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Ajmer S. Bhagsari and Doyle A. Ashley

Field experiments with 15 sweet potato [Ipomoea batatas L. (Lam.)] genotypes were conducted to study the physiological basis of yield in 1981 and 1982. The leaf area index differed significantly among the sweet potato genotypes during early and late phases of growth, hut showed an inconsistent relationship with yield. Single leaf net photosynthesis ranged from 0.74 to 1.12 mg CO2/m' per sec. Canopy photosynthesis for sweet potato genotypes differed significantly in 1981, but not in 1982. It ranged from 0.81 to 1.16 mg CO2/m2 per sec in Aug. 1981. and from 0.63 to 0.88 mg CO2/m2 per sec in 1982. Four hours after “C-labeling, 14C-assimilate translocation from the treated leaf ranged from 21% to 46%, but did not differ significantly among the genotypes. At final harvest, harvest index [HI, defined as (storage root yield/total biological yield) × 100] of the genotypes varied from 43% to 77% and 31% to 75% for 1981 and 1982, respectively. Canopy photosynthesis during September was significantly correlated with storage root dry matter yield (r = 0.54*) in 1981 and with phytomass (above-ground biomass plus storage roots) (r = 0.60*) in 1982. Both phytomass and HI were significantly correlated with storage root matter yield. Canopy photosynthetic evaluation of sweet potato germplasm may be-more relevant when the storage root sinks are at an advanced stage of development. Our study suggests that yield is poorly predicted by Pn, particularly when the genotypes have different leaf sizes.

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D.G. Mortley, C.K. Bonsi, P.A. Loretan, W.A. Hill, and C.E. Morris

Growth chamber experiments were conducted to study the physiological and growth response of peanut (Arachis hypogaea L.) to 50% and 85% relative humidity (RH). The objective was to determine the effects of RH on pod and seed yield, harvest index, and flowering of peanut grown by the nutrient film technique (NFT). `Georgia Red' peanut plants (14 days old) were planted into growth channels (0.15 × 0.15 × 1.2 m). Plants were spaced 25 cm apart with 15 cm between channels. A modified half-Hoagland solution with an additional 2 mm Ca was used. Solution pH was maintained between 6.4 and 6.7, and electrical conductivity (EC) ranged between 1100 and 1200 μS·cm–1. Temperature regimes of 28/22 °C were maintained during the light/dark periods (12 hours each) with photosynthetic photon flux (PPF) at canopy level of 500 μmol·m–2·s–1. Foliage and pod fresh and dry weights, total seed yield, harvest index (HI), and seed maturity were greater at high than at low RH. Plants grown at 85% RH had greater total and individual leaflet area and stomatal conductance, flowered 3 days earlier and had a greater number of flowers reaching anthesis. Gynophores grew more rapidly at 85% than at 50% RH.

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B.T. Scully and D.H. Wallace

A diverse set of 112 common bean (Paseolus vulgaris L.) accessions were evaluated for variation in eight traits related to yield over a 2-year period. Days to flower, days of pod fill, and days to maturity ranged from 25 to 66, 44 to 83, and 70 to 133, respectively, in upstate New York: Yield and biomass ranged from 81 to 387 and 270 to 1087 g•m-2, respectively. Harvest index ranged from 12% to 65%. The biomass (biomass/days to maturity) and seed (yield/days of pod fill) growth rates ranged from 3.2 to 9.3 and 1.2 to 9.5 g•m-2 -day-1, respectively. The economic growth rate (yield/days to maturity) extended from 0.6 to 5.7 g•m-2 -day-1. The growth rates, biomass, and days of pod fill were linearly and positively related to yield. Biomass and the growth rates explained a large amount of the variation in yield, with r 2 values between 0.71 and 0.84; days of pod fill explained the least, with r 2 = 0.09. Yield followed a curvilinear relationship with days to flower and days to maturity; yield was maximized at 48.5 days to flower and 112.2 days to maturity. Yield was a quadratic function of harvest index and maximized at 57.2%. Among these three curvilinear traits, days to flower explained 80% of the variation in yield, while days to maturity and harvest index accounted for 25% and 12.5%, respectively. The “ideal” genotype for New York was defined at these maximum values for harvest index, days to maturity, days to flower, and at 63.7 days of pod fill. Additionally, a simple equation is proposed to aid breeders in the selection of common bean accessions with strong sink strength. It is defined as “relative sink strength”: RSS = seed growth rate/biomass growth rate. Values > 1.0 implied strong sink capacity in common beans.

