IMPACTS OF WATER CHARACTERISTICS CHANGES ON THE DISTRIBUTION OF WATER PLANTS IN LAKE BURULLUS, EGYPT دراسة تاثير التغيرات في خصائص المياة علي انتشارالنباتات المائية في بحيرة البرلس في مصر

Document Type : Original Article

Abstract

This study was conducted to evaluate the impacts of water characteristics changes on the growth and distribution of water plants present in lake Burullus protected area. Najas armata, Ceratophyllum demersum, Pistia stratiotes and Myriophyllum spicatum growth rate were declined and completely disappeared from the eastern part of the lake and became very rare across the lake as a results of clearing and shallwing process of this part of the lake which leads to increasing in water salinity, depth, dissolved oxygen and decreasing in biological oxygen demand with changeable pH values. Water depth, TDS, salinity, ammonium and phosphate were the key factors that control the growth and distribution of aquatic macrophytes in lake burrullus.
ملخص البحث:
تهدف هذه الدراسة الي تقييم تأثير التغيرات في خصائص المياه علي النمو والانتشار للنباتات المائية في بحيرة البرلس حيث اوضحت النتائج ان زيادة العمق والتطهير في الجانب الشرقي لبحيرة البرلس ادى الي اختفاء بعض الانواع النباتية مثل ( نبات الحريشة  Najas armata, نخشوش الحوت  Ceratophyllum demersum خس الماء  Pistia stratiotes , Myriophyllum spicatum وندرة تواجدها في بقية اجزاء البحيرة و هناک انواع قل تواجدها.   من الجانب الشرقي للبحيرة
واوضحت النتايج ان الملوحة ارتفعت ارتفاع ملحوظ في البحيرة وخاصة الجانب الشرقي  وارتفاع نسبي في بقية اجزاء البحيرة مما ادي الي اختفاء تلک النباتات وندرتها في البحيرة وتغير الترکيب الفلوري للبحيرة . 

Keywords

Main Subjects


 

 

Impacts of water characteristics changes on the distribution of water plants in lake Burullus, Egypt

Elsayed M. A. Nafea

Aquatic Environment Department, Faculty of Fish Resources, Suez University, Suez, Egypt

E-mail: elsayed.nafea@suezuniv.edu.eg

ABSTRACT:

This study was conducted to evaluate the impacts of water characteristics changes on the growth and distribution of water plants present in lake Burullus protected area. Najas armata, Ceratophyllum demersum, Pistia stratiotes and Myriophyllum spicatum growth rate were declined and completely disappeared from the eastern part of the lake and became very rare across the lake as a results of clearing and shallwing process of this part of the lake which leads to increasing in water salinity, depth, dissolved oxygen and decreasing in biological oxygen demand with changeable pH values. Water depth, TDS, salinity, ammonium and phosphate were the key factors that control the growth and distribution of aquatic macrophytes in lake burrullus.

Keywards : Lake Burullus, aquatic plants , water characteristics, salinty , water depth  ,  nutreints


INTRODUCTION

Egypt has five lakes or lagoons in the northern coast. These lakes are: Bardawil, Manzala, Burullus, Edku, and Mariut, and considered the most important sites in the Egyptian Mediterranean coastal water. Lake Burullus is located between the two main Egyptian Delta Rosetta and Damietta branches and is a Ramsar site which declared as a protected area since 1998. Because of the presence of habitat variety of Lake Burullus, a variety of biodiversity inhabits the lake.

In the recent years, the amounts of agricultural and sewage wastewater entering the lake through several drains at the southern part changed their physico-chemical and limnological features and decreasing the levels of salinity across the Lake, which caused shifting in their biodiversity. The Egyptian Ministry of Environmental Affairs and Egyptian Environmental Affairs Agency updated the National Biodiversity, Strategy and Action Plan (NBSAP). One of the important goals of this strategy is to minimize the rate of lake degradation and improve the water quality. The major concern in Lake Burullus toward achieving the National Biodiversity Strategy is to decreasing the anthropogenic activities and land runoffs by restoring salinity level by clearing and shallower the eastern part of the lake to make water current and increasing salinity, the mechanical removal of reeds form 50 cm under water surface causing recycling of water across the lake, maintain the sea outlet (El-Boughaz) open and clear to ease seawater and fish enter the lake.

Water quality and consequent Macrophytes growth are continuously affected by physical, chemical and biological variables including nutrient availability, water flow, turbulence, water salinity, temperature, depth, sediments characteristics and epiphytic growth (Duarte et al., 1994; Wetzel, 2001). The abundance and biomass production of several plant species in according to physico-chemical variation were observed by Lacoul&Freedman, (2006) and Rolon & Maltchik (2006). Such studies provide the opportunity for species richness assessment in relation to environment in particular the factors that determine aquatic plant diversity (Murphy et al., 2003).

Biotic factor such as competition and herbivores can also be considered as one of significant factors that affect the abundance and distribution of macrophytes (Titus & Stephen, 1983; Rasch et al., 2004). On the other hand macrophytes communities have their impacts on the aquatic habitats by influences the ecosystem functions through modifying , flow pattern (Sand-Jensen & Pedersen, 1999), sediment process (Clarke & Wharton, 2001), oxygen dynamics (Uehlinger et al., 2000) and nutrients cycles (Wilcock et al., 2004). The extent to which macrophytes could affect the aquatic system is by their interaction in physical, chemical and biological process depending mainly on; biomass density, composition, and species morphology (Sand-Jensen & Mebus, 1996). The understanding of the interaction between aquatic environment and macrophytes is essential if the macrophytes community includes a rare or highly valued (environmentally and/or economically) species, for example, Najas aramata, Pistia stratiotes and Lemna gibba as they are vital for fish feeding and water treatment, Younis & Nafea (2014), Potamogeton pectinatus is important tool for water purification from heavy metals (Nafea &Zyada, 2015).  Najas  armata can help to retain soil moisture for short periods before it rots down, so, ironically, it helps promoting the early growth of grass (Belal et al., 2009). Natural and anthropogenic impacts put macrophytes under pressure and reduce in many ways their growth and productivity in shallow water areas in Lake Burullus.

