A. Alonsomejia et al., USE OF LIPID RESERVES BY MONARCH BUTTERFLIES OVERWINTERING IN MEXICO - IMPLICATIONS FOR CONSERVATION, Ecological applications, 7(3), 1997, pp. 934-947
During their 5-mo overwintering period in Mexico, tens of millions of
monarch butterflies (Danaus plexippus) form dense aggregations in fore
sts dominated by oyamel fir trees (Abies religiosa). These forests pro
vide a cool, moist environment that most monarchs use to maintain a st
ate of reproductive diapause and to remain largely inactive until Marc
h, when they migrate back to the southern United States. In 1986, the
Mexican government created the Monarch Butterfly Special Biosphere Res
erve (MBSBR), but it is under pressure to allow forest extractions fro
m core areas of the reserve. A recent argument to justify logging main
tains that tree extraction would benefit monarchs by creating forest o
penings in which more plants would flower. The increased availability
of nectar might mean that fewer monarchs would deplete their lipid con
tents, and therefore, more monarchs would survive the overwintering pe
riod. We investigated this hypothesis by comparing, throughout the ove
rwintering period, lipid utilization and three other physical characte
ristics of monarch butterflies that were clustered on trees vs. monarc
hs that were collected while they visited flowers. Comparisons were al
so made with autumn migrants collected in Texas, successful spring mig
rants collected in the southern United States, and reproductively acti
ve summer generations collected in Wisconsin and Minnesota. We also ex
amined changes in lipid mass during the annual cycle of eastern North
American monarch populations. We found that clustered butterflies had
significantly higher lipid mass, water content, lean mass, and larger
wings than did monarchs collected from flowers. These differences were
consistent throughout the overwintering period. Clustered monarchs co
nsumed their lipid reserves passively in relation to the ambient tempe
rature, as would be expected based on their resting metabolic rate. In
contrast, a high proportion of flower-visiting monarchs had lipid mas
ses close to zero; very few had medium or high lipid levels. This sugg
ests that flower-visiting monarchs either maintained their lipid reser
ves at low levels by visiting flowers, but were unable to reach levels
found in clustered monarchs, or that, as the flower-visiting monarchs
died, clustered monarchs with low lipid reserves departed from their
roosting trees to visit flowers. Migrating monarchs collected in April
in the southern United Stales had significantly higher Lipid masses t
han did flower-visiting monarchs collected in March at the overwinteri
ng site. Furthermore, migrating monarchs arrived in the southern Unite
d States with <50% of the lipid mass found in clustered, overwintering
monarchs in March. Due to this apparent cost of migration, we hypothe
size that the cohorts of monarchs visiting flowers at the overwinterin
g site may not be able to migrate successfully to breeding areas in th
e southern United States. Our data do not support the hypothesis that
there is a need to create open areas in the core zones of the MBSBR to
promote flower production for monarchs overwintering in Mexico. To th
e contrary, the pattern of lipid loss observed in monarchs clustered i
n shaded areas is consistent with the hypothesis that intact, closed f
orest is necessary for successful overwintering because it permits mon
archs to conserve their lipid reserves for the spring migration.