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1.
The direct and semi-direct radiative effects of anthropogenic aerosols on the radiative transfer and cloud fields in the Western United States (WUS) according to seasonal aerosol optical depth (AOD) and regional climate are examined using a regional climate model (RCM) in conjunction with the aerosol fields from a GEOS-Chem chemical-transport model (CTM) simulation. The two radiative effects cannot be separated within the experimental design in this study, thus the combined direct- and semi-direct effects are called radiative effects hereafter. The CTM shows that the AOD associated with the anthropogenic aerosols is chiefly due to sulfates with minor contributions from black carbon (BC) and that the AOD of the anthropogenic aerosol varies according to local emissions and the seasonal low-level winds. The RCM-simulated anthropogenic aerosol radiative effects vary according to the characteristics of regional climate, in addition to the AOD. The effects on the top of the atmosphere (TOA) outgoing shortwave radiation (OSRT) range from ?0.2?Wm?2 to ?1?Wm?2. In Northwestern US (NWUS), the maximum and minimum impact of anthropogenic aerosols on OSRT occurs in summer and winter, respectively, following the seasonal AOD. In Arizona-New Mexico (AZNM), the effect of anthropogenic sulfates on OSRT shows a bimodal distribution with winter/summer minima and spring/fall maxima, while the effect of anthropogenic BC shows a single peak in summer. The anthropogenic aerosols affect surface insolation range from ?0.6?Wm?2 to ?2.4?Wm?2, with similar variations found for the effects on OSRT except that the radiative effects of anthropogenic BC over AZNM show a bimodal distribution with spring/fall maxima and summer/winter minima. The radiative effects of anthropogenic sulfates on TOA outgoing longwave radiation (OLR) and the surface downward longwave radiation (DLRS) are notable only in summer and are characterized by strong geographical contrasts; the summer OLR in NWUS (AZNM) is reduced (enhanced) by 0.52?Wm?2 (1.14?Wm?2). The anthropogenic sulfates enhance (reduce) summer DLRS by 0.2?Wm?2 (0.65?Wm?2) in NWUS (AZNM). The anthropogenic BC affect DLRS noticeably only in AZNM during summer. The anthropogenic aerosols affect the cloud water path (CWP) and the radiative transfer noticeably only in summer when convective clouds are dominant. Primarily shortwave-reflecting anthropogenic sulfates decrease and increase CWP in AZNM and NWUS, respectively, however, the shortwave-absorbing anthropogenic BC reduces CWP in both regions. Due to strong feedback via convective clouds, the radiative effects of anthropogenic aerosols on the summer radiation field are more closely correlated with the changes in CWP than the AOD. The radiative effect of the total anthropogenic aerosols is dominated by the anthropogenic sulfates that contribute more than 80% of the total AOD associated with the anthropogenic aerosols.  相似文献   

2.
对气溶胶气候效应开展分类评估并探讨诊断方法的合理性。人为气溶胶辐射效应对计算云辐射强迫的影响为0.38 W·m~(-2)。诊断评估气溶胶对云辐射强迫的影响需要排除这个偏差。两种基于不同试验设计诊断得出的半直接效应分别为0.21和0.09 W·m~(-2),存在显著差异。主要原因可能是人为气溶胶影响云辐射强迫的不同机制之间在模式模拟过程中不断地相互交织,不是简单的线性叠加关系。模式诊断得出的Twomey效应不仅包括Twomey效应本身,还包括Twomey效应引起的部分快速调整。总之,利用模式评估分析人为气溶胶气候效应需要注意审查试验设计和诊断方法的合理性。  相似文献   

