<p>Ово истраживање има за циљ да процени резерве органског угљеника у земљишту и представи његову просторну дистрибуцију у земљиштима Републике Србије, као и да утврди зависност садржаја органског угљеника у земљишту од типа земљишта, температуре, падавина, надморске висине, начина коришћења земљишта и морфогенетских карактеристика рељефа. Резерве органског угљеника у земљишту процењене су за слој 0-30 cm и 0-100 cm дубине на основу резултата из базе података уз коришћење педолошке карте и карте коришћења земљишта. За потребе утврђивања зависности садржаја органског угљеника и типа земљишта педолошка карта Србије је прилагођена WRB класификацији и садржи 15.437 полигона. Примењена методологија за процену резерве органског угљеника за дату дубину је базирана на сумирању резерве органског угљеника по слојевима земљишта која се добија на основу запреминске масе, вредности садржаја органског угљеника и дебљине слоја. Прорачун је урађен за сваки профил посебно, затим је урађена калкулација за сваку референтну групу земљишта на основу резултата средњих вредности садржаја органског угљеника до 30 cm и 100 cm дубине за главне референтне групе и њихових површина. На основу површина референтних група земљишта, површине Републике Србије и вредности садржаја за сваку референтну групу, добијене су укупне резерве органског угљеника до 30 cm дубине које износе 0,71 Pg. Резултати анализе резерве органског угљеника до 100 cm дубине показују вредност 1,16 Pg.<br />На основу Corine Land Cover (CLC) базе података за 2006. годину издвојене су површине главних категорија начина коришћења земљишта. На основу резултата средњих вредности садржаја органског угљеника до 30 и 100 cm дубине и површине коју заузима Corine Land Cover категорија начина коришћења земљишта израчуната је укупна вредност резерве органског угљеника за пољопривредна земљишта, шуме и полуприродна подручја и вештачке површине.<br />Резултати показују да су резерве органског угљеника у оквиру категорије пољопривредних површина 303,22 x 1012g (Tg) до 30 cm дубине и 600,25 x 1012g (Tg) до 100 cm дубине. Категорије шуме и полуприродна подручја имају резерве од основних климатских елемената температуре и падавина и надморске висине показује да постоји средње јака до јака статистичка зависност у оквиру испитивања реализованих до 30 и 100 cm дубине.</p><p>органског угљеника 345,26 x 1012g (Tg) угљеника до 30 cm и 457,55 x 1012g (Tg) до 100 cm дубине. Резултати показују вредности резерве органског угљеника у категорији вештачке површине која углавном обухватају локалитете у оквиру зелених урбаних подручја и рекреационих површина 19,21 x 1012g (Tg) до 30 cm и 41,50 x 1012g (Tg) до 100 cm дубине.<br />Анализа садржаја резерве органског угљеника према начину коришћења земљишта показује да су вредности садржаја органског угљеника веће у шумама и полуприродним подручјима у односу на пољопривредне површине и то за 40,71 % до 30 cm, односно за 11,43 % до 100 cm дубине. Прорачун губитка резерве органског угљеника у земљишту на подручјима где је извршена пренамена пољопривредних површина, шума и полуприродних подручја у урбано земљиште, без категорије зелена урбана подручја, у периоду 1990-2006. године показује укупну вредности од 0,92 Mt С, односно 1,49 Mt С за дубинe до 30 cm, односно до 100 cm.<br />Утврђивање статистичке зависности садржаја органског угљеника у земљиштуод основних климатских елемената температуре и падавина и надморске висине показује да постоји средње јака до јака статистичка зависност у оквиру испитивања реализованих до 30 и 100 cm дубине.</p><p>Прорачун садржаја резерве органског угљеника у земљишту у зависности од морфометријских карактеристика рељефа показујe да резерва садржаја органског угљеника у земљишту расте са порастом надморске висине. Највеће средње вредности садржаја измерене су на терену који обухвата планине са надморским висинама од 1.000-2.000 m и који обухвата 11,5 % територије Републике Србије</p> / <p>Ovo istraživanje ima za cilj da proceni rezerve organskog ugljenika u zemljištu i predstavi njegovu prostornu distribuciju u zemljištima Republike Srbije, kao i da utvrdi zavisnost sadržaja organskog ugljenika u zemljištu od tipa zemljišta, temperature, padavina, nadmorske visine, načina korišćenja zemljišta i morfogenetskih karakteristika reljefa. Rezerve organskog ugljenika u zemljištu procenjene su za sloj 0-30 cm i 0-100 cm dubine na osnovu rezultata iz baze podataka uz korišćenje pedološke karte i karte korišćenja zemljišta. Za potrebe utvrđivanja zavisnosti sadržaja organskog ugljenika i tipa zemljišta pedološka karta Srbije je prilagođena WRB klasifikaciji i sadrži 15.437 poligona. Primenjena metodologija za procenu rezerve organskog ugljenika za datu