Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Macrofossil evidence for a rapid and severe Cretaceous–Paleogene mass extinction in Antarctica


Debate continues about the nature of the Cretaceous–Paleogene (K–Pg) mass extinction event. An abrupt crisis triggered by a bolide impact contrasts with ideas of a more gradual extinction involving flood volcanism or climatic changes. Evidence from high latitudes has also been used to suggest that the severity of the extinction decreased from low latitudes towards the poles. Here we present a record of the K–Pg extinction based on extensive assemblages of marine macrofossils (primarily new data from benthic molluscs) from a highly expanded Cretaceous–Paleogene succession: the López de Bertodano Formation of Seymour Island, Antarctica. We show that the extinction was rapid and severe in Antarctica, with no significant biotic decline during the latest Cretaceous, contrary to previous studies. These data are consistent with a catastrophic driver for the extinction, such as bolide impact, rather than a significant contribution from Deccan Traps volcanism during the late Maastrichtian.


The Cretaceous–Paleogene (K–Pg) mass extinction at 66 Ma is the most intensively studied of the ‘Big Five’ crises to have affected life during the Phanerozoic1,2,3,4,5,6,7,8. The extinction led to a fundamental restructuring of global ecosystems and the rise of modern taxonomic groups7,9,10,11. Despite this interest, debate continues as to the duration of the crisis as well as the relative contributions of the bolide impact at Chicxulub1,4, voluminous eruptions from the Deccan Traps large igneous province12,13, and dynamic climate instability during the preceding Maastrichtian stage (72.1–66 Ma)6,14. Parts of this discourse have particularly focused on the Antarctic fossil record. Previous studies on high southern latitude biotas have claimed the extinction to be either a gradual diversity decline15,16, a series of extinction pulses linked to episodes of Deccan volcanism17 or, for ammonites at least, a single rapid event18. In addition, it has been suggested that the intensity of the extinction and environmental stress varied with latitude and was related to the proximity of the impact site or the volcanism (both at mid to low latitudes)19,20. As a result, the high southern latitudes are thought to have weathered the crisis better than lower latitude regions15,21,22.

The López de Bertodano Formation of southern Seymour Island, Antarctica (Fig. 1) represents one of the most highly expanded onshore Maastrichtian–Danian sedimentary successions in the world with 1,000 m of sedimentation in 4 Myr (refs 17, 23, 24). At a palaeolatitude of 65° S during the latest Cretaceous25, this succession represents a true high latitude record of events during this critical time period. The succession exposed on Seymour Island is dominated by silty-clays with occasional, thin glauconite-rich sandstone horizons becoming more prevalent in the uppermost 300 m, along with indurated layers formed of early diagenetic concretions and thin bioturbated sands26,27,28. Despite the lithological homogeneity of the succession, several environmental changes have been proposed that have a bearing on marine biodiversity. The depositional environment of the López de Bertodano Formation is broadly transgressive; the lower portion has been interpreted as relatively shallow water, outer estuarine facies28,29, with a low-energy, marine shelf facies forming the remainder of the succession27,30.

Figure 1: Location map of Seymour Island.

(a) Modern Southern Hemisphere geography showing location of Antarctica, Antarctic Peninsula highlighted. (b) Map of northern Antarctic Peninsula, location of James Ross Basin (JRB) circled and highlighted. (c) Geological map of Seymour Island showing locations of principal lithological units, their ages, as well as the locations of British Antarctic Survey section lines mentioned in the text. Location of K–Pg boundary indicated by dotted line on c. Circled letters in c correspond to individual British Antarctic Survey section lines, A, 1999 field season, B, 2006 field season, C, 2010 field season. Scale bar, 5 km. See Supplementary Figs 1–4 for more details.

Here we address these debates on the timing and intensity of Antarctic marine extinctions with a detailed analysis of marine diversity trends during the Maastrichtian to earliest Paleocene 70–65.6 Ma (ref. 23) from the López de Bertodano Formation. We evaluate the nature of the K–Pg extinction, its abruptness and intensity in this region. In addition, we test the relationship between palaeoenvironmental changes and diversity, using pyrite petrography as an indicator of palaeoenvironmental conditions. Besides comparisons of existing low-resolution faunal range charts with oxygen isotope data as a proxy for marine palaeotemperature trends17, there have been few previous attempts to relate faunal diversity trends in this succession to other local environmental conditions, for example benthic redox changes. We suggest that the K–Pg extinction in Antarctica was as rapid and severe as that seen at lower latitudes, with no evidence for significant precursor extinction events during the latest Maastrichtian, which can be related to the onset of Deccan volcanism or climatic instability.


Fossil evidence for diversity and extinction

The primary data for this study comprises >6,000 benthic molluscan fossils (bivalves and gastropods) from 377 individual sampling stations accurately located within a series of detailed measured sedimentary sections through the López de Bertodano Formation (Fig. 1; Supplementary Figs 1–4). Species range charts based on these collections were combined and compared directly with data from nektonic and nekto-benthic cephalopod molluscs from the same sections18 (Fig. 2) and from previous studies of the K–Pg boundary interval on Seymour Island undertaken by Zinsmeister et al.16 (Supplementary Fig. 6). The K–Pg boundary on Seymour Island occurs in a 2.5–3-m-thick glauconite-rich horizon 1,007.5 m above the base of our composite section, based on biostratigraphic data from marine palynology24,30,31 (Fig. 2; Supplementary Figs 1–5) and the presence in a parallel section of the globally recognized iridium (Ir) anomaly used as a marker for the K–Pg boundary30,32 (Fig. 3). Besides an abundant and diverse molluscan fauna, other common faunal elements found throughout the Maastrichtian portion of the López de Bertodano Formation include serpulid worm tubes (Rotularia), cidaroid echinoid spines, scaphopods, rare solitary corals, decapod crustaceans, marine reptiles, shark vertebrae and fossil wood bored by Teredolites26,27,33. Recent work has also revealed the presence of fossil methane seeps, which are periodically developed on the Maastrichtian sea-floor and are characterized by a distinctive benthic molluscan fauna34.

Figure 2: Composite stratigraphic range data for molluscan taxa from the López de Bertodano formation.

Range data is plotted against composite lithostratigraphy and age model. Includes new data from this study (see Methods and Supplementary Figs 1–4), and from refs 16, 18 (see also Supplementary Fig. 5). Separated into bivalves (B) (1–32), gastropods (G) (33–51), and cephalopods (A and N) (52–66), with taxa ordered by first appearance in the composite section. Range extensions calculated based on a literature review of molluscan occurrences from underlying formations (Supplementary Table 1), in addition to collections from overlying Paleocene strata24,44. Also illustrated are the stratigraphic ranges of marine reptile fossils (MR), lamniform shark vertebrae (S), echinoid spines (E) and serpulid worm tubes (Rotularia .spp (R) in the composite section. Age model is derived from ref. 23 (see Supplementary Fig. 1 for detailed explanation). Time scale is based on Sr isotope chemostratigraphy (italicized A–C)68 and magnetostratigraphy17, updated with ages from the Geological Time Scale 2012 (ref. 69) and using the K–Pg boundary datum. G, glauconite-rich intervals. S, Sobral Formation. See Supplementary Note 1 for details of species identifications.

