26 results on '"Nierop, K."'
Search Results
2. Heating histories and taphonomy of ancient fireplaces: A multi-proxy case study from the Upper Palaeolithic sequence of Abri Pataud (Les Eyzies-de-Tayac, France)
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Braadbaart, F., Reidsma, F. H., Roebroeks, W., Chiotti, L., Slon, V., Meyer, M., Théry-Parisot, I., van Hoesel, A., Nierop, K. G.J., Kaal, J., van Os, B., Marquer, L., Organic geochemistry, Paleomagnetism, GeoLab Algemeen, Organic geochemistry & molecular biogeology, Organic geochemistry, Paleomagnetism, GeoLab Algemeen, Organic geochemistry & molecular biogeology, Leiden University, Utrecht University [Utrecht], Universiteit Leiden [Leiden], Histoire naturelle de l'Homme préhistorique (HNHP), Muséum national d'Histoire naturelle (MNHN)-Université de Perpignan Via Domitia (UPVD)-Centre National de la Recherche Scientifique (CNRS), Max Planck Institute for Evolutionary Anthropology [Leipzig], Max-Planck-Gesellschaft, Culture et Environnements, Préhistoire, Antiquité, Moyen-Age (CEPAM), Université Côte d'Azur (UCA)-Centre National de la Recherche Scientifique (CNRS)-Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA), Cultural Heritage Agency of the Netherlands, Consejo Superior de Investigaciones Científicas [Spain] (CSIC), Max Planck Society, and European Research Council
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010506 paleontology ,Archeology ,Taphonomy ,060102 archaeology ,Hearth ,[SHS.ARCHEO]Humanities and Social Sciences/Archaeology and Prehistory ,Excavation ,Upper Palaeolithic ,06 humanities and the arts ,Fuel ,01 natural sciences ,Archaeology ,Diagenesis ,Fireplaces ,0601 history and archaeology ,Sedimentary rock ,Aurignacian ,Geology ,Rock shelter ,ComputingMilieux_MISCELLANEOUS ,0105 earth and related environmental sciences ,Chronology ,Fire use - Abstract
While the use of fire has long been recognised as a crucial innovation in the cultural evolution of humankind, much research has focused on the (debated) chronology of its earliest use and control, and less on the ways in which fire was used in the deep past. At its latest by the Upper Palaeolithic, hunter-gatherers routinely used fire to heat a wide range of materials, adjusting parameters like temperature, exposure time and fuel type to the specific requirements of the treated materials, for instance in food preparation or tool production. Comparing analyses of the chemical and physical properties of modern materials, heated under a range of controlled conditions in a laboratory, to archaeological ones might allow the reconstruction of the “heating history” of excavated materials and hence to infer the function of particular fires in the past - provided changes affecting the properties of the heated archaeological material during burial time are taken into consideration. To investigate the feasibility of such an approach, heated materials sampled from ~40,000 to 25,000 year old fireplaces (hearths) and their sedimentary matrices from the Upper Palaeolithic Abri Pataud rock shelter in South-Western France are used here to study (1) the fuel type(s) used by the site’s occupants, (2) the temperatures reached in fireplaces and (3) the potential changes in human activities related to fireplaces over time, with the influence of post-depositional processes taken into explicit consideration throughout. For this purpose, we used a range of methods to analyse macroscopically visible as well as “invisible” (microscopic and molecular) heat-altered materials. The results suggest that charred organic materials (COM) encountered in the samples predominantly result from the fuel used in fireplaces, including the earliest reported use of dung as fuel. Earlier suggestions about the use of bone as fuel at the Abri Pataud are not supported by this study. The heating temperature of COM increased gradually from 350 °C in the Aurignacian to 450 °C in Gravettian levels. Py-GC–MS studies identified a range of organic compounds, biomolecules derived from plant as well as animal sources, still preserved in the sediments after exposure to heat and burial in the rock shelter more than 20,000 years ago. Mammalian mtDNA was identified in sediment samples retrieved from the fireplaces, including ancient mtDNA fragments that originated from one or more modern human-like mitochondrial genome(s). This makes the Abri Pataud the first archaeological site for which ancient modern human mtDNA has been retrieved from sediment samples. The absence of specific organic compounds (furans) in the Aurignacian levels and their presence in the Gravettian ones, the changes in temperatures reached through the Aurignacian-Gravettian sequence as well as changes in the character of the fireplaces (presence/absence of lining river pebbles) suggest that the functions of hearths changed through time. These results highlight the potential of multi-proxy analyses of macro- and microscopic traces of ancient fireplaces, and especially of a shift in focus towards molecular traces of such activities. Systematic sampling of fireplaces and their sedimentary matrix should become a standard part of the excavation protocol of such features, to improve our understanding of the activities of humans in the deep past., The genetic work was funded by the Max Planck Society and the European Research Council (grant no. 694707 to Svante Pääbo). We thank B. Nickel, J. Richter, B. Schellbach and A. Weihmann for work in the ancient DNA laboratory of the Max Planck Institute for Evolutionary Anthropology at Leipzig.
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- 2020
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3. Composition of soil organic matter and its water-soluble fraction under young vegetation on drift sand, central Netherlands
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NIEROP, K. G. J. and BUURMAN, P.