dubinu je bazirana na sumiranju rezerve organskog ugljenika po slojevima zemljišta koja se dobija na osnovu zapreminske mase, vrednosti sadržaja organskog ugljenika i debljine sloja. Proračun je urađen za svaki profil posebno, zatim je urađena kalkulacija za svaku referentnu grupu zemljišta na osnovu rezultata srednjih vrednosti sadržaja organskog ugljenika do 30 cm i 100 cm dubine za glavne referentne grupe i njihovih površina. Na osnovu površina referentnih grupa zemljišta, površine Republike Srbije i vrednosti sadržaja za svaku referentnu grupu, dobijene su ukupne rezerve organskog ugljenika do 30 cm dubine koje iznose 0,71 Pg. Rezultati analize rezerve organskog ugljenika do 100 cm dubine pokazuju vrednost 1,16 Pg.<br />Na osnovu Corine Land Cover (CLC) baze podataka za 2006. godinu izdvojene su površine glavnih kategorija načina korišćenja zemljišta. Na osnovu rezultata srednjih vrednosti sadržaja organskog ugljenika do 30 i 100 cm dubine i površine koju zauzima Corine Land Cover kategorija načina korišćenja zemljišta izračunata je ukupna vrednost rezerve organskog ugljenika za poljoprivredna zemljišta, šume i poluprirodna područja i veštačke površine.<br />Rezultati pokazuju da su rezerve organskog ugljenika u okviru kategorije poljoprivrednih površina 303,22 x 1012g (Tg) do 30 cm dubine i 600,25 x 1012g (Tg) do 100 cm dubine. Kategorije šume i poluprirodna područja imaju rezerve od osnovnih klimatskih elemenata temperature i padavina i nadmorske visine pokazuje da postoji srednje jaka do jaka statistička zavisnost u okviru ispitivanja realizovanih do 30 i 100 cm dubine.</p><p>organskog ugljenika 345,26 x 1012g (Tg) ugljenika do 30 cm i 457,55 x 1012g (Tg) do 100 cm dubine. Rezultati pokazuju vrednosti rezerve organskog ugljenika u kategoriji veštačke površine koja uglavnom obuhvataju lokalitete u okviru zelenih urbanih područja i rekreacionih površina 19,21 x 1012g (Tg) do 30 cm i 41,50 x 1012g (Tg) do 100 cm dubine.<br />Analiza sadržaja rezerve organskog ugljenika prema načinu korišćenja zemljišta pokazuje da su vrednosti sadržaja organskog ugljenika veće u šumama i poluprirodnim područjima u odnosu na poljoprivredne površine i to za 40,71 % do 30 cm, odnosno za 11,43 % do 100 cm dubine. Proračun gubitka rezerve organskog ugljenika u zemljištu na područjima gde je izvršena prenamena poljoprivrednih površina, šuma i poluprirodnih područja u urbano zemljište, bez kategorije zelena urbana područja, u periodu 1990-2006. godine pokazuje ukupnu vrednosti od 0,92 Mt S, odnosno 1,49 Mt S za dubine do 30 cm, odnosno do 100 cm.<br />Utvrđivanje statističke zavisnosti sadržaja organskog ugljenika u zemljištuod osnovnih klimatskih elemenata temperature i padavina i nadmorske visine pokazuje da postoji srednje jaka do jaka statistička zavisnost u okviru ispitivanja realizovanih do 30 i 100 cm dubine.</p><p>Proračun sadržaja rezerve organskog ugljenika u zemljištu u zavisnosti od morfometrijskih karakteristika reljefa pokazuje da rezerva sadržaja organskog ugljenika u zemljištu raste sa porastom nadmorske visine. Najveće srednje vrednosti sadržaja izmerene su na terenu koji obuhvata planine sa nadmorskim visinama od 1.000-2.000 m i koji obuhvata 11,5 % teritorije Republike Srbije</p> / <p>The aim of this study was to quantify current SOC stocks and present the spatial distribution of organic carbon (SOC) in the soils of Republic of Serbia. The relation of SOC content to soil type, temperature, precipitation, altitude, land use and topography was investigated. Organic carbon stocks were estimated for soil layers 0-30 cm and 0-100 cm based on the results from a database and using soil and land use maps.<br />To establish the relationship between organic carbon content and soil type, a soil map of Serbia was adapted to the WRB classification and divided into 15,437 polygons (map units). The methodology for SOC stocks estimation was based on bulk density, organic carbon content and thickness of the analyzed soil layers. We calculated the values for each reference soil group based on mean values of SOC at 0-30 and 0-100 cm in the main reference groups and their areas. Based on the size of the reference groups, total area of Republic of Serbia, and the SOC values for each reference group, we calculated the total SOC stocks. The obtained values for the soil layers 0-30 cm and 0-100 cm amounted to 0,71 Pg and 1,16 Pg respectively.