Crucian carp (Carassius carassius) increases in body depth in response to c
hemical cues from piscivores and the deeper body constitutes a morphologica
l defence against gape-limited piscivores. In the field, deep-bodied indivi
duals suffer a density-dependent cost when competing with shallow-bodied co
nspecifics. Here, we use hydrodynamic theory and swimming respirometry to i
nvestigate the proposed mechanism underlying this effect, high drag caused
by the deep-bodied morphology. Our study confirms that drag is higher for d
eep-bodied crucian carp, both in terms of estimated theoretical drag and po
wer curve steepness. However, deep-bodied fish swimming at the velocity ass
ociated with minimum cost of transport, U-mc, did not experience higher cos
ts of transport than shallow-bodied fish. Deep-bodied crucian carp had sign
ificantly lower standard metabolic rates, i.e. metabolic rates at rest, and
also lower U-mc, and the resulting costs of transport were similar for the
two morphs. Nevertheless, when deep-bodied individuals deviate from U-mc,
e.g. when increasing foraging effort under competition, their steeper power
curves will cause substantial energy costs relative to shallow-bodied cons
pecifics. Furthermore, there is evidence that reductions in standard metabo
lic rate incur costs in terms of lower stress tolerance, reduced growth rat
e, and life history changes. Thus, this work provides links between hydrody
namics, a cost-reducing mechanism, and a density-dependent fitness cost ass
ociated with an inducible defence.