A supertree is a connected and acyclic hypergraph. For a hypergraph H, the maximal modulus of the eigenvalues of its adjacency tensor is called the spectral radius of H. By applying the operation of moving edges on hy...A supertree is a connected and acyclic hypergraph. For a hypergraph H, the maximal modulus of the eigenvalues of its adjacency tensor is called the spectral radius of H. By applying the operation of moving edges on hypergraphs and the weighted incidence matrix method, we determine the ninth and the tenth k-uniform supertrees with the largest spectral radii among all k-uniform supertrees on n vertices, which extends the known result.展开更多
Let S(m,d,k)be the set of k-uniform supertrees with m edges and diameter d,and S1(m,d,k)be the k-uniform supertree obtained from a loose path u_(1),e_(1),u_(2),e_(2),...,u_(d),e_(d),u_(d+1),with length d by attaching ...Let S(m,d,k)be the set of k-uniform supertrees with m edges and diameter d,and S1(m,d,k)be the k-uniform supertree obtained from a loose path u_(1),e_(1),u_(2),e_(2),...,u_(d),e_(d),u_(d+1),with length d by attaching m-d edges at vertex u_[d/2]+1.In this paper,we mainly determine S1(m,d,k)with the largest signless Laplacian spectral radius in S(m,d,k)for 3≤d≤m-1.We also determine the supertree with the second largest signless Laplacian spectral radius in S(m,3,k).Furthermore,we determine the unique/c-uniform supertree with the largest signless Laplacian spectral radius among all fc-uniform supertrees with n vertices and pendent edges(vertices).展开更多
A supertree is a connected and acyclic hypergraph.We investigate the supertrees with the extremal spectral radii among several kinds of r-uniform supertrees.First,by using the matching polynomials of supertrees,a new ...A supertree is a connected and acyclic hypergraph.We investigate the supertrees with the extremal spectral radii among several kinds of r-uniform supertrees.First,by using the matching polynomials of supertrees,a new and useful grafting operation is proposed for comparing the spectral radii of supertrees,and its applications are shown to obtain the supertrees with the extremal spectral radi among some kinds of r-uniform supertrees.Second,the supertree with the third smallest spectral radius among the r-uniform supertrees is deduced.Third,among the r-uniform supertrees with a given maximum degree,the supertree with the smallest spectral radius is derived.At last,among the r-uniform starlike supert rees,the supertrees with the smallest and the largest spectral radii are characterized.展开更多
In the mid 19th century, systematic biologists realized that observable similarities and differences among a group of related species could be the basis for hypotheses about the evolutionary relationships among the sp...In the mid 19th century, systematic biologists realized that observable similarities and differences among a group of related species could be the basis for hypotheses about the evolutionary relationships among the species and their ancestors. Such hypotheses can be expressed as characters. A character is comprised of two or more character states of species considered to be similar with respect to a basis for comparison. The states of a character may also be arranged into a character state tree to hypothesize speciation events associated with changes from one character state to another. In the mid 20th century, some systematists realized that sometimes pairs of characters (or character state trees) could be incompatible as hypotheses, i.e., they could not both be true. Through the 1950s, '60s and '70s, tests for, and ways to resolve, incompatibilities were used to estimate an ancestor rela-tion based on mutually compatible characters. An estimate was often shown as a diagram connecting ancestors to their immediate descendants (not quite correctly) called a phylogenetic tree. More recently, other applications of compatibility concepts have been developed, including: identify characters that appear to be random in the context of their data set; combine estimates of ancestor relations for subsets of taxa in a larger collection into a single estimate (a so-called supertree) for the whole collection; and interpret geographic patterns in an evolutionary context.展开更多
Aims The aim of this article is 3-fold.First,we present an updated version of a published megaphylogeny of vascular plants that can be used in studies of plant ecology and biogeography.second,we develop a tool that ca...Aims The aim of this article is 3-fold.First,we present an updated version of a published megaphylogeny of vascular plants that can be used in studies of plant ecology and biogeography.second,we develop a tool that can be used by botanists and plant ecologists to generate phylogenetic hypotheses in three scenarios.Third,we use a set of regional assemblages of angiosperm trees in North america as a model system to evaluate the effect of differences in phylogenies generated using the three scenarios on the quantification of phylogenetic properties and the relationship between measures of phylogenetic properties and environment.Methods The taxonomy and nomenclature of plant species in the megaphy-logeny were standardized according to The Plant list(version 1.1).a tool for generating phylogenies was created using the r language.The robustness of derived phylogenies was evaluated using correlation and regression analyses.Important Findingsan updated megaphylogeny of vascular plants(PhytoPhylo)and a tool for reconstructing phylogenies of seed plants(s.Phylomaker)were generated.our study shows that phylogenies generated by s.Phylomaker using the PhytoPhylo megaphylogeny as a backbone are nearly as good as phylogeny resolved at the species level when using derived phylogenies to quantify phylogenetic properties(e.g.phylogenetic diversity and phylogenetic relatedness)of biological assemblages,and that s.Phylomaker-generated phylogenies are robust for studies of community ecology and biogeography,par-ticularly those seeking for patterns of phylogenetic properties along environmental gradients.展开更多
基金This work was supported in part by the National Natural Science Foundation of China (Grant No. 11101263).