<br />Using Corine Land Cover (CLC) database for 2006, we defined areas of the major categories of land use. Based on the obtained mean values of organic carbon content at 0-30 and 0-100 cm and the areas indicated by Corine Land Cover categories of land use, we calculated the organic carbon stocks in agricultural land, forest land, semi-natural areas, and artificial areas. The results showed that the organic carbon stocks in the category of agricultural land were 303.22 x 1012 g (Tg) and 600.25 x 1012 g (Tg) at 0-30 cm and 0-100 cm, respectively. In the category of forests and semi-natural areas, the organic carbon stocks were 345.26 x 1012 g (Tg) and 457.55 x 1012 g (Tg) at 0-30 cm and 0-100 cm, respectively. In the category of artificial areas, which mainly included sites within urban green areas and recreational areas, the organic carbon stocks were 19.21 x 1012 g (Tg) and 41.50 x 1012 g (Tg) at 0-30 cm and 0-100 cm, respectively. The map of organic carbon distribution depending on land use method indicated that organic carbon stocks were higher in forests and semi-natural areas than in agricultural land, up to 40.71% and 11.43% at 0-30 cm and 0-100 cm, respectively.<br />SOC loss amount to 0,92 Mt С at 0-30 cm layer and 1,49 Mt С at 0-100 cm layer in the period 1990-2006 as a results of conversion from agricultural land, forestland and semi-natural areas to artificial areas.<br />For soil layers 0-30 and 0-100 cm, a medium to strong statistical relationship between temperature, precipitation and altitude and amount of organic carbon in soil is indicated. The soil organic carbon density was significantly affected by altitude. SOC content increased with increasing altitude.<br />The highest mean values of organic carbon content were found in the mountainous areas within the elevation of 1000-2000 m, which covers 11,5 % of the territory of the Republic of Serbia.</p>

Le recyclage des résidus organiques (RO) en agriculture pourrait permettre de limiter l’utilisation des ressources minérales de phosphore (P), à condition de déterminer leur efficacité pour fournir du P aux cultures. L’objectif de ce travail était donc d’étudier les mécanismes déterminant l’effet des RO apportés au sol sur la biodisponibilité du P pour la plante (phytodisponibilité). Ce travail a été basé sur cinq essais de terrain à La Réunion, fertilisés sur une décennie avec des fertilisants organiques ou minéraux, et sur des expérimentations d’incubations en conditions contrôlées et de cultures de plantes en pot. Le P inorganique (Pi) et organique (Po) disponible du sol a été déterminé par des extractions (eau, Olsen), la technique des diffusive gradients in thin films (DGT) et la dilution isotopique associée à des membranes échangeuses d’ions. La capacité de sorption en Pi des sols a été évaluée avec des courbes de sorption. Le P phytodisponible a été déterminé en mesurant le P prélevé par la plante. Dans les différents types de sol (andosol, andique cambisol, nitisol et arenosol), l’apport de RO a augmenté le Pi disponible relativement au Po, suggérant que la minéralisation du Po issu des RO n’est pas un facteur limitant la disponibilité du Pi. Les RO ont augmenté le Pi disponible principalement par l’augmentation du pH du sol et par conséquent la diminution de sa capacité de sorption de Pi. Le P phytodisponible a augmenté avec le Pi disponible du sol, mais a diminué avec l’augmentation du pH du sol. Au-delà de la dose de P, l’effet de l’apport de RO à long-terme sur la phytodisponibilité du P semble principalement contrôlé par l’évolution induite du pH du sol. / Application of organic residues (OR) on agricultural soils could reduce the use of mineral phosphorus (P) fertilizers, but this implies to determine the efficiency of OR to meet crop requirements. We thus aimed to study mechanisms determining the effects of OR on P bioavailability to plants (phytoavailability). Our work was based on five field trials with decadal organic or mineral fertilization located in Réunion island, and on incubations and plant growth experiments under controlled conditions. Available inorganic P (Pi) and organic P (Po) was determined using extractions (water, Olsen), the diffusive gradients in thin films technique (DGT) and the isotopic dilution associated to anion exchange membranes (EAEM). Phytoavailable P was determined as the plant P uptake. Soil Pi sorption capacity was determined using sorption curves. For all soil types studied (andosol, andic cambisol, nitisol, and arenosol), RO increased mainly available Pi and had few effects on available Po, which suggests that mineralization of Po applied with RO does not limit Pi availability. Application of RO increased available Pi mainly by increasing soil pH and consequently by decreasing soil Pi sorption capacity. Phytoavailable P increased with soil available Pi, but decreased with increasing soil pH. Our work suggests that except the dose of P applied, effect of RO on P phytoavailability depends mainly on soil pH changes induced.

