- Catégorie parente: Revue des bioressources
NEDJIMI B.1*, GUIT B.1, TOUMI M.2 et DAOUD Y.3
1. Université de Djelfa, Laboratoire d’Exploration et de Valorisation des Écosystèmes Steppiques, Faculté des Sciences de la Nature et de la Vie, Algérie,
2. Ecole Normale Supérieure Bachir El Ibrahimi BP. 92 Kouba 16050 Alger, Algérie.
3. Ecole Nationale Supérieure Agronomique, Département de Sciences du Sol, El-Harrach Alger 16000, Algérie.
Abstract: Lygeum spartum L. (Poaceae) is a perennial rhizomatous grass, which is widely distributed in the Algerian steppes. This species can tolerate extreme conditions of aridity and high temperatures and it has been used as raw material for manufacturing paper. The seeds of L. spartum were collected from the area of Aïn Maâbed in the province of Djelfa (Algeria). Theobjective of the present work was to analyse plant water relations of this speciesin the presence of NaCl at different concentrations in order to evaluate the tolerance of the plant to salt stress. L. spartum seedlings were grown in hydroponic culture with Hoagland nutrient solution. After 13 days of growth, plants were treated with 0, 50 and 100 mM NaCl. The effect of NaCl on water relation parameters were measured after 7 days of the treatments. NaCl exposure of L. spartum produced a decrease in root hydraulic conductivity (L0), with the highest NaCl concentration (100mM NaCl) causing 79% decrease of L0. Transpiration was reduced by about 22% and 48% as compared to control plants, respectively, at 50 and 100mM NaCl. No change was observed in the turgor potential (Ψτ). Based upon these results, the ability to tolerate moderate saltinity renders this species a promising pasture plant for increasing forage production in salt-affected soils.
Key words: Lygeum spartum L., steppe, salinity, root hydraulic conductivity, turgor potential, transpiration.
SATATUT HYDRIQUE DU Lygeum spartum L. SOUS STRESS SALIN
Résumé : Le sparte (Lygeum spartum L.) fait partie des espèces graminées pérennes des steppes semi arides algériennes. Dotée d’une biomasse aérienne et racinaire assez importante, il constitue un outil efficace et relativement peu coûteux dans la lutte contre la désertification et dans la réhabilitation des terres dégradées. En Afrique du Nord, il constitue une ressources importantes en fibres pour l‘industrie papetière. Des plantules de L. spartum ont été cultivées en condition hydroponique pour étudier l'effet de l’addition du NaCl dans la solution nutritive sur le statut hydrique de cette espèce. Les traitements utilisés sont 0, 50 et 100 mM NaCl. Les résultats obtenus ont montré que le NaCl entraîne une réduction de la conductivité hydraulique des racines (L0) de l’ordre de 79% par rapport au témoin pour la concentration la plus stressante (100mM NaCl). La transpiration se trouve sévèrement diminuée en présence de NaCl dans le milieu de culture. Cette diminution peut atteindre jusqu’à 22% et 48% par rapport au témoin respectivement pour 50 et 100 mM NaCl. Alors que pour le potentiel de turgescence (Ψτ) une certaine stabilité a été enregistrée. Cette espèce peut être employée localement pour le repeuplement des terres affectées par la salinité, en vue de leur réhabilitation, notamment en tant que parcours.
Mots clefs : Lygeum spartum L., steppe, salinité, transpiration, conductivité hydraulique des racines, potentiel de turgescence, transpiration.
Salinity, one of the major factors limiting crop production, may reduce plant growth by water deficit, ion toxicity, ion imbalance or a combination of these factors . Some plants are able to tolerate salinity stresses by reducing the cellular osmotic potential as a consequence of a net increase in solute accumulation .
Lygeum spartum L. (Poaceae) is one of the most abundant and widespread perennial rhizomatous grasses found in the Algerian steppes. This species can tolerate extreme conditions of aridity and high temperatures, the maximal temperatures growth ranging between 40 and 45 °C [3,4].Its extensive root system plays a significant role in preventing desertification, by stabilising the sand. It has been used as a fodder for domestic livestock and for rehabilitation of degraded lands.
