Electronic Journal of Polish Agricultural Universities (EJPAU) founded by all Polish Agriculture Universities presents original papers and review articles relevant to all aspects of agricultural sciences. It is target for persons working both in science and industry,regulatory agencies or teaching in agricultural sector. Covered by IFIS Publishing (Food Science and Technology Abstracts), ELSEVIER Science - Food Science and Technology Program, CAS USA (Chemical Abstracts), CABI Publishing UK and ALPSP (Association of Learned and Professional Society Publisher - full membership). Presented in the Master List of Thomson ISI.
2005
Volume 8
Issue 4
Topic:
Horticulture
ELECTRONIC
JOURNAL OF
POLISH
AGRICULTURAL
UNIVERSITIES
Jamiołkowska A. , Wagner A. 2005. FUNGAL COMMUNITIES FROM THE RHIZOSPHERE OF TOMATO CULTIVATED CONVENTIONALLY AND WITH RYE AS COVER CROP, EJPAU 8(4), #23.
Available Online: http://www.ejpau.media.pl/volume8/issue4/art-23.html

FUNGAL COMMUNITIES FROM THE RHIZOSPHERE OF TOMATO CULTIVATED CONVENTIONALLY AND WITH RYE AS COVER CROP

Agnieszka Jamiołkowska1, Anna Wagner2
1 Department of Plant Protection and Quarantine, Faculty of Horticulture and Landscape Architecture, University of Life Sciences in Lublin, Poland
2 Department of Plant Protection and Quarantine, University of Life Sciences in Lublin, Poland

 

ABSTRACT

Fungal communities from the rhizosphere of tomato grown conventionally and in rye mulch were analyzed in 1998-2000. Their compositions depended on the type of cultivation and development phase of plant. The frequency of Fusarium equiseti, Aureobasidium pullulans, Talaromyces flavus and Penicillium spp. was higher in the soil amended with rye. Trichoderma spp. populations were similar in both environments but more numerous in August than in June. Rye mulch significantly affected the number of Fusarium oxysporum f.sp. lycopersici. The number of its isolates observed in the soil with cover crop was significantly lower than in control field.

Key words: cover crop, rye, tomato, soil-borne fungi, Fusarium oxysporum f.sp. lycopersici.

INTRODUCTION

In Poland the interest in alternate methods of vegetables cultivation is increasing recently due to the necessity of developing sustainable agricultural systems reducing chemical control of weeds and plant pathogens [7]. One of these methods is using cover crops to grow vegetables without tillage what not only reduce production costs but also increase soil fertility and suppress weeds [1, 2].

Grass crops protect the soil against erosion and nutrient leaching. By improving water infiltration they are conducive to early cultivation of vegetables in temperate climate. Rye is one of grass crops recommended both as off-season crop and as mulch for many cash crops. Apart from improving soil proprieties, cover crops can play an important role in the control of soil-borne pathogens [3, 16, 18]. The aim of this work was to investigate fungal communities developing in soil environment of tomato grown conventionally and in rye mulch without tillage.

MATERIALS AND METHODS

The experiments were conducted in 1998-2000 in the Felin Experimental Farm (near Lublin) on loess soil. Tomato plants of cv. Rumba were grown in two ways: conventionally (control) and with rye mulch without tillage on the plots of 100 m2 each. Rye of cv. Dankowskie was sown the previous autumn and in the spring, when plants were 50 cm high, it was treated with Roundup 360 SL (1444 g·ha-1). After two weeks, when dry mulch covered fully the surface, tomato seedlings were planted directly into the mulch. Control field was prepared in the traditional way. In 2nd and 5th weeks tomato plants were fertilized with Norway and lime salpetre (50 kg·ha-1).

Soil from tomato rhizosphere was sampled twice a year (1st week of June and 3rd week of August) according to the method described by Lemańczyk and Sadowski [12]. Fungi isolation was carried out using Warcup’s plate method modified by Mańka [13]. Plates (50 for each combination) containing about 25 mg of soil-sand mixture were filled with Martin medium [14], incubated for 5 days and then the colonies of fungi were transferred into the tubes with PDA slants. Fungi growing from soil were identified with mycological monographs.

