scholarly journals A maximal zero-free interval for chromatic polynomials of bipartite planar graphs

2008 ◽  
Vol 308 (11) ◽  
pp. 2285-2287 ◽  
Author(s):  
F.M. Dong ◽  
K.M. Koh
1992 ◽  
Vol 101 (1-3) ◽  
pp. 333-341 ◽  
Author(s):  
D.R. Woodall

2018 ◽  
Vol 27 (6) ◽  
pp. 988-998 ◽  
Author(s):  
THOMAS J. PERRETT ◽  
CARSTEN THOMASSEN

We prove that the roots of the chromatic polynomials of planar graphs are dense in the interval between 32/27 and 4, except possibly in a small interval around τ + 2 where τ is the golden ratio. This interval arises due to a classical result of Tutte, which states that the chromatic polynomial of every planar graph takes a positive value at τ + 2. Our results lead us to conjecture that τ + 2 is the only such number less than 4.


1954 ◽  
Vol 6 ◽  
pp. 80-91 ◽  
Author(s):  
W. T. Tutte

SummaryTwo polynomials θ(G, n) and ϕ(G, n) connected with the colourings of a graph G or of associated maps are discussed. A result believed to be new is proved for the lesser-known polynomial ϕ(G, n). Attention is called to some unsolved problems concerning ϕ(G, n) which are natural generalizations of the Four Colour Problem from planar graphs to general graphs. A polynomial χ(G, x, y) in two variables x and y, which can be regarded as generalizing both θ(G, n) and ϕ(G, n) is studied. For a connected graph χ(G, x, y) is defined in terms of the “spanning” trees of G (which include every vertex) and in terms of a fixed enumeration of the edges.


1993 ◽  
Vol 2 (3) ◽  
pp. 325-336 ◽  
Author(s):  
Bill Jackson

LetGbe a graph andP(G, t) be the chromatic polynomial ofG. It is known thatP(G, t) has no zeros in the intervals (−∞, 0) and (0, 1). We shall show thatP(G, t) has no zeros in (1, 32/27]. In addition, we shall construct graphs whose chromatic polynomials have zeros arbitrarily close to 32/27.


1986 ◽  
Vol 56 (03) ◽  
pp. 268-270 ◽  
Author(s):  
M Morfini ◽  
D Rafanelli ◽  
G Longo ◽  
A Messori ◽  
P Rossi Ferrini

SummaryPost-infusion hepatitis is known to occur very frequently in haemophiliacs after treatment with unheated commercial clotting factor concentrates, obtained from large plasma donation pool. On the contrary, single-donor cryoprecipitate is likely to carry a lower risk of transmitting hepatitis.To evaluate this hypothesis, we retrospectively reviewed the medical records of 25 first infused haemophiliacs (from 1981 to 1984) treated with unheated commercial clotting factor concentrates (n = 19) or cryoprecipitate (n = 6).The hepatitis-free interval after the beginning of therapy was expressed as exposure days. The end point of each patient, i.e. the hepatitis occurrence, was defined as an increase of aminotransferases (ALT and AST) and/or the seroconversion of HBV-markers, which were checked every three months.The life-table method and log-rank test showed that cryo-precipitates had a significantly longer hepatitis-free interval (p = 0.0131, log-rank test) and a lower risk of transmitting hepatitis (p = 0.01-0.05, life-table method) than the commercial concentrates. However, the safety of cryoprecipitate therapy was shown to cover only a few exposure days, and so the real advantage of this product depends on the bleeding frequency of the patient concerned.We believe that these methods and our findings may be useful to assess and compare the safety of the new “heat-treated” clotting factor concentrates.


Author(s):  
Akane SETO ◽  
Aleksandar SHURBEVSKI ◽  
Hiroshi NAGAMOCHI ◽  
Peter EADES

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