Several cotton experiments have been conducted at the University of Arizona's Maricopa Agricultural Center from which datasets have been obtained documenting cotton responses to elevated CO2 concentrations, water supply, nitrogen fertilizer, and planting density. In particular, these experiments included FACE (free-air CO2 enrichment; CO2, water; 10 treatment-years), AgIIS (Agricultural Irrigation Imaging System, pronounced Ag Eyes; nitrogen fertilizer, water supply; 4 treatment-years), and FISE (FAO-56 Irrigation Scheduling Experiments; irrigation scheduling method, planting density, nitrogen fertilizer; 24 treatment-years). Besides achieving the experimental objectives of determining cotton's response to the several variables, as well as testing remote sensing techniques, the comprehensive datasets are suitable for validating plant growth models because they include weather, soils, management, growth, yield and other data.
Field experimental data of five experiments covering a wide range of growing conditions are assembled for wheat growth and cropping systems modeling. The data include an experiment on interactive effects of elevated CO2 by water and elevated CO2 by nitrogen fertilizer application from a Free-Air Carbon Dioxide Enrichment experiment (FACE) at Arizona in USA; a nitrogen rate fertilizer experiment from three locations and two years in The Netherlands; water deficit experiments at Lincoln in New Zealand and at Cunderdin in Australia; and a temperature sensitivity experiment at Obregon in Mexico. The data consist of 65 experimental treatments with more than 1000 detailed observations, with time series of development and growth, soil water and soil nitrogen dynamics, yield and yield components, daily weather, soil characteristics, and cultivar descriptions. These data have been used in various previous agronomic and crop modeling studies. Assembled data are quality checked and supplied in Agricultural Model Inter-comparison and Improvement (AgMIP) format. Data access via DOI 10.7910/DVN/V4P6PU.
Despite widespread application in studying climate change impacts, most crop models ignore complex interactions among air temperature, crop and soil water status, CO2 concentration and atmospheric conditions that influence crop canopy temperature. The current study extended previous studies by evaluating Tc simulations from nine crop models at six locations across environmental and production conditions. Each crop model implemented one of an empirical (EMP), an energy balance assuming neutral stability (EBN) or an energy balance correcting for atmospheric stability conditions (EBSC) approach to simulate Tc. Model performance in predicting Tc was evaluated for two experiments in continental North America with various water, nitrogen and CO2 treatments. An empirical model fit to one dataset had the best performance, followed by the EBSC models. Stability conditions explained much of the differences between modeling approaches. More accurate simulation of heat stress will likely require use of energy balance approaches that consider atmospheric stability conditions.
The rationale for this study is found in the probable higher temperatures and changes in rainfall patterns that are expected in the future as a result of increasing levels of CO2 in the atmosphere. In particular, higher air temperatures may cause an increase in evapotranspiration demand while a reduction in rainfall could increase the severity and duration of drought in arid and semi-arid regions. Representation of the water transfer scheme includes water uptake by roots and the interaction between evapotranspiration and CO2 enrichment. The predicted response of a spring wheat (Triticum aestivum L. cv. Yecora rojo) canopy in terms of energy exchange processes to elevated atmospheric CO2 level was tested against measurements collected at the FACE (Free Air Enrichment Experiment) site in 1994. Simulated and measured canopy conductances were reduced by about 30% under elevated [CO2] under optimum conditions of water supply. Reductions in latent heat fluxes under elevated instead of ambient [CO2] caused reductions in both simulated and measured seasonal water use of 6% under optimum and 2% under suboptimum irrigation. The soil–plant–atmosphere water transfer scheme proposed here offers several advances in the simulation of land surface interactions. First, the stomatal resistance model minimizes assumptions in existing land surface schemes about the effects of interactions among environmental conditions (radiation, temperature, CO2) upon stomatal behavior. These interactions are resolved in the calculation of CO2 in which processes are already well understood.
