesting by the common raven ( Corvus corax )

Common ravens are usually rather shy birds around their nests and avoid nesting too near human activity. We here report the use of overpasses along heavily traveled Interstate Highway 84 in Idaho and Utah for nest placement. Nests are within 6 m of passing vehicles.     

Breeding biology of Mountain Plovers ( Charadrius montanus ) in the Uinta Basin

The known Mountain Plover population breeding on the Myton Bench, Duchesne County, Utah, is small, composed roughly of 30 adults and young after each breeding season. Currently, its location is peripheral to the species main range. This shrub-steppe breeding habitat differs from the shortgrass prairie habitat with which this bird is historically associated. Between 1996 and 1998 we made observations at nesting sites located consistently in 2 concentrated areas surrounded by large tracts of similar habitat. Activity may be focused in these specific areas because of breeding-site fidelity; this behavior is common among most shorebirds and has been documented for the Mountain Plover in Colorado. Also, Mountain Plovers are social and tend to choose nest sites near others. Most nests in Utah were located within close proximity of mounds of white-tailed prairie dogs ( Cynomys leucurus ), and all were situated near roadways or oil well pads. Mountain Plovers were often observed with broods on these bare areas at night. We conclude that Mountain Plovers on the Myton Bench are distributed in clumped breeding colonies within large areas of apparently favorable habitat.     

Alteration in crossbridge kinetics caused by mutations in actin

The generation of force during muscle contraction results from the interaction of myosin and actin. The kinetics of this force generation vary between different muscle types and within the same muscle type in different species. Most attention has focused on the role of myosin isoforms in determining these differences. The role of actin isoforms has received little attention, largely because of the lack of a suitable cell type in which the myosin isoform remains constant yet the actin isoforms vary. An alternative approach would be to examine the effect of actin mutations, however, most of these cause such gross disruption of muscle structure that mechanical measurements are impossible. We have now identified two actin mutations which, despite involving conserved amino acids, can assemble into virtually normal myofibrils. These amino-acid changes in actin significantly affect the kinetics of force generation by muscle fibres. One of the mutations is not in the putative myosin-binding site, demonstrating the importance of long-range effects of amino acids on actin function.     

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

Haemophilia A is the most common inherited bleeding disorder in man, affecting approximately 1 male in 10,000. The disease is caused by a deficiency in the gene for factor VIII, a component of the intrinsic coagulation pathway. Due to the broad range of clotting activity in normal and heterozygous females, it is often difficult to confirm the status of women at risk for carrying the disease. A genetic marker in the form of a restriction fragment length polymorphism (RFLP) within or tightly linked to the factor VIII gene would serve as a tag for the haemophilia gene, thus allowing both accurate carrier detection and improved, earlier prenatal diagnosis by chorionic villi sampling. The recent isolation of the factor VIII gene has allowed a search for RFLPs within the gene, and we report here the identification of a common polymorphism within the factor VIII gene, revealed by the restriction enzyme BclI, which can be used diagnostically in about 42% of all families. Although the disease haemophilia A has been mapped to the distal portion of Xq, the BclI RFLP makes possible higher-resolution genetic linkage mapping with respect to other polymorphic markers on this portion of the X chromosome. We have established close linkage of the factor VIII gene to several useful RFLP markers, including the highly informative marker St14. These markers should also be useful for prenatal diagnosis of haemophilia A and for detection of its carriers.     

The effect of moderate hemodilution with fluosol-DA or normal saline on acetaminophen disposition in the rat

Hemodilution with 40 ml/kg of Fluosol or saline reduced the acetaminophen Vd and the acetaminophen sulfate ClM at 48 or 72 h, respectively. Fluosol hemodilution increased the acetaminophen renal excretion at 24 and 72 h. But at 48 h, Fluosol hemodilution either inhibited the renal secretion of acetaminophen or enhanced its reabsorption.     

Preliminary observations of a bacteriophage infectingXenorhabdus luminescens (Enterobacteriaceae)

A bacteriophage infective toXenorhabdus luminescens, a bacterial symbiont of heterorhabditid nematodes, was recovered from insects that supported poor nematode development. Plaque tests showed the phage particles to be infective only to primary and not secondary colonies ofX. luminescens. The phage was not infective toX. nenatophilus primaries or secondaries. The bacteriophage particles ranged 80–90 nm in length, with the head ranging from 40 to 50 nm in diameter. Restriction analysis was performed on isolated bacteriophage DNA. This first report of a bacteriophage fromXenorhabdus species has pratical implications since it could be detrimental to cultures ofHeterorhabditis nematodes that are being produced throughout the world for the biological control of insects.