HOME JOURNALS CONTACT

International Journal of Botany

Year: 2008 | Volume: 4 | Issue: 2 | Page No.: 151-163
DOI: 10.3923/ijb.2008.151.163
Ecological Studies on the Aquatic Vegetation in North East Nile Delta, Egypt
M.E. Abu Ziada, I.A. Mashaly and M. Torky

Abstract: The present research comprises an investigation of the vegetation analysis, a quantitative assessment of the soil and water characteristics and an evaluation of the relationship between the major identified vegetation groups and the environmental attributes of the canals, drains and their wet shorelines at four governorates in North East Nile Delta, namely: Damietta, El Dakahlya, El Sharkia and Al Qaliopia. Vegetation, soil and water were sampled in 65 representative stands. The floristic categories, life span and life-forms of the recorded species were described. The soil and water characteristics were determined for each stand. The vegetation analysis was carried out using the multivariate techniques. The classification (TWINSPAN) and ordination (DCA) techniques of the stands led to recognition of four vegetation groups: group A codominated by Veronica anagallis-aquatica, Potulaca oleracea and Cynodon dactylon, group B codominated by Rumex dentatus, Phragmites australis and Cynodon dactylon, group C codominated by Phragmites australis and Echinochloa stagnina and group D codominated by Phragmites australis and Bolboschoenus glaucus. Canonical Correspondence Analysis (CCA) was applied to detect the main environmental factors influencing the vegetation groups. The electrical conductivity, calcium, sodium, potassium, magnesium, total nitrogen, chlorides and bicarbonates are the most effective environmental variables, which showed significant correlations with the first and second ordination axes. Accordingly, these soil and water variables seem to be the major ecological factors control the distribution of vegetation in the study area.

Fulltext PDF Fulltext HTML

How to cite this article
M.E. Abu Ziada, I.A. Mashaly and M. Torky, 2008. Ecological Studies on the Aquatic Vegetation in North East Nile Delta, Egypt. International Journal of Botany, 4: 151-163.

Keywords: environmental variables and Aquatic vegetation

INTRODUCTION

The irrigation and drainage systems of the Egyptian cultivated land comprise approximately 47000 km of waterways (El-Sherbeny, 2003). The canals and drains are infested with most types of aquatic weeds. The increasing spread of aquatic weeds was attributed to the deep penetration of sun-light in water, decrease of water fluctuations and less disturbed habitat was created, increasing fertilization of farm land and pesticides application lead to eutrophication of canals and drains, excess of algal growth leading to deoxygenation of water and increasing pollution from industrial centers and human activities along canals and drains cause environmental physico-chemical alteration (Seiki et al., 1991; Edwin, 1996; Khedr and El-Demerdash, 1997; Wang et al., 1997). The problems created by these plants are many such as, constituting a health hazard by providing mosquitoes larvae with an ideal breeding place, causing oxygen depletion, obstructing drainage and flow of water in irrigation canals, decreasing phytoplankton production, polluting water supplies, increasing sedimentation by trapping silt particles and causing loss of water through evapotranspiration (Idso, 1981; Zahran et al., 1998). Aquatic plants have received great attention, not only for the magnitude of problems caused by them in the management of water resources, but also for promise they hold as a new source, for such diverse uses as animal feed, compost, paper, fiber, bioenergy and above all the possibility of using them as biofilter for improving water quality and removing heavy metals (Pieterse and Murphy, 1990; Sajwan and Ornes, 1997; Rice et al., 1997; Samecka-Cyerman and Kempers, 2001; El-Sherbeny, 2003). Various ecological studies have been concerned with aquatic and canal banks weeds in the Nile Delta as example Shaltout and El-Sheikh (1991) and Shaltout et al. (1994) gave information about the vegetation of some canals and drains along Cairo-Alexandria agriculture road. Also, they evaluated the behavior of some common species distributed along canals and drains in the middle of Nile Delta. Shalaby (1995) recorded the flora of canals banks at Kafr El-Sheikh governorate. The vegetation analysis of canals, drains and lacks of northern part of Nile Delta region was studied by Al-Sodany (1998). To evaluate the relationship between the vegetation components of canals, drains and shorelines in Northeast Nile Delta and their environmental conditions, the multivariate techniques (classification and ordination) have been used.

