Outi Meinander

Dr. Outi Meinander

orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 September 2022 in Atmospheric Chemistry and Physics
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OMOuti Meinander
Outi Meinander
PWPavla Dagsson Waldhauserova
Pavla Dagsson Waldhauserova
PAPavel Amosov
Pavel Amosov
EAElena Aseyeva
Elena Aseyeva
CACliff Atkins
Cliff Atkins
AVAna Vukovic Vimic
Ana Vukovic Vimic
Dust particles from high latitudes have a potentially large local, regional, and global significance to climate and the environment as short-lived climate forcers, air pollutants, and nutrient sources. Identifying the locations of local dust sources and their emission, transport, and deposition processes is important for understanding the multiple impacts of high-latitude dust (HLD) on the Earth's systems. Here, we identify, describe, and quantify the source intensity (SI) values, which show the potential of soil surfaces for dust emission scaled to values 0 to 1 concerning globally best productive sources, using the Global Sand and Dust Storms Source Base Map (G-SDS-SBM). This includes 64 HLD sources in our collection for the northern (Alaska, Canada, Denmark, Greenland, Iceland, Svalbard, Sweden, and Russia) and southern (Antarctica and Patagonia) high latitudes. Activity from most of these HLD sources shows seasonal character. It is estimated that high-latitude land areas with higher (SI ≥0.5), very high (SI ≥0.7), and the highest potential (SI ≥0.9) for dust emission cover >1 670 000 km2, >560 000 km2, and >240 000 km2, respectively. In the Arctic HLD region (≥60 ∘ N), land area with SI ≥0.5 is 5.5 % (1 035 059 km2), area with SI ≥0.7 is 2.3 % (440 804 km2), and area with SI ≥0.9 is 1.1 % (208 701 km2). Minimum SI values in the northern HLD region are about 3 orders of magnitude smaller, indicating that the dust sources of this region greatly depend on weather conditions. Our spatial dust source distribution analysis modeling results showed evidence supporting a northern HLD belt, defined as the area north of 50∘ N, with a “transitional HLD-source area” extending at latitudes 50–58∘ N in Eurasia and 50–55∘ N in Canada and a “cold HLD-source area” including areas north of 60∘ N in Eurasia and north of 58∘ N in Canada, with currently “no dust source” area between the HLD and low-latitude dust (LLD) dust belt, except for British Columbia. Using the global atmospheric transport model SILAM, we estimated that 1.0 % of the global dust emission originated from the high-latitude regions. About 57 % of the dust deposition in snow- and ice-covered Arctic regions was from HLD sources. In the southern HLD region, soil surface conditions are favorable for dust emission during the whole year. Climate change can cause a decrease in the duration of snow cover, retreat of glaciers, and an increase in drought, heatwave intensity, and frequency, leading to the increasing frequency of topsoil conditions favorable for dust emission, which increases the probability of dust storms. Our study provides a step forward to improve the representation of HLD in models and to monitor, quantify, and assess the environmental and climate significance of HLD.

14 February 2019 in Atmospheric Chemistry and Physics
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Michael BoyMichael Boy
Michael Boy
ETErik S. Thomson
Erik S. Thomson
JNJuan-C. Acosta Navarro
Juan-C. Acosta Navarro
OAOlafur Arnalds
Olafur Arnalds
EBEkaterina Batchvarova
Ekaterina Batchvarova
MKMarkku Kulmala
Markku Kulmala
The Nordic Centre of Excellence CRAICC (Cryosphere–Atmosphere Interactions in a Changing Arctic Climate), funded by NordForsk in the years 2011–2016, is the largest joint Nordic research and innovation initiative to date, aiming to strengthen research and innovation regarding climate change issues in the Nordic region. CRAICC gathered more than 100 scientists from all Nordic countries in a virtual centre with the objectives of identifying and quantifying the major processes controlling Arctic warming and related feedback mechanisms, outlining strategies to mitigate Arctic warming, and developing Nordic Earth system modelling with a focus on short-lived climate forcers (SLCFs), including natural and anthropogenic aerosols. The outcome of CRAICC is reflected in more than 150 peer-reviewed scientific publications, most of which are in the CRAICC special issue of the journal Atmospheric Chemistry and Physics. This paper presents an overview of the main scientific topics investigated in the centre and provides the reader with a state-of-the-art comprehensive summary of what has been achieved in CRAICC with links to the particular publications for further detail. Faced with a vast amount of scientific discovery, we do not claim to completely summarize the results from CRAICC within this paper, but rather concentrate here on the main results which are related to feedback loops in climate change–cryosphere interactions that affect Arctic amplification.