Figure 3: Molluscan diversity and extinction data compared with evidence for Cretaceous–Paleogene palaeoenvironmental change.

(a) Molluscan diversity for benthos (bivalves and gastropods) and nekton (ammonites and nautiloid) measured as standing species richness in the composite section (Supplementary Data 1), plotted against age model and lithostratigraphy. Composite standing species richness for all molluscan groups plotted as solid black line. Note all nektonic molluscan taxa disappear at the K–Pg boundary (grey dashed line, defined by dinoflagellate cyst biostratigraphy and iridium (Ir) anomaly in paralell section16,30,31. All nekton data species richness and extinction data reanalysed from Witts et al.18. (b) Extinction and origination rates through time based on boundary-crosser methodology38, calculated for the entire molluscan fauna (both benthic and nektonic taxa) in 10 m bins (Methods and Supplementary Data 1). See Supplementary Fig. 6 for metrics calculated for benthos and nekton individually. (c) Analysis of extinction pattern based on ‘Meldahl’s method’40,41 with last occurrences (LO) in the composite section plotted against stratigraphic abundance S (measured as a %), separated into benthos (bivalves and gastropods) and nekton (ammonites and nautiloid). Numbers in parentheses indicate number of overlapping data points (that is, where taxa have the same value of S). Data are consistent with a single mass extinction event affecting common molluscan taxa (those with a higher value of S) coincident with the K–Pg boundary. (d) Palaeoclimate interpretation based on published data from multiple sections on Seymour Island17,23,51,65. Snowflake symbols are ‘cold snaps’ of Bowman et al.23, red arrow labelled DT, approximate duration of the main phase of Deccan Trap volcanism (correlated to section and age model using magnetostratigraphy, based on Schoene et al.12 and Renne et al.13). Dashed red line and ? illustrates uncertainty surrounding the timing of initial onset of Deccan volcanism12,70. Yellow star, position of Ir anomaly at the K–Pg boundary in a parallel section30 taken as a global marker of the Chicxulub impact event32 (see Supplementary Figs 6 and 7 for further information).

On the basis of the combined data sets, a total of 44 species and 39 genera of benthic molluscs occur within the Maastrichtian portion of the López de Bertodano Formation (Fig. 2) along with 15 species and 9 genera of nektonic and nekto-benthic cephalopods18. Focusing on the benthos, a total of 25 out of 37 benthic molluscan species (67%) have their last occurrence at or below the K–Pg boundary and 15 out of 35 benthic molluscan genera disappear during the Maastrichtian (43%) (excluding those represented by a single occurrence: 7 species and 4 genera, respectively). Standing species richness based on range-through data gives a good approximation of taxonomic diversity, and indicates an overall increase in benthic molluscan diversity up-section from the base of the López de Bertodano Formation, culminating in a maximum of 33 species at 690 m (310 m below the K–Pg boundary in our composite section) (Fig. 3a). Many of the benthic molluscan genera and species present in the López de Bertodano Formation are also known from the underlying Santonian-early Maastrichtian Santa Marta and Snow Hill Island formations35,36,37 (Supplementary Table 1). However, a similar increase in species richness is also seen in the cephalopod fauna during the same interval18 (Figs 2 and 3), suggesting that this early Maastrichtian diversity increase represents a true ecological signal. Rates of turnover (extinction and origination38) generally remain low throughout the Maastrichtian (Fig. 3b) for benthic molluscs in particular (Supplementary Fig. 7), with two periods of slightly elevated extinction rates in the benthos between 850 and 890 m, and at 960 m.

Standing species richness of bivalve and gastropod faunas remains stable until a level 40 m below the K–Pg interval (Figs 2 and 3). Above this horizon, there is a slight decline due to the apparent loss of six species, before a significant extinction event between 1,000 and 1,007.5 m in our composite section (that is, the interval directly beneath the K–Pg boundary) where 11 benthic species disappear along with all eight remaining species and genera of cephalopods18 (Fig. 2; Supplementary Fig. 7). Turnover metrics clearly indicate a significant peak in extinction rate at this level, which is apparent in both a combined analysis (Fig. 3a,b) and when data are separated into benthos and nekton (Supplementary Fig. 7). Two bivalve species (Panopea clausa and Seymourtula antarctica) range into the glauconite-rich beds in the earliest Paleocene before disappearing, and based on existing data from Zinsmeister et al.16, another species (Surobula nucleus) also shows this pattern (Supplementary Fig. 6). These taxa are classed as additional victims of the extinction (Fig. 2). Thus combined raw stratigraphic range data suggest the benthic molluscan community at Seymour Island saw a species-level extinction of 56% (14 out of 25 species) at the K–Pg event. Local generic level extinction was lower at only 30% (9 out of 30 genera), although several genera (Cryptorhytis, Haustator) were extirpated in Antarctica but may have survived the K–Pg event at lower latitudes10.

These are also likely to be conservative estimates because many of the taxa that disappear within the Maastrichtian are rare and could therefore be under-sampled with respect to their true stratigraphic range (that is, the ‘Signor-Lipps’ effect)39. To examine this phenomenon, we first employed a modified version of Meldahl’s method40,41 to our combined records (see Methods). Significantly, the majority of the most common molluscs (those most likely to give a true picture of their stratigraphic range40) disappear immediately below the K–Pg boundary (Fig. 3c). This suggests that the preceding decline is likely due to the apparent loss of rare taxa, known as ‘backward smearing’39,40,41. Application of confidence intervals to raw range and occurrence data in the two longest stratigraphic sections (A and B in Fig. 1c and Supplementary Fig. 1) in the form of range extensions42 support this assertion, showing a cluster of both 50 and 95% confidence intervals around the K–Pg boundary interval outlined above (Supplementary Figs 2 and 3). Only two benthic taxa with a stratigraphic abundance >10 (Austroaporrhais sp. and Eselaevitrigonia regina) disappear >10 m below the K–Pg boundary, and only one of these disappearances is close to the interval identified by Tobin et al.17 as containing a supposed precursor extinction event (see Supplementary Data 1 for more details). Furthermore, extension of their 95% confidence intervals into the K–Pg interval in the two BAS section lines suggests that both these taxa, plus a further rare species of bivalve (Dozyia drygalskiana), could be additional victims of extinction in the boundary interval. Assuming this is the case would raise the species-level extinction to 61% (17 out of 28) and generic-level extinction to 36% (12 out of 33).

Directly above the K–Pg boundary a low-diversity molluscan assemblage occurs, dominated by large numbers of the bivalves Lahillia larseni and Cucullaea ellioti, along with the gastropod Struthiochenopus hurleyi27,43. Beds immediately above the Ir anomaly level also contain a large number of diagenetic concretions containing articulated and disarticulated fish remains16, the only such horizon in the Seymour Island succession. A total of eight benthic molluscan species range through the K–Pg boundary and occur in the 60-m-thick Paleocene portion of the López de Bertodano Formation. This number increases to 11 when taxa that disappear in the Maastrichtian but reappear in the overlying Paleocene Sobral Formation are included43,44 (Figs 2 and 3; Supplementary Data 1). Origination rates peak in the interval containing the extinction horizon and directly above in the earliest Paleocene, and seven benthic molluscan species make their first appearances in the 60-m between the K–Pg boundary and the base of the Sobral Formation, an interval that represents 350 kyr (refs 17, 23, 24) with only one of these taxa disappearing during the same interval (Figs 2 and 3). However, diversity of the molluscan fauna fails to recover to levels attained during the Maastrichtian.