3.
Current global climate models cannot resolve the complex topography over the Tibetan Plateau (TP) due to their coarse resolution. This study investigates the impacts of horizontal resolution on simulating aerosol and its direct radiative effect (DRE) over the TP by applying two horizontal resolutions of about 100 km and 25 km to the Chinese Academy of Sciences Flexible Global Ocean-Atmosphere Land System (CAS FGOALS-f3) over a 10-year period. Compared to the AErosol RObotic NETwork observations, a high-resolution model (HRM) can better reproduce the spatial distribution and seasonal cycles of aerosol optical depth (AOD) compared to a low-resolution model (LRM). The HRM bias and RMSE of AOD decreased by 0.08 and 0.12, and the correlation coefficient increased by 0.22 compared to the LRM. An LRM is not sufficient to reproduce the aerosol variations associated with fine-scale topographic forcing, such as in the eastern marginal region of the TP. The difference between hydrophilic aerosols in an HRM and LRM is caused by the divergence of the simulated relative humidity (RH). More reasonable distributions and variations of RH are conducive to simulating hydrophilic aerosols. An increase of the 10-m wind speed in winter by an HRM leads to increased dust emissions. The simulated aerosol DREs at the top of the atmosphere (TOA) and at the surface by the HRM are –0.76 W m–2 and –8.72 W m–2 over the TP, respectively. Both resolution models can capture the key feature that dust TOA DRE transitions from positive in spring to negative in the other seasons.  相似文献   

4.
Taking winter and summer in eastern China as an example application, a grid-cell method of aerosol direct radiative forcing(ADRF) calculation is examined using the Santa Barbara DISORT Atmospheric Radiative Transfer(SBDART) model with inputs from MODIS and AERONET observations and reanalysis data. Results show that there are significant seasonal and regional differences in climatological mean aerosol optical parameters and ADRF. Higher aerosol optical depth(AOD)occurs in summer and two prominent high aerosol loading centers are observed. Higher single scattering albedo(SSA) in summer is likely associated with the weak absorbing secondary aerosols. SSA is higher in North China during summer but higher in South China during winter. Aerosols induce negative forcing at the top of the atmosphere(TOA) and surface during both winter and summer, which may be responsible for the decrease in temperature and the increase in relative humidity.Values of ADRF at the surface are four times stronger than those at the TOA. Both AOD and ADRF present strong interannual variations; however, their amplitudes are larger in summer. Moreover, patterns and trends of ADRF do not always correspond well to those of AOD. Differences in the spatial distributions of ADRF between strong and weak monsoon years are captured effectively. Generally, the present results justify that to calculate grid-cell ADRF at a large scale using the SBDART model with observational aerosol optical properties and reanalysis data is an effective approach.  相似文献   

5.
Anthropogenic aerosols play an important role in the atmospheric energy balance. Anthropogenic aerosol optical depth (AOD) and its accompanying shortwave radiative forcing (RF) are usually simulated by nu- merical models. Recently, with the development of space-borne instruments and sophisticated retrieval algorithms, it has become possible to estimate aerosol radiative forcing based on satellite observations. In this study, we have estimated shortwave direct radiative forcing due to anthropogenic aerosols over oceans in all-sky conditions by combining clouds and the Single Scanner Footprint data of the Clouds and Earth’s Radiant Energy System (CERES/SSF) experiment, which provide measurements of upward shortwave fluxes at the top of atmosphere, with Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol and cloud products. We found that globally averaged aerosol radiative forcing over oceans in the clear-sky conditions and all-sky conditions were -1.03±0.48 W m-2 and -0.34 ±0.16 W m-2, respectively. Direct radiative forcing by anthropogenic aerosols shows large regional and seasonal variations. In some regions and in particular seasons, the magnitude of direct forcing by anthropogenic aerosols can be comparable to the forcing of greenhouse gases. However, it shows that aerosols caused the cooling effect, rather than warming effect from global scale, which is different from greenhouse gases.  相似文献   

