| 1. |
- Myers-Smith, Isla H., et al.
(författare)
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Complexity revealed in the greening of the Arctic
- 2020
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Ingår i: Nature Climate Change. - : Springer Science and Business Media LLC. - 1758-678X .- 1758-6798. ; 10:2, s. 106-117
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Tidskriftsartikel (refereegranskat)abstract
- As the Arctic warms, vegetation is responding, and satellite measures indicate widespread greening at high latitudes. This ‘greening of the Arctic’ is among the world’s most important large-scale ecological responses to global climate change. However, a consensus is emerging that the underlying causes and future dynamics of so-called Arctic greening and browning trends are more complex, variable and inherently scale-dependent than previously thought. Here we summarize the complexities of observing and interpreting high-latitude greening to identify priorities for future research. Incorporating satellite and proximal remote sensing with in-situ data, while accounting for uncertainties and scale issues, will advance the study of past, present and future Arctic vegetation change.
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| 2. |
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| 3. |
- Olvmo, Mats, 1956, et al.
(författare)
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Sub-arctic palsa degradation and the role of climatic drivers in the largest coherent palsa mire complex in Sweden (Vissatvuopmi), 1955-2016
- 2020
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Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 10:1
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Tidskriftsartikel (refereegranskat)abstract
- Substantial palsa degradation has occurred in Fennoscandia, which is considered to be driven by global climate change. Deeper understanding of the role of different climatic drivers on palsa decay, however, is lacking. We use meteorological data and aerial photographs from 1955 to 2016 to statistically identify the most important climatic drivers affecting changes in lateral-temporal palsa decay rates in the largest coherent palsa complex in Sweden, Vissatvuopmi. We show that wetter, warmer and shorter winters are the main causes of large and rapid changes in lateral-palsa extent since the mid-1950s. By analyzing meteorological data from the 1880s to present, we show that average annual temperature conditions have been unfavourable for palsas for more than a century and average annual precipitation conditions have been unfavourable since the 1940s. The decay rates have likely been amplified over the past 50-60 years, and in particular over the most recent decades, due to the combined effect of adverse air temperature and precipitation conditions. Palsa loss is expected to continue, most likely at a higher rate than today, with serious ecological impacts as a consequence.
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| 4. |
- Zhang, Yi Ge, et al.
(författare)
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Refining the alkenone-pCO2 method II : Towards resolving the physiological parameter ‘b’
- 2020
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Ingår i: Geochimica et Cosmochimica Acta. - : Elsevier BV. - 0016-7037 .- 1872-9533. ; 281, s. 118-134
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Tidskriftsartikel (refereegranskat)abstract
- Haptophyte algal biomarkers called alkenones are widely used to reconstruct atmospheric CO2 in Earth’s Cenozoic history. This method is based on the notion that the algal carbon isotope fractionation during photosynthesis, as represented by ep37:2, is a function of seawater CO2 concentration and algal physiology. Constraining the algal physiological parameter, known as the ‘b’ term, is the key for successful applications of the alkenone-CO2 method. Using sensitivity analyses, we show that the growth rate (µ), cell size (r), and membrane permeability (P) are the most important variables to determine b. For all life on Earth, body size is a key factor that regulates metabolic rates. Exploiting the interdependence between phytoplankton cell size and growth rate, and specifically, the r – µ relationship for coccolithophores, we show that the length of fossil coccoliths (Lcoccolith) produced by ancient alkenone-synthesizers can be used to estimate r and therefore µ. Combining our new Lcoccolith data and published ep37:2 from the South China Sea Site MD01-2392, existing results from ODP Site 925, and ice core CO2, we determined the cell membrane permeability (P = 5.09 10-5 m s-1) for the Pleistocene community employing a bootstrap resampling technique. These new methods of constraining r, µ and P, combined with proxy-derived temperature (T), led us to rebuild b as a variable for each sample individually, which is subsequently used for alkenone-CO2 calculations. Application of this approach established pCO2 of the last 3 glacial-interglacial cycles, which turns out to be comparable with the ice core data in both the amplitude of changes and absolute values. It also reconciles the published Eocene – Oligocene alkenone-CO2 data which showed large geographical differences, with the new estimates much more consistent among different sites, and in line with other proxy-based results and ice sheet model predictions.
