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1.
The character of turbulent overturns in a weakly stratified deep-sea is investigated in some detail using 144 high-resolution temperature sensors at 0.7 m intervals, starting 5 m above the bottom. A 9-day, 1 Hz sampled record from the 912 m depth flat-bottom (<0.5% bottom-slope) mooring site in the central-north Alboran Sea (W-Mediterranean) demonstrates an overall conservative temperature range of only 0.05 °C, a typical mean buoyancy period as large as 3 h and a 1 Hz-profile-vertically-averaged turbulence dissipation rate maximum of only 10−8 m2 s−3. Nonetheless, this ‘boundary layer’ varies in height between <6 and >104 m above the bottom and is thus not homogeneous throughout; the temperature variations are seldom quiescent and are generally turbulent in appearance, well exceeding noise levels. The turbulence character is associated with small-scale internal waves; examples are found of both shear- and convection-driven turbulence; particular association, although not phase-locked, is found between turbulence variations and tidal rather than with inertial motions; the mean buoyancy frequency of a few times the inertial frequency implies the importance of ‘slantwise convection’ in the direction of the earth rotational vector rather than in the direction of gravity. Such convection is observed both in near-homogeneous and weakly stratified form. 相似文献
2.
Concentrations and flux densities of methane were determined during a Lagrangian study of an advective filament in the permanent upwelling region off western Mauritania. Newly upwelled waters were dominated by the presence of North Atlantic Central Water and surface CH4 concentrations of 2.2 ± 0.3 nmol L−1 were largely in equilibrium with atmospheric values, with surface saturations of 101.7 ± 14%. As the upwelling filament aged and was advected offshore, CH4 enriched South Atlantic Central Water from intermediate depths of 100–350 m was entrained into the surface mixed layer of the filament following intense mixing associated with the shelf break. Surface saturations increased to 198.9 ± 15% and flux densities increased from a mean value over the shelf of 2.0 ± 1.1 μmol m−2 d−1 to a maximum of 22.6 μmol m−2 d−1. Annual CH4 emissions for this persistent filament were estimated at 0.77 ± 0.64 Gg which equates to a maximum of 0.35% of the global oceanic budget. This raises the known outgassing intensity of this area and highlights the importance of advecting filaments from upwelling waters as efficient vehicles for air-sea exchange. 相似文献
3.
Below-cloud aerosol scavenging is generally estimated from field measurements using advanced instruments that measure changes in aerosol distributions with respect to rainfall. In this study, we discuss various scavenging mechanisms and scavenging coefficients from past laboratory and field measurements. Scavenging coefficients derived from field measurements (representing natural aerosols scavenging) are two orders higher than that of theoretical ones for smaller particles (Dp < 2 μm). Measured size-resolved scavenging coefficients can be served as a better option to the default scavenging coefficient (e.g. a constant of 10?4 s?1 for all size of aerosols, as used in the CALPUFF model) for representing below-cloud aerosol scavenging. We propose scavenging correction parameter (CR) as an exponential function of size-resolved scavenging coefficients, winds and width in the downwind of the source–receptor system. For a wind speed of 3 m s?1, CR decrease with the width in the downwind for particles of diameters Dp < 0.1 μm but CR does not vary much for particles in the accumulation mode (0.1 < Dp < 2 μm). For a typical urban aerosol distribution, assuming 3 m s?1 air-flow in the source–receptor system, 10 km downwind width, 2.84 mm h?1 of rainfall and using aerosol size dependent scavenging coefficients in the CR, scavenging of aerosols is found to be 16% in number and 24% in volume of total aerosols. Using the default scavenging coefficient (10?4 s?1) in the CALPUFF model, it is found to be 64% in both number and volume of total aerosols. 相似文献
4.