RESULTS

Over three years of investigations, in June 697 fungal isolates were obtained from rye mulch field and 614 from control field. This compares to 1073 isolates in August from cover crop field and 645 from control field in August (tab. 1, 2). Fungal communities isolated from the soil with rye mulch contained more species than those from the control field. The composition of communities differed also between June and August although some species were common in both seasons. The highest number of colonies belonged to Fusarium spp., Penicillium spp., Trichoderma spp., Aureobasidium pullulans and Talaromyces flavus. Among pathogenic fungi, F. oxysporum f.sp. lycopersici was isolated from all soil samples. However, the population of this pathogen in soil amended with rye mulch was less numerous (1.4-1.5% of all isolates) than in soil from control field (6.4-12.6%). The pathogen was isolated most frequently in August 1999 from control field, while at the same time its population was the smallest in the soil amended with rye mulch. F. solani occurred in control field in all years of investigations but from the field with cover crop that fungus was isolated only in 1999. F. culmorum was obtained more frequently only in June 1998 from rye mulch field. In other fungal communities it occurred sporadically. Non pathogenic to tomato F. equiseti predominated in August 1998 in both combinations but in other years that species occurred only in the rhizosphere of tomato grown with cover crop (tab. 1, 2).

Table 1. Fungi isolated from rhizosphere of tomato grown conventionally and in rye mulch in June

Species of fungi

Rye

Control

1998

1999

2000

S

%

1998

1999

2000

S

%

Alternaria alternata (Fr.) Keiss.

1

 

11

12

1.7

1

   

1

0.2

Aureobasidium pullulans (de By) Am

1

26

26

53

7.6

5

38

4

47

7.6

Fusarium culmorum (Smith) Sacc.

 

1

 

1

0.1

 

1

 

1

0.2

Fusarium equiseti (Corda) Sacc.

3

   

3

0.4

4

 

4

8

1.3

Fusarium oxysporum Schlecht.

3

4

3

10

1.4

12

14

13

39

6.4

Fusarium solani (Mart.) Sacc.

 

4

 

4

0.6

 

6

 

6

1.0

Gliocladium fimbriatum Gilman et Abbott

   

2

2

0.3

16

   

16

2.6

Gliocladium roseum (Link) Thom

   

10

10

1.4

         

Mortierella isabellina (Oud) Zycha

7

   

7

1.0

24

   

24

3.9

Mortierella pusilla Oud.

9

   

9

1.3

18

   

18

2.9

Penicillium chrysogenum Thom

 

69

 

69

9.9

 

1

 

1

0.2

Penicillium cyclopium West.

3

97

2

102

14.6

 

13

29

42

6.8

Penicillium janczewskii Zaleski

10

54

21

85

12.2

19

73

12

104

16.9

Penicillium janthinellum Biourge

8

7

4

19

2.7

9

14

2

25

4.1

Penicillium restrictum Gilman et Abbott

 

80

3

83

11.9

 

79

21

100

16.3

Talaromyces flavus (Klöcker) Stolk et Samson

3

32

5

40

5.7

 

34

 

35

5.7

Trichoderma aureoviride Rifai

2

7

4

13

1.9

 

20

 

20

3.3

Trichoderma hamatum (Bonord) Bain

2

16

 

18

2.6

1

20

2

23

3.7

Trichoderma harzianum Rifai

1

44

12

57

8.2

 

12

30

42

6.8

Trichoderma koningii Oud.

2

8

 

10

1.4

3

11

 

14

2.3

Trichoderma longibrachiatum Rifai

 

15

 

15

2.2

         

Trichoderma viride Pers.