文摘A supertree is a connected and acyclic hypergraph. For a hypergraph H, the maximal modulus of the eigenvalues of its adjacency tensor is called the spectral radius of H. By applying the operation of moving edges on hypergraphs and the weighted incidence matrix method, we determine the ninth and the tenth k-uniform supertrees with the largest spectral radii among all k-uniform supertrees on n vertices, which extends the known result.
基金supported in part by the National Natural Science Foundation of China(Grant No.11871398)the Natural Science Foundation of Shaanxi Province(Nos.2020JQ-107,2020JQ-696)the Seed Foundation of Innovation and Creation for Graduate Students in Northwestern Polytechnical University(Nos.ZZ2018171,CX2020190).
文摘Let S(m,d,k)be the set of k-uniform supertrees with m edges and diameter d,and S1(m,d,k)be the k-uniform supertree obtained from a loose path u_(1),e_(1),u_(2),e_(2),...,u_(d),e_(d),u_(d+1),with length d by attaching m-d edges at vertex u_[d/2]+1.In this paper,we mainly determine S1(m,d,k)with the largest signless Laplacian spectral radius in S(m,d,k)for 3≤d≤m-1.We also determine the supertree with the second largest signless Laplacian spectral radius in S(m,3,k).Furthermore,we determine the unique/c-uniform supertree with the largest signless Laplacian spectral radius among all fc-uniform supertrees with n vertices and pendent edges(vertices).
基金supported by the National Natural Science Foundation of China(Grant Nos.11871040,11001166).
文摘A supertree is a connected and acyclic hypergraph.We investigate the supertrees with the extremal spectral radii among several kinds of r-uniform supertrees.First,by using the matching polynomials of supertrees,a new and useful grafting operation is proposed for comparing the spectral radii of supertrees,and its applications are shown to obtain the supertrees with the extremal spectral radi among some kinds of r-uniform supertrees.Second,the supertree with the third smallest spectral radius among the r-uniform supertrees is deduced.Third,among the r-uniform supertrees with a given maximum degree,the supertree with the smallest spectral radius is derived.At last,among the r-uniform starlike supert rees,the supertrees with the smallest and the largest spectral radii are characterized.
文摘In the mid 19th century, systematic biologists realized that observable similarities and differences among a group of related species could be the basis for hypotheses about the evolutionary relationships among the species and their ancestors. Such hypotheses can be expressed as characters. A character is comprised of two or more character states of species considered to be similar with respect to a basis for comparison. The states of a character may also be arranged into a character state tree to hypothesize speciation events associated with changes from one character state to another. In the mid 20th century, some systematists realized that sometimes pairs of characters (or character state trees) could be incompatible as hypotheses, i.e., they could not both be true. Through the 1950s, '60s and '70s, tests for, and ways to resolve, incompatibilities were used to estimate an ancestor rela-tion based on mutually compatible characters. An estimate was often shown as a diagram connecting ancestors to their immediate descendants (not quite correctly) called a phylogenetic tree. More recently, other applications of compatibility concepts have been developed, including: identify characters that appear to be random in the context of their data set; combine estimates of ancestor relations for subsets of taxa in a larger collection into a single estimate (a so-called supertree) for the whole collection; and interpret geographic patterns in an evolutionary context.
文摘Aims The aim of this article is 3-fold.First,we present an updated version of a published megaphylogeny of vascular plants that can be used in studies of plant ecology and biogeography.second,we develop a tool that can be used by botanists and plant ecologists to generate phylogenetic hypotheses in three scenarios.Third,we use a set of regional assemblages of angiosperm trees in North america as a model system to evaluate the effect of differences in phylogenies generated using the three scenarios on the quantification of phylogenetic properties and the relationship between measures of phylogenetic properties and environment.Methods The taxonomy and nomenclature of plant species in the megaphy-logeny were standardized according to The Plant list(version 1.1).a tool for generating phylogenies was created using the r language.The robustness of derived phylogenies was evaluated using correlation and regression analyses.Important Findingsan updated megaphylogeny of vascular plants(PhytoPhylo)and a tool for reconstructing phylogenies of seed plants(s.Phylomaker)were generated.our study shows that phylogenies generated by s.Phylomaker using the PhytoPhylo megaphylogeny as a backbone are nearly as good as phylogeny resolved at the species level when using derived phylogenies to quantify phylogenetic properties(e.g.phylogenetic diversity and phylogenetic relatedness)of biological assemblages,and that s.Phylomaker-generated phylogenies are robust for studies of community ecology and biogeography,par-ticularly those seeking for patterns of phylogenetic properties along environmental gradients.