Abstract
A detailed uplift history of the Tibetan Plateau is essential for disentangling the proposed geodynamical models and assessing its impacts on climate and biodiversity. However, when and how the plateau formed remains highly controversial. Here, we present unusual geochemical indicators of marine signatures in the Cenozoic terrestrial strata of the Qaidam Basin, northern Tibetan Plateau, with strong implications for the basin altitude. Our investigations across the basin reveal typical marine alkenones and anomalously high carbonate carbon isotopic values during the mid-Miocene, but not at earlier stages, which are accompanied by a divergent trend in the paired carbonate oxygen and leaf wax hydrogen isotopic records. We infer an incursion of seawater into the Qaidam Basin, thus constraining the mid-Miocene basin altitude close to sea level. Hence, much of the substantial northern plateau uplift afterwards appears to be associated with the outward growth of the Tibetan Plateau.
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Introduction
The collision of Indian and Eurasian plates, since ~55 ± 10 million years ago (Ma)1, generated the most prominent elevated landmass on Earth, the Himalaya-Tibetan Plateau, thought to have reshaped Asian and even global atmospheric circulation and ecosystems2,3,4. Hypotheses evolved from earlier proposal of plateau uplift as a whole block5 to diachronous models, the latter type including northward propagation of stepwise growth6 and outward growth of a “proto-Tibetan Plateau” at its present center1. The recent discovery of a central deep valley in the Lunpola Basin by the early Miocene7, possibly bounded by pre-existing mountain ranges before the collision4, implies that the relatively flat modern plateau topography is only a recent geological phenomenon. During the mid-Miocene, approximately around 15 Ma, a profound geodynamic event seems to have occurred, as evidenced by the outward growth of the plateau and widespread normal faulting in the plateau interior (summarized in ref. 8,9,10), indicating a change in style of plateau deformation, perhaps from previous crustal shortening and thickening to extension and thinning8,9,10,11.
Tectonic end-member models predict competing temporal-spatial evolution patterns for the northern Tibetan Plateau (NTP, north of the Kunlun Mountains) across a distance of at least ~1500‒2000 km from the collision zone in the south (Fig. 1a): the early surface rise since the terminal collision5, versus delayed orographic development in the context of stepwise growth6. Determining the detailed topographic history of the NTP would provide vital insights into underlying mechanisms of plateau uplift. Despite active research, when and how the NTP was uplifted remains contentious1,4,5,6,7,8,9,10,11,12,13,14,15,16,17. Particularly, the mid-Miocene southern Tarim Basin was suggested to be at sea level and connected to open marine waters, inferred from planktonic foraminifers discovered at the Miran River section17 (Fig. 1b). The topographic evolution of the Qaidam Basin (QB) on the NTP, with present altitudes of ~3,000 m above sea level (Fig. 1b), also remains controversial, ranging from substantial uplift since the mid-Miocene18,19,20 to near-present elevation by the early Oligocene21. These discrepancies are rooted in uncertainties in quantitative constraints on surface uplift from the isotope paleoaltimetry and plant fossils used4, representative with assumptions regarding climatic tolerance of fossil species21, preservation conditions of fossil leaves21, temporally and spatially varying isotopic values18,19, and complex moisture transport pathways18,19. We here report unusual geochemical indicators, bearing marine signatures, discovered in the thick Cenozoic QB strata (Methods). Our new results, corroborated with the independent constraint for the southern Tarim Basin17 (Fig. 1b), offer a new perspective on the QB altitude during the mid-Miocene18,19,20,21.
