Hydroxylated isoprenoid GDGTs in Chinese coastal seas and their potential as a paleotemperature proxy for mid-to-low latitude marginal seas
Introduction
Archaea of the phylum Thaumarchaeota (Brochier-Armanet et al., 2008, Spang et al., 2010) are ubiquitous in marine environments and account for up to 20–40% of marine picoplankton (DeLong, 1992, Fuhrman et al., 1992, Karner et al., 2001, DeLong, 1998, Schattenhofer et al., 2009). The predominant membrane lipids of Thaumarchaeota are isoprenoid glycerol dialkyl glycerol tetraethers (iGDGTs; e.g., Schouten et al., 2008, Pitcher et al., 2011). It is assumed that the mesophilic planktonic Thaumarchaeota adjust the number of cyclopentyl rings in their GDGT membrane lipids in response to change in temperature, as demonstrated for several mesophilic and thermophilic archaeal cultures of the phyla Thaumarchaeota, Euryarchaeota and Crenarchaeota (de Rosa et al., 1980, Gliozzi et al., 1983, Uda et al., 2001, Uda et al., 2004, Lai et al., 2007, Boyd et al., 2011, Elling et al., 2015). The observation that the degree of cyclization of GDGTs found in surface sediments correlates with sea surface temperature (SST) led to the proposal for a novel proxy, TEX86 (Schouten et al., 2002, Wuchter et al., 2004), which showed potential in SST reconstruction (cf. Pearson and Ingalls, 2013, Schouten et al., 2013 and references therein). However, in coastal and lacustrine environments, the TEX86 signal may be biased by the presence of terrigenous organic matter (OM) containing GDGTs derived from soil Thaumarchaeota and other archaeal groups (e.g. Weijers et al., 2006, Sinninghe Damsté et al., 2010). The branched and isoprenoid tetraether (BIT) index (Hopmans et al., 2004) has been used as a tool for assessing the input of terrigenous OM and thus a potential bias in the TEX86 signal (e.g. Weijers et al., 2006, Zhu et al., 2011). However, in situ production of marine/lacustrine branched GDGTs, as well as very low BIT values in soils from semi-arid and arid regions (e.g. Peterse et al., 2009, Sinninghe Damsté et al., 2009, Zhu et al., 2011; Yang et al., 2014) may complicate application of the BIT index to constrain terrigenous input, hindering TEX86-based SST reconstruction severely in some environments (e.g. Fietz et al., 2012, Smith et al., 2012, Ge et al., 2014).
The hydroxylated GDGTs (OH-GDGTs), initially detected in subsurface sediments by Lipp and Hinrichs (2009) and subsequently identified by Liu et al. (2012), are a suite of GDGTs with up to two OH groups in one of their alkyl chains (structures in Fig. 1) and are widespread in marine sediments (Liu et al., 2012, Huguet et al., 2013, Fietz et al., 2013). Those in marine sediments likely originate from planktonic Thaumarchaeota, though their presence in a thermophilic euryarchaeon hints at a wider taxonomic distribution and possibly points to multiple sources of OH-GDGTs in environmental samples (cf. Liu et al., 2012). Within the Thaumarchaeota, OH-GDGT biosynthesis has only been observed in cultivated representatives of Group 1.1a (Pitcher et al., 2011, Liu et al., 2012, Elling et al., 2014, Elling et al., 2015) but not in strains affiliated to Group 1.1b (Sinninghe Damsté et al., 2012), which represent the dominant thaumarchaeotal group in most soils (Bates et al., 2011, Bartossek et al., 2012). Therefore, OH-GDGTs are thought to be primarily of planktonic origin and have potential for use as biomarkers for thaumarchaeotal taxonomy (Liu et al., 2012, Sinninghe Damsté et al., 2012). In addition, the presence of OH-GDGTs in ancient downcore sediments (Liu et al., 2012) suggests potential for these compounds for paleoenvironmental applications. The relative abundance of OH-GDGTs vs. iGDGTs in marine surface sediments was found to increase with increasing latitude and showed a significant correlation with sea surface temperature (SST; Huguet et al., 2013). In addition, Fietz et al. (2013) observed that the relative number of cyclopentane rings in OH-GDGTs increased with increasing SST in subpolar and polar regions, and suggested that the number of rings could be used as a proxy for tracing SST in polar seas. The