Yi Ge Zhang’s research while affiliated with Guangzhou Institute of Technology and other places

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Publications (57)


Fig. 2. Structures of tetraether lipids discussed in this study. Three main groups of non-isoprenoid branched glycerol dialkyl glycerol tetraethers (brGDGTs) discussed in this study are (1) regular branched GDGTs (B-GDGTs), (2) derivatives with fewer methylated branches, called sparsely-branched GDGTs (SBGDGTs), and (3) derivatives with a higher number of methylated branches, called overly-branched GDGTs (OB-GDGTs). Mass-to-charge (m/z) ratios for each molecule are labeled on the upper right. The numbers labeled in front of each molecule represent a varying number of methylated branches. For B-GDGTs, structures for C5-methylated (left column) and C6-methylated (right column) B-GDGTs are shown separately.
Information for study sites with GDGT measurements
Methylation index of Overly Branched tetraether lipids (MOB): a proxy for deep ocean (de)oxygenation?
  • Preprint
  • File available

April 2024

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184 Reads

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Yi Ge Zhang

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[...]

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Tiegang Li

Branched glycerol dialkyl glycerol tetraethers (brGDGTs) with lower (sparsely-branched; SB-) and higher (overly-branched; OB-) numbers of methylated branches relative to the “regular” brGDGTs (B-GDGTs) are abundant in anoxic waters in the Black Sea. Observed changes in abundances and numbers of methylated branches of the entire series OB-GDGTs, B-GDGTs, and SB-GDGTs relative to dissolved oxygen (DO) levels in anoxic waters suggest that these compounds can potentially track changes in oceanic DO levels through time. To explore this, we determine the entire brGDGT series in surface or near-surface sediments from sites with different DO distributions in marine waters and sediments, extending the limited core-top collection of these lipids. We propose a modified methylation index based on only OB-GDGTs, called MOB, to avoid the potential impacts of terrestrial-derived B-GDGTs. Interestingly, MOB values in our extended core-top collection are strongly related to changes in bottom-water DO concentrations rather than the site-specific minimum DO values, i.e. usually within mid-depth oxygen minimum zones (OMZs). This suggests that sedimentary lipids are likely derived from heterotrophic bacteria living at the sediment-water boundary in sediments while lipids produced within mid-depth OMZs are not effectively exported to deep oceans. Analysis of MOB values in ancient sediments in the East Equatorial Pacific shows a gradual decline in bottom water DO, correlating with the progressive increase in global export productivity, organic carbon burial, and elevated level of deep-water nutrient contents since the middle Miocene. These findings highlight the potential of MOB as a tool for reconstructing past oceanic (de)oxygenation events.

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Toward a Cenozoic history of atmospheric CO2

December 2023

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1,723 Reads

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100 Citations

Science

The geological record encodes the relationship between climate and atmospheric carbon dioxide (CO 2 ) over long and short timescales, as well as potential drivers of evolutionary transitions. However, reconstructing CO 2 beyond direct measurements requires the use of paleoproxies and herein lies the challenge, as proxies differ in their assumptions, degree of understanding, and even reconstructed values. In this study, we critically evaluated, categorized, and integrated available proxies to create a high-fidelity and transparently constructed atmospheric CO 2 record spanning the past 66 million years. This newly constructed record provides clearer evidence for higher Earth system sensitivity in the past and for the role of CO 2 thresholds in biological and cryosphere evolution.




Location of our studied sediment core R07 (red dot) on Chukchi Sea shelf. Surface currents were modified from Grebmeier et al. (2006). The base map was generated with the Ocean Data View software (Schlitzer, 2016).
Annual vertical profiles of nitrate, silicate, phosphate, salinity and temperature along 73°N transect. These data were downloaded from WOA 2018 in the National Centers for Environmental Information (NCEI; https://www.ncei.noaa.gov/access/world-ocean-atlas-2018/).
Temporal variations in brassicasterol/dinosterol (B/D) ratio, concentrations of long-chain n-alkanes, n-alkanols, n-alkanoic acids, and C32 1,15-diol in the R07 core, and summer AO index. Red (blue) bar in AO index indicates positive (negative) value, and black line represents the 3-years running mean. The AO index data were obtained from NOAA Climate Prediction Center (https://www.cpc.ncep.noaa.gov/products/precip/CWlink/daily_ao_index/ao.shtml).
Temporal variations in concentrations of brassicasterol, dinosterol, and C30 diols, TOC from R07, and SST/SIC at the study area. a. TOC from Zhang et al. (2018); b. The blue solid line represents the download satellite SIC data, and the blue dash line represents the SIC data calculated based on SST. The satellite SIC data are from the National Snow and Ice Data Center (NSIDC; Cavalieri et al., 1996). Historical SST data were obtained from the NOAA ERSST V5 (https://www.esrl.noaa.gov/psd/data/gridded/data.noaa.ersst.v5.html; Huang et al., 2017).
Biomarker evidence of the water mass structure and primary productivity changes in the Chukchi Sea over the past 70 years

