Pub Date : 2001-12-01DOI: 10.1016/S0003-5017(01)72084-3
Dunia Bouaoun, J. Aoun
{"title":"Étude en microscopie électronique et application d’une biomasse nitrifiante sur gels de polyacrylamide","authors":"Dunia Bouaoun, J. Aoun","doi":"10.1016/S0003-5017(01)72084-3","DOIUrl":"10.1016/S0003-5017(01)72084-3","url":null,"abstract":"","PeriodicalId":78387,"journal":{"name":"L' Annee biologique","volume":"40 ","pages":"Pages 43-54"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0003-5017(01)72084-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115840336","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0003-5017(01)72083-1
Pascal Collin
Plant adaptations to environmental conditions
In response to extreme conditions, plants exhibit a variety of adaptations that are important in the maintenance of plant community. Adaptation may be defined as heritable modifications in physiological or developmental attributes that improve the fitness of an organism under conditions of its environment. Adaptations are selected by three types of constraint: climatic, edaphic and biotic. Water act as a key element in the plant distribution and many morphophysiological traits are conditioned by water, directly or indirectly. Plant have developed a wide variety of mechanisms for surviving in habitats exposed to episodic or prolonged periods of frost. The extreme altitude and latitude reached by plants are revealing of the capacity of some plants to resist to cold. The photosynthetic apparatus of plants is capable of optimally efficient absorption and utilization of visible radiation because light availability vary considerably in intensity, duration, and space. Nutrient-poor environments or toxic soils have a well adapted plant community like carnivorous plants in peat swamp land and halophytes in salted soils. In habitats exposed to stress, the interplay of numerous stressors restricts the area on which a particular plant species can survive. Morphological and biochemical traits as been selected to withstand constraints under given conditions and thus plants possess various adaptations. Global changes in the atmospheric composition and climate are able to affect vegetation dynamics and could induce changes in plant distribution. Adaptation will therefore be a key element in the survival of the plant community.
{"title":"L’adaptation au milieu chez les plantes vasculaires","authors":"Pascal Collin","doi":"10.1016/S0003-5017(01)72083-1","DOIUrl":"10.1016/S0003-5017(01)72083-1","url":null,"abstract":"<div><h3>Plant adaptations to environmental conditions</h3><p>In response to extreme conditions, plants exhibit a variety of adaptations that are important in the maintenance of plant community. Adaptation may be defined as heritable modifications in physiological or developmental attributes that improve the fitness of an organism under conditions of its environment. Adaptations are selected by three types of constraint: climatic, edaphic and biotic. Water act as a key element in the plant distribution and many morphophysiological traits are conditioned by water, directly or indirectly. Plant have developed a wide variety of mechanisms for surviving in habitats exposed to episodic or prolonged periods of frost. The extreme altitude and latitude reached by plants are revealing of the capacity of some plants to resist to cold. The photosynthetic apparatus of plants is capable of optimally efficient absorption and utilization of visible radiation because light availability vary considerably in intensity, duration, and space. Nutrient-poor environments or toxic soils have a well adapted plant community like carnivorous plants in peat swamp land and halophytes in salted soils. In habitats exposed to stress, the interplay of numerous stressors restricts the area on which a particular plant species can survive. Morphological and biochemical traits as been selected to withstand constraints under given conditions and thus plants possess various adaptations. Global changes in the atmospheric composition and climate are able to affect vegetation dynamics and could induce changes in plant distribution. Adaptation will therefore be a key element in the survival of the plant community.</p></div>","PeriodicalId":78387,"journal":{"name":"L' Annee biologique","volume":"40 ","pages":"Pages 21-42"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0003-5017(01)72083-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115480848","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0003-5017(01)72082-X
Marc-André Selosse , François Le Tacon
{"title":"Les stratégies symbiotiques de conquête du milieu terrestre par les végétaux","authors":"Marc-André Selosse , François Le Tacon","doi":"10.1016/S0003-5017(01)72082-X","DOIUrl":"10.1016/S0003-5017(01)72082-X","url":null,"abstract":"","PeriodicalId":78387,"journal":{"name":"L' Annee biologique","volume":"40 ","pages":"Pages 3-20"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0003-5017(01)72082-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124977324","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0003-5017(01)72086-7
Julien Hasler , Claude Penel , Thomas Gaspar , Michèle Crèvecœur
Programmed cell death (PCD) in plants has been the subject of controversy for a long time. There is no more doubts nowadays of the occurrence of such a phenomenon during normal plant development or during the plant responses to pathogens. There are some analogies between plant programmed cell death and animal cell's apoptosis, although plant PCD may occur through different morphological patterns. The initial molecular mechanisms leading to PCD during plant normal development and defense responses might be common but with various morphological manifestations depending upon the plant needs.