Ziel der Arbeit ist die Gesamtbilanzierung der Treibhausgasemissionen eines Anbausystems unter Bewässerung auf einem Sandboden. Die dazu aufgestellte Treibhausgasbilanz basiert auf langjährigen Datenreihen zu Erträgen und Corg-Vorräten eines Dauerfeldversuchs sowie auf zweijährigen im Feldversuch durchgeführten N2O-Messungen. Die durchgeführten Untersuchungen zum Einfluss der Bewässerung auf die Corg-Vorräte zeigen, dass der Einsatz von mineralischem Stickstoffdünger und Bewässerung auf einem leichten Standort unter den klimatischen Bedingungen Nord-Ost-Deutschlands positive Effekte hat. Die N2O-Emissionen eines Sandbodens unter den klimatischen Bedingungen Brandenburgs sind sehr niedrig. Die Applikation von mineralischem Stickstoffdünger hat nur schwache und Bewässerung hat aufgrund der der hohen Bodendurchlüftung des Sandbodens keine Effekte auf die Höhe der N2O-Emissionen. Die direkten und indirekten Emissionen aus dem Maschinen- und Betriebsmitteleinsatz erhöhen sich bei Bewässerung und steigender Stickstoffdüngung deutlich. Bei den indirekten Treibhausgasemissionen nehmen die Emissionen der Herstellung des mineralischen Stickstoffdüngers einen bedeutenden Anteil der Gesamttreibhausgasemissionen ein. Bewässerung führt durch den erhöhten Dieselverbrauch hauptsächlich zu einer Erhöhung der direkten Emissionen. Unter Bewässerung kann jedoch ein Teil der Emissionen durch zunehmende Corg-Vorräte kompensiert werden. Somit sind in einigen Fällen die Gesamttreibhausgasemissionen pro Hektar bei Bewässerung geringer als ohne Bewässerung. Die aus Stickstoffdüngung und Bewässerung resultierenden Ertragserhöhungen führen dazu, dass die Gesamttreibhausgasemissionen bezogen auf die Ertragseinheit in den meisten bewässerten Varianten deutlich geringer sind als in den unbewässerten. Daraus lässt sich ableiten, dass Bewässerung auf einem Sandboden zu einer Verminderung der Treibhausgasemissionen beitragen kann. / The aim of this work is the estimation of the net greenhouse gas emissions by a greenhouse balance for an irrigated cropping system on a sandy soil in north-east Germany under various nitrogen fertilizer intensities. The balances are based on data of yields and SOC stocks of an irrigated long term field experiment as well as on results of N2O-measurements over two years. The results of the analysis of the long term response of irrigation and nitrogen fertilization have shown that irrigation and mineral nitrogen fertilization led to significant increases in yields and harvest residues. The increased carbon inputs from above ground harvest residues had positive effects on the SOC stocks. The results of N2O measurements indicated that N2O emissions from a sandy soil are very low. Mineral nitrogen fertilization had only marginal effects. Irrigation showed no effects on the amount of N2O emissions. On the one hand the analysis of the prepared greenhouse gas balances showed that irrigation and increased nitrogen fertilization lead to a strong increase of direct and indirect emissions from machinery and maintenance resource use. The indirect emissions of nitrogen fertilizer production took up a main part of the net greenhouse gas emissions. Irrigation mainly increased greenhouse gas emissions of fuel use and fuel production as well as the emissions of the machinery production. On the other hand the increasing SOC stocks especially in the fertilized variants under irrigation led to a compensation of a huge part of the additional emissions. Thus, in many cases the net greenhouse gas emissions per unit area was lower under irrigation. Due to the increased yields under irrigation the net greenhouse gas emissions per unit yield were lower than that under non-irrigated conditions.

The primary objective of this study was to evaluate the rates of nitrate removal for a nitrate containing, low organic carbon wastewater interacting with four different carbon-containing solid substrates (alder woodchips, corn silage, manure and woodchip biochar). Batch systems were tested for nitrate removal, and systems with a combination of three carbon substrates (75% woodchips, 12.5% silage, and 12.5% manure or woodchip biochar by mass) produced average nitrate removal rates of 571 and 275 mg-N L⁻¹ D⁻¹, and systems containing the carbon substrates individually produced rates between 11.4 - 3.3 mg-N L⁻¹ D⁻¹. Silage proved to be the dominant carbon substrate providing high quantities of organic carbon to fuel denitrification. With the introduction of semi-continuous flow, all systems had nitrate removal rates that converged to 13.3 – 6.4 mg-N L⁻¹ D⁻¹, which is approximately two orders of magnitude smaller than the rates of the mixture systems in the batch experiment. Silage appeared to be removed