January 2023

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172 Reads

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1 Citation

The Chukchi Sea has experienced significant changes under global warming in the Common Era, including the shift of primary productivity. However, modern observations are too short to fully investigate the effects of environmental changes in this area. Here, we analyzed lipid biomarkers (e.g. long-chain n-alkanes, n-alkanols, n-alkanoic acids, diols, and sterols) from a sediment core (R07) collected from the Chukchi Sea shelf to determine phytoplankton primary productivity variations and factors influencing these changes over the past 70 years. Similar trends of the abundance of terrestrial ecosystem-derived compounds (e.g. long-chain n-alkanes, n-alkanols, n-alkanoic acids, and C32 1,15-diol) indicate that terrigenous input increased from ca. 1946 towards ca. 1983 and then decreased thereafter. In comparison, biomarkers with marine origin indicate that the ratio of diatoms to dinoflagellates increased after ca. 1983 towards the core-top (ca. 2011). Concurrent changes in terrigenous input and phytoplankton community indicated a shift in water mass structure at ca. 1983 (i.e. the Alaska Coastal Water decreased and the Bering Sea Water increased), which may be attributed to the phase shift of the Arctic Oscillation and/or unsynchronized flow changes in different water masses. Owing to the different water mass properties, the change of water mass structure caused intense water mixing and the resulting high turbidity in the study area, which led to light limitation for phytoplankton growth. These conditions probably account for the reduced phytoplankton primary productivity from ca. 1983 to ca. 2000 in the general trend of increasing. The results indicate that, in addition to global warming and sea ice retreat, other factors, such as change in regional water mass structure (i.e. different water masses), may also have a significant influence on the primary productivity and the phytoplankton community in the Chukchi Sea shelf.


Location of our studied sites overlaid on the Longhurst biogeochemical provinces
The Longhurst map defines 56 coherent provinces from the modern biogeochemistry perspective³⁰, which were simplified to 27 provinces used in this study (Extended Data Table 1). The original provinces were merged on the basis of their geographical proximity and biogeochemical similarity to ensure that each new province is represented by at least one site over the Neogene. Different shapes and colours denote IODP (International Ocean Discovery Program and Integrated Ocean Drilling Program, red diamonds), ODP (maroon dots) and DSDP (blue squares) sites.
Provincial OC burial changes and their contribution to the global burial
a, Relative changes of provincial OC burial rates over time, with the ‘modern’ (Pleistocene) value defined as 1. b, Provincial contribution to the global OC burial rates during the Neogene (total 100%), with the leftmost column representing the modern burial of Dunne et al.³¹. The provinces presented here are identical to those shown in Fig. 1. Details for each province and the IODP sites used to construct the provincial records are provided in Extended Data Table 1.
Neogene OC burial in the global ocean
a, Burial rates calculated using different definitions of provinces, including Longhurst (black curve with uncertainty envelope, ±1σ in purple and ±2σ in pale lilac), Oceans (blue curve) and FAO Fishing (orange curve) approaches. b, Comparisons of global OC MAR between our record and the output of commonly used global carbon cycle models (COPSE⁷, GEOCARBSULFOR⁸ and Li & Elderfield⁹). All relative changes were normalized to the modern (Pleistocene) level.
Neogene climate and carbon cycle changes
a, A stacked deep-sea benthic foraminiferal δ¹⁸O curve⁵². b, Benthic δ¹³C stack⁵². c, 3 Ma moving average of δ¹³CCO2 (ref. ⁴⁰). d, Atmospheric CO2 reconstructions based on marine proxies including the alkenone (green hollow squares) and boron (solid blue squares) methods⁵³. Sky blue line is the locally estimated scatter plot smoothing fit curve. e, Neogene OC burial in the global ocean with ±1σ uncertainty envelope. f, Ratio between OC and carbonate carbon burial (OC:IC). Carbonate burial⁴⁶ was calculated on the basis of two carbonate compensation depth scenarios. g, Calculated flux of total carbon input to Earth’s surficial system. Absolute burial rates were adjusted to match the assumption that the modern (2.5–0.5 Ma) burial ratio between inorganic and organic carbon is 4:1. h. Calculated δ¹³C of the total carbon input to Earth’s surficial system. The changing inorganic versus organic burial ratio during the Neogene, together with δ¹³CIC (ref. ⁴⁸) and δ¹³Corg (ref. ⁴⁷) data were used to obtain this record using equation (2). Pink and blue vertical bars highlight the timing of the Miocene Climatic Optimum (MCO) and Middle Miocene Climate Transition (MMCT).
Neogene burial of organic carbon in the global ocean

