“…It is evident though that many aquatic carnivorous plant species in their typical habitats do not comply, as irradiance is often low and sometimes also free CO 2 is sub-optimal, though [CO 2 ] is commonly high (> 0.1 mM; see e.g., Hough & Fornwall 1988, Adamec 1997b, Adamec & Lev 2002. In aquatic Utricularia species, the structural and maintenance costs of traps are considerable (Friday 1992, Knight 1992, Adamec 2006, Porembski et al 2006), but the plants are able to change the proportion of their resources invested in traps (their 'investment in carnivory') to match variations in habitat factors: particularly water chemistry, prey availability, and level of irradiance (Knight & Frost 1991, Knight 1992, Guisande et al 2000, Richards 2001, Englund & Harms 2003, Manjarrés-Hernández et al 2006. In three aquatic Utricularia species with homogeneous, non-differentiated shoots (U. australis, U. gibba, U. refl exa) and in the epiphytic U. quelchii with carnivorous shoots living in the leaf water reservoirs of bromeliads, Porembski et al (2006) found the contribution of traps to the total plant biomass to be 11-20 % and 30 %, respectively.…”