The water plants of Lake Burullus have been investigated by Younis & Nafea (2012) and Shaltout & Khalil (2005) and Al-Sodany (1992). The number of the recorded aquatic plants in Lake Burullus, as estimated by Nafea (2005) was 26 species: 4 submerged species, 8 floating species, and 14 emerged species. The salinity and water depth of water of Lake Burullus appears to be the most important factor affecting the distribution and abundance of hydrophytes communities in the lake. Younis & Nafea (2012) stated that water plants in Lake Burullus can grouped into three categories, some are restricted to the more saline water e.g. Ruppia maritima, while others occur more abundantly in freshwater and slightly brackish water, e.g. Myriophylum spicatum, Pistia stratiotes and Najas armata and others have wide salinity tolerance e.g. Potamogeton pectinatus, Phragmites australis, and Typha domingenssis. High drainage water from agricultural and aquaculture projects at south of the lake caused reduction of many species to one or two populations with few individuals on the shores of Lake Burullus (Khedr & Lovett-Doust, 2000). Freshwater origin species Myriophylum spicatum was recorded in front of Brimbal Canal and around the outlets of southern drains where the water salinity was relatively low. (Younis &Nafea, 2012).

This work aimed mainly to evaluate the water variables that positively and negatively impact the growth and distribution of water plants in Lake Burullus.

MATERIALS AND METHODS
The study area

Lake Burullus is one of the delta lakes located between Rosetta and Damietta branches and between longitude 30° 30` and 31° 10`E, and latitude 31° 21` and 31° 35` N. It is elongated in shape and connected to the sea through a narrow (50 m wide) opening called Boughaz Al-Burullus. This lake is a Ramsar site and has been declared as a protected area since 1998. Fig (1).

 

Fig (1) Map represent the lake burullus

 

Table (1): The studied sites in lake Burullus protected area

no

Section

Location description

position

a-

Eastern section

 

 

1

El-Boughaz area

Boughaz bridge connect the Medit. and the lake Burullus

N=31º 34´

E=30º 59´

2

Emade

Beside the international road receive domestic waste water

N=31º 33´

E=30º 59´

3

Mouth of  drain El-Burullus

Mixed   Drainage water of El-Burullus drain

N=31º  33´

E=31º  04´

4

Mouth of El-Gharbia drain

Mixed  Drainage water of  El-Gharbia drain

N= 31º  31´

E=31º  04´

5

Mishkhilah

Mixed  Drainage water of Terra drain

N=31º 30´

E=30º 57´

b-

Middle section

 

 

6

shallow

Area covered with hydrophytes

N=31º 32´

E=30º 58

7

El-Kom El-Akhder

Mixed Drainage water of  Drain 8 .

N=31º 24´

E=30º 43´

8

El-Zanka

Near El-Zanka island brackish water at lake center.

N=31º 32´

E=30º 47´

9

Kodaa

Mid. northern section area covered with hydrophytes.

N=31º 36 ´

E=31º 01´

10

El-Maksabah

Mixed drainage waterof El-Maksabah village

N=31º 29´

E=30º 45

c-

Western section

 

 

11

Deshemi

Near Deshemi islands area covered with hydrophytes

N=31º 20´

E=30º 37

12

El-Tawilla

Near El-Tawilla island at the mid. of the lake

N=31º 26´

E=30º 44´

13

Abo-Amer

Area covered with hydrophytes near Abo-Amer island

N=31º 25´

E=30º 40´

14

Sakkarana

Near Sakkarana village and covered with hydrophytes.

N=31º 24´

E=30º 37´ 

15

Brimbal canal

mixed fresh water form Brimbal canal.

N=31º 24 ´  E=30º 35´

 


FIELD SURVEY AND FLORISTIC COMPOSITION

15 sampling sites were set up across the lake as; five sites on the eastern section, five in the middle and five in the western one. The vegetation survey was carried out in three trips from March 2018 to April 2019, where most of water plants were sufficiently developed. Sites were selected randomly representing all most aquatic habitats in the lake. The location of each site was determined by a Garman GPS. Plant species were identified after Boulus (1999, 2000, 2001, 2005 and 2009).

All aquatic species were listed and the cover percentage for each species was estimated. The cover of macrophytes species was calculated using one square meter quadrate. (Murphy et al., 1981). The results were represented by tables and figures. In all the selected sites detailed studies including floristic composition and physico- chemical properties of water were carried out.

PHYSICO - CHEMICAL  VARIABLES OF WATER

The pH values and temperatures (°C) were determined using Misuraline model ML 1010. Depth (m) and transparency were measured using a Secchi disc. Total dissolved salts (mg l-1) and conductivity (μS/cm-1) were measured with an electronic TDS meter (HANNA, model HI 99300). Dissolved oxygen (mg/l-1 and saturation percentage) was measured using the model HI 9146 by HANNA. Soluble reactive phosphate was determined by the molybdate blue method (Allen et al., 1986). Nitrate was determined by means of chromic acid method (APHA, 1985). Sodium salicylate is added to an aliquot of filtered water samples. Nitrite was determined by the modified Griess-Ilosvary method (APHA, 1985). Ammonia was determined by Nessler’s method, in which an alkaline solution of mercury chloride is used as a reagent for the colourimetric determination (APHA, 1985). Sulphate was determined by the turbidimetric method using NaCl/HCl - glycerol-ethanol reagent and barium chloride crystals (Rossum and Villarruz, 1961).

RESULTS AND DISCUSSION

The obtained results revealed that 28 water plant species belonging to 21 genera and 17 families were recorded in the Lake Burullus during the period from March 2018 to April 2019 from which; 7 submerged, 8 floating and 13 emerged species.

It was observed that the clearing and shallower process in the eastern section of   Lake Burullus leads to an  increase of water characteristics as ; depth, pH , salinity, aeration, Dissolve Oxygen percentage from the northern to southern part of the lake, but the western and middle section  still shallow with dense growth of macrophytes and relatively low  salinity. Table,(1).

The freshwater origin species Ceratophyllum demersum, Najas armata, Myriophyllum  spicatum and Pistia stratiotes prefer more sheltered areas at the southern and western margins of the lake  around the outlets of drains where the water salinity is relatively low.