January 2023

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811 Reads

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58 Citations

Nature

Organic carbon buried in marine sediment serves as a net sink for atmospheric carbon dioxide and a source of oxygen1,2. The rate of organic carbon burial through geologic history is conventionally established by using the mass balance between inorganic and organic carbon, each with distinct carbon isotopic values (δ13C)3,4. This method is complicated by large uncertainties, however, and has not been tested with organic carbon accumulation data5,6. Here we report a ‘bottom-up’ approach for calculating the rate of organic carbon burial that is independent from mass balance calculations. We use data from 81 globally distributed sites to establish the history of organic carbon burial during the Neogene (roughly 23–3 Ma). Our results show larger spatiotemporal variability of organic carbon burial than previously estimated7–9. Globally, the burial rate is high towards the early Miocene and Pliocene and lowest during the mid-Miocene, with the latter period characterized by the lowest ratio of organic-to-carbonate burial rates. This is in contrast to earlier work that interpreted enriched carbonate 13C values of the mid-Miocene as massive organic carbon burial (that is, the Monterey Hypothesis)10,11. Suppressed organic carbon burial during the warm mid-Miocene is probably related to temperature-dependent bacterial degradation of organic matter12,13, suggesting that the organic carbon cycle acted as positive feedback of past global warming. A ‘bottom-up’ approach for calculating the rate of organic carbon burial in the global ocean shows larger variability than has been previously estimated, suggesting that the organic carbon cycle acted as positive feedback of past global warming.


The PhanSST global database of Phanerozoic sea surface temperature proxy data

December 2022

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1,407 Reads

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25 Citations

Scientific Data

Paleotemperature proxy data form the cornerstone of paleoclimate research and are integral to understanding the evolution of the Earth system across the Phanerozoic Eon. Here, we present PhanSST, a database containing over 150,000 data points from five proxy systems that can be used to estimate past sea surface temperature. The geochemical data have a near-global spatial distribution and temporally span most of the Phanerozoic. Each proxy value is associated with consistent and queryable metadata fields, including information about the location, age, and taxonomy of the organism from which the data derive. To promote transparency and reproducibility, we include all available published data, regardless of interpreted preservation state or vital effects. However, we also provide expert-assigned diagenetic assessments, ecological and environmental flags, and other proxy-specific fields, which facilitate informed and responsible reuse of the database. The data are quality control checked and the foraminiferal taxonomy has been updated. PhanSST will serve as a valuable resource to the paleoclimate community and has myriad applications, including evolutionary, geochemical, diagenetic, and proxy calibration studies.


Persistent high latitude amplification of the Pacific Ocean over the past 10 million years

November 2022

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405 Reads

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19 Citations

While high latitude amplification is seen in modern observations, paleoclimate records, and climate modeling, better constraints on the magnitude and pattern of amplification would provide insights into the mechanisms that drive it, which remain actively debated. Here we present multi-proxy multi-site paleotemperature records over the last 10 million years from the Western Pacific Warm Pool (WPWP) – the warmest endmember of the global ocean that is uniquely important in the global radiative feedback change. These sea surface temperature records, based on lipid biomarkers and seawater Mg/Ca-adjusted foraminiferal Mg/Ca, unequivocally show warmer WPWP in the past, and a secular cooling over the last 10 million years. Compiling these data with existing records reveals a persistent, nearly stationary, extratropical response pattern in the Pacific in which high latitude (~50°N) temperatures increase by ~2.4° for each degree of WPWP warming. This relative warming pattern is also evident in model outputs of millennium-long climate simulations with quadrupling atmospheric CO 2 , therefore providing a strong constraint on the future equilibrium response of the Earth System.


