模拟降雨变化对古尔班通古特沙漠土壤养分及酶活性的影响

土壤酶参与土壤系统的养分循环过程,是联系植物和土壤养分的关键纽带。土壤酶活性对降水格局变化响应敏感,这种响应对于缺水且养分贫瘠的荒漠生态系统显得尤为重要。然而,早春积雪完全融化后首次降雨时间及降雨量如何影响土壤养分及土壤酶活性还鲜见相关报道。以新疆古尔班通古特沙漠为研究区,在早春积雪完全融化后,设置3个首次降雨时间(积雪完全融化后第10天、20天和30天)和3个降雨梯度(5 mm、10 mm和15 mm),于植物生长旺季采集土壤样品,研究土壤养分含量和土壤酶活性的响应特征。结果表明：积雪完全融化后不同首次降雨时间下5mm降雨处理以及积雪完全融化后第30天下各降雨量处理对土壤养分和酶活性影响不显著。积雪完全融化后第10天,随降雨量增加,土壤全碳呈显著先下降后增加趋势,全钾呈显著增加趋势,而土壤微生物量碳呈显著降低趋势;积雪完全融化后第20天,随降雨量增加,速效氮、土壤蔗糖酶活性、土壤微生物量碳氮呈先下降后增加趋势,土壤全碳和多酚氧化酶活性显著下降,土壤全钾和碱性磷酸酶活性显著增加。模拟10 mm降雨,随首次降雨时间推迟,土壤全氮、速效氮、速效磷、土壤蔗糖酶活性和土壤微生物量碳呈增加趋势;...     

长沙市不同污染程度区域桂花和香樟叶表面PM2.5吸附量及其影响因素

为阐释不同污染程度下城市绿化植物吸滞PM_2.5机理、解析污染物来源,应用气溶胶再发生器定量测定长沙市常见的2种园林绿化树种(桂花和香樟)植物叶片PM_2.5吸附量,同时应用原子力显微镜(AFM)观察了不同污染区(交通区、文教区、清洁区)植被的叶表面微形态特征,使用离子色谱仪测定样品中水溶性离子含量.结果表明: 污染程度与植物叶表面PM_2.5吸附量呈正相关,不同植物单位叶面积PM_2.5吸附量全年均值表现为交通区(0.56±0.04 μg·cm^-2)＞文教区(0.48±0.06 μg·cm^-2)＞清洁区(0.33±0.02 μg·cm^-2),植物单位叶面积PM_2.5吸附量季节变化为冬季(0.70±0.10 μg·cm^-2)＞春季(0.43±0.14 μg·cm^-2)＞秋季(0.39±0.12 μg·cm^-2)＞夏季(0.31±0.09 μg·cm^-2),桂花的单位叶面积PM_2.5吸附量大于香樟;污染程度轻的区域的植物叶片比较光滑,污染程度重的区域的叶片较粗糙,植物粗糙度排序为交通区(195.45±16.09 nm)＞文教区(176.99±8.45 nm)＞清洁区(131.88±12.98 nm);不同污染程度地区PM_2.5离子含量均表现为冬季最大,其次是春季和秋季,夏季最低;3个污染区PM_2.5离子成分均以Na⁺、NH₄⁺、Cl^-和Br^-这4种离子为主,不同程度污染区PM_2.5污染均以移动源污染为主.     

丹参氮、磷肥效效应及最佳施肥模式研究

在陕西省商州市山阳县不同肥力土壤上,采用N、P二因素五水平最优设计,进行了丹参氮、磷优化配方施肥模式研究的多点田问试验。根据田间试验结果,求得不同土壤肥力水平下的N、P肥效反应方程,根据方程提出丹参不同产量水平的N、P合理配比和肥料用量。寻优结果表明,在山阳低肥力土壤目标产量10000～11500kg／hm^2之间的施氮为88．17～165．7kg／hm^2,施磷(P2O4)为88．18～165．7kg／hm^2;中肥力土壤目标产量在11000～14000kg／hm^2之间的施N量为108．5～187．4kg／hm^2,施磷(P2O5)为105．1～179．5kg／hm^2;高肥力土壤目标产量在20000～25000kg／hm^2之间的施N量为85．4～173．1kg／hm^2,施磷(P2O5)为121．95～179．01kg／hm^2。合理施用N、P肥有利于提高丹参产量,但过量施肥会造成丹参减产。     

Sperm ultrastructure, morphometry, and abnormal morphology in American black bears (Ursus americanus)

