The Chicxulub crater was formed by an asteroid impact at ca. 66 Ma. The impact is considered to have contributed to the end-Cretaceous mass extinction and reduced productivity in the world’s oceans due to a transient cessation of photosynthesis. Here, biomarker profiles extracted from crater core material reveal exceptional insights into the post-impact upheaval and rapid recovery of microbial life. In the immediate hours to days after the impact, ocean resurge flooded the crater and a subsequent tsunami delivered debris from the surrounding carbonate ramp. Deposited material, including biomarkers diagnostic for land plants, cyanobacteria, and photosynthetic sulfur bacteria, appears to have been mobilized by wave energy from coastal microbial mats. As that energy subsided, days to months later, blooms of unicellular cyanobacteria were fueled by terrigenous nutrients. Approximately 200 k.y. later, the nutrient supply waned and the basin returned to oligotrophic conditions, as evident from N2-fixing cyanobacteria biomarkers. At 1 m.y. after impact, the abundance of photosynthetic sulfur bacteria supported the development of water-column photic zone euxinia within the crater.

The impact crater at Chicxulub (Yucatán Peninsula, México) is the only terrestrial crater on Earth with a well-preserved peak ring (Hildebrand et al., 1991; Schulte et al., 2010; Morgan et al., 2016; Kring et al., 2017; Gulick et al., 2019). The asteroid impact is linked to the end-Cretaceous mass extinction event, which wiped out 76% of all species worldwide (Sepkoski, 1996), along with a near-global loss of vegetation (Kring, 2007; Vajda and Bercovici, 2014; Brugger et al., 2017). A collapse in phytoplankton productivity in the world’s oceans (Hsü et al., 1982; Zachos and Arthur, 1986; Sepúlveda et al., 2009) occurred due to the sudden decline in photosynthesis as atmospheric particulates lowered light levels for years after the impact (Bardeen et al., 2017). In 2016, the peak ring of the Chicxulub crater was cored (Fig. 1) by the International Ocean Discovery Program (IODP) and International Continental Scientific Drilling Program Expedition 364 (see the GSA Data Repository1). A 130-m-thick interval of impact melt rock and upward-fining suevite, which overlies fractured basement rock, was deposited immediately after impact. The lower suevite, rich in impact melt rock, is directly overlain by material transported via ocean resurge and then by seiches and a tsunami deposit (Grice et al., 2009; Gulick et al., 2019; Osinski et al., 2019; Whalen, 2019, personal commun.). The overlying 0.75-m-thick, fine-grained, brown micritic limestone (“transitional unit”), deposited in days to years after the impact by continuing seiches and tsunami, contains microfossils of calcareous plankton and trace fossils of burrowing organisms (Whalen et al., 2017; Lowery et al., 2018; Gulick et al., 2019). The transitional unit is overlain by a thin green marlstone, followed by the deposition of “white” micritic limestone (616.55–616.24 m below seafloor [mbsf]) within 30–200 k.y., representing the base of the succeeding pelagic-hemipelagic limestone deposit. Data to support the geology and relative timing of these events have been published by Gulick et al. (2019) and Lowery et al. (2018).

Evidence of ancient life is generally preserved in sediments as morphological fossils, trace fossils, and molecular fossils (biomarkers). Biomarkers are often well preserved in sediments even where visible mineralized fossils are absent, representing valuable signs of past life, especially microbial life. For example, in the Fiskeler Member in the end-Cretaceous boundary layer at Kulstirenden, Denmark, biomarkers showed that marine productivity recovered within a century following the Chicxulub impact (Sepúlveda et al., 2009). Here, we present biomarker distributions and sulfur isotopes of pyrite between 619 mbsf and 608 mbsf at IODP Site M0077A (21.45°N, 89.95°W). Our aim was to use biomarkers to reconstruct the origin, recovery, and development of microbial life and to determine the paleoenvironmental conditions in the crater from the time of impact to up to ∼4 m.y. after the impact (Figs. 2 and 3).

