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93

August 2018

M. javanica

or mixed populations. Several of the weed species

screened were excellent and/or good hosts of either

M. incognita

,

M. javanica

and/or mixed populations of the two species.

Although

T. minuta

is generally being referred to as a non- or

poor host for a variety of nematode pests, results from this study

showed that it has the potential to serve as a good host for mono-

culture

M. javanica

populations as well as mixed populations of

M. incog-nita

and

M. javanica

.

Future prospects

Notwithstanding this study on weeds, variable host efficiency of

root-knot nematodes has been demonstrated for a range of crops

by other authors. A probable explanation for this is the exposure

of weeds to different populations of

M. javanica

and

M. incognita

and/or mixed root-knot nematode species (

M. incognit

a and

M. javanica

) as a result of our study.

The occurrence of mixed root-knot nematode species populations

in particular is experienced in South African agricultural soils,

where

M. incognita

and

M. javanica

often occur together.

The phenomenon of variable host suitability needs to be studied ex-

tensively by screening the weed species to different

populations of

Meloidogyne

species, since such an

approach will provide more insight in this regard.

WEED SPECIES

KURUMAN

NELSPRUIT

POTCHEFSTROOM

Amaranthus cruentus (Arusha)

11,4 (41 125) ef

7,6 (832) bcde

8 (1 336) ab

Amaranthus hybridus

7,5 (461) abc

8,1 (605) bcdef

8,8 (931) ab

Amaranthus tricolor

9,8 (659) cdef

8,1 (1 260) bcdef

8,8 (3 043) ab

Bidens bipinnata

5,6 (134) a

5,8 (10 925) abc

7,2 (203 ab

Chenopodium carinatum

8,2 (2 276) abcd

8,3 (2 981) bcdefg

8 (638) ab

Cleome gynandra

8,9 (1 800) abc

8 (823) bcdef

7,5 (348) ab

Corchorus trilocularis

10,5 (10 704) def

9,7 (48 431) efgh

7,9 (391) ab

Crotalaria sphaerocarpa

7 (263) abc

10,5 (4 2685) efgh

8,3 (356) ab

Cynodon dactylon

8,3 (668) abcd

6,2 (116) abcd

8,5 (519) ab

Cyperus rotundus

9 (3 475) bcde

5,8 (121) abc

7,6 (1 318) ab

Datura ferox

7,6 (792) abcd

5,9 (79) abc

7 (489) ab

Datura stramonium

7,1 (1 194) abc

6,1 (97) abcd

7,9 (338) ab

Eleusine corocana

9,9 (66 810) cdef

5,3 (155) ab

7,7(297) ab

Hibiscus trionum

1

12,5 (34 649) a

12,3 (32 882) h

12,4 (27 344) c

Ipomoea purpurea

8,7 (1 091) bcde

11 (21 322) fgh

9,3 (1 628) bc

Sorghum bicolor

6,6 (228) ab

3,1 (214) a

7,7 (18 043) ab

Solanum nigrum

8,8 (4 568) abcde

11,5 (32 854) gh

9,5 (70 763) bc

Solanum retroflexum

12,5 (171 746) a

9,2 (274) defgh

9,3 (11 177) bc

Tagetes minuta

2

8 (2 390) abcd

8,6 (1 821) cdefg

5,6 (50) a

Urochloa panicoides

7,3 (58) abc

9,2 (47) defgh

6,6 (215) ab

P value

0,0000

0,0000

0,0000

F ratio

9,255

14,37

4,268

1

Good-host standard;

2

Poor-host standard;

3

Ln(x+1) transformed data with real means in parenthesis

Figure 1: Principal Component

Analysis (PCA) indicating (A)

the relative position of the dif-

ferent

Meloidogyne

species with

regards to the host reaction of

20 weed species that were evalu-

ated against, at three on-farm field

sites and (B) the difference in

susceptibility levels of the weed

species to these root-knot nema-

tode species.

Table 1: Root-knot nematode eggs and second-stage juvenile (J2) population levels 50 g/roots of 20 weed species

grown in field, three sites.