This dissertation examines Moche (A.D. 300-900) sociopolitical organization in northern Peru at the previously unexplored site of Licapa II, a mid-sized ceremonial center in the Chicama Valley. Moche’s distinct archaeological signatures, chiefly, ceramics and architecture, have long been seen as emblematic of an ethnic and political reality and defined as evidence for the first South American state although recent scholarship has begun to view Moche as a more complex mosaic of interacting settlements across a landscape. My research at Licapa II is the first study of a site of its size and kind, thus constituting a novel contribution to the paradigm shift in Moche research. My excavations, surface collections, and geophysical surveys contributed to understanding the nature of the site and the activities performed there. Licapa II consists of two pyramids (huacas), a canal, and other buildings. I show that the two major structures, Huaca A and Huaca B, are characterized by different material culture, are different in form, and date to different time periods. Huaca A has local ceramics and was mainly used before A.D. 600. Huaca B has Moche IV and V style ceramics and was in use after A.D. 600. Based on my evaluation of radiocarbon dates, the changes in buildings and ceramics seen at Licapa II around A.D. 600 also occurred throughout the Moche world and included the adoption of Moche IV ceramics and soon after, in some places, Moche V. I also show that the Moche V style likely originated in the northern Chicama Valley and spread from there circa A.D. 650. I also argue that political organization in Moche times may have been similar to colonial era organization, based on nested moieties organized around the irrigation system. Overall, in this dissertation I demonstrate that Licapa II was an independent center intimately connected to a dynamic landscape of interconnected nodes in an ever- changing and complex network of sites. Simplistic models based on the concept of large Moche states thus should be discarded. / Anthropology

Permafrost soils in the Arctic store large quantities of organic matter, roughly twice the amount of carbon that was present in the atmosphere before the industrial revolution. This freeze-locked carbon pool is susceptible to thawing caused by amplified global warming at high latitudes. The remobilization of old permafrost carbon facilitates its degradation to carbon dioxide and methane, thereby providing a positive feedback to climate change. Accelerating coastal erosion in addition to projected rising river discharge with enhancing sediment loads are anticipated to transport increasing amounts of land-derived organic carbon (OC) to the Arctic Ocean. On its shallow continental shelves, this material may be remineralized in the water column or in the sediments, transported without being altered off shelf towards the deep sea of the Arctic Interior or buried in marine sediments and hence sequestered from the contemporary carbon cycle. The fate of terrigenous material in the marine environment, though offering potentially important mechanisms to either strengthen or attenuate the permafrost-carbon climate feedback, is so far insufficiently understood. In this doctoral thesis, sediments from the wide East Siberian Arctic Shelf, the world’s largest shelf-sea system, were used to investigate some of the key processes for OC cycling. A range of bulk sediment properties, carbon isotopes and molecular markers were employed to elucidate the relative importance of different organic matter sources, the role of cross-shelf transport and the relevance of degradation during transport and after burial. Overall, OC released from thawing permafrost constitutes a significant proportion of the sedimentary organic matter on the East Siberian Arctic Shelf. Two sediment cores from the inner and outer East Siberian Sea recorded no substantial changes in source material or clear trends in degradation status for the last century. With increasing distance from the coast, however, strong gradients were detected towards lower concentrations of increasingly reworked land-derived OC. The time spent during cross-shelf transport was consequently found to exert first-order control on degradation. Compound-specific radiocarbon dating on terrigenous biomarkers revealed a net transport time of ~4 000 years across the 600 km wide Laptev Sea shelf, yielding degradation rate constants for bulk terrigenous OC and specific biomarkers on the order of 2-4 kyr-1. From these results, the carbon flux released by degradation of terrigenous OC in surface sediments was estimated to be ~1.7 Gg yr-1, several orders of magnitude lower than what had been quantified earlier for dissolved and particulate OC in the water column. Lower oxygen availability and close associations with the mineral matrix may protect sedimentary OC from remineralization and thereby weaken the permafrost-carbon feedback to present climate change. / <p>At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Submitted. Paper 4: Manuscript.</p>