《Atmospheric Research》2009,91(2-4):243-252
Aerosol size distributions were measured with Micro Orifice Uniform Deposit Impactor (MOUDI) cascade impactors at the rural Angiola and urban Fresno Supersites in California's San Joaquin Valley during the California Regional PM10/PM2.5 Air Quality Study (CRPAQS) winter campaign from December 15, 2000 to February 3, 2001. PM2.5 filter samples were collected concurrently at both sites with Sequential Filter Samplers (SFS). MOUDI nitrate (NO3−) concentrations reached 66 μg/m3 on January 6, 2001 during the 1000–1600 PST (GMT-8) period. Pair-wise comparisons between PM2.5 MOUDI and SFS concentrations revealed high correlations at the Angiola site (r > 0.93) but more variability (r < 0.85) at the Fresno site for NO3−, sulfate (SO4=), and ammonium (NH4+). Correlations were higher at Fresno (r > 0.87) than at Angiola (r < 0.7) for organic carbon (OC), elemental carbon (EC), and total carbon (TC). NO3− and SO4= size distributions in Fresno were multi-modal and wider than the uni-modal distributions observed at Angiola. Geometric mean diameters (GMD) were smaller for OC and EC than for NO3− and SO4= at both sites. OC and EC were more concentrated on the lowest MOUDI stage (0.056 µm) at Angiola than at Fresno. The NO3− GMD increased from 0.97 to 1.02 µm as the NO3− concentration at Angiola increased from 43 to 66 µg m− 3 during a PM2.5 episode from January 4–7, 2001. There was a direct relationship between GMD and NO3− and SO4= concentrations at Angiola but no such relationships for OC or EC. This demonstrates that secondary aerosol formation increases both concentration and particle size for the rural California environment. 相似文献
5.
The samples of water-soluble inorganic ions (WSIs), including anions (F?, Cl?, SO42?, NO3?) and cations (NH4+, K+, Na+, Ca2+, Mg2+) in 8 size-segregated particle matter (PM), were collected using a sampler (with 8 nominal cut-sizes ranged from 0.43 to 9.0 μm) from October 2008 to September 2009 at five sites in both polluted and background regions of a coastal city, Xiamen. The results showed that particulate matters in the fine mode (PM2.1, Dp < 2.1 μm) comprised large part of mass concentrations of aerosols, which accounted for 45.56–51.27%, 40.04–60.81%, 42.02–60.81%, and 40.46–57.07% of the total particulate mass in spring, summer, autumn, and winter, respectively. The water-soluble ionic species in the fine mode at five sampling sites varied from 15.33 to 33.82 (spring), 14.03 to 28.06 (summer), 33.47 to 72.52 (autumn), and 48.39 to 69.75 μg m? 3 (winter), respectively, which accounted for 57.30 ± 6.51% of the PM2.1 mass concentrations. Secondary pollutants of NH4+, SO42? and NO3? were the dominant contributors of WSIs, which suggested that pollutants from anthropogenic activities, such as SO2, NOx were formed in aerosols by photochemical reactions. The size distributions of Na+, Cl?, SO42? and NO3? were bimodal, peaking at 0.43–0.65 μm and 3.3–5.8 μm. Although some ions, such as NH4+ presented bimodal distributions, the coarse mode was insignificant compared to the fine mode. Ca2+ and Mg2+ exhibited unimodal distributions at all sampling sites, peaking at 2.1–3.3 μm, while K+ having a bimodal distributions with a major peak at 0.43–0.65 μm and a minor one at 3.3–4.7 μm, were used in most of samples. Seasonal and spatial variations in the size-distribution profiles suggested that meteorological conditions (seasonal patterns) and sampling locations (geographical patterns) were the main factors determining the formation of secondary aerosols and characteristics of size distributions for WSIs. 相似文献
6.
