We examined the effect of harvest schedule on the yield of ‘Red Russian’ kale (Brassica napus ssp. napus var. pabularia) grown during the winter in 16 × 32-ft high tunnels in northern New Mexico. We conducted the study for two growing seasons: 2013–14 and 2014–15. All plots were sown on 16 Oct. and harvested four times according to four harvest schedules: A) 8, 16, 20, and 24 weeks after sowing; B) 10, 17, 21, and 25 weeks after sowing; C) 12, 18, 22, and 26 weeks after sowing; and D) 14, 19, 23, and 27 weeks after sowing. The first harvest of each treatment was the greatest, averaging 216 g/ft2, compared with 88, 109, and 104 g/ft2 for harvests 2, 3, and 4, respectively. Season total yield of treatments B, C, and D (harvests beginning at 10, 12, and 14 weeks after sowing) yielded significantly more than treatment A, but only in year 2, when delayed growth resulted in very low yields for treatment A at harvest 1. Considering the entire 240-ft2 cropped area of the high tunnel, staggered harvests of 60 ft2 at a time can yield 2.6 to 17.5 kg per harvest or up to 124 kg over an entire season. Although we examined the yield of mature leaves, harvests could possibly begin earlier than in this study for “baby” kale or salad mixes, and the area harvested could be tailored to plant growth stage and market demand.
Robert F. Heyduck, Dawn VanLeeuwen, and Steven J. Guldan
Geno A. Picchioni, Sharon A. Martinez, John G. Mexal, and Dawn M. VanLeeuwen
Commercial production of pecan [Carya illinoinensis (Wangenh.) K. Koch.] generates significant woody biomass from hedge prunings with little economic value. Value-added uses could aid pecan growers, and one possible use is wood chips for potting substrates to lessen dependence on peatmoss, thereby aiding greenhouse growers. We evaluated vegetative growth and leaf nutrient responses of ‘Carpino’ garden chrysanthemum (Dendranthema ×grandiflorum) over a 60-day period. Plants were grown in five pecan wood chip substrate levels that substituted 0%, 25%, 50%, 75%, and 100% of peatmoss by volume. Three water soluble fertilizer (WSF) rates—N at 0, 200, or 400 mg·L−1 (0–N, 200–N, and 400–N, respectively)—were applied with each irrigation and to each of the wood substitution treatments. The WSF and wood substitution treatments interacted strongly. In the presence of wood, (25−100% substitution levels), increasing WSF to 400–N increased cumulative evapotranspiration (ET), crop height, total leaf number and area, total leaf and stem dry weight, and leaf N and P concentrations. However, with 0% wood substitution, 400−N provided little or no such enhancements. With 25% to 50% wood substitution, root dry weight increased by 61% to 91% from 0–N to 200–N, which may be an adaptive response to nutrient-limiting conditions at 200–N. Appearance of a white rot fungal species in and atop pecan wood-supplemented substrate supports the likelihood that microbial activity was, at least in part, responsible for the nutrient limitations. High WSF at 400–N in combination with 25% pecan wood substitution maintained adequate fertility and shoot growth that was comparable to the conventional peat-only substrate at 200–N. With low to moderate amounts of pecan wood, further adjustments to WSF rate and irrigation volume would support sustainable fertigation practices, reduce dependence on peatmoss by greenhouse industry, and provide a value-added recycling option for pecan growers.
Yuqing Wang, Richard J. Heerema, James L. Walworth, Barry Dungan, Dawn VanLeeuwen, and F. Omar Holguin
Pecan (Carya illinoinensis) has high kernel antioxidant activity and unsaturated fatty acid content, which contribute to its nutraceutical properties. In the western United States, where soils are typically alkaline, pecan trees require frequent zinc (Zn) fertilizer applications to maintain normal canopy growth and nut production. Our objective was to investigate the effects of tree Zn fertilization on nutraceutical properties of ‘Wichita’ and ‘Western’ pecan kernels. Trees were fertilized with ethylenediaminetetraacetic acid (EDTA) chelated Zn, which was applied to the soil at one of three seasonal rates for a total of three treatments: 0 (control), 2.2, or 4.4 kg·ha−1 Zn. Nut samples were collected and homogenized for analyses of kernel oil yield, hydrophilic antioxidant capacity, fatty acid profile, and γ-tocopherol content. Although soil Zn treatments did not significantly affect antioxidant capacity of defatted pecan kernels, Zn application had significant positive effects on both total kernel oil yield and γ-tocopherol content compared with the control. In conclusion, soil application of Zn fertilizer may increase the human health-promoting aspects of pecan kernels, a valuable attribute among health-conscious consumers.
