Login       Friday, September 03, 2010     Search  
   Grey Leaf Spot of Maize Minimize  

GREY LEAF SPOT OF MAIZEkzn-coat-of-arms.gif
by Dr Julian Ward


Introduction

Grey leaf spot (GLS) of maize is caused by the fungus Cercospora zeae-maydis. The disease is now recognised as one of the most significant yield-limiting diseases of maize worldwide and certainly in the province of KwaZulu-Natal (see Table 1). Not only is it a threat to maize production in the commercial farming sector, it also reduces yields of maize on small-scale farms. The disease was first identified in KwaZulu-Natal in 1989/90 and has since spread to neighbouring provinces and most maize producing countries in Africa.

Symptoms

Symptoms are initially first observed on the lower leaves of the maize plant. The immature lesions are similar to lesions caused by other foliar maize pathogens, and first appear as small tan spots about 1 to 3 mm in size and are irregular in shape. The tan spots usually have yellow or chlorotic borders and, are more easily observed when the leaf is held to light

 

Mature lesions are readily distinguished from other pathogen symptoms and are distinctly rectangular in shape (5 to 70 mm long and 2 to 4 mm wide), and run parallel with leaf-veins.

 

Lesions, tan in colour, assume a grey sheen or caste when sporulating. As disease progresses, lesions coalesce and blighting of the whole leaf may result.

 

Under favourable conditions, blighting progresses upwards on the plant.

 

and the whole plant may die before the crop reaches maturity,

 

and serious yield losses may result.

 

Under these conditions, the maize plant may be pre-disposed to stalk-rotting fungal attack and resultant severe lodging adding further to the yield losses.

 

 

Disease Cycle

Grey leaf spot is highly dependant on favourable weather conditions. It requires frequent and prolonged periods of high humidity and warm temperatures (20E to 30EC) to complete spore gemination and the infection process. Spores (conidia) are produced from infested residues of previous maize crops in spring under conditions of high humidity and these are windblown to infect the newly planted maize crop. The lower leaves are usually the site of primary infection.

 

 

Lesions resulting from the initial infection produce spores that are wind- or rain-splashed to the upper leaves. (Ward et al 1999). Under unfavourable conditions (hot, dry weather), the fungus can remain dormant and then resume rapid development as soon as favourable weather conditions return (Latterall and Rossi, 1988). In mid- to late-season plantings and under favourable conditions, lesions may first appear on the mid- to upper-canopy as a result of wind-blown spores from adjacent infected maize. Such late season infections may be serious because it is the upper canopy that contributes 75 to 90% of the photosynthate for grain fill (Allison and Watson, 1966).

The occurrence of fewer and/or shorter periods of high humidity early in the growing season may account for the slower rate of early-season disease development (during the months of November and December). In contrast, good early season rains and more periods of high humidity (in November and December) have led to a higher frequency of early-season lesions (and more severe disease) (Ringer and Grybauskas, 1995).

 

Disease Management

As maize is the only known host for GLS, and the pathogen is not known to be seedborne, GLS is only able to survive from one season to the next on maize debris from a previously infected crop. It is spores produced in the infected debris in spring that are wind-blown to the newly planted maize that triggers the new epidemic.

Agronomic Practices
Tillage practices aimed at reducing initial inoculum by burying infested debris are classical methods of control and have been demonstrated to be effective in managing GLS (Latterell and Rossi, 1983). However, ploughing is less effective in managing the disease in areas with high levels of inoculum and where GLS is already established (Perkins et al., 1995). This is because inoculum from neighbouring infected fields, may be wind-blown to infect maize grown under conventional tillage systems. Further, other sources of inoculum may result from production practices used in South Africa. For example the practice of allowing maize to dry down to about 13,5% moisture in the field before harvesting, allows equinoxial winds to remove infected leaf tissue, which may be deposited on contours and headlands in and around maize fields. Such debris, and stubble remaining on the soil surface after ploughing, may act as an important source of inoculum to infect newly planted maize in the late Spring (Ward, 1996). Observations at Cedara have indicated that in dry seasons GLS may be detected three weeks earlier in no-till maize than in conventionally tilled maize. However, the improved moisture conservation under no-till, more than offsets the adverse effects of earlier GLS infection. In seasons favourable for GLS there is little or no difference between no-till and conventional tillage in the time the GLS infects maize.

