scholarly journals The singular acyclic matrices of even order with a P-set of maximum size

Filomat ◽  
2016 ◽  
Vol 30 (13) ◽  
pp. 3403-3409 ◽  
Author(s):  
Zhibin Du ◽  
Fonseca da
Keyword(s):  
Nonempty Subset ◽  
Symmetric Matrix ◽  
Maximum Size ◽  
Principal Submatrix ◽  
Even Order

Let mA(0) denote the nullity of a given n-by-n symmetric matrix A. Set A(?) for the principal submatrix of A obtained after deleting the rows and columns indexed by the nonempty subset ? of {1,...,n}. When mA(?)(0) = mA(0) + |?|, we call ? a P-set of A. The maximum size of a P-set of A is denoted by Ps(A). It is known that Ps(A) ? ?n/2? and this bound is not sharp for singular acyclic matrices of even order. In this paper, we find the bound for this case and classify all of the underlying trees. Some illustrative examples are provided.

scholarly journals The characterization of elliptic curves over finite fields

1988 ◽  
Vol 45 (2) ◽  
pp. 275-286 ◽  
Author(s):  
J. W. P. Hirschfeld ◽  
J. F. Voloch
Keyword(s):  
Elliptic Curves ◽  
Finite Fields ◽  
Sufficient Conditions ◽  
Maximum Size ◽  
Desarguesian Plane ◽  
Cubic Curve ◽  
Odd Order ◽  
Even Order ◽  
Curves Over Finite Fields

AbstractIn a finite Desarguesian plane of odd order, it was shown by Segre thirty years ago that a set of maximum size with at most two points on a line is a conic. Here, in a plane of odd or even order, sufficient conditions are given for a set with at most three points on a line to be a cubic curve. The case of an elliptic curve is of particular interest.

scholarly journals The Sharp Threshold for Maximum-Size Sum-Free Subsets in Even-Order Abelian Groups

2015 ◽  
Vol 24 (4) ◽  
pp. 609-640 ◽  
Author(s):  
NEAL BUSHAW ◽  
MAURÍCIO COLLARES NETO ◽  
ROBERT MORRIS ◽  
PAUL SMITH
Keyword(s):  
Recent Work ◽  
Abelian Groups ◽  
Maximum Size ◽  
Constant Factor ◽  
Sharp Threshold ◽  
Even Order ◽  
Free Subset ◽  
Free Sets

We study sum-free sets in sparse random subsets of even-order abelian groups. In particular, we determine the sharp threshold for the following property: the largest such set is contained in some maximum-size sum-free subset of the group. This theorem extends recent work of Balogh, Morris and Samotij, who resolved the caseG= ℤ2n, and who obtained a weaker threshold (up to a constant factor) in general.

scholarly journals A note on skew-symmetric determinants

1993 ◽  
Vol 36 (2) ◽  
pp. 335-338 ◽  
Author(s):  
Walter Ledermann
Keyword(s):  
Classical Result ◽  
Short Proof ◽  
Symmetric Matrix ◽  
Schur Complement ◽  
Even Order ◽  
Skew Symmetric Matrix

A short proof, based on the Schur complement, is given of the classical result that the determinant of a skew-symmetric matrix of even order is the square of a polynomial in its coefficients.

Continuous Quantitative Monitoring of Mural, Platelet-Dependent, Thrombus Kinetics in the Crushed Rat Femoral Vein

1991 ◽  
Vol 65 (04) ◽  
pp. 425-431 ◽  
Author(s):  
F Stockmans ◽  
H Deckmyn ◽  
J Gruwez ◽  
J Vermylen ◽  
R Acland
Keyword(s):  
Thrombus Formation ◽  
Femoral Vein ◽  
Maximum Size ◽  
Digital Analysis ◽  
Video Recordings ◽  
Quantitative Monitoring ◽  
Set Up ◽  
Kinetics Of ◽  
Quantitative Nature

SummaryA new in vivo method to study the size and dynamics of a growing mural thrombus was set up in the rat femoral vein. The method uses a standardized crush injury to induce a thrombus, and a newly developed transilluminator combined with digital analysis of video recordings. Thrombi in this model formed rapidly, reaching a maximum size 391 ± 35 sec following injury, after which they degraded with a half-life of 197 ± 31 sec. Histological examination indicated that the thrombi consisted mainly of platelets. The quantitative nature of the transillumination technique was demonstrated by simultaneous measurement of the incorporation of 111In labeled platelets into the thrombus. Thrombus formation, studied at 30 min interval in both femoral veins, showed satisfactory reproducibility overall and within a given animalWith this method we were able to induce a thrombus using a clinically relevant injury and to monitor continuously and reproducibly the kinetics of thrombus formation in a vessel of clinically and surgically relevant size

