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Halophytes : Ecological Anatomy Aspects

By Grigore, Marius, Nicusor, Ph.D.

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Book Id: WPLBN0002828067
Format Type: PDF (eBook)
File Size: 19.27 mb
Reproduction Date: 5/6/2010

Title: Halophytes : Ecological Anatomy Aspects  
Author: Grigore, Marius, Nicusor, Ph.D.
Language: Moldovan
Subject: Non Fiction, Science, Plant anatomy, halophytes
Collections: Science, Science Fiction Collection, Health and Safety Technology, Biochemistry, Business Strategy, Authors Community, Environmental Economics, Medicine, Geography, Technology, Chemistry, Agriculture, Economics, Biology, Anthropology, Most Popular Books in China, Management, Fine Arts, Literature, Finance, Economy, Language
Publication Date:
Publisher: Edit. Univ. Alexandru Ioan Cuza, Iasi
Member Page: Marius Nicusor Grigore


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Grigore, Ph.D, M. N. (2010). Halophytes : Ecological Anatomy Aspects. Retrieved from

An original book focused on the anatomical features in halophytes from Romania. A very good tool for understanding the ecological value of adaptations in plants vegetating on saline habitats. It comprises 500 original photos taken on light microscope - all being original contribution. Coming with an English abstract.

Salinisation is currently one of the biggest problems facing Earth agriculture. In a continuous increase of world population, obtaining of salt tolerant crops represents a true priority. Halophytes have been defined as salt-tolerant plants having therefore, cellular, biochemical, physiological and anatomical mechanisms allowing them to survive in high salinity conditions. This work represents an anatomical and ecological monograph of halophyte species from Moldova (North-Eastern Romania), representing the results of investigations conducted over many years. Thus, 26 taxa were investigated; these species belong to different botanical families and constitute a heterogeneous group of plants collected from different saline - some dry, others wet habitats. Ecological anatomy approach involves a correlation between structure and habitat, between certain well-defined anatomical adaptations and some environmental factors such as salinity, soil moisture or dryness. In some cases, finding such correlations has been proved facile, while in other cases, some anatomical adaptations remain controversial, because their function is not fully elucidated. In the introductory part of the book, we have discussed some theoretical issues related to definition and classification of halophytes and the relationship between halophytes and salt stress, the latter one being one of the most intensely studied in plant biology field. We are keeping open the question whether anatomical adaptations of halophytes are the result of formative effect of salts, salt stress damage or an expression of positive adaptation, allowing plants to withstand in hypersaline environments. The proper part of the work refers to the histo-anatomical study of halophyte species. Ecological interpretations were made whenever possible, in concordance with the evidenced and discussed structure. As a general rule, we have seen that in most cases, histo-anatomical features are logically linked to environmental factors, thus being the effect of environmental factors. We found that taxa included in the Chenopodiaceae (Atriplex littoralis, A. prostrata, A. tatarica, Camphorosma annua, Halimione verrucifera, Petrosimonia oppositifolia, P. triandra, Salicornia europaea, Suaeda maritima) show successive cambia phenomenon on vegetative axial organs (root, stem) level. Regarded by many authors as a structural anomaly, the connection of this phenomenon with salinity factor remains unclear. Although the interpretation of this phenomenon is very difficult to be done in ecological and adaptive direction, because here is almost a completely lack in some studies, so we tried, as a hypothesis, to explain this phenomenon. We have assumed that additional cambia phenomenon might be a mechanism involved in regulation of salt content, thus having an adaptive and ecologic significance. Certainly, it is has been sometimes shown the fact that the intense lignification which is provided by the activity of successive cambia can be stimulated by salinity. Therefore, this could confer mechanical resistance of cells to high osmotic pressure of soil solution. Halophyte species collected from wet habitats (Aster tripolium ssp. pannonicus, Juncus grardi, Spergularia media) present aerenchyma, especially in underground organs (rhizome, root). This feature is a common adaptation in species vegetating in such habitats, supplying the plant with oxygen during the possible hypoxia conditions. Another interesting anatomical feature is a well developed endodermis, evidenced in some species (Artemisia santonicum, Juncus gerardi, Lactuca saligna, Salicornia europaea, Suaeda maritima, Bolboschoenus maritimus), on axial vegetative organs level. We have viewed this structure as a barrier that controls and limits the salt penetration in plant body. Other adaptation, relatively common on halophytes and intensely discussed, is the shoot succulence. We have evidenced this feature, expressed by a water storage tissue and sometimes by a well-developed palisade tissue, in: Salicornia europaea, Suaeda maritima, Petrosimonia oppositifolia, P. triandra and Spergularia media. On halophyte species growing in wet habitats (Suaeda, Salicornia), the succulence ensures the erect position of plant and the potential dilution of toxic salts. In addition, the succulence can be induced and developed by chlorine ions as it is known that the two species listed above have been included in the chloruric plant associations. In xero-halophytes (Petrosimonia oppositifolia and P. triandra) the water storage tissues constitute, in the same time, a water reservoir needed in the dry seasons. Moreover, at these species, the succulence also facilitates the salt dilution, because in dry conditions salts become more concentrated in root zone. Traheids occuring in succulent tissues of Salicornia are very interesting but also controversial structures. It is assumed that these tracheids are involved in plant water balance, salt tolerance, mechanical support and water or air storage. They are located among the palisade cells, approximately perpendicular to the epidermis, with no direct conection neither with epidermis, on the one hand, neither with vascular system of plant, on the other hand. The vezicular, salt-secreting hairs (bladders) of Atriplex tatarica and Halimione verrucifera, evidenced in the leaf structure, are highly specialized structures, involved in the accumulation and subsequent removal of salts in excess. They are characteristic mainly in the Chenopodiaceae, and consist in a stalk-cell and a vezicular (bladder) cell, where salts are accumulated in order to be eliminated on leaf surface. The secretory pathway, chosen by many halophyte species (crynohalophytes) represents an important adaptive strategy in salt tolerant plants life. Another adaptive mechanism related to the C4 photosynthesis, is the so-called Kranz Anatomy configuration, in the leaf structure of some Chenopodiaceae species. Thus, we have described the atriplicoid sub-type on Atriplex tatarica, meaning that here is a sheath formed by izodiametric cells that form a layer more or less continuous around the vascular bundles. On Petrosimonia opositifolia, P. triandra and Camphorosma annua we have described the kochioid sub-type included in Kranz anatomy. This means, mainly, the following tissues dispozition: epidermis (with hypodermis on Camphorosma), external chlorenchyma (palisade tissue), internal clorenchyma (a layer of more or less cubic cells) and central, water storage tissue in which usually here a great vascular bundle is located. The two chlorenchyma tissues are arranged in two discontinuous layers, arround the leaf. We have also evidenced bulliform cells (Puccinellia distans, Juncus gerardi, Bolboschoenus maritimus, Carex distans), at leaf epidermis level; these cells are mostly involved in leaves rolling in dry habitat conditions. But, apparently, their role is more complex and subtle than at first sight. Although they are considered a xerophytic character, we have evidenced them on hygro-halophyte species. In such a context, we think that here is not relevant to consider one single environmental factor, seen stable and fixed, but its fluctuation during one growing season. The plants listed above have been called amphibious halophytes, due to their ability to survive in dry soil conditions, and this real possibility requires, in addition, the presence of xeromorphytic features. In general, as a result of our investigations, we can say that there are some obvious anatomical adaptations of halophytes, well defined, enabling them to survive in hypersaline environments. These features characterize the „obligatory” halophytes - species adapted to high salinity conditions, which are strictly restricted to salty areas, and are not found on other soil types than the saline ones. These observations allowed us to formulate a hypothesis regarding the „extreme” adaptations of halophytes to salinity. The most evident and „spectacular” characters, linked to halophilous profile were observed on halophyte species adapted to higher salinity conditions (and usually on the species that occur only in high salinized areas). Following our investigations and given interpretations, we have proposed a new system of halophytes classification, based on the relevance of anatomical adaptations correlated with the intensity of environmental factors (most oftenly, soil salinity). Thus, the Chenopodiaceae succulent species best adapted to high salinity conditions (Salicornia, Suaeda, Halimione, Petrosimonia oppositifolia and P. triandra) were nominated as extremohalophytes; in addition, because they grow only in very salinized environments, we apllied to them the term irreversible halophytes. Atriplex littoralis, A. prostrata, A. tatarica, Bassia hirsuta, Camphorosma annua species, which have a large ecological spectrum and they are not so strictly related to increased salinity, were called by us as reversible halophytes. These species may also pass in less salinized environments. The suporting, accidental or preferential halophytes which don’t have histo-anatomical characters very clearly correlated to salinity factor were called mesohalophytes. They are more subjected to multiple influences of environmental factors, including soil salinity, but this is not the major factor inducing spectacular adaptations within this group of halophyte species. In the mesohalophytes group, the above mentioned amphibious halophytes could be included. Our investigations and observations suggest that here is a relevant correlation between histo-anatomical features of halophytes and ecological factors of environments where they vegetate.