Results and discussion
Unusual geochemical signatures
Marine biomarker Group III alkenones, anomalously high carbonate carbon isotopic (δ13Ccarb) values, and paired carbonate oxygen isotopic (δ18Ocarb) and leaf wax hydrogen isotopic (δDalk) values, were identified from the Cenozoic Dahonggou (DHG) and Honggou (HG) sections in the northern QB (Methods, Fig. 1, Supplementary Fig. 1, Supplementary Data). Alkenones were detected exclusively in the interval from the uppermost Xia Youshashan and lowermost Shang Youshashan formations (Fig. 1c), the ages of which are constrained to the mid-Miocene (~15‒11 Ma)16,22 or the late Miocene (~9‒7.5 Ma)23 (Supplementary Figs. 2, 3), with the former being our preferred age model (Methods, Fig. 2). They were captured by 45 of 450 samples in the DHG and 13 of 177 in the HG section. Within the mid-Miocene interval, alkenones were detected in relatively deep lake facies24 (Supplementary Figs. 4, 5). Meanwhile, in the older Ganchaigou Formation of the Hongliugou Section (Supplementary Fig. 1), with relatively deep lacustrine facies developed25, alkenones were not detected in 216 samples analyzed. Identified alkenones in most DHG and HG samples belong to Group III Isochrysidales26, typically living in marine settings, and Group II alkenones, found in lacustrine and coastal settings, appeared briefly at ~11 Ma (with one exception at ~15 Ma at HG) (Fig. 2a, b, Supplementary Fig. 6, Supplementary Note 1). Similarly, at the depo-center KC-1 well in the western QB (Fig. 1b), saturated ketones, diagenetic products of alkenones, also occurred during ~15‒6 Ma, but not before (~18‒15 Ma)27 (Fig. 2c). Within the interval of ~15‒6 Ma, alkenones occurred in relatively shallow lake facies27, in contrast with the DHG and HG sections (Supplementary Fig. 5). Most of them were also produced by Group III Isochrysidales (Supplementary Note 1), with some around ~6 Ma from Group II27 (Fig. 2c). Group III alkenones hence appear to have occurred basinwide around ~15 Ma. C37 alkenone concentrations range from trace to ~450 and ~2900 ng g−1 in the DHG and HG sections respectively (Fig. 2a, b) and C37 saturated ketones in KC-1 could be up to 120 ng- g−1 (Fig. 2c), comparable to or slightly higher than those reported from mid-Miocene marine sediments28 (mostly within 100 ng g−1 and up to 400 ng g−1). Surface water temperatures estimated from Group III alkenones range from ~24 to 29 °C in the DHG and HG sections (Methods) and display roughly a cooling trend (Fig. 2d), perhaps corresponding to global cooling during the mid-Miocene Climate Transition28,29.
Cenozoic δ13Ccarb records in both sections display substantial fluctuations, varying mostly between −7‰ and −2‰. Except for the mid-Miocene interval (~15‒11 Ma), all δ13Ccarb values are < −1.3‰. During the mid-Miocene interval when the basinwide occurrence of Group III alkenones was observed, δ13Ccarb values reach 0.3‒0.8‰ for the DHG and −0.5‰ for the less-sampled HG section (Fig. 2e). The δDalk values (Methods) vary from −224‰ to −132‰ and −210‰ to −125‰ for the HG and DHG sections respectively, showing considerable similarity in the temporal trends throughout the Cenozoic. Before ~15 Ma, δDalk records resemble δ18Ocarb from the same DHG section24, including both the long-term trend and short-term fluctuations (Fig. 3b). However, after ~15 Ma, δDalk values became substantially more negative, ~45‰ less than the mean value before ~15 Ma and even lower than late Eocene values, while δ18Ocarb became progressively more positive as in many lacustrine and pedogenic carbonate records30. The paired isotopic records thus display a strong divergent trend after ~15 Ma (Fig. 3b, c).