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- 1998
4. Radiocarbon dating of late pleistocene marine shells from the southern north sea
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Busschers, F. S., Wesselingh, F. P., Kars, R. H., Versluijs-Helder, M., Wallinga, J., Bosch, J. H A, Timmner, J., Nierop, K. G. J., Meijer, T., Bunnik, F. P M, De Wolf, H., Inorganic Chemistry and Catalysis, Marine Palynology, Sub Inorganic Chemistry and Catalysis, Organic geochemistry, Inorganic Chemistry and Catalysis, Marine Palynology, Sub Inorganic Chemistry and Catalysis, and Organic geochemistry
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010506 paleontology ,Archeology ,010504 meteorology & atmospheric sciences ,Pleistocene ,Energy / Geological Survey Netherlands ,pyrolysis-gas chromatography ,Geological Survey Netherlands ,Earth and Planetary Sciences(all) ,Context (language use) ,quartz osl ages ,Biostratigraphy ,Feldspar ,cosmogenic nuclides ,01 natural sciences ,law.invention ,chemistry.chemical_compound ,Paleontology ,law ,calcium-carbonate ,Radiocarbon dating ,GM - Geomodelling AEC - Applied Environmental Chemistry ,Sea level ,Holocene ,luminescence signals ,0105 earth and related environmental sciences ,regenerative-dose protocol ,level change ,Earth / Environmental ,central netherlands ,Bodemgeografie en Landschap ,chemistry ,Archaeology ,rhine-meuse system ,visual_art ,climate-change ,visual_art.visual_art_medium ,Soil Geography and Landscape ,General Earth and Planetary Sciences ,Carbonate ,ELSS - Earth, Life and Social Sciences ,Geology ,Geosciences - Abstract
This article presents a set of Late Pleistocene marine mollusk radiocarbon (AMS) age estimates of 30–5014C kyr BP, whereas a MIS5 age (>75 ka) is indicated by quartz and feldspar OSL dating, biostratigraphy, U-Th dating, and age-depth relationships with sea level. These results indicate that the14C dates represent minimum ages. The age discrepancy suggests that the shells are contaminated by younger carbon following shell death. The enigmatic14C dates cannot be “solved” by removing part of the shell by stepwise dissolution. SEM analysis of the Late Pleistocene shells within a context of geologically younger (recent/modern, Holocene) and older (Pliocene) shells shows the presence of considerable amounts of an intracrystalline secondary carbonate precipitate. The presence of this precipitate is not visible using XRD since it is of the same (aragonitic) polymorph as the original shell carbonate. The combination of nanospherulitic-shaped carbonate crystals, typical cavities, and the presence of fatty acids leads to the conclusion that the secondary carbonate, and hence the addition of younger carbon, has a bacterial origin. As shell material was studied, this study recommends an assessment of possible bacterial imprints in other materials like bone collagen as well.
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- 2014
5. Bioavailability of HOCs related to soil organic matter composition
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Cuypers, M.P., Grotenhuis, J.T.C., Nierop, K., Maneiro, E., Dijkema, C., and Rulkens, W.H.
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WIMEK ,Environmental Technology ,Life Science ,Milieutechnologie - Published
- 2000
6. Origin and fate of organic matter in sandy soils along a primary vegetation succession
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Nierop, K., Agricultural University, N. van Breemen, and P. Buurman
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WIMEK ,decomposition ,Laboratorium voor Bodemkunde en geologie ,zandgronden ,organische stof ,vegetation types ,Laboratory of Soil Science and Geology ,plant succession ,decompositie ,organic horizons ,vegetatie ,plantensuccessie ,vegetation ,vegetatietypen ,organische horizonten ,sandy soils ,deterioration ,achteruitgang (deterioration) ,organic matter - Abstract
Until now little is known about the role vegetation plays in the organic matter formation, particularly at the molecular level. Most ecosystems have a long history, which is unknown or too complex to find distinct relations between vegetation and the chemical composition of soil organic matter. To gain a better insight in such relationships, the relative simple soil-vegetation system of the Hulshorster Sands and Leuvenum Forest is used. The complete vegetation succession has been investigated, making it possible to monitor the organic matter development. During the succession, thus with time, the pH decreases, the ectorganic layer becomes thicker and the soil develops towards a micro-podzol.Chapter 2 describes the organic matter composition and relation to the first stages of vegetation development in the pre-podzol phase. In the Ah horizon under grass ( Corynephorus canescens ), the organic matter has virtually no contribution of the covering vegetation. Algae, from an earlier stage, and mosses ( Polytrichum piliferum and Bryum sp.), from adjacent spots, are the main suppliers. Under mosses, the organic matter is very similar to that of the original species. An aliphatic biopolymer, derived from mosses, that produces a series of branched alkene/alkane doublets (C 20 -C 32 ) together with a homologous series of n -alkenes and n -alkanes (C 10 up to C 34 ) upon pyrolysis, appears to be very recalcitrant in the first stages of succession.In the vegetation stages following mosses, these aliphatic macromolecules are still an important source of the aliphatic part of organic matter. Apart from the aliphatic moss contribution, the organic matter under Callunavulgaris and Pinus sylvestris has a close relationship with the contributing plant parts: flowers, leaves and branches dominate the organic layer under Calluna , needles predominate the ectorganic horizon under pines, and the soil organic matter in the Ah horizons in both cases is almost completely determined by roots.In Chapter 3 the water soluble organic matter (WSOM) of the Ah horizons is compared with the bulk horizons. The WSOM contains little lignin, also when this compound was present in significant amounts in the Ah horizons. In contrast, the moss-derived