 

Table (2): Floristic list and mean cover % of aquatic  Macrophytes in lake Burullus    

 E=Eastern section      M=Middle  section       W= Western section

no

species

cover % Nafea (2005) before clearing and shallower

cover % in 2019

after clearing and shallower

a-

Submerged species

E

M

W

E

M

W

1

Ceratophyllum demersum

95

90

85

5

85

95

2

Ceratophyllum submersum

70

75

65

0

20

35

3

Potamogeton pectinatus      

95

98

95

10

75

95

4

Potamogeton crispus             

60

70

75

0

35

35

5

Myriophylum spicatum

35

30

65

0

35

75

6

Najas armata 

55

65

75

0

30

45

7

Najas minor

30

25

55

0

15

20

b-

Floating species

 

 

 

 

 

 

1

Eichhornia crassipes

35

40

65

0

55

65

2

Lemna gibba

45

65

60

5

65

70

3

Lemna minor

30

35

30

5

35

30

4

Nymphaea caerulea

10

5

35

0

15

15

5

Pistia stratiotes

15

5

20

0

3

2

6

Marsilea aegyptiaca  

15

10

30

0

15

35

7

Azolla filiculoides

10

10

15

1

15

25

8

Spirodela polyrrhiza

15

10

15

0

15

10

c-

Emerged species

 

 

 

 

 

 

1

Phragmites australis

90

95

75

10

75

85

2

Typha domingensis

85

75

50

15

78

90

3

Panicum repens

50

45

55

5

65

70

4

Ludwigia stolonifera

55

65

65

5

65

90

5

Persicaria salicifolia

50

35

55

4

45

55

6

Persicaria senegalensis

15

55

65

0

35

45

7

Saccharum spontaneum

35

45

40

0

25

35

8

Echinochloa stagnina          

30

35

30

5

10

15

9

Scirpus maritimus

35

35

40

3

25

25

10

Scirpus littoralis

25

25

30

5

25

65

11

Juncus rigidus

55

45

30

5

35

55

12

Juncus subulatus

55

20

15

8

35

45

13

Cyperus articulatus

20

5

5

5

35

35


 

 

Some of aquatic plants were disappeared and not recorded in the eastern section and became very rare  in the  middle and western section after the process of clearing the Boughaz and eastern section due to the increasing salinity level, lake depth and decreasing the nutreints sources and the eastern section became clear and seemed to be open water with no hydrophytes except near the shore and around the ilands , This agreed with William et al. (1974), who stated that increase of salinity reduced the growth of macrophytes where it is toxic to most of them as, Pistia stratiotes, Eichhornia crassipes, Myriopyllum specatum, Najas aramata and Azolla  filiculoides. Younis and Nafea (2012), documented that freshwater origin species Myriophylum spicatum, Ceratophyllum demersum, Najas armata, and Panicum repens were recorded in front of Brimbal Canal and around the outlets of southern drains where the water salinity was relatively low and they prefer more sheltered areas at the southern and western margins of the lake Table (1).  Stoler et al. (2018) documented that salts from roads and turbidity have negative impacts on the productivity and growth rate of Ceratophyllum demersum and Myriophyllum spicatum species and have a positive impacts on the growth and productivity of other water plants as Lemna gibba. Hadad et al. (2017) confirmed that floating plants

 

 

(Pistia sratiotes and Eichhornia crassipes) cannot tolerate the high range of salinity (2,000; 3,000; 4,000; 6,000; and 8,000 mg/ L and high range of pH (8, 9, 10 and 11) while emerged macrophytes   (Typha sp. and Phragmites australis) can tolerate the high ranges of pH and salinity.

Najas armata is more frequent than Najas minor and dominates the middle area of Lake Burrullus where it is present in 6 stations (45 % cover) and Najas minor was rare as it is grow only in four sites (20% cover).The fishermen collect and use the Najas spp. as a mixture: they call Najas armata Horisha Abu Shouk (spiny) and Najas minor-Horisha Naema (smooth) self-communication with local fishermen. The maximum growth rate of Najas armata was on the middle and western sections of the lake where salinity level is low and the water is not deep, in contrast the Najas armata and other Macrophytes became very rare in  the eastern section due to it became deep and highly saline water (Stelzer et al., 2005; Torn et al., 2006). Also low water velocity (Birket et al., 2007) and low nutrients input (Horppila and Nurminer, 2005). Myriophylum spicatum is the most frequent species occupying 3 sites in the western section; it forms pure stands in many areas in western parts of the lake and not present in eastern section.


 

 

 

 

 

 

 

 

Table (3): Physico- chemical properties of Lake Burullus water in the studied sites before clearing and shallower after Nafea 2005.

Parameters

Eastern section

 

Middle section

 

Western section

 

1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

Depth cm

190

180

175

165

140

56

145

115

130

189

120

190

215

225

195

Temperature C

33

32

32

31

32

28

31

32

31

32

29

32

31

32

31

Transparency cm

25

43

45

55

60

20

55

60

70

55

65

50

72

45

55

pH

6.6

8.4

8.7

8.6

7.5

8.5

8.6

8.4

6.3

7.6

7.8

9.5

9.1

8.9

8.7

EC g/ l

9.6

8.6

8.4

5.7

8.2

1.0

3.2

3.7

3.1

3.2

1.0

2.4

1.1

1.2

1.7

TDS  g/ l

2.5

2.4.

2.2

1.4

2.3

0.7

1.6

1.4

1.7

1.5

0.4

1.1

0.6

0.7

1.0

DO mg/ l

5.6

6.5

5.7

7.6

6.9

2.5

3.6

5.7

3.6

5.3

6.4

8.4

7.5

8.6

8.3

BOD  mg/ l

3.7

3.8

3.8

2.9

2.9

6.3

7.9

4.9

5.3

4.3

2.2

6.6

3.4

2.3

1.8

PO4  µg/ l

1.9

3.2

4.3

2.2

1.5

1.4

2.3

2.4

1.8

1.4

11.5

19

11

17

16

NH4  µg/ l

1.8

1.4

1.9

2.6

1.4

1.2

3.1

1.4

1.4

1.3

1.2

1.3

1.4

1.2

1.4

NO3  µg/ l

1.2

1.4

2.3

1.7

1.3

1.6

1.7

2.4

2.4

3.2

13.4

10.0

8.9

7.4

8.1

NO2  µg/ l

1.7

0.8

1.2

1.2

1.1

0.5

2.4

1.6

1.9

2.8

8.4

11.3

8

8

7.4

SiO2  µg/ l

21

31

34

37

27

24

36

43

29

26

34

37

31

21

23

 

Table (4): Physico- chemical properties of Lake Burullus water in the studied sites in the lake 2019.