The objective of this study was to describe sperm ultrastructure, morphometry, and abnormal morphology in American black bears. Electroejaculation was successful in 53.8% (7/13) of the attempts, but urine contamination was common. Epididymal sperm samples were also obtained from five bears. Sperm had a paddle-like head shape and the ultrastructure was similar to that of most other mammals. The most striking particularity of black bear sperm ultrastructure was a tightening of the nucleus in the equatorial region. Although the differences were not significant in all bears, the overall decrease in sperm nucleus dimensions during transport from the caput epididymis to the cauda suggested increasing compaction of the nucleus during maturation. For ejaculated sperm, nucleus length, width, and base width were 4.9, 3.7, and 1.8 μm, respectively, whereas sperm head length, width, and base width were 6.6, 4.8, and 2.3 μm, and midpiece, tail (including midpiece), and total sperm lengths were 9.8, 68.8, and 75.3 μm. Evaluation of sperm cytoplasmic droplets in the epididymis revealed that proximal droplets start migrating toward a distal position in the caput epididymis and that the process was mostly completed by the time sperm reached the cauda epididymis. The proportion of morphologically normal sperm in the ejaculate was 35.6%; the most prevalent sperm defects were distal cytoplasmic droplets and bent/coiled tails. The morphology of abnormal sperm and the underlying ultrastructural defects were similar to that in other large domestic animals thus suggesting similar underlying pathogenesis of specific sperm defects and similar effects on fertility.     

Spermatogenesis and distinctive mature sperm in the giant freshwater prawn, Macrobrachium rosenbergii (De Man, 1879)

The structures of differentiating male germ cells in the testis of the giant freshwater prawn, Macrobrachium rosenbergii, were studied by light and electron microscopy. Based on ultrastructural characteristics, the developing male germ cells are classified into 12 stages, including spermatogonia, six phases of primary spermatocytes (leptotene, zygotene, pachytene, diplotene, diakinesis and metaphase), secondary spermatocyte, three stages of spermatids and mature sperm. During spermatogenesis, the differentiating germ cells have characteristics similar to those of other invertebrates, but they exhibit some unique characteristics during spermiogenesis. In particular, an early spermatid has a round nucleus with highly condensed heterochromatin, appearing as thick interconnecting cords throughout the nucleus. In contrast to most invertebrates and vertebrates, the chromatin begins to decondense in one-half of the nucleus at the mid spermatid stage. In the late spermatid, the chromatin becomes almost entirely decondensed with only a small crescent-shaped heterochromatin patch remaining at the anterior pole of the nucleus. Mature sperm possess an everted umbrella-shaped plate with a spike covering the anterior pole of the nucleus, whose chromatin is totally decondensed as only small traces of histones H3 and H2B remain. The acrosome appears at the ruffled border of the spike plate as small sac-like structures. Few mitochondria remain in the cytoplasm at the posterior pole.     

施钾对强筋小麦生理特性及产量的效应

以强筋面包小麦临优145为试验材料,于大田生产条件下研究了施用钾肥对强筋小麦叶片光合、膜脂氧化及产量特性的影响.结果显示,适量施钾能显著降低开花14d以后旗叶中超氧阴离子的产生强度和MDA含量,并显著提高旗叶的叶绿素含量、光合速率和籽粒灌浆速率,显著增加千粒重;在施钾(K2O)37.5~150.0kg/hm2范围内,随施钾量增加,各处理产量呈先上升后下降趋势且均比对照极显著增产14.5%~30.7%,各处理间产量差异显著,以施钾(K2O)112.5kg/hm2时籽粒产量最高.结果表明,中产条件下施用钾肥可显著提高强筋小麦籽粒产量,且以施钾(K2O)103.0~112.5kg/hm2为宜.     

Shaping mitotic chromosomes: From classical concepts to molecular mechanisms

How eukaryotic genomes are packaged into compact cylindrical chromosomes in preparation for cell divisions has remained one of the major unsolved questions of cell biology. Novel approaches to study the topology of DNA helices inside the nuclei of intact cells, paired with computational modeling and precise biomechanical measurements of isolated chromosomes, have advanced our understanding of mitotic chromosome architecture. In this Review Essay, we discuss – in light of these recent insights – the role of chromatin architecture and the functions and possible mechanisms of SMC protein complexes and other molecular machines in the formation of mitotic chromosomes. Based on the information available, we propose a stepwise model of mitotic chromosome condensation that envisions the sequential generation of intra‐chromosomal linkages by condensin complexes in the context of cohesin‐mediated inter‐chromosomal linkages, assisted by topoisomerase II. The described scenario results in rod‐shaped metaphase chromosomes ready for their segregation to the cell poles.