MATERIALS AND METHODS

Sixty-five sampling stands were selected to cover the irrigation and drainage canals in the study area (Fig. 1). The sampling processes of the plants, soil and water have been carried out during the year 2005-2006. In each stand, the plant species were recorded in five plots (25 m2 each). The identification and nomenclature of the plants were following Tackholm (1974) and Boulos (1999-2005). The description and classification of life forms were according to Raunkiaer (1937). The soil samples were collected at a depth of 0-20 cm then dried, thoroughly mixed and passed through a 2 mm sieve to be ready for physical and chemical analyses. Soil texture was determined using sieve method for coarse soil and Bouyoucous hydrometer for the heavy soil samples. Moisture content, porosity and water holding capacity were determined according to Piper (1947). Organic carbon was determined using Walkly and Black rapid titration method (Black, 1979). Calcium carbonate was determined as described by Jackson (1962). Soil salinity (EC) and soil reaction (pH) were estimated in 1:5 soil-water extract using the conductivity and pH meters, respectively. Chloride was determined by titration against N/35.5 AgNO3. Sulphate was estimated gravimetrically using 5% barium chloride. Carbonate and bicarbonate were determined using 0.1 N HCl. The cations Na+, K+, Ca++, Mg++ were estimated using flame photometer as described by Allen et al. (1974).

The chemical characteristics of the water samples were determined according to the methods previously applied in the soil analysis.

Two trends of multivariate analysis were applied, namely; classification and ordination. The classification technique applied here was the two-way indicator species analysis TWINSPAN-a fortran program (Hill, 1979; Gauch, 1982). While ordination techniques applied were the Detrended Correspondence Analysis (DCA) and the Canonical Correspondence Analysis (CCA) using CANOCO-a fortran program (Ter Braak, 1987, 1988). The relationships between vegetation gradients and environmental variables can be indicated on the ordination diagram produced by Canonical Correspondence Analysis (CCA biplot), on which points represent species and arrows represent environmental variables. The angle between an arrow and each axis is a reflection of its degree of correlation with the axis. The statistical treatments applied were according to Snedecor and Cochran (1967) and Nie et al. (1975).

Fig. 1: Location map showing the selected stands (●) of the different governorates (*) in the study area

RESULTS

Floristic composition and features: The vegetation analysis of the selected stands revealed that, the total number of hydrophytic and canal bank species was 116 (Table 1). The recorded species in the different governorates were 71 in Damietta, 49 in El Dakahlyia, 44 in El Sharkia and 62 in Al Qaliopia. These species could be classified into three major groups according to their duration (life span): 67 perennials (57.76%), 5 biennials (4.31%) and 44 annuals (37.93%). Out of the perennials, sixteen species have wide ecological amplitude; they have been recorded in the four governorates. The five biennials have been recorded only in Damietta, El Sharkia and Al Qaliopia. Among the annuals, seven species have been found in all governorates and two species in three governorates. Concerning the life-forms Table 1 show that the recorded species are grouped under five types: therophytes (48 species = 41.38%), cryptophytes comprising geophytes, helophytes and hydrophytes collectively (38 species = 32.76%), hemicryptophytes (14 species = 12.07%), chamaeophytes (10 species = 8.62%) and phanerophytes (6 species = 5.17%).

