Hundreds of fossil marine vertebrates cropping out at Cerro Colorado (Pisco Basin, Peru) are identified and reported on a 1:6500 scale geological map and in a joined stratigraphic section. All the fossils are from the lower strata of the Pisco Formation, dated in this area to the late middle or early late Miocene. They are particularly concentrated (88%) in the stratigraphic interval from 40 to 75 m above the unconformity with the underlying Chilcatay Formation. The impressive fossil assemblage includes more than 300 specimens preserved as bone elements belonging mostly to cetaceans (81%), represented by mysticetes (cetotheriids and balaenopteroids) and odontocetes (kentriodontid-like delphinidans, pontoporiids, ziphiids, and physeteroids, including the giant raptorial sperm whale Livyatan melvillei). Seals, crocodiles, sea turtles, seabirds, bony fish, and sharks are also reported. Isolated large teeth of Carcharocles and Cosmopolitodus are common throughout the investigated stratigraphical interval, whereas other shark teeth, mostly of carcharinids, are concentrated in one sandy interval. This work represents a first detailed census of the extraordinary paleontological heritage of the Pisco Basin and the basis for future taphonomic, paleoecological, and systematic studies, as well as a much needed conservation effort for this extremely rich paleontological site.

Eight skulls of beaked whales (Cetacea, Odontoceti, Ziphiidae), in six cases associated with elements of the mandible, were collected from a limited area (about 1.5 km²) and roughly from the same stratigraphic horizon at Cerro Colorado, 35 km south-south-west of the city of Ica (Peru), where the late Middle Miocene basal strata of the Pisco Formation crop out. They represent the highest concentration reported of fossil Ziphiidae. These finely preserved Cerro Colorado fossils are described and assigned to a new species Messapicetus gregarius, together with another specimen collected from sediments of the same age at Cerro la Bruja (33 km south-east to Cerro Colorado). Messapicetus gregarius shares with M. longirostris Bianucci, Landini and Varola, 1992 (Tortonian of Italy), an extremely elongated rostrum, but is clearly different from the Italian species in the more distinct maxillary tubercle and prominential notch, the more robust premaxillary crest, and the abrupt ventrolateral descent of the medial margin of the maxilla from the vertex. A parsimony analysis reveals that Messapicetus belongs to a basal clade, which includes other ziphiids with a dorsally closed mesorostral groove and prenarial basin. The high concentration of specimens belonging to the same species (some of them tentatively identified as adult males and females), combined with the presence of a calf, supports the hypothesis of site fidelity; these cetaceans might have lived in a limited region for a long period for both breeding and feeding. Besides the eight specimens of M. gregarius, strata at Cerro Colorado include many other cetacean remains (with several specimens of the pontoporiid Brachydelphis including a foetus), pinnipeds, turtles, fishes, and birds.

One-hundred and ninety-two fossil marine vertebrate specimens, preserved as bone elements cropping out at Cerro Los Quesos (Pisco Basin, Peru), are identified and reported on a 1:4,000 scale geological map and in the corresponding stratigraphic section. All the fossils originate from the Pisco Formation, which is dated in this area to the late Miocene (from 7.55 Ma to ≥6.71 Ma, based on ⁴⁰Ar/³⁹Ar analyses of three volcanic ash layers along the section). Specimens are particularly concentrated near the top of the two main hills, where the geologically youngest portion of the examined section crops out. The impressive fossil assemblage includes cetaceans (91.6%), represented by mysticetes (balaenopteroids and cetotheriids) and odontocetes (phocoenids, physeteroids, and ziphiids, including the holotype of Nazcacetus urbinai). Seals, a crocodile, a seabird, bony fish, and sharks are also reported. Isolated large teeth of Carcharocles and Cosmopolitodus are common and, in several instances, associated to mysticete skeletons. Together with a similar work recently published for the other late Miocene locality of Cerro Colorado, this work represents a case study for the detailed inventory of the extraordinary paleontological heritage of the Pisco Basin. As such, it constitutes the basis for future taphonomic, paleoecological, and systematic studies, as well as for a much-needed conservation effort.

Massive salt accumulations, or salt giants, have formed in highly restricted marine basins throughout geological history, but their impact on biodiversity has been only patchily studied. The salt giant in the Mediterranean Sea formed as a result of the restriction of its gateway to the Atlantic during the Messinian Salinity Crisis (MSC) 5.97 to 5.33 million years ago. Here, we quantify the biodiversity changes associated with the MSC based on a compilation of the Mediterranean fossil record. We conclude that 86 endemic species of the 2006 pre-MSC marine species survived the crisis, and that the present eastward-decreasing richness gradient in the Mediterranean was established after the MSC.

Mystacodon selenensis Lambert, Martínez-Cáceres, Bianucci, Di Celma, Salas-Gismondi, Steurbaut, Urbina & Muizon, 2017 is a toothed mysticete that represents the earliest member of the suborder in the current state of knowledge. Its holotype is a relatively complete skeleton from the upper Eocene (early Priabonian, c. 36.4 Ma) Yumaque Member of the Paracas Formation from the southern coast of Peru. The thorough description of this specimen is presented here and reveals numerous similarities with the contemporaneous basilosaurids including the retention of an innominate that originally articulated to the unpreserved hind limb. However, several characters of M. selenensis clearly relate this taxon to the mysticetes, such as the large palate with a dorsoventrally flattened rostrum, the posterior extension of the palate with an infraorbital plate of the maxilla, the shortening of the premaxillary part of the rostrum, the zygomatic process of the squamosal being closely apposed to the postorbital process of the frontal, and the humeral head being oriented more proximally than posteriorly. A parsimony analysis retrieves Mystacodon as the earliest diverging branch of the Mysticeti with no close phylogenetic relationship with Llanocetus the second oldest known mysticete (c. 34.2 Ma). The dental formula of M. selenensis is that of basilosaurids (I 3/3, C 1/1, P 4/4, M 2/3). The anterior teeth (incisors and canine) are distinctly proportionally smaller than in basilosaurids, whereas the cheek teeth are very close in relative length, but are relatively larger than in most other toothed mysticetes (except Coronodon). The large cheek teeth of Mystacodon suggest a raptorial feeding strategy, probably assisted with some degree of suction, as indicated by the large size of the palate. The anterior teeth of the holotype display a subhorizontal apical wear facet and the cheek teeth a moderately sloping wear surface, differing from the subvertical attrition facets of basilosaurids. This pattern suggests an efficient dental abrasion resulting from feeding upon abrasive food items or/and from the ingestion of sediment during prey capture, which could indicate some degree of bottom feeding. On the forelimb, the size and orientation of the acromion, the great length of the deltopectoral crest, the massiveness of the olecranon of the ulna, and the strong radial anterior process indicate powerful shoulder movements, which suggest an active use of the forelimb when foraging for food on the sea floor. The robustness of digits and the pachyosteosclerosis of ribs with pestle-like distal end corroborate such a scenario. Mystacodon selenensis represents a first step in the evolutionary history of feeding adaptations of early mysticetes; the latter are likely to have experimented an abundant set of feeding strategies and were probably very eclectic in prey choice and capture before hyperspecialized filter feeding became widespread in the suborder.