Benthic environmental conditions from pyrite petrography

Pyrite petrography was undertaken according to the established procedures45. This revealed highly variable pyrite abundance with framboids either being absent (in 10 samples) or present in abundance (in 13 samples). When present, the framboid populations have small mean diameters varying between 4 and 7 μm, and often a considerable ‘tail’ of large examples (Supplementary Fig. 8; Supplementary Table 2); this size range is typical of dysoxic (low oxygen) environments in modern settings46. Samples with abundant framboid populations are more common in the lower part of the López de Bertodano Formation. Several samples, from closer to the base of the formation, have a narrow size distribution of framboids (minimum diameter 1.5 μm, maximum diameter 14 μm) and a smaller s.d. (1.5–2), more typical of modern anoxic–euxinic environments46 (Fig. 4). It is notable that samples from both of the glauconite-rich sandstone units examined in the petrographic analysis, including the interval that yields articulated fish remains immediately above the K–Pg boundary, also have a framboid population typical of rapid fluctuations between dysoxic and anoxic conditions. However, samples from the latest Maastrichtian strata and those above the glauconite-rich interval in the earliest Danian do not contain framboids, possibly indicating that fully oxygenated conditions prevailed on the sea-floor both before and after the K–Pg boundary.

Figure 4: Mean versus s.d. plot of framboid populations from the López de Bertodano Formation.

Samples ordered stratigraphically in composite section. Dashed line separates redox conditions and is based on modern calibration46. Samples plot in both oxic–dysoxic and anoxic–euxinic fields, indicating rapid redox fluctuations. Inset represents pyrite framboids from sample D5.481.2 (158 m). Scale bar, 10 μm. See Supplementary Fig. 8 and Supplementary Table 2 for more detailed information.


In contrast to all previous studies on the molluscan fauna from Seymour Island15,17,30, our results identify a single, severe K–Pg extinction event in Antarctica affecting both benthic and nektonic taxa, without precursor extinction events. In contrast, Tobin et al.17 argued for two extinction events, one at the K–Pg boundary itself, and an earlier extinction 40 m below (300 kyr prior to the K–Pg boundary), which primarily affected benthic taxa. Tobin and colleagues argued that the earlier crisis was related to a phase of climate warming that has been linked to the onset of Deccan Traps eruptions prior to the K–Pg boundary47,48. However, there remains significant uncertainty in the precise timing of the main phase of Deccan eruptions relative to the K–Pg extinction12,13, as well as the magnitude and potential for global environmental change driven by this volcanism49, and even the possibility of a cause-and-effect relationship between Deccan eruptions and the Chicxulub impact event50. In addition, marine and terrestrial proxy data indicate evidence for regional climate warming in the Antarctic Peninsula region commencing up to 2 million years prior to the K–Pg boundary23,51 (Fig. 3d). It seems unlikely that any late Maastrichtian warming event significantly stressed the marine fauna. Throughout this interval of warming temperatures, macrofaunal diversity in our composite section remained stable, and extinction rates were low in both the benthic and nekton/nekto-benthic molluscan faunas (Figs 2 and 3; Supplementary Fig. 7). The difference in findings compared with previous studies15,17 can be explained by our much expanded fossil data set from Seymour Island, which has extended stratigraphic ranges through both the Maastrichtian and the Early Paleocene, and the addition of updated taxonomic information, in particular for benthic molluscs44,52 (Supplementary Note 1).

The majority of macrofaunal last occurrences are confined to a short interval directly beneath the K–Pg boundary where previously common benthic, and all nektonic molluscs disappear alongside evidence for severe losses in the wider marine community (Figs 2 and 3). For example, remains of large marine vertebrates (marine reptiles, lamniform sharks) are present until the extinction interval, with marine reptiles disappearing only 1 m beneath the K–Pg boundary on Seymour Island16,53. Providing further evidence for a major benthic disruption, serpulid worm tubes (Rotularia spp.) and cidaroid echinoid spines, the most common of all Maastrichtian benthic fossils on Seymour Island, temporarily disappear from the succession at the K–Pg boundary16 (Supplementary Fig. 6), only reappearing in the basal levels of the Sobral Formation some 350 kyr later (Fig. 2). The record from microfossils is more equivocal. In common with low latitude sections, dinoflagellate cysts exhibit a turnover of taxa at the K–Pg boundary on Seymour Island, but show no significant extinction events24,30,31, as do diatoms54. This may be due to the ability to encyst (dinoflagellates) or create resting spores (diatoms) during periods of environmental stress55,56. Cretaceous planktonic and benthic foraminifera also disappear beneath the K–Pg boundary following a long period of apparent faunal stability in the López de Bertodano Formation57. Silicoflagellate assemblages show a similar pattern of stasis followed by an abrupt turnover coincident with the K–Pg boundary on Seymour Island54.

The 30–43% extinction of bivalves and gastropods at generic level on Seymour Island is similar to that seen in other Southern Hemisphere molluscan faunas (for example, 21.7–32.1% in Patagonia10) These values are also comparable to extinction estimates from Northern Hemisphere K–Pg boundary sections (for example, 30.5% for bivalves and gastropods in the clastic facies of the Gulf Coast, USA10,58, and 22.5% for bivalves in the chalk facies of Stevns Klint, Denmark10,59). Estimates for the magnitude of the extinction are similar despite significant differences in the diversity (in terms of generic richness) of these different benthic molluscan faunas from different palaeolatitudes10,44,58,59,60. Our data are thus also in broad agreement with the suggestion made using global databases, albeit analysed at stage level, that there was no latitudinal variation to the K–Pg losses in these groups60. A latitudinal diversity gradient provided no protection against mass extinction for molluscs at the K–Pg boundary, with the polar regions seemingly no safer than the tropics.

Previous studies have postulated that longer-term biotic changes recorded in the James Ross Basin, such as changes in molluscan faunas during the Campanian–Maastrichtian interval, were ‘harbingers’ of the K–Pg extinction itself15,30,61. We infer that these changes are more likely recording high-latitude biotic response to environmental perturbations on a longer time-scale, such as the long-term global cooling trend evident at this time18,62,63, and are thus independent of events at the K–Pg boundary.