Parameters

Eastern section

 

Middle section

 

Western section

 

1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

Depth cm

210

180

230

180

165

60

140

120

125

190

190

230

210

230

225

Temperature C

30

33

32

31

32

28

31

32

31

32

29

32

31

32

31

Transparency cm

73

100

65

70

95

20

55

60

70

55

65

50

72

45

55

pH

7.3

8.1

8.3

7.6

7.9

7.5

8.6

8.4

6.3

8.9

7.8

9.3

9.1

8.9

8.7

EC g/ l

25

23

21

16

12

1.0

3.2

3.5

4.1

4.2

1.1

2.6

1.2

1.1

1.4

TDS  g/ l

2.3

17.6

10

8

6.4

1.2

1.9

1.4

1.8

1.9

0.6

1.0

1.0

0.9

1.0

DO mg/ l

5.6

9.5

6.4

7.2

8.1

2.3

3.4

5.1

4.6

4.3

6.8

9.4

7.8

9.1

7.6

BOD  mg/ l

2.7

2.3

2.8

2.6

1.9

6.3

6.9

4.7

5.9

6.3

1.2

5.6

3.2

2.4

1.9

PO4  µg/ l

2.7

3.2

4.3

2.2

1.5

1.4

2.3

2.4

1.7

1.8

16.5

21

13

15

12

NH4  µg/ l

2.1

1.4

1.5

2.3

1.7

1.1

2.3

1.5

1.7

1.3

12

21.5

13

12

14

NO3  µg/ l

1.1

1.3

2.1

1.4

1.2

1.3

1.9

2.1

2.3

2.1

11.3

9.0

8.7

8.4

9.1

NO2  µg/ l

1.2

0.9

1.1

1.3

1.2

0.4

2.1

1.4

1.7

1.8

9.0

13.3

10

9.4

7.9

SiO2  µg/ l

19

21

26

30

24

20

43

22

25

31

34

32.4

22

19

23

 


The temporal and spatial variations in water depth were clear and highly related to Lake water level. High depth was recorded (230 cm) in western part. The shallow sites were in the middle parts. Water temperature did not varied significantly due to location. In general, lower temperature was recorded in sites located at western of Burrullus which characterized by shallow water and occupied by dense Macrophytes growth, (30 and 31 °C,) respectively). Maximum mean value of water temperature (33 °C) was recorded in eastern section, while the minimum (30 C), in middle section.  Water was alkaline, where the mean pH values were 7.3 and 7.5, respectively. The most alkaline sites in burullus were western part; recording pH values of 9.3 in most sites, pH values were higher in July than in other sampling months.

Total dissolved solids ranged between 1.2 in western and 17.6 g/l, in eastern. There is no certain pattern of spatial variation, but in general it shows reverse variation from pH. Total dissolved solids showed lower values in sites with intensive plant growth in western part. The variation in water conductivity was highly related to water dissolved salts. It was lower in western part and higher in the eastern part of the lake   according to direct connection to the sea through the boughaz.

The total dissolved oxygen showed clear spatial variation. Oxygen content ranged between 3.7 to 7.3 mg/l. The highest mean value was recorded in eastern part and the lowest at middle part. In general, water is more aerated in sites with less dense growth of Macrophytes recording 9.4and 9.5 mg/l, respectively. It was observed that site (which recorded lowest oxygen content, 3.7 mg/l) was occupied by damaged and decayed aquatic plants due to fishing boats impact. In most sites, the highest dissolved oxygen values were recorded in July, and the lowest was in May. Water phosphate showed low spatial variation with mean values varying between 0.04 and 0.3 mg/l. Minimum values were in eastern parts, while the maximum was at western. It was noticed during the field work that the two sites of minimum phosphate content were characterized by high epiphytic growth, forming a layer on the macrophytes species. Clear difference in water phosphate was recorded between the three samples. High phosphate content was in July with few exceptions (no difference between the three samplings: 0.04 mg/l).

Ammonia concentrations showed a much clearer spatial variation, Water ammonia content in ranged between the lowest of 1.1 mg/l in most sites and the highest of 40 mg/l in the western section.

It was observed that Macrophytes flourish in July and remarkably reduce in the other sampling months. Migratory water birds like White Pelican, Cormorants, White Stork and Flamingo are one of the causes of aquatic plants decline. The migratory birds are common visitors to Lake Burullus as it is a Ramsar site (Younis and Nafea, 2012; Younis &Nafea, 2015) in dense flocks and resting at the shores of Lake Burullus from November till April. Although previous studies indicated the positive role of water birds on the aquatic habitat e.g. their role for dispersal of plants propagates (Green et al., 2002), rising water productivity (Little, 1979); water birds, particularly large ones (White Pelican and Flamingo), caused serious mechanical damage for aquatic macrophytes (by cutting during their movements, feeding and grazing) and dispersion of the bottom sediment, increasing the water turbidity. Our results support those of Agami and Waisel (1984), who found that Najas armata, is eaten and exposed to damage by water birds, such as Gallinula chloropus Linnaeus 1758 and Fulica atra Linnaeus 1758, causing a serious reduction on plant growth, explaining minimum macrophytes density at seasons of migration compared to other sampling seasons. Field surveys support these findings. On the other side, migratory birds that grazing on Macrophytes may have a positive role of enhance the seeds germination (following exposure to bird's digestive system). Such results are not exclusive related to seeds of aquatic macrophytes, but also to the ones of terrestrial plants (Koller and Cohen, 1959). Growth and distribution of Macrophytes in lake burullus are influenced by natural and anthropogenic environmental conditions. The natural ones include dense growth of epiphytes, invasion of other plants as Myriophyllim spicatum, and the impact of water birds. The study confirmed that the high salinity levels reduced the plants growth and caused a decline in macrophytes. The anthropogenic impacts caused a significant variation in water conditions, limiting the growth of many species and providing the opportunity for Myriophyllum spicatum to compete with native species. This conclusion is in consistence with Agami and Waisel (1985, 2002), who found that the competitive relationship between Myriophyllum spicatum and Najas armata developed as a result of resources exploitation and  environmental deterioration, where the competition between the two species is usually in the benefit of Myriophyllum specatum, causing the reduction of Najas armata. Myriophyllum showed a higher flexibility toward unfavorable conditions, making the plant more qualified to survive in such conditions than Najas spp. the leaves forms and lacunae of Myriophyllum spicatum provide low resistance to oxygen diffusion between leaves and make the plant able to benefit of the low oxygen contents (Laskov et al., 2006).