aliphatics are prominently present in the WSOM. Their presence in water is probably due to the formation of micelle-like arrangements in which the hydrophobic parts are inside a hydrophilic mantle resulting into 'soluble' aliphatics.Chapter 4 deals with the fractionation of three H horizons under different vegetation in the forest with incipient podzolization: a water soluble fraction, a NaOH soluble fraction and the residue, the insoluble fraction (humin). The water soluble fractions are very similar to each other with regard to their chemical composition, and so are the NaOH soluble factions. The insoluble fractions differ in particular in their aliphatic part. During beech forest development, an increasing amount of suberin, mainly derived from beech roots, is observed. The bulk of the organic matter in the H horizons, however, appears to have a pine origin as concluded from the chemical data. Pollen analysis supports that beech litter did not contribute to the H horizons.Chapter 5 addresses the analysis (composition of polysaccharides, NMR, pyrolysis and thermochemolysis) and the unraveling of the origin of the ectorganic layers in the succession from pine to beech forest. Under pine, the bulk organic matter shows only little effect of the ground vegetation Deschampsia and Empetrum respectively. The chemical composition of the L and F1 horizons are very similar to each other, but towards the H horizons an increase of aliphatics, a decrease of polysaccharides and a more or less constant fraction of aromatic compounds is noticed. The lignin composition is dominated by guaiacol building blocks, and hardly any angiosperm-lignin is present in the ectorganic layers implying no significant contributions of the undergrowth. This contrasts with macromorphological analyses, because abundant above- and below-ground parts of Deschampsia and Empetrum are present in the organic horizons suggesting an important input of the understorey. The composition of the aliphatic fraction also shows an effect of the undergrowth.The distribution of cutin and suberin building blocks as measured upon thermochemolysis reveals the clear impact of Deschampsia and Empetrum in addition to pine, especially in the F1 and F2 horizons. The transition towards the beech forest is characterized by a more distinct influence of beech litter. From L to H horizons polysaccharide contents decrease clearly, aromatics remain constant and the amounts of aliphatic compounds increase relatively.Furthermore, with depth a clear decrease of syringyl lignin compared with guaiacyl lignin is observed. The latter is mainly due to a decrease of beech litter towards the H horizon: the L consists only of beech litter, the F is also dominated by beech litter in addition to beech roots, and the H horizon is virtually only derived from pine litter. Nevertheless, the composition of the H horizons is affected by beech through their roots, which is clearly marked by the presence of beech-suberin, and the contents of that biopolymer increases from younger to older beech stands.In Chapter 6 the WSOM fractions from L, F, and H horizons are compared on their chemical composition with those of the bulk of B horizons and fibers of incipient podzols. The WSOM shows hardly any resemblance with the B horizons, whereas it appears to be very similar to the fibers. This strongly suggests that in the initial phases of podzolization almost all WSOM moves through the B horizons and accumulates when the water movement stops resulting into the formation of humus fibers. In Chapter 7 it is elucidated that the organic matter in the B horizons is mainly composed of root-derived material, whereas hardly any organic matter is complexed with metals or clay. The organic matter in B horizons is highly aliphatic, consisting partly of suberan-like polymers and partly of suberin, whereas lignin and polysaccharides are virtually absent. In Chapter 8, the chemical implications of the negligible organic matter sources of both illuviation as mixing of above-ground litter is described. The clear chemical evidence of root-derived organic matter could be established.
- Published
- 1999
7. Thermally assisted hydrolysis and methylation of organic matter in two allophanic volcanic ash soils from the Azores Islands.
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Arnalds, Ó., Óskarsson, H., Bartoli, F., Stoops, G., García-Rodeja, E., Nierop, K. G. J., and Buurman, P.
- Abstract
Thermally assisted Hydrolysis and Methylation was used to analyse in more detail the aromatic and aliphatic building blocks of the organic matter of two soil profiles from the Azores. Both Ah horizons showed significant contributions of lignin, tannins, cutin and suberin, which were virtually absent from the underlying horizons. Alkanoic acids were present throughout both soil profiles, with long-chain acids (>C20) decreasing with depth in comparison with short-chain acids in EUR05, whereas having a relative minimum in AB2 and 2Bw1 horizons in EUR06. Despite the huge potential of Andosols to store carbon, the studied soils did not exhibit a great preservation potential of plant-derived molecules (lignin, cutin/suberin-derived lipids, C26 alkanol) in comparison with other soils as studied by THM. By contrast, bacterial-derived branched alkanoic acids are better preserved than the plant-derived alkanoic acids, which confirms the high degree of microbial and insect-derived OM in the Andosols studied. [ABSTRACT FROM AUTHOR]
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- 2007
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8. NaOH and Na-Na4P2O7-extractable organic matter in two allophanic volcanic ash soils of the Azores Islands — quantified pyrolysis-GC/MS data and factor analysis.
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Arnalds, Ó., Óskarsson, H., Bartoli, F., Stoops, G., García-Rodeja, E., Buurman, P., and Nierop, K. G. J.
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- 2007
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9. Chapter 10: Molecular chemistry by pyrolysis-GC/MS of selected samples of the Penido Vello peat deposit, Galicia, NW Spain.