Table 1: Floristic composition and distribution of the plant life in the study area
Ph = Phanerophytes, Ch = Chamaeophytes, H = Hemicryptophytes, G = Geophytes, He = Helophytes, Hy = Hydrophytes, Th = Therophytes, COSM = Cosmopolitan, PAN = Pantropical, PAL = Palaeotropical, NEO = Neotropical, ME = Mediterranean, ER-SR = Euro-Siberian, SA-SI = Saharo-Sindian, IR-TR = Irano-Turanian, S-Z = Sudano-Zambezian, Nat. = Naturalized, Cult. = Cultivated, Dam. = Damietta, Dak. = El-Dakahlyia, Sha. = El-Sharkia, Qua. = Al-Qualiopia, P = Presence and P% = Presence percentage

Table 2: The principal floristic categories of the families in the study area

Floristic analysis: The recorded plant species (116) in the study area are belonging to 90 genera and related to 39 families (Table 2). Gramineae (26 species), Compositae (14 species) and Chenopodianceae (10 species) are represented collectively by 50 species or about 43.1% of the total number of the recorded species. Cyperaceae (7 species), Polygonaceae (6 species), Amaranthaceae (5 species), Euphorbiaceae and Leguminosae (4 species each) and Convolvulaceae (3 species) comprise 25%. The remaining families (30) are either represented by two or one species. Floristically, Table 2 reveals that the most common floristic elements of Gramineae are: Pantropical (9 species), Cosmopolitan and Palaeotropical (4 species each) and Pluriregional (3 species). In compositae, the most common chorotypes are: Pluriregional (4 species) and Neotropical (3 species). The abundant floristic elements in Chenopodiaceae are Pluriregional (4 species) and Cosmopolitan (3 species). In Cyperaceae, Polygonaceae and Leguminosae, The common element is Palaeotropical (3 species each). Other families comprise different types of floristic elements, which are represented by a few numbers of species. The floristic analysis of the study area as shown in Table 2 reveals that 41 species (35.34%) are Mediterranean taxa. They are either pluriregional (25 species), Biregional (14 species) or monoregional (2 species). Also, 63 species of the recorded plants are either Cosmoplitan (17.24%), Pantropical and palaeotropical (16.38% each) or Neotropical (4.31%). The other floristic categories are poorly represented.

Fig. 2: Two Way Indicator Species Analysis (TWINSPAN) dendrogram of the 65 sampled stands based on the importance values of the 116 species

Vegetation analysis
Classification of stands:
The application of TWINSPAN classification led to the recognition of four vegetation groups (Fig. 2). The vegetational composition of these groups is presented in Table 3. Group A comprises 8 stands codominated by Veronica anagallis-aquatica, Portulaca oleracea and Cynodon dactylon. The important species in this group include Sonchus oleraceous (indicator species), Cyperus rotundus and Amaranthus lividus. Group B comprises 19 stands codominated by Rumex dentantus, which also identified as indicator species, Phragmites australis and Cynodon dactylon. The important species in this group comprise Malva parviflora, Sonchus oleraceus, Echhornia crassipes and Echinochloa stangnina. Other indicator species are Plantago major, Chenopodium album and Bidens pilosa. Group C includes 33 stands codominated by Pharagmites australis and Echinochloa stagnina. The most common species in this group are: Myriophyllum spicatum, Cynodon dactylon, Cyperus alopecuroides, Nymphaea lotus (indicator species), Ludwigia stolonifera and Ipomoea carnea. Group D includes 5 stands codominated by Phragmites australis and Bolboschoenus glaucus. The most important species are Paspalidium geminatum, Cynanchum acutum, Leptochloa fusca, Panicum repens and Atriplex portulacoides. No indicator species have been identified in this group.

Table 3:
Mean value and coefficient of variation (value between brackets) of the importance values of indicator and preferential plants in the different vegetation groups resulting from TWINSPAN classification in the study area

Ordination of stands: The ordination of the surveyed stands given by Detrended Correspondence Analysis (DCA) is shown in Fig. 3. It is obvious that, the vegetation groups obtained by TWINSPAN classification are distinguishable and having a clear pattern of segregation on the ordination planes. Group A is separated at the right side of the DCA diagram, while group B is separated at the middle position of the DCA diagram. On the other hand, Group C is segregated at the lower left side. And Group D at the upper left side of the DCA diagram.