Marisa Y. Thompson, Jennifer J. Randall, Dawn VanLeeuwen, and Richard J. Heerema
Regarding pecan (Carya illinoinensis), alternate bearing, which is a biennial fluctuation of crop yield, is a major hindrance for the pecan industry. Little is known about the internal cues that trigger pecan shoots to become reproductive. This 2-year study approached the mysteries of alternate bearing of pecan by determining whether pecan homologs of three genes known to control floral initiation in other species are expressed differently at various times of the growing season or in distinct plant tissues, and whether expression of these genes can be manipulated by plant growth regulator (PGR) application when compared with an untreated control group. The flowering genes of interest were pecan homologs of leafy (CpLFY), apetala1 (CpAP1), and flowering locus t (CpFT). During year 1 (2014), PGRs ethephon and gibberellin GA3 were applied at the shoot level 1 week before each of three tissue sampling dates (13 June, 3 July, 29 July). During the following year (2015), two more PGRs were added to the study [a second double rate (2X) of gibberellin GA3 and ethylene inhibitor aminoethoxyvinylglycine (AVG)] for a total of four PGRs (applied on 10 June, 1 July, and 23 July) plus the untreated control. Experimental leaf and bud tissues were sampled from fruiting and nonfruiting shoots on mature ‘Western’ pecan trees and analyzed separately. Normalized expression levels of CpLFY and CpAP1 were significantly higher in buds than in leaves. Normalized expression of CpLFY in bud tissues differed statistically based on the sampling date in 2014, with the earliest date (13 June) having higher expression than the two later dates that year. In 2015, a treatment × date interaction revealed that, compared with the untreated control, CpLFY expression was significantly lower in shoots treated with both gibberellin GA3 dosages on 1 July. A few weeks later (23 July), CpLFY expression was lower in the 2X GA3 treatment group and higher in samples treated with AVG. In 2014, CpAP1 expression in buds was significant, with a treatment × date interaction in which ethephon increased CpAP1 expression, but only on one date (29 July). In 2015, bud CpAP1 expression was significantly higher in fruiting than in nonfruiting shoots; however, again, only on one date. The results reveal differential expression of these key flowering genes based on tissue type, sampling date, and fruiting status of the shoot and PGR treatment. Results suggest that more research of the effects of PGRs is necessary for understanding the flowering behavior of pecan and mitigating the intensity of alternate bearing.
Jacqueline Cormier, Robert Heyduck, Steven Guldan, Shengrui Yao, Dawn VanLeeuwen, and Ivette Guzman
A decrease in available farmland worldwide has prompted interest in polyculture systems such as intercropping where two or more crops are grown simultaneously on the same land to increase the yield per farm area. In Alcalde, NM, a year-round intercropping system was designed to evaluate organically produced blackberry cultivars (Rubus, subgenus Rubus) and winter greens in a high tunnel over a 2-year period. Two floricane fruiting blackberry cultivars, Chester Thornless and Triple Crown, were grown intercropped with ‘Red Russian’ kale (Brassica napus) and ‘Bloomsdale’ spinach (Spinacia oleracea) in a high tunnel. In an adjacent field, the planting of blackberry was repeated with no winter intercrop and no high tunnel. Both cultivars of blackberry were harvested July to September, and fresh weights were measured to determine suitability to the intercropping system in the high tunnel. Both species of winter greens were harvested January to April, and fresh yield weights were measured to discern fitness as possible intercrops in this system. Row covers were used for kale and spinach, and air temperatures were monitored November to April inside the high tunnel. High tunnel temperatures were within acceptable ranges for the production of greens with the use of rowcovers. Yield data from this study indicates that ‘Triple Crown’ blackberry outperformed ‘Chester Thornless’ blackberry in both the high tunnel and field trials with significant difference in the second season. Additionally, blackberry yields from both cultivars were observed to be higher in the field than in the high tunnel for both years. High temperature damage to high tunnel berry canes was noticed for both cultivars, with observed yield decreases in the second year in the high tunnel. Overall, this study indicates that the phenology and climate needs of the two winter greens and blackberry cultivars were not compatible for sustaining year-round organic high tunnel production.
