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PE EIE[R-Rg RESEARCH ON - HJ Andrews Experimental Forest

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condition differ) ; the turnover rate o f<br />

the population, and the intensity o f<br />

metabolism of different groups of animals<br />

. . . Whilst it is not difficult to estimate<br />

the intensity of metabolism of certain<br />

species in a calorimetric chamber, i t<br />

is practically impossible to estimate the<br />

loss of energy by a bat, a mole, or a<br />

dolphin in the process of their natura l<br />

life activity .<br />

In the light of these considerations we wil l<br />

examine our preliminary data and, through a<br />

comparison of actual and needful information,<br />

delineate the work still to be done .<br />

Small Mammal Studies<br />

Since small mammals are generally inconspicuous,<br />

and do not make readily detectable<br />

signs, the determination of species presence<br />

and especially population density is widely<br />

recognized as a difficult problem .<br />

The most commonly used method fo r<br />

estimating population densities in smal l<br />

mammals is to capture, mark, and release a<br />

sample, and then capture a second sampl e<br />

containing both marked and unmarked individuals<br />

. Several underlying assumption s<br />

(Leslie 1952) are : all individuals have equa l<br />

probabilities of capture, released individual s<br />

disperse randomly into the populations, an d<br />

there is no mortality, natality, or significan t<br />

ingress or egress during the experimenta l<br />

period .<br />

Since these assumptions were not war -<br />

ranted in our case, and since we needed to<br />

collect specimens for data on weight, foo d<br />

habits, and reproduction, we considered intensive<br />

removal methods . Grodzinski et al .<br />

(1966) proposed such a method for IBP smal l<br />

mammal studies. They suggested intensive<br />

kill-trapping following a prebaiting period on<br />

a defined grid of locations . This provided data<br />

for an estimation procedure in which a regression<br />

line, plotted for the number of animals<br />

caught each day (on the ordinate axis) against<br />

the cumulative number previously caught ,<br />

would provide an estimate of populatio n<br />

density (the point where the regression line<br />

intersected the abscissa) . Earlier work on this<br />

approach was that of DeLury (1947), Hayn e<br />

(1949), and Zippin (1958) .<br />

The major flaw in the method of Grodzinski<br />

et al. (1966) is that it gives no accurat e<br />

estimate of the area sampled by the grid, be -<br />

cause the small mammals move some unknown<br />

distance to the trapping point . Sinc e<br />

the area sampled is not defined, populatio n<br />

densities cannot be determined .<br />

Adamczyk and Ryszkowski (1968) suggested<br />

that the sample grid be surrounded o n<br />

each side by an external belt of trapping locations<br />

to catch animals moving toward th e<br />

inner grid before they could reach it, thereb y<br />

controlling the "periphery effect ."<br />

The data provided by the external trappin g<br />

belt cannot be used, because the distance<br />

travelled by each animal before being caught<br />

is highly variable (Miller 1970) .<br />

Adamczyk and Ryszkowski (1968) recommend<br />

a 5-day prebaiting period to accusto m<br />

the mammals to the trap locations, followe d<br />

by a 5-day period of removal trapping . Their<br />

basic assumptions are : (1) all residents of the<br />

inner grid are captured, (2) prebaiting does<br />

not increase the resident density, and (3) individuals<br />

not resident on the inner grid are no t<br />

captured on the inner grid ; immigrants and<br />

individuals resident in the outer grid will b e<br />

captured, if at all, in the outer grid .<br />

Of these three assumptions, we could tes t<br />

only the second . Adopting a 5-day prebaiting<br />

period, we ran pairs of trap-lines-one pre -<br />

baited and one control-in each case . Total<br />

catches over 5 days were not different,<br />

though prebaited lines took a higher proportion<br />

of the catch on the first day (Mille r<br />

1970) . This finding corroborates that o f<br />

Babinska and Bock (1969), who showed tha t<br />

prebaiting did not significantly increase th e<br />

density of resident small mammals .<br />

Our trapping procedure was as follows : a<br />

5 .94-ha (12 .4-acre) sample area was divide d<br />

into 256 stations, 16 rows by 16 lines, wit h<br />

15 .2-meter spacing . Anchored at each statio n<br />

was a paper plate which was baited with oatmeal,<br />

millet, sunflower seeds, oats, and wheat<br />

for 5 days . Then the remaining bait was removed<br />

and two mouse traps were placed on<br />

each plate, one trap baited with a peanut<br />

butter-bacon grease mixture, and the other<br />

200

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