Variations in soil variables: The soil variables of the four groups of stands which derived from TWINSPAN classification are shown in Table 4, it is notable that most of the soil variables showed a little variation between the different groups of stands. The soils of the four groups have coarse sandy texture with sand fraction more than 80%. The fine fractions (silt and clay) were relatively high in group B than in the other groups. The highest mean value of water holding capacity was attained in group A (56.13%). However, the lowest mean value in group D (47.24%). The mean values of soil pore spaces are obviously comparable at all groups. The percentages of calcium carbonate content are high in groups D and B as compared with the A and C groups. Organic carbon contents are obviously comparable in all groups. The pH values indicate that the soil reaction is slightly alkaline in all groups. It is clear that, the mean values of electrical conductivity, chloride, bicarbonate, total nitrogen content and concentration of extractable cations: Na+, K+, Ca++ and Mg++ are obviously high in group D and low in group A. The phosphate and total phosphorus contents are highly represented in group B.

Table 4: Mean value and standard error (±) of the different soil variables in the stands representing the different vegetation groups obtained by TWINSPAN classification in the study area

Fig. 3: Detrended Correspondence Analysis (DCA) ordination of the 65 stands

Variation in water variables: Table 5 shows the means of water variables of the four vegetation groups. It is obvious that the water reaction is weakly alkaline with pH values ranged between 7.98 in group B and 8.68 in group D. Also, it has been found that the highest mean values of electrical conductivity, dissolved oxygen, chlorides, sulphates, total nitrogen, organic carbon, sodium, potassium, calcium and magnesium are attained in group D. On the other hand, the most mean values of the previous variables are attained in group B except organic carbon, chloride, total nitrogen, calcium and magnesium in group A. The total phosphorous in water reached the highest concentration in group C and the lowest concentration in group B.

Table 5: Mean value and standard error (±) of the different water variables in the stands representing the different vegetation groups obtained by TWINSPAN classification in the study area

Fig. 4:
Canonical Correspondence Analysis (CCA) ordination diagram with hydrosoil variables represented by arrows. The indicator and preferential species are abbreviated to the first three letters of each of the genus and species

Relation between vegetation and environment: The correlation between vegetation and environment is indicated on the ordination diagram produced by Canonical Correspondence Analysis (CCA) of the biplot of species-environment as shown in Fig. 4 and 5 for the soil and water, respectively. It is notable that, electrical conductivity, the percentages of calcium, sodium, potassium, magnesium, total nitrogen, chlorides, bicarbonates, calcium carbonates, sulphate, organic carbon, sand, clay and silt are effective soil variables which show relatively high significant correlations with the first and second axis of CCA ordination diagram. The codominant species of the most identified groups, Veronica anagllis-aquatica and Rumex dentatus as well as the important species Cyperus rotundus, Amaranthus lividus, Malva parviflora, Chenopodium album, Myriophullum spicatum (indicator species) and Eichhornia crassipes are separated at the upper right side of CCA biplot diagram. These species showed a close relationship with sodium, total nitrogen, bicarbonate, calcium carbonate, organic carbon and porosity. While the codominant species Bolboschoenus glaucus as well as the indicator species Plantago major, Bidens pilosa and Ipomoea carnea are segregated at the lower right side of the CCA-bipilot diagram. These species exhibit a clear relationship with electrical conductivity, calcium, potassium, magnesium, chlorides and sulphates. Cynodon dactylon as a codominant species in group A and B and as an important species in group C and Echinochloa stagnina as a codominant species in group C and as an important species in group B are separated at the upper left side of the CCA-biplot diagram. These species showed a clear relationship with silt and water holding capacity. Cyperus alopecuroides as an important species in group C is separated at the lower side of the CCA-biplot diagram and showed a distinct relationship with soil reaction.