1

16

 

17

2.3

 

5

 

5

0.8

Others*

32

2

24

58

8.3

31

3

9

43

7.0

Total

88

482

127

697

 

143

344

126

614

 
*Other non pathogenic less frequent fungi:
Mucor hiemalis Wehmer – 9, Penicillium fellutanum Biourge – 9, Mortierella subtillissima Oudemans – 8, Zygorhynchus heterogamus (Vuill.) Vuill. – 7, Verticillium tenerum Ness – 6, Chaetomium funicola Cooke – 5, Cladosporium cladosporioides (Fres.) de Vries – 5, Humicola grisea Domsch – 5, Mammaria echinobotryoides Ces. – 4, Microdochium nivale (Fr.) Samuels et Hallet – 5, Penicillium canescens Sopp – 4, Aspergillus fumigatus Fres. – 3, Humicola brevis Gilman et Abbott – 3, Humicola fuscoatra Traaen – 3, Sepedonium chrysospermum (Bulliard) Fries – 3, Acremonium strictum W. Gams – 2, Epicoccum purpurascens Ehr. Ex Schlecht. – 2, Gilmaniella humicola Barron – 2, Gliocladium penicillioides Corda – 2, Hormiactis candida v. Höhnel – 1, Phoma destructiva Plowr. – 1, Phoma medicaginis Malbr. et Roum. – 1, Scopulariopsis brumptii Salvanet-Duval – 1, non sporulating – 10.

Table 2. Fungi isolated from rhizosphere of tomato grown conventionally and in rye mulch in August

Species of fungi

Rye

Control

1998

1999

2000

S

%

1998

1999

2000

S

%

Alternaria alternata (Fr.) Keiss.

15

1

1

17

1.6

13

1

 

14

2.2

Aspergillus flavus Link ex Gray

 

28

1

29

2.7

 

64

 

64

9.9

Aureobasidium pullulans (de By) Arn

 

17

5

22

2.1

         

Botrytis cinerea Pers.

         

2

   

2

0.3

Fusarium culmorum (Smith) Sacc.

12

   

12

1.1

1

   

1

0.2

Fusarium equiseti (Corda) Sacc.

106

3

2

111

10.3

34

   

34

5.3

Fusarium oxysporum Schlecht.

5

5

6

16

1.5

3

68

10

81

12.6

Fusarium solani (Mart.) Sacc.

 

10

 

10

0.9

6

 

13

19

2.9

Gliocladium fimbriatum Gilman et Abbott

 

9

16

25

2.3

1

 

1

2

0.3

Humicola grisea Domsch

8

6

 

14

1.3

8

   

8

1.2

Mortierella pusilla Oud.

7

   

7

0.7

26

 

3

29

4.5

Mucor hiemalis Wehm.

19

   

19

1.8

8

 

1

9

1.4

Penicillium cyclopium Westl.

100

14

40

154

14.4

81

 

30

111

17.2

Penicillium janthinellum Biourge

 

2

23

25

2.3

8

15

 

23

3.6

Penicillium janczewskii Zaleski

 

80

76

156

14.6

 

5

5

10

1.6

Penicillium restrictum Gilman et Abbott

 

137

1

138

12.9

         

Sclerotinia sclerotiorum (Lib.) de By

1

   

1

0.1

         

Talaromyces flavus (Klöcker) Stolk et Samson

 

56

1

57

5.3

   

1

1

0.2

Trichoderma aureoviride Rifai

 

1

 

1

0.1

 

50

 

50

7.8

Trichoderma hamatum (Bonord) Bain

10

39

49

98

9.1

8

86

1

95

14.7

Trichoderma harzianum Rifai

 

15

55

60

5.6

4

9

43

56

8.7

Trichoderma koningii Oud.

4

 

45

49

4.6

4

 

4

8

1.2

Others*

24

7

11

42

3.9

13

5

6

24

3.7

Total

311

430

332

1073

 

220

303

118

641

 
*Other non pathogenic less frequent fungi:
Gliocladium roseum (Link) Thom – 9, Mucor circinelloides van Tiegh. – 9, Penicillium granulatum Bain. – 8, Zygorhynchus heterogamus (Vuill.) Vuill. – 7, Penicillium ochraceum (Bain.) Thom – 4, Chaetomium funicola Cooke – 2, Penicillium aurantio-violaceum Biourge – 2, Penicillium chermesinum Biourge – 2, Scopulariopsis brevicaulis (Sacc.) Bain. – 2, Acremonium roseum (Oud.) W. Gams – 1, Gliocladium catenulatum Gilman et Abbott – 1, Mucor globosus Fisch. – 1, Penicillium funiculosum Thom – 1, Penicillium viridicatum Westl. – 1, Trichoderma viride Pers. – 1, non sporulating – 15.

