994 resultados para 13-123


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◾ Report of Opening Session (p. 1) ◾ Report of Governing Council (p. 15) ◾ Report of the Finance and Administration Committee (p. 47) ◾ Reports of Science Board and Committees: Science Board Inter-sessional Meeting (p. 63); Science Board (p. 73); Biological Oceanography Committee (p. 87); Fishery Science Committee (p. 95); Marine Environmental Quality Committee (p. 105); MONITOR Technical Committee (p. 115); Physical Oceanography and Climate Committee (p. 125); Technical Committee on Data Exchange (p. 133) ◾ Reports of Sections, Working and Study Groups: Section on Carbon and Climate (p. 139); Section on Ecology of Harmful Algal Blooms in the North Pacific (p. 143); Working Group 18 on Mariculture in the 21st Century - The Intersection Between Ecology, Socio-economics and Production (p. 147); Working Group 19 on Ecosystem-Based Management Science and its Application to the North Pacific (p. 151); Working Group 20 on Evaluations of Climate Change Projections (p. 157); Working Group 21 on Non-indigenous Aquatic Species (p. 159); Study Group to Develop a Strategy for GOOS (p. 165) ◾ Reports of the Climate Change and Carrying Capacity Scientific Program: Implementation Panel on the CCCC Program (p. 169); CFAME Task Team (p. 175); MODEL Task Team (p. 181) ◾ Reports of Advisory Panels: Advisory Panel for a CREAMS/PICES Program in East Asian Marginal Seas (p. 187); Advisory Panel on Continuous Plankton Recorder Survey in the North Pacific (p. 193); Advisory Panel on Iron Fertilization Experiment in the Subarctic Pacific Ocean (p. 197); Advisory Panel on Marine Birds and Mammals (p. 201); Advisory Panel on Micronekton Sampling Inter-calibration Experiment (p. 205) ◾ Summary of Scientific Sessions and Workshops (p. 209) ◾ Membership List (p. 259) ◾ List of Participants (p. 277) ◾ List of PICES Acronyms (p. 301) ◾ List of Acronyms (p. 303)

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This workshop was convened to begin building a foundation of understanding for developing and evaluating proposed measures for the rational management of the blue crab fishery in Chesapeake Bay. Our goal was to generate a summary of knowledge of blue crab stock dynamics. Specifically, we intended to address, and hoped to estimate, the basic parameters of an exploited stock - growth, mortality, natality, migration rates, sex ratios and abundance. In one sense these objectives were simply a means for organizing our discussions. A second objective was to compile at the workshop pertinent data held by the major research institutions on Chesapeake Bay so all participants could see the kinds and extent of existing data. As with many stock assessment problems, tailoring an estimating procedure around known existing data can be more productive than deciding on a procedure and then trying to find the required data in someone else's files. Authors of papers contributed to the report: B.S. Hester and P.R. Mundy (p. 50); Qisheng Tang (p. 86); L. Eugene Cronin (p. 111); J.R. McConaugha (p. 128); Cluney Stagg and Phil Jones (p. 153).

