Preferred direction site of the sugar-cane field to infestation by Pulvinaria tenuivalvata (Newstead) and its relation with parasitized Coccophagus scutellaris Hymenoptera Aphelinidae

Document Type : Original Article

Author

Crop Pest Research Department, Plant Protection Research Institute, Agriculture Research Center, Dokki, Giza, Egypt.

Abstract

This research aims to evaluate the effects of biotic factors on the population density of the sugar cane soft scale
P. tenuivalvata. Population estimation was performed in different sites of the sugar cane field, i.e, east, north, south,
west and field center. Results show that, scales proportionally increased from May to December in all field sites
and the scales spread intensively through September, October and November. Tt was found that plants locating in
west site intensively harbored the highest population of scales followed by north site. The number of scales on
plant in west and south sites was approximately similar. The field center harbored the lowest scale population.
These results reveal that the west direction followed by north are preferred by this insect in its various stages. This
could be attributed to the direction of the wind which always blows from north to west carrying crawlers to these
directions where it may aggregate for feeding and growth. During the two successive seasons of the study, data
also revealed the incidence of the Aphelinidae parasite Coccophagus scutellaris (Aphelinidae: Hymenoptera)
parasitizing the different immature stages (except 1st instar) and mature stage (Adult females). The influence of
such parasite on the insect was significant in both seasons. In conclusion, there are many biotic factors that
can affect the population density of the sugar cane soft scale P. tenuivalvata. This can assist to avoid the
difficult application of the insecticide and minimize the population of the environment by natural
enemies.

Keywords


INTRODUCTION

The wide distribution of Pulvinaria tenuivalvata (Newstead) was observed for the first time by Ali et al (1997). in sugar cane fields at Atfeh locality, Giza Governorate, El-minia, Sohage, Quena, Luxor and Aswan. This reflects the seventy dangerous and bad situations of this pest on sugar-cane in Upper Egypt.

Sugar cane is cultivated in large contiguous areas and remains in the field for the whole year. Therefore, a wide range of insect species cause the most significant losses. Some of the insects are major pests of regular occurrence and cause survivor damage, others are minor species. Among these insect pests are soft scale insects Maareg et al (1992).

In 1995, 1996 season, the first noticed in sugar cane fields in Giza separated widely and quickly to cover of about 18 thousand feddaen in all sugarcane plantation in (2015-2016) season Besheit (2002). The nymph and adult females were found clustering on both leaf surface. They are arranged as a line near the edge of the leaf blade Mau (1992)

P. tenuivalvata causes severe damage due to the sucking leaf juice, leading to a loss of leaves, tender young stems, stored plants growth and even death of the plant (Valand et al. 1989). The chemical control in sugar cane fields is very difficult due to foliage intensity and crowded plants. At the same time, many parasitoids are already found, amongst these parasitoids, Coccophagus scutellaris (Dolman) are the major attackers and represent a big portion of P. tenuivalvata population (Hindawy et al., 2002).

Shalaby (2002) found that, this parasitism ranged between 60.1 in August to 33.1 in December, 1997, but in sugar cane season of 1998, the parasitism activity was higher and ranged between 66.7 – 72.2.

This research aims to evaluate the effects of biotic factors on the population density of the sugar cane soft scale P. tenuivalvata. This can assist to avoid the difficult application of the insecticide and minimize the population of the environment. natural enemies (parasites).  

MATERIAL AND METHODS

Spread pattern of insect all over the sugar cane field

One Fadden was selected for this study at Awadlah, Edfo, belonging to Aswan Governorate. During the period extending from May to January, regular intervals sample of sugar can plant leaves were collected from the field border 1,2,3,4 and 5 m. towards the field center. Sample were taken from the different directions of the sugar–cane field representing east, west, north and south directions, in addition to the center site of the field. For each direction, 20 plants were selected randomly and 3 leaves from each plant (lower, mid, and upper levels) were cut – off, kept in muslin bags and transferred to the laboratory. Regular inspection of P. tenuivalvata scales infesting sugarcane plants in (Edfo-Aswan) Governorate during (2015 and 2016) seasons revealed the incidence of the Aphelinidae parasite Coccophagus scutellaris. Data on the parasite activity was based on 2 weekly counts of parasitized scales. The wide distribution of P. tenuivalvata (Newstead) was observed for the first time by Ali et al.1 in sugar cane fields at Atfeh locality, Giza Governorate, El-minia, Sohage, Quena, Luxor and Aswan. These results reflect the dangerous and bad effect of this pest on sugar-cane in Upper Egypt.