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Buurman, P., Nierop, K. G. J., Pontevedra-Pombal, X., and A. Martínez Cortizas
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Chapter 10 of the book "Peatlands: Evolution and Records of Environmental and Climate Changes," by I. P. Martini, A. Martínez Cortizas and W. Chesworth is presented. It describes the organic chemistry of peatlands in Galicia, Spain. It discusses the difference between extracted and non-extractable peat and the presence of polysaccharides, alkanes, and alkeness in larger molecular units.
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- 2007
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10. Microbial bioavailability regulates organic matter preservation in marine sediments.
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Koho, K. A., Nierop, K. G. J., Moodley, L., Middelburg, J. J., Pozzato, L., Soetaert, K., van der Plicht, J., and Reichart, G.-J.
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COMPOSITION of marine sediments ,ORGANIC compounds ,CARBON cycle ,BIOCHEMISTRY ,BIODEGRADATION - Abstract
Burial of organic matter (OM) plays an important role in marine sediments, linking the short-term, biological carbon cycle with the long-term, geological subsurface cycle. It is well established that low-oxygen conditions promote organic carbon burial in marine sediments. However, the mechanism remains enigmatic. Here we report biochemical quality, microbial degradability, OM preservation and accumulation along an oxygen gradient in the Indian Ocean. Our results show that more OM, with biochemically higher quality, accumulates under low oxygen conditions. Nevertheless, microbial degradability does not correlate with the biochemical quality of OM. This decoupling of OM biochemical quality and microbial degradability, or bioavailability, violates the ruling paradigm that higher quality implies higher microbial processing. The inhibition of bacterial OM remineralisation may play an important role in the burial of organic matter in marine sediments and formation of oil source rocks. [ABSTRACT FROM AUTHOR]
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- 2013
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11. Microbial bioavailability regulates organic matter preservation in marine sediments.
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Koho, K. A., Nierop, K. G. J., Moodley, L., Middelburg, J. J., Pozzato, L., Soetaert, K., van der Plicht, J., and Reichart, G.-J.
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BIOAVAILABILITY ,ORGANIC compounds ,MARINE sediments ,CARBON cycle ,MICROBIAL diversity - Abstract
Burial of organic matter (OM) plays an important role in marine sediments, linking the short-term, biological carbon cycle with the long-term, geological subsurface cycle. It is well established that low-oxygen conditions promote organic carbon burial in marine sediments. However, the mechanism remains enigmatic. Here we report bio- chemical quality, microbial degradability, OM preservation and accumulation along an oxygen gradient in the Indian Ocean. Our results show that more OM, and of biochemically higher quality, accumulates under low oxygen conditions. Nevertheless, microbial degradability does not correlate with the biochemical quality of OM. This decoupling of OM biochemical quality and microbial degradability, or bioavailability, violates the ruling paradigm that higher quality implies higher microbial processing. The inhibition of bacterial OM remineralisation may play an important role in the burial of organic matter in marine sediments and formation of oil source rocks. [ABSTRACT FROM AUTHOR]
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- 2012
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12. Towards understanding of carbon stocks and stabilization in volcanic ash soils in natural Andean ecosystems of northern Ecuador.
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Tonneijck, F. H., Jansen, B., Nierop, K. G. J., Verstraten, J. M., Sevink, J., and De Lange, L.
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BIOTIC communities ,SOILS & climate ,VEGETATION & climate ,AGRICULTURAL climatology - Abstract
Volcanic ash soils contain very large stocks of soil organic matter (SOM) per unit area. Consequently, they constitute potential sources or sinks for the greenhouse gas carbon dioxide. Whether soils become a net carbon source or sink with climate and/or land-use change depends on the stability of SOM against decomposition, which is influenced by stabilization mechanisms in the soil. To quantify organic carbon stocks and to clarify the importance of chemical and physical soil characteristics for carbon stabilization in volcanic ash soils, we applied selective extraction techniques, performed X-ray diffraction analysis of the clay fraction and estimated pore-size distribution of soils under natural upper montane forest and grassland (páramo) in the Ecuadorian Andes. Our results show that organic carbon stocks under both vegetation types are roughly twice as large as previously reported global averages for volcanic ash soils. SOM stabilization is suggested to be dominantly influenced by the following chemical and physical soil characteristics: (i) direct stabilization of SOM in organo-metallic (Al-humus) complexes, explaining at most 40% of carbon accumulation, (ii) indirect protection of SOM (notably aliphatic compounds) through low soil pH and toxic levels of Al, and probably also (iii) physical protection of SOM caused by a very large micro-porosity. Moreover, in the case of the forest soils, inherent recalcitrance of OM itself was responsible for substantial accumulation in ectorganic horizons. Both vegetation types contributed to soil acidification, thus increasing SOM accumulation. [ABSTRACT FROM AUTHOR]
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- 2010
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13. Mechanisms controlling the mobility of dissolved organic matter, aluminium and iron in podzol B horizons.
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Jansen, B., Nierop, K. G. J., and Verstraten, J. M.