In North Africa, it has been used as raw material for manufacturing paper . However, as far as we know, there is little published information pertaining to the effect of salinity on L. spartum, in regard to the possibility of using it in arid zones [5,6]. Therefore, the objective of the present work was to evaluate the water status of L. spartum seedlings in the presence of NaCl.
1. Materials and methods
1.1. Plant material and growth conditions
The seeds of L. spartum were collected from the area of Aïn Maâbed in the province of Djelfa (Algeria) (2°39'E longitude, 34°50'N latitude and 934 m elevation). Seeds were pre-hydrated with de-ionised water for 12 h and germinated in vermiculite, at 28°C in an incubator, for 2 days. They were then transferred to a controlled-environment chamber with a 16h light – 8h dark cycle and air temperatures of 25 and 20 °C, respectively. The relative humidity (RH) was 60% (in day) and 80% (at night) and photosynthetically-active radiation (PAR) was 400 μmol m-2 s-1, provided by fluorescent tubes.
After 7 days, the seedlings were placed in 15 Liters containers with modified, continuously-aerated Hoagland nutrient solution : Ca(NO3)2 (2 mMole), K2HPO4 (0.5 mMole), MgSO4 (0.5 mMole), H3BO3 (25 μMole), MnSO4 (2 μMole), ZnSO4 (2 μMole), CuSO4 (0.5 μMole), (NH4)6Mo7O24 (0.5 μMole) and Fe-EDDHA [ethylendiamino-di(o-hydroxyphenylacetic) acid] (20 μMole).
The solution was replaced completely every week. After 13 days (when plants were 20 days-old).
Plants were treated with 0, 50 and 100 mM NaCl, the concentration of NaCl used in this experiment was similar to the level that can be found on Algerian saline steppes .
Transpiration, turgor potential (Ψτ) and root hydraulic conductance (Lo) were measured after 7 days of the treatments.
The hydraulic conductance (L0) of roots was measured by pressurising the roots using the Scholander chamber .
For transpiration, each pot containing one plant was covered with a plastic bag, secured around the stem base. The water transpired was estimated under controlled light from the weight loss over a 6-h period (10:00–16:00 h). The mean transpiration rate (per g fresh weight) was calculated based on the amount of transpired water and total fresh weight at the sampling time.
Turgor potential (Ψτ) was calculated as the difference between leaf water potential and osmotic potential.
1.3. Data analysis
The experiment was set up as a completely randomised design, with five replications of each treatment. Data were analysed statistically, using the SPSS 7.5 software package, by ANOVA and by Tukey´s multiple range test, to determine differences between means.
2. Results and discussion
After 30 days of treatment, all plants remained alive until the end of the experiment. The root hydraulic conductance (L0) was measured from 11 to 13 h, when transpiration was maximal. Compared with the control, root hydraulic conductivity (P<0.01) in L. spartum seedlings declined significantly with the increase of salinity (figure 1).
A significant reduction of transpiration (P<0.01) occurred in plants treated with NaCl, both sodium chloride treatments decreased this parameter, the reduction being greater at 100 mM NaCl (figure 2).
There were no significant differences (P>0.05) between the turgor potential (Ψτ) values of the control and treated plants (figure 3).
The effects of increased salinity on L0 have been widely reported and it has been suggested [2,10] that they are due to the high concentrations of Na+ and Cl- in the cytoplasm, that reduce water transport through the plasma membrane aquaporins . Our experiments showed a strong decrease of L0 in roots of L. spartum plants when NaCl was applied (figure 1).
The large reductions in root hydraulic conductance for salinized plants were related closely to the decrease in the activity or concentration of aquaporins in the root plasma membrane [6,10], this effect being due mainly to the specific toxicity of Na+and Cl- .