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| 5. |
- Wang, Xuan, et al.
(författare)
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Effects of Anthropogenic Chlorine on PM2.5 and Ozone Air Quality in China
- 2020
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Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 54:16, s. 9908-9916
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Tidskriftsartikel (refereegranskat)abstract
- China has large anthropogenic chlorine emissions from agricultural fires, residential biofuel, waste incineration, coal combustion, and industrial processes. Here we quantify the effects of chlorine on fine particulate matter (PM2.5) and ozone air quality across China by using the GEOS-Chem chemical transport model with comprehensive anthropogenic emissions and detailed representation of gas-phase and heterogeneous chlorine chemistry. Comparison of the model to observed ClNO2, HCl, and particulate Cl- concentrations shows that reactive chlorine in China is mainly anthropogenic, unlike in other continental regions where it is mostly of marine origin. The model is successful in reproducing observed concentrations and their distributions, lending confidence in the anthropogenic chlorine emission estimates and the resulting chemistry. We find that anthropogenic chlorine emissions increase total inorganic PM2.5 by as much as 3.2 μg m-3 on an annual mean basis through the formation of ammonium chloride, partly compensated by a decrease of nitrate because ClNO2 formation competes with N2O5 hydrolysis. Annual mean MDA8 surface ozone increases by up to 1.9 ppb, mainly from ClNO2 chemistry, while reactivities of volatile organic compounds increase (by up to 48% for ethane). We find that a sufficient representation of chlorine chemistry in air quality models can be obtained from consideration of HCl/Cl- thermodynamics and ClNO2 chemistry, because other more complicated aspects of chlorine chemistry have a relatively minor effect.
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| 6. |
- Wang, Y. J., et al.
(författare)
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Comparative Study of Particulate Organosulfates in Contrasting Atmospheric Environments: Field Evidence for the Significant Influence of Anthropogenic Sulfate and NOx
- 2020
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Ingår i: Environmental Science & Technology Letters. - : American Chemical Society (ACS). - 2328-8930. ; 7:11, s. 787-794
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Tidskriftsartikel (refereegranskat)abstract
- Organosulfates (OSs) are an important group of secondary organic aerosols, but the key influential factors of their formation in polluted atmospheres are not well understood. In this study, we monitored particulate OSs (carboxy OSs, hydroxyacetone sulfate, and isoprene- and monoterpene-derived OSs) at an urban site and a regional site in Beijing and examined their compositions and formation pathways under contrasting atmospheric conditions. The quantified OSs were most abundant in the summer at the regional site due to higher biogenic emissions and favorable formation conditions (higher aerosol acidity and humidity), followed by urban summer and winter conditions. Larger fractions of inorganic sulfate were converted to organosulfur when sulfate was less abundant. This implies that OSs would play more important roles in aerosol properties as the decline of sulfate. Monoterpene-derived nitrooxy-OSs were enhanced via NO3 oxidation in the summer under high-NOx conditions at night, while the day-night variations in the winter were not as obvious. Among isoprene-OSs, IEPOX (isoprene epoxydiols)-OS formation was clearly suppressed under high-NOx conditions, while other isoprene-OSs that are favored under high-NOx conditions showed increasing formation with NOx. The results highlight that isoprene-OS formation pathways in polluted atmospheres could be different from the IEPOX-dominated regions reported for the low-NOx environments in the literature.
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| 7. |
- Ickes, Luisa, 1986, et al.