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ORGANIC compounds , *ALUMINUM , *IRON , *PODZOL , *SOILS - Abstract
The processes governing the (im)mobilization of Al, Fe and dissolved organic matter (DOM) in podzols are still subject to debate. In this study we investigated the mechanisms of (im)mobilization of Al, Fe and organic matter in the upper and lower B horizons of two podzols from the Netherlands that are in different stages of development. We equilibrated batches of soil material from each horizon with DOM solutions obtained from the Oh horizon of the corresponding soil profiles. We determined the amount of (im)mobilized Al, Fe and DOM after addition of Al and Fe at pH 4.0 and 4.5 and initial dissolved organic carbon (DOC) concentrations of 10 mg C litre−1 or 30 mg C litre−1, respectively. At the combination of pH and DOC concentrations most realistic for the field situation, organic matter was retained in all horizons, the most being retained in the lower B horizon of the well-developed soil and the least in the upper B horizon of the younger profile. Organic matter solubility seemed to be controlled mainly by precipitation as organo-metal complexes and/or by adsorption on freshly precipitated solid Al- and Fe-phases. In the lower B horizons, at pH 4.5, solubility of Al and Fe appeared to be controlled mainly by the equilibrium with secondary solid Al- and Fe-phases. In the upper B horizons, the solubility of Al was controlled by adsorption processes, while Fe still precipitated as inorganic complexes as well as organic complexes in spite of the prevailing more acidic pH. Combined with a previous study of eluvial horizons from the same profiles, the results confirm the important role of organic matter in the transport of Al and Fe to create illuvial B horizons initially and subsequently deepening and differentiating them into Bh and Bs horizons. [ABSTRACT FROM AUTHOR]
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- 2005
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14. Mobilization of dissolved organic matter, aluminium and iron in podzol eluvial horizons as affected by formation of metal-organic complexes and interactions with solid soil material.
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Jansen, B., Nierop, K. G. J., and Verstraten, J. M.
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SOILS , *HUMUS , *SOIL testing , *SOIL composition , *AGRICULTURAL chemistry , *AGRICULTURAL chemicals - Abstract
Interactions with dissolved organic matter (DOM) are generally believed to play a crucial role in the translocation of Al and Fe in acid sandy soils. Binding of Al and Fe to DOM affects their mobility in soils by altering sorption equilibria of charged sites on solid soil material, inducing precipitation of organo-metallic complexes and preventing the formation of inorganic Al and Fe phases. The relative importance of the different processes, especially with respect to the translocation of Al, Fe and organic matter in podzols, remains unresolved. We determined the effect of the presence of solid soil material from the eluvial (AhE and AE, respectively) horizons of a Fimic Anthrosol and a Haplic Podzol on the metal-to-organic carbon (M/C) ratio in solution and the formation of dissolved organic Al and Fe complexes. Furthermore, we assessed the resulting influence on the mobilization of Al, Fe and DOM. Even under considerable metal loading, the M/C ratios and ‘free’ metal fractions in solution remained low and relatively constant, due to an apparent buffering by the solid phase and the formation of organo-metal complexes in solution. The M/C ratios remained so low that significant precipitation of organo-metal complexes due to saturation with metals was not found. The apparent buffering by the solid phase can be explained by a strong release of organic matter from solid soil material and adsorption of non-complexed Al and Fe on solid organic matter upon metal addition. Adsorption of organo-metal complexes most likely played only a minor role. The observations confirm the expected mobilization of Al, Fe and DOM in eluvial horizons and seem to indicate that even under fluctuating input of Al, Fe and DOM the soil solution will have a constant composition with respect to M/C ratios and percentage of Al and Fe present in dissolved organo-metal complexes. [ABSTRACT FROM AUTHOR]
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- 2004
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15. Liming effects on the chemical composition of the organic surface layer of a mature Norway spruce stand (Picea abies [L.] Karst.).
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Rosenberg, W., Nierop, K. G. J., Knicker, H., de Jager, P. A., Kreutzer, K., and Weiß, T.
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LIMING of soils , *HUMUS - Abstract
The application of lime in a mature Norway spruce (Picea abies [L.] Karst.) forest in southern Germany induced major changes in the activity of soil organisms and root growth. Since this may influence the chemical compostion of the soil organic matter (SOM) of the organic surface layer, its composition and changes due to the treatment were examined in this study. Fine roots of Norway spruce have a relatively low content of extractable lipids, a low alkyl C content (13C CPMAS NMR) and a high ratio of non-cellulosic to cellulosic carbohydrates (NC/CC, carbohydrate determination by MBTH and gas chromatography analyses) as compared to needles. Furthermore, they show high ratios of suberin/cutin compounds (thermally assisted hydrolysis and methylation, (THM)) and high ratios of eicosanic acid/phytadiene I in their lipid extracts (pyrolysis-GC/MS).Liming (4 t ha−1 dolomite) of a Norway spruce organic surface layer decreased the proportion of alkyl C, the alkyl C/O-alkyl C ratio, and the content of extractable lipids. The NC/CC ratio and the abundance of suberin relative to cutin components increased. The contribution of the chlorophyll component phytadiene I decreased in relation to eicosanic acid. These changes are attributed to increased fine root formation in the organic layer after liming. Furthermore, the presence of less degraded lignin (THM, peak ratio of 3,4-dimethoxybenzoic acid, methyl ester/3,4-dimethoxy-benzaldehyde) on the limed plot is explained by the increased input of relatively fresh fine root material. On the other hand, the decrease in the carbon-to-nitrogen ratio may be attributed to the higher microbial activity after liming. [Copyright &y& Elsevier]
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- 2003
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16. Degradation of Biomacromolecules during High‐Rate Composting of Wheat Straw–Amended Feces.