6.
西北地区气溶胶光学特性及辐射影响   总被引：3，自引：1，他引：2  
利用SACOL（兰州大学半干旱气候与环境观测站）2006~2012年AERONET（全球气溶胶自动监测网）level 2.0和太阳短波辐射计资料,分析了中国西北地区气溶胶的光学特性与辐射影响。利用辐射传输模式SBDART（平面平行大气辐射传输模式）检验TOA（大气层顶）处辐射强迫为正的原因。BOA（地表）、TOA、Atmosphere（大气）的辐射强迫年均值分别是-59.43 W m-2、-17.03 W m-2、42.40 W m-2,AOD（光学厚度,550 nm）年均值0.37,α（波段的波长指数,440~675 nm）年均值0.91,变化趋势与AOD位相相反,当AOD为0.3~2.2时,α很小（0.0~0.2）,表明粒子尺度很大。SSA（单次散射反照率,675 nm）年均值0.93,g（不对称因子,675 nm）年均值0.68,复折射指数（675 nm）实部年均值1.48,虚部0.007。复折射指数实部的年变化趋势与AOD一致,虚部与AOD反位相,所以西北地区多为粗模态散射性气溶胶。气溶胶对大气的加热率最大值出现在0~2 km,随高度递减。冬、夏半年在地表加热率分别是2.6 K d-1和0.6 K d-1;季节变化中,冬季、秋季、春季和夏季,在地表的加热率依次是2.5 K d-1、1.4 K d-1、1.2 K d-1和0.2 K d-1,主要因为秋季气溶胶的吸收性大于春季。地表反照率和SSA对TOA正辐射强迫贡献率分别是22.5%和77.5%。  相似文献   

7.
利用SBDART（Santa Barbara DISORT Atmospheric Radiative Transfer）辐射传输模式,结合AERONET（Aerosol Robotic Network）北京站观测的气溶胶光学特性数据,评估北京地区近十年气溶胶以及黑碳气溶胶的辐射强迫,主要研究结果如下:北京近十年气溶胶平均光学厚度（aerosol optical depth, AOD440nm）为0.61±0.56,?ngstr?m波长指数均值为1.09,单次散射反照率（single scattering albedo, SSA440nm）的均值为0.888±0.045;AOD呈现下降趋势,SSA呈上升趋势,表明该区域气溶胶污染有所改善。晴空条件下,大气层顶、地面和大气的气溶胶直接辐射强迫多年均值分别为?24.91±19.80 W m?2、?65.52±43.78 W m?2、40.61±28.62 W m?2,即气溶胶对大气层顶和地表为冷却效应,对大气产生加热作用。气溶胶和黑碳气溶胶的直接辐射强迫绝对值的年际变化表现为微弱的下降趋势,季节变化特征为春夏季高,冬季低,这与AOD的变化规律一致。并且黑碳气溶胶的直接辐射强迫下降趋势与SSA的上升趋势呈现较好的反位相关系。  相似文献   

8.
The environmental impact of aerosols is currently a hot issue that has received worldwide attention. Lacking simultaneous observations of aerosols and carbon flux, the understanding of the aerosol radiative effect of urban agglomeration on the net ecosystem carbon exchange(NEE) is restricted. In 2009-2010, an observation of the aerosol optical property and CO_2 flux was carried out at the Dongguan Meteorological Bureau Station(DMBS) using a sun photometer and eddy covariance systems. The different components of photosynthetically active radiation(PAR),including global PAR(GPAR), direct PAR(DPAR), and scattered PAR(FPAR), were calculated using the Santa Barbara DISORT Atmospheric Radiative Transfer(SBDART) model. The effects of PAR on the NEE between land-atmosphere systems were investigated. The results demonstrated that during the study period the aerosol optical depth(AOD)reduced the DPAR by 519.28±232.89 μmol photons · m~(-2)s~(-1);, but increased the FPAR by 324.93±169.85μmol photons ·m~(-2)s~(-1);, ultimately leading to 194.34±92.62 μmol photons · m~(-2)s~(-1); decrease in the GPAR. All the PARs(including GPAR,DPAR, and FPAR) resulted in increases in the NEE(improved carbon absorption), but the FPAR has the strongest effect with the light use efficiency(LUE) being 1.12 times the values for the DPAR. The absorption of DPAR by the vegetation exhibited photo-inhibition in the radiation intensity 600 photons · m~(-2)s~(-1); in contrast, the absorptions of FPAR did not exhibit apparent photo-inhibition. Compared with the FPAR caused by aerosols, the DPAR was not the primary factor affecting the NEE. On the contrary, the increase in AOD significantly increased the FPAR, enhancing the LUE of vegetation ecosystems and finally promoting the photosynthetic CO_2 absorption.  相似文献   