The response of whole-canopy net CO 2 exchange rate (CER) and canopy architecture to CO 2 enrichment and N stress during 1996 and 1997 for open-field-grown wheat ecosystem ( Triticum aestivum L. cv. Yecora Rojo) are described. Every Control (C) and FACE (F) CO 2 treatment (defined as ambient and ambient +200 μmol mol −1 , respectively) contained a Low- and High-N treatment. Low-N treatments constituted initial soil content amended with supplemental nitrogen applied at a rate of 70 kg N ha −1 (1996) and 15 kg N ha −1 (1997), whereas High-N treatments were supplemented with 350 kg N ha −1 (1996 and 1997). Elevated CO 2 enhanced season-long carbon accumulation by 8% and 16% under Low-N and High-N, respectively. N-stress reduced season-long carbon accumulation 14% under ambient CO 2 , but by as much as 22% under CO 2 enrichment. Averaging both years, green plant area index (GPAI) peaked approximately 76 days after planting at 7.13 for FH, 6.00 for CH, 3.89 for FL, and 3.89 for CL treatments. Leaf tip angle distribution (LTA) indicated that Low-N canopies were more erectophile than those of High-N canopies: 48° for FH, 52° for CH, and 58° for both FL and CL treatments. Temporal trends in canopy greenness indicated a decrease in leaf chlorophyll content from the flag to flag-2 leaves of 25% for FH, 28% for CH, 17% for CL, and 33% for FL during 1997. These results indicate that significant modifications of canopy architecture occurs in response to both CO 2 and N-stress. Optimization of canopy architecture may serve as a mechanism to diminish CO 2 and N-stress effects on CER.
We have examined the photosynthetic acclimation of wheat leaves grown at an elevated CO(2) concentration, and ample and limiting N supplies, within a field experiment using free-air CO(2) enrichment (FACE). To understand how leaf age and developmental stage affected any acclimation response, measurements were made on a vertical profile of leaves every week from tillering until maturity. The response of assimilation (A) to internal CO(2) concentration (C(i)) was used to estimate the in vivo carboxylation capacity (Vc(max)) and maximum rate of ribulose-1,5-bisphosphate limited photosynthesis (A (sat)). The total activity of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco), and leaf content of Rubisco and the Light Harvesting Chlorophyll a/b protein associated with Photosystem II (LHC II), were determined. Elevated CO(2) did not alter Vc(max) in the flag leaf at either low or high N. In the older shaded leaves lower in the canopy, acclimatory decline in Vc(max) and A (sat) was observed, and was found to correlate with reduced Rubisco activity and content. The dependency of acclimation on N supply was different at each developmental stage. With adequate N supply, acclimation to elevated CO(2) was also accompanied by an increased LHC II/Rubisco ratio. At low N supply, contents of Rubisco and LHC II were reduced in all leaves, although an increased LHC II/Rubisco ratio under elevated CO(2) was still observed. These results underscore the importance of leaf position, leaf age and crop developmental stage in understanding the acclimation of photosynthesis to elevated CO(2) and nutrient stress.
Atmospheric CO2 concentration continues to rise. It is important, therefore, to determine what acclimatory changes will occur within the photosynthetic apparatus of wheat (Triticum aestivum L. cv. Yecora Rojo) grown in a future high-CO2 world at ample and limited soil N contents. Wheat was grown in an open field exposed to the CO2 concentration of ambient air [370 μmol (CO2) mol−1; Control] and air enriched to ∼200 μmol (CO2) mol−1 above ambient using a Free-Air CO2 Enrichment (FACE) apparatus (main plot). A High (35 g m−2) or Low (7 and 1.5 g m−2 for 1996 and 1997, respectfully) level of N was applied to each half of the main CO2 treatment plots (split-plot). Under High-N, FACE reduced stomatal conductance (g s) by 30% at mid-morning (2 h prior to solar noon), 36% at midday (solar noon) and 27% at mid-afternoon (2.5 h after solar noon), whereas under Low-N, g s was reduced by as much as 31% at mid-morning, 44% at midday and 28% at mid-afternoon compared with Control. But, no significant CO2 × N interaction effects occurred. Across seasons and growth stages, daily accumulation of carbon (A′) was 27% greater in FACE than Control. High-N increased A′ by 18% compared with Low-N. In contrast to results for g s, however, significant CO2 × N interaction effects occurred because FACE increased A′ by 30% at High-N, but by only 23% at Low-N. FACE enhanced the seasonal accumulation of carbon (A′′) by 29% during 1996 (moderate N-stress), but by only 21% during 1997 (severe N-stress). These results support the premise that in a future high-CO2 world an acclimatory (down-regulation) response in the photosynthetic apparatus of field-grown wheat is anticipated. They also demonstrate, however, that the stimulatory effect of a rise in atmospheric CO2 on carbon gain in wheat can be maintained if nutrients such as nitrogen are in ample supply.
