David H. Barker

Photochemistry and xanthophyll cycle-dependent energy dissipation in differently oriented cladodes of Opuntia stricta during the winter

The photosynthetic and energy dissipation responses of four differently oriented photosynthetic surfaces (cladodes) from the cactus Opuntia stricta (Haw.) Haw. were studied in the field during the winter in Australia. Even under very low PFD (i.e. -2 s-1) all surfaces experienced a dramatic decline in photosystem II (PSII) efficiency during the morning period when temperatures were below freezing. However, light energy absorbed during the warmer afternoon period was more efficiently utilised for photochemistry with less diversion through the thermal energy dissipation pathway. Low temperature presumably reduced the proportion of excitation energy that could be utilised photosynthetically, resulting in a high rate of energy dissipation with a concomitant decline in PSII efficiency. A lag in the diurnal de-acidification of malic acid, and therefore the availability of endogenous CO2, may have also contributed to the low rate of photochemistry during the morning period. We interpret the increase in energy dissipation and decline in PSII efficiency as a controlled response of PSII that is dependent upon the de-epoxidised components of the xanthophyll cycle under conditions when the absorption of light exceeds the capacity of the photosynthetic apparatus to process the excitation energy through photochemistry.

Changes in photosynthetic pigment composition and absorbed energy allocation during salt stress and CAM induction in Mesembryanthemum crystallinum

Mesembryanthemum crystallinum L. undergoes a transition from the C3 photosynthetic pathway to crassulacean acid metabolism (CAM) in response to increasing salinity. As a consequence, growth is greatly reduced and less light energy is utilised in carbon fixation, leading to an increase in dissipation of thermal energy to remove potentially dangerous excess excitation energy. The pigment composition of plants grown for 4 weeks at 20 mm (low) and 400 mm (high) NaCl was sampled, and photochemical performance, tissue acidity and growth were sampled at 2 and 4 weeks. High-salt-grown plants, which switched to CAM, accumulated only 25% of the fresh weight of low-salt-grown plants, which maintained C3 photosynthesis. Predawn Fv / Fm and de-epoxidation of violaxanthin [(A + Z) / (V + A + Z)] was similar between plants after 2 and 4 weeks, revealing no sustained depression in PSII efficiency under the high-salt treatment. However, at midday under high photosynthetic photon flux densities (PPFD) high-salt plants displayed lower PSII efficiency, higher (A + Z) / (V + A + Z) and greater allocation of energy to thermal dissipation over photochemistry than low-salt plants. Pigment contents were similar between treatments for the first 3 weeks, but after 4 weeks high-salt plants had accumulated significantly less chlorophyll and lutein than low-salt plants. However, V + A + Z content did not differ. High-salt treatment, leading to CAM photosynthesis and substantial reduction in growth, was associated with increased allocation of energy to xanthophyll cycle-dependent energy dissipation at high light and adjustment of thylakoid pigment composition.