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Veeken, A. H. M., Adani, F., Nierop, K. G. J., Jager, P. A., and Hamelers, H. V. M.
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BIOMACROMOLECULES ,MAGIC angle spinning ,COMPOSTING ,LIGNOCELLULOSE ,NUCLEAR magnetic resonance ,HEMICELLULOSE ,WHEAT straw ,FECES - Abstract
Pig (Sus scrofa) feces, separately collected and amended with wheat straw, was composted in a tunnel reactor connected with a cooler. The composting process was monitored for 4 wk and the degradation of organic matter was studied by two chemical extraction methods, 13C cross polarization magic angle spinning (CPMAS) nuclear magnetic resonance (NMR) and pyrolysis gas chromatography–mass spectrometry (GC–MS). Wet‐chemical extraction methods were not adequate to study the degradation of specific organic compounds as the extraction reagents did not give selective separation of hemicellulose, cellulose, proteins, and lignins. A new method was proposed to calculate the contribution of four biomacromolecules (aliphatics, proteins, polysaccharides, and lignin) from the 13C CPMAS NMR spectrum. Pyrolysis GC–MS allowed identification of the composition of the biomacromolecules. The biomacromolecules showed different rates of degradation during composting. High initial degradation rates of aliphatics, hemicellulose, and proteins were observed, where aliphatics were completely degraded and hemicellulose and proteins were partly recalcitrant during the four weeks of composting. The degradation rate of cellulose was much lower and degradation was not completed within the four weeks of composting. Lignin was not degraded during the thermophilic stage of composting but started to degrade slowly during the mesophilic stage. A combination of 13C CPMAS NMR and pyrolysis GC–MS gave good qualitative and semiquantitative assessments of the degradation of biomacromolecules during composting. [ABSTRACT FROM AUTHOR]
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- 2001
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17. Water-soluble organic matter in incipient podzols: accumulation in B horizons or in fibres?
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Nierop, K. G. J. and Buurman, P.
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PODZOL , *ORGANIC compound content of soils , *HUMUS , *SOIL horizons - Abstract
To elucidate the mechanism of podzolization in its first stages we studied the fate of the water-soluble organic matter (WSOM) in incipient podzols in sandy soils by comparing the composition of the WSOM from L, F and H horizons with that in the bulk of the Bh horizons and fibres of three profiles. The WSOM appeared to consist significantly of ligno-cellulose and proteins, but these biopolymers were hardly present in the Bh horizons. The material of the fibres, however, greatly resembled the WSOM composition, thereby suggesting that in these soils most of the WSOM is transported through the B horizon and accumulates hardly changed in thin bands where the water stops moving. This implies that in the early steps of podzolization, accumulation of organic matter in the B horizon is not likely to be caused by water-soluble material. [ABSTRACT FROM AUTHOR]
- Published
- 1999
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18. Synthesis and photopolymerization of cholesteric liquid crystalline diacrylates.
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Lub, J., Broer, D. J., Hikmet, R. A. M., and Nierop, K. G. J.
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- 1995
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19. Letters to the Editor.
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Nierop, K. G. J. and Buurman, P.
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HUMUS , *FIELD ionization mass spectrometry , *ALIPHATIC compounds - Abstract
Presents a reply to the comments on the composition of soil organic matter and its water-soluble fraction under young vegetation on drift sand in central Netherlands. Importance of pyrolysis-field ionization mass spectrometry in analyzing aliphatic compound; Use of tetramethylammonium hydroxide as methylation agent in the analyses of aliphatics.
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- 1999
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20. What potential do mosses have as biomonitors of POPs? A comparative study of hexachlorocyclohexane sorption.
- Author
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Chaos Z, Fernández JA, Balseiro-Romero M, Celeiro M, García-Jares C, Méndez A, Pérez-Alonso P, Estébanez B, Kaal J, Nierop KGJ, Aboal JR, and Monterroso C
- Subjects
- Adsorption, Bryophyta chemistry, Environmental Pollutants analysis, Biological Monitoring methods, Sphagnopsida chemistry, Hexachlorocyclohexane analysis, Environmental Monitoring methods
- Abstract
Persistent organic pollutants (POPs) pose a significant global threat to human health and the environment, and require continuous monitoring due to their ability to migrate long distances. Active biomonitoring using cloned mosses is an inexpensive but underexplored method to assess POPs, mainly due to the poor understanding of the loading mechanisms of these pollutants in mosses. In this work, Fontinalis antipyretica (aquatic moss) and Sphagnum palustre (terrestrial moss) were evaluated as potential biomonitors of hexachlorocyclohexanes (HCHs: α-, β-, γ-, δ-HCH), crucial POPs. Moss clones, grown in photobioreactors and subsequently oven-dried, were used. Their lipid composition and distribution were characterized through molecular and histochemical studies. Adsorption experiments were carried out in the aqueous phase using the repeated additions method and in the gas phase using an active air sampling technique based on solid-phase extraction, a pioneering approach in moss research. F. antipyretica exhibited greater lipid content in the walls of most cells and higher adsorption capacity for all HCH isomers in both gaseous and liquid environments. These findings highlight the need for further investigation of POP loading mechanisms in mosses and open the door to explore other species based on their lipid content., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
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21. Application of pyrolysis-gas chromatography/mass spectrometry to study changes in the organic matter of macro- and microaggregates of a Mediterranean soil upon heating.