from of the systems with liquid exchange potentially causing the rate decreases. Columns filled with various volume fractions of woodchips (100%, 25%, 12.5%, and 0%) produced nitrate removal rates between 30.8 – 2.4 mg-N L⁻¹ D⁻¹ at a 24 hour and 12 hour hydraulic residence time (HRT). Greater nitrate removal was achieved with higher HRTs and larger fractions of woodchips (the 100% woodchip system at a 24 hour HRT produced the fastest nitrate removal rate of 30.8 mg-N L⁻¹ D⁻¹). When rates were normalized to the amount of woodchips in each column, higher efficiency was found in lower woodchip fraction systems (the 12.5% woodchip column produced the highest normalized nitrate removal rate of 56 mg-N L⁻¹ D⁻¹ L[subscript woodchips]⁻¹). Woodchips proved to be best suited as a long term carbon substrate for nitrate removal in a system containing a nitrate concentrated, low organic carbon wastewater. However, large amounts of woodchips were necessary to achieve nitrate removal greater than 50%. A 41 acre hypothetical wetland with a 3.3 day HRT and a nitrate influent concentration of 45 mg-N L⁻¹ would require 30,000 yd³ of woodchips to achieve 68% nitrate removal based on the values obtained in the bench scale column experiment. / Graduation date: 2012

La comunitat bentònica dels ecosistemes fluvials processa una gran quantitat de la matèria orgànica que arriba als rius. L'origen de les entrades de material (autòctones o al·lòctones), la seva composició química i la seva quantitat (freqüència de les entrades i concentració assolida en el riu), determinen l'estructura de la comunitat bentònica autotròfica i heterotròfica, les seves relacions tròfiques i les seves interaccions potencials (competència, sinergisme). L'objectiu d'aquesta tesi és posar de manifest la utilització de la matèria orgànica dissolta (MOD) per part dels biofilms bacterians bentònics fluvials i determinar l'eficiència del sistema fluvial en l'ús dels diferents materials que hi circulen. Amb aquesta finalitat s'han portat a terme diversos experiments, tant de camp com de laboratori, per tal de conèixer els efectes de la disponibilitat de la matèria orgànica (quantitat) i la seva qualitat (composició química i biodegradabilitat) i els efectes deguts a l'augment de temperatura de l'aigua del riu. / The benthic community in river ecosystems processes a large amount of organic matter entering the river. The input sources (autochthonous and allochthonous) as well as their chemical composition and amount (frequency of inputs and concentrations reaching the river), determine the structure of the autotrophic and heterotrophic benthic community, their trophic relationships and their potential interactions (competition, synergism). The aim of this thesis is to elucidate the use of dissolved organic matter (DOM) by the benthic stream microbial biofilms and determine the efficiency of the fluvial system in the use of the different materials that circulate through it. Different experiments were developed in the field and others in laboratory conditions to control the respective effects of organic matter availability (quantity) and quality (chemical composition and lability), as well as the effects of increasing river water temperature.

Characterization and Source Apportionment of Ambient PM2.5 in Atlanta, Georgia: On-Road Emission, Biomass Burning and SOA Impact Bo Yan 260 Pages Directed by Drs. Armistead G. Russell and Mei Zheng Various airborne PM2.5 samples were collected in the metropolitan Atlanta and surrounding areas, which are directly impacted or dominated by on-road mobile and other typical urban emissions, regional transport sources, prescribed burning plumes, wildfire plumes, as well as secondary sources with anthropogenic and biogenic nature in origin. Detailed PM2.5 chemical speciation was conducted including over one hundred of GC/MS-quantified organic compounds, organic carbon (OC), water-soluble organic carbon (WSOC), elemental carbon (EC), ionic species, and tens of trace metals. Day-night, seasonal and spatial variations of PM2.5 characterization were also studied. Contributions of PM2.5 major sources were identified quantitatively through the receptor source apportionment models. These modeling results, especially on-road mobile source contributions and secondary organic carbon (SOC) were assessed by multiple approaches. Furthermore, new season- and location-specific source profiles were developed in this research to reflect real-world and representative local emission characterizations of on-road mobile sources, aged prescribed burning plumes, and wildfire plumes. Secondary organic aerosol (SOA), a major component of PM2.5 in the summer, was also explored for sources and contributions.

