Quantitative evaluation of intraspecific genetic diversity in a natural fish population using environmental DNA analysis

Recent advances in environmental DNA (eDNA) analysis using high‐throughput sequencing (HTS) enable evaluation of intraspecific genetic diversity in a population. As the intraspecific genetic diversity provides invaluable information for wildlife conservation and management, there is an increasing demand to apply eDNA analysis to population genetics and the phylogeography by quantitative evaluation of intraspecific diversity. However, quantitative evaluations of intraspecific genetic diversity using eDNA is not straightforward because the number of eDNA sequence reads obtained by HTS may not be an index of the quantity of eDNA. In this study, to quantitatively evaluate genetic diversity using eDNA analysis, we applied a quantitative eDNA metabarcoding method using the internal standard DNAs. We targeted Ayu (Plecoglossus altivelis altivelis) and added internal standard DNAs with known copy numbers to each eDNA sample obtained from three rivers during the library preparation process. The sequence reads of each Ayu haplotype were successfully converted to DNA copy numbers based on the relationship between the copy numbers and sequence reads of the internal standard DNAs. In all rivers, the calculated copy number of each haplotype showed a significant positive correlation with the haplotype frequency estimated by a capture‐based survey. Furthermore, estimates of genetic indicators such as nucleotide diversity based on the eDNA copy numbers were comparable with those estimated based on a capture‐based study. Our results demonstrate that eDNA analysis with internal standard DNAs enables reasonable quantification of intraspecific genetic diversity, and this method could thus be a promising tool in the field of population genetics and phylogeography.     

Determination of absolute configuration of photo-degraded catechinopyranocyanidin A by modified Mosher's method

Catechinopyranocyanidins A and B (cpcA and cpcB) are two purple pigments present in the seed-coat of red adzuki bean, Vigna angularis, of which cpcA is the major pigment, containing two chiral carbons in the catechin part. Their absolute configurations were determined by comparison of their experimental and quantum chemical calculated electronic circular dichroisms (ECDs). These purple pigments are labile on light irradiation and easily decompose to photo-degraded catechinopyranocyanidins A and B (pdcpcA and pdcpcB), while retaining the stereostructure of the catechin residue. We applied modified Mosher's method for determining the chirality of the secondary alcohol in pdcpcA. Hexamethylation of pdcpcA by diazomethane followed by esterification using (S)- and (R)-MTPACl gave (R)- and (S)-MTPA esters, respectively. By analysis of the NMR spectra of (R)- and (S)-MTPA esters of tetramethylated (+)-catechin, the chirality of pdcpcA was determined to be 2R, 3S, same as the absolute configuration of cpcA.     

Diagrammatic scale for severity evaluation of the Eremanthus erythropappus–Puccinia velata pathosystem

Candeia (Eremanthus erythropappus (DC.) MacLeish), a native forest species from South America, has garnered commercial interest due to its production of essential oil that contains alpha-bisabolol. This compound is widely used in the pharmaceutical and cosmetics industry, with approximately 80% of Brazilian production being exported. Since candeia rust (Puccinia velata) has only been reported in Brazil, little is known about its epidemiology and control. There is no methodology to quantify rust severity in candeia, justifying the elaboration and validation of a diagrammatic scale containing eight levels of disease severity based on leaf area coverage (0.25%, 0.5%, 1%, 2%, 4%, 8%, 16% and 32%). In a natural sampling of disease in the field, 95% of the leaves showed severity below 16%, with the remaining 5% showing severities between 16% and 32% of leaf area. Validation of the proposed diagrammatic scale was performed by assessing the results from 10 inexperienced evaluators, performing evaluations of three leaves with different severity levels. The evaluations were performed at 7-day intervals; in the first instance, severity values were assigned without the diagrammatic scale, and for the second attempt, the scale proposed in this study was used. The accuracy and precision of the severity estimates produced by each evaluator compared to the real severity was analysed by linear regression and by Lin's statistics. The reproducibility of the estimates was evaluated by analysing the coefficient of determination of linear regressions by pairs of evaluators. The scale provided adequate levels of accuracy, precision, repeatability and reproducibility, indicating the proposed scale was a suitable method for quantifying the severity of candeia rust.     