<p>Wood combustion is mainly used in cold regions as a primary or supplemental space heating source in residential areas. In several industrialized countries, there is a renewed interest in residential wood combustion (RWC) as an alternative to fossil fuel and nuclear power consumption. The main objective of this thesis was to investigate the impact of RWC on the air quality in urban areas. To this end, a field campaign was conducted in Northern Sweden during wintertime to characterize atmospheric aerosol particles and polycyclic aromatic hydrocarbons (PAH) and to determine their source apportionment.</p><p>A large day-to-day and hour-to-hour variability in aerosol concentrations was observed during the intensive field campaign. On average, total carbon contributed a substantial fraction of PM10 mass concentrations (46%) and aerosol particles were mostly in the fine fraction (PM1 accounted for 76% of PM10). Evening aerosol concentrations were significantly higher on weekends than on weekdays which could be associated to the use of wood burning for recreational purposes or higher space heat demand when inhabitants spend longer time at home. It has been shown that continuous aerosol particle number size distribution measurements successfully provided source apportionment of atmospheric aerosol with high temporal resolution. The first compound-specific radiocarbon analysis (CSRA) of atmospheric PAH demonstrated its potential to provide quantitative information on the RWC contribution to individual PAH. RWC accounted for a large fraction of particle number concentrations in the size range 25-606 nm (44-57%), PM10 (36-82%), PM1 (31-83%), light-absorbing carbon (40-76%) and individual PAH (71-87%) mass concentrations.</p><p>These studies have demonstrated that the impact of RWC on air quality in an urban location can be very important and largely exceed the contribution of vehicle emissions during winter, particularly under very stable atmospheric conditions.</p>

Wood combustion is mainly used in cold regions as a primary or supplemental space heating source in residential areas. In several industrialized countries, there is a renewed interest in residential wood combustion (RWC) as an alternative to fossil fuel and nuclear power consumption. The main objective of this thesis was to investigate the impact of RWC on the air quality in urban areas. To this end, a field campaign was conducted in Northern Sweden during wintertime to characterize atmospheric aerosol particles and polycyclic aromatic hydrocarbons (PAH) and to determine their source apportionment. A large day-to-day and hour-to-hour variability in aerosol concentrations was observed during the intensive field campaign. On average, total carbon contributed a substantial fraction of PM10 mass concentrations (46%) and aerosol particles were mostly in the fine fraction (PM1 accounted for 76% of PM10). Evening aerosol concentrations were significantly higher on weekends than on weekdays which could be associated to the use of wood burning for recreational purposes or higher space heat demand when inhabitants spend longer time at home. It has been shown that continuous aerosol particle number size distribution measurements successfully provided source apportionment of atmospheric aerosol with high temporal resolution. The first compound-specific radiocarbon analysis (CSRA) of atmospheric PAH demonstrated its potential to provide quantitative information on the RWC contribution to individual PAH. RWC accounted for a large fraction of particle number concentrations in the size range 25-606 nm (44-57%), PM10 (36-82%), PM1 (31-83%), light-absorbing carbon (40-76%) and individual PAH (71-87%) mass concentrations. These studies have demonstrated that the impact of RWC on air quality in an urban location can be very important and largely exceed the contribution of vehicle emissions during winter, particularly under very stable atmospheric conditions.

La connaissance des principales sources de l’aérosol permet d’améliorer, d’adapter et de cibler les mesures prises pour réduire les concentrations de particules fines. Ainsi, l’identification et la hiérarchisation des sources de particules fines sont des étapes essentielles à la mise en place d'une politique efficace d'amélioration de la qualité de l'air. Le travail mené durant cette thèse s’inscrit dans cette démarche puisqu'il avait pour objectif de quantifier les sources de PM2.5 en milieu industriel. Afin de répondre à cet objectif, deux campagnes de prélèvements ont été réalisés dont une sous les vents des principales activités industrielles afin de caractériser leurs émissions (profils) et une en zones urbaines caractéristiques de l’exposition de la population aux particules fines. Les résultats ont permis d'obtenir des empreintes représentatives des principales activités industrielles de la zone d'étude. L’analyse ME-2 menée a permis, avec la combinaison d’analyses radiocarbones, de déterminer que la source de combustion de biomasse est la source majoritaire pendant l’automne et l’hiver où les épisodes de PM2.5 ont été observés. La source industrielle est la source majoritaire des PM2.5 au printemps et en été mais ne constitue pas un driver fort de la concentration des PM2.5. Toutefois, cette étude a montré que les sources industrielles impactent significativement la population de particules (taille, composition, etc.) dans la zone d’étude. / In order to limit the impact of air quality on human health, public authorities need reliable and accurate information on the sources contribution. So, the identification of the main sources of PM2.5 is the first step to adopt efficient mitigation policies. This work carry out in this thesis take place in this issue and was to determine the main sources of PM2.5 inside an industrial area. To determinate the main sources of PM2.5, two campaigns were lead to collect daily PM2.5 to: 1/ determine the enrichment of atmospheric pollutants downwind from the main industrial activities and 2/ collect PM2.5 in urban areas characteristic of the population exposition. Results allowed to obtain very representative profiles for the main industrial activities implanted inside the studied area. ME-2 analysis, combined to radiocarbon measurements, allowed to highlight the very high impact of Biomass Burning sources for all the PM2.5 pollution events recorded from early autumn to March. This study showed that industrial sources, even if they are the major sources during spring and summer, are not the major PM2.5 driver. However, this study highlights that industrial sources impact significantly the aerosol population (size, composition, etc.) in the studied area.