- Author
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Campo J, Nierop KG, Cammeraat E, Andreu V, and Rubio JL
- Subjects
- Fires, Hot Temperature, Mediterranean Region, Organic Chemicals metabolism, Principal Component Analysis, Quercus, Trees, Ecological and Environmental Phenomena, Gas Chromatography-Mass Spectrometry methods, Organic Chemicals analysis, Soil chemistry
- Abstract
The heating effect on the soil organic matter (SOM) of a Mediterranean soil was studied in two fractions (macro- and microaggregates) and in two environments (soil under canopy of Quercus coccifera and bare soil between plants). Samples were heated under laboratory conditions at different temperatures (220, 380 and 500°C) to establish their effects on the SOM quality and quantity by comparison with unheated control samples (25°C). The SOM content in the soil under canopy was higher than in the bare one and in the microaggregate fractions than in the macroaggregate ones. Increasing temperatures caused, in general, the decrease of SOM content in both soils as well as in both aggregate classes. The quality of SOM was determined after extraction with 0.1 M NaOH and analysed by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). Obtained pyrolysates were characterized by the presence of polyphenols and other aromatic pyrolysis products (lipids, polysaccharides, proteins and lignin derivatives). Some of the products in these control samples, and furthermore the presence of black carbon (BC) markers (e.g. benzene, pyridine and toluene), confirmed the occurrence of past wildfires in the study zone. The composition of the SOM extracted from the soils heated at 220°C, was quite similar to that obtained from unheated soils. The products derived from polysaccharides and lignin, and some coming from polyphenols, were not detected in the pyrolysates of the soil heated at 380 and 500°C., (Copyright © 2011 Elsevier B.V. All rights reserved.)
- Published
- 2011
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22. Soil organic matter from pioneer species and its implications to phytostabilization of mined sites in the Sierra de Cartagena (Spain).
- Author
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Ottenhof CJ, Faz Cano A, Arocena JM, Nierop KG, Verstraten JM, and van Mourik JM
- Subjects
- Amaranthaceae chemistry, Biodegradation, Environmental, Poaceae chemistry, Spain, Amaranthaceae growth & development, Humic Substances analysis, Industrial Waste analysis, Mining, Poaceae growth & development, Soil analysis, Soil standards, Soil Pollutants analysis
- Abstract
Pioneer plant species were observed growing on mined areas despite unfavourable conditions such as extreme pH, high salinity and phytotoxic levels of several elements. This study evaluated the contribution of pioneer species to the accumulation of soil organic matter (SOM). We collected 51 samples from 17 non-vegetated, natural and pioneer-vegetated sites in five highly saline mined areas in the Sierra de Cartagena (Spain). The composition of SOM was determined using total C, N and S elemental anlayzer, pyrolysis and solid state (13)C NMR spectroscopy. Results showed that pioneer species like Lygeum spartum had contributed approximately 11 kg SOM kg(-1) soil into the Balsa Rosa sites since 1991; it will take approximately 120 years of continuous growth for this plant to increase the SOM level comparable to natural site. In the Portman Bay area, Sarconia ramosissima and Phragmites australis can contribute SOM equivalent to present day SOM in natural sites in the next 30 years. Low quality SOM (C/N>20) deposited by pioneer plants was dominated by lignin-derived organic compounds such as phenols, guaiacols, syringols and aromatics while polyssacharides and alkyls were the major components in high quality SOM (C/N<20). The addition of SOM to mine wastes is similar to early stages of soil formation and with time, we expect the formation of well-developed Ah horizon on the surface of mine wastes. The presence of P. australis on several sites makes it a very good candidate for successful revegetation of hostile conditions found in many mined sites.
- Published
- 2007
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23. Lysosomal destabilization contributes to apoptosis of germinal center B-lymphocytes.
- Author
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van Nierop K, Muller FJ, Stap J, Van Noorden CJ, van Eijk M, and de Groot C
- Subjects
- Amides pharmacology, Apoptosis drug effects, B-Lymphocytes cytology, B-Lymphocytes drug effects, CD40 Antigens metabolism, Caspase 3 metabolism, Caspase 8 metabolism, Cells, Cultured, DNA Fragmentation drug effects, Dendritic Cells, Follicular metabolism, Germinal Center cytology, Humans, Lysosomes drug effects, Mitochondria drug effects, Mitochondria metabolism, Phosphatidylserines metabolism, Serine analogs & derivatives, Serine pharmacology, Apoptosis physiology, B-Lymphocytes metabolism, Germinal Center metabolism, Lysosomes metabolism
- Abstract
During germinal center (GC) reactions, B-lymphocytes with high-affinity B-cell receptors are selected. Regulation of apoptosis is a key process in selecting such wanted B-cells and in eliminating B-cells with unwanted specificities. In this paper, we show that apoptosis in human GC B-cells involves lysosomal destabilization, which is strictly controlled by caspase-8 activity, but not by caspase-9 activity. Ligation of CD40 provides resistance to lysosomal destabilization. Experimental lysosomal rupture by the lysosomotropic drug O-methyl-l-serine dodecylamide hydrochloride (MSDH) induces apoptosis in GC B-cells, including phosphatidyl serine exposure, mitochondrial inactivation, and DNA fragmentation. These apoptotic features occur in the absence of caspase-3 activity. Follicular dendritic cells (FDCs) protect binding B-lymphocytes from lysosomal destabilization, in both the absence and the presence of MSDH. Our study demonstrates that lysosomal leakage induces apoptosis of GC B-cells in a caspase-3-independent manner and that high-affinity binding to FDCsprevents lysosomal leakage and apoptosis in GC B-cells.