{"title":"Mort cellulaire programmée, apoptose, …et cellules végétales","authors":"Julien Hasler , Claude Penel , Thomas Gaspar , Michèle Crèvecœur","doi":"10.1016/S0003-5017(01)72086-7","DOIUrl":"10.1016/S0003-5017(01)72086-7","url":null,"abstract":"<div><p>Programmed cell death (PCD) in plants has been the subject of controversy for a long time. There is no more doubts nowadays of the occurrence of such a phenomenon during normal plant development or during the plant responses to pathogens. There are some analogies between plant programmed cell death and animal cell's apoptosis, although plant PCD may occur through different morphological patterns. The initial molecular mechanisms leading to PCD during plant normal development and defense responses might be common but with various morphological manifestations depending upon the plant needs.</p></div>","PeriodicalId":78387,"journal":{"name":"L' Annee biologique","volume":"40 ","pages":"Pages 75-95"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0003-5017(01)72086-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122358242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0003-5017(01)72085-5
Charles Descoins Jr.
Antifeeding agents are mainly organic compounds issued from the metabolic pathways of plants that interrupt food intake by phytophagous insects. These substances can be toxic but generally do not directly kill the insect; it will die by inanition. Antifeeding agents are recognized by taste receptors located on the maxilla and epipharynx. In caterpillars, the two medial and lateral sensilla, the main organs involved in chemoreception, are located on the galea. They are uniporous at their apical extremity and contain four bipolar gustatory neurones, and another one that is a mecanoreceptor. As for olfactory organs, the dendritic parts of these neurones are soaked in a sensory liquor that transports chemical stimuli from outside to the membranous receptors. Antifeeding agents belong to various classes of chemicals and it is not possible to correlate their biological activity with common structural features. Main representatives are terpenoids (drimanes, clerodanes, limonoids, agarofurans) and steroids (phytoecdysteroids). Antifeeding activities can be evaluated by the amount of treated food eaten by a caterpillar in comparison with the reference. Antifeeding agents can be classified by their feeding ratio 50: FR50 or by their antifeedant index 50: AFI50. These values must be calculated for each studied species, each one showing different sensitivity for the same compound. Responses of gustatory neurones to a stimulation with an antifeeding agent can be recorded at the extracellular level by electrophysiological techniques, derived from the pioneer work of Hodgson. When stimulated, these neurones respond by characteristic spikes that depend of the recognition capacity of the neurone, and many hypotheses have been formulated to explain the modalities of this recognition. The most commonly accepted is that antifeeding agents selectively stimulate a special gustatory cell: the deterrent cell. Activation of this cell is often associated with simultaneous inhibition of other gustatory cells involved in perception of phagostimulants like sugars and free aminoacids. The occurrence of the deterrent cell has been demonstrated for many phytophagous caterpillars and can explain repellence for the non-host plants. Phytoecdysteroids are secondary metabolites widely spread in the plant kingdom and it has been hypothesized that they act as defensive substances against herbivorous. Two categories of caterpillars in relation to their sensitivity to the substance have been proposed: the tolerant ones that accept relatively large amounts of phytoecdysteroids in their diet, and the sensitive ones that reject diet with even low amounts. According to this classification, polyphagous species must be tolerant, and at the opposite monophagous species sensitive (diet breadth hypothesis). To verify this hypothesis, the antifeeding activity of three phytoecdysteroids (ecdysone: E, 20-hydroxyecdysone: 20E, and ponasterone: A ponA)
