Endosymbiosis with chemosynthetic bacteria has enabled many deep-sea invertebrates to thrive at hydrothermal vents and cold seeps, but most previous studies on this mutualism have focused on the bacteria only. Vesicomyid clams dominate global deep-sea chemosynthesis-based ecosystems. They differ from most deep-sea symbiotic animals in passing their symbionts from parent to offspring, enabling intricate co-evolution between the host and the symbiont. Here, we sequenced the genomes of the clam Archivesica marissinica (Bivalvia: Vesicomyidae) and its bacterial symbiont to understand the genomic/metabolic integration behind this symbiosis. At 1.52 gigabases, the clam genome encodes 28 genes horizontally transferred from bacteria, a large number of pseudogenes and transposable elements whose massive expansion corresponded to the timing of the rise and subsequent divergence of symbiont-bearing vesicomyids. The genome exhibits gene family expansion in cellular processes that likely facilitate chemoautotrophy, including gas delivery to support energy and carbon production, metabolite exchange with the symbiont, and regulation of the bacteriocyte population. Contraction in cellulase genes is likely adaptive to the shift from phytoplankton-derived to bacteria-based food. It also shows contraction in bacterial recognition gene familie, indicative of suppressed immune response to the endosymbiont. The gammaproteobacterium endosymbiont has a reduced genome of 1.03 megabases but retains complete pathways for sulfur oxidation, carbon fixation, and biosynthesis of 20 common amino acids, indicating the host’s high dependence on the symbiont for nutrition. Overall, the host-symbiont genomes show not only tight metabolic complementarity, but also distinct signatures of co-evolution allowing the vesicomyids to thrive in chemosynthesis-based ecosystems.
In 2018, the Institute of Deep Sea Science and Engineering investigated the “HaiMa” cold seeps in the northwestern part of the South China Sea using R/V “TanSuoYiHao” with manned submersible “ShenHaiYongShi.” Ten dives were conducted to make seafloor observations at six cold seeps (HM‐1 to HM‐6). By combining multibeam echosounder data and seismic profiles, a systematic study was made to understand fluid migration, accumulation, and eruption and their impact on the ecosystem. Location of gas flares observed in the multibeam echosounder data obtained in 2016 and 2018 is different, indicating a year‐level spatiotemporal variation of the cold seep activities. Seafloor observation shows that massive carbonates occur in HM‐1 and HM‐5, indicating two long‐term existed cold seeps (several thousands of years). Mussels covered large areas of HM‐2, HM‐3, and HM‐6, suggesting young active seeps. Elevated seabed with broken edges, mud cones, clay pools, and sudden increased water turbidity and temperature was encountered in multiple areas, which are inferred to be associated with shallow gas accumulation and eruption. Methane content of the headspace gas from shallow sediment at HM‐2 is higher than 99.5% with δ13C‐CH4 of −71.5‰ to 72.3‰, indicating a biogenic gas origin. It is inferred that the gas is sourced by reservoirs at ~1,280 mbsf, which are characterized by low frequency in the seismic profiles. Gas migrates from the gas reservoir to the top of the Basel uplift along the slope. High‐angle faults are widely developed between 800 and 240 mbsf, facilitating gas migration from the top of the Basel uplift to the shallow sediment. Most of the faults did not reach the seafloor; therefore, gas accumulated at shallow depth exhibits bright spots in the seismic profiles. When the pore pressure overcomes the overburden sediment, fractures will be created for gas entering the water column. Gas emission provides a pressure release mechanism; therefore, most fractures did not reach the seafloor as observed in the seismic profiles. However, it is speculated that gas emission will stop with growth of gas hydrates and authigenic carbonates, which continuously decrease the permeability of the original fractures. Pressure will be built up, and new fractures will be generated, leading to the formation of new seeps. This mechanism is inferred to result in the spatiotemporal variation of cold seep activity and affects the development of the cold seep ecosystem.
Cold seeps frequently occur at the seafloor along continental margins. The dominant biogeochemical processes at cold seeps are the combined anaerobic oxidation of methane and sulfate reduction, which can significantly impact the global carbon and sulfur cycles. The circulation of methane-rich fluids at margins is highly variable in time and space, and assessing past seepage activity requires the use of specific geochemical markers. In this study, we report multiple sedimentary proxy records for three piston gravity cores (QDN-14A, QDN-14B, and QDN-31) from the Haima seep of the South China Sea (SCS). By combining total organic carbon (TOC), total inorganic carbon (TIC), total nitrogen (TN), total sulfur (TS), acid insoluble carbon and sulfur isotope (δ13Corganic carbon and δ34Sacid-insoluble), and δ34S values of chromium reducibility sulfur (δ34SCRS), as well as carbon isotopes of TIC (δ13CTIC) in sediments, our aim was to provide constraints on methane seepage dynamics in this area. We identified three sediment layers at about 260-300 cm, 380-420 cm and 480-520 cm sediment depth, characterized by particular anomalies of low δ13CTIC values and high TS content, high TS and CRS contents, and high δ34Sacid-insoluble and δ34SCRS values, respectively. On this basis, we propose that these sediment horizons correspond to distinct methane release events preserved in the sediment record. While the exact mechanisms accounting for the presence (or absence) of these particular geochemical signals in the sediment are not known, we propose that they correspond to variations in methane flux and their duration through time. Overall, our results suggest that sedimentary carbon and sulfur and their isotopes are useful tracers for better understanding of methane seepage dynamics over time. Please note that this is an author-produced PDF of an article accepted for publication following peer review. The definitive publisher-authenticated version is available on the publisher Web site.
High temperature stress has a significant impact on plant growth and development. Herbaceous peony (Paeonia lactiflora Pall.) is a very important landscape plant used in greenbelt whose growth is restrained seriously by high summer temperature, but little is known about relevant solving measures. In order to find an effective measure, this paper studied the effect of black shading net with about 60% transmittance on alleviating the thermal damage of P. lactiflora under field conditions. The results showed that P. lactiflora physiological indices were higher in shaded plants than those in sun-exposured plants especially in the late stages of higher temperature, such as chlorophyll (Chl) a, Chl b, Chl a+b, soluble sugar, soluble protein contents; whereas the exception to the trend was in Chl a/b and malondialdehyde (MDA) content. Moreover, compared with sun exposure, shade increased P. lactiflora protective enzymes activities, made mesophyll cell ultrastructures more intact, the chloroplasts more round and the grana lamellaes arrange relatively neatly, which led to enhance its photosynthesis rate (Pn) and transpiration rate (Tr). Additionally, the full-length cDNA of a heat shock protein gene (HSP70) containing 2195 bp nucleotides was obtained from P. lactiflora, and the expression analysis of PlHSP60, PlHSP70 and PlHSP90 in four developmental stages showed that shade caused PlHSP60 and PlHSP70 expression levels to rise especially in the late stages. These results indicated that shade alleviated the thermal damage of high temperature stress to P. lactiflora through scavenging reactive oxygen species, protecting cell structures, enhancing photosynthesis and the expression levels of HSP under high temperature stress, which might lay a theoretical foundation for P. lactiflora safe over summering and cultivated form in summer.
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