Concentrations of dissolved organic carbon (DOC) measured within water bodies have been increasing on a global scale over the last two decades. Changes in temperature and rainfall have been shown to increase the production and export of DOC from catchments with peat soils in the UK (Freeman et al., 2001). However it is not clear whether increases in DOC concentrations are caused by production increases induced by temperature changes or by a greater incidence of high flows induced by rainfall changes. Increases in both temperature and rainfall have been predicted in Scotland over the next few decades (Kerr et al., 1999) which may further increase current DOC concentrations and exports. The implications of this include both a decrease in water quality and an increase in mobility of metals in upland water bodies. The overall aim of the thesis is to determine if the relationship between dissolved organic carbon (DOC) concentrations and discharge has changed over a 20 year period in small stream catchments in Scotland, in order to better understand the role of hydrology, in driving changes in DOC concentration. To achieve this streams draining two coniferous forest sites and one moorland site were monitored intensively between June 2004 and February 2006. Analysis of the relationship between DOC and discharge, within the catchments, identified the importance of the amount of precipitation falling on the catchment, antecedent precipitation and season, on the concentration of DOC that was measured within the stream. Models were then developed using variables to represent these drivers in terms of both the production (seasonal sine values and 14 day average temperatures) and movement (log of discharge (log Q), days since previous storm event and rising or falling stage) of DOC. In the Ochil Hills catchment, the best predictive model, used 4 hour average discharge and 1 day average 30cm soil temperatures (R2= 0.88). In the Duchray and Elrig catchments, the best predictive models produced used discharge and seasonal sine values; the strength of the model was greater in the Elrig (R2= 0.80) than the Duchray (R2= 0.48) catchment. The strength of the regression models produced highlighted the importance of precipitation in the movement of DOC to the stream and temperature variables representing production in the surrounding catchment. To determine if dissolved organic carbon (DOC) concentrations had changed within the three study catchments, since previous research was conducted at the same sites in the early 1980s and 1990s (Grieve, 1984a; Grieve, 1994), then regression analysis conducted in the previous research was repeated, so changes in the DOC and discharge relationship could be identified. Analysis of the Ochil Hills regression equations identified higher log of discharge and lower temperature and seasonal sine values in the present study (2004-06), when compared to the previous study (1982-83). This suggests that more DOC is now available for movement from the soil, and that the difference between winter and summer DOC production has decreased, potentially because of increasing temperatures. This would explain the limited increase in DOC concentration within the Ochil Hills stream. In the Duchray and Elrig streams, a large increase in DOC was identified at all discharges when all the models produced were compared between the two sampling periods (1989-90 and 2004-06). The increasing trend in DOC concentrations is too large to have been produced by change in temperature alone and it is suggested that the measured reduction in acidic deposition has resulted in the increased DOC concentrations measured in the Duchray and Elrig. The results from this research have identified that concentrations of DOC have increased in Scottish streams over the last 20 years and that the increases in DOC have been induced, potentially by temperature changes in climate. However, changes in temperature are not the only driver of this change as the reduction in acidic deposition is potentially more important, specifically in areas with base poor geology such as the Duchray and Elrig catchments.

During the last three decades, a number of studies based on national environmental monitoring data have found increased concentrations of total organic carbon (TOC) in surface waters in much of the northern hemisphere including Sweden. There are many hypothesis of what has been the main cause of this trend, including changes in land use, decreased atmospheric deposition of acidifying compounds and climate change. Different hypothesis may have different implications for quantifying pre-industrial levels and for future predictions of TOC concentrations, which in turn will have different implications for water classification according to the European Water Framework Directive, water management and drinking water treatment. To analyse the long term effects of industrialisation and climate change on TOC in surface waters there is a need for long term time series of data. Since environmental monitoring data in Sweden only extends back to the mid-1980s, other techniques must be used in order to reconstruct data. In this study, sediment cores from 17 lakes along a climatic and deposition gradient in Sweden were collected and analysed with visible near infrared spectroscopy (VNIRS), an analytical technique that makes it possible to reconstruct historic surface water concentrations of TOC to pre-industrial conditions. A previous study with VNIRS showed that TOC concentrations declined in response to sulfate deposition until peak sulfur deposition in 1980, and thereafter increased as a result of sharp reductions of sulfate emissions. It was noted that the rate of increase of TOC after 1980 was faster than the rate of decrease due to sulfate deposition before 1980. The purpose of this study was therefore to explore the hypothesis that increasing TOC concentrations have not only been due to recovery from acidification, but also due to changes in climate. It was possible to analyse the long term effects of industrialisation and climate change on surface water TOC by analysing the reconstructed TOC data together with climate data from