Genetic diversity of Puccinia kuehnii,the causal agent of orange rust of sugarcane,from Brazil

The use of resistant genotypes is the preferred method to control orange rust of sugarcane (Saccharum spp) caused by Puccinia kuehnii. This approach has been adopted in Brazil but outbreaks of the disease on previously resistant varieties showed that the efficacy of this method is limited and requires a better understanding of pathogen diversity. Nevertheless, adequate molecular markers for examining pathogen diversity at population level are not available, which limits the success of orange rust control by genetic resistance. Therefore, two independent investigations were conducted to examine genetic diversity of P. kuehnii from São Paulo state, the most important sugarcane growing state of Brazil. First, simple-sequence repeat (SSR) markers were developed in the present work and genotypic diversity of orange rust isolates from different locations investigated. Second, phenotypic diversity was examined by the single-pustule inoculation technique on P. kuehnii isolates retrieved from three susceptible commercial sugarcane cultivars. A total of 96 SSR markers were generated and tested for this species. Subsequently, 29 isolates of P. kuehnii were fingerprinted with nine SSR markers to estimate the genotypic diversity by neighbour-joining and 3D principal coordinates. The 29 isolates of the pathogen clustered into four main groups, which were identified by three SSR markers (NPRL_PK_108a, NPRL_PK_162_spka and NPRL_PK_221_spka). Phenotypic data at 21 days after the single-pustule inoculation showed that P. kuehnii from highly susceptible commercial cultivars harboured a small proportion of variants capable of causing disease on resistant cultivars. A differential reaction was demonstrated for the most virulent variant in a repeated experiment confirming the existence of races within P. kuehnii in Brazil.     

Integrative structure and function of the yeast exocyst complex

Exocyst is an evolutionarily conserved hetero‐octameric tethering complex that plays a variety of roles in membrane trafficking, including exocytosis, endocytosis, autophagy, cell polarization, cytokinesis, pathogen invasion, and metastasis. Exocyst serves as a platform for interactions between the Rab, Rho, and Ral small GTPases, SNARE proteins, and Sec1/Munc18 regulators that coordinate spatial and temporal fidelity of membrane fusion. However, its mechanism is poorly described at the molecular level. Here, we determine the molecular architecture of the yeast exocyst complex by an integrative approach, based on a 3D density map from negative‐stain electron microscopy (EM) at ~16 Å resolution, 434 disuccinimidyl suberate and 1‐ethyl‐3‐(3‐dimethylaminopropyl)carbodiimide hydrochloride cross‐links from chemical‐crosslinking mass spectrometry, and partial atomic models of the eight subunits. The integrative structure is validated by a previously determined cryo‐EM structure, cross‐links, and distances from in vivo fluorescence microscopy. Our subunit configuration is consistent with the cryo‐EM structure, except for Sec5. While not observed in the cryo‐EM map, the integrative model localizes the N‐terminal half of Sec3 near the Sec6 subunit. Limited proteolysis experiments suggest that the conformation of Exo70 is dynamic, which may have functional implications for SNARE and membrane interactions. This study illustrates how integrative modeling based on varied low‐resolution structural data can inform biologically relevant hypotheses, even in the absence of high‐resolution data.     

基于机会成本法的海洋保护区生态保护补偿标准

建立海洋保护区已被公认为维持海洋生物多样性和防止海洋生态环境恶化的重要途径,而合理实施生态保护补偿是确保海洋保护区建设和管理成效、促进区域经济发展机会公平的关键手段。以土地、海域为载体,从机会成本补偿的角度出发,分别设置了机会成本补偿基数、区域调整系数、分区补偿系数和开发限度补偿系数,构建了海洋保护区生态保护补偿标准测算方法,并选取全国8个省(市)14个国家级海洋自然保护区开展了实证分析。结果表明:2015年案例区的机会成本补偿测算结果介于0.66×10~4—10.69×10~4元/km~2之间,河北昌黎黄金海岸国家级自然保护区和天津古海岸与湿地国家级自然保护区的补偿金额显著高于其他保护区,分别为10.69×10~4元/km~2和10.47×10~4元/km~2,相比之下,其余12个保护区的平均补偿金额为1.70×10~4元/km~2。     

