During the Early Jurassic, reefs in the shallow seas of the Atlas Rift experienced substantial changes as they recovered from the end-Triassic mass extinction. Excellent Lower Jurassic reef deposits documenting this change occur in the Central High Atlas region of Morocco, and herein we describe Owl Olistolith, a micro-olistolith found in lower Pliensbachian-aged (∼ 188.7 million years ago) Moroccan strata. The olistolith records the composition of a reef that grew within the Atlas rift zone and represents a snapshot of reef recovery ∼ 10 million years after the end-Triassic mass extinction. Owl Olistolith is derived from a reef that was originally situated on an outer platform within fair weather wave base; it broke loose and was transported to deeper water and deposited amongst marls. Corals and microbialites formed the primary framework of the reef; microproblematica, foraminifera, and other minor components were also present. The reef can be divided into two dominant facies: a microbialite facies that contains no corals (54%–94% microbialites), and a coral-microbialite facies with substantial proportions of both microbialite (23%–50%) and corals (14%–72%). The micro-olistolith contains at least 15 distinct coral types. In this study, seven coral genera were identified, three of which represent taxa that span the Triassic/Jurassic boundary, including Coryphyllia, Stylophyllopsis, and Margarosmilia. These results indicate that, although surviving taxa played a significant role, newly evolved corals were the most important taxa in the reestablishment of reef ecosystems in the Early Jurassic of Morocco.

Sea turtles are characterized by a wide variety of invertebrate ectoparasites. Few of these ectoparasites leave a permanent indication of their presence on the skeletal remains of their host taxa and thus represent ecological information doomed to be lost in the paleontological record. Some barnacle taxa provide an exception to this, in that they cause the formation of small, subcircular to circular divots, pits, and holes on the skull, mandible, carapace or plastron of sea turtles. Loggerhead Sea Turtle (Caretta caretta) skeletons from Cumberland Island, Georgia, USA were examined to assess the presence, frequency, and loci of occurrence of barnacle pits, and to establish which taxa are involved in pit development.

Six types of divot and pit attributed to barnacles are identified in this study. Type I traces are shallow, oval/semicircular in outline, with smooth, gently sloped bases. Type II traces are deep, hemispherical pits with smooth bases. Type III traces are deep, circular to subcircular pits with flat bases. Type IV traces are deep, circular to subcircular pits with multiple (4–6) small sub-pits on their bases. Type V traces are cylindrical, penetrative holes. Type VI traces comprise shallow ring-shaped grooves on the surface of the bone. Type I through III traces are identical to the ichnotaxon Karethraichnus lakkos. Type IV traces have not, as yet, been described in the rock record. Type V traces are identical to K. fiale. Type VI traces are identical to Thatchtelithichnus holmani. Barnacle taxa identified as emplacing non-penetrative divots and pits on C. caretta skulls, mandibles, and shell bones include Chelonibia caretta (Type I), Platylepas hexastylos (Types I–IV), Calyptolepas bjorndalae (Types I and II), and Stomatolepas elegans (Types I and II). Type V traces were most likely emplaced by either Stephanolepas muricata or Chelolepas cheloniae. Type VI traces reflect the former attachment of balanid or lepadid barnacles. Embedded barnacles were observed in epidermal material associated with Types I through IV traces but not for Type V and VI traces and thus the relationship is inferred for these latter traces.

Barnacle-related pits, divots, and holes are believed to result from barnacle mediated chemical corrosion into the outer surface of sea turtle bone. The occurrence of these traces provides one of the few preservable lines of evidence of barnacle interactions with sea turtle hosts. Identification of definitive barnacle borings in fossil material will provide evidence of the evolution of platylepadid barnacles and the development of their commensal relationship with chelonid turtles.

The late Paleozoic transition is well represented by the upper Pennsylvanian to lower Permian Conemaugh, Monongahela, and Dunkard groups of the western Appalachian Basin (U.S.A.). These units contain abundant paleosols possessing suites of ichnofossils that serve as indicators of soil moisture, soil organic content, water table level, precipitation, and landscape stability. Analysis of these units can, therefore, be used to refine the details of how late Paleozoic terrestrial landscapes changed through time. A study along a 50 km west-east and a 40 km north-south transect through southeast Ohio and southwest West Virginia resulted in the recognition of 24 pedotypes with distinct ichnofossil assemblages. Ichnofossils include rhizoliths, Planolites, Palaeophycus, Taenidium, Scoyenia, Macanopsis, Skolithos, Cylindricum, cf. Psilonichnus, Arenicolites, mottles, and coprolites produced by various plants, gastropods, and larval-to-adult soil arthropods. Soil-forming environments include palustrine, levee, proximal to distal floodplain, interfluve, backswamp, marsh, and fen settings. An up-section shift in pedotypes from Argillisols to Vertisols and Calcisols as well as an overall increase in the diversity of pedotypes recorded a change in soil-forming conditions, resulting in a diverse landscape that changed significantly as mean annual precipitation rose and fell. An up-section increase in ichnofossil diversity in the paleosols and changes in ichnocoenoses suggests an increased dependence on the soil as a refuge and as a food resource. Overall, growing instability of the climate during the Pennsylvanian–Permian transition led to a more heterogeneous landscape that helped to promote colonization of a more diverse assemblage of soil organisms.

Here we describe an epibiont association between conulariids and holdfast producers, with attachment scars resembling those of the tubular epibiont, Sphenothallus, from the Silurian (late Telychian Series) Brandon Bridge Formation, Wisconsin. The conulariid population represents the most abundant sessile organisms in the Waukesha Biota and consists of two species, Conularia niagarensis Hall, 1852 and Metaconularia cf. manni (Roy, 1935). Attachment scars present on the conulariid test offer a unique glimpse into the paleoecology of this Silurian benthic assemblage. However, body fossils of the attached epibiont are scarce and have not been observed attached or near conulariid specimens. This study evaluates the identity and paleoecological relationship between the conulariids and their enigmatic epibionts. Statistical analyses of attachment trace size, frequency, and distribution on the conulariid test gives insight to the nature of their symbiotic relationship. Our results did not find any significant support for a parasitic relationship. However, commensalism cannot be ruled out and serves as an alternative explanation for the relationship between these two organisms.