The Use of Remote Sensing and GIS in the Sustainable Management of Tropical Coastal Ecosystems

The sustainable use and management of important tropical coastal ecosystems (mangrove forests, seagrass beds and coral reefs) cannot be done without understanding the direct and indirect impacts of man. The ecosystem's resilience and recovery capacity following such impacts must be determined. The efficacy of mitigation measures must also be considered. Remote sensing and geographic information systems (GIS) are excellent tools to use in such studies. This paper reviews the state of the art and application of these tools in tropical coastal zones, and illustrates their relevance in sustainable development. It highlights a selected number of remote sensing case-studies on land cover patterns, population structure and dynamics, and stand characteristics from South-East Asia, Africa and South-America, with a particular emphasis on mangroves. It further shows how remote sensing technology and other scientific tools can be integrated in long-term studies, both retrospective and predictive, in order to anticipate degradation and to take mitigating measures at an early stage. The paper also highlights the guidelines for sustainable management that can result from remote sensing and GIS studies, and identifies existent gaps and research priorities.There is a need for more comprehensive approaches that deal with new remote sensing technologies and analysis in a GIS-environment, and that integrate findings collected over longer periods with the aim of prediction. It is also imperative to collect and integrate data from different disciplines. These are essential in the spirit of sustainable development and management, particularly in developing countries, which are often more vulnerable to environmental degradation.     

Dandy – Walker syndrome and corpus callosum agenesis in 5p deletion

5p deletion syndrome commonly known as cri du chat is well described in affected neonates with catlike cry and hypotonia. Karyotyping will usually show a deletion of the short arm of one chromosome 5 with variable breakpoints. Only a few cases have been reported prenatally, and the fetal form of the syndrome has not been clearly individualised. We report a new case of 5p deletion syndrome diagnosed prenatally in association with Dandy–Walker syndrome and agenesis of the corpus callosum. Other brain anomalies have been reported previously, but this unusual association suggests the use of a specific probe in the investigation of these malformations. Copyright © 2005 John Wiley & Sons, Ltd.     

Fetal phenotype of Prader–Willi syndrome due to maternal disomy for chromosome 15

Prader–Willi syndrome (PWS) results from either paternal deletion of 15q11–q13, or maternal uniparental disomy (UPD) of chromosome 15 or imprinting center mutation. Prenatal diagnosis of PWS is currently indicated for chromosomal parental translocation involving chromosome 15 and for decreased fetal movements during the third trimester of gestation. Here we present the prenatal diagnosis of PWS during the first trimester of gestation and autopsy findings. Chorionic villus sampling (CVS) was performed for advanced maternal age at 13 weeks' gestation. CVS showed mosaicism including cells with a normal karyotype and cells with trisomy 15. Amniocentesis showed cells with a normal karyotype. Molecular analysis demonstrated that the fetus had a typical PWS abnormal methylation profile and maternal disomy for chromosome 15. Fetal ultrasound examination showed slightly enlarged lateral ventricles and hypoplasic male external genitalia without intra-uterine growth retardation. The autopsy showed a eutrophic male fetus with facial dysmorphy, hypoplasic genitalia, abnormal position of both feet and posterior hypoplasia of the corpus callosum. This report points out that in a karyotypically normal fetus with ambiguous male external genitalia and cerebral anomalies, extensive cytogenetic and molecular biology studies are strongly recommended because of risk of PWS. Copyright © 2003 John Wiley & Sons, Ltd.     

Prenatal diagnosis of Juberg–Hayward syndrome

Juberg–Hayward syndrome is a rare autosomal recessive syndrome characterised by the association of growth retardation, microcephaly, cleft lip and palate, and thumb and radial ray abnormalities. To date, no prenatal cases have been reported. Here, we report on the first prenatal case of Juberg–Hayward syndrome. The diagnosis was established following fetopathological study. Besides the cardinal features of the syndrome, this prenatal case was remarkable for the severity of the short arm malformation and by the finding of big toe agenesis and cerebral abnormalities including hydrocephalus, agenesis of corpus callosum, and cerebellar hypoplasia. We conclude that the diagnosis of Juberg–Hayward syndrome can be discussed prenatally following ultrasound diagnosis of the association of intrauterine growth restriction, microcephaly, thumb/radial anomalies, and cleft lip/palate. Copyright © 2005 John Wiley & Sons, Ltd.     

人口流动规律及其政策含义

人口流动是人力资源配轩优化的根本创新路径,人口流动的一般规律是:如果流动人口为理性行为选择者,在社会制度安排许可的发展环境下,当不同区域和不同产业间形成比较收益差异,存在着流动收益大于流动成本的潜在和现实的各种获利机会时,就必定驱使人们由低收益领域向高必益领域流动,而且比较收益差异量与流动人口的流速、流量正相关,并必然导致产生收益率及人口分布走向平均化的趋势,社会发展也将获得最优化的人力资源配置结果.其相关政策含义:一是人口流动是流动人口的理性选择;二是切实保障公民的自由流动权利;三是利用比较利益差别促进人口流动;四是降低各种不必要的流动成本和流动风险;五是建构人口流动的有效率社会发展框架.     

节水灌溉措施下湘东北丘陵林-稻汇水区复合系统铅的迁移

铅通过食物链的迁移和积累对人类健康的毒害作用日益为社会所重视,而水稻是人类铅摄入的主要途径之一,因此,对稻田土壤铅的迁入途径及其过程特征的研究十分必要.为了探明湖南地区远离城镇、工矿区的丘陵稻区铅的输入、迁移、滞留机制,选择位于湘东北地域的汩罗市桃林林场的林地-山塘-稻田汇水区系统作为研究对象,在水稻大田生长期间,原位研究其大气沉降、岗地径流、山塘水、稻田水、水稻生长等过程的铅通量.结果表明：①输入系统的铅源是大气沉降,其中,在水稻生育前期通过东南季风输入的区域外源铅占90%;②山塘是大气沉降铅的主要集纳地貌单元,存留了大气沉降输入岗地和山塘总铅的66%;③林-稻汇水区系统岗地铅净留存28.8~57.7 g·hm^-2,山塘铅净留存604.3~961.9 g·hm^-2,稻田铅净留存89.6~90.9 g·hm^-2;而对照系统岗地铅净输出173.3 g·hm^-2,山塘净留存3427.6 g·hm^-2,稻田净留存87.1 g·hm^-2;④岗地和山塘对铅的截留量能够互补;⑤从岗地通过径流-山塘水过程迁移到稻田的大分子有机物能够增强稻田对铅的截留.综上所述,丘陵林-稻汇水区系统中铅的循环与大气沉降有关,系统内岗地森林类型、郁闭度、降水产流及泥沙、有机物的输出都会影响铅在系统中的迁移和分配.