Detailed materials and methods are provided in the Data Repository. Briefly, samples were Soxhlet extracted, and the extracts were separated into apolar and polar fractions and analyzed by gas chromatography–mass spectrometry (GC-MS), metastable reaction monitoring (MRM), and high-performance liquid chromatography–tandem mass spectrometry (HPLC-MS2). The δ13C and δ34S values were measured on extracted residues. Total organic carbon (TOC) was determined by an elemental analyzer. Typical traces of GC-MS and MRM for procedural blanks and samples are given in Figures DR1–DR4 in the Data Repository.

The TOC content (Fig. 2A) in the entire interval was low (0.06–0.2 wt%), consistent with carbonate dilution (see the Data Repository). The homohopane ratios [i.e., 22S/(22S + 22R)], were ≤ 0.6, supporting a low thermal maturity through the section (see Fig. DR5; Peters et al., 2005). Despite low organic matter content and low abundances of biomarkers (Figs. 2 and 3), the record provided insights into the evolution of microbial communities in this exotic habitat.

First Days After Impact (619.31–617.33 mbsf)

The uppermost suevite was deposited by a tsunami within the first day after impact (Gulick et al., 2019). This tsunami transported reworked organic matter from outside the crater, as evidenced by the abundance and distribution of perylene and charcoal (Grice et al., 2009; Gulick et al., 2019). Reworked marine inputs shown by biomarkers included dominant n-C17/n-C19 alkanes, indicative of algae or cyanophytes (Fig. 2G). Further, abundant C29 steranes from green algae and/or land plants (Fig. 2F) reflect a mixture of marine and terrigenous inputs. This interval also contains biomarkers derived from anoxygenic photosynthetic sulfur bacteria (i.e., isorenieratane, β-isorenieratane, and traces of chlorobactane and okenane; Summons and Powell, 1987; Brocks et al., 2005; Grice et al., 2005, 1996; Figs. 3B–3D). In addition, cyanobacterial biomarkers in the form of 2α-methylhopanes (2α-MeH; Summons et al., 1999; Welander et al., 2010) and heterocyst glycolipids (HGs) were observed. The latter, diagnostic for N2-fixing cyanobacteria, represent the oldest reported intact HGs (Fig. 2D; Bauersachs et al., 2010). From the presence of terrestrial signatures and the depositional regime, we infer that all the organic signatures are reworked materials, likely derived from carbonate platforms and coastal environments close to the site. The biomarkers listed above were also identified in overlying sediments (617.33–608.48 mbsf), where they represent organisms living within the nascent crater. Here, we evaluate the oceanographic and redox conditions in the impact basin as inferred from the biological origins of these compounds.

Recovery—The First 200 k.y. (617.33–616.24 mbsf)

The interval deposited immediately after impact is represented by the transitional unit (617.33–616.58 mbsf) of fine-grained brown micrite and overlying green marlstone, and it is likely to contain the first record of microbial life after the impact (Lowery et al., 2018; Bralower, 2019, personal commun.). The succeeding “white micrite” is possibly a result of calcite formed photosynthetically by cyanobacteria that replaced the calcareous nanoplankton and other algae across the Cretaceous-Paleogene boundary (Bralower, 2019, personal commun.).

Our study provides the first evidence of cyanobacteria 30 k.y. after impact at 617.33–616.58 mbsf, from abundant C31+ hopanes (Figs. 2B and 2C; Rohmer et al., 1984; Summons et al., 1999; Brocks, 2018). The 2α-MeH ratios (1.9 and 4.2; Fig. 2C), in agreement with those reported for the Fiskeler Member boundary layer, are typical of marine conditions (Sepúlveda et al., 2009). However, the ratios observed here are significantly lower than those reported in Permian-Triassic (Cao et al., 2009) and Triassic-Jurassic (Kasprak et al., 2015) boundary sections.