Nevertheless, existing geochemical, palaeontological and sedimentological data sets from Seymour Island support ideas of a relationship between local palaeoenvironmental changes and marine diversity during the Maastrichtian–Paleocene interval in Antarctica. The lower part of the succession on Seymour Island contains evidence for predominantly cool ocean temperatures during the early Maastrichtian17,23,64 (Fig. 2; Supplementary Fig. 7) supporting records from lower latitudes62,63. Although lithological homogeneity and lack of key horizons makes a detailed analysis of water depth changes difficult, the shallow water setting proposed for this interval26,28,29, correlates to a period of low molluscan diversity in our sections (Figs 2 and 3; Supplementary Fig. 7). A transition to a more offshore environment occurred during the mid Maastrichtian26,28,29, under a variable temperate climate with fluctuating temperatures and occasional ‘cold-snaps’ when sea ice may have developed on the Antarctic margin17,23,51. This interval is linked to an increase in diversity and establishment of a more diverse and stable benthic and nektonic molluscan fauna (Figs 2 and 3). Warming in the late Maastrichtian occurred alongside a slight facies change, with more frequent deposition of glauconite-rich horizons perhaps indicative of subtle changes in water depth and the nature of the substrate26. This may account for the minor increase in benthic extinction rates recorded in this interval (Supplementary Fig. 7). Warming is followed by further cooling in the latest Maastrichtian17,24,51,65, and evidence for an overall shallowing of the basin into the Paleocene26,29,30. The cluster of last occurrences at the K–Pg boundary appear unrelated to significant facies change.

Integration of our new pyrite petrographic analysis with these data reveals a broadly inverse relationship between diversity in the López de Bertodano Formation and the occurrence of framboid-rich samples. This suggests that, contrary to previous studies of the López de Bertodano Formation that assumed fully oxic conditions throughout deposition16,26,29, fluctuating redox conditions on the Maastrichtian sea-floor may have been a further factor influencing benthic diversity.

Initial low molluscan diversity during the early Maastrichtian also corresponded with evidence for the periodic development of shallow water dysoxia, anoxia and even euxinia (Fig. 4; Supplementary Fig. 8). Significantly, the apparent reappearance of a large number of range-through taxa from underlying formations (Supplementary Table 1) in the mid-López de Bertodano Formation indicates that early Maastrichtian environmental fluctuations were not accompanied by any significant extinction events, at least in the benthos, and any reduction in diversity was temporary (Figs 2 and 3). Oxygenation levels and benthic diversity subsequently improved, although framboid evidence for redox conditions fluctuating between dysoxia and anoxia–euxinia is present in samples in at least three distinct levels in the upper López de Bertodano Formation (Fig. 4; Supplementary Fig. 8).

Interestingly, these include the glauconite-rich sandstone horizons immediately above the K–Pg boundary, suggesting the development of local bottom-water anoxia in the aftermath of the extinction. Although the occurrence of similar conditions associated with another, older, glauconite-rich horizon in the Maastrichtian suggest this is not unusual (Supplementary Fig. 8), certain characteristics of the extinction interval suggest the development of harsh conditions in the water column as well as on the sea-floor at this time. These include the loss of pelagic and nektonic/nektobenthic macrofauna18,53 (Fig. 2), disruption to planktonic microfauna and flora31,54,57, and occurrence of large numbers of articulated fish remains immediately above the K–Pg boundary on Seymour Island16. The origin of recurrent ‘fish-kill’ events in this short stratigraphic interval is unclear; Zinsmeister16 suggested they may have resulted from large-scale algal or bacterial blooms, or unspecified changes in water chemistry following the end-Cretaceous impact event. Such blooms of opportunistic primary producers and geographically heterogeneous high-stress marine conditions have been hypothesized worldwide in the aftermath of the Chicxulub impact66, following perturbation or collapse of the global marine food web due to mass extinction of many groups of phytoplankton4. In Antarctica, local benthic anoxia likely led to enhanced preservation potential for victims of the subsequent ‘fish-kills’ by limiting the activity of benthic scavengers. The loss of common scavenging taxa such as many epifaunal gastropods and echinoids in the aftermath of the extinction event on Seymour Island (Fig. 2), may also have favoured enhanced preservation of fish carcasses. The benthos of this immediate post-extinction interval is also characterized by unusual high abundance ‘blooms’ of presumably opportunistic molluscan taxa, primarily represented by the infaunal bivalve Lahillia larseni and the aporrhaid gastropod Struthiochenopus hurleyi27,43.

Pyrite framboid data probably indicate a return to oxygenated sea-floor conditions above the boundary interval (Supplementary Fig. 8). However, successive acmes of several species of dinoflagellate cyst31, and an increase in diatom resting spores54 in the 60 m stratigraphic interval above the K–Pg boundary may indicate the persistence of unstable marine conditions and a perturbed marine ecosystem following the extinction on Seymour Island. Despite a peak in origination rates at and above the K–Pg interval (Fig. 3), significant recovery of benthic species richness only commenced, 350 kyr after the extinction, just prior to initial deposition of the Sobral Formation24,44. This provides some support for the hypothesized continuation of unusual environmental conditions into the early Danian.

In summary, intensive collecting of marine fossils from the Maastrichtian-earliest Paleocene López de Bertodano Formation on Seymour Island, Antarctica, reveals that, contrary to all previous studies, there was a single, abrupt extinction at the end of the Cretaceous at this location. We find no counter-evidence for any precursor biotic crises at this high southern palaeolatitude. Our results support the idea that a sudden event such as the Chicxulub bolide impact and associated rapid environmental deterioration4,22,32 was the most probable cause of the K–Pg mass extinction. Although recent dating estimates for onset of the main phase of the Deccan Traps large igneous province do suggest a complex temporal coincidence between volcanism and impact at this time12,13, the precise environmental effects of this volcanism on global ecosystems remain unclear49.

Prior to the K–Pg extinction interval, minor diversity fluctuations in Antarctica were linked to local water depth changes with associated changes in seawater temperature. Pyrite framboid data indicates fluctuations in local benthic oxygenation levels may also have played a role in controlling diversity of the marine fauna. In conjunction with the temporary absence of scavenging benthic taxa in the immediate aftermath of the mass extinction event, this provided favourable conditions for fossilization of well-preserved fish directly above the K–Pg boundary in Antarctica, perhaps related to transient unstable marine conditions following the Chicxulub impact. Although evidence for rapid climate oscillations and a late Maastrichtian warming event are present on Seymour Island17,23,51, they are not associated with any significant diversity decline in the marine macrofauna prior to the K–Pg boundary. This argues against models that invoke rapid Maastrichtian climate changes as a significant stressor on pre-extinction communities6,14. The losses among the benthic invertebrates in Antarctica due to the K–Pg extinction are closely comparable with those recorded from lower latitudes, despite the overall lower diversity of the Antarctic molluscan fauna, and do not support the theory of latitudinal extinction selectivity during this major mass extinction event22,60.


Sampling strategy

Our primary data are derived from extensive macrofossil collecting in three sedimentary section lines spanning the López de Bertodano Formation and K–Pg interval. All sub-sections that comprise the composite section were measured perpendicular to strike using a Jacob’s staff and tape measure. Fieldwork was undertaken during three field seasons to Seymour Island and encompassed the main outcrop of the López de Bertodano Formation in the southern part of the island24,27,44,51. The island is ice-free and exposure excellent. Sections DJ.959, DJ.957, DJ.952 and DJ.953 were made during the 1999 field season, and are located close to the central portion of the outcrop, commencing in the mid-levels of the López de Bertodano Formation representing the informal mapping units Klb7–9 and Ktplb10 of Macellari26 (Fig. 1). Section D5.251 (comprising sub-sections D5.212, D5.215, D5.218, D5.219, D5.220, D5.222 and D5.229) was measured and sampled during the 2006 field season and runs perpendicular to strike and approximately parallel to the southern coast of the island, beginning within the uppermost levels of the Snow Hill Island Formation. Sections D9.205, D9.206 and D9.207 were located at the northern end of the outcrop during the 2010 field season, and begin immediately below the K–Pg boundary. All three composite sections extend through the K–Pg boundary and the informal mapping unit Ktplb10 to the unconformable contact with the overlying Sobral Formation (Supplementary Figs 1–4).