Permian–Triassic chronology, stable isotope and lipid biomarker stratigraphic records from Shangsi section, China
a, Litho- and biostratigraphy, lithology and extinction rate (black dashed curve) with a two-pulse pattern² (EP1, EP2). b, Carbonate carbon isotopic compositions (δ¹³Ccarb, blue squares). c, Bulk organic carbon isotopic compositions (δ¹³Corg) together with weight percentage total organic carbon (%TOC, grey circles, size of symbol proportional to %) and phytane carbon isotopic compositions (δ¹³Cphy, blue triangles). Horizontal error bars represent 1σ of the mean (n = 2). d, εp (blue diamonds) calculated from δ¹³Cphy and δ¹³C of dissolved CO2 determined from b. Horizontal error bars represent 1σ uncertainty in εp calculation based on Monte Carlo simulations with 10,000 times (Methods). e, Bulk nitrogen isotopic compositions (δ¹⁵NTN) together with weight percentage total nitrogen (%TN, red circles, size of symbol proportional to %). f, Porphyrin nitrogen isotopic compositions (δ¹⁵Npor, red triangles). Horizontal error bars represent fully propagated errors of blank-corrected isotopic uncertainty and the standard deviation of the mean (n = 2). Vertical error bars represent the range of two adjacent sample positions combined due to the low porphyrin concentration. g, The isotopic offset between bulk sediment and porphyrin (εpor, red diamonds) and the corresponding fraction of cyanobacterial export based on the endmembers of 0 ± 2‰ for marine cyanobacteria and 5 ± 2‰ for eukaryotic algae³⁰. Blue (d) and red (g) dashed lines represent the locally estimated scatterplot smoothing (LOESS) function (Methods). Latest geochronology from ref. ¹³. Volcanism information from ref. ³². C.Z., conodont zones13–15; C.s., Clarkina subcarinata; C.ch, Clarkina changxingensis; C.y., Clarkina yini; C.m., Clarkina meishanensis; H.ch, Hindeodus changxingensis; H.p., Hindeodus parvus; I.l, Isarcicella lobata; I.i., Isarcicella isarcica. Data in Supplementary Table 1.
Estimates of atmospheric CO2 and the fraction of cyanobacterial versus eukaryotic export across the P–Tr mass extinction
a, Litho- and biostratigraphy, lithology and extinction rate² (black dashed curve). b, High-resolution pCO2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p_{{\mathrm{CO}}_2}$$\end{document} estimates based on εp. Shaded grey areas represent 68% (dark grey) and 95% (light grey) confidence intervals of pCO2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p_{{\mathrm{CO}}_2}$$\end{document} estimation based on Monte Carlo simulations (Methods). c, The fractional export production of cyanobacteria and eukaryotes based on εpor. d, The degree of ocean stratification based on gammacerane¹⁵. e, Seawater pH record based on boron isotope data⁷. f, Mercury evidence for the timing and strength of volcanism²⁴. Dashed lines represent the LOESS smoothing function. Position of P/Tr boundary based on ref. ¹³ in Shangsi section or based on first occurrence of Hindeodus parvus (leftmost *), a global marker for recognition of the boundary in other sections. H.praep., Hindeodus praeparvus. Other conodont zone abbreviations, refer to Fig. 1.
Model Predictions
a–d, LOSCAR model results of P–Tr variation in atmospheric CO2 (b), ocean surface pH (c) and ocean δ¹³C DIC (d) in response to carbon emission (red) and decrease in export biopump parameter (blue) (a). b, pCO2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p_{{\mathrm{CO}}_2}$$\end{document} simulations (solid and dashed lines) versus pCO2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p_{{\mathrm{CO}}_2}$$\end{document} estimates by εp (grey circles). Shaded grey area represents 68% confidence intervals of pCO2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p_{{\mathrm{CO}}_2}$$\end{document} estimation based on Monte Carlo simulations. c, pH simulations (solid and dashed lines) versus the change in δ¹¹B-derived seawater ΔpH from ref. ⁷ (grey diamonds). Blue bands highlight the fitness between the predicted results and geological data points. d, δ¹³CDIC simulations with different external carbon sources versus CIE in Shangsi carbonate records (red diamonds).
Early and late phases of the Permian–Triassic mass extinction marked by different atmospheric CO2 regimes

