The Cretaceous–Paleogene boundary (K–Pg) crops out on Seymour Island in the upper levels of the Lopez de Bertodano Formation.[3] A small (but significant) iridium anomaly occurs at the boundary on Seymour Island, as at lower latitudes, thought to be fallout from the Chicxulub impactor in the Gulf of Mexico.[4] Directly above the boundary a layer of disarticulated fish fossils occurs, victims of a disturbed ecosystem immediately following the impact event.[3] Multiple reports have described evidence for climatic changes in Antarctica prior to the mass extinction,[5] but the extent to which these affected marine biodiversity is debated. Based on extensive marine fossil collections from Seymour Island, recent work has confirmed that a single and severe mass extinction event occurred at this time in Antarctica just as at lower latitudes.[6]
Climate
During the Maastrichtian, Seymour Island was located within the Antarctic polar circle at around ~65°S latitude.[7] Chemical studies on oxygen-18 isotopes found in shells and benthic foraminifera have calculated intermediate-depth and deep-sea ocean temperatures at a mean average of 6 °C (43 °F) with fluctuations of 4–12 °C (39–54 °F) throughout the Maastrichtian; one of the same studies has also suggested that sea surface temperatures may have been colder, possibly dropping below freezing and forming sea ice at times.[8][9] Alternatively, a study using data acquired from ancient bacterial membrane lipids yielded a slightly warmer temperature of 12 ± 5 °C (54 ± 9 °F) around 66 Ma. Nevertheless, these estimated climates characterize primarily cool temperate environments with possible subpolar and warm episodes.[7]
Dinosaur remains are among the fossils that have been recovered from the formation[14] and include at least two and probably as much as six lineages of indisputably modern birds: one related to waterfowl, a primitive shorebird or related form, 1 to 2 species of possible loons, a large and possibly flightless bird belonging to a lineage extinct today as well as a partial skull that might belong to either of the smaller species or represent yet another one. The formation also contains a rich fossil invertebrate fauna, including bivalves, gastropods,[15] and cephalopods (ammonites and nautiloids).[16]
The fish assemblage of the López de Bertodano Formation was dominated by Enchodus and ichthyodectiformes, accounting for 21.95% and 45.6% of local fish diversity respectively. Of the remaining percentages, sand sharks made up 10.5%, the cow shark Notidanodon 6.8%, chimaeras 3.9%, saw sharks 2.7%, various other teleost fish 2.4%, and the remaining 6% were shared between other sharks like Paraorthacodus, frilled sharks, Protosqualus, and Cretalamna.[17]
MLP 98-I-10-47, MLP 98-I-10-50, MLP 98-I-10-52, MLP 98-I-10-76: tarsometatarsus;MLP 98-I-10-59: diaphysis of left tibiotarsus; MLP 98-I-10-51: proximal end of left femur; MLP 98-I-10-48: distal end of left tibiotarsus; MLP 98-I-10-60 and MLP 98-I-10-61: distal end and partial corpus of pedal phalanges.[23]
Initially identified as a fossil of a member of Cariamae,[27] but subsequently reinterpreted as a fossil of an unnamed large-bodied member of the genus Vegavis.[28]
Two left upper lateral teeth preserving one root branch and lateral denticle, MLP 13-XI-29-35, MLP 13-XI-29-37; one right upper lateral tooth preserving one root branch and lateral denticle, MLP 13-XI-29-36; several fragmentary teeth, MLP 13-XI29-4, MLP13-XI-29-44 to46, MLP13-XI-29-16, MLP 13-XI-29-13 to 14.[17]
MLP 82-I-28-1, an incomplete skeleton comprising 15 cervical, three pectorals, 21 dorsal, three sacral, and 22 caudal vertebrae, an almost complete left hind limb, some dorsal ribs, incomplete coracoids and fragments of the scapulae
SGO.PV.6523, postcranial remains of a single adult individual, including remains of 9 mid-to-posterior cervical vertebrae (6 of them preserving parts of their centra), the right scapula, several fragments of ribs and gastralia, and one phalanx.