The transpiration rates of our plants seemed to reflect the effects observed for L0. This may be due to the possibility that lowered water potentials in the roots can trigger a signal from root to shoot. This signal might be hydrostatic  or involve organic molecules such as ABA, as previous authors have claimed .
Osmotic adjustment involves the net accumulation of solutes in cells in response to a fall in the water potential of their environment. As a consequence of this net accumulation, the cell osmotic potential is lowered and turgor pressure tends to be maintained. The fact that there were no changes in turgor in the plants, in response to the treatments of our experiment, indicates a certain level of osmotic adjustment .
In summary, salinity significantly decreased transpiration and root hydraulic conductance in L. spartum plants. However, turgor potential was not significantly changed by salinity. These results indicate the possibility of introducing this plant as a source of fodder or forage in moderate salt-affected soils which are inadequate for traditional agricultural uses.
The Algerian Ministry of Higher Education and Scientific Research are gratefully acknowledged (CNEPRU Projet code F–02820100012).
 Munns R. 2002. Comparative physiology of salt and water stress. Plant Cell Environment; 25: 239-250.
 Nedjimi B., Daoud Y. 2009.Effects of calcium chloride on growth, membrane permeability and root hydraulic conductivity in two Atriplex species grown at high (sodium chloride) salinity. Journal of Plant Nutrition; 32: 1818–1830
 Djabeur A., Kaid-Harche M., Côme D., Corbineau F. 2010. Environmental control of germination and dormancy of seeds of two cytotypes of Lygeum spartum L., a perennial grass of semi-arid and arid areas in Algeria. Ecologia Mediterranea; 36 (1): 89 – 98.
 Le Houérou H.N. 1995.Bioclimatologie et biogéographie des steppes aride du Nord de l'Afrique-Diversité biologique, développement durable et désetisation. Options Méditerranéennes. 10:1-397.
 Nedjimi B. 2009.Salt tolerance strategies of Lygeum spartum L.: A new fodder crop for Algerian saline steppes. Flora;204: 747–754
 Nedjimi B., Daoud Y., Carvajal M., Martínez-Ballesta M.C. 2010. Improvement of the adaptation of Lygeum spartum L. to salinity under the presence of calcium. Communications in Soil Science and Plant Analysis; 41(19): 2301-2317.
 Hoagland D.R., Arnon D.I. 1938. The water culture method for growing plants without soil. California Agriculture Experiment Station Circular; 347:1–39.
 Pouget M. 1973.Salinity on the quaternary glacis in Algerian calcareous soils. Bulletin de la Société Naturelle d’Afrique du Nord ; 64: 15–24.
 Jackson M.B., Davies W.J., Else M.A. 1996. Pressure-flow relationships, xylem solutes and root hydraulic conductance in flooded tomato plants. Annals of Botany; 77:17–24.
 Martinez-Ballesta M.C., Aparicio F., Pallas V., Martinez V., Carvajal M. 2003. Influence of saline stress on root hydraulic conductance and PIP expression in Arabidopsis. Journal of Plant Physiology; 160: 689–697.
 Martinez-Ballesta M.C., Silva C., Lopez-Berenguer C., Cabañero F.J., Carvajal M. 2006. Plant aquaporins: New perspectives on water and nutrient uptake in saline environment. Plant Biology; 8: 535–546.
 Martinez-Ballesta M.C., Martinez V., Carvajal M. 2004.Osmotic adjustment, water relations and gas exchange in pepper plants grown under NaCl or KCl. Environmental and Experimental Botany; 52: 161–174.
 Carvajal M., Cooke D.T., Clarkson D.T. 1996. Responses of wheat plants to nutrient deprivation may involve the regulation of water-channel function. Planta;199: 372–381.
Sibole J.V., Cabot C., Poschenrieder C., Barcelo J. 2003.Efficient leaf ion partitioning, an overriding condition for abscisic acid-controlled stomatal and leaf growth responses to NaCl salinization in two legumes. Journal ofExperimental Botany; 54: 2111–2119.