Abstract. Azooxanthellate cold-water corals (CWCs) have a global
distribution and have commonly been found in areas of active fluid seepage.
The relationship between the CWCs and these fluids, however, is not well
understood. This study aims to unravel the relationship between CWC
development and hydrocarbon-rich seepage in Pompeia Province (Gulf of
Cádiz, Atlantic Ocean). This region is comprised of mud volcanoes (MVs), coral
ridges and fields of coral mounds, which are all affected by the
tectonically driven seepage of hydrocarbon-rich fluids. These types of seepage, for example, focused, scattered, diffused or eruptive, is tightly controlled by a
complex system of faults and diapirs. Early diagenetic carbonates from the
currently active Al Gacel MV exhibit δ13C signatures down to
−28.77 ‰ Vienna Pee Dee Belemnite (VPDB), which indicate biologically derived methane
as the main carbon source. The same samples contain 13C-depleted lipid
biomarkers diagnostic for archaea such as crocetane (δ13C down
to −101.2 ‰ VPDB) and pentamethylicosane (PMI) (δ13C down to
−102.9 ‰ VPDB), which is evidence of microbially mediated
anaerobic oxidation of methane (AOM). This is further supported by next
generation DNA sequencing data, demonstrating the presence of AOM-related
microorganisms (ANMEs, archaea, sulfate-reducing bacteria) in the carbonate.
Embedded corals in some of the carbonates and CWC fragments exhibit less
negative δ13C values (−8.08 ‰ to −1.39 ‰ VPDB), pointing against the use of methane as the carbon source. Likewise,
the absence of DNA from methane- and sulfide-oxidizing microbes in sampled
coral does not support the idea of these organisms having a chemosynthetic lifestyle.
In light of these findings, it appears that the CWCs benefit rather indirectly
from hydrocarbon-rich seepage by using methane-derived authigenic carbonates
as a substratum for colonization. At the same time, chemosynthetic organisms
at active sites prevent coral dissolution and necrosis by feeding on the
seeping fluids (i.e., methane, sulfate, hydrogen sulfide), allowing
cold-water corals to colonize carbonates currently affected by
hydrocarbon-rich seepage.
Carbonate minerals such as dolomite, kutnahorite or rhodochrosite are frequently, but not exclusively generated by microbial processes. In recent anoxic sediments, Mn(II)carbonate minerals (e.g. rhodochrosite, kutnahorite) derive mainly from the reduction of Mn(IV) compounds by anaerobic respiration. The formation of huge manganese-rich (carbonate) deposits requires effective manganese redox cycling in an oxygenated atmosphere. However, putative anaerobic pathways such as microbial nitrate-dependent manganese oxidation, anoxygenic photosynthesis and oxidation in ultraviolet light may facilitate manganese cycling even in an early Archean environment, without the availability of oxygen. In addition, manganese carbonates precipitate by microbially induced processes without change of the oxidation state, e.g. by pH shift. Hence, there are several ways how these minerals could have been formed biogenically and deposited in Precambrian sediments. We will summarize microbially induced manganese carbonate deposition in the presence and absence of atmospheric oxygen and we will make some considerations about the biogenic deposition of manganese carbonates in early Archean settings.
Siboglinids were sampled from four mud volcanoes in the Gulf of Cádiz (El Cid MV, Bonjardim MV, Al Gacel MV, and Anastasya MV). These invertebrates are characteristic to cold seeps and are known to host chemosynthetic endosymbionts in a dedicated trophosome organ. However, little is known about their tube as a potential niche for other microorganisms. Analyses by scanning and transmission electron microscopy showed dense biofilms on the tube in Al Gacel MV and Anastasya MV specimens by prokaryotic cells. Methanotrophic bacteria were the most abundant forming these biofilms as further supported by 16S rRNA sequence analysis. Furthermore, elemental analyses with electron microscopy and energy-dispersive X-ray spectroscopy point to the mineralization and silicification of the tube, most likely induced by the microbial metabolisms. Bacterial and archaeal 16S rRNA sequence libraries revealed abundant microorganisms related to these siboglinid specimens and certain variations in microbial communities among samples. Thus, the tube remarkably increases the microbial biomass related to the worms and provides an additional microbial niche in deep-sea ecosystems.
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