(författare)
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The ice-nucleating activity of Arctic sea surface microlayer samples and marine algal cultures
- 2020
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Ingår i: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 20:18, s. 11089-11117
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Tidskriftsartikel (refereegranskat)abstract
- In recent years, sea spray as well as the biological material it contains has received increased attention as a source of ice-nucleating particles (INPs). Such INPs may play a role in remote marine regions, where other sources of INPs are scarce or absent. In the Arctic, these INPs can influence water-ice partitioning in low-level clouds and thereby the cloud lifetime, with consequences for the surface energy budget, sea ice formation and melt, and climate. Marine aerosol is of a diverse nature, so identifying sources of INPs is challenging. One fraction of marine bioaerosol (phytoplankton and their exudates) has been a particular focus of marine INP research. In our study we attempt to address three main questions. Firstly, we compare the ice-nucleating ability of two common phytoplankton species with Arctic seawater microlayer samples using the same instrumentation to see if these phytoplankton species produce ice-nucleating material with sufficient activity to account for the ice nucleation observed in Arctic microlayer samples. We present the first measurements of the ice-nucleating ability of two predominant phytoplankton species: Melosira arctica, a common Arctic diatom species, and Skeletonema marinoi, a ubiquitous diatom species across oceans worldwide. To determine the potential effect of nutrient conditions and characteristics of the algal culture, such as the amount of organic carbon associated with algal cells, on the ice nucleation activity, Skeletonema marinoi was grown under different nutrient regimes. From comparison of the ice nucleation data of the algal cultures to those obtained from a range of sea surface microlayer (SML) samples obtained during three different field expeditions to the Arctic (ACCACIA, NETCARE, and ASCOS), we found that they were not as ice active as the investigated microlayer samples, although these diatoms do produce ice-nucleating material. Secondly, to improve our understanding of local Arctic marine sources as atmospheric INPs we applied two aerosolization techniques to analyse the ice-nucleating ability of aerosolized microlayer and algal samples. The aerosols were generated either by direct nebulization of the undiluted bulk solutions or by the addition of the samples to a sea spray simulation chamber filled with artificial seawater. The latter method generates aerosol particles using a plunging jet to mimic the process of oceanic wave breaking. We observed that the aerosols produced using this approach can be ice active, indicating that the ice-nucleating material in seawater can indeed transfer to the aerosol phase. Thirdly, we attempted to measure ice nucleation activity across the entire temperature range relevant for mixed-phase clouds using a suite of ice nucleation measurement techniques - an expansion cloud chamber, a continuous-flow diffusion chamber, and a cold stage. In order to compare the measurements made using the different instruments, we have normalized the data in relation to the mass of salt present in the nascent sea spray aerosol. At temperatures above 248K some of the SML samples were very effective at nucleating ice, but there was substantial variability between the different samples. In contrast, there was much less variability between samples below 248 K. We discuss our results in the context of aerosol-cloud interactions in the Arctic with a focus on furthering our understanding of which INP types may be important in the Arctic atmosphere.
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| 8. |
- Lindborg, Tobias, et al.
(författare)
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A carbon mass-balance budget for a periglacial catchment in West Greenland : Linking the terrestrial and aquatic systems
- 2020
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Ingår i: Science of the Total Environment. - : Elsevier. - 0048-9697 .- 1879-1026. ; 711
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Tidskriftsartikel (refereegranskat)abstract
- Climate change is predicted to have far reaching consequences for the mobility of carbon in arctic landscapes. On a regional scale, carbon cycling is highly dependent on interactions between terrestrial and aquatic parts of a catchment. Despite this, studies that integrate the terrestrial and aquatic systems and study entire catchments using site-specific data are rare. In this work, we use data partly published by Lindborg et al. (2016a) to calculate a whole-catchment carbon mass-balance budget for a periglacial catchment in West Greenland. Our budget shows that terrestrial net primary production is the main input of carbon (99% of input), and that most carbon leaves the system through soil respiration (90% of total export/storage). The largest carbon pools are active layer soils (53% of total carbon stock or 13 kg C m (2)), permafrost soils (30% of total carbon stock or 7.6 kg C m (2)) and lake sediments (13% of total carbon stock or 10 kg C m (2)). Hydrological transport of carbon from the terrestrial to aquatic system is lower than in wetter climates, but the annual input of 4100 kg C yr (1) (or 3.5 g C m (2) yr (1)) that enters the lake via runoff is still three times larger than the eolian input of terrestrial carbon. Due to the dry conditions, the hydrological export of carbon from the catchment is limited (5% of aquatic export/storage or 0.1% of total export/storage). Instead, CO2 evasion from the lake surface and sediment burial accounts for 57% and 38% of aquatic export/storage, respectively (or 0.8% and 0.5% of total export/storage), and Two-Boat Lake acts as a net source of carbon to the atmosphere. The limited export of carbon to downstream water bodies make our study system different from wetter arctic environments, where hydrological transport is an important export pathway for carbon.