RESULTS AND DISCUSSION

Data in Table (1 and 2) summarizes the changes in the population density of P. tenuivalvata expressed as monthly numbers of insect

As it appears from Table (1) result for 2015 indicate the presence of this insect during the main period of activity which extended from the first week of May to end of December.

Results also showed that P. tenuivalvata appeared for the first time, in a few numbers during the first week of May (79 insects), in all directions and increased gradually, afterwards. The insect reached the highest peak during the first period of September (445 insects). The population density of P. tenuivalvata decreased until the last period of December (117 insects).

The same trend was detected during the second year (2016) as showed in Table (2). The population of the insect increased gradually starting from June (99 Insects) and reached the maximum number at end of October (331 insects). After that, it decreased to reach (64 insects) on December. Tables (1 and 2) and Figs (1 and 2) summarizes the changes in the population density of P. tenuivalvata and parasites distribution in the different. directions of sugarcane field in Awadlah village (Edfo, Aswan) in 2015 and 2016 seasons.

As it appears from Tables (3 and4) and Figs (1 and 2) a significant positive relationship holds between the numbers of insects and parasites in both years such relationship seemed to be stronger in 2015 than 2016.

Numbers of scale insect, Coccophagus scutellaris and the parasite Coccophagus Scutellaris were estimated from May to December in sugar cane field during 2015 and 2016 seasons.

Data in Table (1) showed, the numbers of P. tenuivalvata and Coccophagus scutellaris distribution in different direction of sugar cane field in Awadlah, Edfo Aswan Governorate during 2015 season.

Results on parasitism in 2015 season in sugar cane field indicated that, the its activity increased of July by increasing the numbers of Pulvinaria tenuivalvata especially at the West direction then decreased at the end of December the data in Table (1) also showed that’s the parasite activity increased in September at the West and North directions compared with other directions during 2015 season.

The highest total number of parasites appeared in west direction (359) during the whole season of 2015. The lowest total number of parasites appeared in South direction (87) during the whole season of 2015.

Parasitoid activity fluvtuted during the activity period of P. tenuivalvata (June- December).

The data recorded high abundance in September in West direction (64 parasite with 168 insect pest).

Data in Table (2) clarified, the relationship between P. tenuivalvata and Coccophagus Scutellaris as a parasite in Awadlah, Edfo, Aswan Governorate during season 2016.

The highest population of Pulvinaria tenuivalvata and their parasite was recorded at the West direction then North direction.

The lowest population of P. tenuivalvata and their parasite was recorded at the East and south directions during season 2016.

The data indicated that the numbers of parasite were gradually increased in all directions by increasing their host P. tenuivalvata fromat the first of June till the first of December. Hot months (July, August, September and October) had considerable high populationof P. tenuivalvata scales, consequently, the number of parasites increased a close relationship between the parasite activity and the population density of insect pests especially at the west and north directions 2015 and 2016 seasons. 

The highest total number of insect pests was recorded at the North and West directions (371and 676 insect), while the highest number of parasites was recorded at the West and North directions (369 and 219 insect) during 2016 season. (Table 2).

The highest number of insect pest recorded at the West and North direction (766 and 437 insect), while the highest number of parasites recorded at the west and north direction (359 and 197 insect during 2015 season (Table 1).

In 2015 sugar cane season, the parasitoid activity was higher than 2016 season, the parasitoid activated one week earlier than 2015. Number of parasitized increased steadily in the following months particular during July, August and September. The numbers scales were estimated from May to December of cane season 2015 and 2016. It was estimated in different sites of cane– fields, i.e. East, North, south west, and Center.