Crop rotations have shown that even a single year of alternative crops away from maize can reduce initial inoculum. Rotations also provide additional benefits by improving soil quality, conserving soil water content and may reduce maize soil pathogens.

Other practices such as time of planting, plant density and timing of irrigation applications may all play a role in reducing disease severity.

Genetic Resistance
Hybrid resistance is perhaps the most cost-effective strategy of managing GLS. However, few hybrids have sufficient resistance to prevent yield losses due to GLS in commercial maize production. Resistance is due to several genes which are additive in effect, and each of which adds small increments of resistance to the hybrid. Breeders have found that if too high a level of resistance is required, breeding would be time consuming and other genetic characteristics such as yield or growing season length may be sacrificed. This can be observed in Table 1, where the more resistant hybrids, have in general a lower yield potential than hybrids more susceptible to disease. However, each season, more GLS resistant hybrids are being evaluated and their yield potential continues to improve.

Fungicide Control
Although efforts to improve genetic resistance to GLS in maize hybrids, it can be seen that even the most resistant hybrids still respond to fungicide treatment.

 

Table 1.  Cedara Cultivar Trial: 1999 / 2000 

Cultivar

Maturity(1)

Lodging
%

AUDPC(2)

Unsprayed Yield

Sprayed Yield

Yield Loss due to GLS

kg

%

SC

627

157

7

143

8683

9913

1230

12,4

SC

602

150

36

189

11807

12632

825

6,5

CRN

3308

146

2

219

10780

11028

248

2,2

SC

709

165

12

335

8814

10460

1646

15,7

SC

513

145

38

415

7730

9375

1645

17,5

PAN

6777

154

12

621

9267

11016

1749

15,9

PAN

6335

144

11

816

7273

10816

3543

32,8

PAN

6479

148

8

954

7316

10415

3099

29,8

PAN

6573

151

13

965

7945

11348

3403

30,0

PAN

6243

155

6

1023

7585

10358

2773

26,8

PAN

6823

148

10

1080

7900

10253

2353

23,0

PAN

6633

146

24

1193

7143

10911

3768

34,5

PAN

6480

150

10

1224

7578

10233

2655

26,0

PAN

6615

146

30

1335

5954

11001

5047

45,9

SC

407

138

15

1351

8037

9252

1215

13,1

SC

405

138

8

1368

6531

9991

3460

34,6

PAN

6043

147

44

1410

6777

9993

3216

32,2

PAN

6568

155

13

1446

7942

12558

4616

36,8

PAN

6414

154

22

1448

7346

10883

3537

32,5

LS

8503

161

61

1450

5921

10204

4283

42,0

SNK

2911

138

18

1494

6674

9978

3304

33,1

QS

7608

154

23

1503

6197

9661

3464

35,9

PHI

3203

141

7

1507

7019

11269

4250

37,7

LS

8502

151

6

1538

6296

10637

4341

40,8

NS

9100

155

22

1556

5429

10129

4700

46,4

SNK

2972

147

41

1580

6527

10560

4033

38,2

CRN

3891

152

19

1617

6009

10766

4757

44,2

SNK

2021

143

16

1661

5918

10294

4376

42,5

SNK

2778

154

8

1749

8027

11474

3447

30,0

SNK

2266

148

8

1779

6314

10479

4165

39,7

PAN

6146

148

35

1792

5044

11908

6858

57,6

SNK

2969

151

31

1816

5036

9859

4833

49,0

CRN

3760

157

5

1819

6214

12132

5918

48,8

CRN

4502

144

27

1836

5885

10505

4620

44,0

SNK

2959

154

61

1844

4254

9278

5024

54,1

CRN

7821 BT

137

14

1845

5850

10313

4463

43,3

SNK

2682

149

28

1852

6048

11029

4981

45,2

SNK

2340

146

52

1866

5977

11042

5065

45,9

SNK

2472

148

34

1876

6367

11214

4847

43,2

SNK

2957

150

41

1877

5427

11036

5609

50,8

