Marine Sclerobiofacies: Encrusting and Endolithic Communities on Shells Through Time and Space

The concept of sclerobiofacies is defined herein as suites of sclerobiont encrusters and endiont borers (collectively sclerobionts) preserved on skeletons that characterize particular facies/environments. Skeletal components provide biologically standardized substrates; when possible, comparison of encrusting assemblages on fossil shells of the same or closely related eurytopic species provides a degree of substrate control comparable to modern experimentally deployed shells. Taxonomic composition of sclerobiont suites varies rather predictably among marine environments (e.g., based upon depth) but is primarily useful for comparisons of environments within local areas and limited time frames. Parameters that may be used to compare sclerobiofacies across broader spatial and temporal dimensions include: per shell and cumulative species richness (diversity), frequency of encrustation, areal coverage, and guild structure of encrusting taxa. Herein, we summarize characteristic sclerobiofacies in a series of Recent and ancient examples. Modern subtropical marine encrusters, documented on experimentally deployed molluscan shells at sites ranging from 15 to over 200 m, show high biont richness in shallow subtidal areas. Maximal areal coverages in Bahamian samples occur at about 20–30 m, whereas species richness increases downward to the deeper euphotic zone (∼75–80 m). Below this level, rapid decline in both richness and percent coverage results in deeper Dysphotic–Aphotic zone samples yielding only a few species with coverage rarely exceeding 5%. Burial is also a key factor such that rapidly buried shells in the Shallow Euphotic zone have species coverages, richnesses, and taxonomic compositions resembling long-exposed shells in deeper areas below the euphotic zone. Shelly substrates from the Cambrian to Early Ordovician exhibit only minor encrustation by solitary attached taxa, especially echinoderms; however, by the Late Ordovician various solitary (e.g., cornulitids, craniid brachiopods) and colonial forms (e.g., trepostome and tubuliporate bryozoans) form distinctive sclerobiofacies. Photic zone-related environments, judged independently on the basis of microendoliths, show overall lower taxonomic richness than modern counterparts. However, they also show common patterns, including a general decrease of richness and percent encrustation from Shallow Euphotic to Dysphotic/Aphotic zones. Comparable trends are seen in Middle Devonian exemplars from New York State. Not only were there consistent trends toward lowered diversity/coverage into deep-water settings but also an additional factor related to turbidity and/or sedimentation rate was identified from assemblages at comparable depths arrayed along a distal to proximal gradient with respect to siliciclastic input sources. Carboniferous sclerobiont suites from varied sites in North America show many of the same traits as their Devonian counterparts, although detailed depth zonations are not documented at present. The Permo-Triassic extinctions appear to have had a strong impact on the taxonomic composition of marine sclerobiofacies, although a paucity of studies obscures details of Mesozoic and Cenozoic sclerobiofacies. In general, they appear to have taxonomic compositions and patterns similar to those observed in the Recent. The concept of sclerobiofacies provides another tool for paleoenvironmental analysis. Together with litho-, ichno-, bio-, and taphofacies, the properties of shell encrusting assemblages will yield detailed further insights into ancient environmental gradients

A highly diverse siliceous sponge fauna (Porifera: Hexactinellida, Demospongiae) from the Eocene of north-eastern Italy: systematics and palaeoecology

A siliceous sponge fauna, consisting of more than 900 specimens, is described from an early Lutetian tuffite horizon in the Chiampo Valley, Lessini Mountains, north-eastern Italy. Thirty-two taxa (15 Hexactinellida, 17 Demospongiae) are determined and illustrated, belonging to 24 genera, two of which are new (Rigonia gen. nov. and Coronispongia gen. nov.). Among these, 10 new species are proposed: Stauractinella eocenica sp. nov., Rigonia plicata gen. et sp. nov., Hexactinella clampensis sp. nov., Camerospongia visentinae sp. nov., C. tuberculata sp. nov., Toulminia italica sp. nov., Coronispongia confossa gen. et sp. nov., Cavispongia scarpai sp. nov., Corallistes multiosculata sp. nov. and Bolidium bertii sp. nov. Of the genera identified at Chiampo, 14 range back to the Cretaceous, three to the Jurassic and one to the Triassic, while six are still extant. The studied fauna shows affinities with sponges from the Eocene of Spain and the Cretaceous of Germany. The sponge fossils are uncompressed and bodily preserved, but the original siliceous skeleton is dissolved and substituted by calcite. Delicate attachments can be nevertheless documented: some sponges attached to a hard substrate by encrustation, while others were anchored on soft sediments by root-like structures. The presence of different modes of attachment suggests heterogeneous substrate conditions. Small, possibly young, sponges are recorded too. The sponge fauna is essentially autochthonous and lived in the middle-outer part of a carbonate ramp, where it formed clusters. This study extends the geographical and stratigraphical range of many sponge taxa, including Camerospongia, Toulminia, Ozotrachelus and Bolidium, previously documented only from the Cretaceous. The Recent calcified demosponge genus Astrosclera is reported here in the Cenozoic for the first time, having been reported previously in the Triassic only. Additionally, this study documents the second worldwide occurrence of the Recent sphinctozoan genus Vaceletia in the Palaeogene, formerly recorded exclusively in Australia. http://zoobank.org/urn:lsid:zoobank.org:pub:B3466955-8E20-429A-89BE-42BAEB4002E8 \ua9 2016, \ua9 The Trustees of the Natural History Museum, London 2016. All Rights Reserved