Abstract

Abstract. Ladderane fatty acids are commonly used as biomarkers for bacteria involved in anaerobic ammonium oxidation (anammox). These lipids have been experimentally shown to undergo aerobic microbial degradation to form short chain ladderane fatty acids. However, nothing is known of the production or the distribution of these oxic biodegradation products in the natural environment. In this study, we analysed marine water column particulate matter and sediment from three different oceanic regimes for the presence of ladderane oxidation products (C14 ladderane fatty acids) and of original ladderane fatty acids (C18 and C20 ladderane fatty acids). We found that ladderane oxidation products, i.e. C14 ladderane fatty acids, are already produced within the water column of the Arabian Sea oxygen minimum zone (OMZ) and thus only low amounts of oxygen (< 3 μM) are needed for the β-oxidation of original ladderane fatty acids to proceed. However, no short chain ladderane fatty acids were detected in the Cariaco Basin water column, where oxygen concentrations were below detection limit, suggesting that the β-oxidation pathway is inhibited by the absence of molecular oxygen, or that the microbes performing the degradation are not proliferating under these conditions. Comparison of distributions of ladderane fatty acids indicates that short chain ladderane fatty acids are mostly produced in the water column and at the sediment surface, before being preserved deeper in the sediments. Short chain ladderane fatty acids were abundant in Arabian Sea and Peru Margin sediments (ODP Leg 201), often in higher concentrations than the original ladderane fatty acids. In a sediment core taken from within the Arabian Sea OMZ, short chain ladderanes made up more than 90% of the total ladderanes at depths greater than 5 cm below sea floor. We also found short chain ladderanes in higher concentrations in hydrolysed sediment residues compared to those freely occurring in lipid extracts, suggesting that they had become bound to the sediment matrix. Furthermore, these matrix-bound short chain ladderanes were found at greater sediment depths than short chain ladderanes in the lipid extract, suggesting that binding to the sediment matrix aids the preservation of these lipids. Though sedimentary degradation of short chain ladderane fatty acids did occur, it appeared to be at a slower rate than that of the original ladderane fatty acids, and short chain ladderane fatty acids were found in sediments from the Late Pleistocene (~ 100 kyr). Together these results suggest that the oxic degradation products of ladderane fatty acids may be suitable biomarkers for past anammox activity in OMZs.

Highlights

  • Anaerobic ammonium oxidation is the conversion of ammonium through nitrite reduction to dinitrogen gas, performed by select Planctomycetes bacteria

  • As previous reported by Wakeham et al (2012), the original C18 and C20 ladderane fatty acids were not detected within the oxic Cariaco Basin (CB) waters, and were only detected in suspended particulate matter (SPM) at 205 m water depth (Fig. 3a; dissolved O2 = 18 μM), and in relatively low concentrations (0.07 ng l−1; Fig. 3c)

  • Our analyses showed that short chain ladderane fatty acids were not detected in any CB SPM

Read more

Summary

Introduction

Anaerobic ammonium oxidation (anammox) is the conversion of ammonium through nitrite reduction to dinitrogen gas, performed by select Planctomycetes bacteria. Anammox bacterial cells contain characteristic biomarker lipids, called ladderane lipids, which are comprised of concatenated cyclobutane moieties (Sinninghe Damsteet al., 2002). C18 and C20 ladderane fatty acids with either 3 or 5 cyclobutane moieties (Fig. 1, IV–VII) have been used to trace anammox (Hopmans et al, 2006; Kuypers et al, 2003, 2005; Jaeschke et al, 2009a), and the preservation of ladderane lipids in sediments may indicate past anammox activity (Jaeschke et al, 2009b). Relatively little is known about their fate in the water column or in the sediment

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call