DIET,HOME RANGE,HUNTING AND REPRODUCTIVE BEHAVIOUR OF A PAIR OF DICKINSON'S KESTREL FALCO DZCKZNSONZ IN THE KRUGER NATIONAL PARK,SOUTH AFRICA

Summary

BENN, G.A. &; KEMP, A.C. 1995. Diet, home range, hunting and reproductive behaviour of a pair of Dickinson's Kestrel Falco dickinsoni in the Kruger National Park, South Africa. Ostrich 66: 81–91.

During July-December 1992, the diet, home range, hunting and reproductive behaviour of a pair of Dickinson's Kestrel Falco dickinsoni was recorded in the Kruger National Park, South Africa. Numerically, for both sexes combined, invertebrates formed the majority (56%) of the diet, while separately the female caught 75% and the male 49% invertebrate prey. During courtship and incubation the male supplied the female with primarily vertebrate prey and both provisioned mainly vertebrates to the nestlings (male = 80%; female = 57%). The non-breeding home range of the female was 27.8 km², and the breeding home range of the male was 26.3 km2. Both utilised their home ranges differentially, the area within a 2 km radius of the nest (12.6 km²) being used proportionally more than the remaining area. The home range of the female was compared to that of other Falco spp. and was larger than would be expected based on body weight. Perch-hunting was the only technique utilised by both sexes, with 79–80% of observed strike attempts from dead trees. During the day, the 9.emale spent 87% and the male 77% of the time perch-hunting, with respective hunting success rates of 69% and 58%. During courtship, the female spent much of her time (94%) close to the nest, where the male supplied her with prey. During incubation, the male spent 95% of his time within 2 km of the nest tree, where he hunted to supply the female with prey at a rate of 0.3 items.hr^?1 and assisted in nest defence. On occasion the male entered the nest to relieve the female, and remained in the cavity on average for 134 min (n = 5). As the young got older, the female spent less time at the nest and provisioned more items to the nestlings. Overall, there was an increase in the rate of prey provisioning to the nestlings from 0.45 items.hr^?1 (10 days old) to 0.85 items.hr^?1 (21 days old). The male initially passed prey to the female but provisioned directly to older nestlings.     

Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.

Angelman syndrome (AS) most frequently results from large (> or = 5 Mb) de novo deletions of chromosome 15q11-q13. The deletions are exclusively of maternal origin, and a few cases of paternal uniparental disomy of chromosome 15 have been reported. The latter finding indicates that AS is caused by the absence of a maternal contribution to the imprinted 15q11-q13 region. Failure to inherit a paternal 15q11-q13 contribution results in the clinically distinct disorder of Prader-Willi syndrome. Cases of AS resulting from translocations or pericentric inversions have been observed to be associated with deletions, and there have been no confirmed reports of balanced rearrangements in AS. We report the first such case involving a paracentric inversion with a breakpoint located approximately 25 kb proximal to the reference marker D15S10. This inversion has been inherited from a phenotypically normal mother. No deletion is evident by molecular analysis in this case, by use of cloned fragments mapped to within approximately 1 kb of the inversion breakpoint. Several hypotheses are discussed to explain the relationship between the inversion and the AS phenotype.     

The conversion of potassium allylglucosinolate to 3,4-epithiobutanenitrile by Crambe abyssinica seed flour

An aqueous suspension of Crambe abyssinica seed flour efficiently converted potassium allylglucosinolate (sinigrin) into 3,4-epithiobutanenitrile.     

Characterization of differentiated quiescent and nonquiescent cells in yeast stationary-phase cultures

Cells in glucose-limited Saccharomyces cerevisiae cultures differentiate into quiescent (Q) and nonquiescent (NQ) fractions before entering stationary phase. To understand this differentiation, Q and NQ cells from 101 deletion-mutant strains were tested for viability and reproductive capacity. Eleven mutants that affected one or both phenotypes in Q or NQ fractions were identified. NQ fractions exhibit a high level of petite colonies, and nine mutants affecting this phenotype were identified. Microarray analysis revealed >1300 mRNAs distinguished Q from NQ fractions. Q cell-specific mRNAs encode proteins involved in membrane maintenance, oxidative stress response, and signal transduction. NQ-cell mRNAs, consistent with apoptosis in these cells, encode proteins involved in Ty-element transposition and DNA recombination. More than 2000 protease-released mRNAs were identified only in Q cells, consistent with these cells being physiologically poised to respond to environmental changes. Our results indicate that Q and NQ cells differentiate significantly, with Q cells providing genomic stability and NQ cells providing nutrients to Q cells and a regular source of genetic diversity through mutation and transposition. These studies are relevant to chronological aging, cell cycle, and genome evolution, and they provide insight into complex responses that even simple organisms have to starvation.     

