Programmed cell death, mitochondria and the plant hypersensitive response.

The plant response to attempted infection by microbial pathogens is often accompanied by rapid cell death in and around the initial infection site, a reaction known as the hypersensitive response. This response is associated with restricted pathogen growth and represents a form of programmed cell death (PCD). Recent pharmacological and molecular studies have provided functional evidence for the conservation of some of the basic regulatory mechanisms underlying the response to pathogens and the activation of PCD in animal and plant systems. In animals, the mitochondrion integrates diverse cellular stress signals and initiates the death execution pathway, and studies indicate a similar involvement for mitochondria in regulating PCD in plants. But many of the cell-death regulators that have been characterized in humans, worms and flies are absent from the Arabidopsis genome, indicating that plants probably use other regulators to control this process.     

Movements and home ranges of San Joaquin kit foxes ( Vulpes macrotis mutica ) relative to oil-field development

We examined the effect of oil-field development on movements and patterns of spatial use of San Joaquin kit foxes ( Vulpes macrotis mutica ) on the Naval Petroleum Reserves in California (NPRC) in the San Joaquin Valley. To do this, we compared movements and home ranges of kit foxes from June 1984 to September 1985 in areas developed for petroleum production (30% of native habitat lost to production facilities) and areas with little development (3%). Distances traveled nightly by kit foxes did not differ between levels of petroleum development or between sexes ( P > 0.2). Mean length of nightly movements during breeding (14.6 km) was longer than during pup-rearing (10.7 km) and pup-dispersal (9.4 km) periods ( P = 0.01). Mean size of home ranges was 4.6 ± 0.4 ( s￣x ) km 2 ( n = 21) and did not differ between levels of petroleum development and sexes ( P > 0.2). Overlap of home ranges of foxes from the same social group (78 ± 4.3%) was greater than that of same-sex foxes (35 ± 7.8%) and males and females of different social groups (32 ± 8.0%, P P > 0.4). Despite extensive overlap of home ranges, kit foxes on NPRC maintained relatively exclusive core areas, particularly adjacent foxes of the same sex. Future studies should examine which levels of habitat conversion impact spatial use of kit foxes.