30 June 2008 in Atmospheric Chemistry and Physics
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KLKaisa Lakkala
Kaisa Lakkala
AAAntti Arola
Antti Arola
AHA. Heikkilä
A. Heikkilä
JKJ. Kaurola
J. Kaurola
TKT. Koskela
T. Koskela
GHG. Hülsen
G. Hülsen
The quality assurance of the two Brewer spectrophotometers of the Finnish Meteorological Institute is discussed in this paper. The complete data processing chain from raw signal to high quality spectra is presented. The quality assurance includes daily maintenance, laboratory characterizations, calculation of long-term spectral responsivity, data processing and quality assessment. The cosine correction of the measurements is based on a new method, and is included in the data processing software. The results showed that the actual cosine correction factor of the two Finnish Brewers can vary between 1.08–1.13 and 1.08–1.12, respectively, depending on the sky radiance distribution and wavelength. The temperature characterization showed a linear temperature dependence between the instruments' internal temperature and the photon counts per cycle, and a temperature correction was used for correcting the measurements. The long-term spectral responsivity was calculated using the time series of several lamps using two slightly different methods. The long-term spectral responsivity was scaled to the irradiance scale of the Helsinki University of Technology (HUT) for the whole of the measurement time-periods 1990–2006 and 1995–2006 for Sodankylä and Jokioinen, respectively. Both Brewers have participated in many international spectroradiometer comparisons, and have shown good stability. The differences between the Brewers and the portable reference spectroradiometer QASUME have been within 5% during 2002–2007.

10 April 2013 in Atmospheric Chemistry and Physics
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OMOuti Meinander
Outi Meinander
Stelios KazadzisStelios Kazadzis
Stelios Kazadzis
AAAntti Arola
Antti Arola
ARAku Riihelä
Aku Riihelä
PRPetri Räisänen
Petri Räisänen
OHO. Hautecoeur
O. Hautecoeur
We have measured spectral albedo, as well as ancillary parameters, of seasonal European Arctic snow at Sodankylä, Finland (67°22' N, 26°39' E). The springtime intensive melt period was observed during the Snow Reflectance Transition Experiment (SNORTEX) in April 2009. The upwelling and downwelling spectral irradiance, measured at 290–550 nm with a double monochromator spectroradiometer, revealed albedo values of ~0.5–0.7 for the ultraviolet and visible range, both under clear sky and variable cloudiness. During the most intensive snowmelt period of four days, albedo decreased from 0.65 to 0.45 at 330 nm, and from 0.72 to 0.53 at 450 nm. In the literature, the UV and VIS albedo for clean snow are ~0.97–0.99, consistent with the extremely small absorption coefficient of ice in this spectral region. Our low albedo values were supported by two independent simultaneous broadband albedo measurements, and simulated albedo data. We explain the low albedo values to be due to (i) large snow grain sizes up to ~3 mm in diameter; (ii) meltwater surrounding the grains and increasing the effective grain size; (iii) absorption caused by impurities in the snow, with concentration of elemental carbon (black carbon) in snow of 87 ppb, and organic carbon 2894 ppb, at the time of albedo measurements. The high concentrations of carbon, detected by the thermal–optical method, were due to air masses originating from the Kola Peninsula, Russia, where mining and refining industries are located.

11 December 2015 in The Cryosphere
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JPJouni Peltoniemi
Jouni Peltoniemi
MGMaria Gritsevich
Maria Gritsevich
THTeemu Hakala
Teemu Hakala
PWPavla Dagsson Waldhauserova
Pavla Dagsson Waldhauserova
ÓAÓ. Arnalds
Ó. Arnalds
Gerrit de LeeuwGerrit de Leeuw
Gerrit de Leeuw
In order to quantify the effects of absorbing contaminants on snow, a series of spectral reflectance measurements were conducted. Chimney soot, volcanic sand, and glaciogenic silt were deposited on a natural snow surface in a controlled way as a part of the Soot on Snow (SoS) campaign. The bidirectional reflectance factors of these soiled surfaces and untouched snow were measured using the Finnish Geodetic Institute's Field Goniospectropolariradiometer, FIGIFIGO. A remarkable feature is the fact that the absorbing contaminants on snow enhanced the metamorphism of snow under strong sunlight in our experiments. Immediately after deposition, the contaminated snow surface appeared darker than the natural snow in all viewing directions, but the absorbing particles sank deep into the snow in minutes. The nadir measurement remained the darkest, but at larger zenith angles, the surface of the contaminated snow changed back to almost as white as clean snow. Thus, for a ground observer the darkening caused by impurities can be completely invisible, overestimating the albedo, but a nadir-observing satellite sees the darkest points, underestimating the albedo. Through a reciprocity argument, we predict that at noon, the albedo perturbation should be lower than in the morning or afternoon. When sunlight stimulates sinking more than melting, the albedo should be higher in the afternoon than in the morning, and vice versa when melting dominates. However, differences in the hydrophobic properties, porosity, clumping, or size of the impurities may cause different results than observed in these measurements.

1 March 2015 in Aeolian Research
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PWPavla Dagsson Waldhauserova
Pavla Dagsson Waldhauserova
OAOlafur Arnalds
Olafur Arnalds
HOHaraldur Olafsson
Haraldur Olafsson
JHJindrich Hladil
Jindrich Hladil
Roman SkalaRoman Skala
Roman Skala
OMOuti Meinander
Outi Meinander