大兴安岭泥炭地不同菌根类型木本植物叶片凋落物分解及其温度敏感性差异

以我国大兴安岭多年冻土区泥炭地常见的3种外生菌根木本植物(细叶沼柳Salix rosmarinifolia、白桦Betula platyphylla和柴桦B.fruticosa)和4种欧石楠菌根木本植物(笃斯越桔Vaccinium uliginosum、狭叶杜香Ledum palustre、甸杜Chamaedaphne calyculata和小叶杜鹃Rhododendron parrifolum)为研究对象,通过315天培养试验测定10和20℃叶片凋落物分解过程中的碳(C)累积矿化量和重量损失,并分析其温度敏感性。结果表明:外生菌根植物叶片凋落物的C矿化量和重量损失在10和20℃均高于欧石楠菌根植物;外生菌根植物凋落物分解过程中C矿化量的温度敏感性系数高于欧石楠菌根植物,但重量损失的温度敏感性系数低于欧石楠菌根植物;在每一培养温度下,C矿化量和重量损失均与凋落物全氮(N)和全磷(P)浓度呈正相关,与C/N和C/P呈负相关;尽管C矿化量的温度敏感性系数与凋落物初始化学组成无显著相关性,但重量损失的温度敏感性系数与凋落物全N和全P浓度呈负相关,与C/N和C/P呈正相关。本研究结果为认识和预测气候变暖及其引起的物种组成变化对北方泥炭地植物凋落物分解的影响提供理论依据。     

基于综合评价法的洞庭湖区绿地生态网络构建

绿地生态网络对于改善区域生态空间破碎化、生物多样性降低、生态系统服务供需不平衡及保障区域生态安全具有重要意义。本研究以洞庭湖区为例,在3S技术支持下,从生态系统服务功能、潜在生物多样性、形态空间格局的角度综合评价和识别生态源地及计算栅格单元的基本生态阻力;利用夜间灯光指数修正基本生态阻力;运用最小累积阻力模型识别生态廊道;构建加权评价模型,对源地的聚合度、离散度及廊道的生态连接贡献度进行评价;利用结构特征指数对综合网络、“源-汇”潜在网络及规划网络进行对比分析和评价。结果表明: 源地空间分布不均衡,林地、灌丛与水域三者面积之和占源地总面积的95.9%,位于研究区中部的洞庭湖湿地生态风险较高;源地离生态网络系统中心位置越近及到其他源地的平均最小累积阻力越小,聚合及离散的优势越强;高生态质量源地周围的中、高生态质量源地分布越密集,其聚合度、离散度越高;廊道离高生态质量的源地越近,表现为生态连接贡献度越大;林地、灌丛,尤其是河道在自然生态系统与人类社会系统之间起着非常重要的生态连接作用;“源-汇”规划绿道对“源-汇”潜在生态廊道形成了良好补充,与“源-汇”潜在网络相比,综合网络的α、β、γ、ρ指数分别提高123.1%、25.8%、26.2%、74.6%;与“源-汇”规划网络相比,α、β、γ、ρ指数分别提高了190.0%、31.1%、32.5%、114.6%。本研究结果能为洞庭湖区绿地生态网络构建、国土空间规划提供参考。     

基于多源数据的福州市中心城区人居环境质量评价

城市内部居住环境的客观性评价有助于发现城市发展中暴露出的问题,有针对性地进行调整进而改善城市环境。以福州市中心城区为研究区,居住区为研究单元,利用气象监测数据、遥感影像数据、地图兴趣点数据、国土规划数据等多源数据,从环境健康舒适性、交通便捷性、城市安全性和生活方便性4方面构建城市人居环境监测体系,并使用优劣解距离法进行人居环境质量综合评价。结果表明: 福州市中心城区人居环境水平差异性较大,整体上呈现出中心区域高、边缘地区低的特点。城区中部人居环境指数较高,东部和南部区域较低,西部和北部区域人居环境高值与低值混杂分布。各指标层中,交通便捷性和生活方便性的高-高集聚以及低-低集聚特征与人居环境高低值聚类分布较为一致,便捷的交通以及完备的服务设施对人居环境评价的影响较大;环境健康舒适性呈现城市内部低、边缘高的特点,而城市安全性呈现内部高、边缘低的特点。