Interpretations of geochemical indicators
Alkenones produced by Group III Isochrysidales are ubiquitous in marine settings, but not in modern inland lakes31. Hence, as the QB became a terrestrial sedimentary basin after the early Cenozoic32, the basinwide occurrence of Group III alkenones during the mid-Miocene needs to be critically assessed. Sediment reworking of nearby pre-Cenozoic marine strata can confidently be excluded based on alkenone concentrations, the shift from Group III to Group II alkenones, variable temperatures estimated from marine alkenones (Fig. 2), and alkenone occurrence in contrasting lake facies at the three sections (Supplementary Figs. 4, 5). These observations thus strongly indicate in situ production of alkenones (Supplementary Note 2). Regarding how marine Isochrysidales might have arrived in the mid-Miocene QB initially that served as the “seed” for alkenone production, a proposal of the remnant species associated with the last major marine transgression during the late Eocene33 could be refuted due to no alkenones detected in a wider range of lake facies before ~15 Ma (Fig. 2, Supplementary Fig. 1). Possibly remnant Isochrysidales could not survive in a highly unstable lacustrine system for an extended period34,35. Less plausibly or even implausibly, marine Isochrysidales were carried by birds or winds and then survived in the mid-Miocene QB by chance. Alternatively, marine Isochrysidales could evolve themselves in a lacustrine system with water chemistry similar to oceans. For instance, thick-boned fish fossil reported from the arid Pliocene Qaidam Basin is similar to the one found in the Mediterranean Sea during the Messinian desiccation period36. However, as marine Isochrysidales are not observed in any modern inland lakes with very diverse lake water chemistry including those similar to oceans31, we consider either scenario unlikely. Instead, Group III alkenones are common in coastal oceans31,37 (i.e., Black Sea) (Supplementary Note 2). The unusual marine signature found in the QB strata thus suggests possible seawater incursion during the mid-Miocene.
The abnormally high δ13Ccarb values within the mid-Miocene differ substantially from those (<−2‰) in Cenozoic pedogenic30 and lacustrine carbonates on the Tibetan Plateau38,39. Cenozoic lacustrine δ13Ccarb values of > 0‰ have been reported from the plateau, but are usually accompanied by elevated δ18Ocarb values, indicating a strong lake evaporative effect38,39, although paired δ13Ccarb/δ18Ocarb values in Oligocene-Miocene lacustrine limestones in southern Nevada40, also interpreted to be deposited in restricted, high-salinity lake basins, are similar to those in the mid-Miocene DHG section. We consider that the evaporative effect could not account for the abnormally high δ13Ccarb values for the mid-Miocene DHG section as multiple proxies suggest not particularly arid environment at the time24 (Fig. 3, Supplementary Fig. 5), which can also be refuted by the lower δ13Ccarb values with enhanced regional aridification after ~11 Ma24 (Fig. 2e). Elevated δ13Ccarb values could also be found in special settings, such as geothermal springs, volcanic and anoxic environment, however, the mid-Miocene DHG strata appear to be normal lacustrine/deltaic settings (Supplementary Fig. 1). Lastly, the paired δ13Ccarb/δ18Ocarb values resemble those of marine carbonates39,41. Meanwhile, corroborated by the concurrence of marine alkenones, the marine signal originating from ancient marine carbonates can be excluded, as those values can only be preserved without being altered/diluted by soil and lake processes, like the desert environment39. This leaves mid-Miocene seawater incursion as the most viable explanation. The Z value42 (Methods) was proposed to differentiate marine vs. terrestrial environment earlier. With the confounding lake salinization effect excluded (Supplementary Fig. 5), Z values >120 (in the range of 120‒125) within the mid-Miocene QB strata (Supplementary Data) may also indicate a marine signal42. Hence, the identified Group III alkenones and abnormal δ13Ccarb values in QB strata, together with the reported planktonic foraminifers from the southern Tarim Basin17 (Figs. 2, 3), all suggest a possible mid-Miocene seawater incursion.
