মরুজ উদ্ভিদ: সংশোধিত সংস্করণের মধ্যে পার্থক্য

উইকিপিডিয়া, মুক্ত বিশ্বকোষ থেকে
বিষয়বস্তু বিয়োগ হয়েছে বিষয়বস্তু যোগ হয়েছে
Jdebabrata (আলোচনা | অবদান)
সম্পাদনা সারাংশ নেই
Jdebabrata (আলোচনা | অবদান)
সম্পাদনা সারাংশ নেই
৪৪ নং লাইন: ৪৪ নং লাইন:


Bushes, also called semi-shrubs often occur in sandy desert region, mostly in deep sandy soils at the edges of the dunes. One example is the ''[[Reaumuria soongorica]]'', a perennial resurrection semi-shrub. Compared to other dominant arid xerophytes, an adult ''R. soongorica'', bush has a strong resistance to [[water scarcity]], hence, it is considered a super-xerophytes.<ref name=":0" />
Bushes, also called semi-shrubs often occur in sandy desert region, mostly in deep sandy soils at the edges of the dunes. One example is the ''[[Reaumuria soongorica]]'', a perennial resurrection semi-shrub. Compared to other dominant arid xerophytes, an adult ''R. soongorica'', bush has a strong resistance to [[water scarcity]], hence, it is considered a super-xerophytes.<ref name=":0" />


== Importance of water conservation ==

If the [[water potential]] (or strictly, water vapour potential) inside a leaf is higher than outside, the water vapour will [[diffusion|diffuse]] out of the leaf down this gradient. This loss of water vapour from the leaves is called [[transpiration]], and the water vapour diffuses through the open [[stomata]]. Transpiration is natural and inevitable for plants; a significant amount of water is lost through this process. However, it is vital that plants living in dry conditions are adapted so as to decrease the size of the open stomata, lower the rate of transpiration, and consequently reduce water loss to the environment. Without sufficient water, plant cells lose [[turgor]]. This is known as [[plasmolysis]]. If the plant loses too much water, it will pass its [[permanent wilting point]], and die.<ref>{{Cite web|url=http://plantsinaction.science.uq.edu.au/content/314-turgor-loss-cytorrhysis-and-plasmolysis|title=3.1.4 - Turgor loss, cytorrhysis, and plasmolysis {{!}} Plants in Action|website=plantsinaction.science.uq.edu.au|language=en|access-date=2018-03-21}}</ref>

In brief, the rate of transpiration is governed by the number of [[stomata]], stomatal aperture i.e. the size of the stoma opening, leaf area (allowing for more stomata), temperature differential, the relative humidity, the presence of wind or air movement, the light intensity, and the presence of a waxy cuticle. It is important to note, that whilst it is vital to keep stomata closed, they have to be opened for gaseous exchange in respiration and photosynthesis.

== Morphological adaptations ==

{{multiple image
| width = 200
| footer = The cactus ''[[Cereus peruvianus]]'' looks superficially very similar to ''[[Euphorbia virosa]]'' due to [[convergent evolution]].
| image1 = Cereus_peruvians_(cropped).jpg
| alt1 =
| caption1 = ''Cereus peruvianus''
| image2 = Euphorbia-virosa.jpg
| alt2 =
| caption2 = ''Euphorbia virosa''
}}
Xerophytic plants may have similar shapes, forms, and structures and look very similar, even if the plants are not very closely related, through a process called [[convergent evolution]]. For example, some species of [[cacti]], which evolved only in the Americas, may appear similar to [[euphorbia]]s, which are distributed worldwide. An unrelated species of [[caudiciform]]s plants with swollen bases that are used to store water, may also display some similarities.

Under conditions of water scarcity, the seeds of different xerophytic plants behave differently, which means that they have different rates of germination since water availability is a major limiting factor. These dissimilarities are due to [[natural selection]] and eco-adaptation as the seeds and plants of each species evolve to suit their surrounding.<ref>{{cite journal|last1=Ibañez|first1=A.N.|last2=Passera|first2=C.B.|title=Factors affecting the germination of albaida (Anthyllis cytisoidesL.), a forage legume of the Mediterranean coast|journal=Journal of Arid Environments|date=February 1997|volume=35|issue=2|pages=225–231|doi=10.1006/jare.1995.0142}}</ref>

=== Reduction of surface area ===

Xerophytic plants can have less overall [[surface area]] than other plants, so reducing the area that is exposed to the air and reducing water loss by transpiration and evaporation. They can also have smaller leaves or fewer branches than other plants. An example of leaf surface reduction are the [[Thorns, spines, and prickles|spines]] of a cactus, while the effects of compaction and reduction of branching can be seen in the [[barrel cactus|barrel cacti]]. Other xerophytes may have their leaves compacted at the base, as in a [[basal rosette]], which may be smaller than the plant's flower. This adaptation is exhibited by some ''[[Agave]]'' and ''[[Eriogonum]]'' species, which can be found growing near [[Death Valley]].