9.
Aerosol and its effects, especially its indirect effects, on climate have drawn more and more attention in recent years. In this study, the first indirect radiative forcing (RF) of sulfate aerosol and its impacts on the regional climate in East Asia during the period from December 2008 to November 2009 were investigated. Affected by the general circulation and the conversion efficiency from SO2 to SO4 2? in aqueous phase, a remarkable seasonal variation of sulfate was found. The results show that the highest sulfate concentration as large as 24 g m?2 appears in the summer. The indirect RF due to sulfate aerosol at the top of atmosphere (TOA) and the surface is negative, which leads to a cooling effect on the surface by 0.12°C and a reduction of precipitation by 0.01 mm d?1. The tendencies of temperature and rainfall have significant diversity in space and time. The cloud feedback, associated with the hydrologic cycle and energy budget, is responsible for this discordant distribution. The variation of low cloud dominates the change of surface temperature. The subsidence due to the cooling effect in the mid atmosphere restrained and reduced the low clouds, leading to an apparent warm effect on the surface in Northeast Mongolia.  相似文献   

10.
It is well established that aerosols affect the climate in a variety of ways. In order to understand these effects, we require an insight into the properties of aerosols. In this paper we present a study of aerosol properties such as aerosol optical depth (AOD), single scattering albedo (SSA) and aerosol radiative forcing (ARF) over mega city of Lahore (Pakistan). The data from Aerosol Robotic Network (AERONET) have been used for the period December 2009 to October 2011. The seasonal average values of AOD, asymmetry parameter (ASY) and volume size distribution in coarse mode were observed to be highest in summer. On the other hand, the average values of Angstrom exponent (AE) and imaginary part of refractive index (RI) were found to be maximum in winter. The average value of real part of RI was found to be higher in spring than in all other seasons. The SSA exhibited an increasing trend with wavelength in the range 440 nm–1020 nm in spring, summer and fall indicating the dominance of coarse particles (usually dust). However, a decreasing trend was found in winter in the range 675 nm–1020 nm pointing towards the dominance of biomass and urban/industrial aerosols. As far as aerosol radiative forcing (ARF) is concerned, we have found that during the spring season ARF was lowest at the surface of Earth and highest at top of the atmosphere (TOA). This indicates that the atmosphere was warmer in spring than in all the remaining seasons.  相似文献   

11.
A regional climate model is employed to simulate the aerosols(dust,sulfate,black carbon,and organic carbon) and their direct effect on the climate over China.The emphasis is on the direct radiative forcing due to the change in mixing state of aerosols.The results show that direct radiative forcing is significantly different between externally and internally mixed aerosols.At the top of the atmosphere(TOA),the radiative forcing of externally mixed aerosols is larger than that of internally mixed ones,especially in the Tarim desert region where the difference is about 0.7 W m 2.At the surface,however,the situation becomes opposite,especially in the Sichuan basin where the difference is about-1.4 W m 2.Nonetheless,either externally or internally mixed aerosols in China can result in a significant cooling effect,except for the warming in South China in winter and the slight warming in North China in February.The cooling effect induced by externally mixed aerosols is weaker than that induced by internally mixed aerosols,and this is more obvious in spring and winter than in summer and autumn.In spring and summer,the inhibiting effect of externally mixed aerosols on precipitation is less than that of internally mixed aerosols,whereas in autumn and winter the difference is not obvious.  相似文献   

12.

