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Titlebook: Algal Chemical Ecology; Charles D. Amsler Book 20081st edition Springer-Verlag Berlin Heidelberg 2008 Algen.Algenkunde.Meeres?kologie.Phyt

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樓主: Menthol
21#
發(fā)表于 2025-3-25 05:02:56 | 只看該作者
22#
發(fā)表于 2025-3-25 10:36:24 | 只看該作者
Secondary Metabolite Defenses Against Pathogens and Biofoulers, . (Sawabe et al. 1998) is caused by . bacteria; similarly, white rot disease in the kelp . is caused by an . sp. bacterium (Andrews 1977). Some bacteria act as secondary pathogens, accelerating disease progression following attack of a primary pathogen (Correa et al. 1994). Fungi can also act as se
23#
發(fā)表于 2025-3-25 13:29:21 | 只看該作者
Oxidative Burst and Related Responses in Biotic Interactions of Algae,d epidemics has increased in recent decades and sessile invertebrate and algal populations will have to adapt their defense strategies to cope with new challenges (Harvell et al. 1999, 2002; Mydlarz et al. 2006). Marine algae have evolved a variety of defensive mechanisms against grazers and pathoge
24#
發(fā)表于 2025-3-25 17:24:58 | 只看該作者
Algal Sensory Chemical Ecology,ted by chapters on sensory chemical ecology (cf. more focused works by Roitberg and Isman 1992; Eisner and Meinwald 1995; Cardé and Millar 2004; Dicke and Takken 2006). Even in nonalgal marine chemical ecology, sensory ecology is relatively well studied, particularly with respect to prey detection v
25#
發(fā)表于 2025-3-25 20:17:40 | 只看該作者
https://doi.org/10.1007/978-3-031-39821-6ver evolutionary timescales, for the presence of diverse and effective chemical defenses. In this scenario of bottom-up control, a number of counteradaptations are supposed to have occurred in herbivores, including feeding specialization and sequestration of defenses, which represent potential steps
26#
發(fā)表于 2025-3-26 03:18:23 | 只看該作者
Database and Expert Systems Applicationslished studies of polar macroalgal chemical defenses featured herein, only 3 were completed before 2001. Likewise, potential ecological roles of some Antarctic macroalgal secondary metabolites have been determined in recent years (Ankisetty et al. 2004; Lebar et al. 2007), but there are still relati
27#
發(fā)表于 2025-3-26 04:50:27 | 只看該作者
https://doi.org/10.1007/978-3-319-22852-5inen 2005; Dworjanyn et al. 2006b; Ianora et al. 2006). However, the response of algal secondary metabolites to stimuli is a complex process, and these models do not consistently predict patterns of macroalgal metabolite production.
28#
發(fā)表于 2025-3-26 10:51:02 | 只看該作者
https://doi.org/10.1007/978-3-319-22852-5bolites was as a defense against consumers (Dethier 1954; Fraenkel 1959) led ecologists to formulate a series of general defense models, especially during the 1970s and 1980s, to explain the distribution and variation of secondary metabolites. These defense models have allowed natural product chemis
29#
發(fā)表于 2025-3-26 12:45:39 | 只看該作者
30#
發(fā)表于 2025-3-26 19:36:02 | 只看該作者
An Object Behavior Modeling Method . (Sawabe et al. 1998) is caused by . bacteria; similarly, white rot disease in the kelp . is caused by an . sp. bacterium (Andrews 1977). Some bacteria act as secondary pathogens, accelerating disease progression following attack of a primary pathogen (Correa et al. 1994). Fungi can also act as se
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