In this paper we determine the torsion free rank of the group of endotrivial modules for any finite group of Lie type, in both defining and non-defining characteristic. On our way to proving this, we classify the maximal rank 2 elementary abelian ℓ-subgroups in any finite group of Lie type, for any prime ℓ, which may be of independent interest.
Abstract. We determine the torsion subgroup of the group of endotrivial modules for a finite solvable group in characteristic p. We also prove that our result would hold for p-solvable groups, provided a conjecture can be proved for the case of p-nilpotent groups.
Abstract. We complete a classification of the groups of endotrivial modules for the modular group algebras of symmetric groups and alternating groups. We show that for n ≥ p 2 the torsion subgroup of the group of endotrivial modules for the symmetric groups is generated by the sign representation. The torsion subgroup is trivial for the alternating groups.
We complete a classification of the groups of endotrivial modules for the modular group algebras of symmetric groups and alternating groups. We show that, for n p 2 , the torsion subgroup of the group of endotrivial modules for the symmetric groups is generated by the sign representation. The torsion subgroup is trivial for the alternating groups. The torsion-free part of the group is free abelian of rank 1 if n p 2 + p and has rank 2 if p 2 n < p 2 + p. This completes the work begun earlier by Carlson, Mazza and Nakano.
= Hom B (µ, ResHowever, a direct computation shows that Res J A J A ∩B χ is not trivial. So we have a contradiction to the assumption that Y A is endotrivial.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.