The function of acquired algal secondary metabolites in sea hares is the su
bject of debate, in part because the dynamics/processing of metabolites by
sea hares is poorly understood. This study investigates the dynamics of red
algal secondary metabolites in two sea hares, Aplysia parvula and Aplysia
dactylomela. Secondary metabolite levels were quantified for the dietary re
d algae Laurencia obtusa and Delisea pulchra and for sea hares collected fr
om these seaweeds in the field. The patterns and dynamics of algal secondar
y metabolites were further investigated in the laboratory by quantitative a
nalysis of secondary metabolites in sea hares grown on diets of L. obtusa,
D. pulchra, or the green alga Ulva sp. Sea hares accumulated the most abund
ant metabolites from each red alga, the terpene palisadin A from L. obtusa,
and the halogenated furanone 3 from D. pulchra, and stored a greater propo
rtion of these metabolites than other algal metabolites. A. parvula accumul
ated D. pulchra metabolites at much higher levels than L. obtusa metabolite
s. A. dactylomela accumulated similar concentrations of L. obtusa metabolit
es to A. parvula. The loss of L. obtusa metabolites by A. dactylomela match
ed that expected for dilution of metabolites via growth of the sea hares. H
owever, the loss of L, obtusa metabolites by A. parvula was faster than pre
dicted for growth alone, suggesting that metabolites were actively metaboli
zed or excreted. Data for the loss of D, pulchra metabolites by A. parvula
was equivocal. The secretions of A. parvula fed D. pulchra or L. obtusa wer
e analyzed for the presence of algal secondary metabolites to investigate o
ne possible path of excretion. L. obtusa secondary metabolites were detecte
d in the mucous and opaline secretions of A. parvula, but D. pulchra metabo
lites were not detected in any secretions. The deployment of L. obtusa seco
ndary metabolites in secretions by A. parvula may explain the more rapid ra
te of loss of these compounds and is consistent with a possible defensive r
ole for acquired metabolites.