"Most of water on the earth is salty and yet most of the land is not. Over the millennia, salts have been washed from rocks and soils into the oceans where they have accumulated. Where the oceans meet the land then saline areas can form that have an unusual flora, one that tolerates salt concentrations lethal to most of our plant species. These salt-tolerant plants are called halophytes. Halophytes were recognised in the late 1700s, but it took a further hundred years or so before their scientific study began. Since then, there has been a small but steady increase in the numbers of scientific publications on the biochemistry, physiology, ecology and potential economic uses of halophytes. In recent years, the need to feed a burgeoning world population has focussed attention on limitations to agricultural production and the part halophytes might play in our ability to raise crops on saline soils. The saline fringes of the oceans constitute a small proportion of the world’s land surface and are not particularly important agriculturally. However, these saline fringes are not the only salt-affected soils on the world’s land surface. Saline soils can also be found in other, often arid, areas - sometimes as a result of the presence of underlying ancient oceans. Yet other saline areas are the consequence of human activity and have been created either though irrigation or forest clearance. The continuous application of irrigation water with small concentrations of dissolved salts can, over time, lead to the build-up of salts in the soil as the water is transpired or evaporated; furthermore, water is often left in the soil creating saline water-logging. Secondary salinisation can also arise through forest clearance, which brings saline water tables into the root zone. It has proven difficult to assess the extent of primary and of secondary salinisation, because measuring the salinity of a soil has been a slow process. Nevertheless, estimates abound in the literature, with values for the area of salt-affected soils in the world ranging from about 350 to 1000 million hectares: at maximum this is about 6% of the world’s land surface. However, as far as agricultural production is concerned, it is not the majority of this land that is important, but that part which is irrigated, since salinisation reduces crop yields and irrigated farmland can be the most productive on earth. The effect of salinity on plants is generally described in terms of growth, using words such as sensitive, resistant or tolerant. Those plants that survive in seawater are clearly halophytes and ‘tolerant’; those that are killed by one tenth the salt concentrations found in seawater are clearly sensitive (and called glycophytes, plants of sweet – or fresh – water). However, there is no clear demarcation between halophytes and glycophytes; salt sensitivity/tolerance varies continuously amongst plant species. Drawing a dividing line in any continuous distribution is somewhat arbitrary and so it is not surprising that different authors have separated halophytes from glycophytes at different salt concentrations. Describing the response of plants is also made complex by variation not only between, but within species. This can lead to semantic problems with terms such as resistant or tolerant glycophytes. However, what is clear is that there is a small group of plants that are highly tolerant of salts around their roots. The number of these halophytic species is not known with certainty because of lack of data, but is likely to be about 500 - of the approximately 250,000 plant species. This makes halophytes relatively rare amongst flowering plants. However, it is the study of these species that will, in my view, inform us of the nature of salt tolerance and help us in our quest to increase the tolerance of existing crops – for it has not proven easy to change the tolerance of any crop species. Not only can the study of halophytes enlighten our understanding of what makes one species salt tolerant and another salt sensitive, but halophytes have their own potential as crops and as a resource in the management and reclamation of saline land. So, I warmly welcome this book and the scientific study of halophytes". T J Flowers, University of Sussex March 2010


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