Fig. 5:
Canonical Correspondence Analysis (CCA) ordination diagram with water variables represented by arrows. The indicator and preferential species are abbreviated to the first three letters of each of the genus and species

It is obvious that, electrical conductivity, potassium, sodium, bicarbonate, chlorides, magnesium, total nitrogen, sulphates, calcium, pH, carbonate and dissolved oxygen are the most important water variables which exhibited a relatively high significant correlation with the first and second axes of the CCA-biplot diagram (Fig. 5). The codominant Veronica anagallis-aquatica of group A and Rumex dentatus of group B, the important species Amaranthus lividus of group A, Malva parviflora and Echhornia crassipes of group B, Myriophyllum spicatum and Nymphaea lotus of group C, Paspalidium geminatum, Cynanchum acutum and Atriplex portulacoides of group D, also the indicator species Chenopodium album of group B are collectively segregated at the upper right side of the CCA-biplot diagram. These species show a close relation with the high contents of K+, Na+, HCO3, Cl, Mg2+, total N and Ca2+. However, Portulaca oleracea, Phragmites australis and Bolboschoenus glaucus are in groups A, B, C and D, respectively. And the indicator species Sonchus oleraceus in group A, Plantago major and Bidens pilosa in group B and Ipomoea carnea in group C are separated at the lower right side of CCA-biplot and showed a distinct relationship with EC, SO4– –, pH, dissolved O2 and CO3– –. On the other hand, a few species: Cynodon dactylon, Solanum nigrum, Echinochloa stagnina and Sorghum virgatum are obviously segregated at the upper left side, while Cyperus alopecuroides alone in the lower left side.

DISCUSSION

The present study reveals that the eastern section of the Nile Dalta, which comprises Damietta, El Dakahlyia, El Sharkia and Al Qaliopia governorates, is rich in its flora on specific generic and families levels. The total number of macrohydrophytes of the irrigations and drainage canals and weeds of its shores is 116 species belonging to ninety genera grouped under thirty-nine families. Graminae, Compositae, Chenopodiaceae, Cyperaceae, Polygonaceae, Amaranthaceae, Euphorbiaceae, Leguminosae and Convolvulaceae constitute the major part of its floristic composition. The cause of interspecific association are varied, but are usually related to similar response of species to the environmental variables. The degree of water availability and the sandy texture of the soil activated the therophytes to maintain predominance over other life forms. Cryptophytes are the second active life form. This could be emphasized through consideration of both its growth habit and the nature of the soil of its habitat. This trend is similar to spectra reported by Mashaly (1987). From the floristic point of view, about 35.34% of the total number of the recorded species are Mediterranean taxa. The other floristic elements are Cosmopolitan, Palaeotropical, Pantropical, Neotropical, Irano-Turanian, Saharo-Sindian, Euro-Seberian and Sudano-Zambesion are represented by varying number of species, reflection their different capability to penetrate the region. Similar investigations have been described by El Ameir (2005). The application of TWINSPAN technique has proved useful in classifying stands, on objective basis, into four vegetational groups, although these groups are not absolutely distinct because the member of some groups are linked together by having one of the dominant species in common. The recognized vegetational groups named after their codominant species as follows: Veronica anagallis-aquatica, Portulaca oleracea and Cynodon dactylon (group A), Rumex dentatus, Phragmites australis and Cynodon dactylon (group B), Phragmites australis and Echinochloa stagnina (group C), Phragmites australis and Bolboschoenus glaucus (group D). Comparable groups have been described in the Nile Delta by El-Sheikh (1989), Al-Sodany (1992), Khedr and El Demerdash (1997) and Mashaly et al. (2001). The CCA-biplot ordination diagrams indicated that the effective soil and water variables which significantly correlated with the abundance and distribution of vegetation groups in the study area are numerous such as Salinity (EC), soil fractions (sand, silt and clay), pH value, soil fertility (organic carbon, phosphorus and nitrogen contents), dissolved oxygen, calcium carbonate, soluble anions (chlorides and sulphates) and extractable cations (sodium, potassium, calcium and magnesium). Several studies confirmed this trend such as those of El-Shiekh (1989) and Shaltout and El-Sheikh (1991). Veronica anagallis-aquatica as codominant in group A and Rumex dentatus as codominant in group B showed a close relationship with sodium, bicarbonate, total nitrogen, calcium carbonate, organic carbon and porosity. However, Cynodon dactylon as codominant in group A and B and Echinochloa stagnina as codominant in group C exhibited a close relationship with silt and water holding capacity. Phragmites australis as codominant in groups B, C and D, Bolboschoenus glaucus as codominant in group D and Portulaca oleracea as codominant in group A showed a close relationship with electrical conductivity, sulphates, pH value, chlorides, dissolved oxygen. It may be concluded that the most important soil variables which correlated with the distribution and abundance of the aquatic and canal banks weeds in the Nile Delta are: soil salinity (EC), sodium, calcium, potassium, chloride, soil fertility (organic carbon, nitrogen and phosphorus contents) and fine fraction (clay). The most important water variables are salinity, potassium, sodium, bicarbonate, chloride, nitrogen content and pH.

