標(biāo)題: Titlebook: Algal Chemical Ecology; Charles D. Amsler Book 20081st edition Springer-Verlag Berlin Heidelberg 2008 Algen.Algenkunde.Meeres?kologie.Phyt [打印本頁(yè)] 作者: Menthol 時(shí)間: 2025-3-21 19:12
書(shū)目名稱(chēng)Algal Chemical Ecology影響因子(影響力)
書(shū)目名稱(chēng)Algal Chemical Ecology影響因子(影響力)學(xué)科排名
書(shū)目名稱(chēng)Algal Chemical Ecology網(wǎng)絡(luò)公開(kāi)度
書(shū)目名稱(chēng)Algal Chemical Ecology網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱(chēng)Algal Chemical Ecology被引頻次
書(shū)目名稱(chēng)Algal Chemical Ecology被引頻次學(xué)科排名
書(shū)目名稱(chēng)Algal Chemical Ecology年度引用
書(shū)目名稱(chēng)Algal Chemical Ecology年度引用學(xué)科排名
書(shū)目名稱(chēng)Algal Chemical Ecology讀者反饋
書(shū)目名稱(chēng)Algal Chemical Ecology讀者反饋學(xué)科排名
作者: bibliophile 時(shí)間: 2025-3-21 23:33 作者: Phonophobia 時(shí)間: 2025-3-22 03:53
Macroalgal Chemical Defenses and Their Roles in Structuring Temperate Marine Communities,rce for a species-rich fauna (reviewed in Underwood 2000; Menge and Branch 2001). In such a diverse community, interactions within and between trophic levels become important for the regulation of the structure and function of both the producer and consumer assemblages (Duffy 2002; Worm and Duffy 2003).作者: 上下倒置 時(shí)間: 2025-3-22 07:38 作者: 割讓 時(shí)間: 2025-3-22 09:42
Hieu Hanh Le,Satoshi Hikida,Haruo Yokotadiversity, concentrations, and distributions of algal secondary metabolites within and across seaweed individuals, and in many cases, which of these algal compounds deter particular herbivores (Cronin 2001; Van Alstyne et al. 2001; Amsler and Fairhead 2006).作者: 共同確定為確 時(shí)間: 2025-3-22 13:35 作者: 危機(jī) 時(shí)間: 2025-3-22 18:46
and for marine ecologists and algal biologists seeking an iStudies of biotic interactions of algae that involve chemical defenses or signals are currently vibrant, active components of both marine ecological and phycological research. This field is rapidly growing, not only by delving deeper into r作者: Scintigraphy 時(shí)間: 2025-3-22 21:18 作者: 改良 時(shí)間: 2025-3-23 02:21
Soumaya Guesmi,Chiraz Trabelsi,Chiraz Latiriual increase in photosynthetically produced oxygen over millions of years was accompanied by a strong enrichment of it in the atmosphere, which ultimately acted as precursor for the ozone (O3) layer in the stratosphere.作者: arthroplasty 時(shí)間: 2025-3-23 07:08 作者: puzzle 時(shí)間: 2025-3-23 12:33
Defense Strategies of Algae and Cyanobacteria Against Solar Ultraviolet Radiation,ual increase in photosynthetically produced oxygen over millions of years was accompanied by a strong enrichment of it in the atmosphere, which ultimately acted as precursor for the ozone (O3) layer in the stratosphere.作者: Assault 時(shí)間: 2025-3-23 16:12
Lecture Notes in Computer Scienced as an overview of natural product chemistry with an emphasis on the chemical aspects of algal defensive metabolites. It is our hope that algal ecologists will gain insight into the chemistry in the same manner that chemists will acquire a deeper understanding of the ecology from the remaining chapters of this book.作者: considerable 時(shí)間: 2025-3-23 18:39 作者: BUDGE 時(shí)間: 2025-3-24 00:43 作者: Guaff豪情痛飲 時(shí)間: 2025-3-24 05:40
Book 20081st edition Likewise, algal natural products chemistry is not emphasized in most chapters but the book begins with an introduction to the chemistry of algal defenses that is intended as a primer on natural products chemistry for algal ecologists. In addition, although intended to be broad, it could not be so c作者: 果仁 時(shí)間: 2025-3-24 06:44 作者: 賞心悅目 時(shí)間: 2025-3-24 12:31
Macroalgal Chemical Defenses and Their Roles in Structuring Tropical Marine Communities,ver 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作者: invade 時(shí)間: 2025-3-24 18:47 作者: 加劇 時(shí)間: 2025-3-24 22:51
New Perspectives for Addressing Patterns of Secondary Metabolites in Marine Macroalgae,inen 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.作者: 奇思怪想 時(shí)間: 2025-3-25 00:35
Macroalgal Models in Testing and Extending Defense Theories,bolites 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作者: 血友病 時(shí)間: 2025-3-25 05:02 作者: collagen 時(shí)間: 2025-3-25 10:36
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作者: 噱頭 時(shí)間: 2025-3-25 13:29
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作者: Processes 時(shí)間: 2025-3-25 17:24
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作者: 預(yù)定 時(shí)間: 2025-3-25 20:17
