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pdf, 57.71Mb - Entomological Society of Canada

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376 W. G. H. Ives and J. A. Muldrew<br />

Sorex cinereus<br />

cinereus Kerr<br />

(lnsedivora: Sorlddae)<br />

Evaluation <strong>of</strong> Control Attempts<br />

The masked shrew, introduced into Newfoundland in 1958, has continued to spread.<br />

Survey reports for 1969 and 1970 (Anon. 1970-79) mentioned the concern <strong>of</strong> local<br />

residents as high initial numbers were noted in each area: by 1971 the shrew had spread<br />

over 95% <strong>of</strong> the island. Populations on the island, excluding the first 2 or 3 years' data,<br />

averaged about eight shrews per hectare, which seems to be unusually high. However,<br />

the 18-year average populations <strong>of</strong> the masked shrew in the Rennie life-table plot (Ives<br />

1981) was 5.2/ha. If one includes populations <strong>of</strong> the closely related arctic shrew, Sora<br />

arcticus Kerr, which averaged 1.8/ha, the total <strong>of</strong> 7.01ba is comparable. Populations <strong>of</strong><br />

the masked shrew in Newfoundland therefore seem to have stabilized, and can be<br />

expected to fluctuate in the future in response to environmental conditions.<br />

O. benefactor and larch sawfly populations have probably not yet reached an equilibrium,<br />

even at the original release point near Pine Falls. As shown in Fig. 19, the level <strong>of</strong> O.<br />

benefactor parasitism at or near the release point reached 90% in 1967. It remained at or<br />

near this level until 1972, but larch.sawfly populations collapsed in 1973, presumably as a<br />

result <strong>of</strong> the continued high rates <strong>of</strong> parasitism (rves 1976). No larvae or cocoons were<br />

obtained near the plot in 1973 or 1974, although intensive sampling was conducted<br />

(Muldrew in press). Detailed studies were discontinued after 1974, and further trends<br />

are based on limited sampling. In 1977, a collection <strong>of</strong> 72 fourth- and fifth-instar larvae<br />

was made near the original release site at Pine Falls. None was parasitized by O.<br />

benefactor. In 1978, collections <strong>of</strong> larvae from the same area yielded 1730 cocoons.<br />

Parasitism by O. benefactor was 1.5%, hyperparasitism by Mesochorus dimidiatus was<br />

86%. A total <strong>of</strong> 237 third- to fifth-instar larvae collected 8 km north <strong>of</strong> the release point in<br />

1978 contained no O. benefactor, but 19% <strong>of</strong> 424 fourth- and fifth-instar larvae from an<br />

area 8 km south <strong>of</strong> the release point were parasitized. NinetY7three per cent <strong>of</strong> these O.<br />

benefactor larvae were parasitized by M. dimidiatus. In 1980, a total <strong>of</strong> 535 cocoons<br />

was obtained from the same location; 15% <strong>of</strong> these contained O. benefactor, <strong>of</strong> which<br />

75% were parasitized by M. dimidiatus. No O. benefactor were present in 150 cocoons<br />

obtained by rearing late-instar larvae collected in 1980 near the Seddon's Comer lifetable<br />

plot, about 70 km south <strong>of</strong> the Pine Falls release point.<br />

Although the above data are rather fragmented, there is some evidence that O.<br />

benefactor is in danger <strong>of</strong> local extinction over a fairly wide area. Should this happen, it<br />

is possible that the larch sawfly may increase in abundance if environmental conditions<br />

are favourable. No population sampling <strong>of</strong> the larch sawfly was done in the Pine Falls<br />

release area in 1980, but observations by Ives indicated that this population increase<br />

may already be taking place. It remains to be seen whether or not O. benefactor will be<br />

able to prevent an outbreak in spite <strong>of</strong> the adverse influence <strong>of</strong> M. dimidiatus. O.<br />

benefactor is host specific, but M. dimidiatus is not (Pschorn-Walcher & Zinnert 1971).<br />

Because <strong>of</strong> this, one would expect M. dimidiatus to be able to persist on alternate hosts,<br />

thus obtaining a "head start" on any re-invading O. benefactor. Under these circumstances,<br />

M. dimidiatus would probably be able to control O. benefactor, thus permitting larch<br />

sawfly populations to reach outbreak proportions. However, a crude model developed<br />

by Ives (1976) indicated that the two parasitoids should reach an equilibrium with each<br />

other and with the larch sawfly. According to the model, the larch sawfly populations<br />

would fluctuate in response to density-independent environmental factors, but should not<br />

reach outbreak proportions in the presence <strong>of</strong> O. benefactor, even when M. dimidiatus is<br />

present. It is too early to tell which hypothesis is correct.<br />

The impact <strong>of</strong> the masked shrew on larch sawfly populations in Newfoundland has not<br />

been assessed in detail (Warren 1971). The fact that larch sawfly infestations reached

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