Size-segregated aerosol particles were collected using a high volume MOUDI sampler at a coastal urban site in Xiamen Bay, China, from March 2018 to June 2020 to examine the seasonal characteristics of aerosol and water-soluble inorganic ions (WSIIs) and the dry deposition of nitrogen species. During the study period, the annual average concentrations of PM1, PM2.5, PM10, and TSP were 14.8?±?5.6, 21.1?±?9.0, 35.4?±?14.2 μg m?3, and 45.2?±?21.3 μg m?3, respectively. The seasonal variations of aerosol concentrations were impacted by the monsoon with the lowest value in summer and the higher values in other seasons. For WSIIs, the annual average concentrations were 6.3?±?3.3, 2.1?±?1.2, 3.3?±?1.5, and 1.6?±?0.8 μg m?3 in PM1, PM1-2.5, PM2.5–10, and PM>10, respectively. In addition, pronounced seasonal variations of WSIIs in PM1 and PM1-2.5 were observed, with the highest concentration in spring-winter and the lowest in summer. The size distribution showed that SO42?, NH4+ and K+ were consistently present in the submicron particles while Ca2+, Mg2+, Na+ and Cl? mainly accumulated in the size range of 2.5–10 μm, reflecting their different dominant sources. In spring, fall and winter, a bimodal distribution of NO3? was observed with one peak at 2.5–10 μm and another peak at 0.44–1 μm. In summer, however, the fine mode peak disappeared, likely due to the unfavorable conditions for the formation of NH4NO3. For NH4+ and SO42?, their dominant peak at 0.25–0.44 μm in summer and fall shifted to 0.44–1 μm in spring and winter. Although the concentration of NO3–N was lower than NH4–N, the dry deposition flux of NO3–N (35.77?±?24.49 μmol N m?2 d?1) was much higher than that of NH4–N (10.95?±?11.89 μmol N m?2 d?1), mainly due to the larger deposition velocities of NO3–N. The contribution of sea-salt particles to the total particulate inorganic N deposition was estimated to be 23.9—52.8%. Dry deposition of particulate inorganic N accounted for 0.95% of other terrestrial N influxes. The annual total N deposition can create a new productivity of 3.55 mgC m?2 d?1, accounting for 1.3–4.7% of the primary productivity in Xiamen Bay. In light of these results, atmospheric N deposition could have a significant influence on biogeochemistry cycle of nutrients with respect to projected increase of anthropogenic emissions from mobile sources in coastal region.

  相似文献   

13.
A Regional Climate Chemistry Modeling System that employed empirical parameterizations of aerosol-cloud microphysics was applied to investigate the spatial distribution, radiative forcing (RF), and climate effects of black carbon (BC) over China. Results showed high levels of BC in Southwest, Central, and East China, with maximum surface concentrations, column burden, and optical depth (AOD) up to 14 μg?m?3, 8 mg?m?2, and 0.11, respectively. Black carbon was found to result in a positive RF at the top of the atmosphere (TOA) due to its direct effect while a negative RF due to its indirect effect. The regional-averaged direct and indirect RF of BC in China was about +0.81 and ?0.95 W?m?2, respectively, leading to a net RF of ?0.15 W?m?2 at the TOA. The BC indirect RF was larger than its direct RF in South China. Due to BC absorption of solar radiation, cloudiness was decreased by 1.33 %, further resulting in an increase of solar radiation and subsequently a surface warming over most parts of China, which was opposite to BC’s indirect effect. Further, the net effect of BC might cause a decrease of precipitation of ?7.39 % over China. Investigations also suggested large uncertainties and non-linearity in BC’s indirect effect on regional climate. Results suggested that: (a) changes in cloud cover might be more affected by BC’s direct effect, while changes in surface air temperature and precipitation might be influenced by BC’s indirect effect; and (b) BC second indirect effect might have more influence on cloud cover and water content compared to first indirect effect. This study highlighted a substantial role of BC on regional climate changes.  相似文献   

14.
Global aerosol and ozone distributions and their associated radiative forcings were simulated between 1850 and 2100 following a recent historical emission dataset and under the representative concentration pathways (RCP) for the future. These simulations were used in an Earth System Model to account for the changes in both radiatively and chemically active compounds, when simulating the climate evolution. The past negative stratospheric ozone trends result in a negative climate forcing culminating at ?0.15 W m?2 in the 1990s. In the meantime, the tropospheric ozone burden increase generates a positive climate forcing peaking at 0.41 W m?2. The future evolution of ozone strongly depends on the RCP scenario considered. In RCP4.5 and RCP6.0, the evolution of both stratospheric and tropospheric ozone generate relatively weak radiative forcing changes until 2060–2070 followed by a relative 30 % decrease in radiative forcing by 2100. In contrast, RCP8.5 and RCP2.6 model projections exhibit strongly different ozone radiative forcing trajectories. In the RCP2.6 scenario, both effects (stratospheric ozone, a negative forcing, and tropospheric ozone, a positive forcing) decline towards 1950s values while they both get stronger in the RCP8.5 scenario. Over the twentieth century, the evolution of the total aerosol burden is characterized by a strong increase after World War II until the middle of the 1980s followed by a stabilization during the last decade due to the strong decrease in sulfates in OECD countries since the 1970s. The cooling effects reach their maximal values in 1980, with ?0.34 and ?0.28 W m?2 respectively for direct and indirect total radiative forcings. According to the RCP scenarios, the aerosol content, after peaking around 2010, is projected to decline strongly and monotonically during the twenty-first century for the RCP8.5, 4.5 and 2.6 scenarios. While for RCP6.0 the decline occurs later, after peaking around 2050. As a consequence the relative importance of the total cooling effect of aerosols becomes weaker throughout the twenty-first century compared with the positive forcing of greenhouse gases. Nevertheless, both surface ozone and aerosol content show very different regional features depending on the future scenario considered. Hence, in 2050, surface ozone changes vary between ?12 and +12 ppbv over Asia depending on the RCP projection, whereas the regional direct aerosol radiative forcing can locally exceed ?3 W m?2.  相似文献   