October 2022

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1,667 Reads

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19 Citations

The Permian–Triassic mass extinction is characterized by a massive injection of carbon dioxide associated with Siberian Traps volcanism, pronounced global warming and ocean acidification. However, in the absence of high-resolution records of atmospheric CO2 (pCO2), detailed changes in the carbon cycle and their relationship to biosphere perturbations remain unresolved. Here we present a continuous and high-resolution pCO2 record and quantitative estimates of marine phytoplankton community structure across this interval, using carbon and nitrogen isotope analyses of chlorophyll degradation products from the Shangsi section, China. We find that the first extinction pulse in the latest Permian coincided with a minimum in pCO2, which was followed by a rapid rise to a prolonged high pCO2 interval that persisted through the second extinction pulse in the Early Triassic, and that cyanobacteria increasingly dominated marine export production between these two pulses. While the first extinction appears to have been associated with intense initial weathering that briefly suppressed the pCO2 rise and promoted eutrophy and anoxia-driven habitat loss, incorporating our observations into a biogeochemical model indicates the second extinction was sustained by reduced export production driven by the expansion of bacterial production in response to oligotrophic conditions. Such conditions were potentially caused by a long-term failure of the weathering feedback and may mark a catastrophic combination of food web collapse, hyperthermal climate and hypercapnia. The first pulse of the Permian–Triassic mass extinction was driven by intense weathering, suppressing CO2, while food web collapse and prolonged warming drove the second pulse, according to a high-resolution record from the Shangsi section, China


Fig. 1. (Left) Ranges and distributions of GDGT-2/GDGT-3 ratios from different archives and (Right) structures of common GDGTs found in marine settings. (A) Cultures of thermophilic Thermoproteia (syn. Crenarchaeota). (B) Cultures of thermophilic AOA strains. (C) Environmental samples from terrestrial hot spring mats from sites with pH 6.5. (D) Cultures of known shallow AOA strains. Globally distributed SPM from (E) above (shallow SPM) and (G) below (deep SPM) the permanent pycnocline. Globally distributed surface (core top) sediments from sites sitting (F) above (shallow core tops) and (H) below (deep core tops) the permanent pycnocline. Open marine sediments from different geologic time intervals: (I) late Cenozoic (Oligocene-Holocene; 34 to 0 Ma), (J) early Cenozoic (Paleocene-Eocene; 66 to 34 Ma), and (K) Mesozoic (Early Jurassic-Cretaceous; 192 to 66 Ma). The median values (white dots), the interquartile range (black bars) of GDGT-2/GDGT-3 ratios, and the number of observations (n) associated with each group are also reported. Structures of six common GDGTs found in marine settings discussed throughout the main text are presented on the right. Stereochemistries of GDGTs shown here are based on revised structures following refs. 18-20.
Fig. 2. Thermal and nonthermal behaviors of GDGTs from different archives. Scatterplots of GDGT-2/GDGT-3 ratios versus TEX 86 . Panels with data from cultured samples are highlighted, while the rest of data are all from environmental samples. The order and colors of all subplots correspond to Fig. 1. GDGTs derived from (A) Cultures of thermophilic Thermoproteia, (B) pure cultures of thermophilic AOA, (C) hot spring mats, (D) cultures of shallow water AOA, (E) shallow SPM, and (F) shallow core top sediments follow the PTD trend. GDGTs from (G) deep SPM and (H) deep core top sediments show trends that deviate from the PTD trend. Samples from the (K) Mesozoic (Early Jurassic-Cretaceous; 192 to 66 Ma) and the (J) early Cenozoic (Paleocene-Eocene; 66 to 34 Ma) also largely follow the PTD trend, while the (I) late Cenozoic (Oligocene-Holocene; 34 to 0 Ma) pattern resembles modern deep sediments and SPM. Red dots in E-H are data from the SCS. Contour plots of joint KDE (shaded, colored regions) are plotted with a contour interval of 0.1 from the joint density of 0.1 (outer rim) to 0.9 (core). Dashed gray lines in all subplots show the established PTD trend. Shaded gray areas represent ranges of OD PTD that approximately follow thermal (0 OD PTD 0.5) behaviors.
Archaeal lipids trace ecology and evolution of marine ammonia-oxidizing archaea