《Atmospheric Research》2009,91(2-4):195-202
We present results of direct aerosol radiative forcing over a French Mediterranean coastal zone based on one year of continuous observations of aerosol optical properties during 2005–2006. Monthly-mean aerosol optical depth at 440 nm ranged between 0.1 and 0.34, with high Angstrom coefficient (α > 1.2). The single scattering albedo (at 525 nm) estimated at the surface ranged between 0.7 and 0.8, indicating significant absorption. The presence of aerosols over the Mediterranean zone during summer decreases the shortwave radiation reaching the surface by as much as 26 ± 3.9 W m− 2, and increases the top of the atmosphere reflected radiation by as much as 5.2 ± 1.0 W m− 2. The shortwave atmospheric absorption translates to an atmospheric heating of 2.5 to 4.6 K day− 1. Concerted efforts are needed for investigating the possible impact of the increase in heating rate on the maintenance of heat-waves frequently occurring over this coastal region during summer time. 相似文献
7.
In October 7–9, 2016, Hurricane Matthew moved along the southeastern coast of the U.S., causing major flooding and significant damage, even to locations farther north well away from the storm’s winds. Various observations, such as tide gauge data, cable measurements of the Florida Current (FC) transport, satellite altimeter data and high-frequency radar data, were analyzed to evaluate the impact of the storm. The data show a dramatic decline in the FC flow and increased coastal sea level along the U.S. coast. Weakening of the Gulf Stream (GS) downstream from the storm’s area contributed to high coastal sea levels farther north. Analyses of simulations of an operational hurricane-ocean coupled model reveal the disruption that the hurricane caused to the GS flow, including a decline in transport of ∼20 Sv (1 Sv = 106 m3 s−1). In comparison, the observed FC reached a maximum transport of ∼40 Sv before the storm on September 10 and a minimum of ∼20 Sv after the storm on October 12. The hurricane impacts both the geostrophic part of the GS and the wind-driven currents, generating inertial oscillations with velocities of up to ±1 m s−1. Analysis of the observed FC transport since 1982 indicated that the magnitude of the current weakening in October 2016 was quite rare (outside 3 standard deviations from the mean). Such a large FC weakening in the past occurred more often in October and November, but is extremely rare in June-August. Similar impacts on the FC from past tropical storms and hurricanes suggest that storms may contribute to seasonal and interannual variations in the FC. The results also demonstrated the extended range of coastal impacts that remote storms can cause through their influence on ocean currents. 相似文献
8.
A new methodology is proposed to estimate the strength of the South Atlantic Anticyclone (SAA), using the gridded sea level pressure (SLP) of the National Centers for Environmental Prediction/National Center for Atmospheric Research (NCEP/NCAR) Reanalysis data. The top quartile (1017.3 hPa) of the SLP data was found a reasonable criterion to delimit the SAA area. Consequently, we defined the SAA area as the quadrangle containing 80% of the observations with pressure >1017.3 hPa. In this quadrangle, an area weighted pressure gradient (AWPG) was computed for the whole area and for the north–south and west–east halves. When compared with maximum pressure, the AWPG showed a better correlation with the significant wave height (SWH) and wind speed (WS) derived from altimetry. The mean value of the AWPG was 8 × 10−4 Pa/m, with representative values of 9.1 × 10−4 Pa/m and 7.4 × 10−4 Pa/m for austral winter and summer, respectively. The phase difference between the monthly AWPG in the north and south sub-quadrangles accounts for the evolution of the spatial pattern of the anticyclone throughout a year. This quantitative approach proved to be a useful estimate of the strength of South Atlantic Anticyclone. Further improvements of this approach are discussed. 相似文献
9.
The variability of sea surface Total Alkalinity (TA) and sea surface Total Inorganic Carbon (CT) is examined using all available data in the western tropical Atlantic (WTA: 20°S-20°N, 60°W-20°W). Lowest TA and CT are observed for the region located between 0°N-15°N/60°W-50°W and are explained by the influence of the Amazon plume during boreal summer. In the southern part of the area, 20°S-10°S/40°W-60°W, the highest values of TA and CT are linked to the CO2–rich waters due to the equatorial upwelling, which are transported by the South Equatorial Current (SEC) flowing from the African coast to the Brazilian shore. An increase of CT of 0.9 ± 0.3 μmol kg−1yr−1 has been observed in the SEC region and is consistent with previous published estimates. A revised CT-Sea Surface Salinity (SSS) relationship is proposed for the WTA to take into account the variability of CT at low salinities. This new CT-SSS relationship together with a published TA-SSS relationship allow to calculate pCO2 values that compare well with observed pCO2 (R2 = 0.90). 相似文献
10.