Saprobiotic fungi predominated in all fungal communities. Penicillium spp. occurred in all soil samples but they were isolated more frequently from rye mulch field, especially in 1999. The populations of these fungi in the soil from cover crop field was generally similar in both seasons even if there were differences in species composition, while in control field Penicillium spp. were less numerous in August (with the exception of P. cyclopium in 1998). The frequency and species composition of Trichoderma spp. differed from year to year but generally the populations of these fungi were similar in both combinations. However, at earlier phase of tomato growth, more Trichoderma isolates were collected from rye mulch field. Aureobasidium pullulans amounted to similar percentage of all isolates in both investigated soils in June but in August that species was isolated only from cover crop field in 1999 and 2000. In the soil amended with rye, T. flavus populations were numerous in June 1999 as well as in August 1998 and 2000 while in control field it occurred only in June 1999. Regarding other saprobiotic fungi, the differences in their numbers were noticed between seasons, years and types of cultivation.

DISCUSSION

The research showed the influence of type of cultivation on fungal communities in tomato rhizosphere. Fungal communities from the soil under tomato grown in rye mulch were more diversified but some fungi occurred every year in both fields, particularly Fusarium spp., Penicillium spp., Trichoderma spp., A. pullulans and T. flavus. Those fungi are typical colonizers of soil environment of many crops, including tomato [11, 19]. However, the frequency of F. oxysporum f. sp. lycopersici was significantly lower in the rhizosphere of tomato grown in rye mulch. Rye could influence soil mycoflora both as living crop and as mulch. Root exudates of rye contain some compounds that can directly induce plant resistance [4]. Rye residues and components produced during decay process are also nutrient basis for many soil-borne microorganisms, what results in the increase of their populations [8, 16]. As rye prevents leaching of nitrogen, it could be responsible for numerous colonies of nitrofilious Penicillium spp. [15, 17]. Some of these species are antagonistic to F. oxysporum [9, 11], therefore their presence in tomato rizosphere can reduce the population of pathogen both by competition and by antibiosis. The same conditions favor T. flavus, frequently isolated, particularly in summer, from the rhizosphere of tomato grown in rye mulch.

Species of Trichoderma were isolated more frequently in August, probably due to higher soil temperature [10]. Their ability to produce antibiotics is enhanced in higher temperature. However, the production and activity of antibiotics is decreasing with the increase of soil pH [6]. The pH of investigated soil amounted to 5.5, what together with lower temperature in spring could have an adverse effect on Trichoderma activity in the rhizosphere. Numerous isolates of A. pullulans in rye mulch field are due to earlier colonization of rye roots [19]. F. equiseti is also related to cereals soil environment [12], therefore the numerous population of this fungus in rye amended soil is easy to explain. The presence of F. equiseti, a plant growth promoting fungus, can indicate an inhibitory effect of rye mulch. Horinouchi and Hyakumachi [5] proved a suppressive effect of this species on F. oxysporum f. sp. lycopersici.

CONCLUSIONS

  1. Effect of rye, as cover crop on the population of F. oxysporum in tomato rhizosphere was significant. The number of F. oxysporum isolates collected from this environment was significantly lower than those obtained from the soil under tomato grown conventionally.

  2. The populations of F. equiseti, Penicillium spp., A. pullulans and T. flavous were more numerous in the soil amended with rye mulch.

  3. Trichoderma spp. colonized the rhizosphere of tomato every year irrespective of type of cultivation but their frequency was higher in August.


REFERENCES

  1. Abdul-Baki A.A., Teasdale J.R., Korcak R., Chitwood D.J., Huettel R.N., 1996. Fresh market tomato production in a low-input alternative system using cover crop mulch. HortScience 31, 65-69.

  2. Borowy A., Jelonkiewicz M., 1998. Weed infestation and yielding of three vegetable crops in no-tillage cultivation using rye seeded in the spring as a cover crop. Acta Horticulturae et Regioculturae I, 181-182.

  3. Bottenberg H., Masiunas J., Eastman C., Eastburn D., 1997. The impact of rye cover crops on weeds, insects and diseases in snapbean cropping systems. Journal of Sustainable Agriculture 9 (2/3), 131-155.

  4. Funck-Jensen D., Hockenhull D., 1984. Root exudation, rhizosphere microorganisms and disease control. Vaxtskyddsnotiser 48, 49-54.

  5. Horinouchi H., Hyakumachi M., 2002. Control of Fusarium wilt of tomato in soil system by combination of plant growth promoting fungus, Fusarium equisei, and biodegradable pots. IOBC wprs Bulletin 25 (10), 207-210.

  6. Howell C.R., 1998. In: Harman G.E. and Kubicek C.P. (eds), Trichoderma and Gliocladium. Vol. 2. Taylor & Francis, London, UK and Bristol, USA, pp. 173-184.

  7. Hoyt G.D., Hargrove W.L., 1986. Legume cover crops for improving crop and soil management in southern United States. HortScience 21, 397-401.

  8. Huber D., Watson R.D., 1970. Effects of organic amendments on soil-borne pathogens. Phytopathology 60, 22-26.

  9. Jamiołkowska A., Wagner A., 2003. Effect of field pea (Pisum arvense) as cover crop on fungal communities from soil environment of tomato and their influence on Fusarium oxysporum growth. Phytopathologia Polonica 30, 37-50.

  10. Kredics L., Manczinger L., Antal Z., Molnar A., Kevei F., Nagy E., 2002. Effects of abiotic and biotic factors on Trichoderma strains with biocontrol potential. IOBC wprs Bulletin 25 (10), 407-410.

  11. Kurzawińska H., Pacyna E., 2000. Fungi isolated from substrate of tomato plants and their effect on the growth of two tomato pathogens. Phytopathologia Polonica 20, 115-121.

  12. Lemańczyk G., Sadowski C. K., 2000. The effect of different forecrops on the occurrence of Fusarium spp. in winter wheat rhizosphere. Phytopathologia Polonica 20, 131-138.

  13. Mańka K., 1974. Zbiorowiska grzybów jako kryterium oceny wpływu środowiska na choroby roślin (Fungal communities as an evaluation test of environment impact on plant diseases). Zesz. Problem. Postęp. Nauk Roln. 160, 9-23.

  14. Martin J.P., 1950. Use of acid, rose-bengal and streptomycin in the plate method estimating soil fungi. Soil Sci. 69, 215-232.

  15. Mc Cracken D.V., Smith M.S., Grove J.H., MacKown C.T., Blevins R.L., 1994. Nitrate leaching as influenced by cover cropping and nitrogen source. Soil Science Society of America Journal 58, 1476-1483.

  16. Pięta D., Pastucha A., Patkowska E., 1999. The effect of organic substance on the healthiness and yielding of soybean (Glycine max (L.) Merrill). Annals of Agricultural Sciences, S. E: Plant Protection 28 (1/2).

  17. Pląskowska E., 1997. Effect of communities of soil fungi on the growth of some pathogens which cause foot-rot complex in wheat cultivated after different crops. Phytopathologia Polonica 13, 109-132.

  18. Smeda R.J., Weller S.C., 1996. Potential of rye (Secale cereale) for weed management in transplant tomatoes (Lycopersicum esculentum). Weed Science 44, 596-602.

  19. Wagner A., 1996. Effect of fungal communities from soil environment of winter wheat (Triticum aestivum L.) grown in crop rotation and monoculture on the growth of Rhizoctonia solani Kühn. Phytopathologia Polonica 11, 67-83.


Agnieszka Jamiołkowska
Department of Plant Protection and Quarantine, Faculty of Horticulture and Landscape Architecture, University of Life Sciences in Lublin, Poland
phone: (+48 81) 532-30-47
7 Leszczynskiego Street
20-069 Lublin
Poland
email: aguto@wp.pl

Anna Wagner
Department of Plant Protection and Quarantine,
University of Life Sciences in Lublin, Poland
phone: (+48 81) 524 81 32
email: aguto@wp.pl

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