=== Forming water vapour-rich environment ===

Some xerophytes have tiny hairs on their surfaces to provide a wind break and reduce air flow, thereby reducing the rate of evaporation. When a plant surface is covered with tiny hairs, it is called tomentose. Stomata are located in these hairs or in pits to reduce their exposure to wind. This enables them to maintain a humid environment around them.

In a still, windless environment, the areas under the leaves or spines where transpiration takes place form a small localised environment that is more saturated with water vapour than normal. If this concentration of water vapour is maintained, the external water vapour potential gradient near the stomata is reduced, thus, reducing transpiration. In a windier situation, this localisation is blown away and so the external water vapour gradient remains low, which makes the loss of water vapour from plant stomata easier. Spines and hairs trap a layer of moisture and slows air movement over tissues.

=== Reflective features ===
[[File:Dudleya Brittonii.jpg|thumb|right|The succulent leaves of ''[[Dudleya brittonii]]'' are visibly coated with a 'powdery' white which is the epicuticular wax.]]
The color of a plant, or of the waxes or hairs on its surface, may serve to reflect sunlight and reduce transpiration. An example is the white chalky [[epicuticular wax]] coating of ''[[Dudleya brittonii]]'', which has the highest [[ultraviolet light]] (UV) [[reflectivity]] of any known naturally-occurring biological substance.<ref>{{cite journal|last=Mulroy|first=Thomas W.|title=Spectral properties of heavily glaucous and non-glaucous leaves of a succulent rosette-plant|journal=Oecologia|date=1979|volume=38|issue=3|pages=349–357|doi=10.1007/BF00345193|pmid=28309493}}</ref>

=== Cuticles ===

Many xerophytic species have thick [[plant cuticle|cuticles]]. Just like human skin, a plant's cuticles are the first line of defense for its aerial parts. As mentioned above, the cuticle contains wax for protection against [[Biotic component|biotic]] and [[abiotic component|abiotic]] factors. The [[ultrastructure]] of the cuticles varies in different species. Some examples are ''[[Antizoma miersiana]]'', ''[https://www.ispotnature.org/communities/southern-africa/species-dictionary/26483/hermannia-disermifolia Hermannia disermifolia]'' and ''[[Galenia africana]]'' which are xerophytes from the same region in [[Namaqualand]], but have different cuticle ultrastructures.

''A. miersiana'' has thick cuticle as expected to be found on xerophytes, but ''H. disermifolia'' and ''G. africana'' have thin cuticles. Since resources are scarce in arid regions, there is selection for plants having thin and efficient cuticles to limit the nutritional and energy costs for the cuticle construction.

In periods of severe water stress and stomata closure, the cuticle's low water permeability is considered as one of the most vital factor in ensuring the survival of the plant. The rate of transpiration of the cuticles of xerophytes is 25 times lower than that of stomatal transpiration. To give an idea of how low this is, the rate of transpiration of the cuticles of mesophytes is only 2 to 5 times lower than stomatal transpiration.
<ref>{{cite journal|last1=Jordaan|first1=A.|last2=Kruger|first2=H.|title=Notes on the cuticular ultrastructure of six xerophytes from southern Africa|journal=South African Journal of Botany|date=February 1998|volume=64|issue=1|pages=82–85|doi=10.1016/S0254-6299(15)30829-2|doi-access=free}}</ref>





০৬:৩২, ৪ সেপ্টেম্বর ২০২০ তারিখে সংশোধিত সংস্করণ

A মরুজ উদ্ভিদ বা জেরোফাইট (গ্রীক থেকে ξηρός xeros dry, φυτόν phuton plant) is a species of plant that has adaptations to survive in an environment with little liquid water, such as a desert or an ice- or snow-covered region in the Alps or the Arctic. Popular examples of xerophytes are cacti, pineapple and some Gymnosperm plants.