We analyzed a 20-year time series (January 1st, 1993 through December 31st, 2012) of Loop Current (LC) surface area derived from satellite altimetry in the eastern Gulf of Mexico to estimate kinematical metrics of this potent flow. On average the LC intrudes to its maximum northward position about 216 ± 126 days after the previous eddy separation; and ∼30 ± 31 days later sheds a large anticyclonic eddy. When the northern extent of the LC intrusion following the previous eddy separation is greater than 27°N, the current retreats very quickly until it sheds another eddy with the entire separation process occurring on the order of 30 days. To first order the change in areal extent of the LC during intrusion into the Gulf occurs at an average rate of 225 km2 day−1, which corresponds to an intrusion velocity of 1.7 cm s−1 of the LC front, and adds Caribbean water to the Gulf at a rate of 2.6 ± 0.7 Sv. 相似文献
11.
In this study, total suspended particles (TSP) and size-segregated atmospheric aerosol samples were measured on Qianliyan Island in the Yellow Sea in spring (April–May), summer (July–August) and fall (October–November) of 2006 and in water (January–February) of 2007. The mass concentration of the TSP varied from 75.6 to 132.0 μg/m3. The average concentration were 9.37 ± 7.56 μg/m3 and 5.32 ± 4.25 μg/m3 for nitrate and ammonium in the TSP, respectively. TSP concentration showed a significant correlation with those of nitrate (n = 27, r = 0.73) and ammonium (n = 27, r = 0.60). The mass-size distribution of atmospheric particles exhibited two modes with an accumulation mode at 0.43–1.1 μm and a coarse mode at 3.3–4.7 μm throughout the sampling months. A bi-modal size distribution of nitrate in concentration occurred in the April–May, October–November and January–February, but a uni-modal size distribution occurred in the August. The uni-modal size distribution of ammonium at 0.43–0.65 μm was observed throughout the sampling months. The average of inorganic nitrogen in mass concentration accounted for 4.0% of the total mass of aerosol particles while ammonium-N was the dominant fraction of TIN (Total Inorganic Nitrogen), contributing to 62–71% of the TIN. 相似文献
12.
The relationships between meteorological conditions (temperature, wind-speed and direction, relative humidity, surface-inversion depth and strength, and stability) and PM2.5 concentrations in Fairbanks, Alaska were investigated using ten years of observational data. The results show that during wintertime (November through February) PM2.5 concentrations exceeding the 24 h National Air Quality Standard (35 μg/m3) occurred under calm wind, extremely low temperature (≤20 °C) and moisture (water-vapor pressure < 2 hPa) multiday surface-inversion conditions that trap the pollutants in the breathing level and inhibit transport of polluted air out of Fairbanks. PM2.5 concentrations tend to be higher under stable than other conditions, but are not sensitive to the degree of stability. The presence of a surface inversion and calm wind are necessary, but in combination with low temperatures and humidity, the conditions are sufficient for high PM2.5 concentrations. The low temperatures are required because they lead to increased emission rates from domestic heating and power production. During multiday inversions with temperatures above ? 20 °C, high relative humidity (> 75%) partly caused by water-vapor emission reduces PM2.5 concentrations. 相似文献
13.