CRN

3604

152

10

1888

5451

10455

5004

47,9

SNK

2721

144

17

1888

5169

10581

5412

51,2

PAN

6710

138

15

1901

6648

11596

5308

44,4

CRN

3815

140

60

1913

4457

8381

3924

43,2

PAN

6364

138

39

1921

5255

9085

3830

42,2

CRN

3549

150

11

1945

4788

10429

5641

54,1

CRN

3524

143

27

1948

5118

10370

5252

50,6

CRN

3818

150

19

1991

4397

11200

6803

60,7

PAN

6242

153

21

1999

5302

11068

5766

52,1

PAN

6332

143

14

2028

5262

10361

5099

49,2

PHI

3442

147

19

2056

3787

10009

6222

62,2

CRN

3414

151

13

2056

4221

10817

6596

61,0

SNK

2041

138

29

2069

5083

10470

5387

51,5

SNK

2945

150

34

2108

4330

9756

5426

55,6

PHI

P30H22

148

24

2221

3939

11926

7987

67,0

PHI

P33A14

134

9

2223

4677

9887

5210

52,7

1  Maturity in days after planting

2  AUDPC is the area under disease progress curve, the lower the value, the less susceptible to GLS.

Fungicide sprays are therefore still necessary to maintain maize yield potentials in most circumstances. Combination products belonging to the triazole and benzimidazole chemical groups have been registered for use. The reason for use of combination fungicides is part of resistance management strategies aimed at preventing or delaying pathogen-resistance build-up to the fungicides used. The possibility of development of pathogen resistance is much greater if fungicides of a single chemical group (such as the benzimidazoles) are applied alone. Such irresponsible practices could jeopardise future effectiveness of fungicide control.

Details of fungicide spraying appear in "Fungicide Control of Grey Leaf Spot of Maize".

Bibliography

Allison, J.C., and Watson, D.J. 1966. The production and distribution of dry matter in maize after floweing. Ann. Bot. (London) 30: 365-381.

Latterell, F.M., and Rossi, A.E. 1983. Grey leaf spot of maize: A disease on the move. Pant Dis. 67:842-847.

Perkins, J.M., Smith, D.R., Kinsey, J.G. and Dowden, D.C. 1995. Prevalence and control of grey leaf spot. Pages 177-185 in: Prc. Annu. Conf. ILL. Maize Breeders School 31, University of Illinois, Urbana.

Ringer, C.E., and Grybauskas, A.P. 1995. Infection cycle components and disease progress of grey leaf spot on field cover. Plant Dis. 79:24-28.

Ward, J.M.J. 1996. Epidemiology of grey leaf spot: A new disease of maize in South Africa. Ph.D. Thesis. University of Natal. Pietermaritzburg, 3200, South Africa.

Ward, J.M.J., Stromberg, E.L., Nowell, D.C., and Nutter, F.W. Grey leaf spot, a disease of global importance in maize production. Plant Dis. 83:884-895.

     
      
Allelopathy Acid Soils & Liming Animal Requirements Apples & Pears in KZN - IPDM Bananas in KwaZulu-Natal Cashmere Production from Goats Cherries in KZN - IPDM Cowpeas - Production in KZN Crop Residues for Animal Feeding Cyperus esculentus - Yellow nutsedge Cyperus rotundus - Purple nutsedge Subsistence Dairying in KZN Electric Fencing in Agriculture Farm Business Strategy - Planning Farming with Fish Feedlot Options for Small Scale Farmers Fertilizer usage in KwaZulu-Natal Fertilizers Fodder Radish (Japanese Radish) Forage Sorghum Cultivars - Evaluation Goat Production in KwaZulu-Natal Grey Leaf Spot of Maize Grazing Habits of Different Animals Grazing Capacity - Calculation Grazing Capacity Holistic Resource Management Identification Markings Insect Pests of Maize in KwaZulu-Natal Establishment of Kikuyu Reproduction in Livestock Macadamia Fertilization
Copyright 2005 by DAEA    Privacy Statement