Mid-Miocene QB at sea level altitude
Following the previous proposal that the southern Tarim Basin was connected to open marine waters17, we further suggest that mid-Miocene Paratethyan seawater entered the QB through the Pamir salient, southern Tarim Basin, and along the Altyn Tagn Fault (ATF) (Fig. 4a). The mid-Miocene QB may have resembled the recent Black Sea, and been impacted by seawater incursion37. The northward propagation of Pamir salient by the mid-Miocene43,44 might still allow the Tarim Basin to be connected to the Paratethyan Sea17. A pre-Quaternary east-west paleoriver along the southern Tarim Basin existed, carrying detritus from the arcuate Pamir belt to the QB through the ATF34. At ~24‒15 Ma, the rapid left-lateral offset of the reactivated ATF12,13,14 (Fig. 4b) might have further deepened channels to allow a connection. In the QB, the sedimentary basin experienced earlier flexural subsidence and perhaps remained at or near sea level, with isolation and partition after the mid-Miocene16.
This interpretation is supported by our paired δ18Ocarb and δDalk records from the DHG section (Fig. 3). The divergent trend since the mid-Miocene may have resulted from the altitudinal effect of the uplifting basin and surrounding mountains, reflected in the δDalk trend, while δ18Ocarb, similar to other lacustrine and pedogenic δ18Ocarb records24,30, is more affected by regional aridification, overprinting the altitudinal effect (Supplementary Note 3). Alkenone temperature (Fig. 2) is not used as independent evidence to infer QB altitude here due to large uncertainty in estimates of mid-Miocene terrestrial temperature and altitudinal temperature gradient. Nonetheless, those warm temperatures, similar to mid-latitude ocean temperatures28,29, do not contradict a sea level altitude. Moreover, higher global sea level, rising by ~40‒70 m during the mid-Miocene45, might have made connection of the QB to Paratethys possible or enhanced the connection (further discussion in Supplementary Note 4). We note that the interval of alkenone occurrence at all three localities, ~15–11 Ma, does not exactly match the period of higher global sea level45 (Fig. 3). The exact reason remains unclear. Apart from chronological uncertainty, we speculate that marine Isochrysidales might need time to adapt new environment in a lacustrine system or the seawater pathway was disconnected during the early part of the mid-Miocene. It also remains unclear whether multiple or persistent seawater incursions occurred during the whole interval of ~15‒11 Ma, as marine Isochrysidales, once entering the QB, might have existed for many generations if lake conditions did not change dramatically. Hence, with details to be explored (Supplementary Note 4), we consider seawater incursion as an accidental event, coincident with mid-Miocene sea level rise and reactivated offset along the ATF serving to deepen connecting channels.
Implications for Tibetan Plateau uplift
The unusual marine signatures identified in QB strata effectively constrain the basin altitude to sea level by the mid-Miocene. Thus, uplift to the present basin altitude, ~3000 m, mostly occurred subsequently. Although our findings do not provide a direct constraint on the altitude of surrounding mountain ranges, numerous lines of evidence accumulated over the past decades, based on analyses of low-temperature thermochronology, sedimentation, and stratigraphy, indicate accelerated uplift of various parts of the NTP since the mid-Miocene8,9,10,11,12,13,14,15,16 (Fig. 4b, Supplementary Note 5), while only minor pre-Miocene relief existed surrounding the QB16. With isostatic balance ~1100 m rise of the QB since the Miocene can be attributed to sediment infill20. With the new constraint at sea level, about 2/3 of the present QB altitude may result from crustal shortening and thickening9,10,11, implying a similar magnitude of uplift for surrounding mountain ranges. Hence, collective evidence suggests the NTP as a whole uplifted substantially since ~15 Ma.