Climate output from the UK Hadley Centre's HadCM2 and HadCM3 experiments for the period 1860 to 2100, with IS92a greenhouse gas forcing, together with predicted patterns of N deposition and increasing CO2, were input (offline) to the dynamic vegetation model, Hybrid v4.1 (Friend et al., 1997; Friend and White, 1999). This model represents biogeochemical, biophysical and biogeographical processes, coupling the carbon, nitrogen and water cycles on a sub-daily timestep, simulating potential vegetation and transient changes in annual growth and competition between eight generalized plant types in response to climate.Global vegetation carbon was predicted to rise from about 600 to 800 PgC (or to 650 PgC for HadCM3) while the soil carbon pool of about 1100 PgC decreased by about 8%. By the 2080s, climate change caused a partial loss of Amazonian rainforest, C4 grasslands and temperate forest in areas of southern Europe and eastern USA, but an expansion in the boreal forest area. These changes were accompanied by a decrease in net primary productivity (NPP) of vegetation in many tropical areas, southern Europe and eastern USA (in response to warming and a decrease in rainfall), but an increase in NPP of boreal forests. Global NPP increased from 45 to 50 PgC y−1 in the 1990s to about 65 PgC y−1 in the 2080s (about 58 PgC y−1 for HadCM3). Global net ecosystem productivity (NEP) increased from about 1.3 PgC y−1 in the 1990s to about 3.6 PgC y−1 in the 2030s and then declined to zero by 2100 owing to a loss of carbon from declining forests in the tropics and at warm temperate latitudes — despite strengthening of the carbon sink at northern high latitudes. HadCM3 gave a more erratic temporal evolution of NEP than HadCM2, with a dramatic collapse in NEP in the 2050s. 相似文献
14.
《Atmospheric Research》2009,91(2-4):253-263
A high-volume cascade impactor, equipped with a PM10 inlet, was used to collect size-segregated aerosol samples during the summer of 2004 at two Portuguese locations: a coastal-rural area (Moitinhos) and an urban area (Oporto). Concentrations of airborne particulate matter (PM), total carbon (TC), organic carbon (OC), elemental carbon (EC), and water-soluble organic carbon (WSOC) were determined for the following particle size ranges: < 0.49, 0.49–0.95, 0.95–3.0, and 3.0–10 µm. The total PM mass concentrations at the urban and coastal-rural sites ranged from 22.8 to 79.6 μg m− 3 and 19.9 to 28.2 μg m− 3, respectively, and more than 56% of the total aerosol mass was found in the fractions below 3.0 μm. At both locations the highest concentrations of OC and EC were found in the submicrometer size range. The regional variability for the OC and EC concentrations, with the highest concentrations being found in the urban area, was related to the contribution of local primary sources (mostly traffic emissions). It was also verified an enrichment of the small size particles in WSOC, representing on average 37.3(± 12.4)% and 59.7(± 18.0)% of OC in the very fine aerosol at the coastal-rural and urban areas, respectively. The amount of secondary OC calculated by the minimum OC/EC ratio method indicates that secondary organic aerosol formation was important throughout the study at both sites. The obtained results suggest that long-range transport and favourable summer conditions for photochemical oxidation are key factors determining secondary OC formation in the coastal-rural and urban areas. The ultraviolet absorption properties of the chromophoric constituents of the WSOC fractions were also different among the different particle size ranges and also between the two sampling locations, thus suggesting the strong impact of the diverse emission sources into the composition of the size-segregated organic aerosol. 相似文献
15.
