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Welcome to the 31st IUBS General Assembly and Conference on ...

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c<strong>on</strong>diti<strong>on</strong>s of C. megacephala protein. Optimizati<strong>on</strong><br />

fac<str<strong>on</strong>g>to</str<strong>on</strong>g>rs were enzyme dosage (5–7%), level of water added<br />

(20–30 mL/g), pH (8–9) <str<strong>on</strong>g>and</str<strong>on</strong>g> temperature (50–60℃)<br />

while investigated resp<strong>on</strong>se was <str<strong>on</strong>g>the</str<strong>on</strong>g> degree of hydrolysis<br />

(DH%). An optimal design, with 4 variables <str<strong>on</strong>g>and</str<strong>on</strong>g> <strong>on</strong>e<br />

resp<strong>on</strong>se functi<strong>on</strong>, was employed <str<strong>on</strong>g>to</str<strong>on</strong>g> study <str<strong>on</strong>g>the</str<strong>on</strong>g> effect of <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

individual variables <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g> resp<strong>on</strong>se functi<strong>on</strong>. For each<br />

resp<strong>on</strong>se, sec<strong>on</strong>d‐order polynomial models were<br />

developed using multiple linear regressi<strong>on</strong> analysis. The<br />

degree of hydrolysis was significantly affected by <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

enzyme dosage, pH <str<strong>on</strong>g>and</str<strong>on</strong>g> temperature. Applying<br />

desirability functi<strong>on</strong> method, optimum hydrolysis<br />

operating c<strong>on</strong>diti<strong>on</strong>s were found <str<strong>on</strong>g>to</str<strong>on</strong>g> be enzyme dosage of<br />

7%, level of water added of 25 mL/g, pH of 9.0 <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

temperature of 59.87℃. At this optimum point, <str<strong>on</strong>g>the</str<strong>on</strong>g> actual<br />

degree of hydrolysis was found <str<strong>on</strong>g>to</str<strong>on</strong>g> be 23.30%, <str<strong>on</strong>g>and</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

predicted value 22.66%. The results presented in this<br />

work show a fast, simple <str<strong>on</strong>g>and</str<strong>on</strong>g> easy enzymatic hydrolysis<br />

process of C. megacephala protein.<br />

Patterns determinants <str<strong>on</strong>g>and</str<strong>on</strong>g>c<strong>on</strong>servati<strong>on</strong> of<br />

vascular plants <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g> Tibetan Plateau<br />

Yujing YAN <str<strong>on</strong>g>and</str<strong>on</strong>g> Zhiyao TANG<br />

Department of Ecology, College of Urban <str<strong>on</strong>g>and</str<strong>on</strong>g> Envir<strong>on</strong>mental<br />

Science, Peking University, Beijing 100871, China. Email:<br />

africarugu@gmail.com<br />

Large‐scale patter of species richness <str<strong>on</strong>g>and</str<strong>on</strong>g> its<br />

determinants have l<strong>on</strong>g been <str<strong>on</strong>g>the</str<strong>on</strong>g> central issues in<br />

biogeography <str<strong>on</strong>g>and</str<strong>on</strong>g> macroecology. The Tibetan Plateau is<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> highest plateau in <str<strong>on</strong>g>the</str<strong>on</strong>g> world; it provides habitats for<br />

about 8000 vascular plants, of which about 17% are<br />

endemic <str<strong>on</strong>g>to</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> plateau. The plateau is undergoing<br />

remarkable climate change. To underst<str<strong>on</strong>g>and</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> resp<strong>on</strong>se<br />

of ecosystems <str<strong>on</strong>g>to</str<strong>on</strong>g> climate change <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g> Tibetan Plateau, it<br />

is <str<strong>on</strong>g>the</str<strong>on</strong>g>refore necessary <str<strong>on</strong>g>to</str<strong>on</strong>g> explore <str<strong>on</strong>g>the</str<strong>on</strong>g> patterns <str<strong>on</strong>g>and</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

fac<str<strong>on</strong>g>to</str<strong>on</strong>g>rs determine <str<strong>on</strong>g>the</str<strong>on</strong>g>se patterns of <str<strong>on</strong>g>the</str<strong>on</strong>g> biodiversity. Here,<br />

we studied patterns of richness of <str<strong>on</strong>g>the</str<strong>on</strong>g> vascular plant,<br />

based <strong>on</strong> a high resoluti<strong>on</strong> distributi<strong>on</strong> database of<br />

vascular plants. The results show that most of <str<strong>on</strong>g>the</str<strong>on</strong>g> vascular<br />

plants are distributed <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g> eastern part of <str<strong>on</strong>g>the</str<strong>on</strong>g> plateau<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> in <str<strong>on</strong>g>the</str<strong>on</strong>g> main mountain areas, while <str<strong>on</strong>g>the</str<strong>on</strong>g> species<br />

endemic <str<strong>on</strong>g>to</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> Tibetan Plateau are mostly distributed<br />

al<strong>on</strong>g <str<strong>on</strong>g>the</str<strong>on</strong>g> HimalayaMountains. The complimentary<br />

algorithm revealed that ‘hotspots’ of endemic plants are<br />

mainly located in <str<strong>on</strong>g>the</str<strong>on</strong>g> sou<str<strong>on</strong>g>the</str<strong>on</strong>g>astern part of <str<strong>on</strong>g>the</str<strong>on</strong>g> plateau.<br />