Richard J. Heerema, Dawn VanLeeuwen, Marisa Y. Thompson, Joshua D. Sherman, Mary J. Comeau, and James L. Walworth
Zinc deficiency is common in pecan (Carya illinoinensis) grown in alkaline, calcareous soils. Zinc (Zn)-deficient pecan leaves exhibit interveinal chlorosis, decreased leaf thickness, and reduced photosynthetic capacity. Low photosynthesis (Pn) contributes to restricted vegetative growth, flowering, and fruiting of Zn-deficient pecan trees. Our objectives were to measure effects of soil-applied ethylenediaminetetraacetic acid (EDTA)-chelated Zn fertilizer on gas exchange of immature ‘Wichita’ pecan and characterize the relationship between leaf Zn concentration and Pn. The study orchard had alkaline and calcareous soils and was planted in Spring 2011. Zinc was applied throughout each growing season as Zn EDTA through microsprinklers at rates of 0 (Control), 2.2, or 4.4 kg·ha−1 Zn. Leaf gas exchange and SPAD were measured on one occasion in the 2012 growing season, four in 2013, and five in 2014. Soil Zn-EDTA applications significantly increased the leaf tissue Zn concentration throughout the study. On all measurement occasions, net Pn was significantly increased by soil-applied Zn EDTA compared with the control, but Pn was not different between the two soil-applied Zn-EDTA treatments. Leaf Pn in midseason did not increase at leaf tissue Zn concentrations above 14–22 mg·kg−1. Leaf SPAD consistently followed a similar pattern to Pn. Soil Zn-EDTA application increased leaf stomatal conductance (g S) compared with the Control early through midseason but not after August. Intercellular CO2 concentration was significantly lower for Zn-EDTA-treated trees than the Control even on dates when there was no significant difference in g s, which suggests that soil application of Zn-EDTA alleviated nonstomatal limitations to Pn caused by Zn deficiency.
Cyrus A. Smith, Dawn VanLeeuwen, Richard J. Heerema, Joshua D. Sherman, Mary J. Comeau, and James L. Walworth
Analysis of composite pecan leaf samples typically used to determine need for nutrient applications does not account for variability among trees in the sampled area. To account for this unmeasured variability, pecan orchard block nutrient standards are greater than actual single tree nutrient requirements. In 2018 and 2019, we measured variability in a pecan orchard block by evaluating nutrient status of all trees in a study area consisting of two cultivars (Wichita and Western) grafted on open-pollinated ‘Ideal’ seedlings. Foliar zinc (Zn) coefficient of variation (cv) ranged from 0.186 to 0.255 within individual cultivars and years but was as high as 0.30 when combining cultivars within a year. The ‘Western’ cultivar had higher foliar Zn concentrations than ‘Wichita’, but Zn concentrations were not consistently associated with other leaf nutrient levels, soil Zn status, or other soil properties. Using observed foliar Zn variability, we determined that it is necessary to sample 35 trees for a composite sample to achieve a relative margin of error of 10% and 95% confidence level in a pecan orchard block with more than 1000 trees. We developed field scale foliar Zn recommendations based on individual tree research that indicates a minimum acceptable leaf Zn concentration of ≈15 mg·kg–1 is needed to maintain optimal photosynthetic function in Zn chelate fertigated pecan trees. Assuming a Zn cv of 0.30 and a composite sample comprised of leaves from 35 trees, the minimum acceptable orchard block Zn level to ensure that less than 5% of trees had suboptimal levels of Zn was 27.6 mg·kg–1. An orchard block Zn level below 23.4 mg·kg–1 indicates that more than 5% of trees in the block had suboptimal foliar Zn concentrations.
Mark E. Uchanski, Dawn M. VanLeeuwen, Steven J. Guldan, Constance L. Falk, Manoj Shukla, and Juliette Enfield
Replicated temperature data from passively heated high tunnels are lacking, especially in the southwestern United States. Field studies were conducted over three seasons in two locations in New Mexico—a southern site in Las Cruces and a northern site in Alcalde—to characterize the crop environment in three high-tunnel designs during the winter growing season (October–March). High tunnels were 16 × 32 ft and oriented with the long edge running east to west. Heavyweight woven plastic covered the single-layer (SL) high-tunnel design. Double-layer designs (DL) were covered with a lightweight woven plastic on the bottom, followed by a second layer of the heavyweight plastic inflated with a fan. A heat sink was created using 16 55-gal barrels painted black, filled with water, and aligned along the north side of the double layer for the DL+B design. Soil temperature (3 inches deep) and air temperature (1 ft above the soil surface) were recorded inside the high tunnel, inside the high tunnel under a floating rowcover, and outside the high tunnel. In addition, photosynthetically active radiation (PAR) was recorded inside and outside the high tunnels during or near the winter solstice each year of the study. Daily air and soil temperature minimums were highest in the DL+B design and lowest in the SL design. Maximum air and soil temperatures did not significantly differ between high-tunnel designs, although the DL+B design measurements were consistently lower. During season 1, the SL design had significantly higher PAR transmission than the other two designs. In the northern location, the difference became insignificant during seasons 2 and 3, likely due to dust accumulation and plastic aging. In the southern location, the SL design maintained higher PAR transmission throughout the study, possibly due to plastic cleaning. Data collected in this study can help inform the decisions of high-tunnel growers and researchers in the region.