Human Activities on the Deep Seafloor in the North East Atlantic: An Assessment of Spatial Extent

Background

Environmental impacts of human activities on the deep seafloor are of increasing concern. While activities within waters shallower than 200 m have been the focus of previous assessments of anthropogenic impacts, no study has quantified the extent of individual activities or determined the relative severity of each type of impact in the deep sea.

Methodology

The OSPAR maritime area of the North East Atlantic was chosen for the study because it is considered to be one of the most heavily impacted by human activities. In addition, it was assumed data would be accessible and comprehensive. Using the available data we map and estimate the spatial extent of five major human activities in the North East Atlantic that impact the deep seafloor: submarine communication cables, marine scientific research, oil and gas industry, bottom trawling and the historical dumping of radioactive waste, munitions and chemical weapons. It was not possible to map military activities. The extent of each activity has been quantified for a single year, 2005.

Principal Findings

Human activities on the deep seafloor of the OSPAR area of the North Atlantic are significant but their footprints vary. Some activities have an immediate impact after which seafloor communities could re-establish, while others can continue to make an impact for many years and the impact could extend far beyond the physical disturbance. The spatial extent of waste disposal, telecommunication cables, the hydrocarbon industry and marine research activities is relatively small. The extent of bottom trawling is very significant and, even on the lowest possible estimates, is an order of magnitude greater than the total extent of all the other activities.

Conclusions/Significance

To meet future ecosystem-based management and governance objectives for the deep sea significant improvements are required in data collection and availability as well as a greater awareness of the relative impact of each human activity.     

Status of Golden Eagle Aquila chrysaetos in Britain in 2015

Capsule: A complete survey of Golden Eagles Aquila chrysaetos in Britain in 2015 found that the population had increased by 15% since 2003 to 508 territorial pairs.

Aims: The survey aimed to investigate the population size, distribution and breeding success of Golden Eagles in Britain, and to compare results with similar surveys since the early 1980s.

Methods: Every home range was visited on a minimum of three occasions between January and August 2015. First, to look for eagles or signs of their presence (January–March), then to look for evidence of breeding or further checks for occupation (April–June) and finally to record productivity of nesting pairs (July–August).

Results: The figure of 508 territorial pairs represents a 15% increase in the population from 442 pairs in 2003. The proportion of home ranges occupied was 70%. The largest increases in the proportion of occupied home ranges were in south-central Highlands (71%), northern moors and flows (38%) and northwest Highlands (29%), with modest increases of up to 10% in the other regions. Productivity was lower in 2015 than in 2003, and there was significant variation in breeding success between regions.

Conclusion: The British Golden Eagle population has increased since 2003, although the species is absent from England and Wales. The population now meets the abundance target identified to define favourable conservation status in Scotland, and while home range occupancy has increased there is regional variation, with some regions falling below the target levels. A combination of increased annual monitoring and tagging of eagles, as well as the introduction of new legislation, may serve as effective deterrents against persecution of eagles thus facilitating this population increase. However, concerns remain over low levels of home range occupancy particularly in the east Highlands, but also the proportion of sub-adult pairs holding territory in that region and in the south-central Highlands. Persecution associated with grouse moor management has been highlighted as a particular population constraint in both of these areas.     

BAG-1L promotes keratinocyte differentiation in organotypic culture models and changes in relative BAG-1 isoform abundance may lead to defective stratification

In keratinocytes the human Bag-1 gene produces three different protein isoforms from a single messenger RNA, BAG-1L, BAG-1M and BAG-1S. In this study we questioned whether BAG-1L or the shorter isoforms would promote keratinocyte differentiation in organotypic cultures of HaCaT. HaCaT parental and vector cells showed stratification, but terminal differentiation was not complete. Cultures overexpressing BAG-1L isoform-specifically were of increased thickness, demonstrated pronounced expression of basal cytokeratin 5 and β1-integrin, suprabasal involucrin, cytokeratin 1 and plasma membrane-localised filaggrin, and a marked keratinized layer of cells at the surface. We were unable to overexpress BAG-1S and BAG-1M isoform-specifically. Overexpression of BAG-1M gave rise to organotypic cultures intermediate in differentiation to controls and those overexpressing BAG-1L. Cells overexpressing BAG-1S also exhibited elevated endogenous BAG-1. These produced slow growing cultures with high levels of basal cytokeratin 5, but little involucrin or cytokeratin 1. Suprabasal β1-integrin and Ki67 positive cells indicated defective stratification. The results suggest that BAG-1L potentiates epidermal differentiation, but disruption in the relative balance of isoforms towards overexpression of BAG-1S can lead to defective tissue patterning. Hence, a delicate balance of BAG-1 isoforms may be required to regulate normal epidermal stratification and differentiation, with important implications for aberrant differentiation in cancer.