Macrofossil collections were made systematically at varying scales during the different field seasons, with sample bins ranging on average from 1 m to intervals 10–15 m thick (see Supplementary Figs 2–4 and Supplementary Data 1 for illustration of sampling intervals and bin length in each individual section line). Changes in the size of sample bins within and between individual section lines were necessary during field collecting due to the nature of the ‘scarp and dip-slope’ topography that predominates on southern Seymour Island, whereby fossils are invariably more common on dip-slopes than scarps. Collections were made at each station until a representative collection of all the obvious macrofossil types had been obtained; just as it was not possible to standardize sample bin size, so it was not possible to use a standard collecting time either. For these reasons we chose to focus only on range-through data and standing species richness to estimate changes in taxonomic diversity across the K–Pg boundary. In Supplementary Fig. 7, we have plotted variations in sample species richness through all three of our sections, including data from Zinsmeister16 (Supplementary Fig. 6). These all show fairly regular variation around a sample mean, but no major trends that could be linked to any obvious form of either local or global environmental variation. Such small-scale fluctuations in species richness are an inevitable consequence of specimen collection in a scarp and dip-slope terrain, and are unlikely to represent any true response to environmental change.

Correlation between section lines and the construction of a composite section was achieved using several stratigraphic tie-points, notably the glauconite-rich beds that mark the K–Pg boundary and a further prominent glauconite-rich horizon present in all section lines 174 m below the K–Pg. To enable a full analysis of extinction patterns at the K–Pg boundary, field data derived from British Antarctic Survey sampling was also supplemented with additional data from Zinsmeister16 (Supplementary Fig. 6). Zinsmeister’s16 macrofossil collections were taken from a series of short (20 m) sections measured and sampled during a detailed along-strike mapping study of the K–Pg boundary across 5.5 km of southern Seymour Island. When plotting these additional fossil occurrences the base of the ‘Lower Glauconite’ horizon of Zinsmeister16 is taken as a reference plane, and assumed to be equivalent to the base of the glauconite-rich beds and K–Pg boundary in our composite measured section at a stratigraphic height of 1,007.5 m (refs 31, 51). For all these stratigraphic correlations, we assume planar bedding along strike. The unconformable contact at the base of the Sobral Formation is also useful as a tie-point, although it can be demonstrated that on a regional scale the degree of erosion of the upper levels of the López de Bertodano Formation changes subtly along strike across the island26,67.

The occurrence of glauconite-rich horizons, such as those that mark the K–Pg interval, suggest periods of slower, condensed sedimentation. The base of these units appears gradational in the field16,24,27,30 and high-resolution palynological studies18,23,24 show they are not associated with significant sedimentary hiatuses in the studied sections, but probably represent conformable facies boundaries24.

Fossil data analysis

Over 6,000 fossils of benthic molluscs (bivalves and gastropods) were examined during this study, with 5,710 identified to at least generic level, these have been combined with >700 cephalopod macrofossils18 for an examination of overall diversity of the molluscan fauna. Following taxonomic identification and reassessment (Supplementary Note 1), first and last occurrence data from individual section lines were used to construct a composite range chart using the stratigraphic tie points outlined above. Changes in stratigraphic bin size were accounted for by taking the base of the stratigraphic bin in which a species first occurred as the first appearance, and the top of the stratigraphic bin in which a species last occurred as the last appearance. While this introduces a degree of error into the results (for example, where a sampling bin straddles the K–Pg boundary in a single stratigraphic section), it is negligible given the expanded nature of the succession. A presence–absence data set based on this range data (Supplementary Data 1) was used to calculate standing species richness variations throughout the section, supplemented with additional collections from the overlying Paleocene Sobral Formation24,44 and a literature review to identify range-through taxa from older, underlying formations (Supplementary Table 1). To assess changing rates of biotic turnover through the succession, the presence–absence data set was split into 10 m bins and both extinction (Er) and origination (Or) rates calculated for each 10 m bin using the boundary-crosser methodology outlined by Foote38:

where Nbt=number of range-through taxa, Nft=number of taxa that originate within any given 10 m bin and cross the top boundary of that bin and Nbl=number of taxa that cross the bottom boundary of the bin but have their last occurrence within the bin. These should be considered as ‘extinction’ and ‘origination’ rates only in the local context, and are not expressed relative to bin duration. Available evidence suggests overall sedimentation rates remained high throughout deposition of the López de Bertodano Formation at 0.1–0.2 mm per year (ref. 17) (Supplementary Fig. 5) indicating that any variation in bin duration is likely to have a negligible effect on the magnitude of biotic turnover rates.

To test the hypothesis of multiple extinction events and visually assess the pattern of taxonomic turnover more generally through the Maastrichtian, we also employed the stratigraphic abundance method of Meldahl40. Stratigraphic abundance (S, the percentage of sample intervals in which a given taxon occurs) was calculated using a recently modified method41 to enable us to include data from all three studied sedimentary sections in addition to data from Zinsmeister16:

where Noccurrence 1 is the number of occurrences of a given species in section 1, and Nsample 1 is the number of samples in section 1. A plot of S versus last occurrence provides a visual estimate of the likely position of an extinction horizon based on the disappearance of the most common taxa in an assemblage (Fig. 3c), and along with a plot of the frequency distribution of last occurrences in a stratigraphic section (Supplementary Fig. 7), can be compared with simulated models of sudden and gradual extinction40. We included all molluscan taxa in this analysis, including a reanalysis of the nekton to include additional data from field collections made in 2010 (data reanalysed from ref. 18). To investigate the extent to which the data is influenced by the ‘Signor-Lipps Effect’39 due to the sampling strategy, 50 and 95% confidence intervals were calculated for all benthic taxa with >5 occurrences during the Maastrichtian within two BAS section lines (sections A and B, Fig. 1c). We applied the ‘classical’ method as summarised by Marshall42, and illustrate these confidence intervals as range extensions (Supplementary Figs 3 and 4) using the following equation:

Average gap size between fossil occurrences also provides an unbiased point estimate of the true time of appearance or disappearance in any given stratigraphic section assuming random fossil recovery42, and was calculated for the same taxa using:

where rC,i is the length of the range extension, runbiased is the average gap between fossil occurrences as a percentage of that taxon’s stratigraphic range, C is the desired confidence level (expressed as a decimal; 0.5 and 0.95), H is the number of observed fossil occurrences for a species in an individual section line and R is the observed stratigraphic range of the taxon in the same section line. Confidence intervals were only calculated for data from two sections directly sampled by the authors (sections A and B, Fig. 1c), both of which have extended records from the Maastrichtian into the Paleocene. Because of the constraints of the sampling strategy outlined above, confidence intervals were not applied to any composite data set that is derived only from range-through data (Fig. 2).