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本论文对沿阶草族Ophiopogoneae(Endl.)Kunth的研究历史作了回顾,从染色体、形态学和解剖学角度对此族作了研究,并作了数值分类和分支 系统学分析的尝试,在此基础上探讨了这个族的系统学问题. 1)本论文对此族三属37种123居群的染色体数目、基数及核型不对称性作了研究,其中19种的染色体为首次报道.它们是:P.macrostegiaHance, P.yunnanensis Wang et Tang,P.ophiopogonoides Wang et Tang,O. sarmentosus Wang et Dai,O.tienensis Wang et Tang, O.sylvicola Wang et Tang, O.fooningensis Wang et Dai, O.mairei L6vl.,O.szechuanensis Wang et Tang, O.angustiatus (Wang et Tang) S.C.Chen, O.amblyphyllus Wang et Dai,O.clavatus Wright ex Oliver,O.clivioidesD.M.Zhang et Hong, O.longiscaposus D.M.Zhang et Hong,O.umbraticola Hance,O.fuiD.M.Zhang ntHong,O.zingiberaceus Wang et Dai,O.gangxiensisd.M.Zhang et Hong,O. lo fouense L6vl. 2)在此族中首次报道了2n = 2x = 34的异基数二倍体,同时在O.umbraticola,O.japonicus,O.cLarkei中报道了2n=68的异基数二倍体,过核型和减数分裂等证明异基数是在二倍体水平上形成,并发展成倍性系列的. 3)在此族中首次报道了B染色体的存在,已确证了两种(P.macrostegia和D.tienensis).一种尚需进一步确证(O.Larkei). 4)通过对随体位置的系统研究,发现在此族中随体位置具有分类价值. 5)通过对8个种内多倍体、4个多倍体种的研究,表明多倍体分布于较北、海拔较高的地方,而亚洲热带地区的种,则无多倍体,同时在具异基数种类和核型较不对称种类上亦有这种分布特征;在确定了分布的多度中心的基础上,提出喜马拉雅_横断山脉到川西、川南一带是沿阶草属和山麦冬属的近代分化中心. 6)通过染色体结构和数目几个角度的研究,表明球子草属与其他两属在。染色体水平上已发生很大分化,但其属内的分化则不表现在染色体上.其他二属内部则有基数、倍性和核型不对称方面的分化.综观此族,染色体具有由核 型对称向不对称、由二倍体向多倍体、由种内多倍体向多倍体种,由单一基数向种内异基数几个方向进化的趋势. 7)通过对此族的形态观察和分析,提出茎或根状茎分枝方式是属下分类的重要依据;认为本族植物的花序是由圆锥花序简化而来,但残留着圆锥花序特征;并提出了本族花、茎、叶、根几个方面的形态演化趋势. 8)通过对此族二属21种的子房解剖,发现三属均有半下位子房,因而认为子房半下位作为分属检索性状是不合适的.此外还观察到子房着生位置在种内亦有变异,对这种变异的意义进行了探讨. 9)通过此族三属46种2变种的数值分类处理,表明本族由球子草群和沿阶草一山麦冬群两大类群组成,山麦冬属仅是与沿阶草属一个组(葶花组)并列的分类单元,其内部分化较小,而沿阶草属则较大. 10)通过46个性状计算了山麦冬属和沿阶草属共6个广布的“群内总体相 似度”(IOS),表明山麦冬属3个种种内个体之间、种间个体之间的分化很小,且可能有杂交现象,结合染色体资料和分布特征,认为这个属的发生是个相当晚近的事件. 11)本文从形态和染色体角度,认为沿阶草族是一个自然类群;由分支系 统学分析表明,此族由二个单系类群(球子草属和沿阶草属)组成,沿阶草属含两个单系的组,其中各含3个系,山麦冬属为其中一个系.这一结果与数值 分类结果和染色体资料相符. 12)为避免单一分类方法可能导致的不合理结果,本文以自拟的一种综合分类方法,把谱系、进化、分化诸因素均予考虑,得出一个三维图象,以图象 上相对等径的球作为分类依据,得出的结果与分支系统学和数值分类结果基本一致.因此,山麦冬属作为与沿阶草属等阶的分类地位,应予重新考虑. 13)本文最后对这个族的全面修订提出几点建议. 14)此外,本文还描述了沿阶草属4个新种.

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EXTRACT (SEE PDF FOR FULL ABSTRACT): Pollen from the upper 2.75 m of a core taken 200 km west of the Golfo de Guayaquil, Ecuador (Trident 163-13, 3° S, 84° W, 3,000 m water depth) documents changes in Andean vegetation and climate of the Cordillera Occidental for ~17,000 years before and after the last glacial maximum.

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  全新世是与人类关系最密切的地质时期,重建全新世气候变化的历史,对人类的生产生活有重要的意义。植被是自然界中对气候变化反映最灵敏的指示物,通过地层剖面中的花粉分析,可以揭示古代植物区系,恢复古植被,因此,孢粉分析被用作研究植被演化、环境变迁的重要手段。   本文选取吉林哈尼湖钻孔剖面837~304cm(13.1~4.5cal.kaB.P.)沉积物进行孢粉分析,共采集样品123个,平均时间分辨率为69年。建立了早中全新世以来东北地区的孢粉组合序列,恢复了这一时段的植被演替序列,在此基础上,重点研究讨论了早中全新世气候事件在东北地区植被演替中的响应,为全新世古环境和气候变化的演变提供孢粉学证据。   研究结果表明:哈尼地区早中全新世以来气候演化有以下特征:13.1~11.9cal.kaB.P.为疏林草原景观,从11.9cal.kaB.P.开始逐渐发展成山地寒温性针叶林,至9.3cal.kaB.P.演化成栎为主的落叶阔叶林,5.5cal.kaB.P后松增加,发展成针阔混交林。从植被的变化推测,本区的气候经历了四个阶段的变化:冷干——冷湿——暖湿——凉干,虽然存在着冷暖干湿的变化,但自然环境基本为湿润状态,较稳定地保持了森林景观,气候变化相对温和。本区在进入大暖期以来气候并不稳定,分别在6.8、6.1、5.5、4.7cal kaB.P有不同程度的冷湿和冷干事件。频谱分析表明,本区在13.1~4.5cal.kaB.P.存在1100、700、500及300年的气候变化的准周期。