15.
The atmospheric aerosols can absorb moisture from the environment due to their hydrophilicity and thus affect atmospheric radiation fluxes. In this article, the ultraviolet radiation and relative humidity (RH) data from ground observations and a radiative transfer model were used to examine the influence of RH on ultraviolet radiation flux and aerosol direct radiative forcing under the clear-sky conditions. The results show that RH has a significant influence on ultraviolet radiation because of aerosol hygroscopicity. The relationship between attenuation rate and RH can be fitted logarithmically and all of the R2 of the 4 sets of samples are high, i.e. 0.87, 0.96, 0.9, and 0.9, respectively. When the RH is 60%, 70%, 80% and 90%, the mean aerosol direct radiative forcing in ultraviolet is ?4.22W m?2, ?4.5W m?2, ?4.82W m?2 and ?5.4W m?2, respectively. For the selected polluted air samples the growth factor for computing aerosol direct radiative forcing in the ultraviolet for the RH of 80% varies from 1.19 to 1.53, with an average of 1.31.  相似文献   

16.
PM10 samples were collected to characterize the seasonal and annual trends of carbonaceous content in PM10 at an urban site of megacity Delhi, India from January 2010 to December 2017. Organic carbon (OC) and elemental carbon (EC) concentrations were quantified by thermal-optical transmission (TOT) method of PM10 samples collected at Delhi. The average concentrations of PM10, OC, EC and TCA (total carbonaceous aerosol) were 222?±?87 (range: 48.2–583.8 μg m?3), 25.6?±?14.0 (range: 4.2–82.5 μg m?3), 8.7?±?5.8 (range: 0.8–35.6 μg m?3) and 54.7?±?30.6 μg m?3 (range: 8.4–175.2 μg m?3), respectively during entire sampling period. The average secondary organic carbon (SOC) concentration ranged from 2.5–9.1 μg m?3 in PM10, accounting from 14 to 28% of total OC mass concentration of PM10. Significant seasonal variations were recorded in concentrations of PM10, OC, EC and TCA with maxima during winter and minima during monsoon seasons. In the present study, the positive linear trend between OC and EC were recorded during winter (R2?=?0.53), summer (R2?=?0.59) and monsoon (R2?=?0.78) seasons. This behaviour suggests the contribution of similar sources and common atmospheric processes in both the fractions. OC/EC weight ratio suggested that vehicular emissions, fossil fuel combustion and biomass burning could be the major sources of carbonaceous aerosols of PM10 at the megacity Delhi, India. Trajectory analysis indicates that the air mass approches to the sampling site is mainly from Indo Gangetic plain (IGP) region (Uttar Pradesh, Haryana and Punjab etc.), Thar desert, Afghanistan, Pakistan and surrounding areas.  相似文献   