Abstract Previous studies of photosynthetic acclimation to elevated CO2 have focused on the most recently expanded, sunlit leaves in the canopy. We examined acclimation in a vertical profile of leaves through a canopy of wheat (Triticum aestivum L.). The crop was grown at an elevated CO2 partial pressure of 55 Pa within a replicated field experiment using free-air CO2 enrichment. Gas exchange was used to estimate in vivo carboxylation capacity and the maximum rate of ribulose-1,5-bisphosphate-limited photosynthesis. Net photosynthetic CO2 uptake was measured for leaves in situ within the canopy. Leaf contents of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco), light-harvesting-complex (LHC) proteins, and total N were determined. Elevated CO2 did not affect carboxylation capacity in the most recently expanded leaves but led to a decrease in lower, shaded leaves during grain development. Despite this acclimation, in situ photosynthetic CO2 uptake remained higher under elevated CO2. Acclimation at elevated CO2 was accompanied by decreases in both Rubisco and total leaf N contents and an increase in LHC content. Elevated CO2 led to a larger increase in LHC/Rubisco in lower canopy leaves than in the uppermost leaf. Acclimation of leaf photosynthesis to elevated CO2 therefore depended on both vertical position within the canopy and the developmental stage.
To quantify the growth and yield responses to CO2 enrichment in an open field setting, freeair CO2 enrichment (FACE) technology was used to expose a cotton (Gossypium hirsutum L.) crop to 550 γmol mol−2 CO2 throughout the growing seasons of 1989, 1990 and 1991 in fields near Maricopa, Arizona. In 1990 and 1991 a water stress treatment was also imposed. Response data for all years were consistent, and the data for 1991 were the least compromised by unusual weather or equipment failures. In that season the biomass was increased 37% by the 48% increase in CO2 concentration. Harvestable yield was increased 43%. The increase in biomass and yield was attributed to increased early leaf area, more profuse flowering and a longer period of fruit retention. The FACE treatment increased water-use efficiency (WUE) to the same amount in the well-irrigated plots as in the water-stressed plots. The increase in WUE was due to the increase in biomass production rather than a reduction of consumptive use.
CO2 treatment level control and CO2 use are reported for free-air carbon dioxide enrichment (FACE) facility operations at the University of Arizona's Maricopa Agricultural Center in 1990 and 1991. These are required for evaluation of the validity of biological experiments conducted in four replicates of paired experimental and control plots in a large cotton field and the cost-effectiveness of the plant fumigation facility. Gas concentration was controlled to 550 γmol mol-1 at the center of each experimental plot, just above the canopy. In both years, season-long (April–September) average CO2 levels during treatment hours (05:00–19:00 h Mountain Standard Time) were 550 γmol mol−1 measured at treatment plot centers when the facility was operating. Including downtime, the season average was 548 γmol mol−1 in 1991. In 1990, the season averages for the four elevated CO2 treatments varied from 522 to 544 γmol mol−1, owing to extended periods of downtime after lightning damage. Ambient CO2 concentration during treatment was 370 γmol mol−1. Instantaneous measurements of CO2 concentration were within 10% of the target concentration of 550 γmol mol−1 more than 65% of the time when the facility was operating, and 1 min averages were within 10% of the target concentration for 90% of the time. The long-term average of CO2 concentration measured over the 20 m diameter experimental area of one array at the height of the canopy was in the range 550–580 γmol mol−1 during July 1991, with the higher values near the edges. In 1991, CO2 demand averaged 1250 kg per array per 14 h treatment day, or 4 kg m−2 of fumigated plant canopy. The FACE facility provided good temporal and spatial control of CO2 concentration and was a cost-effective method for large-scale field evaluations of the biological effects of CO2.