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作者: infinite 時(shí)間: 2025-3-26 03:18
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作者: 值得贊賞 時(shí)間: 2025-3-26 04:50
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.作者: Alveoli 時(shí)間: 2025-3-26 10:51
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作者: outskirts 時(shí)間: 2025-3-26 12:45 作者: 內(nèi)向者 時(shí)間: 2025-3-26 19:36
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作者: inspired 時(shí)間: 2025-3-27 00:27
Yongrui Qin,Lina Yao,Quan Z. Shengd 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作者: 新鮮 時(shí)間: 2025-3-27 01:14
Lecture Notes in Computer Scienceted 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作者: DAFT 時(shí)間: 2025-3-27 09:03 作者: nostrum 時(shí)間: 2025-3-27 09:38
Macroalgal Chemical Defenses and Their Roles in Structuring Tropical Marine Communities,96; Harborne et al. 2006; Vinueza et al. 2006), probably because of their profound effects in both temperate and tropical communities and their importance as major conduits of energy between autotrophs and the rest of the food web. Nonetheless, very little is understood about how macroalgal chemical作者: refine 時(shí)間: 2025-3-27 16:30 作者: 動(dòng)脈 時(shí)間: 2025-3-27 21:21 作者: Vaginismus 時(shí)間: 2025-3-27 23:07
Macroalgal and Cyanobacterial Chemical Defenses in Freshwater Communities,dissolved oxygen concentration, and nutrient recycling in those habitats (Howarth et al. 1988; Schippers et al. 2004). In recent years, these groups have garnered much negative attention as a result of their ability to dominate aquatic systems receiving chronic nutrient inputs. Freshwater blooms of 作者: Provenance 時(shí)間: 2025-3-28 05:40 作者: 預(yù)測(cè) 時(shí)間: 2025-3-28 08:22
Macroalgal Models in Testing and Extending Defense Theories,e decades. They have also become one of the most theory-laden fields of plant ecology, if not ecology in general, with a number of general models (theories) seeking to explain and predict patterns of chemical defenses in plants. (We use the terms model or theory rather than hypothesis because we def作者: hallow 時(shí)間: 2025-3-28 12:05 作者: 障礙 時(shí)間: 2025-3-28 18:25 作者: crutch 時(shí)間: 2025-3-28 20:55
Herbivore Offense in the Sea: The Detoxifi cation and Transport of Secondary Metabolites,al and morphological mechanisms that algae use to protect themselves from being consumed by their herbivores (Hay and Fenical 1988; Paul 1992; Steinberg 1992; Paul et al. 2001; Paul and Puglisi 2004; Paul et al. 2006; see Chaps. 2–6). In particular, we have a tremendous amount of information on the 作者: Frenetic 時(shí)間: 2025-3-29 00:45 作者: 勉勵(lì) 時(shí)間: 2025-3-29 04:03
Oxidative Burst and Related Responses in Biotic Interactions of Algae,his was exemplified in kelp forests by dramatic changes associated with the reduction or extinction of local populations of some key predators controlling macroalgal grazers (Estes and Duggins 1995), or in coral reef ecosystems, where coralline lethal orange disease (CLOD), a disease affecting vario作者: Lethargic 時(shí)間: 2025-3-29 08:10 作者: colony 時(shí)間: 2025-3-29 13:45
Algal Sensory Chemical Ecology,onment by organisms. Algae are well known to have numerous physiological responses to variations in their chemical environment, particularly with respect to nutrients (Lobban and Harrison 1994). However, with respect to environmental sensing it is typical for “chemical ecology” to be restricted to b作者: 定點(diǎn) 時(shí)間: 2025-3-29 15:33 作者: avulsion 時(shí)間: 2025-3-29 21:45
http://image.papertrans.cn/a/image/152407.jpg作者: INCH 時(shí)間: 2025-3-30 03:45
Lecture Notes in Computer Sciencee, agriculture, and engineering. It is fundamentally a basic science, involved in the discovery, characterization and cataloging of new chemical substances found in nature. Among other basic scientists, biologists and ecologists recognized some time ago that natural products might help explain speci作者: 愛(ài)得痛了 時(shí)間: 2025-3-30 07:45 作者: incontinence 時(shí)間: 2025-3-30 10:13
Elyas Rashno,Farhana Zulkernineuna occasionally complemented with larger herbivores, and predators. Diversity in the producer assemblage is generated by small-scale heterogeneity in substrate characteristics, seasonal variation in growing conditions, and the depth gradient. Abiotic disturbances, mainly in the form of wave energy,作者: 我不明白 時(shí)間: 2025-3-30 15:30
