Eco county construction in China

１　ＩｎｔｒｏｄｕｃｔｉｏｎＩｎＣｈｉｎａ，ｃｏｕｎｔｙｉｓｔｈｅｍｏｓｔｅｌｅｍｅｎｔａｒｙｕｎｉｔｉｎａｄｍｉｎｉｓｔｒａｔｉｏｎ．Ｉｔｈａｓｔｈｅｒｅｌａｔｉｖｅｌｙｉｎｄｅｐｅｎｄｅｎｔａｕｔｈｏｒｉｚａｔｉｏｎｉｎｐｏｌｉｃｙｍａｋｉｎｇａｎｄａｄｍｉｎｉｓｔｒａｔｉｖｅｍａｎａｇｅｍｅｎｔ．Ｉｎｇｅｎｅｒａｌ，ａｃｏｕｎｔｙｈａｓａｌａｎｄａｒｅａｏｆ１０００—４０００ｋｍ２ｗｉｔｈａｐｏｐｕｌａｔｉｏｎｏｆ０－２—０－８ｍｉｌｌｉｏｎ．Ｓｉｎｃｅｔｈｅ１９９０ｓ，ｃｏｕｎｔｙｉｓｒ…     

Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhood

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a potentially fatal inherited disease with a carrier frequency of approximately 1:100 in most Caucasian populations. The disease is implicated in sudden unexpected death in childhood. A prevalent disease-causing point mutation (A985G) in the MCAD gene has been characterized, thus rendering diagnosis easy in the majority of cases. Since the clinical spectrum of MCAD deficiency ranges from death in the first days of life to an asymptomatic life, there are probably other genetic factors—in addition to MCAD mutations—involved in the expression of the disease. Thus, families who have experienced the death of a child from MCAD deficiency might have an increased risk of a seriously affected subsequent child. In such a family we have therefore performed a prenatal diagnosis on a chorionic villus sample by a highly specific and sensitive polymerase chain reaction (PCR) assay for the G985 mutation. The analysis was positive and resulted in abortion. We verified the diagnosis by direct analysis on blood spots and other tissue material from the aborted fetus and from family members.     

Maternal serum inhibin levels in second-trimester down's syndrome pregnancies

Maternal serum inhibin levels were measured in 19 second-trimester pregnancies affected by fetal Down's syndrome and 95 unaffected control pregnancies matched for gestational age. A statistically significant elevation was found in the affected pregnancies compared with the controls (Wilcoxon rank sum test: one-tail P=0·02). The median level in the cases was 1·3 times that in the controls, with 95 per cent confidence limits of 0·9–1·9. Although the inhibin levels were unrelated to those of alpha-fetoprotein and unconjugated oestriol in the same samples, there was a statistically significant correlation with human chorionic gonadotropin. This together with the relatively small elevation in cases suggests that inhibin would be of limited value in maternal serum screening for Down's syndrome.     

近百年中国亚热带地区农业气候带界限动态变化及其对农业生产的影响

本文利用我国东部亚热带地区315个站点的资料,采用农业气候带分界指标,分析了北亚热带北界、中亚热带北界、南亚热带北界3个界限近百年的动态变化以及农业气候带界限波动变化对农业生产的影响。     

Association of generalized dystrophic epidermolysis bullosa with positive acetylcholinesterase and markedly elevated maternal serum and amniotic fluid alpha-fetoprotein

A case of fatal generalized dystrophic epidermolysis bullosa is described in a prematurely born female whose mother had strikingly elevated mid-trimester serum and amniotic fluid alpha-fetoprotein concentrations, a positive amniotic fluid acetylcholinesterase band, and negative serial ultrasound studies. This case lends further support to an association between autosomal recessive generalized dystrophic epidermolysis bullosa and increased levels of alpha-fetoprotein, positive amniotic fluid acetylcholines'terase, and normal ultrasound findings.     

Early amniocentesis at 11–14 weeks' gestation for the diagnosis of fetal chromosomal abnormality—a clinical evaluation

Early arnniocentesis between 11 and 14 weeks' gestation was offered to 110 women at risk of a chromosomally abnormal fetus due to maternal age. Four were found to be unsuitable for the procedure, and 106 early amniocenteses were performed. In 102 cases, clear amniotic fluid was obtained with a single tap. There were two dry taps and two bloodstained tapis; sampling was repeated in three of these cases before 15 weeks. In the fourth case, placental biopsy was performed at 16 weeks. Thus, we were able to obtain a satisfactory sample in all but three cases(2.8 percent). Karyotyping of cells harvested from the early amniotic fluid samples was successful in all the 105 cases. Cell culture from the initial samples revealed a normal karyotype in 99 cases, two balanced translocations, two tetraploid karyotypes, and two cases of pseudomosaicism. Of the 105 pregnancies successfully sampled, there have been two losses to date (1–8 per cent). Two further patients presented with premature rupture of membranes, both pregnancies having successful outcomes. Sixty-two babies have delivered to date, with four congenital anomalies. There were no respiratory problems. Twenty-nine pregnancies are continuing without known complications, and details are not yet available on the remaining 12. The results indicate that early arnniocentesis may replace the traditional test at 15–17 weeks.     

Chance-constrained programming (CCP)abatement of SO_2 emission for acid deposition control in Liuzhou City

A deterministic linear programming model which optimizes the abatement of each SO2 emission source, is extended into a CCP form by introducing equations of probabilistic constrained through the incorporation of uncertainty in the source-receptor-specific transfer coefficients. Based on the calculation of SO2 and sulfate average residence time for Liuzhou City, a sulfur deposition model has been developed and the distribution of transfer coefficients have been found to be approximately log-normal. Sulfur removal minimization of the model shows that the abatement of emission sources in the city is more effective, while control cost optimization provides the lowest cost programmes for source abatement at each allowable deposition limit under varied environmental risk levels. Finally a practicable programme is recommended.     

赣江流域山丘荒地的形成、危害和开发途径

赣江流域的山丘荒地总面积约为 2902×10⁴亩,除 35×10⁴亩属于“十边草地”零星分布于路边、河边、田边、村边、沟边之外,比较成片的约有 2867×10⁴亩（见表 1）,略多于现有耕地,而且相当于现有林地的一半。这些荒地 3/4以上分布在红壤丘陵（低丘岗地 388×10⁴亩,占13.5％;中低丘1236×10⁴亩,占43.1％;高丘605×10⁴亩,占21.2％;山地638×10⁴亩,占22.3％）,而且主要分于于上、中游地区（上游地区占60.2％,中游地区占25.4％,下游地区占14.4％）。综合开发治理、合理利用这些山丘荒地,是赣江流域、特别是上、中游地区的农民摆脱贫穷落后困境、实现小康目标的重要环节之一。     

A study on Se application for improving the soil in the environment at lower Se level

A result that application of sodium selenite or fly ash to some of soilin loess plateau can increase Se content in wheat grain has been demonstrated by the pot and field experiments, and added Se in soil can last its availability for 3 years. So this is a good measure for improving the low Se soils and preventing the Kaschin-Beck disease.     

Iniencephaly is not uniformly fatal

Iniencephaly is an uncommon, but not rare, lesion involving a fusion between the posterior occipital bone and the cervical spine. Many cases are associated with other cranio-cervical abnormalities and anencephaly, and most are associated with other structural abnormalities. The prognosis is thought to be dismal. We describe a male infant, one of twins, who was diagnosed prenatally as having iniencephaly. The child was born without complication and has grown and thrived. This is the fourth patient with long-term survival with iniencephaly. We recommend that non-directive counselling be applied when presenting the findings of iniencephaly to parents.