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A fossil mysticete was discovered along the southwestern coast of Spain, occurring in a block detached from the Neogene deposits exposed along a coastal cliff at the locality of Conil de la Frontera (Cádiz, Spain). These deposits range from Pliocene to Pleistocene in age and include shallow-marine, mixed carbonate–siliciclastic sediments, with the whale being found in occurrence of a stratigraphic unconformity marked by Thalassinoides burrows. 87Sr/86Sr analyses on oyster shells associated with the skeleton suggest an Early Pliocene age, in agreement with the age of the lowermost unit cropping out at the study site. The studied cetacean specimen consists of an articulated, almost complete balaenopteroid skeleton exposed in the field dorsal side up; being contained in an upside-down block, however, it is preserved in ventral disposition. Bones exhibit a low degree of preservation of the cortical bone tissue, which locally features shark bite marks and Osedax traces as well as abundant encrustations of barnacles and ostreids. Two shark teeth were also found near the skeleton. Bones have preserved their main histological features, even though they locally exhibit microcracks, dissolution, substitution by Fe oxides, and microborings. Sediment particles and late diagenetic cements fill the medullary cavities. We propose that the whale carcass experienced refloating before sinking to the seafloor and that the skeleton was probably exposed on the seafloor for some time before being eventually buried. [ABSTRACT FROM AUTHOR]

Acorn barnacles are sessile crustaceans common in shallow-water settings, both in modern oceans and in the Miocene geological record. Barnacle-rich facies occur from polar to equatorial latitudes, generally associated with shallow-water, high-energy, hard substrates. The aim of this work is to investigate this type of facies by analysing, from the palaeontological, sedimentological and petrographical points of view, early Miocene examples from Northern Italy, Southern France and South-western Peru. Our results are then compared with the existing information on both modern and fossil barnacle-rich deposits. The studied facies can be divided into two groups. The first one consists of very shallow, nearshore assemblages where barnacles are associated with an abundant hard-substrate biota (e.g., barnamol). The second one includes a barnacle-coralline algae association, here named “barnalgal” (= barnacle / red algal dominated), related to a deeper setting. The same pattern occurs in the distribution of both fossil and recent barnacle facies. The majority of them are related to very shallow, high-energy, hard-substrate, a setting that represents the environmental optimum for the development of barnacle facies, but exceptions do occur. These atypical facies can be identified through a complete analysis of both the skeletal assemblage and the barnacle association, showing that barnacle palaeontology can be a powerful tool for palaeoenvironmental reconstruction.

Many biotite phenocrysts from marine tephra layers have substoichiometric potassium concentrations and alkali occupation <<2.0 atoms per formula unit. Diagenetic alteration is an expected effect of exposure of fresh magmatic minerals to interstitial water and brine intrusions after the deposition and burial of sediments. To test the effect of diagenetic alteration on potassium-argon ages, we irradiated and step heated untreated Fish Canyon biotite (t = 28.2 Ma) and several aliquots leached to various extents in strong and weak acids. Laboratory alteration caused loss of K, age spectrum discordance, high step ages and total gas ages, Ar release at lower furnace temperature, higher Cl/K and Ca/K, and a slight decrease in 36Ar concentration. Potassium loss was always higher than 40Ar* loss. Electron microprobe element maps document that acids preferentially penetrated in phyllosilicate interlayers, removing K (and Na). Because Ar* is removed to a lesser extent than K, we propose that natural 40K decay partly implants radiogenic Ar* into the tetrahedral-octahedral-tetrahedral (T-O-T) phyllosilicate layer, where Ar is shielded from interlayer leaching. The recoiled 39Ar, which was produced by irradiation after the leaching, also partitioned between T-O-T and the interlayer; age spectrum discordance was probably enhanced by the heterogeneous partition of 39Ar and 40Ar* in leached samples. [ABSTRACT FROM AUTHOR]

In spite of the widespread occurrence of epibiotic turtle barnacles (Coronuloidea: Chelonibiidae and Platylepadidae) on extant marine turtles (Chelonioidea: Cheloniidae and Dermochelyidae), and although the association between these cirripedes and their chelonian hosts has existed for more than 30 million years, only a few studies have investigated the deep past of this iconic symbiotic relationship on palaeontological grounds. We describe probable platylepadid attachment scars in the form of hemispherical/hemiellipsoidal borings on an Upper Miocene (Tortonian) fragmentary turtle carapace, identified herein as belonging to Cheloniidae, from the Pisco Lagerstätte (East Pisco Basin, southern Peru). When coupled with the available molecular data, this and other similar ichnofossils allow for hypothesising that platylepadid symbionts were hosted by sea turtles as early as in early Oligocene times and became relatively widespread during the subsequent Miocene epoch. Chelonian fossils that preserve evidence of colonisation by platylepadid epibionts in the form of pits on the turtle shell should be regarded as fossil holobionts, i.e., palaeontological witnesses of discrete communal ecological units formed by a basibiont and the associated symbionts (including the epibiota). A greater attention to the bone modifications that may be detected on fossil turtle bones is expected to contribute significantly to the emerging field of palaeosymbiology. [ABSTRACT FROM AUTHOR]