In this study, 24-h PM2.5 samples were collected using Harvard Honeycomb denuder/filter-pack system during different seasons in 2006 and 2007 at an urban site in Guangzhou, China. The particles collected in this study were generally acidic (average strong acidity ([H+]) ~ 70 nmol m? 3). Interestingly, aerosol sulfate was not fully neutralized in the ammonia-rich atmosphere (NH3 ~ 30 ppb) and even when NH4+]/[SO42?] was larger than 2. Consequently, strong acidity ([H+]) as high as 170 nmol m? 3 was observed in these samples. The kinetic rate of neutralization of acidity (acidic sulfate) by ambient ammonia was significantly higher than the rate of formation of ammonium nitrate involving HNO3 and NH3 for [NH4+]/[SO42?] ≤ 1.5 and much lower for NH4+]/[SO42?] > 1.5. Therefore, higher nitrate principally formed via homogeneous gas phase reactions involving ammonia and nitric acid were observed for [NH4+]/[SO42?] > 1.5. However, little nitrate, probably formed via heterogeneous processes e.g. reaction of HNO3 with sea salt or crustal species, was observed for [NH4+]/[SO42?] ≤ 1.5. These demonstrate a clear transition in the pathways of ambient ammonia to form aerosol ammonium at [NH4+]/[SO42?] = 1.5 and evidently explain the observed high acidity due to the unneutralized sulfate in the ammonium-rich aerosol (NH4+]/[SO42?] > 1.5). In fact, the measured acidity was almost similar to the excess acid defined as the acid that remains at [NH4+]/[SO42?] = 1.5 due to the un-neutralized fraction of sulfate ([H+] = 0.5[SO42?]). The presence of high excess acid and ammonium nitrate significantly lowered the deliquescence relative humidity of ammonium sulfate (from 80% to 40%) in the ammonium-rich samples. 相似文献
16.
Yan Wang Jia Guo Tao Wang Aijun Ding Jian Gao Yang Zhou Jeffrey L. Collett Wenxing Wang 《Atmospheric Research》2011,99(3-4):434-442
Cloud/fog samples were collected during spring of 2007 in the highly polluted North China Plain in order to examine the impact of pollution and dust particles on cloud water chemistry. The volume weighted mean pH of cloud water was 3.68. The cloud acidity was shown to be associated with air mass origins. Cloud water with its air mass trajectories originating from the southern part of China was more acidic than those from northern China. Anthropogenic source and dust had obvious impact on cloud water composition as indicated by the very high mean concentrations of SO42? (1331.65 μeq L? 1), NO3? (772.44 μeq L? 1), NH4+ (1375.92 μeq L? 1) and Ca2+ (625.81 μeq L? 1) in the observation periods. During sandstorm days, cloud pH values were relatively high, and the concentrations of all the ions in cloud water reached unusual high levels. Significant decreases in the mass concentrations of PM2.5 and PM10 were observed during cloud events. The average scavenging ratio for PM2.5 and PM10 was 52.0% and 55.7%, respectively. Among the soluble ions in fine particles, NO3?, K+ and NH4+ tend to be more easily scavenged than Ca2+ and Na+. 相似文献
17.
Conventional surface data and quantitative estimations of precipitation are used to document the occurrence and spatial distribution of severe weather phenomena associated with deep moist convection over southeastern South America.Data used in this paper are 24-hour rainfall, maximum hourly gusts and present weather reports from the surface station network for Argentina to the north of 40°S and cover the period 2000–2005. Hourly rainfall estimated with the CMORPH technique (CPC MORPHing technique, R. J. Joyce et al., 2004) is included in the analysis in order to increase the density of the precipitation database from January 2003 to December 2005. Extreme events are detected by means of a 95th-percentile analysis of the 24-hour rainfall and wind; values greater than 30 mm and 25 m s?1 respectively are considered extreme in the study area. These results are related to the presence of deep convection by considering the 235 K and 218 K cloud shield evolution in Geostationary Operational Environmental Satellite-12 Infrared (GOES-IR) imagery evaluated by the Forecasting and Tracking of Cloud Cluster (FORTRACC) technique. Rainfall above 30 mm day?1 and present convection-related weather events tend to occur in the northeast of the country.Finally, an analysis is made of the relationship between severe phenomena and the location and lifecycle of Mesoscale Convective Systems (MCSs) defined by the 218 K or 235 K levels. According to the reports, favorable locations for severe weather concentrate to the northeast of the cloud shield anvil centroid although most of the cases are found in the northwest. This feature can be seen in systems with anvil areas larger than 250,000 km2 in association to the predominant mid-level wind shear direction from the northwest over the area. Moreover, systems with centers located north of 30°S present a more circular shape while those to the south are more elongated with a NW–SE main axis clearly related to the presence and interaction with frontal zones over the area. Most of the events occur previous to the moment when the systems reach their maximum extension, between 2 and 10 h after the initiation of the system depending on the size of the MCSs. 相似文献
18.
