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V P Gutschick

Publications and source records attributed to V P Gutschick.

3 recordsLinked to original sources

Nonrecirculating hydroponic system suitable for uptake studies at very low nutrient concentrations.

We describe the mechanical, electronic, hydraulic, and structural design of a nonrecirculating hydroponic system. The system is particularly suited to studies at very low nutrient concentrations, for which on-line concentration monitoring methods either do not exist or are costly and limited to monitoring relatively few individual plants. Solutions are mixed automatically to chosen concentrations, which can be set differently for every pump fed from a master supply of deionized water and nutrient concentrates. Pumping rates can be varied over a 50-fold range, up to 400 liters per day, which suffices to maintain a number of large, post-seedling plants in rapid growth at (sub)micromolar levels of N and P. The outflow of each pump is divided among as many as 12 separate root chambers. In each chamber one may monitor uptake by individual plant roots or segments thereof, by measuring nutrient depletion in batch samples of solution. The system is constructed from nontoxic materials that do not adsorb nutrient ions; no transient shifts of nitrate and phosphate concentrations are observable at the submicromolar level. Nonrecirculation of solutions limits problems of pH shifts, microbial contamination, and cumulative imbalances in unmonitored nutrients. We note several disadvantages, principally related to high consumption of deionized water and solutes. The reciprocating pumps can be constructed inexpensively, particularly by the researcher. We also report previously unattainable control of passive temperature rise of chambers exposed to full sunlight, by use of white epoxy paint.

Journal Article↗

Concentration quenching in chlorophyll-alpha and relation to functional charge transfer in vivo.

Chlorophyll-alpha in ordinary solvents exhibits concentration quenching. Dimeric chlorophyll is reasonably well confirmed as the quenching species, by a critical reanalysis of available data on concentration dependence and on spectral features, in ordinary solvents, and in several analogous quenching environments. This quenching in the dimer in vitro is somewhat less firmly analyzed as due to a new fast internal conversion. Much peripheral evidence supports transient charge transfer as the cause of internal conversion. The same evidence points to a strong similarity to functional charge transfer in vivo. I suggest that inability to extract P680 may be due to its conversion to a form resembling P700 by addition of water. A number of straightforward experiments are suggested to test these proposals. In particular, it is desirable to test for the existence of a vibronic perturbation (from a higher npi* state) in the dimer, as an alternative to charge transfer for explaining the "observed" internal conversion. Such a vibronic cause would raise interesting problems for phototrap function in vivo.

Chlorophyll↗