The structural features (morphology) and fundamental chemical processes (physiology) of xerophytes are variously adapted to conserve water, also common to store large quantities of water, during dry periods. Other species are able to survive long periods of extreme dryness or desiccation of their tissues, during which their metabolic activity may effectively shut down. Plants with such morphological and physiological adaptations are xeromorphic.[১] Xerophytes such as cacti are capable of withstanding extended periods of dry conditions as they have deep-spreading roots and capacity to store water. The leaves are waxy and thorny that prevents loss of water and moisture. Even their fleshy stems can store water.

পরিচিতি

Ramonda serbica a.k.a. Serbian phoenix flower
The structural adaptations of these two resurrection plants are very similar. They can be found on the grounds of Bulgaria and Greece.

Plants absorb water from the soil, which then evaporates from their shoots and leaves; this process is known as transpiration. In dry environments, a typical mesophytic plant would evaporate water faster than the rate of water uptake from the soil, leading to wilting and even death.

Xerophytic plants exhibit a diversity of specialized adaptations to survive in such water-limiting conditions. They may use water from their own storage, allocate water specifically to sites of new tissue growth, or lose less water to the atmosphere and so channel a greater proportion of water from the soil to photosynthesis and growth. Different plant species possess different qualities and mechanisms to manage water supply, enabling them to survive.

Cacti and other succulents are commonly found in deserts, where there is little rainfall. Other xerophytes, such as certain bromeliads, can survive through both extremely wet and extremely dry periods and can be found in seasonally-moist habitats such as tropical forests, exploiting niches where water supplies are too intermittent for mesophytic plants to survive. Likewise, chaparral plants are adapted to Mediterranean climates, which have wet winters and dry summers.

Plants that live under arctic conditions also have a need for xerophytic adaptations, since water is unavailable for uptake when the ground is frozen, such as the European resurrection plants Haberlea rhodopensis and Ramonda serbica.[২]

In an environment with very high salinity such as mangrove swamps and semi-deserts, water uptake by plants is a challenge due to the high salt ion levels. Besides that, such environments may cause an excess of ions to accumulate in the cells, which is very damaging.[৩] Halophytes and xerophytes evolved to survive in such environments. Some xerophytes may also be considered halophytes, however, halophytes are not necessarily xerophytes. The succulent xerophyte Zygophyllum xanthoxylum, for example, has specialised protein transporters in their cells which allow storage of excess ions in their vacuole to maintain normal cytosolic pH and ionic composition.[৪][৫]

There are many factors which affect water availability, which is the major limiting factor of seed germination, seedling survival, and plant growth. These factors include infrequent raining, intense sunlight and very warm weather leading to faster water evaporation. An extreme environmental pH and high salt content of water also disrupt plants' water uptake.

প্রকারভেদ

Cistus albidus is a xerophyte which grows in European countries such as France, and Italy and North African countries like Morocco.

Succulent plants store water in their stems or leaves. These include plants from the family Cactaceae, which have round stems and can store a lot of water. The leaves are often vestigial, as in the case of cacti, wherein the leaves are reduced to spines, or they do not have leaves at all. These include the C4 perennial woody plant, Haloxylon ammodendron which is a native of northwest China.

Non-succulent perennials successfully endure long and continuous shortage of water in the soil. These are hence called 'true xerophytes' or euxerophytes. Water deficiency usually reaches 60–70% of their fresh weight, as a result of which the growth process of the whole plant is hindered during cell elongation. The plants which survive drought are, understandably, small and weak.

Ephemerals are the 'drought escaping' kind, and not true xerophytes. They do not really endure drought, only escape it. With the onset of rainfall, the plant seeds germinate, quickly grow to maturity, flower, and set seed, i.e., the entire life cycle is completed before the soil dries out again. Most of these plants are small, roundish, dense shrubs represented by species of Papilionaceae, some inconspicuous Compositae, a few Zygophyllaceae and some grasses. Water is stored in the bulbs of some plants, or at below ground level. They may be dormant during drought conditions and are, therefore, known as drought evaders.

