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Does Darwin Belong in Business? The Danger and Comfort of the Evolutionary Metaphor

The metaphor of Darwinism has been extensively researched and analysed in other research disciplines. The usage of the biological metaphor of “Darwinism” in ITrelated headlines is documented and reviewed. The use of the Darwinian metaphor in business studies has changed from its usage by Veblen and Stamp as a descriptor for the scientific method. More recently its meaning has been transformed to synonymy with the “struggle for existence”. The use of this metaphor in IT carries with it a reassurance, which can endanger consumer requirements for performance and accountability

Systems of Winter Milk Production based on all Autumn Calving Cows

End of Project ReportA supply of winter milk is needed by certain milk processors for the production of high value dairy products with a short shelf life to balance the high level of commodity based products which are mainly manufactured from seasonal milk produced from spring calving herds. Winter milk is generally produced by suppliers with split calving herds. A proportion of the cows (30-50%) calve in Autumn (September-December) to supply winter milk for which they receive a winter bonus for a contracted supply for the months of October to February. The remainder of the herd calve in Spring (Feb-April) and produce milk mainly off grass for which no bonus is paid. This system evens out the supply of milk throughout the year but complicates management, as it involves running two herds on the farm, with two calving seasons, two breeding seasons and two sets of replacement heifers to be reared. Also there is no break from milking. A system of winter milk production based on calving all of the cows in Autumn would be simpler, as it would involve only one herd, with a break from milking in late Summer and would appeal to many winter milk producers. In this study the feasibility of operating an all Autumn calving herd was examined, in terms of management, calving, winter feeding, reproduction and summer grazing. The herd was located in the Ballyderown farm attached to the Moorepark Research Centre. Alternative winter feeding systems were put in place over a three year period to compare the feed requirements and milk production of each system. A control system based on grass silage as the sole forage was compared with one where grass silage was supplemented with extended grazing of grass in late Autumn and early Spring or with a system based on a mixed forage diet based on grass silage, maize silage, brewers grains or a brewers grains/beet pulp mix. Grass silage and maize silage was produced within each system and the cows on each system were grazed separately within their own farmlets. The overall stocking rate for each system was 2.7 cows/ha using 350 kg N fertiliser/ha in addition to cattle slurry. Cows were dried off in mid-late July and were grazed tightly until calving down. The calving season extended from early September to early December. Most cows calved down outdoors at pasture or in a calving paddock without assistance. Cows were housed from early November to late March and were allocated to their respective diets in batches according to milk yield, lactation number and calving date. The cows given access to winter grass were given a daily allocation of grass (6-8 kg DM/cow) and grazed between morning and evening milking

Integral constraints on the monodromy group of the hyperkahler resolution of a symmetric product of a K3 surface

Let M be a 2n-dimensional Kahler manifold deformation equivalent to the Hilbert scheme of length n subschemes of a K3 surface S. Let Mon be the group of automorphisms of the cohomology ring of M, which are induced by monodromy operators. The second integral cohomology of M is endowed with the Beauville-Bogomolov bilinear form. We prove that the restriction homomorphism from Mon to the isometry group O[H^2(M)] is injective, for infinitely many n, and its kernel has order at most 2, in the remaining cases. For all n, the image of Mon in O[H^2(M)] is the subgroup generated by reflections with respect to +2 and -2 classes. As a consequence, we get counter examples to a version of the weight 2 Torelli question, when n-1 is not a prime power.Comment: Version 3: Latex, 54 pages. Expository change

Measurement of the B Semileptonic Branching Fraction with Lepton Tags

We have used the CLEO II detector and 2.06fb^(-1) of ϒ(4S) data to measure the B-meson semileptonic branching fraction. The B→Xeν momentum spectrum was obtained over nearly the full momentum range by using charge and kinematic correlations in events with a high-momentum lepton tag and an additional electron. We find B(B→Xeν) = (10.49±0.17±0.43)%, with overall systematic uncertainties less than those of untagged single-lepton measurements. We use this result to calculate the magnitude of the Cabibbo-Kobayashi-Maskawa matrix element V_(cb) and to set an upper limit on the fraction of ϒ(4S) decays to final states other than BB̅

Observation of the Cabibbo-suppressed charmed baryon decay Λ_c^+→pφ

We report the observation of the Cabibbo-suppressed decays Λ_c^+→pK^-K^+ and Λ_c^+→pφ using data collected with the CLEO II detector at CESR. The latter mode, observed for the first time with significant statistics, is of interest as a test of color suppression in charm decays. We have determined the branching ratios for these modes relative to Λ_c^+→pK^-π^+ and compared our results with theory

Some Direct Gillnet Selectivity Tests for Brown Trout Populations

Direct gillnet selectivity tests for introduced brown trout populations in three Irish lakes are outlined. The net gangs and netting procedure utilised are described. Data indicates that the gear used was capable of capturing a random cross section of a trout stock in the length frequency range 19.8 to 47.7 centimetres

Measurement of B(D^0 → K^-π^+) Using Partial Reconstruction of B̅ → D^(*+)Xℓ^-ν̅

We present a measurement of the absolute branching fraction for D^0→K^-π^+ using the reconstruction of the decay chain B̅ →D^(*+)Xℓ^-ν̅ , D^(*+)→D^0π^+ where only the lepton and the low-momentum pion from the D^(*+) are detected. With data collected by the CLEO II detector at the Cornell Electron Storage Ring, we have determined B(D^0→K^-π^+) = [3.81±0.15(stat)±0.16(syst)]%

Ecological Changes over 21 Years Caused by Drainage of a salmonid stream, the Trimblestown River

A site on the Trimblestown River (Boyne Catchment) studied by McCarthy (1977 and 1983), pre- and post-drainage (1968 to 1974), was re-examined by the author in 1989. Changes in the nature of the stream bed, in-stream and bank flora and fish stocks over the entire period (1968 to 1989) are reviewed. Data indicate a general ecological recovery of the site 17 years after drainage works