碳素纤维在近岸海洋污染物磷酸盐、硅酸盐处理中的应用

对碳素纤维进行氧化改性,利用改性后的碳素纤维处理近岸污染海水,重点研究了改性碳素纤维对海水中活性磷酸盐和活性硅酸盐的吸附作用。考察了碳素纤维液相改性时间、碳素纤维投加量、活性磷酸盐初始浓度、活性硅酸盐初始浓度、吸附时间、海况、pH值等单因素对近岸海洋污染物磷酸盐、硅酸盐吸附效果的影响。研究结果表明:改性碳素纤维对硅酸盐的吸附效果较好,去除率可达70%,对活性磷酸盐的去除率为31%左右。通过正交实验确定改性碳素纤维材料修复模拟近岸海水的优化条件为:碳素纤维改性时间为1.5 h,投加量为0.01 g,硅酸盐初始浓度为3mg/L,磷酸盐初始浓度为20 mg/L,海况为3级,pH值为8,吸附时间为3 h。在此条件下,碳素纤维对磷酸盐的去除率可达31.06%,硅酸盐去除率可达70.88%。     

Sulphate, Nitrogen and Base Cation Budgets at 21 Forested Catchments in Canada, the United States and Europe

To assess the concern over declining base cation levels in forest soils caused by acid deposition, input-output budgets (1990s average) for sulphate (SO₄), inorganic nitrogen (NO₃-N; NH₄-N), calcium (Ca), magnesium (Mg) and potassium (K) were synthesised for 21 forested catchments from 17 regions in Canada, the United States and Europe. Trend analysis was conducted on monthly ion concentrations in deposition and runoff when more than 9 years of data were available (14 regions, 17 sites). Annual average SO₄ deposition during the 1990s ranged between 7.3 and 28.4 kg ha⁻¹ per year, and inorganic nitrogen (N) deposition was between 2.8 and 13.8 kg ha⁻¹ per year, of which 41–67% was nitrate (NO₃-N). Over the period of record, SO₄ concentration in deposition decreased in 13/14 (13 out of 14 total) regions and SO₄ in runoff decreased at 14/17 catchments. In contrast, NO₃-N concentrations in deposition decreased in only 1/14 regions, while NH₄-N concentration patterns varied; increasing at 3/14 regions and decreasing at 2/14 regions. Nitrate concentrations in runoff decreased at 4/17 catchments and increased at only 1 site, whereas runoff levels of NH₄-N increased at 5/17 catchments. Decreasing trends in deposition were also recorded for Ca, Mg, and K at many of the catchments and on an equivalent basis, accounted for up to 131% (median 22%) of the decrease in acid anion deposition. Base cation concentrations in streams generally declined over time, with significant decreases in Ca, Mg and K occurring at 8, 9 and 7 of 17 sites respectively, which accounted for up to 133% (median 48%) of the decrease in acid anion concentration. Sulphate export exceeded input at 18/21 catchments, likely due to dry deposition and/or internal sources. The majority of N in deposition (31–100%; median 94%) was retained in the catchments, although there was a tendency for greater NO₃-N leaching at sites receiving higher (<7 kg ha^-1 per year) bulk inorganic N deposition. Mass balance calculations show that export of Ca and Mg in runoff exceeds input at all 21 catchments, but K export only exceeds input at 16/21 sites. Estimates of base cation weathering were available for 18 sites. When included in the mass balance calculation, Ca, Mg and K exports exceeded inputs at 14, 10 and 2 sites respectively. Annual Ca and Mg losses represent appreciable proportions of the current exchangeable soil Ca and Mg pools, although losses at some of the sites likely occur from weathering reactions beneath the rooting zone and there is considerable uncertainty associated with mineral weathering estimates. Critical loads for sulphur (S) and N, using a critical base cation to aluminium ratio of 10 in soil solution, are currently exceeded at 7 of the 18 sites with base cation weathering estimates. Despite reductions in SO₄ and H⁺ deposition, mass balance estimates indicate that acid deposition continues to acidify soils in many regions with losses of Ca and Mg of primary concern. The U.S. Government's right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged. The Canadian Crown reserves the right to retain a non-exclusive, royalty free licence in and to any copyright.     

二氧化氯消毒前后污水毒性的变化及消毒条件的影响

采用发光细菌试验和umu试验,分别考察了二氧化氯投加量和反应时间对污水二氧化氯消毒后急性毒性和遗传毒性变化的影响.结果表明,随着二氧化氯消毒剂投加量的增加,消毒后水样的急性毒性不断增大,但遗传毒性逐渐减小后趋于稳定.随着反应时间的延长,二氧化氯的消耗量不断增大,消毒后水样的急性毒性先增大后减小,遗传毒性逐渐减小后趋于稳定.由于消毒条件对污水急性毒性和遗传毒性有着不同的影响,说明污水中产生急性毒性和产生遗传毒性的物质不同,对于某一种污水,通过控制消毒条件可以使消毒后污水的急性毒性和遗传毒性都较低.     

