Pests and diseases of forestry in New Zealand
Gum Emperor-moth
Gum Emporer Moth
Forest and Timber Insects in New
Zealand No. 7
Based on P.J. Alma (1977)
Revised 2009
Insect
Opodiphthera eucalypti Scott (Lepidoptera :
Saturniidae)
Fig. 1 - Caterpillar of the gum emperor-moth in natural position
upside-down on twig of
eucalypt.
Type of injury
The caterpillar of the gum emperor-moth feeds on the foliage of the
host plants.
Hosts
The main hosts are eucalypts. The moth, however, appears to be
selective when laying eggs and
caterpillars have been recorded from only 24 of the 60 species of
Eucalyptus
that have been
examined in New Zealand. Of the species that have been considered
promising for plantations in
New Zealand (
E. delegatensis, E. fastigata, E. obliqua, E.regnans, E. saligna, E.
botryoides, E.
muellerana, E. pilularis, E. nitens, and
E. oreades
), only E. obliqua and E. muellerana have not
yet been attacked. The gum emperor-moth has also been recorded in
New Zealand on
Schinus
molle (pepper tree), on which it can complete its development
from egg to adult, and on
Liquidambar styraciflua (liquidambar),
Prunus
armeniaca
(apricot),
Betula pendula
(silver
birch), and some cultivars of
Malus sylvestris (apple), on which it is possible that only older
caterpillars can survive. It has been recorded in Australia
feeding on
Pinus radiata (radiata pine),
although apparently only after passing the early stages on
eucalypt undercoppice.
Distribution
The gum emperor-moth is a native of eastern Australia and was
probably introduced into New
Zealand as pupae on imported hardwood poles. The moth was first found
in Wanganui in 1915
and has since spread slowly from that area. By 1960 it had become
distributed in the wide
coastal strip from New Plymouth through Palmerston North to Levin, with
records also from
Wellington, isolated areas on the east coast of the North Island up to
Ruatoria, and the Waikato
region centred on Cambridge. The insect has frequently been used for
biology studies in schools
and teacher training establishments, as well as in the home. Much of
the spread of the moth has
resulted from intentional or accidental releases from these situations.
The gum emperor-moth
was first recorded as being established in the South Island in Nelson
in 1968. It is now found throughout
most of the North Island, wherever eucalypts are grown, as well as in
Nelson in the South Island.
Economic importance
Caterpillars defoliate their host plants (Fig. 3) and will affect the
growth rate and crown-form of
the trees (repeated defoliation causes a proliferation of branching and
consequent bushy
appearance). Severe defoliation may kill trees. Damage so far has
usually been seen in
ornamental, shade, and shelter belt trees. It is not possible to
predict how serious the effects of
the insect might be if eucalypts were planted more widely.

Fig.3 -
Eucalyptus pilularis defoliated by caterpillars of the gum
emperor-moth.
Description, life history, and
habits
The eggs, caterpillar, cocoon, and moth are readily identified and
unlikely to be confused with
any other species found in New Zealand.
The wing colour of the adult is pale brown, often with a rosy tinge.
The wing is clothed with soft
setae (bristles), giving it a furry appearance. The wing-span of the
male is 85-110 mm, that of the
female 95-130 mm. The most prominent features on both pairs of wings
are the eye spots (Fig.4).
On the forewings these are about 7 mm in diameter, ringed in
reddish-brown with pink centres.
In the hind wings the spots are larger (10 mm), ringed in black with
orange centres. In the middle
of both pairs of eye spots there is usually a white dot. A pair of
black or reddish-brown stripes
may be seen on both pairs of wings, one on either side of the eye
spots. The undersides of the
wings are essentially similar to the upper surfaces. The antennae are
pectinate (comb-like), the
pectinationsof the male being about three times as long as those of the
female.

Fig.4 - Above – Gum emperor-moth; male above, female below.
This photo shows approximate maximum wingspan of female.
The eggs are oval and are laid in rows on their sides, often along leaf
margins. They are
approximately 2 mm long and vary from light brown to pale yellow in
colour (Fig. 5).