Results presented in Table (1) and (2) showed that this pest increased from May to December in all field sites, while scales numbers were intensively through August, September and October (322,445, and 359n respectively). The same trend was exhibited in 2016, reached to 231,309, and 331 respectively in the same months.

Hot months with high relative humidity (July, August and September) had considerable high population of P. tenuivalvata scales, consequently, the number of parasitized scales increased the relationship between the parasite activity and the population density of insect pests.

The Aphelinidae parasites particularly these of Coccophagus spp. play a great role in management of soft scale insect population. Coccophagus lymenia is an internal parasite of the immature stage of Parthenalecanium quercifex, Fex attacking willow Oak in Virginia (USA) and parasitism rate averaged 10-60 %. Concerning P. tenuivalvatascale insects, Blumberg et al. (1984). In Egypt two species Coccophagus bivittatus and Coccophagus lycinnie were recorded by Abd- Rabou et al. (1998) on Coccus hesperidus and known as internalparasites of different insect scale species. No other species rather than C. scutellaris could be detected as parasiteof P. tenuivalvata in sugar cane plantation.

Mahmoud (1981)showed that Nymphal stage tended to be concentrated in northern- west of sugar- cane field. The plants locating in this site may heavily suffer from being infested by this pest.

In the meantime, P. tenuivalvata is distributed in different sites of cane field. It was found that plants located in west site were intensively infested and recorded the highest population of scales (95.8 mean scales/leaf) followed by north site (54.4 mean scales/leaf). Other fields sites showed lower infestation plants locating in field center received the lowest scales population (21.1 mean scales/leaf). East and south received approximately similar population number (Table 1). In 2016 season, insect heavily existed sugar cane plants locating in west and north sites (676 and 371 scales/leaf. Moderately infestation was found in east and center (154 and 131 scale /leaf). The lowest population was recorded in south (105 scale/leaf) (Table 1) and 2). Sugar–cane plants infested with P. tenuivalvata showedconsiderable variation in the insect distribution, not only on plant leaves, but also in different field sites.

CONCLUSION

The herein investigation indicated that, there are many biotic factors that can affect the population density of the sugar cane soft scale P. tenuivalvata. This can assist to avoid the difficult application of the insecticide and minimize the population of the environment. natural enemies (parasites).

REFERENCES

Abdo Rabou, S.S., 1998. The species of Metaphycus Marcet (Hymenoptera Encyrtidae) recorded from Egypt. Bull. Ent. Soc. Egypt, 7, 67-76.

Ali, M.A., El-Khouly, A.S., El_Metwally, F.E., Shalaby, M.S., 1997. First recorded of the sugar-cane scale, saccharolecanium krugeri (Zehntner) in Giza, Egypt. Bull. Ent. Soc. Egypt, 75, 156-159.

Besheit, S.Y., Abaziad. A.A., Gomaa, A.M.E.S., El-Hamd, A.S., 2002. The influence of the infestation by the soft scale insect. Pulvanaria tenuivalvata (Newested) Coccidae: Homoptera on sugarcane stalk weight., juice quality and sugar yield in Upper Egypt, Assut J. Agric. Sci., 33 (4),17-28.

Blumberg, D.S., Swirski, E.A., 1984. Response of three soft scales (Homoptera: Coccidea) to parasitization by Metaphycus Smrskii. Phytoparasitica. 12 (1), 29-35.

Hindawy, A.S., Abd El-Samea, S.E., 2002. Scientific not Coccophagus scutellaris (Dalman) (Hymenoptera: Aphelinidae), a new record parasitoid attacking sugarcane soft scale Pulvanaria tenuivalvata (Newested) in Egypt. Egypt. J. Agric.Res., 80 (1), 219-222.

Maareg, M.F., Hassanein, M.A., Abu Dooh, A.M., 1992. Preliminary survey of the scale Insects attacking sugar cane in Egypt. Commun. Sci. Dev. Res., 495, 223-230.

