Tudies addressing the CNBH and GDBH have focused on phenolics [54], making studies of other classes of defense important. Terpenoids are especially interesting because they are produced by the mevalonic acid pathway, and defenses from this pathway do not fit predictions of the CNBH and GDBH as well as the phenolics produced via the shikimic acid pathway [20,54?6]. We tested the hypothesis that saponin production in P. macroloba seedlings incurs both physiological (photosynthetic) and allocation (biomass) costs. We measured saponin and flavan production under different light regimes in response to changes in nutrients and plant density to test ecological predictions made by the CNBH and GDBH. Tests of the CNBH and GDBH have been criticized for not measuring 94-09-7 web complete costs of secondary defenses [57]; by quantifying relationships between two separate classes of defense, as well as photosynthesis and growth, we do not escape this criticism, but attempt to provide a more complete measure of these trade-offs.Materials and MethodsWe collected seeds of Pentaclethra macroloba from JI 101 biological activity multiple individuals distributed throughout the forest of La Tirimbina Rainforest Center, Sarapiqui, Heredia, Costa Rica (10u 23 N, 84u8 W) in January 2008. Pentaclethra macroloba was selected for this study because of its dominance in tropical forests where it is found [58], its diverse defensive chemistry, and the ease with which seeds can be found and propagated. La Tirimbina contains 345 ha of tropical wet forest (sensu [59]) with an average of 4000 mm annual precipitation, 26uC mean annual temperature, and an average day length of 12 hours.Planting DesignOne hundred eighty seeds were planted in 60 6-liter pots with 1.5 kg of sterile peat moss (Berger BM4: Sphagnum peat moss (coarse), 18055761 dolomitic and calcitic lime, initial fertilizer charge, wetting agent; pH 5.4?). A general fertilizer containing 25 phosphate, 41 potassium, 0.02 boron, 15755315 8.27 sulfur, 0.1 iron, 0.05 copper, 0.05 magnesium, 0.05 zinc, 0.001 molybdenum, and 25.459 inert ingredients (Miller Chemical and Fertilizer Corporation) was added to each pot at a concentration of 0.35 g/kg soil. Three levels of nitrogen fertilizer (urea: (NH2)2CO) were also applied: low = 0.002 N, intermediate = 0.004 N, and high = 0.008 N (20 pots per treatment). Seeds were planted alone (30 pots) and in competition pots (30 pots? seeds per pot). Half of the pots were then placed in full sunlight (,1175 PAR (mmol/m2/s)) and half at 24 full sunlight (,282 PAR) in a shadehouse at La Tirimbina (Figure 1). The plants in full sun were exposed to natural rain, and those in the shadehouse were watered regularly to ensure they received adequate moisture. 
The seedlings never appeared water-stressed. Only one shadehouse was available at the research station, so seedlings exposed to low light were grown together. Therefore, the two levels of the light treatment were analyzed as separate experiments to avoid pseudoreplication. Within each light regime, each combination of the nitrogen and competition treatments was replicated five times, with an individual pot as a replicate. Fertilizer was applied a second time in May 2008. Seedlings were routinely examined, and aboveground herbivore damage was notVariation in Costs of Terpenoids and PhenolicsFigure 1. Schematic of experimental design. Seeds were planted individually or in competition 
with four conspecific neighbors and growth at low, intermediate, or high nitrogen levels. Ther.Tudies addressing the CNBH and GDBH have focused on phenolics [54], making studies of other classes of defense important. Terpenoids are especially interesting because they are produced by the mevalonic acid pathway, and defenses from this pathway do not fit predictions of the CNBH and GDBH as well as the phenolics produced via the shikimic acid pathway [20,54?6]. We tested the hypothesis that saponin production in P. macroloba seedlings incurs both physiological (photosynthetic) and allocation (biomass) costs. We measured saponin and flavan production under different light regimes in response to changes in nutrients and plant density to test ecological predictions made by the CNBH and GDBH. Tests of the CNBH and GDBH have been criticized for not measuring complete costs of secondary defenses [57]; by quantifying relationships between two separate classes of defense, as well as photosynthesis and growth, we do not escape this criticism, but attempt to provide a more complete measure of these trade-offs.Materials and MethodsWe collected seeds of Pentaclethra macroloba from multiple individuals distributed throughout the forest of La Tirimbina Rainforest Center, Sarapiqui, Heredia, Costa Rica (10u 23 N, 84u8 W) in January 2008. Pentaclethra macroloba was selected for this study because of its dominance in tropical forests where it is found [58], its diverse defensive chemistry, and the ease with which seeds can be found and propagated. La Tirimbina contains 345 ha of tropical wet forest (sensu [59]) with an average of 4000 mm annual precipitation, 26uC mean annual temperature, and an average day length of 12 hours.Planting DesignOne hundred eighty seeds were planted in 60 6-liter pots with 1.5 kg of sterile peat moss (Berger BM4: Sphagnum peat moss (coarse), 18055761 dolomitic and calcitic lime, initial fertilizer charge, wetting agent; pH 5.4?). A general fertilizer containing 25 phosphate, 41 potassium, 0.02 boron, 15755315 8.27 sulfur, 0.1 iron, 0.05 copper, 0.05 magnesium, 0.05 zinc, 0.001 molybdenum, and 25.459 inert ingredients (Miller Chemical and Fertilizer Corporation) was added to each pot at a concentration of 0.35 g/kg soil. Three levels of nitrogen fertilizer (urea: (NH2)2CO) were also applied: low = 0.002 N, intermediate = 0.004 N, and high = 0.008 N (20 pots per treatment). Seeds were planted alone (30 pots) and in competition pots (30 pots? seeds per pot). Half of the pots were then placed in full sunlight (,1175 PAR (mmol/m2/s)) and half at 24 full sunlight (,282 PAR) in a shadehouse at La Tirimbina (Figure 1). The plants in full sun were exposed to natural rain, and those in the shadehouse were watered regularly to ensure they received adequate moisture. The seedlings never appeared water-stressed. Only one shadehouse was available at the research station, so seedlings exposed to low light were grown together. Therefore, the two levels of the light treatment were analyzed as separate experiments to avoid pseudoreplication. Within each light regime, each combination of the nitrogen and competition treatments was replicated five times, with an individual pot as a replicate. Fertilizer was applied a second time in May 2008. Seedlings were routinely examined, and aboveground herbivore damage was notVariation in Costs of Terpenoids and PhenolicsFigure 1. Schematic of experimental design. Seeds were planted individually or in competition with four conspecific neighbors and growth at low, intermediate, or high nitrogen levels. Ther.