Fig.5 - Eggs of the gum emperor-moth on eucalypt leaf.

Fig. 6 - Young caterpillars of the gum emperor-moth.
The first- and second-stage caterpillars are basically black, with two
yellow stripes along the top
and one along each side of the abdomen (Fig. 6). The prothorax is
orange-brown and the head
black. Small tufted projections occur along the stripes on each segment
and give the caterpillar a
hairy appearance.
In their final three stages of growth the caterpillars are bright
green, the colour resembling the
foliage of most eucalypts. The upper surface is slightly lighter and
more blue-green than the
underside. As the caterpillars then normally feed hanging upside-down
on twigs, this difference
in colour intensity aids their camouflage (they are much more
conspicuous if twigs on which
they are feeding are held the other way up). A pale yellow stripe
extends down the side of the
body, bearing a tufted blue projection on each segment. Similar
projections are found all around
the thoracic and abdominal segments and may be red, blue, or blue and
red. The fully grown
caterpillar may be up to 120 mm long (Fig. 1).
Pupation takes place in a tough silken cocoon amongst the leaves, or
more usually on twigs and
small branches. Setae from the caterpillar, and twigs or leaves may
adhere to the brown fibrous
silk of the cocoon (Fig. 7).

Fig.7 - Gum emperor-moth cocoon.
In spring and early summer the adult within the cocoon regurgitates a
fluid which softens the silk;
it then emerges by cutting a hole with a sharp book on the base of each
forewing. The moth has
poorly developed mouth-parts and is unable to feed. Mating occurs soon
after emergence and the
eggs are then laid. Caterpillars are usually found from
mid-December and pupate from
approximately mid- January to the end of August. Some adults may emerge
in late February to
mid-March and produce a second generation of caterpillars, but the
pupae produced in mid-
January to August normally overwinter. Some variation in the life cycle
may be expected under
climatic conditions other than those of the Manawatu area where the
life history was elucidated.
White (1972) considers that were it to spread to North Auckland it
might have two distinct
generations in that region.
Control
Widespread outbreaks of the gum emperor-moth have not been recorded,
and it is thought that
populations are probably regulated by natural biological control
agents. Caterpillars are often
found infected with a polyhedral virus (Fig. 8) and, under conditions
suitable for mycelial
growth, may succumb to a parasitic fungus (
Beauveria
sp.) (Fig.9). Also, magpies break open the
cocoons and eat the contents. Control should readily be obtained
with an insecticide designed for
leaf-eating insects if it is applied in December when the caterpillars
are actively feeding. It is
probable that such control would be reasonably long-lasting as the
moths disperse slowly.

Fig.8 - Caterpillar of the gum emperor-moth infected with a virus
(compare with healthy
specimen in Fig. 1).

Fig. 9 - Caterpillar of the gum emperor-moth killed by a fungus.
Bibliography
Alma, P.J. 1977:
Antheraea eucalypti Scott (Lepidoptera: Saturniidae). Gum
Emperor-moth.
New Zealand Forest Service, Forest and Timber Insects in New Zealand
No. 7.
Emberson, R.M. 1984. Forest and timber insects. In: Scott, R.R. (ed)
New Zealand Pest and
Beneficial Insects. Lincoln University, Canterbury, New Zealand. P
191-204.
Meyer-Rochow, V. B. and Ward, D. 1981: Gum emperor moth caterpillars
not only feed on gum-tree
leaves - a possible threat to the foliage of introduced deciduous
trees.
Weta 4(2): 17.
Meyer-Rochow, V. B. and Ward, D. 1986: Further observations on gum
emperor moth caterpillars
feeding on the foliage of birch trees.
Weta 9(1): 7-9.
White, T.C.R., 1972. The distribution, dispersal and host range
of
Antheraea eucalypti
(Lepidoptera: Saturniidae) in New Zealand.
Pacific Insects 14: 669-73.