Asude Hanedar Kadir Alp Burcak Kaynak Jaemeen Baek Edip Avsar M. Talat Odman 《Atmospheric Research》2011,99(3-4):391-399
The chemical mass balance model was applied to atmospheric Polycyclic Aromatic Hydrocarbons (PAHs) in Istanbul, Turkey. A total of 326 airborne samples were collected and analyzed for 16 PAHs and Total Suspended Particles (TSP) in the September 2006–December 2007 period at three monitoring stations: Yildiz, DMO (urban sites) and Kilyos (rural site). The total average PAH concentrations were 100.66 ± 61.26, 84.63 ± 46.66 and 25.12 ± 13.34 ng m?3 and the TSP concentrations were 101.16 ± 53.22, 152.31 ± 99.12, 49.84 ± 18.58 μg m?3 for Yildiz, DMO and Kilyos stations respectively. At all the sites, the lighter compounds were the most abundant, notably Nap, AcPy and PA. The average correlation values between TSP and total heavier PAH were greater than 0.5 for Yildiz and DMO stations. The patterns of PAH and TSP concentrations showed spatial and temporal variations. PAH concentrations were evaluated for the PAH contribution from four sources (diesel engines, gasoline engines, natural gas combustion, and coal + wood burning). Vehicle emissions appear to be the major source with contributions of 61.2%, 63.3% and 54.1% for Yildiz, DMO and Kilyos stations respectively. Seasonal and yearly variations had different trends for all sites. 相似文献
19.
Oil palm production expanded 1.2 million hectares in sub-Saharan Africa since 1990, with expansion accelerating in several heavily forested countries since 2000. Despite a narrative of expansion driven by multinational corporations, we provide evidence of a dynamic non-industrial oil palm production sector linked to a burgeoning informal milling enterprise. Surveys were conducted with oil palm farmers in Cameroon (n = 546), the third largest palm oil producer on the continent with the greatest amount of deforestation due to recent expansion, to determine who is expanding into forest. Seventy-three percent of survey respondents reported clearing forest, the magnitude of which was explained by differences in milling strategies and supply chain integration. Large-scale, non-industrial producers played a disproportionate role in deforestation, many of which were engaged in informal supply chains through the use of non-industrial mills. Farms associated with more clearing tended to use high-yielding seedlings. Even the highest yielding farms, however, averaged only 7.7 tons fresh fruit bunches (FFBs) ha−1 yr−1, well below the potential 20 tons FFBs ha−1 yr−1 yield for Cameroon. We also found a strong relationship between deforestation and land claims. Most farms claimed ownership of their land, although only 5% had official land titles. Conservation challenges in the region arise from land tenure laws that incentivize forest clearing. This study sheds light on the role of informal supply chains in deforestation and highlights the need for strict implementation and enforcement of land use zoning policies. 相似文献
20.
Urban growth is increasing the demand for freshwater resources, yet surprisingly the water sources of the world's large cities have never been globally assessed, hampering efforts to assess the distribution and causes of urban water stress. We conducted the first global survey of the large cities’ water sources, and show that previous global hydrologic models that ignored urban water infrastructure significantly overestimated urban water stress. Large cities obtain 78 ± 3% of their water from surface sources, some of which are far away: cumulatively, large cities moved 504 billion liters a day (184 km3 yr−1) a distance of 27,000 ± 3800 km, and the upstream contributing area of urban water sources is 41% of the global land surface. Despite this infrastructure, one in four cities, containing $4.8 ± 0.7 trillion in economic activity, remain water stressed due to geographical and financial limitations. The strategic management of these cities’ water sources is therefore important for the future of the global economy. 相似文献