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- 2006
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24. Retention of tannic acid and condensed tannin by Fe-oxide-coated quartz sand.
- Author
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Kaal J, Nierop KG, and Verstraten JM
- Subjects
- Adsorption, Carbohydrate Sequence, Iron Compounds chemistry, Minerals, Molecular Sequence Data, Molecular Structure, Surface Properties, Ferric Compounds chemistry, Proanthocyanidins chemistry, Quartz chemistry, Tannins chemistry
- Abstract
This paper intends to shed light on the interactions between tannin and mineral soil particles. For that purpose, aqueous solution of condensed tannin (CT) (derived from Black pine (Pinus nigra var. maritima)) and commercially available tannic acid (TA) were added to purified quartz (Qtz) sand and quartz sand coated with either goethite (Gt) or ferrihydrite (Fh). After solvent removal by evaporation the samples were extracted by water. The extracts were analysed for organic carbon, total phenolics and CT. The extractability of the two tannins was small and increased in the order Qtz-Fh < Qtz-Gt < Qtz. For all mineral samples, TA was more extractable than CT. Bonding of tannins to the mineral samples and the partial peptisation of the Fe oxide coatings upon the binding resulted in complex tannin release curves. Our results suggest that the inextractability of tannins from natural soils and the absence of tannins in soil leachates might be caused by strong adsorption on soil minerals such as Qtz and Fe (oxy)(hydr)oxides. The results of competition experiments with mixtures of both tannins demonstrate that the CTs, and TA in particular, can release large amounts of Fe (oxides), suggesting that the tannins are excellent metal-mobilising agents. We therefore suggest that the fate of tannins in the mineral soil environment is highly dependent on the abundance of weakly bonded secondary oxides.
- Published
- 2005
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25. Human follicular dendritic cells: function, origin and development.
- Author
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van Nierop K and de Groot C
- Subjects
- Animals, Antigen Presentation, Autoimmune Diseases immunology, Autoimmune Diseases pathology, Germinal Center immunology, Humans, Dendritic Cells, Follicular immunology, Germinal Center cytology
- Abstract
Follicular dendritic cells (FDCs) have important functions in the selection of memory B lymphocytes during germinal center reactions (GCR). They present native antigens to potential memory cells, of which only B cells with high affinity B cell receptors (BCR) can bind. These B lymphocytes survive, whereas nonbinding B cells undergo apoptotic cell death. FDCs are present in follicles of any secondary lymphoid organ and belong to the stromal cells of these organs. Ectopic FDC-formation can be found in a number of autoimmune diseases and/or chronic inflammatory situations. This indicates that the development of FDCs is not restricted to secondary lymphoid organs, but that it is rather a matter of local conditions that drives a precursor cell type into FDC-maturation. A precursor of FDCs has presently not been identified, but phenotypic marker studies, in vitro experiments with fibroblast-like cell lines, and recent data on mesenchymal precursor cells from the peripheral blood suggest a close relation to fibroblast-like cells.
- Published
- 2002
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26. Ribosomal scanning on the highly structured insulin-like growth factor II-leader 1.
- Author
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van der Velden AW, van Nierop K, Voorma HO, and Thomas AA
- Subjects
- Animals, COS Cells, Genes, Reporter, Humans, Insulin-Like Growth Factor II metabolism, Nucleic Acid Conformation, Peptide Chain Initiation, Translational, 5' Untranslated Regions genetics, Insulin-Like Growth Factor II genetics, Ribosomes metabolism
- Abstract
The complex architecture of human insulin-like growth factor (IGF) II-leader 1 of 592 nucleotides (nt), with one open reading frame (ORF), and the potential to fold into stable structures makes efficient linear ribosomal scanning difficult to comprehend. Indeed, leader 1-driven reporter expression is low in rabbit reticulocyte lysate. Contrarily, leader 1 is very efficient in cells. Therefore, we tested whether this 5'UTR uses an alternative mechanism for translation initiation in vivo, internal entry or ribosomal shunting. Internal initiation was tested by introducing leader 1 into the intercistronic region of a bicistronic vector. Second cistron expression, driven by leader 1, was lower than by the intercistronic beta-globin 5'UTR, indicating that leader 1 does not contain an internal ribosomal entry site (IRES). Shunting was tested by inserting hairpin (HP) structures, capable of blocking ribosomal scanning, at eight positions in leader 1. After transfection, these mutant 5'UTRs were incapable of directing reporter expression. Less stable HPs at the same positions increased the activity to 50% of wild-type activity, indicating that insertions at these positions are not disastrous for initiation. These data indicate that the translational machinery encounters major parts of leader 1. As scanning seems unlikely, and internal entry and shunting were shown not to occur, we discuss a modified scanning mechanism for architecturally complex 5'UTRs.
- Published
- 2002
- Full Text
- View/download PDF
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