Pyrite petrography

Polished blocks were made from 21 bulk sediment samples collected throughout composite section D5.251 (Supplementary Table 2). These were examined using an FEI Quanta 650 scanning electron microscope (SEM) in back-scatter mode to identify microfacies and quantify the diameter of pyrite framboid populations. The size and distribution of pyrite framboids in both ancient and modern sediments are interpreted to result from local redox conditions45,46. In modern environments, syngenetic framboids form in a narrow iron reduction region developed at the redox boundary, but cease growing in the underlying fully anoxic sulphate reduction zone. Under fully euxinic conditions (where free H2S occurs in the water column), syngenetic framboids grow to a maximum diameter of 6–7 μm in the water column before gravity causes them to sink to the seabed45. Framboid populations formed under these conditions will exhibit both a small size range and a small s.d. In dysoxic settings, conditions on the seabed are often weakly oxygenated, leading to framboid development in the pore water of the underlying sediments. Here the size range is controlled primarily by the availability of reactants and therefore framboid populations typically grow to larger sizes (up to 20 μm) with a correspondingly higher s.d.46. Supplementary Figure 8 presents a ‘Box and Whisker’ plot showing the stratigraphic distribution of the sampled horizons and illustration of framboid populations.

Data availability

The authors declare that all data supporting the findings of this study are available within the article and its Supplementary Information Files.

Additional information

How to cite this article: Witts, J. D. et al. Macrofossil evidence for a rapid and severe Cretaceous–Paleogene mass extinction in Antarctica. Nat. Commun. 7:11738 doi: 10.1038/ncomms11738 (2016).


  1. 1

    Alvarez, L. W., Alvarez, W., Asaro, F. & Michel, H. V. Extraterrestrial cause for the Cretaceous-Tertiary extinction. Science 208, 1095–1108 (1980).

    CAS  ADS  Article  Google Scholar 

  2. 2

    Raup, D. M. & Sepkoski, J. J. Mass extinctions in the marine fossil record. Science 215, 1501–1503 (1982).

    CAS  ADS  Article  Google Scholar 

  3. 3

    Bambach, R. K. Phanerozoic biodiversity mass extinctions. Annu. Rev. Earth Planet. Sci. 34, 127–155 (2006).

    CAS  ADS  Article  Google Scholar 

  4. 4

    Schulte, P. et al. The Chicxulub asteroid impact and mass extinction at the Cretaceous-Paleogene boundary. Science 327, 1214–1218 (2010).

    CAS  ADS  Article  Google Scholar 

  5. 5

    Keller, G. et al. Cretaceous extinctions: evidence overlooked. Science 328, 974–975 (2010).

    CAS  Article  Google Scholar 

  6. 6

    Archibald, J. D. et al. Cretaceous extinctions: multiple causes. Science 328, 973 (2010).

    CAS  Article  Google Scholar 

  7. 7

    McGhee, G. R., Clapham, M. E., Sheehan, P. M., Bottjer, D. J. & Droser, M. L. A new ecological severity ranking of major Phanerozoic biodiversity crises. Palaeogeogr. Palaeoclimatol. Palaeoecol. 283, 260–270 (2013).

    Article  Google Scholar 

  8. 8

    Brusatte, S. L. et al. The extinction of the dinosaurs. Biol. Rev. 90, 628–642 (2015).

    Article  Google Scholar 

  9. 9

    Krug, A. Z., Jablonski, D. & Valentine, J. W. Signature of the end-Cretaceous mass extinction in the modern biota. Science 323, 767–771 (2009).

    CAS  ADS  Article  Google Scholar 

  10. 10

    Aberhan, M. & Kiessling, W. Rebuilding biodiversity of Patagonian marine molluscs after the end-Cretaceous mass extinction. PLoS ONE 9, e106269 (2014).

    Article  Google Scholar 

  11. 11

    Aberhan, M. & Kiessling, W. Persistent ecological shifts in marine molluscan assemblages across the end-Cretaceous mass extinction. Proc. Natl Acad. Sci. USA 112, 7207–7212 (2015).

    CAS  ADS  Article  Google Scholar 

  12. 12

    Schoene, B. et al. U-Pb geochronology of the Deccan Traps and relation to the end-Cretaceous mass extinction. Science 347, 182–184 (2014).

    ADS  Article  Google Scholar 

  13. 13

    Renne, P. R. et al. State shift in Deccan volcanism at the Cretaceous-Paleogene boundary, possibly induced by impact. Science 350, 76–78 (2015).

    CAS  ADS  Article  Google Scholar 

  14. 14

    Renne, P. R. et al. Time scales of critical events around the Cretaceous-Paleogene boundary. Science 339, 684–687 (2013).

    CAS  ADS  Article  Google Scholar 

  15. 15

    Zinsmeister, W. J., Feldmann, R. M., Woodburne, M. O. & Elliot, D. H. Latest Cretaceous/earliest Tertiary transition on Seymour Island, Antarctica. J. Palaeont. 63, 731–738 (1989).

    Article  Google Scholar 

  16. 16

    Zinsmeister, W. J. Discovery of fish mortality horizon at the K-T boundary on Seymour Island: re-evaluation of events at the end of the Cretaceous. J. Palaeont. 72, 556–571 (1998).

    Article  Google Scholar 

  17. 17

    Tobin, T. S. et al. Extinction patterns, δ18O trends, and magnetostratigraphy from a southern high-latitude Cretaceous-Paleogene section: links with Deccan volcanism. Palaeogeogr. Palaeoclimatol. Palaeoecol. 350–352, 180–188 (2012).

    Article  Google Scholar 

  18. 18

    Witts, J. D. et al. Evolution and extinction of Maastrichtian (Late Cretaceous) cephalopods from the López de Bertodano Formation, Seymour Island, Antarctica. Palaeogeogr. Palaeoclimatol. Palaeoecol. 418, 193–212 (2015).

    Article  Google Scholar 

  19. 19

    Powell, M. G. & MacGregor, J. A geographic test of species selection using planktonic foraminifera during the Cretaceous/Paleogene mass extinction. Paleobiology 37, 426–437 (2011).

    Article  Google Scholar 

  20. 20

    Punekar, J., Mateo, P. & Keller, G. in Volcanism, Impacts, and Mass Extinctions: Causes and Effects vol. 505, eds Keller K., Kerr A. C. SPE504–SPE505Geol. Soc. Am. (2014).

    Google Scholar 

  21. 21

    Jablonski, D. Geographic variation in the molluscan recovery from the end-Cretaceous extinction. Science 279, 1327–1330 (1998).

    CAS  ADS  Article  Google Scholar 

  22. 22

    Jiang, S., Bralower, T. J., Patzkowsky, M. E., Kump, L. R. & Schueth, J. D. Geographic controls on nannoplankton extinction across the Cretaceous/Paleogene boundary. Nat. Geosci. 3, 280–285 (2010).

    CAS  ADS  Article  Google Scholar 

  23. 23

    Bowman, V. C., Francis, J. E. & Riding, J. B. Late Cretaceous winter sea ice in Antarctica? Geology 41, 1227–1230 (2013).