August 2022

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422 Reads

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46 Citations

Proceedings of the National Academy of Sciences

Archaeal membrane lipids are widely used for paleotemperature reconstructions, yet these molecular fossils also bear rich information about ecology and evolution of marine ammonia-oxidizing archaea (AOA). Here we identified thermal and nonthermal behaviors of archaeal glycerol dialkyl glycerol tetraethers (GDGTs) by comparing the GDGT-based temperature index (TEX 86 ) to the ratio of GDGTs with two and three cyclopentane rings (GDGT-2/GDGT-3). Thermal-dependent biosynthesis should increase TEX 86 and decrease GDGT-2/GDGT-3 when the ambient temperature increases. This presumed temperature-dependent (PTD) trend is observed in GDGTs derived from cultures of thermophilic and mesophilic AOA. The distribution of GDGTs in suspended particulate matter (SPM) and sediments collected from above the pycnocline—shallow water samples—also follows the PTD trend. These similar GDGT distributions between AOA cultures and shallow water environmental samples reflect shallow ecotypes of marine AOA. While there are currently no cultures of deep AOA clades, GDGTs derived from deep water SPM and marine sediment samples exhibit nonthermal behavior deviating from the PTD trend. The presence of deep AOA increases the GDGT-2/GDGT-3 ratio and distorts the temperature-controlled correlation between GDGT-2/GDGT-3 and TEX 86 . We then used Gaussian mixture models to statistically characterize these diagnostic patterns of modern AOA ecology from paleo-GDGT records to infer the evolution of marine AOA from the Mid-Mesozoic to the present. Long-term GDGT-2/GDGT-3 trends suggest a suppression of today’s deep water marine AOA during the Mesozoic–early Cenozoic greenhouse climates. Our analysis provides invaluable insights into the evolutionary timeline and the expansion of AOA niches associated with major oceanographic and climate changes.


Citations (39)


... 进入新生代后, 受碳同位素负偏和北大西洋火成岩省侵位事件的影响 [15,16] , 温度 在古近纪的古新世-始新世极热事件(PETM)期间达到最大值(~34℃). 这种高温状态一直持 续到始新世早期, 其变化趋势与 Hönisch 等人重建的大气二氧化碳(CO 2 )浓度变化基本一致 [17] . 晚始新世之后, 温度逐渐下降, 并在经历较长时期的小波动后降至显生宙的最低温度水 平(11℃); 但重建的大气 CO 2 浓度在这个时期基本不变, 这可能反映了海洋环流、反照率和 热量传输变化等因素对气候演变的影响 [18] . ...

Reference:

过去4.85亿年以来全球地表温度演化历史
Toward a Cenozoic history of atmospheric CO2

Science

... The most obvious impact of degradation, therefore, is that the pelagic signal is diluted relative to sedimentary archaeal or soil contributions . For example, Hou et al. (2023) and Kim and Zhang (2023) showed that high values of the MI, Delta Ring index ( ) and BIT index corresponded with an interval of lower absolute concentrations of GDGTs, and in particular a 620 disproportionate decline in the concentration of crenarchaeol. Because these impacts remain incompletely understood or perhaps offer additional environmental insights, we recommend that samples that are removed by screening should still be reported in the data report but excluded from the subsequent temperature reconstruction. ...

Methane Index: Towards a quantitative archaeal lipid biomarker proxy for reconstructing marine sedimentary methane fluxes
  • Citing Article
  • June 2023

Geochimica et Cosmochimica Acta

... An erosive regime could have suppressed marine production in the marginal Gulf Coast region, especially where it has directly impacted the sedimentary system and lithology. Although increased erosion is typically associated with nutrient inputs and high productivity (Li et al., 2024), this would be complicated by high sediment loads that can induce light limitation (Gao et al., 2023). At the same time, persistent inputs of terrestrial sediments could drive shifts in nutrient cycling like those observed in open-ocean oligotrophic ecosystems (Lowery & Bralower, 2022;Lowery, Leckie, et al., 2018;Lowery et al., 2021). ...

Biomarker evidence of the water mass structure and primary productivity changes in the Chukchi Sea over the past 70 years

... Our understanding of ocean temperatures throughout the Phanerozoic is primarily derived from stable oxygen isotope (δ 18 O)-based temperature reconstructions (Gaskell et al., 2022;Grossman and Joachimski, 2022;Judd et al., 2024Judd et al., , 2022Scotese et al., 2021;Veizer and Prokoph, 2015). Stable oxygen isotope data acquired on carbonate or phosphate biominerals represent half of the entries in a recent Phanerozoic-scale compilation of sea-surface temperature (SST) proxy data and constitute the only proxy extending from the Cambrian to Modern (Judd et al., 2024(Judd et al., , 2022. ...

