Root respiration rates of Lolium multiflorum supplied with nitrate or ammonium were measured continuously during several days (Exp. A). Net uptake rate of nitrate was similarly measured by an ion selective nitrate electrode in a system of flowing nutrient solution (Exp. B). Diurnal variation of in vitro nitrate reductase activity and nitrate content of tops and roots were determined (Exp. C). Two levels of irradiance were applied throughout, with day:night of 16:8 h. Root respiration rates showed diurnal patterns, most pronounced in the nitrate treatment, with two peaks appearing about 6 and 16 h after commencement of the photoperiod. Respiration rates were highest in the nitrate treatment and at high irradiance. Respiration rates fell after removal of nitrogen, particularly in the nitrate supplied plant and at high irradiance. Net uptake rate of nitrate exhibited diurnal patterns, often with two peaks occurring at the same times as those of respiration rates. In vitro nitrate reductase activity of tops increased steeply 16 h after commencement of the photoperiod and remained at the high level during the following 8 h of darkness. Nitrate content of tops was highest during the 8 h dark period and fell at the start of the photoperiod. Possible controlling systems of the apparent coincidences of diurnal variation rates, net nitrate uptake and nitrate reduction are discussed.

Continuous measurements of CO2‐exchange were separately carried out on tops and roots of small swards of Lolium multiflorum grown in nutrient solution in growth chamber during 3–4 weeks. From these measurements, a daily carbon balance and accumulated dry matter could be established. The data were used to distinguish between two components of respiration, one proportional to growth or photosynthesis (growth respiration), the other proportional to plant dry weight (maintenance respiration). The separation of respiration in the two components was made by multiple regression analyses with daily photosynthesis or growth rate and accumulated dry matter as the independent variables. To ensure independency between the independent variables during the growth period, photosynthesis was varied by application of alternate three‐day periods of high and low irradiance. From the two regression coefficients, the efficiency of converting assimilates into constructive growth (YG) and the maintenance coefficient (M) could be derived. Three experiments with varying length of photoperiod and dark period were carried out. The analyses were carried out for whole‐plant respiration, respiration of tops and respiration of roots separately. Growth respiration for whole plants as well as for tops and for roots was lower — and hence the efficiencies higher — the longer the photoperiods were. Growth respiration and maintenance respiration were higher for roots than for tops. The high rate of root respiration may originate from release of HCO3− in exchange for NO3−. The parameters found can be utilized quantitatively in computer models of crop photosynthesis and respiration.

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Continuous measurements of CO2‐release from intact roots of Lolium multiflorum growing in nutrient solution were carried out during 3–7 weeks. Periods of days with high level of irradiance and periods with low level alternated. Root respiration rate was found to depend on photosynthesis. The change in root respiration, induced by change in photosynthesis, was delayed. The root respiration rate showed diurnal fluctuations with two characteristic peaks occurring 4–6 and 14–16 hours after onset of the photoperiod. The amplitudes increased with increasing photosynthesis. The frequencies were independent of the length of photoperiod, when this varied between 8 and 16 hours. The fluctuations are discussed in relation to diurnal fluctuations in protein synthesis.

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