Ali & Sotan (2006) also indicated that Myriophyllum showed higher production in water with nitrogen compounds and high organic matter in sediment. Myriophyllum spicatum can be an indicator for eutrophicated conditions represented by high concentrations of ammonia, nitrate and phosphate in both water and sediments while Najas armata and Najas minor were more tolerant to such conditions, their adaptability to deep and eutrophicated waters was lower than that of Myriophyllum spicatum.

Fishing is another form of human activity that creates a destructive impact on Macrophytes from Lake Burrullus.  My study concerns with shallow water fishing (Najas spp. grew in shallow water) which extends from May to July. The results showed a low growth of Najas spp. in May due to boat impacts. One can suggest that Lake Burullus is exposed to constrains, mainly from anthropogenic disturbance, which caused a decline in density and diversity, not only to Najas armata, but also to other Macrophytes species.

 In conclusion; the increasing water depth and water salinity at the eastern section of lake Burullus leads to disappear of some aquatic Macrophytes from this section as; Najas armata, Myriophyllum spicatum , Ceratoplyllum demerssum and Azolla filiculoides. The eastern section became an open water with less turbidity suitable for environmental tourism and increase the fish production from this section. So the sustainable management and development of the rest of the lake must be completed and the process of Deeping and shallower Lake Burrullus must be continuously occurring with regular and strategic plans.    


REFERENCES

Aaron, S.; Kelsey, S.; Joseph, M. and Rick, R., (2018): Interactive effects of road salt    and sediment disturbance on the productivity of seven common aquatic macrophytes freshwater Biology. 2018; 1–12.

Agami, M. and Waisel, Y. (1984): Germination of Najas marina L., Aquatic Botany, 19: 37-44.

 Agami, M. and Waisel, Y. (1985):  Inter-relationships between Najas marina L. and three other Species of aquatic macrophytes, Hydrobiologia, 126: 169-173.

 Agami M. and Waisel Y. (2002):  Competitive relationships between two water plant species: Najas marina L. and Myriophyllum spicatum L., Hydrobiologia, 482: 197-200.

Ali, M. and Soltan, M. (2006):  Expansion of Myriophyllum spicatum (Eurasian water milfoil) into Lake Nasser, Egypt: Invasive capacity and habitat stability, Aquatic Botany, 84: 239-244.

Allen, S. E., Grimshow, H. M., Parkinson, J. A., Quarmby, C. and Roberts, J. D. (1986): Chemical analysis in plant ecology, in: Methods in Plant Ecology, P. D. Moor and S. B. Chapman (eds.). p. 257.

Al-Sodany, Y.M. (1992): Vegetation analysis of the northern part of Nile Delta region. MSc thesis, Faculty of Science, Tanta University, 122 p

APHA-American Public Health Association, (1985): Standard Methods for the Examination of Water and Waste Water, American Public Health Association, Washington D. C., 874 p.

Baha El-Dein, S., Hobbs, J. and Mullie, W. (1989): The Birds of Egypt, Oxford University Press, Oxford, 551 p.

Belal, A., Brigges, J., Sharp, J. and Springuel, I. (2009): Bedouins by the Lake: Environment, change and sustainability in Southern Egypt, The American University in Cairo Press, Cairo, 104-108.

Bini L., Thomaz S., Murphy K. and Camargo A. (1999): Aquatic macrophytes distribution in relation to water and sediment conditions in the Itaipu reservoir, Brazil, Hydrobiologia, 415: 147-154.

Birket, C., Tollner, E. and Gattie, D., (2007): Total suspended solids and flow regime effects on Periphyton development, Trans. Am. Soc. Agric. Engrs., 50 (3): 1095-1104.

Boulos, L. (1995): Flora of Egypt checklist. Cairo, Egypt: Al-Hadara Publishing; 1995

Boulos, L. (1999): Flora of Egypt. Volume 1 Cairo, Egypt: Al-Hadara Publishing; 1999

Boulos, L.(2000): Flora of Egypt. Volume 2 Cairo, Egypt: Al-Hadara Publishing; 2000

Boulos, L.( 2002): Flora of Egypt. Volume 3 Cairo, Egypt: Al-Hadara Publishing; 2002

Boulos, L. (2005): Flora of Egypt. Volume 4 Cairo, Egypt: Al-Hadara Publishing; 2005

Boulos, L.(2009): Flora of Egypt checklist. Cairo, Egypt: Al-Hadara Publishing; 2009.

Clarke, S. and Wharton, G. (2001): Sediment nutrient characteristics and aquatic macrophytes in lowland English rivers, Science of the Total Environment, 266: 103-112.

 

Duarte, C., Planas, D.and Penuelas, J., (1994): Macrophytes taking control of an ancestral home, in: Margalef R. (ed.), Limnology Now: A Paradigm of Planetary Problems, Elsevier Science, Amsterdam, 59-79. 38 H. Yacoub – Najas spp. growth in relation to environmental factors in Wadi Allaqi (1 ~ 40)

Eriksson, B., Sandstorm, A., Isaeus, M., Schreiber, H. and  Karas, P. (2004): Effects of boating Activities on aquatic vegetation in the Stockholm archipelago, Baltic Sea, Estuarine, Coastal and Shelf Science, 61: 339-349.

Green, A., Figuerola, J. and Sanchez, M.( 2002): Implications of water bird ecology for the

Dispersal of aquatic organisms, Acta Oecologica, 23: 177-189.

Hadad, H. R.; Mufarrege, M. M.; Di Luca, G. A.; Maine, M. A. (2017): Salinity and pH effects on floating and emergent macrophytes in a constructed wetland. Water science abd technology 2017(1):wst 2018110.