the beginning of the 1900s, modelled data of atmospheric sulfate deposition and environmental monitoring data, with uni- and multivariate analysis methods. It was found that the recent increase in TOC concentrations could be explained by both decreases in acidifying atmospheric deposition and increased precipitation, while temperature may have a decreasing effect on TOC. It was also found that the rate of increase of TOC-concentrations has been faster in the colder northern parts of Sweden and slower in the warmer south. The results imply that TOC concentrations will continue to rise to unpreceded levels and should be of concern for drinking water treatment plants that will need to adapt their treatment processes in the future. / Under de senaste tre årtiondena har ett flertal studier baserade på data från nationella miljöövervakningsprogram rapporterat ökande koncentrationer av organiskt kol (TOC) i ytvatten på norra halvklotet inklusive Sverige. Det finns många hypoteser om vad som ligger bakom trenden, till exempel förändringar i markanvändning, minskad atmosfärisk deposition av försurande ämnen och klimatförändringar. Olika förklaringar till vad som ligger bakom den ökande trenden ger konsekvenser vid kvantifiering av förindustriella nivåer och för förutsägelser om framtida koncentrationer, vilket i sin tur ger konsekvenser för vattenklassificering enligt Ramvattendirektivet, vattenförvaltning och dricksvattenberedning. För att kunna analysera de långsiktiga effekterna av industrialisering och klimatförändringar på TOC i ytvatten behövs långa tidsserier av data. Då den svenska miljöövervakningen endast sträcker sig tillbaka till mitten av 1980-talet måste andra tekniker användas för att rekonstruera data. I den här studien har sedimentproppar från 17 sjöar längs en klimat- och depositionsgradient analyserats med visible near infrared spektroskopi (VNIRS), en analysteknik som gör det möjligt att rekonstruera TOC-koncentrationer i ytvatten till förindustriell tid. En tidigare studie med VNIRS visade att TOC-koncentrationer sjönk till följd av försurande nedfall fram till 1980 då nedfallet kraftigt minskade, varefter koncentrationer av TOC började öka. Det noterades i studien att ökningen av TOC efter 1980 varit snabbare än vad minskningen var före 1980 på grund av försurande nedfall. Syftet med den här studien var därför att undersöka hypotesen att den senaste tidens ökning av TOC inte bara berott på minskat nedfall av försurande ämnen, utan även på grund av klimatförändringar. Det var möjligt att undersöka de långsiktiga effekterna av industrialisering och klimatförändringar på TOC i ytvatten genom att analysera rekonstruerad TOC data, klimatdata från början av 1900-talet, modellerad sulfatdepositionsdata och miljöövervakningsdata med uni- och multivariata analysmetoder. Resultaten visade att den senaste tidens ökning av TOC kunde förklaras med både en minskande deposition av försurande ämnen och en ökad nederbörd, medan ökande temperaturer kan ha haft en minskande effekt på TOC. Resultaten visade även att förändringshastigheten av TOC-koncentrationer varit snabbare i de norra, kalla delarna av Sverige och långsammare i de varmare södra. Resultaten indikerar att koncentrationer av TOC kommer att öka till nivåer som aldrig tidigare skådats, vilket är något vattenreningsverk kommer att behöva anpassa sina reningsmetoder till i framtiden.

L'obiettivo della ricerca è stato quello di identificare la coltura bioenergetica con il maggior potenziale di sequestro del carbonio (C); sono state considerate tre colture perenni arboree (pioppo, robinia e salice) e tre colture erbacee perenni (canna comune , miscanto e panico ) al sesto anno dal loro impianto e coltivate nello stesso ambiente. In primo luogo sono state misurate le variazioni dei tassi del C organico del suolo (COS) per il primo 1 m, mentre per i primi 30 cm di suolo è stato stimato il grado di stabilita del COS valutando sette frazioni di COS che presentano differenti gradi di stabilizzazione; in secondo luogo, sono stati caratterizzati gli apparati radicali delle sei specie per la stessa profondità di suolo, per valutare dove le specie accumulano la biomassa radicale lungo il profilo di suolo. I risultati confermano che l’impianto di colture bioenergetiche perenni su superfici precedentemente dedite a colture annuali gestite convenzionalmente rappresenta una opzione valida per sequestrare C nel soulo. Tuttavia, è stata osservata una diversa capacità di sequestro di C tra specie arboree ed erbacee: le specie arboree hanno dimostrato aumentre il contenuto di COS nel primo strato di suolo ( 0-10 cm di suolo), ma la loro capacità di allocare biomassa radicale negli strati profondi del suolo è limitata; mentre, la specie erbacee allocano un’alta quantità di biomassa radicale negli strati profondi del suolo, ma solo il panico ed il miscanto hanno aumentato il contenuto di C nel primo strato di suolo. / The objective of the present research was to identify the bioenergy crop with the greatest carbon sequestration potential among three perennial woody crops (poplar, black locust and willow) and three perennial herbaceous crops (giant reed, miscanthus and switchgrass) at the sixth year from plantation and in the same location. First of all the SOC stock variations for the first 1 m soil depth and the quantification of seven soil C fractions related to SOC stabilization level of the first 30 cm of soil were assessed; secondly, a characterization of the root system and the traits which affect the carbon allocation in soil were considered. The results confirm that the establishment of perennial bioenergy crops in previous arable fields can be a suitable option to sequester carbon (C) belowground. However, a different C sequestration capacity was observed between woody and herbaceous crops: woody species showed the greatest SOC sequestration potential in the first soil layer (0-10 cm of soil) but their ability to allocate root biomass in the deeper soil layers was limited; while, the herbaceous species allocated a high amount of root biomass in the deeper soil layers, but only switchgrass and miscanthus sequester C in the first soil layer.