REFERENCES

  • Allen, S.E., 1974. Chemical Analysis of Ecological Materials. Blackwell Scientific Publications, London, UK., Pages: 565
    Direct Link    


  • Al-Sodany, Y.M., 1992. Vegetation analysis of Northern part of Nile Delta region. M.Sc. Thesis, Tanta University, Egypt.


  • Al-Sodany, Y.M., 1998. Vegetation analysis of canals, drains and lakes of Northern part of Nile Delta region. Ph.D. Thesis, Tanta University, Tanta.


  • Black, C.A., 1979. Methods of soil analysis. Am. Soc. Agron., 2: 771-1572.


  • Boulos, L., 1999-2005. Flora of Egypt. Vol. 1-4, Al-Hadara Publication, Cairo, Egypt


  • Edwin, D.O., 1996. Control of water pollution from agriculture-irrigation and drainage. FAO, UN, Rome, pp: 55.


  • El Ameir, Y.A., 2005. Eco-palynological studies of the plant life of the River Nile in Egypt. M.Sc. Thesis, Mansoura University, Egypt.


  • El-Sheikh, M.A., 1989. A study of the vegetation environmental relationships in the canals banks of middle Delta region. M.Sc. Thesis, Tanta University, Egypt.


  • El-Sherbeny, G.A., 2003. Ecological studies on the relationship between some plants and environmental pollution. M.Sc. Thesis, Mansoura University, Egypt.


  • Gauch, H.G., 1982. Multivariate Analysis in Community Ecology (Cambridge Studies in Ecology). 1st Edn., Cambridge University Press, Cambridge


  • Hill, M.O., 1979. TWINSPAN: A FORTRAN Program for Arranging Multivariate Data in an Ordered Two Way Table by Classification of Individual and Attributes Ecology and Systematics. Cornell University, Ithaca, NY., USA., Pages: 90


  • Idso, S.B., 1981. Relative rates of evaporative water losses from open and vegetation covered water bodies. J. Am. Water Resour. Assoc., 17: 46-48.
    CrossRef    Direct Link    


  • Jackson, M.L., 1962. Soil Chemical Analysis. 1st Edn., Prentice Hall, New Jersery, USA., Pages: 498


  • Khedr, A.H.A. and M.A. El-Demerdash, 1997. Distribution of aquatic plants in relation to environmental factors in the Nile Delta. Aquat. Bot., 56: 75-86.
    CrossRef    Direct Link    


  • Mashaly, I.A., 1987. Ecological and floristic studies of dakahlia-damietta region. Ph.D. Thesis, Mansoura University, Egypt.