Hilt S. and Gross E. (2008): Can allelopathically active submerged macrophytes stabilize clear water states in shallow lakes? Basic and Applied Ecology, 9: 422-432.

Khalil, M.T. & El-Dawy, F.A. (2002): Ecological survey of Burullus natural protectorate: fishes and fisheries. MedWetCoast Project, Egyptian Environmental Affairs Agency (EEAA), Cairo

Khedr, A. (1999): Floristic composition and phytosociology in a Medeteranean Deltiac Lake (Lake Burullus), Egypt. Ecol Mediterr 25(1):1–11.

Khedr, A. and Lovett-Doust, J. (2000):  Determinants of floristic diversity and vegetation compo- sition on the islands of Lake Burollos, Egypt. Appl Veg Sci 3:147–156

Krik, J. (1994): Light and photosynthesis in Aquatic ecosystems, Cambridge University Press, Cambridge, 509 p.

Lacoul, P. and Freedman, B. (2006):  Environmental influences on aquatic plants in freshwater ecosystems, Environ. Rev., 14: 89-136.

Laskov, C., Horn, O. and Hupfer, M., (2006): Environmental factors regulating the radial oxygen loss from roots of Myriophyllum spicatum and Potamogeton crispus, Aquatic Botany, 84: 333-340.

Little, E. (1979): Handbook of Utilization of Aquatic Plants, Food and Agriculture Organization of the United Nations, Fish. Tech. Pap., no. 187.

Madsen, T. and Cedergreen, N. (2002): Sources of nutrients to rooted submerged macrophytes growing in a nutrient-rich stream, Freshwater Biology, 47: 283-291.

Malderij, G. (2006): Chemical Warfare in Freshwater-Allelopathic Effects of Macrophytes on Phytoplankton, Ph.D. thesis, Netherlands Institute of Ecology, The Netherlands.

Murphy, J. and Riley, J. (1962): A modified single solution method for the determination of Phosphate in natural waters, Anal. Chem. Acta., 27: 31-38.

Murphy, J., Dickenson, G., Thomaz, S., Bini, L., Dick, K., Greaves, K., Kennedy, M., Livingstone, S., McFerran, H., Milne, J., Oldroyd, J. and Wingfield, R. (2003): Aquatic plant communities and predictors of diversity in a subtropical river floodplain: the upper Rio Parana, Brazil, Aquatic Botany, 77: 257-276.

Nafea, E.M. (2005): On the ecology and sustainable development of the Northern Delta Lakes, Egypt. Ph.D. Thesis, Fac. Sci. Mans. Univ.

Nafea, E.M. (2016): Characterization of environmental conditions required for production of livestock and fish fodder from duckweed (Lemna gibba L.). Journal of Mediterranean Ecology, 14, 5-11.

Rasch, L., Van den Brink, P., Crum,  S. and Woin ,  P. (2004): The effects of pesticides mixture on aquatic ecosystems differing in trophies status: responses of macrophytes Myriophyllum spicatum and the periphytic algal community, Ecotoxicology and Environmental safety, 57: 383-398.

Rolon, A. and  Maltchik, L. (2006): Environmental factors as predictors of macrophytes richness and composition in wetland of southern Brazil, Hydrobiologia, 556: 221-231.

Rossum, J.  R.; Villarruz, P. (1961): Suggested methods for turbedometric determination of sulphate in water, American Water Works Society, 53: 873.

Sand-Jensen, K. and Mebus, J. (1996): Fine-scale patterns of water velocity within macrophytes patches in streams, Oikos, 76: 169-180.

Sand-Jensen, K.; Pedersen, O. (1999): Velocity gradients and turbulence around macrophytes stands in streams, Freshwater Biology, 42: 315-328.

Scheffer, M., de Redlijkheid, M. and  Noppert, F. (1992): Distribution and dynamics of submerged vegetation in a chain of shallow eutrophic lakes, Aquatic Botany, 42: 199-216.

Shaltout, K.H, & Khalil, M.T. (2005): Lake Burullus (Burullus Protected Area). Publication of National Biodiversity Unit (NBU) No 13. Egyptian Environment Affairs Agency (EEAA), Cairo, Egypt, 578 p

Shaltout, K.H.; Al-Sodany, Y.M. (2000): Phytoecology of Lake Burullus Site. MedWetCoast, Global Environmental Facility (GEF) & Egyptian Environmental Affairs Agency (EEAA),Cairo

Standard, J.; Weisner, S. (2001): Morphological plastic responses to water depth and wave exposure in an aquatic plant (Myriophyllum spicatum), Journal of Ecology, 89: 166-175.

Stelzer, D., Schneider, S. and Melzer, A. (2005 ): Macrophyte-based assessment of lakes – a contribution to the implementation of the European Water Framework Directive in Germany, International Review of Hydrobiology, 90 (2): 223-237.

Torn, K., Krause-Jenesen, D. and Martin, G., (2006): Present and past depth distribution of bladder work (Fucus versiculosus) in the Baltic Sea, Aquatic Botany, 84: 53-62.

Van Donk, E. and Van de Bund, W., (2002): Impact of submerged macrophytes including charophytes on phyto- and zooplankton communities: allelopathy verses other mechanisms, Aquatic Botany, 72: 261-274. 40 H. Yacoub–Najas spp. growth in relation to environmental factors in Wadi Allaqi (1 ~ 40).

 Watson, D. (1987): Hydraulic effects of aquatic weeds in Uk rivers, Regulated Rivers: research and Management, 1: 211-227.

Wetzel, R. (2001): Limnology: Lake and River Ecosystems, Academic Press, San Diego.

William, T. Haller; D. L. Sutton; W. C.; Barlowe (1974): Effects of Salinity on Growth of Several Aquatic Macrophytes .Ecology, Vol. 55, No. 4. (Jul., 1974), pp. 891-894.

 Wilcock, R., Scarsbrook, M., Costley, K. and Nagels, J. (2004): Controlled release experiments to determine the effects of shade and plants to nutrient retention in a lowland stream, Hydrobiologia, 485: 153-162.