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| 9. |
- Linkhorst, Annika, et al.
(författare)
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Comparing methane ebullition variability across space and time in a Brazilian reservoir
- 2020
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Ingår i: Limnology and Oceanography. - : Wiley. - 0024-3590 .- 1939-5590. ; 65:7, s. 1623-1634
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Tidskriftsartikel (refereegranskat)abstract
- The potent greenhouse gas methane (CH4) is readily emitted from tropical reservoirs, often via ebullition (bubbles). This highly stochastic emission pathway varies in space and time, however, hampering efforts to accurately assess total CH4 emissions from water bodies. We systematically studied both the spatial and temporal scales of ebullition variability in a river inflow bay of a tropical Brazilian reservoir. We conducted multiple highly resolved spatial surveys of CH4 ebullition using a hydroacoustic approach supplemented with bubble traps over a 12‐month and a 2‐week timescale to evaluate which scale of variation was more important. To quantify the spatial and temporal variability of CH4 ebullition, we used the quartile coefficients of dispersion at each point in space and time and compared their frequency distributions across the various temporal and spatial scales. We found that CH4 ebullition varied more temporally than spatially and that the intra‐annual variability was stronger than daily variability within 2 weeks. We also found that CH4 ebullition was positively related to water temperature increase and pressure decrease, but no consistent relationship with water column depth or sediment characteristics was found, further highlighting that temporal drivers of emissions were stronger than spatial drivers. Annual estimates of CH4 ebullition from our study area may vary by 75–174% if ebullition is not resolved in time and space, but at a minimum we recommend conducting spatially resolved measurements at least once during each major hydrologic season in tropical regions (i.e., in dry and rainy season when water levels are falling and rising, respectively).
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| 10. |
- Lougheed, Bryan C., 1982-, et al.
(författare)
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Re-evaluating 14C dating accuracy in deep-sea sediment archives
- 2020
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Ingår i: Geochronology. - : Copernicus GmbH. - 2628-3719. ; 2:1, s. 17-31
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Tidskriftsartikel (refereegranskat)abstract
- The current geochronological state of the art for applying the radiocarbon (14C) method to deep-sea sediment archives lacks key information on sediment bioturbation. Here, we apply a sediment accumulation model that simulates the sedimentation and bioturbation of millions of foraminifera, whereby realistic 14C activities (i.e. from a 14C calibration curve) are assigned to each single foraminifera based on its simulation time step. We find that the normal distribution of 14C age typically used to represent discrete-depth sediment intervals (based on the reported laboratory 14C age and measurement error) is unlikely to be a faithful reflection of the actual 14C age distribution for a specific depth interval. We also find that this deviation from the actual 14C age distribution is greatly amplified during the calibration process. Specifically, we find a systematic underestimation of total geochronological error in many cases (by up to thousands of years), as well as the generation of age–depth artefacts in downcore calibrated median age. Even in the case of “perfect” simulated sediment archive scenarios, whereby sediment accumulation rate (SAR), bioturbation depth, reservoir age and species abundance are all kept constant, the 14C measurement and calibration processes generate temporally dynamic median age–depth artefacts on the order of hundreds of years – whereby even high SAR scenarios (40 and 60 cm kyr−1) are susceptible. Such age–depth artefacts can be especially pronounced during periods corresponding to dynamic changes in the Earth's Δ14C history, when single foraminifera of varying 14C activity can be incorporated into single discrete-depth sediment intervals. For certain lower-SAR scenarios, we find that downcore discrete-depth true median age can systematically fall outside the calibrated age range predicted by the 14C measurement and calibration processes, thus leading to systematically inaccurate age estimations. In short, our findings suggest the possibility of 14C-derived age–depth artefacts in the literature. Furthermore, since such age–depth artefacts are likely to coincide with large-scale changes in global Δ14C, which themselves can coincide with large-scale changes in global climate (such as the last deglaciation), 14C-derived age–depth artefacts may have been previously incorrectly attributed to changes in SAR coinciding with global climate. Our study highlights the need for the development of improved deep-sea sediment 14C calibration techniques that include an a priori representation of bioturbation for multi-specimen samples.
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