17.
为减少不同气候模式评估气溶胶气候效应的差异,第六次耦合模式比较计划(Coupled Model Intercomparison Project Phase 6,CMIP6)直接给定了人为气溶胶强迫数据。因此,有必要基于此强迫数据重新评估气溶胶气候效应。本研究首先将CMIP6给出的描述人为气溶胶强迫的模块引入南京信息工程大学(Nanjing University of Information Science and Technology,NUIST)的地球系统模式(The NUIST Earth System Model,NESM)。之后,利用NESM模式评估地球辐射收支平衡对此人为气溶胶强迫的响应,并分析模式模拟结果的不确定性。评估给出的人为气溶胶有效辐射强迫为-0. 45(±0. 28) W·m~(-2)。其中,气溶胶直接辐射效应为-0. 34(±0. 01) W·m~(-2),与第二次气溶胶比较计划(The second phase of Aerosol Comparisons between Observations and M odels,Aero ComⅡ)的评估结果基本一致;气溶胶对云辐射强迫的影响(包括半直接效应和间接效应)为-0. 10(±0. 30) W·m~(-2),明显受到模式内部变率的干扰,具有较大的不确定性。  相似文献   

18.
This study is based on ground-based measurements of downward surface shortwave irradiance (SW), columnar water vapour (wv), and aerosol optical depth (τ) obtained at Thule Air Base (Greenland) in 2007–2010, together with MODIS observations of the surface shortwave albedo (A). Radiative transfer model calculations are used in combination with measurements to separate the radiative effect of A (ΔSWA), wv (ΔSWwv), and aerosols (ΔSWτ) in modulating SW in cloud-free conditions. The shortwave radiation at the surface is mainly affected by water vapour absorption, which produces a reduction of SW as low as ?100 Wm?2 (?18%). The seasonal change of A produces an increase of SW by up to +25 Wm?2 (+4.5%). The annual mean radiative effect is estimated to be ?(21–22) Wm?2 for wv, and +(2–3) Wm?2 for A. An increase by +0.065 cm in the annual mean wv, to which corresponds an absolute increase in ΔSWwv by 0.93 Wm?2 (4.3%), has been observed to occur between 2007 and 2010. In the same period, the annual mean A has decreased by ?0.027, with a corresponding decrease in ΔSWA by 0.41 Wm?2 (?14.9%). Atmospheric aerosols produce a reduction of SW as low as ?32 Wm?2 (?6.7%). The instantaneous aerosol radiative forcing (RFτ) reaches values of ?28 Wm?2 and shows a strong dependency on surface albedo. The derived radiative forcing efficiency (FEτ) for solar zenith angles between 55° and 70° is estimated to be (?120.6 ± 4.3) for 0.1 < A < 0.2, and (?41.2 ± 1.6) Wm?2 for 0.5 < A < 0.6.  相似文献   

19.
硫酸盐气溶胶直接辐射效应在线与离线模拟方法的比较   总被引：3，自引：0，他引：3  
利用区域气候模式RegCM 2与大气化学模式连接的模拟系统 ,比较了硫酸盐气溶胶辐射强迫的在线、离线模拟方法的硫酸盐柱含量、大气顶直接辐射强迫及地表温度响应。发现 :在线与离线模拟方法得到的硫酸盐柱含量、有无反馈大气顶直接辐射强迫和地表温度响应在许多地区有很大差异 ,这种差异在较小区域平均的尺度上更显著 ,在全区域平均尺度上也较为明显 ,是不能被忽略的 ;结果显示从硫酸盐含量到辐射强迫和地表温度响应逐渐加大的差异 ,说明硫酸盐气溶胶的辐射强迫与模拟方法有关 ,显示出较大的不确定性。  相似文献   

20.
The aerosol optical properties and direct radiative forcing over the Mu Us desert of northern China, acquired through a CE318 sunphotometer of the ground-based Aerosol Robotic Network (AERONET), are analyzed. The seasonal variations in the aerosol optical properties are examined. The effect of meteorological elements (pressure, temperature, water vapor pressure, relative humidity and wind speed) on the aerosol optical properties is also studied. Then, the sources and optical properties under two different cases, a dust event and a pollution event, are compared. The results show that the high aerosol optical depth (AOD) found in Yulin was mostly attributed to the occurrence of dust events in spring from the Mu Us desert and deserts of West China and Mongolia, as well as the impacts of anthropogenic pollutant particles from the middle part of China in the other seasons. The seasonal variation and the probability distribution of the radiative forcing and the radiative forcing efficiency at the surface and the top of the atmosphere are analyzed and regressed using the linear and Gaussian regression methods.  相似文献   

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