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COCONUT LEAF-MINING BEETLE Promecotheca reichei
Baly -- Chrysomelidae (Contacts) Native to Fiji, the coconut
leaf-mining beetle was originally under natural control by native natural
enemies. However, in the 1880's as
trade developed and coconuts became extensively cultivated, the beetle
gradually became a serious pest (DeBach 1974). Larvae bore within the leaflets and adult beetles feed on the
leaves externally. In heavy
infestations they caused a reduction of ca. 75% in the leaf surface of most
trees in a planting (Taylor 1936, 1937).
Detailed studies of the beetle and its natural
enemies were not made until 1929 when sufficient entomological expertise
became available. It was found that
all severe outbreaks had one unusual feature in common: only one stage of the insect was present
at any one time, and there were no overlapping generations. This was considered atypical in the
tropical climate of Fiji where reproduction can continue year round. Studies showed that beetle outbreaks were
due to the indirect adverse effects of a predatory mite, Pediculoides ventricosus (Newport), on two
native parasitic species which were capable of controlling the beetle in its
absence. The mite was probably
accidentally introduced to Fiji, as it is now known to be cosmopolitan and
feeds on a great variety of insects.
This mite caused an even-brooded condition of the beetle and this
resulted in the native parasitoids being rendered ineffective because they
attacked only the larval stages and these were mostly lacking for long
periods of time because of the even-brooded situation. The mite attacked all larval stages and the
pupae of the beetle but not adults or eggs.
In dry seasons it increased with incredible rapidity and would destroy
all the beetles except eggs and adults in a given locality. The adults laid eggs and died and this
later resulted in the single-stage condition consisting principally of beetle
larvae, but meanwhile the predatory mite population crashed because of food
shortage when only adult beetles and eggs were present (DeBach 1974). With onset of the wet season the beetles
increased very rapidly in the absence of significant parasitism and because
the mite was inactive during wet periods.
Dr. T. H. C. Taylor concluded that the mite would have replaced the
indigenous parasitoids and done effective control had it not been decimated
by wet weather each year. In areas of
Fiji with continuous wet weather the beetle seldom became a serious pest,
probably because the mite was held down and the native parasitoids operated
without interference. It was then considered that new parasitoids be
found, those with a set of quite definite characteristics that could cope
with the single-brooded condition.
These included mainly (1) the parasitoid should have a more rapid rate
of increase relative to the pest than the native parasitoids, and one
generation must require no longer than one month, (2) adults of the
parasitoid should be able to survive the long periods when no individuals of
the pest were in a suitable stage for its attack, and (3) it should
parasitize all larval stages as well as pupae of the host so that suitable
hosts would be available over a much longer period in each pest generation
than for a parasite species which attacked only one stage, and therefore the
period during which the new parasitoid would lack suitable hosts would be
correspondingly shorter. Also it
would be good if the parasitoid were internal, very active and capable of
rapid dispersal and tolerance of the climatic conditions in Fiji. No candidate parasitoids with the above
characteristics were known at the time , but in 1930 R. W. Paine's
investigations in Java resulted in the discovery of a large number of
parasitoids of a related species of Promecotheca
(P. nuciferae Maulik). This beetle occurred throughout Java but
was never a pest. Taylor followed up
with detailed studies of the Javanese parasitoids and concluded that only one
of the parasitoids, Pleurotropis
parvulus Ferriere, met the
conditions desired in a new parasitoid, even though this species was
considered to be one of the least important of the complex controlling its
host in Java. Pleurotropis parvulus
attacks all stages of larvae as well as the pupae of Promecotheca, and many individuals develop in each host
individual giving it a high potential rate of increase with respect to the
host. The life cycle is only about
three weeks long as compared to almost 3 1/2 months for the beetle in Fiji
and more importantly, the adult parasitoids live for 5 1/2 weeks which
enables them to survive periods when suitable stages of the host are rare or
absent. The parasitoids were shipped from Java to Fiji
in six large wire-gauze cages each containing four seedling coconut palms
heavily infested with Promecotheca
nuciferae of all
stages. Parasitoids were included in
the cages and were able to reproduce during the voyage. Taylor left Batavia, Java on April 17,
1933 on the S. S. Van Rees
which traveled from Singapore to Sydney via Java, New Guinea, New Hebrides
and New Caledonia. It was necessary
to trans-ship at Noumea, New Caledonia on May 10 to the S. S. Kareta in order to go on to
Suva, Fiji, where he arrived on May 14.
Before arrival in Noumea (4 days from Fiji) all palms, soil,
containers, etc. were thrown overboard to eliminate any potential pest
hazards, after all parasitoids and parasitized larvae and pupae of the host
had been placed into glass tubes.
From Suva it was necessary to proceed at once on a chartered motor
launch to the Lau group of islands where beetle problems were severe. They arrived at Nabavatu on Vanua Balavu
on May 24 (37 days out of Java), where an insectary were set up. Some 1,200 adults and pupae of P. parvulus arrived in good condition. Taylor also imported the two parasitic
species considered most important in Java as an additional precaution. Only one, Dimmockia javanica
Ferr., was successfully introduced, cultured and liberated in sufficient
numbers, but it failed to establish. The first liberations of P. parvulus
were made on May 26, 1933 and were continued to April 30, 1934, when so many
parasitoids were present in the field that insectary rearing was no longer
necessary. Within a year it had
completely controlled all the severe outbreaks of Promecotheca on Vanua Balavu, Kanacea, Taveuni, Mago,
Lakeba and others. Taylor recorded
that it literally attained 100% parasitism on all trees, even though in many
outbreaks every three over hundreds of acres of land bore about 4,000 beetle
individuals. At the first peak of the
parasitoid explosion, about 5,000 adult parasitoids were emerging per tree
daily and this continued for about 10 days (the parasitoid is
gregarious). Not a single Promecotheca individual escaped
in many outbreak areas and the parasitoid dispersed so well that it
controlled the pest even on isolated coconut trees hidden in the forest
(DeBach 1974). As it turned out the parasitoid had the
disadvantage of being too effective. On
small islets or very isolated spots of coconuts it would exterminate the pest
and then die out itself. This
required reintroduction of the parasitoid if the beetle reinvaded. However, this never occurred on larger
islands or estates, and today the coconut leaf-mining beetle is rare and of
no economic importance. DeBach (1974)
considers this biological control project to be unique in the annals of
biological control, because preselection concentrated on a parasitic species
that was considered of lesser importance in its place of origin. REFERENCES: [Additional
references may be found at: MELVYL
Library ] DeBach,
P. 1974. Biological Control by Natural Enemies. Cambridge University Press, London &
New York. 323 p. Taylor,
T. H. C. 1936. The biological control of the coconut leaf
miner (Promecotheca reichei Baly) in Fiji. Agric. J. Fiji 8: 17-21. Taylor,
T. H. C. 1937. The biological control of an insect in
Fiji. An account of the coconut
leaf-mining beetle and its parasite complex.
Imp. Inst. Ent., London. 239
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