抗摄食剂主要是由植物代谢途径产生的有机化合物,可以阻断食植物昆虫的食物摄取。这些物质可能有毒,但一般不会直接杀死昆虫;它会因缺乏营养而死亡。拒食剂由位于上颌骨和咽上的味觉感受器识别。在毛虫中,两个内侧和外侧的感受器是参与化学接受的主要器官,位于帽状体上。它们的顶端是单孔的,包含四个双极性的味觉神经元,另一个是器官感受器。至于嗅觉器官,这些神经元的树突部分浸泡在一种感觉液体中,这种液体将化学刺激从外部输送到膜受体。抗食剂属于不同种类的化学物质,不可能将它们的生物活性与共同的结构特征联系起来。主要代表是萜类(drimanes, clerodanes, limonids, agarofurans)和类固醇(phytoecdysteroids)。抗摄食活性可通过毛虫进食处理过的食物的数量与对照物进行比较来评价。拒食剂可按其摄食比50:FR50或拒食指数50:AFI50进行分类。这些值必须对每一种被研究的物种进行计算,每一种物种对同一种化合物的敏感性不同。味觉神经元对抗摄食剂刺激的反应可以通过电生理技术在细胞外水平记录下来,这种技术来源于霍奇森的先驱工作。当受到刺激时,这些神经元以依赖于神经元识别能力的特征尖峰反应,并且已经制定了许多假设来解释这种识别的模式。最普遍接受的说法是,拒食剂选择性地刺激一种特殊的味觉细胞:威慑细胞。该细胞的激活通常与其他参与吞噬刺激物(如糖和游离氨基酸)感知的味觉细胞的同时抑制有关。威慑细胞的存在已在许多植食性毛虫中得到证实,并可以解释对非寄主植物的排斥。植物甾体是广泛存在于植物界的次生代谢物,被认为是对草食性植物的防御物质。根据毛虫对该物质的敏感性,人们提出了两类幼虫:耐受型幼虫,它们在饮食中接受相对大量的植物甾体激素;敏感型幼虫,它们拒绝摄入少量的植物甾体激素。根据这一分类,多食物种必须是耐受性的,而在相反的单食物种必须是敏感的(饮食宽度假说)。为了验证这一假设,我们研究了3种植物蜕皮激素(蜕皮激素:E、20-羟基蜕皮激素:20E和ponasterone: A ponA)对4种幼虫(单食家蚕、寡食家蚕、多食滨海夜蛾和nubilalis Ostrinia)的抗摄食活性。通过饲养试验发现,家蚕和芸苔螨的两种末龄幼虫避开含有20E或ponA的饲料,其阈值分别为200和500 ppm,但即使浓度较高,它们也对E不敏感。littoralis幼虫(L4)对这三种甾体激素具有耐受性,但令人惊讶的是,多食性的O. nubilalis幼虫(L5)即使在很低的浓度(25ppm)下也非常敏感。电生理记录与家蚕的内侧感受器和芸苔科的外侧感受器中威慑细胞的出现一致,该细胞响应20E和ponA而不响应E,揭示了类固醇核外侧链上20羟基的重要性。这种阻吓细胞也存在于毛茛的两个感受器中,并以非常低的阈值对三种植物甾体激素作出反应。滨水荆对标准(氯化钾或果糖)的反应无差异。证实了家蚕、芸苔科和滨海夜蛾的食性宽度假说。但对于多食性物种O. nubilalis来说,情况并非如此,根据这一假设,它必须耐受植物甾体激素。问题是要知道nubilalis是否是一个例外,或者在对少数物种进行观察后提出的饮食宽度假设是否适用于大规模。
{"title":"Perception de substances antiappétentes par des chenilles de lépidoptères phytophages","authors":"Charles Descoins Jr.","doi":"10.1016/S0003-5017(01)72085-5","DOIUrl":"10.1016/S0003-5017(01)72085-5","url":null,"abstract":"<div><p>Antifeeding agents are mainly organic compounds issued from the metabolic pathways of plants that interrupt food intake by phytophagous insects. These substances can be toxic but generally do not directly kill the insect; it will die by inanition. Antifeeding agents are recognized by taste receptors located on the maxilla and epipharynx. In caterpillars, the two medial and lateral sensilla, the main organs involved in chemoreception, are located on the galea. They are uniporous at their apical extremity and contain four bipolar gustatory neurones, and another one that is a mecanoreceptor. As for olfactory organs, the dendritic parts of these neurones are soaked in a sensory liquor that transports chemical stimuli from outside to the membranous receptors. Antifeeding agents belong to various classes of chemicals and it is not possible to correlate their biological activity with common structural features. Main representatives are terpenoids (drimanes, clerodanes, limonoids, agarofurans) and steroids (phytoecdysteroids). Antifeeding activities can be evaluated by the amount of treated food eaten by a caterpillar in comparison with the reference. Antifeeding agents can be classified by their feeding ratio 50: <em>FR</em><sub>50</sub> or by their antifeedant index 50: <em>AFI</em><sub>50</sub>. These values must be calculated for each studied species, each one showing different sensitivity for the same compound. Responses of gustatory neurones to a stimulation with an antifeeding agent can be recorded at the extracellular level by electrophysiological techniques, derived from the pioneer work of Hodgson. When stimulated, these neurones respond by characteristic spikes that depend of the recognition capacity of the neurone, and many hypotheses have been formulated to explain the modalities of this recognition. The most commonly accepted is that antifeeding agents selectively stimulate a special gustatory cell: the deterrent cell. Activation of this cell is often associated with simultaneous inhibition of other gustatory cells involved in perception of phagostimulants like sugars and free aminoacids. The occurrence of the deterrent cell has been demonstrated for many phytophagous caterpillars and can explain repellence for the non-host plants. Phytoecdysteroids are secondary metabolites widely spread in the plant kingdom and it has been hypothesized that they act as defensive substances against herbivorous. Two categories of caterpillars in relation to their sensitivity to the substance have been proposed: the tolerant ones that accept relatively large amounts of phytoecdysteroids in their diet, and the sensitive ones that reject diet with even low amounts. According to this classification, polyphagous species must be tolerant, and at the opposite monophagous species sensitive (diet breadth hypothesis). To verify this hypothesis, the antifeeding activity of three phytoecdysteroids (ecdysone: E, 20-hydroxyecdysone: 20E, and ponasterone: A ponA) ","PeriodicalId":78387,"journal":{"name":"L' Annee biologique","volume":"40 ","pages":"Pages 55-73"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0003-5017(01)72085-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55465403","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2001-12-01DOI: 10.1016/S0003-5017(01)72087-9