Moreover, an area occupies approximately 20% of <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

plateau could cover all <str<strong>on</strong>g>the</str<strong>on</strong>g> species endemic <str<strong>on</strong>g>to</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> plateau.<br />

The annual precipitati<strong>on</strong> <str<strong>on</strong>g>and</str<strong>on</strong>g> mean temperature of <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

coldest m<strong>on</strong>th are <str<strong>on</strong>g>the</str<strong>on</strong>g> fac<str<strong>on</strong>g>to</str<strong>on</strong>g>res in shaping <str<strong>on</strong>g>the</str<strong>on</strong>g>se patterns;<br />

whereas <str<strong>on</strong>g>the</str<strong>on</strong>g> habitat hererogeneity played no significant<br />

role in determing this pattern.<br />

Populati<strong>on</strong> dynamics <str<strong>on</strong>g>and</str<strong>on</strong>g> invasive his<str<strong>on</strong>g>to</str<strong>on</strong>g>ry of<br />

red swamp crayfish (Procambarus Clarkii)<br />

Lijun HE 1,2 <str<strong>on</strong>g>and</str<strong>on</strong>g> Min CHAO 2<br />

1State Key Labora<str<strong>on</strong>g>to</str<strong>on</strong>g>ry of Estuarine <str<strong>on</strong>g>and</str<strong>on</strong>g> Coastal Research, East<br />

China Normal University, Shanghai 200062 China <str<strong>on</strong>g>and</str<strong>on</strong>g> 2 East<br />

China Sea Fisheries Research Institute, Chinese Academy of<br />

Fishery Sciences, Shanghai200090, China. Email:<br />

tiger02j@hotmail.com<br />

Since <str<strong>on</strong>g>the</str<strong>on</strong>g> 1900s, human activities have increased<br />

opportunities for biological invasi<strong>on</strong> <str<strong>on</strong>g>and</str<strong>on</strong>g> caused some<br />

severe ec<strong>on</strong>omic <str<strong>on</strong>g>and</str<strong>on</strong>g> ecological questi<strong>on</strong>s in <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

terrestrial ecosystem. In China, red swamp crayfish<br />

(Procambarusclarkii) is an ec<strong>on</strong>omically important<br />

aquatic invasive species. This species has quickly<br />

exp<str<strong>on</strong>g>and</str<strong>on</strong>g>ed <str<strong>on</strong>g>to</str<strong>on</strong>g> almost <str<strong>on</strong>g>the</str<strong>on</strong>g> entire drainage of Yangtze River<br />

through human‐mediated translocati<strong>on</strong>s or natural<br />

migrati<strong>on</strong>s since <str<strong>on</strong>g>the</str<strong>on</strong>g>ir first introducti<strong>on</strong>. To elucidate <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

genetic diversity <str<strong>on</strong>g>and</str<strong>on</strong>g> populati<strong>on</strong> origin of this introduced<br />

crayfish, we obtained samples from 8 sites in China <str<strong>on</strong>g>and</str<strong>on</strong>g> 2<br />

sites in native USA. Segment of mi<str<strong>on</strong>g>to</str<strong>on</strong>g>ch<strong>on</strong>drial<br />

cy<str<strong>on</strong>g>to</str<strong>on</strong>g>chrome oxidase subunit I gene (COI) was amplified,<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> some DNA sequences from o<str<strong>on</strong>g>the</str<strong>on</strong>g>r native populati<strong>on</strong> in<br />

North America <str<strong>on</strong>g>and</str<strong>on</strong>g> alien populati<strong>on</strong> in Europe were also<br />

downloaded from GenBank. A star‐like tree <str<strong>on</strong>g>and</str<strong>on</strong>g> shallow<br />

intraspecific divergence indicate recent populati<strong>on</strong><br />

expansi<strong>on</strong> in native North America. Relative <str<strong>on</strong>g>to</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

native populati<strong>on</strong> in USA <str<strong>on</strong>g>and</str<strong>on</strong>g> Mexico, genetic bottleneck<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> reduced genetic variati<strong>on</strong> were revealed from<br />

populati<strong>on</strong>s in European <str<strong>on</strong>g>and</str<strong>on</strong>g> China. Two of 3 European<br />

haplotypes were shared by Louisiana samples, which<br />

supports <str<strong>on</strong>g>the</str<strong>on</strong>g> records that P. Clarkii was first introduced<br />

from Louisiana <str<strong>on</strong>g>to</str<strong>on</strong>g> Spain in 1973. Only 2 haplotypes<br />

occurred in <str<strong>on</strong>g>the</str<strong>on</strong>g> Chinese samples. One of <str<strong>on</strong>g>the</str<strong>on</strong>g>m was shared<br />

by a dominant <str<strong>on</strong>g>and</str<strong>on</strong>g> central haplotype from Louisiana, <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

o<str<strong>on</strong>g>the</str<strong>on</strong>g>r was shared by a terminal haplotype from<br />

nor<str<strong>on</strong>g>the</str<strong>on</strong>g>astern Mexico, which likely provide direct evidence<br />

111

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