 Younis, A.M, and Nafea, E.M. (2012): Impact of environmental conditions on the biodiversity of Mediterranean Sea Lagoon, Burullus Protected Area, and Egypt. World Appl Sci J 19:1423–1430

Younis, A.M. and  Nafea , E. M. (2015): Heavy metals and nutritional composition of some naturally growing aquatic macrophytes of Northern Egyptian Lakes. J Bio Environ Sci 6(3):16–23

 

 

 

دراسة تاثیر التغیرات فی خصائص المیاة علی انتشارالنباتات المائیة

فی بحیرة البرلس فی مصر

د. السید محمد علی نافع

قسم البیئة المائیة کلیة الثروة السمکیة جامعة السویس مصر

ملخص البحث:

تهدف هذه الدراسة الی تقییم تأثیر التغیرات فی خصائص المیاه علی النمو والانتشار للنباتات المائیة فی بحیرة البرلس حیث اوضحت النتائج ان زیادة العمق والتطهیر فی الجانب الشرقی لبحیرة البرلس ادى الی اختفاء بعض الانواع النباتیة مثل ( نبات الحریشة  Najas armata, نخشوش الحوت  Ceratophyllum demersum خس الماء  Pistia stratiotes , Myriophyllum spicatum وندرة تواجدها فی بقیة اجزاء البحیرة و هناک انواع قل تواجدها.   من الجانب الشرقی للبحیرة

واوضحت النتایج ان الملوحة ارتفعت ارتفاع ملحوظ فی البحیرة وخاصة الجانب الشرقی  وارتفاع نسبی فی بقیة اجزاء البحیرة مما ادی الی اختفاء تلک النباتات وندرتها فی البحیرة وتغیر الترکیب الفلوری للبحیرة . 

REFERENCES
Aaron, S.; Kelsey, S.; Joseph, M. and Rick, R., (2018): Interactive effects of road salt    and sediment disturbance on the productivity of seven common aquatic macrophytes freshwater Biology. 2018; 1–12.
Agami, M. and Waisel, Y. (1984): Germination of Najas marina L., Aquatic Botany, 19: 37-44.
 Agami, M. and Waisel, Y. (1985):  Inter-relationships between Najas marina L. and three other Species of aquatic macrophytes, Hydrobiologia, 126: 169-173.
 Agami M. and Waisel Y. (2002):  Competitive relationships between two water plant species: Najas marina L. and Myriophyllum spicatum L., Hydrobiologia, 482: 197-200.
Ali, M. and Soltan, M. (2006):  Expansion of Myriophyllum spicatum (Eurasian water milfoil) into Lake Nasser, Egypt: Invasive capacity and habitat stability, Aquatic Botany, 84: 239-244.
Allen, S. E., Grimshow, H. M., Parkinson, J. A., Quarmby, C. and Roberts, J. D. (1986): Chemical analysis in plant ecology, in: Methods in Plant Ecology, P. D. Moor and S. B. Chapman (eds.). p. 257.
Al-Sodany, Y.M. (1992): Vegetation analysis of the northern part of Nile Delta region. MSc thesis, Faculty of Science, Tanta University, 122 p
APHA-American Public Health Association, (1985): Standard Methods for the Examination of Water and Waste Water, American Public Health Association, Washington D. C., 874 p.
Baha El-Dein, S., Hobbs, J. and Mullie, W. (1989): The Birds of Egypt, Oxford University Press, Oxford, 551 p.
Belal, A., Brigges, J., Sharp, J. and Springuel, I. (2009): Bedouins by the Lake: Environment, change and sustainability in Southern Egypt, The American University in Cairo Press, Cairo, 104-108.
Bini L., Thomaz S., Murphy K. and Camargo A. (1999): Aquatic macrophytes distribution in relation to water and sediment conditions in the Itaipu reservoir, Brazil, Hydrobiologia, 415: 147-154.
Birket, C., Tollner, E. and Gattie, D., (2007): Total suspended solids and flow regime effects on Periphyton development, Trans. Am. Soc. Agric. Engrs., 50 (3): 1095-1104.
Boulos, L. (1995): Flora of Egypt checklist. Cairo, Egypt: Al-Hadara Publishing; 1995
Boulos, L. (1999): Flora of Egypt. Volume 1 Cairo, Egypt: Al-Hadara Publishing; 1999
Boulos, L.(2000): Flora of Egypt. Volume 2 Cairo, Egypt: Al-Hadara Publishing; 2000
Boulos, L.( 2002): Flora of Egypt. Volume 3 Cairo, Egypt: Al-Hadara Publishing; 2002
Boulos, L. (2005): Flora of Egypt. Volume 4 Cairo, Egypt: Al-Hadara Publishing; 2005
Boulos, L.(2009): Flora of Egypt checklist. Cairo, Egypt: Al-Hadara Publishing; 2009.
Clarke, S. and Wharton, G. (2001): Sediment nutrient characteristics and aquatic macrophytes in lowland English rivers, Science of the Total Environment, 266: 103-112.
 