As the volcanic chain of an Andean-style convergent plate margin, the Gangdese Mountains already attained high altitude prior to India-Asia collision46, the Qiangtang (Tanggula) Mountains reached >5000 m altitude by late Eocene47, while the Himalayas reached their present altitude by mid-Miocene48 (Fig. 5a, additional data summarized in ref. 49,50,51). With the NTP uplifted substantially post mid-Miocene, the available evidence supports diachronous models of the plateau uplift4, predicting a late rise of the NTP. However, none of the current geodynamical models place the mid-Miocene QB at sea level, with most at ~1000‒2000 m altitude instead. Meanwhile, the recently discovered deep central valley in the Lunpola Basin7 (<2300 m), lower altitudes of the Qiabulin Basin52 (<2500 m) and the Hoh Xil Basin53 (~3000 m), and sea level altitude for the QB, together with high relief on the central plateau constrained by isotope paleoaltimetry46,47,48,49,50,51, suggest the existence of a series of east-west orientated deep valleys by the early Miocene (Fig. 5b), providing an ecological niche for Asian biodiversity4. The relatively flat modern topography on the higher plateau appears to have been achieved around ~15 Ma, suggesting prior continuous plateau growth before reaching its highest elevation9,10. The change in style of plateau deformation at ~15 Ma indicates the higher plateau transitioned from previous crustal shortening and thickening to extension and thinning8,9,10,11. This geodynamic event across the plateau can be potentially explained by natural outward growth of the higher plateau, removal of some mantle lithosphere, and outward flow of weakened middle to lower crust8. Considering the magnitude of QB uplift (~3000 m) inferred here, removal of some mantle lithosphere beneath the plateau9,10,11 provides a sensible, but perhaps not unique, solution for the mid-Miocene geodynamic event.
In summary, the unusual marine signatures identified in mid-Miocene QB strata provide new insights into the topographic evolution of the NTP. With careful considerations, the marine signal is best explained by an incursion of Paratethyan seawater into the QB during the mid-Miocene, via a paleochannel (turning into a paleo-seaway temporarily) along southern margin of the Tarim Basin34, analogous to the recent Black Sea. We consider the incursion as an accidental event coincident with global sea level highstand45 and reactivation of tectonic activity along the ATF12,13,14. If correct, our results may constrain the mid-Miocene QB to sea level, postdating all but one17 estimate of NTP paleoaltitude. Both isotopes and plant pollen/fossils, the two main paleoaltimeters used currently to constrain the altitude of bounding mountain ranges and any altitude between the basin and ranges respectively4, could potentially overestimate basin altitudes. The discrepancies of mid-Miocene QB altitude estimates between ours and those from plant fossils21 and isotopes18,19, support this view, although the latter also suggests accelerated uplift post mid-Miocene (Fig. 5). The mid-Miocene QB sea level altitude, attesting the widely reported change in style of plateau deformation8,9,10, can be incorporated into geodynamical models in order to better understand plateau uplift history and mechanisms, with important implications for climatic and ecological impacts.
Methods
Materials and chronologies
The northern Tibetan Plateau is conventionally separated from adjacent regions by three major faults, the Altyn Tagh Fault to the northwest, the Haiyuan Fault to the northeast, and the Kunlun Fault to the south5. The Cenozoic Qaidam Basin (QB), currently at ~3000 m altitude, is the largest basin on the northern Tibetan Plateau, surrounded by the Kunlun Mountains to the south and west, the Altyn Mountains to the north, and the Qilian/Nan Mountains to the north and east (Fig. 1b). It received sedimentation up to 14 km thick in the middle of the basin54. The Dahonggou (DHG, 37.49°N, 95.21°E), Honggou (HG, 37.54°N, 95.17°E), and Hongliugou (HLG, 38.13°N, 94.67°E) sections are well exposed at the eastern side of the QB (Fig. 1b). Specifically, both DHG and HG sections are located in the southern limb of the same Dahonggou anticline, being ~10 km apart from each other (Fig. 1c). The two sections contain >5000 m thick lacustrine, deltaic to braided river deposits and can be divided into six basin-scale lithostratigraphic units, in a geological sequence, including the Lulehe, Xia Ganchaigou, Shang Ganchaigou, Xia Youshashan, Shang Youshashan, and Shizigou Formations (Fm) (Supplementary Fig. 1). Detailed descriptions of lithologies and sediment facies have been provided previously21,22,23,27,32,54.
