2,973 research outputs found
Decline of plum trees caused by Pseudomonas syringae pathovars: a serious threat for plum production in the Netherlands
Lattice Knots in a Slab
In this paper the number and lengths of minimal length lattice knots confined
to slabs of width , is determined. Our data on minimal length verify the
results by Sharein et.al. (2011) for the similar problem, expect in a single
case, where an improvement is found. From our data we construct two models of
grafted knotted ring polymers squeezed between hard walls, or by an external
force. In each model, we determine the entropic forces arising when the lattice
polygon is squeezed by externally applied forces. The profile of forces and
compressibility of several knot types are presented and compared, and in
addition, the total work done on the lattice knots when it is squeezed to a
minimal state is determined
Minimal knotted polygons in cubic lattices
An implementation of BFACF-style algorithms on knotted polygons in the simple
cubic, face centered cubic and body centered cubic lattice is used to estimate
the statistics and writhe of minimal length knotted polygons in each of the
lattices. Data are collected and analysed on minimal length knotted polygons,
their entropy, and their lattice curvature and writhe
Reproductive cycle, nutrition and growth of captive blue spotted stingray, Dasyatis kuhlii (Dasyatidae)
At Burgers' Ocean 7 male and 3 female blue spotted stingrays, Dasyatis kuhlii were born over a period of 4.5 years. This paper describes the experiences of the captive breeding results of this species. The first two young died within 2 days of birth. One of them had an internal yolk sac, which may feed the young in the first few days. The other eight animals started to feed after 4 to 9 days on a variety of food types. Birth size of the young increased with increasing age of the parents. Mating occurred directly after parturition, so no seasonality could be defined. Gestation length ranged between 138 and 169 days, with a mean of 144.9±9.0 days (N = 11). Litter size was one, possibly caused by only one active ovarium. Sexual maturity of the two parent animals is approximately 3.5 years. The average feeding rations for the adults ranged between 10.1% BW week-1 (131 kcal kg BW-1 week-1) and 11.3% BW week-1 (172 kcal kg BW-1 week-1), with a feeding frequency of 4 times per week. The relationship between body weight (BW) and wingspan (WS) is given as BW = 3.6 × 10-5* WS2.940 (R2 = 0.9645; N = 45) (Received December 10 2007) (Accepted April 17 2009) (Online publication August 06 2009
The Compressibility of Minimal Lattice Knots
The (isothermic) compressibility of lattice knots can be examined as a model
of the effects of topology and geometry on the compressibility of ring
polymers. In this paper, the compressibility of minimal length lattice knots in
the simple cubic, face centered cubic and body centered cubic lattices are
determined. Our results show that the compressibility is generally not
monotonic, but in some cases increases with pressure. Differences of the
compressibility for different knot types show that topology is a factor
determining the compressibility of a lattice knot, and differences between the
three lattices show that compressibility is also a function of geometry.Comment: Submitted to J. Stat. Mec
A simple model of a vesicle drop in a confined geometry
We present the exact solution of a two-dimensional directed walk model of a
drop, or half vesicle, confined between two walls, and attached to one wall.
This model is also a generalisation of a polymer model of steric stabilisation
recently investigated. We explore the competition between a sticky potential on
the two walls and the effect of a pressure-like term in the system. We show
that a negative pressure ensures the drop/polymer is unaffected by confinement
when the walls are a macroscopic distance apart
Vermindering van pieken in gasafname en energiebesparing bij gewassen met een lage energiebehoefte : onderzoek 2001-2002
On trivial words in finitely presented groups
We propose a numerical method for studying the cogrowth of finitely presented
groups. To validate our numerical results we compare them against the
corresponding data from groups whose cogrowth series are known exactly.
Further, we add to the set of such groups by finding the cogrowth series for
Baumslag-Solitar groups and prove
that their cogrowth rates are algebraic numbers.Comment: This article has been rewritten as two separate papers, with improved
exposition. The new papers are arXiv:1309.4184 and arXiv:1312.572
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