Patrick Pasques
L’introduction d’organismes génétiquement modifiés (OGM) sur les marchés français et européen, alors que ces organismes étaient déjà bien acceptés aux États-Unis et intégrés à l’économie américaine, a fait l’objet d’un important débat entre les différents acteurs du secteur, débat qui est encore loin d’être terminé. À la différence des États-Unis, l’Union européenne a mis en place un ensemble de directives et de règlements précisant les conditions et les étapes de l’homologation d’OGM ou de produits issus d’OGM. En outre, l’autorisation est limitée dans le temps (10 ans), tandis qu’un contrôle obligatoire après mise sur le marché a été instauré. Les opérations d’évaluation, d’homologation et de contrôle concernent avant tout des plantes transgéniques et les « aliments nouveaux », ainsi que l’utilisation confinée de microorganismes. Dans cet article sont décrits le circuit d’homologation, les conditions à remplir et les étapes à franchir. Les directives européennes et leurs modalités d’application sont présentées, ainsi que les instances consultatives en France (Commission du génie génétique, Commission du génie biomoléculaire, Comité de biovigilance).
{"title":"Circuits d’homologation des OGM","authors":"Patrick Pasques","doi":"10.1016/S0003-5017(01)72087-9","DOIUrl":"10.1016/S0003-5017(01)72087-9","url":null,"abstract":"<div><p>L’introduction d’organismes génétiquement modifiés (OGM) sur les marchés français et européen, alors que ces organismes étaient déjà bien acceptés aux États-Unis et intégrés à l’économie américaine, a fait l’objet d’un important débat entre les différents acteurs du secteur, débat qui est encore loin d’être terminé. À la différence des États-Unis, l’Union européenne a mis en place un ensemble de directives et de règlements précisant les conditions et les étapes de l’homologation d’OGM ou de produits issus d’OGM. En outre, l’autorisation est limitée dans le temps (10 ans), tandis qu’un contrôle obligatoire après mise sur le marché a été instauré. Les opérations d’évaluation, d’homologation et de contrôle concernent avant tout des plantes transgéniques et les « aliments nouveaux », ainsi que l’utilisation confinée de microorganismes. Dans cet article sont décrits le circuit d’homologation, les conditions à remplir et les étapes à franchir. Les directives européennes et leurs modalités d’application sont présentées, ainsi que les instances consultatives en France (Commission du génie génétique, Commission du génie biomoléculaire, Comité de biovigilance).</p></div>","PeriodicalId":78387,"journal":{"name":"L' Annee biologique","volume":"40 ","pages":"Pages 97-106"},"PeriodicalIF":0.0,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0003-5017(01)72087-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117194848","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2000-10-01DOI: 10.1016/S0003-5017(00)90002-3
André-Jean Francez
Sphagnum mires are sink ecosystems for carbon, C-fixation by photosynthesis being higher than organic decay. Total primary production is generally lower than 500 g C·m−2·yr−1, moss layer contribution reaching sometimes 80% of the whole production. Mean annual accumulation in Sphagnum peatlands peat is about 30 g C·m−2, which corresponds approximately to 10% of primary production. Accumulation/production ratio increases from fen to bog and varies with vegetation communities. Methane emissions in the atmosphere from mires are about 39 T g·yr−1 (1 Tg = 1012 g), i.e. 35% of the whole contribution of wetlands. They fluctuate with the types of mires and vegetation and reach sometimes 3 g CH4·m−2·day−1. Mires have been used for agriculture and peat mining. The consequences of drainage and other managements to practise these different uses were carbon emissions of 6 500 Mt from peat, since the beginning of the 19th century. In these conditions, fitting of carbon emissions in the atmosphere shows that disturbed mires could contribute to greenhouse effect as much as coal mining. The influence of increasing atmospheric depositions is not yet well known but seems to be site- and species-dependent. In some European regions, great area of mires have disappeared under the increasing of nitrogen and sulfur depositions. Restoration experiments of mires show that it is possible to regenerate turfigenous process but the time responses for total recovery differ with sites and degrees of disturbance.