Shrubs which grow in arid and semi-arid regions are also xeromorphic. For example, Caragana korshinskii, Artemisia sphaerocephala, and Hedysarum scoparium are shrubs potent in the semi-arid regions of the northwest China desert. These psammophile shrubs are not only edible to grazing animals in the area, they also play a vital role in the stabilisation of desert sand dunes.[৬]

Bushes, also called semi-shrubs often occur in sandy desert region, mostly in deep sandy soils at the edges of the dunes. One example is the Reaumuria soongorica, a perennial resurrection semi-shrub. Compared to other dominant arid xerophytes, an adult R. soongorica, bush has a strong resistance to water scarcity, hence, it is considered a super-xerophytes.[৬]


Importance of water conservation

If the water potential (or strictly, water vapour potential) inside a leaf is higher than outside, the water vapour will diffuse out of the leaf down this gradient. This loss of water vapour from the leaves is called transpiration, and the water vapour diffuses through the open stomata. Transpiration is natural and inevitable for plants; a significant amount of water is lost through this process. However, it is vital that plants living in dry conditions are adapted so as to decrease the size of the open stomata, lower the rate of transpiration, and consequently reduce water loss to the environment. Without sufficient water, plant cells lose turgor. This is known as plasmolysis. If the plant loses too much water, it will pass its permanent wilting point, and die.[৭]

In brief, the rate of transpiration is governed by the number of stomata, stomatal aperture i.e. the size of the stoma opening, leaf area (allowing for more stomata), temperature differential, the relative humidity, the presence of wind or air movement, the light intensity, and the presence of a waxy cuticle. It is important to note, that whilst it is vital to keep stomata closed, they have to be opened for gaseous exchange in respiration and photosynthesis.

Morphological adaptations

Cereus peruvianus
Euphorbia virosa
The cactus Cereus peruvianus looks superficially very similar to Euphorbia virosa due to convergent evolution.

Xerophytic plants may have similar shapes, forms, and structures and look very similar, even if the plants are not very closely related, through a process called convergent evolution. For example, some species of cacti, which evolved only in the Americas, may appear similar to euphorbias, which are distributed worldwide. An unrelated species of caudiciforms plants with swollen bases that are used to store water, may also display some similarities.

Under conditions of water scarcity, the seeds of different xerophytic plants behave differently, which means that they have different rates of germination since water availability is a major limiting factor. These dissimilarities are due to natural selection and eco-adaptation as the seeds and plants of each species evolve to suit their surrounding.[৮]

Reduction of surface area

Xerophytic plants can have less overall surface area than other plants, so reducing the area that is exposed to the air and reducing water loss by transpiration and evaporation. They can also have smaller leaves or fewer branches than other plants. An example of leaf surface reduction are the spines of a cactus, while the effects of compaction and reduction of branching can be seen in the barrel cacti. Other xerophytes may have their leaves compacted at the base, as in a basal rosette, which may be smaller than the plant's flower. This adaptation is exhibited by some Agave and Eriogonum species, which can be found growing near Death Valley.

Forming water vapour-rich environment

Some xerophytes have tiny hairs on their surfaces to provide a wind break and reduce air flow, thereby reducing the rate of evaporation. When a plant surface is covered with tiny hairs, it is called tomentose. Stomata are located in these hairs or in pits to reduce their exposure to wind. This enables them to maintain a humid environment around them.

In a still, windless environment, the areas under the leaves or spines where transpiration takes place form a small localised environment that is more saturated with water vapour than normal. If this concentration of water vapour is maintained, the external water vapour potential gradient near the stomata is reduced, thus, reducing transpiration. In a windier situation, this localisation is blown away and so the external water vapour gradient remains low, which makes the loss of water vapour from plant stomata easier. Spines and hairs trap a layer of moisture and slows air movement over tissues.

Reflective features

The succulent leaves of Dudleya brittonii are visibly coated with a 'powdery' white which is the epicuticular wax.

The color of a plant, or of the waxes or hairs on its surface, may serve to reflect sunlight and reduce transpiration. An example is the white chalky epicuticular wax coating of Dudleya brittonii, which has the highest ultraviolet light (UV) reflectivity of any known naturally-occurring biological substance.[৯]

Cuticles

Many xerophytic species have thick cuticles. Just like human skin, a plant's cuticles are the first line of defense for its aerial parts. As mentioned above, the cuticle contains wax for protection against biotic and abiotic factors. The ultrastructure of the cuticles varies in different species. Some examples are Antizoma miersiana, Hermannia disermifolia and Galenia africana which are xerophytes from the same region in Namaqualand, but have different cuticle ultrastructures.