CCSs, including the Yellow Sea (YS), East China Sea (ECS) and the northern part of the South China Sea (SCS) are marginal seas in the western Pacific Ocean (Fig. 2). The sediments in the CCSs are contributed to mainly by terrigenous input from the Yangtze River, Yellow River and Pearl River (Niino and Emery, 1961, Chen and Zheng, 1985, DeMaster et al., 1985, Milliman et al., 1985a, Milliman et al., 1985b, Zhao and Yan, 1994, Yang and Youn, 2007). The OM in CCS sediments originates generally from both marine authigenic and terrigenous organic input (Lü and Zhai, 2006). If soils contribute GDGTs to marine sediments in the CCSs (cf. Dang et al., 2008, Hu et al., 2013), TEX86 records would likely be biased towards higher values due to a relatively greater contribution from GDGT-1, GDGT-2, GDGT-3 and the crenarchaeol regio isomer from soil Thaumarchaeota (Sinninghe Damsté et al., 2010), especially in areas with a high sedimentation rate (Lü et al., 2014), given the prevalence of a high degree of GDGT cyclization in soil Thaumarchaeota (Sinninghe Damsté et al., 2012). Therefore, it is necessary to develop novel paleotemperature proxies for tracing SST in marginal seas with a high terrigenous input. Here, we have examined the SST proxy potential of OH-GDGTs in surface sediments from the CCSs and propose the ring index as suitable proxy for SST reconstruction in these seas.
Section snippets
Study area
The CCSs are at the western margin of the Pacific Ocean and span temperate and tropical regions. They are influenced by the wet/warm southeast monsoon in summer and the dry/cold northwest monsoon in winter, resulting in a large seasonal variation in SST. In particular, the northern part of the CCSs, i.e. the YS, shows a SST difference of up to 20 °C between summer and winter (Zeng et al., 2006). Other environmental parameters, such as salinity, pH and nutrients change accordingly, causing
Environmental parameters
The mean annual and seasonal SST (Table 1) in the CCS sampling sites is in the range 14.1–27.2 °C (SSTAnnual). The variation (Table 1) is wider in the ECS (14.1–23.7 °C; SSTAnnual) than in the SCS (25.1–27.2 °C; SSTAnnual). Salinity, TAlk and NO3− concentration in the CCSs are in the range 30.5–34.2 psu, 1091–2121 μmol/kg and 0.5–6.2 μmol/l, respectively (Table 1).
Relative abundances of GDGTs
The glycerol tetraether lipid groups iGDGTs, branched GDGTs (brGDGTs), OH-GDGTs and 2OH-GDGTs occurred in all surface sediments from the
Correlation between OH-GDGT distribution and environmental parameters
The CCSs are typical marginal seas of the western Pacific Ocean. Major environmental parameters such as temperature, salinity and nutrients change significantly with latitude (Li et al., 2012; Table 1), thereby providing an excellent framework for studying the influence of environmental gradients on OH-GDGT distribution. In the RDA, the length of the vectors along the X-axis indicates the relative importance of the environmental factors for explaining variation in OH-GDGT indices. In addition,
Conclusions
The tetraether lipid types – iGDGTs, brGDGTs, OH-GDGTs and 2OH-GDGTs – were detected in all of the surface sediments collected from the CCSs, with their relative abundance decreasing sequentially. The OH-GDGTs amounted to 1.8–12.8% of total iGDGTs and increased in relative abundance with latitude. Among the OH-GDGTs, the relative abundance of acyclic OH-GDGT increased significantly with latitude. Redundancy analysis of its abundance with environmental parameters shows that SST is the major
Acknowledgements
This research was funded by the National Natural Science Foundation of China (41376090), the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA11020102), the Research Fund for the Doctoral Program of Higher Education of China (20120145120017) and the Marine Safeguard Project (GZH201200503). Analyses in Bremen were supported through the Gottfried Wilhelm Leibniz Program of the Deutsche Forschungsgemeinschaft (granted to K.-U.H.; HI 616-14). We thank each member of AG
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Current address: Department of Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.