Persistence of giants: population dynamics of the limpet Scutellastra laticostata on rocky shores in Western Australia

2020 ◽  
Vol 646 ◽  
pp. 79-92
Author(s):  
RE Scheibling ◽  
R Black
Keyword(s):  
Population Dynamics ◽  
Western Australia ◽  
Size Structure ◽  
Survival Rates ◽  
Maximum Size ◽  
High Rate ◽  
Adult Survival ◽  
Rocky Shores ◽  
Adult Size ◽  
Decadal Time Scale

Population dynamics and life history traits of the ‘giant’ limpet Scutellastra laticostata on intertidal limestone platforms at Rottnest Island, Western Australia, were recorded by interannual (January/February) monitoring of limpet density and size structure, and relocation of marked individuals, at 3 locations over periods of 13-16 yr between 1993 and 2020. Limpet densities ranged from 4 to 9 ind. m-2 on wave-swept seaward margins of platforms at 2 locations and on a rocky notch at the landward margin of the platform at a third. Juvenile recruits (25-55 mm shell length) were present each year, usually at low densities (<1 m-2), but localized pulses of recruitment occurred in some years. Annual survival rates of marked limpets varied among sites and cohorts, ranging from 0.42 yr-1 at the notch to 0.79 and 0.87 yr-1 on the platforms. A mass mortality of limpets on the platforms occurred in 2003, likely mediated by thermal stress during daytime low tides, coincident with high air temperatures and calm seas. Juveniles grew rapidly to adult size within 2 yr. Asymptotic size (L∞, von Bertalanffy growth model) ranged from 89 to 97 mm, and maximum size from 100 to 113 mm, on platforms. Growth rate and maximum size were lower on the notch. Our empirical observations and simulation models suggest that these populations are relatively stable on a decadal time scale. The frequency and magnitude of recruitment pulses and high rate of adult survival provide considerable inertia, enabling persistence of these populations in the face of sporadic climatic extremes.

scholarly journals Existence of Multiple Positive Solutions for Even Order Multi-Point Boundary Value Problems

2007 ◽  
Vol 14 (4) ◽  
pp. 775-792
Author(s):  
Youyu Wang ◽  
Weigao Ge
Keyword(s):  
Fixed Point ◽  
Fixed Point Theorem ◽  
Boundary Value Problem ◽  
Boundary Value Problems ◽  
Positive Solutions ◽  
Boundary Value ◽  
Sufficient Conditions ◽  
Multiple Positive Solutions ◽  
Point Boundary ◽  
Even Order

Abstract In this paper, we consider the existence of multiple positive solutions for the 2𝑛th order 𝑚-point boundary value problem: where (0,1), 0 < ξ 1 < ξ 2 < ⋯ < ξ 𝑚–2 < 1. Using the Leggett–Williams fixed point theorem, we provide sufficient conditions for the existence of at least three positive solutions to the above boundary value problem. The associated Green's function for the above problem is also given.

scholarly journals ON THE HEIGHT AND RELATIONAL COMPLEXITY OF A FINITE PERMUTATION GROUP

2021 ◽  
pp. 1-40
Author(s):  
NICK GILL ◽  
BIANCA LODÀ ◽  
PABLO SPIGA
Keyword(s):  
Permutation Group ◽  
Model Theory ◽  
Independent Set ◽  
Maximum Size ◽  
Proper Subset ◽  
Permutation Groups ◽  
Finite Permutation Group ◽  
Pointwise Stabilizer ◽  
Relational Complexity

Abstract Let G be a permutation group on a set $\Omega $ of size t. We say that $\Lambda \subseteq \Omega $ is an independent set if its pointwise stabilizer is not equal to the pointwise stabilizer of any proper subset of $\Lambda $ . We define the height of G to be the maximum size of an independent set, and we denote this quantity $\textrm{H}(G)$ . In this paper, we study $\textrm{H}(G)$ for the case when G is primitive. Our main result asserts that either $\textrm{H}(G)< 9\log t$ or else G is in a particular well-studied family (the primitive large–base groups). An immediate corollary of this result is a characterization of primitive permutation groups with large relational complexity, the latter quantity being a statistic introduced by Cherlin in his study of the model theory of permutation groups. We also study $\textrm{I}(G)$ , the maximum length of an irredundant base of G, in which case we prove that if G is primitive, then either $\textrm{I}(G)<7\log t$ or else, again, G is in a particular family (which includes the primitive large–base groups as well as some others).

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