Abstract

Aquatic humic (HA) and fulvic acids (FA) from two different origins were fractionated by the tandem size-exclusion chromatography and polyacrylamide gel electrophoresis (tandem SECPAGE). Three HA and two FA fractions exhibited different molecular sizes, electrophoretic mobilities and structural compositions based on elemental analyses and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) after tetramethyl-ammonium hydroxide (TMAH) treatment. Based on comparison of the size-separates and unfractionated bulk samples, the highest molecular size fractions of aquatic humic substances (HS) appear to be enriched in fatty acids (mainly C16 and C18), which are strictly linked to the humic core. This and the presence of low chain fatty acids and unsaturated and di-tri acids may suggest a microbial rather than a vascular plant origin. Even if the majority of lignin derived components in aquatic HS represent relatively high state of biodegradation (oxidation), a certain variation between different sizefractions also exists, supporting a high heterogeneity and composite nature of aquatic HS. Although SEC-PAGE fractionation appears to produce fairly homogeneous HS fractions, the absorption of some urea into of the separates cannot be completely avoided in this method, which limits its suitability for evaluating, especially the presence of N-containing constituents.

Highlights

  • Humic substances (HS), operationally divided into humic (HA insoluble in water at low pH) and fulvic acids (FA, soluble in water under all pH conditions), are widely distributed in soils, natural waters and sediments being an important component of biospheric organic carbon

  • The polyacrylamide gel electrophoresis (PAGE) of aquatic HS exhibited four narrow colored electrophoretic zones: a starting zone A that did not move into the gel; zone B in the middle part of the gel; and rather poorly separated zones C and D at the bottom of the gel

  • Marked zones from all HA and FA samples had similar electrophoretic mobilities (EM) and the zones C and D were combined in the preparative step due to their incomplete separation

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Summary

Introduction

Humic substances (HS), operationally divided into humic (HA insoluble in water at low pH) and fulvic acids (FA, soluble in water under all pH conditions), are widely distributed in soils, natural waters and sediments being an important component of biospheric organic carbon. A first notable feature in the pyrolysis products of all fractionated size-separates was their higher yields of nitrogen compounds with respect to the corresponding bulk HS samples.

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