泥沼是碳汇生态系统,光合作用对碳的固定高于有机衰变。初级总产量一般低于500 g C·m−2·yr−1,苔藓层的贡献有时可达总产量的80%。泥炭地泥炭年平均积累量约为30 g C·m−2,约相当于初级产量的10%。积累/生产比从沼泽到沼泽增加,并随植被群落而变化。沼泽向大气中排放的甲烷约为39 Tg·yr - 1 (1 Tg = 1012 g),占湿地总排放量的35%。它们随沼泽和植被的类型而波动,有时可达3 g CH4·m−2·day−1。矿坑已被用于农业和泥炭开采。自19世纪初以来,为了实现这些不同的用途,排水和其他管理的后果是泥炭排放了6500万吨碳。在这些条件下,对大气中碳排放的拟合表明,受干扰的矿井可能与煤炭开采一样会造成温室效应。大气沉积增加的影响尚不清楚,但似乎与地点和物种有关。在欧洲一些地区,由于氮和硫沉积的增加,大面积的矿坑已经消失。泥沼恢复实验表明,泥沼恢复是可能的,但泥沼完全恢复的时间响应随场地和扰动程度的不同而不同。
{"title":"La dynamique du carbone dans les tourbières à Sphagnum, de la sphaigne à l'effet de serre","authors":"André-Jean Francez","doi":"10.1016/S0003-5017(00)90002-3","DOIUrl":"10.1016/S0003-5017(00)90002-3","url":null,"abstract":"<div><p><em>Sphagnum</em> mires are sink ecosystems for carbon, C-fixation by photosynthesis being higher than organic decay. Total primary production is generally lower than 500 g C·m<sup>−2</sup>·yr<sup>−1</sup>, moss layer contribution reaching sometimes 80% of the whole production. Mean annual accumulation in <em>Sphagnum</em> peatlands peat is about 30 g C·m<sup>−2</sup>, which corresponds approximately to 10% of primary production. Accumulation/production ratio increases from fen to bog and varies with vegetation communities. Methane emissions in the atmosphere from mires are about 39 T g·yr<sup>−1</sup> (1 Tg = 10<sup>12</sup> g), i.e. 35% of the whole contribution of wetlands. They fluctuate with the types of mires and vegetation and reach sometimes 3 g CH<sub>4</sub>·m<sup>−2</sup>·day<sup>−1</sup>. Mires have been used for agriculture and peat mining. The consequences of drainage and other managements to practise these different uses were carbon emissions of 6 500 Mt from peat, since the beginning of the 19<sup>th</sup> century. In these conditions, fitting of carbon emissions in the atmosphere shows that disturbed mires could contribute to greenhouse effect as much as coal mining. The influence of increasing atmospheric depositions is not yet well known but seems to be site- and species-dependent. In some European regions, great area of mires have disappeared under the increasing of nitrogen and sulfur depositions. Restoration experiments of mires show that it is possible to regenerate turfigenous process but the time responses for total recovery differ with sites and degrees of disturbance.</p></div>","PeriodicalId":78387,"journal":{"name":"L' Annee biologique","volume":"39 4","pages":"Pages 205-270"},"PeriodicalIF":0.0,"publicationDate":"2000-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0003-5017(00)90002-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133104886","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}