Performance of the Button Personal Inhalable Sampler for the measurement of outdoor aeroallergens

No personal aerosol sampler has been evaluated for monitoring aeroallergens in outdoor field conditions and compared to conventional stationary aerobiological samplers. Recently developed Button Personal Inhalable Aerosol Sampler has demonstrated high sampling efficiency for non-biological particles and low sensitivity to the wind direction and velocity. The aim of the present study was to evaluate the Button Sampler for the measurement of outdoor pollen grains and fungal spores side-by-side with the widely used Rotorod Sampler. The sampling was performed for 8 months (spring, summer and fall) at a monitoring station on the roof of a two-storied office building located in the center of the city of Cincinnati. Two identical Button Samplers, one oriented towards the most prevalent wind and the other towards the opposite wind and a Rotorod Sampler were placed side-by-side. The total fungal spore concentration ranged from 129 to 12,980 spores m(-3) (number per cubic meter of air) and the total pollen concentration from 4 to 4536 pollen m(-3). The fungal spore concentrations obtained with the two Button Samplers correlated well (r = 0.95; p<0.0001). The pollen data also showed positive correlation. These findings strongly support the results of earlier studies conducted with non-biological aerosol particles, which demonstrated a low wind dependence of the performance of the Button Sampler compared to other samplers. The Button Sampler's inlet efficiency was found to be more dependent on wind direction when sampling larger sized Pinaceae pollen grains (aerodynamic diameter approximately 65 mum). Compared to Rotorod, both Button Samplers measured significantly higher total fungal spore concentrations. For total pollen count, the Button Sampler facing the prevalent wind showed concentrations levels comparable to that of the Rotorod, but the Button Sampler oriented opposite to the prevalent wind demonstrated lower concentration levels. Overall, it was concluded that the Button Sampler is efficient for the personal sampling of outdoor aeroallergens, and is especially beneficial for aeroallergens of small particle size.     

Assessing the recovery of lakes in southeastern Canada from the effects of acidic deposition

Reductions in North American sulfur dioxide (SO2) emissions promoted expectations that aquatic ecosystems in southeastern Canada would soon recover from acidification. Only lakes located near smelters that have dramatically reduced emissions approach this expectation. Lakes in the Atlantic provinces, Quebec and Ontario affected only by long-range sources show a general decline in sulfate (SO4(2-)) concentrations, but with a relatively smaller compensating increase in pH or alkalinity. Several factors may contribute to the constrained (or most likely delayed) acidity response: declining base cation concentrations, drought-induced mobilization of SO4(2-), damaged internal alkalinity generation mechanisms, and perhaps increasing nitrate or organic anion levels. Monitoring to detect biological recovery in southeastern Canada is extremely limited, but where it occurs, there is little evidence of recovery outside of the Sudbury/Killarney area. Both the occurrence of Atlantic salmon in Nova Scotia rivers and the breeding success of Common Loons in Ontario lakes are in fact declining although factors beyond acidification also play a role. Chemical and biological models predict that much greater SO2 emission reductions than those presently required by legislation will be needed to promote widespread chemical and latterly, biological recovery. It may be unrealistic to expect that pre-industrial chemical and biological conditions can ever be reestablished in many lakes of southeastern Canada.     

ACID PRECIPITATION AND WEATHERING BY ORGANIC ACIDS IN LABRAI)OR LAKE BASINS1

ABSTRACT: Thirty-five lakes in southern Labrador sampled in 1981 were resampled in 1989 and water chemistry values were compared between visits. Results showed higher pH, specific conductance, acid neutralization capacity, color, and base cations values in 1989, though sulfate, the ion most likely to reflect acid precipitation impacts, did not vary. The major ion changes measured were probably due to natural hydrological variations and not to changes in acid inputs. Results from the 1989 data showed a slight, but significant, decrease in water sulfate concentration trend from western to eastern Labrador, though most values, even in the western portion of the study area, fell close to the values considered “background” by Brakke et at. (1989). Base cation concentrations exceeded those which could be predicted from weathering by carbonic and bicarbonic acid. Assuming that little weathering is generated by acid precipitation in this region, the excess cations measured are probably a result of bedrock dissolution from organic acids generated by plant decomposition. Calculations showed that organic acid effect could be responsible for 9 to 52 percent of total weathering in the study basins.     

Status and drivers of food insecurity and adaptation responses under a changing climate among smallholder farmers households in Bagmati Province,Nepal

Environment, Development and Sustainability - Like other low-income countries in Asia and Africa, Nepal still suffers from food insecurity with a large proportion of food-insecure households being...     

2003~2018年干旱对中国森林绿度异常的影响

基于卫星观测和气象再分析数据提取2003~2018年间中国森林绿度异常现象(月尺度LAI长期趋势的累积偏差), 并分析干旱对森林绿度异常影响的时空动态变化, 探究不同森林类型的干旱敏感性.结果表明: ①干旱导致的绿度异常现象频率分布呈现出南高北低的空间格局, 而高强度异常现象主要分布于中国的东北与西南地区.②2003~2018年间绿度异常严重程度呈现显著增加趋势(即绿度异常强度指数下降), 变化率为: -0.06/a(P<0.05), 而绿度异常面积比率下降, 变化率为-0.0049/a.③中国森林对干旱胁迫较为敏感的区域主要分布于云南北部与大兴安岭北部, 这是由区域的地质和气候特点以及植被类型共同作用导致的.④干旱主导区不同森林类型的干旱敏感性依次为: 阔叶林>针叶林>混交林, 绿度异常与SPEI回归斜率依次为1.8>1.3>1.2.⑤针叶林遭受的干旱强度最高, 2003~2018年间统计的SPEI中位数为-1.65, 绿度异常现象也最为严重, 多年绿度异常指数中位数为-1.81, 说明干旱强度而非敏感性主导了森林绿度异常的现象.