At the DHG and HG sections, we collected lacustrine to deltaic mudstones and silty mudstones from the Xia Ganchaigou to Shang Youshashan Fms. For the intervals of fluvial and alluvial deposits, i.e., the Lulehe and Shizigou Fm, mudstone intercalations were sampled in order to achieve sufficient organic materials. In total, 450 and 177 samples have been attained from the DHG and HG sections, respectively. We first took samples at every ~15 m and ~30 m for most of the two sections respectively, and then re-sampled the layers from the upper Xia Youshashan to lower Shang Youshashan Fms at the DHG section, where alkenones were detected. At the HLG section, we collected 216 mudstone samples from the upper Xia Ganchaigou to lower Shang Ganchaigou Fms (~395 m), where sediment facies of this interval is suggested to be deep lacustrine facies25.
A high-resolution magnetostratigraphic study suggests DHG and HG sedimentary successions from ~52 Ma (the base of Lulehe Fm) to ~7 Ma (the lower Shizigou Fm), based on constraints from fossil mammals, ostracods, leaves and pollen22 (Supplementary Fig. 2). The HLG chronology follows a previous high-resolution magnetostratigraphic study which constrains the entire sequence to be ~53.4 Ma (the base of Lulehe Fm) to 2.4 Ma (the upper Shizigou Fm)25,55. Accordingly, our sampled interval at the HLG section is assigned from ~36 to 28 Ma. Recently, the conventional age (~52–7 Ma) of the DHG and HG sections is challenged by a magnetostratigraphic study, which, by applying the newly discovered Honggou fauna as age control, assigned a much younger age of ~26–5 Ma23 (Supplementary Fig. 2), or ~30–5 Ma based on magnetostratigraphy combined with detrital apatite fission-track ages from another section in the region56. In these age models, linear sedimentation rates were assumed between datum ages. Consequently, the interval with alkenone occurrence at the DHG and HG sections would be shifted from ~15–11 Ma with the conventional chronology22 to ~9–7.5 Ma with the revised chronology23.
A recent review16 concludes that the conventional chronology22 fits reasonably well with growth-strata observations and thermochronology data across the basin. The conventional chronology at the DHG and HG sections is also consistent with the one at the HLG section55, anchored by two mammal fossil beds in the Shang Ganchaigou Fm. Paleoclimate studies from the HLG55 and DHG24 sections show good correspondence to global climatic changes if the conventional chronology is used. Further, the chronology at the KC-1 well in the western basin57 is not affected by the controversies in the northern basin22,23, indicating the alkenone occurrence starting from ~15 Ma at this locality27. Hence, to some degree, our main conclusion here, mid-Miocene seawater incursion (Figs. 2, 3), is not significantly impacted by the chronological uncertainty in the northern basin, unless the KC-1 well chronology is also subject to revision (but the mid-Miocene warmer and wetter conditions, indicated by multiple proxies27,57, seem difficult to be shifted to an alternative time interval). With the revised chronology in the northern basin23, it might be inferred that marine Isochrysidales expanded from the western basin to DHG and HG localities at a later time, ~9–7.5 Ma. However, this scenario seems to be less likely considering the regional aridification history24,57. We thus here present our results based on the conventional chronology22, while the revised chronology23 is provided in Supplementary Fig. 2 and our DHG and HG results based on the revised chronology are provided in Supplementary Fig. 3.
Alkenone analysis
Weathered sediments of the studied outcrops were removed before sample collection in the field. In the lab, all samples (from DHG, HG and HLG sections, ~30 g each) were freeze-dried, ground and extracted with CH2Cl2:MeOH (9:1, v/v) using Dionex Accelerated Solvent Extractor (ASE300). Then, we separated the total lipid extraction eluting on a silica gel column with three eluents of n-hexane, CH2Cl2 and MeOH, respectively. Long-chain alkenones and n-alkanes fall in CH2Cl2 and n-hexane fractions, respectively.