TTU P 9239; isolated vertebrae, limb bones, paddle elements, and ribs
Indeterminate
Seymour Island
IAA Pv 443, an incomplete skeleton comprising the mandibular symphysis and part of right and left mandibular rami, cervical and dorsal centra, an incomplete humerus, radius, ulna, ulnare, intermedium, radiale and distal carpal 1, 2 þ 3 and 4, other fragmentary postcranial bones and associated gastroliths[40]
Partially articulated incomplete skeleton including cranial material, many vertebrae, ribs, an ilium, limb bones (right humerus and ulna, a femur), and gastroliths (IAA-Pv 752)
MLP 15-I-7-48, right humerus, ulna, ulnare, intermedium, distal carpal I, distal carpal II+III, pisiform, phalanges and one rib
Indeterminate
Seymour Island
MLP 14-I-20-16, 12 cervical vertebrae, three pectoral vertebrae, 11 dorsal vertebrae, one sacral vertebra, 11 caudal vertebrae, right femur, tibia, fibula and mesopodial elements, fragments of pectoral and pelvic girdles and gastroliths[42]
Mosasaurs
Mosasaurs recorded from Lopez de Bertodano Formation
MLP 80-I-1-1, a cervical vertebra; MLP 80-I-1-2, a mandibular fragment; MLP 80-I-1-3, a cranial fragment; MLP 82-I-28-2, a vertebra; MLP 82-I-3-1/4, four caudal centers[46]
Indeterminate
Seymour Island
DJ.957.133, 18 partially articulated caudal vertebrae, four of which possess transverse process, and DJ.957.505 a caudal vertebra[45]
DJ.1020.2-A, DJ.1020.2-B and DJ.1053.14- A, teeth; MLP 83-X-12-2, a caudal vertebra; MLP 92-XII-30, skull fragments including one tooth and a relatively short, and medially constricted suprastapedial process of the quadrate[45]
M. sp.
Seymour Island
MLP 15-I-24-41, a partial skull including, partial frontal, right postorbital, parietal, right quadrate, right posterior end of basisphenoid, right coronoid, right angular, splenial and right surangular, a broken marginal tooth and several pterygoid teeth have been associated to this specimen.[49]
^ abOlivero, E.B.; Ponce, J.J.; Marsicano, C.A.; Martinioni, D.R. (2007). "Depositional settings of the basal Lopez de Bertodano Formation, Maastrichtian, Antarctica". Revista de la Asociación Geológica Argentina. 62 (4): 521–529.
^ abWeishampel, David B; et al. (2004). "Dinosaur distribution (Late Cretaceous, Antarctica)." In: Weishampel, David B.; Dodson, Peter; and Osmólska, Halszka (eds.): The Dinosauria, 2nd, Berkeley: University of California Press. p. 606. ISBN0-520-24209-2.
^Cordes (2002). "A new charadriiform avian specimen from the Early Maastrichtian of Cape Lamb, Vega Island, Antarctic Peninsula". Journal of Vertebrate Paleontology. 22 (3): 46A.
^Case, J.; Reguero, M.; Martin, J.; Cordes-Person, A. (2006). "A cursorial bird from the Maastrictian of Antarctica". Journal of Vertebrate Paleontology. 26 (3): 48A. doi:10.1080/02724634.2006.10010069. S2CID220413406.
^O'Gorman, J. P., Gasparini, Z., & Salgado, L. (2012). Postcranial morphology of Aristonectes (Plesiosauria, Elasmosauridae) from the Upper Cretaceous of Patagonia and Antarctica. Antarctic Science, 25(1), 71–82. https://doi.org/10.1017/S0954102012000673
^Gasparini, Z.; Del Valle, F.; Goñi, R. (1984). "An elasmosaur (Reptilia, Plesiosauria) of the Upper Cretaceous in the Antarctic". Contribuciones del Instituto Antártico Argentino. 305: 1–24.
Poole, I.; Mennega, A. M. W.; Cantrill, D. J. (2003). "Valdivian ecosystems in the Late Cretaceous and Early Tertiary of Antarctica: further evidence from myrtaceous and eucryphiaceous fossil wood". Review of Palaeobotany and Palynology. 124 (1–2): 9–27. Bibcode:2003RPaPa.124....9P. doi:10.1016/s0034-6667(02)00244-0. hdl:1874/31608. S2CID129281012.