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Despite the importance of Tethys Himalayan or North Himalayan gneiss domes for discussing extrusive flow of the underlying Greater Himalayan Sequence, these metamorphic domes in general remain poorly documented. The main exception is the Kangmar dome. The Malashan metamorphic complex, a newly documented North Himalayan gneiss dome, is shown to have strong similarities with the Kangmar dome, suggesting that the North Himalayan gneiss domes have the following features in common: (i) Barrovian-type metamorphism with grade increasing towards a centrally located two-mica granite; (ii) the presence of two dominant ductile deformation stages, D1 and D2, with D2 showing an increasing strength towards the granite contacts; and (iii) the development of a strong D2 foliation (gneissosity) in the outermost part of the granite cores. In addition, field and bulk-chemical studies show: (i) D2 is associated with a dominant top-to-the-north sense of shear (in disagreement with the most recent kinematic studies in Kangmar dome); (ii) the deposition age of associated metasediments is upper Jurassic suggesting that the Malashan dome is located not at the base, but within the middle section of the Tethys Himalaya; and (iii) in contrast to the Kangmar granitic gneiss that is interpreted as Indian basement, three granitic bodies in Malashan all formed as young intrusive bodies during the Himalayan orogeny. These results suggest that the formation mechanism of the North Himalayan gneiss domes needs to be re-evaluated to test the rigidity of the hanging wall assumed in channel flow models.

The heteromorph ammonite Pravitoceras sigmoidale from the Upper Cretaceous Seidan Formation (Izumi Group) in south-west Japan is frequently encrusted by sessile anomiid bivalves. Fossils of P. sigmoidale with anomiids are often concentrated at the top of or just above turbidite sandstones. Projecting retroversal hooks and apertures of P. sigmoidale are usually intact, and some individuals are associated with jaw apparatuses near apertures. Anomiids are found on both sides and ventral peripheries of P. sigmoidale conchs, attached predominantly to body chambers. These modes of occurrence suggest that the encrustation by anomiids occurred not on post-mortem floating or sunken carcasses but on live conchs and that these organisms were rapidly buried by turbidity current deposits shortly after death. Attachment to both flanks and ventral peripheries of the retroversal hooks may indicate that at least adult individuals of P. sigmoidale did not lie on the sea floor and did not drag their body chambers. It is suggested that fully mature individuals of this ammonite species lived for a long period of time after having formed the retroversal hook because a few generations of anomiids have colonized a single body chamber. Such colonization by anomiids is also observed on Didymoceras awajiense, which is considered to be the closely related ancestral species of P. sigmoidale. This anomiidheteromorph ammonite commensal relationship might continue to persist in descendants during the course of evolution of these heteromorph ammonites.

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