Mahmoud, S.F., 1981. Ecological studies on California red scale and purple scale insects on

Citrus, and the effect of some recent insecticides on them and their parasites. M.Sc. Thesis, Fac. Agric., Cairo Univ., Egypt.

Mau, R.F, Martine Kessing, J.L., 1992. Green shield scale Pulvanaria pasidii (Maskell). crop knowledge Mast. WWW.extento.Hawaii.Edu/Kbse/Crop/Type/Croop-est.htm.

Shalaby, M.S., 2002 Ecological and biological studies on the sugar cane scale Pulvanaria tenuivalvata (Newstead) infesting sugar cane in Giza Governorate. PhD. Thesis, Fac. Agric., Al-Azhar Univ., Cairo, Egypt.

Valand, V.M., Patel, J.I., Mehta, D.M., 1989. Biology of brown scale (Saissetia coffeae) on

pointed gourd (Trichosanthes dioica). Ind. J. Agric. Sci., 59 (9), 610-611.

 

 

 

 

Table 1. Monthly counts P. tenuivalvata distributed in different direction of a sugar–cane fields, in (Edfo- Aswan Governorate (2015) season.

Sampling date

Total number of scales/sugar-cane leaf

-Direction of sugar- cane field.

Total

Mean

East

West

South

North

Center

May

15

33

8

19

4

79

15.8

June

16

46

12

31

7

112

22.4

July

22

93

24

53

22

214

42.8

August

39

137

47

73

26

322

64.4

September

67

168

66

104

40

445

89

October

55

138

48

81

37

359

71.8

November

41

101

36

54

24

256

51.2

December

22

50

14

22

9

117

23.4

Total

277

766

255

437

169

1904

380.8

Mean

34.625

95.75

31.875

54.625

21.125

238

47.6

 

C

A

C

B

D

   

Grouping of number insect of P. tenuivalvata in different sites of sugar cane field (West 95.6 A - North 54.6 B- East 34.6 C- East 34.6 C -South 31.9 C -Center 21.1 D)-

Table 2. Monthly counts P. tenuivalvata distributed in different direction of a sugar – cane fields, in (Edfo- Aswan Governorate (2016) season.

Sampling date

Total number of scales/ sugarcane leaf

-Direction of sugarcane field.

 

Total

 

Mean

East

West

South

North

Center

May

9

26

4

14

2

55

11

June

15

44

7

26

7

99

19.8

July

18

69

16

34

12

149

29.8

August

17

114

16

64

20

231

46.2

September

32

148

22

81

26

309

61.8

October

36

148

25

88

34

331

66.2

November

19

95

11

49

25

199

39.8

December

8

32

4

15

5

64

12.8

Total

154

676

105

371

131

1437

287.4

Mean

19.25

84.5

13.12

46.37

16.37

179.62

35.92

 

C

A

C

B

D

   
                 

Grouping of number of insect P. tenuivalvata in different sites of sugar cane field (-West 84.5 A -North 46.37 B-East 19.25 C-Center 16.37 C -South 13.12 D )-


Table 3. No. of P.tenuivalvate and parasites distribution in different directions of Sugar cane fields in Awadlah village at Edfu district ,Aswan Governorate during (2015) season.

 

Center

North

South

West

East

sampling date

%

Paras.

No. of Insect

%

Paras.

No. of Insect

%

Paras.

No. of Insect

%

Paras.

No. of Insect

%

Paras.

No. of Insect

 

 

0

0

2

33.3

3

9

33.3

1

3

66.6

10

15

37.5

3

8

May

 

100

2

2

40

6

10

40

2

5

42.4

8

18

42.88

3

7

 

33.3

1

3

30.76

4

13

50

2

4

52.38

11

21

62.5

5

8

Jun.

 

50

2

4

50

9

18

37.5

3

8

36

9

25

50

4

8

 

42.85

3

7

48

12

25

26.6

4

10

33.3

15

45

13.3

2

10

Jul.