The sterane/(sterane + hopane) ratios [S/(S + H)] were found to be low (0.17 and 0.7; Fig. 2E), showing low algal inputs relative to bacteria, particularly cyanobacteria (Brocks, 2018). In the Fiskeler Member boundary layer, the lowest S/(S + H) ratio was assigned to a decreased algal input, followed by an immediate increase, suggesting a rapid resurgence of algae when solar irradiance returned to pre-impact levels (Sepúlveda et al., 2009). In the transitional unit, the S/(S + H) ratio changed within multiple intervals, suggesting that the organic matter in the crater was a mixture of transported and autochthonous material, distinct from other Cretaceous-Paleogene sites (Sepúlveda et al., 2009). A similar trend was observed in the 2α-MeH index and the homohopane index (HHI) (Figs. 2B, 2C, and 2E). The HHI (5.8) and 2α-MeH index (4.2) are consistent with anoxic-euxinic conditions (Sepúlveda et al., 2009; Hamilton et al., 2017), which are also reflected by the low pristane/phytane ratios (Figs. 2B, 2C, and 3E). The HHI is based on the increased preservation of extended hopanes (>C33) under euxinic conditions (Peters and Moldowan, 1991) through reduction and cross-linking with reduced sulfur species (Köster et al., 1997). The shifts in high to low S/(S + H) ratios suggest that sedimentation was influenced by water movement, most likely seiches (Gulick et al., 2019) and resuspension (Lowery et al., 2018).

The HGs were observed to be low in abundance (Fig. 2D) in this interval, and exclusively consisted of the HG26 diol and HG26 keto-ol (Fig. DR6), identified in coastal microbial mats (Bauersachs et al., 2011), brackish-marine environments (Sollai et al., 2017), and in axenic cultures of nostocalean cyanobacteria such as Anabaena spp. or Nodularia spp. (Bauersachs et al., 2009, 2017). HG28 triols have been reported in free-living marine cyanobacteria (Bale et al., 2018). It is therefore plausible that the HG26 diol and HG26 keto-ol are also derived from a marine source. The low abundance of both components, however, suggests only low productivity of N2-fixing heterocystous cyanobacteria in the first 200 k.y. after the impact. An increased influx of terrigenous nutrients would have helped to sustain phytoplankton, as shown by the paired increase in the abundance of long-chain waxy n-alkanes (C25–C33) and C29 steranes (0.3–0.56; Figs. 2G and 2F) from plants and green algae (Eglinton and Hamilton, 1967; Volkman, 1986; Kodner et al., 2008). The 3β-MeH index (Fig. 2C) showed an increase at the top of the transitional unit (616.62–616.58 mbsf) and in the white micrite, indicating the presence of methanotrophs (e.g., Ding and Valentine, 2008).

200 k.y. to 4 m.y. After Impact (616.24–608.48 mbsf)

A substantial shift in the microbial community was found in the middle and upper parts of the hemipelagic limestone horizon. The HG distribution patterns and abundances showed considerable changes indicating shifts in the cyanobacterial community and an increase in cyanobacterial productivity by two orders of magnitude (0.23 × 107 area counts/g TOC) compared to the transitional unit, with maximum concentrations at 613.45 mbsf (Fig. 2D; Fig. DR6).

In contrast, the 2α-MeH index remained constant, with a slight increase at 613.45 mbsf, whereas the HHI increased again between 613.45 and 610.72 mbsf. This increase in (cyano) bacterial biomarkers and the concomitant rise in the abundance of N2-fixing heterocystous cyanobacteria suggest a shift toward a nitrogen-limited environment, perhaps triggered by water column stratification. Another possibility is that these organisms were allochthonous and were transported into the crater from microbial mats living in relatively shallow waters. The limestone interval between 613.45 and 610.72 mbsf (ca. 64.4–63.1 Ma) indeed indicated anoxic conditions during deposition, depicted by low pristane/phytane ratios (<1; Fig. 3E), abundant β-carotane from autotrophs, and highly characteristic photic zone euxinia (PZE) biomarkers from green-green and brown-green pigmented Chlorobiaceae (e.g., chlorobactane and isorenieratane), and purple pigmented Chromatiaceae (okenane; Figs. 3A–3D; Imhoff, 2004). Chlorobiaceae and Chromatiaceae are anaerobic photoautotrophs that use hydrogen sulfide (generated by sulfate-reducing bacteria) as an electron donor and biosynthesize specific bacteriochlorophyll and accessory carotenoid pigments to capture longer wavelengths of light energy to fix CO2 (Pfennig, 1978). Such organisms flourish in benthic mats and as plankton concentrated at the chemocline of lakes or restricted marine basins where sulfide concentrations are high within the photic zone; hence, they are indicative of PZE conditions (Pfennig, 1978; Grice et al., 2005; French et al., 2015). In this limestone interval, total reduced inorganic sulfur was abundant, with δ34S values ranging from ∼−22‰ at 613.71 mbsf to −33‰ at ∼611 mbsf, consistent with nonlimiting sulfate concentrations, water-column PZE (Figs. 3G and 3H), and enhanced pyrite burial (Fig. 3H; Lyons, 1997; Böttcher and Lepland, 2000). Similar δ34S values have been reported for reduced sulfur in Cretaceous black shales (Hetzel et al., 2006; Witts et al., 2018). Diagenetic pyrite in shell fillings and sediment matrix indicates recrystallization of primary framboids. The pronounced 34S depletion compared to the estimated value of contemporaneous seawater (15‰–20‰; Strauss, 1997; Witts et al., 2018) signifies that microbial sulfate reduction probably took place in the water column (Figs. 3G and 3H; Strauss, 1997).