Subsequently, the alkenone-containing fraction was analyzed on an Agilent 7890B gas chromatography (GC) with an Agilent J&W column (DB-1, 60 m × 0.25 mm i.d. × 0.1 μm film thickness) and H2 (1.5 ml min−1) as the carrier gas58. The oven temperature program was: 60 °C (2 min) to 270 °C at 15 °C min−1 and then to 310 °C (held 40 min) at 5 °C min−1. n-C36 alkane of a known concentration was used as an internal standard for quantification. Group III and II alkenones from sediments of the South China Sea and Lake Gahai respectively are used for alkenone identification via retention time reference (Supplementary Fig. 6). Additional identification of alkenones was then undertaken by gas chromatography-mass spectrometer (GC-MS), Agilent 7890 A GC coupled to 5975 mass selective detector (MSD). Chromatographic separation was achieved with the aforementioned DB-1 column and its accompanying oven temperature program. Helium was used as carrier gas with a flow rate of 1.0 ml min−1. The MS conditions were: electron impact (EI) mode, 70 eV and 280 °C, scan range m/z 50–650, cycle time 0.65 ms. Detailed peak assignments were conducted by comparing them with previously reported diagnostic fragments in the mass spectra59 (Supplementary Fig. 6).
Finally, for Group III alkenones, the alkenone unsaturation index (UK′37) ratio and surface water temperature were calculated via the equations (Eqs. 1 and 2):
here C37:2 and C37:3 are the concentrations of diunsaturated and triunsaturated C37 alkenones60,61. Group II alkenones were not applied for temperature reconstruction due to the uncertain temperature response induced by phylogenetic diversity62. Analytical uncertainties for lab standards are typically less than 5% for C37 alkenone concentration, and 0.005 units for the UK′37 ratio (equivalent to ~0.2 °C).
Carbonate carbon isotope (δ13Ccarb) analysis
δ13Ccarb analysis for the DHG and HG sections followed the procedure described in ref. 39, with δ18Ocarb from the same analysis at the DHG section reported previously24. In brief, samples (~5 g each) were first grounded in an agate mortar and sieved through a 100 mesh (150 μm) screen. Isotope analysis was achieved using an isotope ratio mass spectrometer (MAT-252, Finnigan) with an automated carbonate preparation device (Kiel II) at the Institute of Earth Environment, Chinese Academy of Sciences. Laboratory standard carbonates (TTB1) with known δ13Ccarb were analyzed daily to ensure instrumental accuracy. International NBS18 and NBS19 standards were used to monitor the long-term instrumental stability. All δ13Ccarb values are reported as per mil deviation relative to the Vienna PeeDee Belemnite (VPDB) standard. Analytical precision for repeated analyses of laboratory standards is generally within ± 0.1‰. The Z value42 is calculated from carbonate δ13C and δ18O values (Eq. 3):
Leaf wax hydrogen isotope (δDalk) analysis
Long-chain n-alkane δDalk for the DHG and HG sections were analyzed using a coupled GC-Delta-V isotope ratio mass spectrometer (IRMS) system (Thermo Finnigan) at the Institute of Earth Environment, Chinese Academy of Sciences. Diagenetic effects and aquatic influences on long-chain n-alkanes are assessed to be minor24. To further minimize their combined effects, samples with low carbon preferential index (CPI < 2) and high proportion of aquatic plants (Paq > 0.3) values were excluded for analysis, mostly occurring in the early interval of the sections63. Detailed hydrogen isotope analysis procedure can be found in ref. 64. Briefly, approximately 300 ng of targeted long-chain n-alkane (C27, C29 and C31) was injected in splitless mode, with the flow rate of carrier gas (He) at 1.0 ml min−1. n-Alkanes were separated by GC and then pyrolyzed into H2 at 1430 °C before transporting into the IRMS for δDalk analysis. The variability of H3+factor was <0.1 ppm nA−1 day−1 during our sample analysis, based on daily measurement using H2 reference gas. The in-house standard n-alkane mixture was measured at every four samples to ensure that the mass spectrometer was stable. δD values of n-alkane standards are close to their supposed/actual values with the ion current intensity at 4000–6000 mV in our lab. We thus reported measured δD values with the current intensity within this range. All δDalk values are expressed in the delta (δ) notation relative to the Vienna Standard Mean Ocean Water (VSMOW) and typical precision for repeated standard analyses is generally better than ± 3‰. δDalk reported here is the average of δD values of C27, C29 and C31 n-alkanes.