 

33.35

5

15

35.71

10

28

42.85

6

14

77.08

37

48

58.3

7

12

 

58.3

7

12

51.51

17

33

38.8

7

18

44.82

26

58

35.7

5

14

Aug

 

50

7

14

30

12

40

34.4

10

29

46.85

37

79

32

8

25

 

55

11

20

29.41

15

51

36.3

12

33

43.75

35

80

48.38

10

31

Sept.

 

45

9

20

39.62

21

53

21.21

7

33

32.95

29

88

38.88

14

36

 

87.7

14

16

62.5

30

48

30.7

8

26

33.23

26

78

40

12

30

Octob.

 

61.9

13

21

66.6

22

33

50

1

22

46.66

28

60

36

9

25

 

53.4

7

13

36.66

11

30

45

9

20

34.88

20

53

64

16

25

Novem.

 

45.3

5

11

37.5

9

24

50

8

16

68.88

31

48

50

8

16

 

33.3

2

6

31.42

10

14

62.5

5

8

93.5

29

31

69.23

9

13

Dec.

 

66.6

2

3

75

6

8

33.3

2

6

42.15

8

19

44.4

4

9

 

-

90

169

-

197

437

-

87

255

-

359

766

-

119

277

Total

 

51.00

5.63

10.56

43.62

12.31

27.31

39.53

5.44

15.94

49.71

22.44

47.88

45.19

7.44

17.31

Mean

 

                                             

Paras. = parasite

 

 

 

 

 


Table 4. No. of P.tenuivalvate and parasites distribution in differcnt directions of Sugar cane fields in Awadlah village at Edfu district ,Aswan 

Governorate during (2016) season.

 

Center

North

South

West

East

sampling date

%

Paras.

No. of Insect

%

Paras.

No. of Insect

%

Paras.

No. of Insect

%

Paras.

No. of Insect

%

Paras.

No. of Insect

 

 

0

0

0

60

3

5

0

0

1

50

6

12

33.3

1

3

May

 

50

1

2

44.4

4

9

66.6

2

3

64.2

9

14

33.3

2

6

 

66.6

2

3

58.3

7

12

100

1

1

60

12

20

42

3

7

Jun.

 

50

2

4

57.1

8

14

66.6

4

6

62.5

15

24

50

4

8

 

66.6

4

6

56.2

9

16

37.5

3

8

68.9

20

29

37.5

3

8

Jul.

 

50

3

6

66.6

12

18

50

4

8

65

26

40

50

5

10

 

62.5

5

8

58.6

17

29

70

7

10

62.5

30

48

37.5

3

8

Aug

 

58.3

7

12

57.1

20

35

66.6

4

6

62.1

41

66

44.4

4

9

 

33.3

4

12

58.9

23

39

60

6

10

62.5

45

72

40

6

15

Sept.

 

57.1

8

14

71.4

30

42

41.6

5

12

39.4

30

76

47

8

17

 

38.8

7

18

60

27

45

60

9

15

52.5

42

80

50

10

20

Octob.

 

56.2

9

16

48.8

21

43

80

8

10

51.4

35

68

56

9

16

 

66.6

10

15

50

15

30

50

3

6

33.8

20

59

45.4

5

11

Novem.

 

90

9

10

63.15

12

19

40

2

5

50

18

36

50

4

8

 

50

2

4

80

8

10

50

2

4

60

12

20

50

3

6

Dec.

 

100

1

1

60

3

5

0

0

0

66.6

8

12

50

1

2

 

-

74

131

-

219

371

-

60

105

-

369

676

-

71

154

Total

 

56.00

4.63

8.19

59.41

13.69

23.19

52.43

3.75

6.56

56.96

23.06

42.25

44.78

4.44

9.63

Mean

 

                                             

Parasite.= paeasites

 

 

 

 

 

 

 

 

Figure1. Relationship between the parasitoid Coccophagus scutellaris and population of P. tenuivalvata on sugar cane fields during 2015 season Awadlah, Edfo Aswan Governorate at different directions.

 

 

 

 

Figure 2. Relationship between the parasitoid Coccophagus scutellaris and population of P. tenuivalvata on sugar cane fields during 2016 season Awadlah, Edfo Aswan Governorate at different directions.