The PhanSST global database of Phanerozoic sea surface temperature proxy data

Scientific Data

... None of these lithologic boundaries match changes in the TEX 86 data or the timing of the LMC (Fig. 2). The modern annual average SST at Site 811 is 26.1°C (Locarnini et al., 2019). The average summer temperature is 28.32°C, and the average winter temperature is 25.09°C (Locarnini et al., 2019). ...

Persistent high latitude amplification of the Pacific Ocean over the past 10 million years

... The burial and release of carbon isotopes in the marine carbon reservoir could lead to the fluctuations of atmospheric CO 2 (Holbourn et al., 2007(Holbourn et al., , 2022Greenop et al., 2014), which could directly or indirectly influence the monsoon system. Li et al. (2023) suggested this process may be associated with the temperature-dependent bacterial degradation of organic matter. The released CO 2 from the enhanced microbial activity during warm intervals acts as a significant driving factor in the East Asian summer monsoon (EASM) system (Wang et al., 2024). ...

Neogene burial of organic carbon in the global ocean

Nature

... Moreover, δ 15 N bulk near to individual airborne and waterborne volcanic ash layers falls sharply (Figs. 2, 3), and abundant cyanobacteria were found in the ash-rich interval through palynological analysis (Fig. 2c, e). Nitrogen fixation by cyanobacteria (i.e., diazotrophy) is the primary source of new bioavailable nitrogen to the oceans [24][25][26][27] . The δ 15 N bulk values of organic matter generated through diazotrophy correlate with atmospheric nitrogen isotopes, exhibiting minimal fractionation, approximately -3‰ to 0‰ [28][29][30] . ...

Early and late phases of the Permian–Triassic mass extinction marked by different atmospheric CO2 regimes

... Some level of translucency is required to observe stomatal traits using conventional transmitted light microscopy. Typically, for a successful preparation, a J o u r n a l P r e -p r o o f Journal Pre-proof combination of acids and bases are needed (Figure 2; Supplemental Table 2), which are effective for clarifying (clearing) and dissolving (cleaning) mesophyll tissue, respectively (Liang et al., 2022a;Liang et al., 2022b). After chemical treatment, if possible, the upper (adaxial) and lower (abaxial) epidermises can be separated using the leaf margin as a hinge. ...

Early Miocene redwood fossils from Inner Mongolia: CO2 reconstructions and paleoclimate effects of a low Mongolian plateau
  • Citing Article
  • August 2022

Review of Palaeobotany and Palynology

... ODP Site 964 still indicates the same trends between CCaT and TEX 86 -based SSTs, only the absolute variability is different. This can partly be explained by a potentially high contribution of deep-water GDGTs reaching this site (Rattanasriampaipong et al., 2022), as indicated by higher iGDGT2/iGDGT3 ratio (ratio >10) at the site when compared to ODP Sites 969 and 987 with iGDGT2/iGDGT3 ratios <10 (Polik et al., 2018). Moreover, ODP Site 964 is situated at deeper water depth (∼3,660 mbsf) than the here studied site M51/3-SL104, which is closer to the water depths of ODP Sites 969 and 987 (water depths of 2,553 and ∼2,200, respectively), and thus we consider ODP Sites 969 and 987 more comparable to our study site. ...

Archaeal lipids trace ecology and evolution of marine ammonia-oxidizing archaea

Proceedings of the National Academy of Sciences

... As a result, hydrate destabilization has long been considered a positive feedback mechanism contributing to carbon cycle perturbations and rapid global warming throughout Earth's history (Deng et al., 2021;Kemp et al., 2005;Kennett et al., 2000Kennett et al., , 2003McInerney & Wing, 2011;Panieri et al., 2023;Zachos et al., 2008). A recent study suggests that ice sheet expansion and associated sea-level lowering triggered methane seepage from marine sediments during the peak of the Oligocene-Miocene transition glaciation, ∼23 million years ago (Ma) (Kim & Zhang, 2022). This destabilization may have acted as a negative feedback loop that facilitated the rapid termination of glaciation in the early Miocene. ...

Methane hydrate dissociation across the Oligocene–Miocene boundary