  • Mashaly, I.A., E.F. El Halawany and G. Omar, 2001. Vegetation analysis along irrigation and drain canals in Damietta Province, Eygpt. J. Biological Sci., 1: 1183-1189.
    CrossRef    Direct Link    


  • Nie, H., C. Hadlaittull, J.G. Jenkins, K. Steinbrenner and H.D. Bent, 1975. Statistical Package for the Social Seciences. 2nd Edn., McGraw-Hill, New York, USA


  • Pieterse, A.H. and K.J. Murphy, 1990. Aquatic Weeds. The Ecology and Management of Nuisance Aquatic Vegetation. 1st Edn., Oxford University Press, New York, USA., pp: 593


  • Piper, C.S., 1947. Soil and Plant Analysis. 1st Ed. Interscience Publishers Inc., New York, USA
    Direct Link    


  • Raunkiaer, C., 1937. Plant Life Forms. 1st Edn., The Clarendon Press, Oxford
    Direct Link    


  • Rice, P.J., T.A. Anderson and J.R. Coats, 1997. Evaluation of the Use of Vegetation for Reducing the Environmental Impact of Deicing Agents. In: Phytoremediation Soil and Water Contaminants, Kruger, E.L., T.A. Anderson and J.R. Coasts (Eds.). American Chemical Society, Washington, DC., USA., ISBN: 08-412-35031, pp: 162-176
    Direct Link    


  • Sajwan, K.S. and W.H. Ornes, 1997. Potential of mosquito fern (Azolla caroliniana willd.) plants as a biofilter for cadmium removal from wastewater. Emerg. Tech. Hazardous Waste Manage., 7: 167-177.
    CrossRef    


  • Samecka-Cyerman, A. and A.J. Kempers, 2001. Bioindication of heavy metals with aquatic macrophytes: The case of a stream polluted with power plant sewages in Poland. J. Toxicol. Enviorn. Health Part A., 62: 57-67.
    PubMed    Direct Link    


  • Seiki, T., E. Date and H. Izawa, 1991. Eutrophication in Hiroshima Bay. Mar. Pollut. Bull., 23: 95-99.
    CrossRef    Direct Link    


  • Shalaby, M.A., 1995. Studies on plant life at Kafr El Sheikh province, Egypt. M.Sc. Thesis, Kafr El Sheikh, Tanta University, Egypt.


  • Shaltout, K.H. and M.A. El-Sheikh, 1991. Gradient analysis of canal vegetation in Nile delta region. Feddes Repertorium, 102: 639-645.
    CrossRef    Direct Link    


  • Shaltout, K.H., A.S. El-Din and M.A. El-Sheikh, 1994. Species richness and phenology of vegetation along irrigation canals and drains in the Nile Delta, Egypt. Vegetatio, 122: 35-43.
    CrossRef    Direct Link    


  • Snedecor, G.W. and W.G. Cochran, 1967. Statistical Methods. 6th Edn., Oxford and IBH Publishing Co. Pvt. Ltd., New Delhi, India, Pages: 593
    Direct Link    


  • Tackholm, V., 1974. Student's Flora of Egypt. 2nd Edn., Cairo University, Egypt


  • Ter Braak, C.J.F., 1987. The analysis of vegetation-environment relationships by canonical correspondence analysis. Adv. Veg. Sci., 8: 69-77.
    CrossRef    Direct Link    


  • Ter Braak, C.J., 1988. CANOCA- a FORTRAN program for canonical community ordination by partial detrended correspondence analysis, principal component analysis and redundancy analysis (Version 2.1). Agric. Math. Group Wageninigen, Netherlands.


  • Wang, W., J.W. Gorsuch and J.S. Hughes, 1997. Plants for Environmental Studies. 1st Edn., CRC Press, New York, USA., ISBN: 1566700280, pp: 563


  • Zahran, M.A., M.S. Serag and S. Bjork, 1998. On the ecology of aquatic plants of the irrigation and drainage canals of Damietta, Egypt. J. Environ. Sci., 16: 77-91.

  • © Science Alert. All Rights Reserved