Les projections concernant les changements climatiques dans les régions arctiques annoncent une augmentation disproportionnée des températures de surface pouvant influencer le cycle hydrologique et la fonte des pergélisols. Les hautes latitudes sont donc perçu comme des environnements potentiellement très sensibles aux modifications du climat. Ces modifications ont la capacité d’impacter les cycles biogéochimiques, en particulier la mobilisation du carbone vers les milieux aquatiques de la zone arctique. Dans les rivières arctiques, la période la plus importante du cycle hydrologique est la crue de printemps qui peut réaliser la majeure partie des transferts annuels de carbone organique vers l’océan dans un lapse de temps très court. L’objectif de cette thèse vise à suivre la dynamique des MOD en termes de quantité et de qualité au cours du cycle hydrologique du fleuve Ienisei, grâce à diverses techniques de caractérisation des MOD permettant de mettre en évidence les variations saisonniéres de leur composition, sources, âge et état de dégradation. La première étape a été d’examiner la large gamme de techniques de caractérisation des MOD dans les rivières du monde afin d’identifier les plus répendues,pértinentes et fiables. Grâce au développement d’une base de données des mesures des qualités des MOD, nous avons pu évaluer la couverture géographique des études de caractérisation des MOD, donner des estimations et gamme de valeurs des principales variables de caractérisation des MOD et observer des tendances générales des qualités des MOD selon un gradient latitudinal. La seconde étape a porté sur l’étude de la dynamique du COD dans le fleuve Ienisei concernant les variations de concentrations et les liens avec la chimie de l’eau et l’hydrologie. Nous avons mené des campagnes d’échantillonnage durant trois années consécutives (2014 à 2016), en couvrant avec une haute fréquence de prélèvement la période de la crue de printemps afin d’en capturer la dynamique rapide. Nous avons observé des concentrations en COD qui suivent l’hydrogramme avec les concentrations maximales mesurées quelques jours avant le pic de crue. Le COD a aussi répondu aux variations de débit (augmentation, probablement liée à des précipitations plus intenses du début d’automne. Nous avons enregistré un flux de COD moyen, durant les trois années de prélèvement, d’environ 4,53 Tg yr-1, ce qui est dans l’ordre de grandeur rapporté dans la littérature. Nous avons également observe ue variabilité interannuelle relativement importante avec les estimations d’exports annuels variant de 5,45 Tg yr-1 en 2014 à 3,57 Tg yr-1 en 2016, certainement influence par l’amplitude de débit. Nous avons confirmé le rôle prédominant de la crue de printemps dans les exports de COD avec en moyenne plus de 65% des exportations ayant lieu Durant cette période (approximatvement mai/juin). Le troisième point a consisté en l’étude de la qualité des MOD présentent dans les eaux du Ienisei et de son évolution durant le cycle hydrologique en combinant différentes outils de caractérisation. Associer les modes de caractérisation aide à renforcer les observations et à valider les interprétations. La plus part des variables mesurées avec les différentes techniques se sont confirmées les unes les autres. L’utilisation des biomarqueurs de la lignine, des propriétés optiques et de la datation 14C ont permis de tracer les sources prédominantes des MOD comme étant principalement dérivées de matières organiques récemment produites lixiviée depuis les litières forestières boréales et des horizons supèrieures pendant la crue de printemps et de matières organiques plus anciennes provenant des horizons plus profonds durant la période des basses eaux. / Arctic regions are expected to be highly sensitive to climate change regarding the prediction of disproportionately large increases in surface temperatures and their related influence over the hydrological cycle and permafrost thaw. These modifications have the potential to impact biogeochemical cycles in these regions and in particular the mobilization of organic carbon into rivers. The most crucial period in arctic rivers hydrological cycle is the spring freshet that can account for most of the annual organic carbon transfers to the ocean in a very short window of time. The focus of this thesis was to monitor the dynamic of DOM in terms of quantity and quality along the hydrological cycle of the Yenisei river, through DOM characterization approaches to reveal seasonal variations in its composition, sources, age and degradation state. The first step was to make a review of the full range of existing DOM characterization approaches in worldwide river systems to identify the most widely used, the most relevant and reliable ones. Through the development of a DOM quality measurements database, we have been able to evaluate the geographical coverage of DOM characterization studies, to give estimates and ranges of values of the main reported DOM characterization variables and to observe global trends of DOM quality across latitudinal gradient. Second stage was to investigate DOC dynamic in the Yenisei river with regard to quantity and links with water chemistry and hydrology. We conducted sampling campaigns during three consecutive years (2014 to 2016), covering with a high sampling frequency the spring flood period to capture its very dynamic evolution. We reported DOC concentrations that followed the hydrograph with highest concentrations observed a few days before peak discharge. DOC concentration also responded to discharge variation (increase, likely due to higher precipitation) in early autumn. We reported average DOC flux over the three sampling years of about 4.53 Tg yr-1 which is within the range of values reported in the literature. We observed interannual variability with annual export estimates ranging from 5.45 Tg yr-1 in 2014 to 3.57 Tg yr-1 in 2016, likely driven by discharge amplitude. We confirmed the important role of spring freshet in DOC export with on average more than 65% occurring during this period (roughly May/June). Third point was to determine DOM quality combining characterization techniques. Combination of approaches helped to strengthen observations and cross validate interpretations. Most of the variables reported from the different characterization techniques confirmed one each other. The use of lignin biomarkers, optical properties and radiocarbon age of DOM allowed us to trace DOM main sources has primarily deriving from recently produced organic matter leached from boreal forest litter and top soil horizon during the spring flood and older organic matter derived from deeper soil horizons during low flow period.