    CAS  ADS  Article  Google Scholar 

  24. 24

    Bowman, V. C. et al. The Paleocene of Antarctica: Dinoflagellate cyst biostratigraphy, chronostratigraphy and implications for the palaeo-Pacific margin of Gondwana. Gondwana Res (in the press).

  25. 25

    Hathway, B. Continental rift to back-arc basin: Jurassic-Cretaceous stratigraphical and structural evolution of the Larsen Basin, Antarctic Peninsula. J. Geol. Soc. London 157, 417–432 (2000).

    Article  Google Scholar 

  26. 26

    Macellari, C. E. Stratigraphy, sedimentology, and paleoecology of Upper Cretaceous/Paleocene shelf-deltaic sediments of Seymour Island. Geol. Soc. Am. Mem. 169, 25–53 (1988).

    Google Scholar 

  27. 27

    Crame, J. A., Francis, J. E., Cantrill, D. J. & Pirrie, D. Maastrichtian stratigraphy of Antarctica. Cretac. Res. 25, 411–423 (2004).

    Article  Google Scholar 

  28. 28

    Olivero, E. B. Sedimentary cycles, ammonite diversity and palaeoenvironmental changes in the Upper Cretaceous Marambio group, Antarctica. Cretac. Res. 34, 348–366 (2012).

    Article  Google Scholar 

  29. 29

    Olivero, E. B., Ponce, J. J., Marsicano, C. & Martinioni, D. R. Depositional settings of the basal López de Bertodano formation, Maastrichtian, Antarctica. Rev. la Asoc. Geol. Argentina 62, 521–529 (2007).

    Google Scholar 

  30. 30

    Elliot, D. H., Askin, R. A., Kyte, F. T. & Zinsmeister, W. J. Iridium and dinocysts at the Cretaceous-Tertiary boundary on Seymour Island, Antarctica: implications for the K-T event. Geology 22, 675–678 (1994).

    CAS  ADS  Article  Google Scholar 

  31. 31

    Bowman, V. C., Francis, J. E., Riding, J. B., Hunter, S. J. & Haywood, A. M. A latest Cretaceous to earliest Paleogene dinoflagellate cyst zonation from Antarctica, and implications for phytoprovincialism in the high southern latitudes. Rev. Palaeobot. Palynol. 171, 40–56 (2012).

    Article  Google Scholar 

  32. 32

    Molina, E. et al. The global boundary stratotype section and point for the base of the Danian stage (Paleocene, Paleogene, ‘Tertiary’, Cenozoic) at El Kef, Tunisia—original definition and revision. Episodes 29, 263–273 (2006).

    Google Scholar 

  33. 33

    Francis, J. E. & Poole, I. Cretaceous and early Tertiary climates of Antarctica: evidence from fossil wood. Palaeogeogr. Palaeoclimatol. Palaeoecol. 182, 47–64 (2002).

    Article  Google Scholar 

  34. 34

    Little, C. T. S. et al. Late Cretaceous (Maastrichtian) shallow water hydrocarbon seeps from Snow Hill and Seymour Islands, James Ross Basin, Antarctica. Palaeogeogr. Palaeoclimatol. Palaeoecol. 418, 213–228 (2015).

    Article  Google Scholar 

  35. 35

    Scasso, R. A., Olivero, E. B. & Buatois, L. Lithofacies, biofacies, and ichnoassemblage evolution of a shallow submarine volcaniclastic fan-shelf depositional system (Upper Cretaceous, James Ross Island, Antarctica). J. South Am. Earth Sci. 4, 239–260 (1991).

    ADS  Article  Google Scholar 

  36. 36

    Pirrie, D., Crame, J. A., Lomas, S. A. & Riding, J. B. Late Cretaceous stratigraphy of the Admiralty Sound region, James Ross Basin, Antarctica. Cretac. Res. 18, 109–137 (1997).

    Article  Google Scholar 

  37. 37

    Stilwell, J. D. Geological exploration of Cockburn Island, Antarctic Peninsula. Polish Polar Res. 23, 47–73 (2002).

    Google Scholar 

  38. 38

    Foote, M. Origination and extinction components of taxonomic diversity: general problems. Paleobiology 26, 74–102 (2000).

    Article  Google Scholar 

  39. 39

    Signor, P. W. & Lipps, J. H. in Geological Implications of Impacts of Large Asteroids and Comets on the Earth vol. 190, eds Silver L. T., Schultz P. H. 291–296Geol. Soc. Am. (1982).

    Article  Google Scholar 

  40. 40

    Meldahl, K. Sampling, species abundance, and the stratigraphic signature of mass extinction: a test using Holocene tidal flat molluscs. Geology 18, 890–893 (1990).

    ADS  Article  Google Scholar 

  41. 41

    Song, H., Wignall, P. B., Tong, J. & Yin, H. Two pulses of extinction during the Permian-Triassic crisis. Nat. Geosci. 6, 52–56 (2012).

    ADS  Article  Google Scholar 

  42. 42

    Marshall, C. R. in Quantitative Methods in Paleobiology vol. 16, eds Alroy J., Hunt G. 291–316The Pal. Soc. (2010).

    Google Scholar 

  43. 43

    Stilwell, J. D., Zinsmeister, W. J. & Oleinik, A. E. Early Paleocene mollusks of Antarctica: systematics, paleoecology and paleogeographic significance. Bull. Am. Paleontol. 367, 1–89 (2004).

    Google Scholar 

  44. 44

    Crame, J. A. et al. The early origins of the Antarctic marine fauna and its evolutionary implications. PLoS ONE 9, e114732 (2014).

    Article  Google Scholar 

  45. 45

    Wignall, P. B. & Newton, R. Pyrite framboid diameter as a measure of oxygen deficiency in ancient mudrocks. Am. J. Sci. 298, 537–552 (1998).

    CAS  ADS  Article  Google Scholar 

  46. 46

    Wilkin, R. T., Barnes, H. L. & Brantley, S. L. The size distribution of framboidal pyrite in modern sediments: an indicator of redox conditions. Geochim. Cosmochim. Acta 60, 3897–3912 (1996).

    CAS  ADS  Article  Google Scholar 

  47. 47

    Thibault, N. & Gardin, S. The nannofossil response to the end-Cretaceous warm event in the tropical Pacific. Palaeogeogr. Palaeoclimatol. Palaeoecol. 291, 239–252 (2010).

    Article  Google Scholar 

  48. 48

    Thibault, N. & Husson, D. Climatic fluctuations and sea-surface water circulation patterns at the end of the Cretaceous era: Calcareous nannofossil response. Palaeogeogr. Palaeoclimatol. Palaeoecol. 441, 152–164 (2016).

    Article  Google Scholar 

  49. 49

    Schmidt, A. et al. Selective environmental stress from sulphur emitted by continental flood basalt eruptions. Nat. Geosci. 9, 77–82 (2016).

    CAS  ADS  Article  Google Scholar 

  50. 50

    Richards, M. A. et al. Triggering of the largest Deccan eruptions by the Chicxulub impact. Geol. Soc. Am. Bull. 127, 1507–1520 (2015).

