Most demersal fishes undergo a dispersal phase as larvae, which strongly influences the connectivity among adult populations and, consequently, their genetic structure and replenishment opportunities. Because this phase is difficult to observe directly, it is frequently simulated through numerical models, most of which consider larvae as passive or only vertically migrating. However, in several...

We prove that given any fixed edge ra in a 4-connected graph G, there exists a cycle C through ra such that G − (V (C) − {r}) is 2-connected. This will provide the first step in a decomposition for 4-connected graphs. We also prove that for any given edge e in a 5-connected graph G there exists an induced cycle C through e in G such that G−V (C) is 2-connected. This provides evidence for a conj...

It was conjectured by Thomassen ([B. Alspach, C. Godsil, Cycle in graphs, Ann. Discrete Math. 27 (1985)], p. 466) that every longest circuit of a 3-connected graph must have a chord. This conjecture is verified for locally 4-connected planar graphs, that is, let N be the set of natural numbers; then there is a function h : N → N such that, for every 4-connected graph G embedded in a surface S w...

Let Tn denote the set of all unrooted and unlabeled trees with n vertices, and (i, j) a double-star. By assuming that every tree of Tn is equally likely, we show that the limiting distribution of the number of occurrences of the double-star (i, j) in Tn is normal. Based on this result, we obtain the asymptotic value of Randić index for trees. Fajtlowicz conjectured that for any connected graph ...

For a 2-connected matroid M , Cunningham and Edmonds gave a tree decomposition that displays all of its 2-separations. When M is 3-connected, two 3-separations are equivalent if one can be obtained from the other by passing through a sequence of 3-separations each of which is obtained from its predecessor by moving a single element from one side of the 3-separation to the other. Oxley, Semple, ...

Let G be a 4-connected graph. For an edge e of G, we do the following operations on G: first, delete the edge e from G, resulting the graph G − e; second, for all the vertices x of degree 3 in G− e, delete x from G− e and then completely connect the 3 neighbors of x by a triangle. If multiple edges occur, we use single edges to replace them. The final resultant graph is denoted by G a e. If G a...

the eccentricity connectivity index of a molecular graph g is defined as (g) = av(g)deg(a)ε(a), where ε(a) is defined as the length of a maximal path connecting a to othervertices of g and deg(a) is degree of vertex a. here, we compute this topological index forsome infinite classes of dendrimer graphs.

Schizophrenia is a psychotic disorder characterized by functional dysconnectivity or abnormal integration between distant brain regions. Recent functional imaging studies have implicated large-scale thalamo-cortical connectivity as being disrupted in patients. However, observed connectivity differences in schizophrenia have been inconsistent between studies, with reports of hyperconnectivity an...

in this paper we present explicit formulas for the eccentric connectivity index of three classesof chain hexagonal cacti. further, it is shown that the extremal chain hexagonal cacti withrespect to the eccentric connectivity index belong to one of the considered types. some openproblems and possible directions of further research are mentioned in the concluding section.

in this paper, we calculate the eccentric connectivity index and the eccentricity sequence of two infinite classes of fullerenes with 50 + 10k and 60 + 12k (k in n) carbon atoms.