ABSTRACT
Quantitative evaluation of ecosystem service value and its spatial mapping is an effective way to determine priority conservation areas of cultural ecosystem services (CES). We used a combination of questionnaires and structured interviews with public participatory GIS (PPGIS) in Gongqing Forest Park in Shanghai to connect non-monetary CES values with spatially explicit information. This method applied spatial indicators of abundance, diversity and rarity to quantitatively assess the value of CES and their spatial distribution, and identified priority CES areas. The results showed the value of CES varied among landscape types. Relatively open grassland, riverside, and shrub areas were associated with high aesthetic value. Riverside areas were associated with the CES category concerned with inspiration and supporting social relationships. High diversity values mainly distributed in riverside areas, while forest and grassland areas were associated with high rarity values. The areas with the highest values for the abundance, diversity, and rarity indices were overlaid with eight gradient thresholds, which indicated that defining the 25% of ecological areas with the highest overall rating as CES priority areas was an effective threshold for CES identification and management. The methodology in this study leveraged PPGIS to spatially refe-rence, quantify, and user perception to establish relationships between landscape attributes, space, and experience. These results could provide an important basis for identifying, planning for, and managing priority conservation areas in urban protected areas.
Subject(s)
Ecosystem , Geographic Information Systems , China , Community Participation , ForestsABSTRACT
BACKGROUND: Early reperfusion can effectively treat acute myocardial infarction (AMI) and reduce the mortality significantly. This study aimed to compare the role of plasma microRNA-1 (miR-1) and cardiac troponin T (cTnT) in early diagnosis of AMI patients. METHODS: From May 2011 to May 2012, plasma samples were collected from 56 AMI patients and 28 non-AMI controls. The expression of plasma miR-1 was measured by quantitative reverse transcription-polymerase chain reaction (qRT-PCR), and the level of plasma cTnT was measured using electrochemiluminescence-based methods on an Elecsys 2010 Immunoassay Analyzer. SPSS 16.0 was used for the statistical analysis of the results. Data were expressed as mean±standard deviation unless otherwise described. The differences about clinical characteristics between the AMI patients and controls were tested using Student's t test or Fisher's exact test. The Mann-Whitney U test was conducted to compare the expression of microRNAs between the AMI patients and controls. MicroRNAs expression between different intervals of the AMI patients was compared using Wilcoxon's signed-rank test. The receiver operating characteristic (ROC) curve was established to discriminate the AMI patients from the controls. RESULTS: In the present study, the expression of plasma miR-1 was significantly increased in the AMI patients compared with the healthy controls (P<0.01). The plasma miR-1 in the AMI patients decreased to the normal level at 14 days (P>0.05). The expression of plasma miR-1 was not related to the clinical characteristics of the study population (P>0.05). ROC curve analyses demonstrated that miR-1 was specific and sensitive for the early diagnosis of AMI, but not superior to cTnT. CONCLUSION: Plasma miR-1 could be used in the early diagnosis of AMI, but it is similar to cTnT.
ABSTRACT
Taq DNA polymerase is one of the most commonly thermostable DNA polymerases in molecular biological researches, which shares its basic characters with others of the family, thereby its purifying strategy could be used not only in itself production but also in the extraction of the others as a reference. At present, the protocols reported for large scale preparation of Taq DNA are high cost, so a cheaper method was described here. In this protocol, by heat denaturation, ammonium sulfate precipitation and cation exchange chromatography of 724 resin, about 18 g powder of Na form resin could recover about 27.07 mg of Taq enzyme. The total activity and specific activity were approximately 2.2 × 105 U and 8131.98 U/mg. The total yield was about 48.92% with 59.35 of purification folds. Analysis of quality of purified enzyme indicated that only one protein 94 kDa was identified against SDS-PAGE and the remnant of DNA nuclease was not detected. For PCR reaction, The amplification ability of purified Taq polymerase was not different from that of the commercially avail-able ones. This method reported in the present study is effective and low cost, making it suitable for general purification in laboratories or business production.