    ADS  Article  Google Scholar 

  51. 51

    Bowman, V. C., Francis, J. E., Askin, R. A., Riding, J. B. & Swindles, G. T. Latest Cretaceous-earliest Paleogene vegetation and climate change at the high southern latitudes: palynological evidence from Seymour Island, Antarctic Peninsula. Palaeogeogr. Palaeoclimatol. Palaeoecol. 408, 26–47 (2014).

    Article  Google Scholar 

  52. 52

    Beu, A. G. Before the ice: biogeography of Antarctic Paleogene molluscan faunas. Palaeogeogr. Palaeoclimatol. Palaeoecol. 284, 191–226 (2009).

    Article  Google Scholar 

  53. 53

    Martin, J. E. Biostratigraphy of the Mosasauridae (Reptilia) from the Cretaceous of Antarctica. Geol. Soc. Lond. Spec. Pub. 258, 101–108 (2006).

    ADS  Article  Google Scholar 

  54. 54

    Harwood, D. M. Upper Cretaceous and lower Paleocene diatom and silicoflagellate biostratigraphy of Seymour Island, eastern Antarctic Peninsula. Geol. Soc. Am. Mem. 169, 55–130 (1988).

    Google Scholar 

  55. 55

    Lewis, J., Harris, A. S. D., Jones, K. J. & Edmonds, R. L. Long term survival of marine planktonic diatoms and dinoflagellates in stored sediment samples. J. Plankton Res. 21, 343–354 (1999).

    Article  Google Scholar 

  56. 56

    Ribeiro, S. et al. Phytoplankton growth after a century of dormancy illuminates past resilience to catastrophic darkness. Nat. Commun. 2, 311 (2011).

    Article  Google Scholar 

  57. 57

    Huber, B. T. Upper Campanian-Paleocene foraminfera from the James Ross Island region, Antarctic Peninsula. Geol. Soc. Am. Mem. 169, 163–252 (1988).

    Google Scholar 

  58. 58

    Hansen, T. A., Farrell, B. R. & Upshaw, B. III. The first 2 million years after the Cretaceous-Tertiary boundary in east Texas: rate and paleoecology of the molluscan recovery. Paleobiology 19, 251–265 (1993).

    Article  Google Scholar 

  59. 59

    Heinberg, C. Lower Danian bivalves, Stevns Klint, Denmark. Continuity across the K/T boundary. Palaeogeogr. Palaeoclimatol. Palaeoecol. 154, 87–106 (1999).

    Article  Google Scholar 

  60. 60

    Raup, D. M. & Jablonski, D. Geography of end-Cretaceous marine bivalve extinctions. Science 260, 971–973 (1993).

    CAS  ADS  Article  Google Scholar 

  61. 61

    Crame, J. A., Lomas, S. A., Pirrie, D. & Luther, A. Late Cretaceous extinction patterns in Antarctica. J. Geol. Soc. Lond. 153, 503–506 (1996).

    Article  Google Scholar 

  62. 62

    Friedrich, O., Norris, R. D. & Erbacher, J. Evolution of middle to Late Cretaceous oceans—a 55 m.y. record of Earth’s temperature and carbon cycle. Geology 40, 107–110 (2012).

    CAS  ADS  Article  Google Scholar 

  63. 63

    Linnert, C. et al. Evidence for global cooling in the Late Cretaceous. Nat. Commun. 5, 1–7 (2014).

    Article  Google Scholar 

  64. 64

    Dutton, A., Huber, B. T., Lohmann, K. C. & Zinsmeister, W. J. High-resolution stable isotope profiles of a dimitobelid belemnite: implications for paleodepth habitat and late Maastrichtian climate seasonality. Palaios 22, 642–650 (2007).

    ADS  Article  Google Scholar 

  65. 65

    Kemp, D. B. et al. A cool temperate climate on the Antarctic Peninsula through the latest Cretaceous to early Paleogene. Geology 42, 583–586 (2014).

    ADS  Article  Google Scholar 

  66. 66

    Alegret, L. & Thomas, E. Food supply to the seafloor in the Pacific Ocean after the Cretaceous/Paleogene boundary event. Mar. Micropaleontol. 73, 105–116 (2009).

    ADS  Article  Google Scholar 

  67. 67

    Montes, N., Nozal, F., Santillana, S., Marenssi, S. A. & Olivero, E. B. Mapa geológioco de la Isla Marambio (Seymour) Escala 1:20,000. Inst. Ant. Arg. Inst. Geol. Min. España (2010).

  68. 68

    McArthur, J. M., Thirlwall, M. F., Engkilde, M., Zinsmeister, W. J. & Howarth, R. J. Strontium isotope profiles across K/T boundary sequences in Denmark and Antarctica. Earth Planet Sci. Lett. 160, 179–192 (1998).

    CAS  ADS  Article  Google Scholar 

  69. 69

    Gradstein, F. M., Ogg, J. G., Schmitz, M. & Ogg, G. The Geological Time Scale 2012 Elsevier Science Ltd (2012).

  70. 70

    Chenet, A. L. et al. Determination of rapid Deccan eruptions across the Cretaceous-Tertiary boundary using paleomagnetic secular variation: 2. constraints from analysis of eight new sections and synthesis for a 3500-m-thick composite section. J. Geophys. Res. 114, BO6103 (2009).

    ADS  Article  Google Scholar 

Download references


Funding for this study was provided by a PhD scholarship from the University of Leeds to J.D.W., and UK Natural Environment Research Council (NERC) grants NE/C506399/1 (Antarctic Funding Initiative) (to J.E.F.) and NE/I00582X/1 (PALEOPOLAR) (to J.A.C.). Fieldwork to Seymour Island was supported logistically by the British Antarctic Survey, and we thank Hilary Blagbrough (BAS, Cambridge, UK) for subsequent laboratory and technical support. We also acknowledge the help of staff at the Paleontological Research Institute (PRI, Ithaca, New York, USA) for assisting with access to the Zinsmeister Fossil Collection. We thank Cris Little and Alex Dunhill (University of Leeds, UK) for their constructive comments on an earlier version of this manuscript, and Jon Ineson (GEUS, Copenhagen, Denmark) as well as other members of the PALEOPOLAR research team, for useful discussions regarding the sedimentology and stratigraphy of Seymour Island.

Author information




Fieldwork and fossil sampling on Seymour Island was conducted by J.A.C., R.J.W., J.E.F. and V.C.B. Macrofossil identifications were made by J.D.W. with assistance from R.J.W. and J.A.C. J.D.W. analysed the data and wrote the manuscript with help and contributions from all co-authors.

Corresponding author

Correspondence to James D. Witts.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Information

Supplementary Figures 1-8, Supplementary Tables 1-2, Supplementary Note 1 and Supplementary References. (PDF 1891 kb)

Supplementary Data 1

Raw field data (sheets A-D), composite range, occurrence, and stratigraphic abundance data (sheets E-F), and turnover metrics (origination and extinction) (sheet G). (XLSX 107 kb)

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Witts, J., Whittle, R., Wignall, P. et al. Macrofossil evidence for a rapid and severe Cretaceous–Paleogene mass extinction in Antarctica. Nat Commun 7, 11738 (2016).

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing