Management Approaches:
Host Plants
Wild Hosts
Most African cereal stem borers are generally polyphagous and have
several graminaceous and other wild hosts, in addition to more than one
cultivated crop. Several non-cultivated wild host plants of
these stem borers have been recorded and documented by various
workers. As might be expected, the spectrum of wild, non-crop
hosts attacked by stem borers is vast. No doubt, the number of
actual wild hosts is even greater, given that stem-borer damage to wild
grasses is unlikely to be investigated. Hosts are found in
three main families - Cyperaceae, Gramineae (Poaceae)
and Typhaceae. An extensive survey carried out by the
International Centre of Insect Physiology and Ecology (ICIPE) scientists
during 1994-1997, were every possible kind of host plant was examined at
different times of the year in various agroecologies throughout Kenya,
resulted in the compilation of Table
2. No plant was given host-plant status until any larva
found in it had been reared through to the adult stage.
In the past, many host-range records did not take into account how the
plant-insect association was determined. In nature, an insect
locates a host plant through a sequence of behavioural
responses. In the laboratory, feeding a larva in a closed
environment ignores the natural feeding process and only measures the
insect's acceptance of the plant as food. Also, increasing
evidence indicates that the host ranges and economic importance of most
insects are dynamic, and often location- and time-specific. For
example, B. fusca, C. orichalcocilieus, E. saccharina
and S. calamistis, the major African stem borers, originally would
have attacked only wild graminaceous plants in tropical and subtropical
parts of the continent. As long as there were only wild plants,
these insects were of no special consequence. After the
introduction and cultivation of maize and extensive planting of sorghum in
vast areas of Africa where they did not occur originally, the insects
followed the cultivated forms of their host plants and became more widely
distributed and of economic importance. In Africa, where the
bulk of maize and sorghum is grown only on small plots surrounded by land
occupied by wild graminaceous plants, these stem borers, which are
normally associated with grasses, infest the cultivated crops in high
populations, due to the presence of wild grass hosts in the immediate
neighbourhood. On the other hand, C. partellus, a
species indigenous to Asia which has become established in East and
Southern Africa, is also polyphagous and attacks several wild host plants.
Some authors have argued that the presence of alternative borer hosts
in cereal-growing areas is detrimental in serving as a stem-borer
reservoir, whereas others have pointed out that natural enemies can
persist and increase their populations during the non-growing season,
thanks to these alternative borer hosts. For example, Napier
grass, Pennisetum purpureum, which is an important pasture grass,
is often encountered as a host of stem borers, and may be important in
some areas as a reservoir host of stem-borer species. Several
wild sedges (Cyperus spp.) are known to be the natural hosts of E.
saccharina. Table
2 summarizes recent surveys, by the second author, of infestation of
wild graminaceous hosts by various borers species in different
agroecological zones in Kenya. These data are far from complete
at this time of writing, and, in particular, the presence of non-economic
species of Busseola and Sesamia, provisionally identified as
B. fusca and S. calamistis, need to be
investigated. In addition, several Chilo species, apart
from C. partellus, are no doubt present, but have not yet been
identified to species level. However, the occurrence of borers,
Phargmataecia boisduvalli (Herrich-Shaeffer) (Cossidae), Bactra
stagnicolana Zellet (Tortricidae) and Poenoma serrata (Hampson)
(Noctuidae) on some of these wild hosts, the first two never found on
cereals, is of interest. Of particular interest is the fact
that some of these borers can and do act as reservoir hosts for natural
enemies of economically important borers; for example, the braconid wasp Stenobracon
rufus attacks P. biosduvalii.
There are plenty of examples illustrating the importance of
uncultivated land as a source of pests for adjacent
crops. However, there is not now, nor does it seem there could
be, a general theory that will predict the role of uncultivated land in
insect invasions and outbreaks in cultivated crops. The overall
value of uncultivated land will have to be judged on a case-by-case basis,
depending on the ecological mechanisms underlying the various
disadvantages and advantages. In cultivated crops, most of
which are short-lived in comparison with natural communities, damage is
typically caused by herbivores that migrate into fields from the
outside. These wild habitats often harbour food sources for
many pest-insect species, and they may encourage insect invasion and
outbreaks in neighbouring agroecosystems. It is also possible
that the presence of wild crop relatives in nearby habitats could result
in the maintenance of genetic diversity in local, relatively non-vagile
insect populations, leading to the emergence of new strains or biotypes
that could overcome host-plant resistance.
On the other hand, wild hosts adjacent to cultivated crops can provide
extremely important refugia for natural enemies, as well as sources of
nectar, pollen and host/alternative prey. There are also
several examples of adjacent wild habitats being used to suppress insect
outbreaks by keeping the pest on the so-called wild trap
plants. Furthermore, non-host plants intercropped with cereals
have also been shown to have a significant effect on stem-borer
damage. In trials at ICIPE, molasses grass (Melinis
minutiflora) intercropped with maize or sorghum significantly
decreased levels of infestation by stem borers and also increased larval
parasitism of stem borers by the braconid, Cotesia sesamiae (Khan
et al., 1997)
During the off-season, when there are no cultivated crops in the field,
in addition to the hibernating or diapausing populations in crop residues,
stem borers remain present on wild host plants and infest the cultivated
hosts after they are planted. Although some basic information
on the wild habitats as hosts of cereal stem borers in Africa is
available, from the applied perpective, a systematic study of the dynamic
relationship between the populations of insects in wild host plants and
those on cultivated crops is important for the development of a
sustainable integrated pest management (IPM) approach for cereal stem
borers. A more complete understanding of the role of such wild
hosts in insect outbreaks will generate suitable management strategies for
stem borers. Appropriate methods of detecting migrants from
wild habitats to cultivated crops and the information on the precise role
of wild habits in stem-borer invasion of cereal crops are
needed. We also need to update and advance our knowledge on the
phenomenon of cereal stem-borer outbreaks in Africa. By
discovering what accoujnts for differencesbetween natural systems and
agroecosystems, we can learn much about the underlying ecological
processes that create the observed patterns of distribution and abundance
of stem borers in nature, and about those chemical features that protect
wild plants from herbivores. Plant breeders and entomologists
can use this information in developing resistant/tolerant crop cultivars.
In addition, the information on the roles of wild habitats in providing
refugia for natural enemies and the possible use of wild hosts in strip
cropping and as trap crops will be helpfull in the management of stem
borers in a cropping system. Such knowledge can be used to
strengthen and sustain the impact of IPM strategies.
Further studies on wild stem-borer hosts, taking into account local
conditions, are currently underway in West Africa (International Institute
of Tropical Agriculture) (IITA, Benin) and East Africa (ICIPE, Kenya).
Major references: Acland
(1971);
Harrison
(1981); Rouanet
(1984); Ibekwe
(1986). |