Data availability
The new data reported in this study (i.e., alkenones, carbonate carbon isotopes and leaf wax hydrogen isotopes from Dahonggou and Honggou sections) are publicly available at https://doi.org/10.6084/m9.figshare.20625810. The modern topographic data can be downloaded from the Shuttle Radar Topography Mission (SRTM) website at: https://srtm.csi.cgiar.org/. Lists of the sources of previously published data supporting the findings of this study are available within the paper, including saturated ketones from the KC-1 well27, carbonate oxygen isotopes from the Dahonggou section24, planktonic foraminifers in the Miran River section17, the Cenozoic global sea level record45, and the Miocene paleotopographic data of Central Asia65. Sources of additional data used in this study are provided in Supplementary References, including the paleoaltitude data of the Tibetan plateau (supplementary ref. 35–38,51–63) summarized in supplementary ref. 34,49,50, the mid- and late Miocene tectonic activities on the northern plateau (supplementary ref. 64–95), and the paleomagnetic data from Dahonggou (supplementary ref. 101) and Honggou (supplementary ref. 102) sections.
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Acknowledgements
The authors thank Profs. Peter Molnar and Jimin Sun for comments on earlier versions of this manuscript and Profs. Brad Ritts and Kevin Theissen and an anonymous reviewer for their constructive reviews. This research was supported by the Strategic Priority Research Program of Chinese Academy of Sciences (XDB40000000), National Natural Science Foundation of China (41820104002, 41807333, 41972035), Hong Kong RGC (17305019), US National Science Foundation (EAR 2022282), and the Second Tibetan Plateau Scientific Expedition and Research Program (2019QZKK0704, 2019QZKK0708). No sampling permissions were required in this work.
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Y.S.: Investigation, Formal analysis, Writing—original draft; Yu Liang: Investigation, Writing- original draft, Writing- reviewing & editing; H.L.: Investigation; Jun Liu: Investigation, Writing—original draft; J.J.: Investigation; X.K.: Investigation; X.L.: Investigation; Y.H.: Investigation; H.W.: Investigation; B.Z.: Investigation; Y.Z.: Investigation; G.Z.: Formal analysis, Writing—reviewing & editing; J.P.: Formal analysis; Yongxiang Li: Formal analysis; C.Q.: Formal analysis, Funding acquisition, Writing—reviewing & editing; Jianxing Li: Formal analysis; J.C.A.: Formal analysis, Writing—reviewing & editing; W.L.: Conceptualization, Formal analysis, Funding acquisition, Writing- original draft; Z.L.: Conceptualization, Formal analysis, Funding acquisition, Writing—original draft, Writing—reviewing & editing.
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Communications Earth & Environment thanks Kevin Theissen, Bradley D. Ritts and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Primary Handling Editors: Maria Laura Balestrieri, Joe Aslin, Heike Langenberg. Peer reviewer reports are available.
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Sun, Y., Liang, Y., Liu, H. et al. Mid-Miocene sea level altitude of the Qaidam Basin, northern Tibetan Plateau. Commun Earth Environ 4, 3 (2023). https://doi.org/10.1038/s43247-022-00671-8
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DOI: https://doi.org/10.1038/s43247-022-00671-8
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