A. miersiana has thick cuticle as expected to be found on xerophytes, but H. disermifolia and G. africana have thin cuticles. Since resources are scarce in arid regions, there is selection for plants having thin and efficient cuticles to limit the nutritional and energy costs for the cuticle construction.

In periods of severe water stress and stomata closure, the cuticle's low water permeability is considered as one of the most vital factor in ensuring the survival of the plant. The rate of transpiration of the cuticles of xerophytes is 25 times lower than that of stomatal transpiration. To give an idea of how low this is, the rate of transpiration of the cuticles of mesophytes is only 2 to 5 times lower than stomatal transpiration. [১০]


তথ্যসূত্র

  1. ” Xeromorphic”, The Cambridge Illustrated Glossary of Botanical Terms, Michael Hickey, Clive King, Cambridge University Press, 2001
  2. Gechev, Tsanko S.; Hille, Jacques; Woerdenbag, Herman J.; Benina, Maria; Mehterov, Nikolay; Toneva, Valentina; Fernie, Alisdair R.; Mueller-Roeber, Bernd (২০১৪-১১-০১)। "Natural products from resurrection plants: Potential for medical applications"। Biotechnology Advances (ইংরেজি ভাষায়)। 32 (6): 1091–1101। আইএসএসএন 0734-9750ডিওআই:10.1016/j.biotechadv.2014.03.005অবাধে প্রবেশযোগ্যপিএমআইডি 24681091 
  3. Liu, Hua; Wang, Qiuqing; Yu, Mengmeng; Zhang, Yanyan; Wu, Yingbao; Zhang, Hongxia (২০০৮)। "Transgenic salt-tolerant sugar beet (Beta vulgaris L.) constitutively expressing an Arabidopsis thaliana vacuolar Na/H antiporter gene, AtNHX3, accumulates more soluble sugar but less salt in storage roots"। Plant, Cell & Environment31 (9): 1325–1334। আইএসএসএন 1365-3040ডিওআই:10.1111/j.1365-3040.2008.01838.xপিএমআইডি 18518917 
  4. Wu, Guo-Qiang; Wang, Qian; Bao, Ai-Ke; Wang, Suo-Min (১ মার্চ ২০১১)। "Amiloride Reduces Sodium Transport and Accumulation in the Succulent Xerophyte Zygophyllum xanthoxylum Under Salt Conditions"। Biological Trace Element Research (English ভাষায়)। 139 (3): 356–367। আইএসএসএন 0163-4984ডিওআই:10.1007/s12011-010-8662-9পিএমআইডি 20352373 
  5. McNair, J.B.। "Hydrophytes, xerophytes and halophytes and the production of alkaloids, cyanogenetic and organic sulphur compounds"। Journal of Natural Products6: 1–17। 
  6. Zeng, Yan Jun; Wang, Yan Rong; Zhang, Ju Ming (এপ্রিল ২০১০)। "Is reduced seed germination due to water limitation a special survival strategy used by xerophytes in arid dunes?"। Journal of Arid Environments74 (4): 508–511। ডিওআই:10.1016/j.jaridenv.2009.09.013 
  7. "3.1.4 - Turgor loss, cytorrhysis, and plasmolysis | Plants in Action"plantsinaction.science.uq.edu.au (ইংরেজি ভাষায়)। সংগ্রহের তারিখ ২০১৮-০৩-২১ 
  8. Ibañez, A.N.; Passera, C.B. (ফেব্রুয়ারি ১৯৯৭)। "Factors affecting the germination of albaida (Anthyllis cytisoidesL.), a forage legume of the Mediterranean coast"। Journal of Arid Environments35 (2): 225–231। ডিওআই:10.1006/jare.1995.0142 
  9. Mulroy, Thomas W. (১৯৭৯)। "Spectral properties of heavily glaucous and non-glaucous leaves of a succulent rosette-plant"। Oecologia38 (3): 349–357। ডিওআই:10.1007/BF00345193পিএমআইডি 28309493 
  10. Jordaan, A.; Kruger, H. (ফেব্রুয়ারি ১৯৯৮)। "Notes on the cuticular ultrastructure of six xerophytes from southern Africa"। South African Journal of Botany64 (1): 82–85। ডিওআই:10.1016/S0254-6299(15)30829-2অবাধে প্রবেশযোগ্য