Duarte, C., Planas, D.and Penuelas, J., (1994): Macrophytes taking control of an ancestral home, in: Margalef R. (ed.), Limnology Now: A Paradigm of Planetary Problems, Elsevier Science, Amsterdam, 59-79. 38 H. Yacoub – Najas spp. growth in relation to environmental factors in Wadi Allaqi (1 ~ 40)
Eriksson, B., Sandstorm, A., Isaeus, M., Schreiber, H. and  Karas, P. (2004): Effects of boating Activities on aquatic vegetation in the Stockholm archipelago, Baltic Sea, Estuarine, Coastal and Shelf Science, 61: 339-349.
Green, A., Figuerola, J. and Sanchez, M.( 2002): Implications of water bird ecology for the
Dispersal of aquatic organisms, Acta Oecologica, 23: 177-189.
Hadad, H. R.; Mufarrege, M. M.; Di Luca, G. A.; Maine, M. A. (2017): Salinity and pH effects on floating and emergent macrophytes in a constructed wetland. Water science abd technology 2017(1):wst 2018110.
Hilt S. and Gross E. (2008): Can allelopathically active submerged macrophytes stabilize clear water states in shallow lakes? Basic and Applied Ecology, 9: 422-432.
Khalil, M.T. & El-Dawy, F.A. (2002): Ecological survey of Burullus natural protectorate: fishes and fisheries. MedWetCoast Project, Egyptian Environmental Affairs Agency (EEAA), Cairo
Khedr, A. (1999): Floristic composition and phytosociology in a Medeteranean Deltiac Lake (Lake Burullus), Egypt. Ecol Mediterr 25(1):1–11.
Khedr, A. and Lovett-Doust, J. (2000):  Determinants of floristic diversity and vegetation compo- sition on the islands of Lake Burollos, Egypt. Appl Veg Sci 3:147–156
Krik, J. (1994): Light and photosynthesis in Aquatic ecosystems, Cambridge University Press, Cambridge, 509 p.
Lacoul, P. and Freedman, B. (2006):  Environmental influences on aquatic plants in freshwater ecosystems, Environ. Rev., 14: 89-136.
Laskov, C., Horn, O. and Hupfer, M., (2006): Environmental factors regulating the radial oxygen loss from roots of Myriophyllum spicatum and Potamogeton crispus, Aquatic Botany, 84: 333-340.
Little, E. (1979): Handbook of Utilization of Aquatic Plants, Food and Agriculture Organization of the United Nations, Fish. Tech. Pap., no. 187.
Madsen, T. and Cedergreen, N. (2002): Sources of nutrients to rooted submerged macrophytes growing in a nutrient-rich stream, Freshwater Biology, 47: 283-291.
Malderij, G. (2006): Chemical Warfare in Freshwater-Allelopathic Effects of Macrophytes on Phytoplankton, Ph.D. thesis, Netherlands Institute of Ecology, The Netherlands.
Murphy, J. and Riley, J. (1962): A modified single solution method for the determination of Phosphate in natural waters, Anal. Chem. Acta., 27: 31-38.
Murphy, J., Dickenson, G., Thomaz, S., Bini, L., Dick, K., Greaves, K., Kennedy, M., Livingstone, S., McFerran, H., Milne, J., Oldroyd, J. and Wingfield, R. (2003): Aquatic plant communities and predictors of diversity in a subtropical river floodplain: the upper Rio Parana, Brazil, Aquatic Botany, 77: 257-276.
Nafea, E.M. (2005): On the ecology and sustainable development of the Northern Delta Lakes, Egypt. Ph.D. Thesis, Fac. Sci. Mans. Univ.
Nafea, E.M. (2016): Characterization of environmental conditions required for production of livestock and fish fodder from duckweed (Lemna gibba L.). Journal of Mediterranean Ecology, 14, 5-11.
Rasch, L., Van den Brink, P., Crum,  S. and Woin ,  P. (2004): The effects of pesticides mixture on aquatic ecosystems differing in trophies status: responses of macrophytes Myriophyllum spicatum and the periphytic algal community, Ecotoxicology and Environmental safety, 57: 383-398.
Rolon, A. and  Maltchik, L. (2006): Environmental factors as predictors of macrophytes richness and composition in wetland of southern Brazil, Hydrobiologia, 556: 221-231.
Rossum, J.  R.; Villarruz, P. (1961): Suggested methods for turbedometric determination of sulphate in water, American Water Works Society, 53: 873.
Sand-Jensen, K. and Mebus, J. (1996): Fine-scale patterns of water velocity within macrophytes patches in streams, Oikos, 76: 169-180.
Sand-Jensen, K.; Pedersen, O. (1999): Velocity gradients and turbulence around macrophytes stands in streams, Freshwater Biology, 42: 315-328.
Scheffer, M., de Redlijkheid, M. and  Noppert, F. (1992): Distribution and dynamics of submerged vegetation in a chain of shallow eutrophic lakes, Aquatic Botany, 42: 199-216.
Shaltout, K.H, & Khalil, M.T. (2005): Lake Burullus (Burullus Protected Area). Publication of National Biodiversity Unit (NBU) No 13. Egyptian Environment Affairs Agency (EEAA), Cairo, Egypt, 578 p
Shaltout, K.H.; Al-Sodany, Y.M. (2000): Phytoecology of Lake Burullus Site. MedWetCoast, Global Environmental Facility (GEF) & Egyptian Environmental Affairs Agency (EEAA),Cairo
Standard, J.; Weisner, S. (2001): Morphological plastic responses to water depth and wave exposure in an aquatic plant (Myriophyllum spicatum), Journal of Ecology, 89: 166-175.
Stelzer, D., Schneider, S. and Melzer, A. (2005 ): Macrophyte-based assessment of lakes – a contribution to the implementation of the European Water Framework Directive in Germany, International Review of Hydrobiology, 90 (2): 223-237.
Torn, K., Krause-Jenesen, D. and Martin, G., (2006): Present and past depth distribution of bladder work (Fucus versiculosus) in the Baltic Sea, Aquatic Botany, 84: 53-62.
Van Donk, E. and Van de Bund, W., (2002): Impact of submerged macrophytes including charophytes on phyto- and zooplankton communities: allelopathy verses other mechanisms, Aquatic Botany, 72: 261-274. 40 H. Yacoub–Najas spp. growth in relation to environmental factors in Wadi Allaqi (1 ~ 40).
 Watson, D. (1987): Hydraulic effects of aquatic weeds in Uk rivers, Regulated Rivers: research and Management, 1: 211-227.
Wetzel, R. (2001): Limnology: Lake and River Ecosystems, Academic Press, San Diego.
William, T. Haller; D. L. Sutton; W. C.; Barlowe (1974): Effects of Salinity on Growth of Several Aquatic Macrophytes .Ecology, Vol. 55, No. 4. (Jul., 1974), pp. 891-894.
 Wilcock, R., Scarsbrook, M., Costley, K. and Nagels, J. (2004): Controlled release experiments to determine the effects of shade and plants to nutrient retention in a lowland stream, Hydrobiologia, 485: 153-162.
 Younis, A.M, and Nafea, E.M. (2012): Impact of environmental conditions on the biodiversity of Mediterranean Sea Lagoon, Burullus Protected Area, and Egypt. World Appl Sci J 19:1423–1430
Younis, A.M. and  Nafea , E. M. (2015): Heavy metals and nutritional composition of some naturally growing aquatic macrophytes of Northern Egyptian Lakes. J Bio Environ Sci 6(3):16–23