Associated with compelling indicators that periodic PZE was prevalent in the Chicxulub crater from ca. 64.4 Ma to 63.1 Ma, the molecular evidence indicates that oxygenated waters overlay the anoxic and sulfidic interval of the water column (Figs. 2B–2D, 3E, 3G, and 3H). During this time interval, methane from anoxic sediments underlying a sulfidic water column likely migrated upward until it was oxidized by microaerophilic methanotrophic bacteria at the chemocline, as evidenced by 3β-MeHI (Fig. 2C). An alternative scenario is the possibility of an oxygen minimum zone (OMZ) existing in the crater water.

The evolution of microbial communities in the Chicxulub crater was investigated using molecular and isotopic signatures, as summarized in Figure 4. We propose a scenario where, in the initial days after the asteroid impact, debris from microbial mats containing N2-fixing heterocystous cyanobacteria and photosynthetic sulfur bacteria was eroded from adjacent carbonate platforms and transported by ocean resurge or tsunamis into the crater. Microbial ecosystem communities were in a constant state of dynamic flux during the early evolution of the crater. Diminution of sunlight following the impact led to a dramatic decline in cyanobacterial productivity in the crater waters. However, rapid recovery of phytoplankton occurred in the first 200 k.y., and marine primary production was fueled by an influx of terrigenous nutrients. Phytoplankton communities continued to experience rapid changes over the following 4 m.y. The nascent Chicxulub crater basin was accompanied by major transitions in nutrient and oxygen supplies (periods of euxinia) that shaped the recovery of microbial life.

The research used samples and data provided by the International Ocean Discovery Program (IODP). Expedition 364 was implemented by the European Consortium for Ocean Research Drilling (ECORD) and jointly funded by the IODP and the International Continental Scientific Drilling Program (ICDP), with contributions and logistical support from the Yucatan State Government and Universidad Nacional Autónoma de México (UNAM). We thank Peter Hopper and Alex Holman for their technical support with GC-MS analyses, and Iris Schmiedinger for isotope mass spectrometric analysis. Grice, Coolen, and Summons thank the Australian Research Council (ARC) for an ARC Discovery grant (DP180100982) titled “The recovery of life recorded at the end-Cretaceous impact crater.” Schaefer thanks Curtin University for an Australian postgraduate award. Coolen and Grice thank IODP and Australian and New Zealand legacy IODP funding (364 postcruise funding, 2016–2018) of “The Chicxulub post-impact crater record: Duration of a giant hydrothermal system and window into the resurgence and evolution of marine and terrestrial life” project. Schwark and Bauersachs received support via Deutsche Forschungsgemeinschaft grant Schw554/26. Freeman and Bralower, Gulick and Lowery, and Whalen were supported by U.S. National Science Foundation grants OCE 1736951, 1737351, and 1737199, respectively. Joanna Morgan was supported by UK NERC grant: NE/P005217/1. Thanks go to Julio Sepúlveda for helpful comments on an earlier version of this manuscript. We thank the anonymous reviewers for their constructive comments, which helped to improve this manuscript. This is University of Texas Institute for Geophysics Contribution #3529.

1GSA Data Repository item 2020087, sample location and description, laboratory and analytical techniques, Figures DR1–DR4 (chromatograms), Figure DR5 (maturity parameters), Figure DR6 (fractional abundance of heterocyst glycolipids), and Figure DR7 (long-chain alkanes versus TOC), is available online at, or on request from
Gold Open Access: This paper is published under the terms of the CC-BY license.