Genetic Relationships Among \u3cem\u3eLeptographium terebrantis\u3c/em\u3e and the Mycangial Fungi of Three Western \u3cem\u3eDendroctonus\u3c/em\u3e Bark Beetles

Morphology, mitochondrial DNA (mtDNA) restriction fragment polymorphisms (RFLPs) and nuclear DNA (nDNA) fingerprinting were used to clarify relationships among the morphologically similar Ophiostoma and Leptographium species associated with mycangia of three Dendroctonus bark beetles (Ophiostoma clavigerum associated with both D. ponderosae and D. jeffreyi, and L. pyrinum associated with D. adjunctus), as well as a closely related nonmycangial bark beetle associate (L. terebrantis). Most isolates of O. clavigerum form long (40-70 μm), septate conidia, while all isolates of L. terebrantis and L. pyrinum form conidia less than 17.0 μm in length. The conidia of L. pyrinum are pyriform, with truncate bases, while the conidia of the other species form only slightly truncate bases. Conidial masses of L. terebrantis are creamy yellow, while the conidial masses of the other species are white. Nuclear DNA fingerprints resulting from probing PstI restrictions with the oligonucleotide probe (CAC)(5) and HaeIII and MspI restrictions of mtDNA, exhibited three major clusters. In the dendrogram developed from mtDNA RFLPs, the L. pyrinum isolates formed one cluster, while the majority of O. clavigerum isolates, including all D. jeffreyi isolates, formed another. A third cluster was composed of all L. terebrantis isolates, as well as several O. clavigerum isolates from D. ponderosae. The inclusion of some O. clavigerum isolates in the L. terebrantis cluster suggests that horizontal transfer of mtDNA has occurred among these fungi. The nDNA dendrogram also exhibited three clusters, and most isolates of L. pyrinum, L. terebrantis and O. clavigerum grouped separately; however, one isolate of O. clavigerum grouped with the L. terebrantis isolates, while one isolate of L. terebrantis grouped with O. clavigerum. No genetic markers were found that distinguished between O. clavigerum associated with D. ponderosae and O. clavigerum associated with D. jeffreyi. Ophiostoma clavigerum might be a recently diverged morphological variant of L. terebrantis, with special adaptations for grazing by young adults of D. jeffreyi and D. ponderosae. The anamorph of O. clavigerum, Graphiocladiella clavigerum, is transferred to Leptographium

Grizzly Bear Scavenging of Carrion on the Northern Yellowstone Winter Range (1997-2012)

The Northern Yellowstone Winter Range (NYWR) in northwestern Wyoming and southwestern Montana is an important winter migratory destination for ungulates.  The NYWR is within the Greater Yellowstone Ecosystem (GYE), a landscape characterized by a complex ecological system of predators, scavengers, and ungulates.  Grizzly bears (Ursus arctos) are dominant members of the scavenging community throughout the spring.  However, little is known about factors associated with grizzly bear use of carcasses.  Of particular interest to managers is how habitat and anthropogenic factors are associated with carcass use.  Such information, for example, may be useful to manage spring recreation in important bear foraging areas to reduce conflict and support conservation efforts.  We used logistic regression to analyze spring survey data from 23 transects located in Yellowstone National Park and the Gallatin National Forest during 1997–2012, to identify factors associated with grizzly bear scavenging of winter- or predator-killed ungulates.  Multi-model inference was used to evaluate relative support for a set of a priori candidate models containing environmental and temporal correlates. Our preliminary findings showed support for models with distance to forest edge, road density, and elevation. Results indicated negative relationships between these factors and probability of carcass use.  Our results suggest that spatial heterogeneity in landscape-level habitat characteristics and human activity affect grizzly bear use of a valuable spring food source

Tribute to Professor Doug Rendleman

A tribute to Professor Doug Rendleman, who served on the faculty of the Washington and Lee University School of Law from 1988 to 2020. Rendleman became Professor of Law, Emeritus in 2020