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B.T. Scully, D.H. Wallace, and D.R. Viands

One-hundred-twelve common bean (Phaseolus vulgaris L.) lines of diverse origin were grown in three environments in 1986 and two environments in 1987. The purpose was to estimate broad-sense heritabilities of nine yield-related traits and the phenotypic, genetic, and environmental correlations among them. The traits and their heritabilities were seed yield (0.90), biomass (0.93), harvest index (0.92), days to maturity (0.96), days to flower (0.98), days of pod fill (0.94), biomass growth rate (biomass/days to maturity) (0.87), seed growth rate (seed yield/days of pod fill) (0.87), and economic growth rate (seed yield/days to maturity) (0.86). These high heritabilities were attributed to the broad genetic diversity and the comparatively small variances associated with the genotype × environment interactions. Genetic correlations of yield were: with biomass, 0.86; harvest index, 0.42; days to maturity, 0.40; days to flower, 0.33; days of pod fill, 0.24; biomass growth rate, 0.92; seed growth rate, 0.84; and the economic growth rate, 0.85. The concomitant phenotypic correlations were mostly equal to the genetic correlations for biomass and the three growth rates, but lower for the phonological traits (days to maturity, flower, and pod fill). Harvest index had the lowest correlations with yield. Correlations were also reported for the other 28 pairwise combinations among these nine traits. Indirect selection was explored with yield as the primary trait and the other eight as secondary traits. Estimates of relative selection efficiency (p) suggested that indirect selection was not a viable option for increasing common bean yields or identifying superior parents.

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D.G. Mortley, C.K. Bonsi, W.A. Hill, and C.E. Morris

`Georgia Red' peanut (Arachis hypogaea L.) was grown hydroponically at 20/16 °C, 24/20 °C, 28/24 °C, and 32/28 °C, day/night air temperatures to evaluate effects on pod and seed yield, flowering, harvest index, and oil content. Ten-day-old peanut seedlings were transplanted into rectangular nutrient film technique troughs (0.15 × 0.15 × 1.2 m) and grown for 110 days. Growth chamber conditions were as follows: photosynthetic photon flux (PPF) mean of 436 μmol·m-2·s-1, 12 h light/12 h dark cycle, and 70% ± 5% relative humidity. The nutrient solution used was a modified half-Hoagland with pH and electrical conductivity maintained between 6.5 to 6.7, and 1000 to 1300 μS·cm-1, respectively, and was replenished weekly. Vegetative growth (foliage, stem growth, total leaf area, and leaf number) was substantially greater at increasingly warmer temperatures. Reproductive growth was significantly influenced by temperature. Flowering was extremely sensitive to temperature as the process was delayed or severely restricted at 20/16 °C. The number of gynophores decreased with temperature and was virtually nonexistent at the lowest temperature. Pod yield increased with temperatures up to 28/24 °C but declined by 15% at the highest temperature (32/28 °C). Seed yield, maturity, and harvest index were highest at 28/24 °C. Oil content (percent crude fat) increased an average of 23% and was highest at the warmest temperature (32/28 °C). These results clearly suggest that vegetative and reproductive growth, as well as oil content of peanut in controlled environments, are best at warmer temperatures of 28/24 °C to 32/28 °C than at cooler temperatures of 20/16 °C to 24/20 °C.

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M. Moriondo, M. Bindi, and T. Sinclair

Crop growth simulation models have been mainly developed to simulate final yield reliably. Thus, a main challenge in these models is the definition of a stable method for expressing the growth of harvested organs (e.g., fruit, seed, tuber, etc.). Generally, two approaches have been used: growth rate analysis of harvested organs [yield growth rate (YGR)] and analysis of harvest index (HI) increase over time (dHI/dt). This work aims to: 1) examine whether YGR and dHI/dt increase linearly over much of growing period, and 2) compare the two growth indices in terms of stability across a number of treatments, in order to identify which is the best indicator of harvest-organ growth. This analysis has already been performed for a large number of field crops, including wheat (Triticum aestivum L.), sunflower (Helianthus annuus L.), soybean [Glycine max L. (Merr.)], and pea (Pisum sativum L.), but it has never been attempted in crops where final yield is not simply seeds. In this study, YGR and dHI/dt performances for tomato (Lycopersicum esculentum Mill.), potato (Solanum tuberosum L.), and eggplant (Solanum melongena L.) were compared using 21, 18, and 4 datasets, respectively. Results indicated that both descriptors of harvest-organ growth increased linearly for most of the growth period, whilst the comparison among the two variables in terms of stability showed that, although a direct statistical test failed, dHI/dt was more suitable to describe harvest-organ growth (smaller coefficient of variability) under a large range of crop management conditions (e.g., irrigation, sowing date, planting density, and water salt concentration).

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Eric T. Stafne and Barbara J. Smith

from the pruning treatments, received the same level of management and environmental exposure. Harvest index was calculated by dividing fruit yield by cane weight ( Price and Munns, 2018 ). The growth index (GI) was calculated as GI = H + [(L + W)/2

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André Pereira and Nilson Villa Nova

over time, C(T) is the correction factor for maintenance respiration, HI is the harvest index, and DM is the dry matter content of the potato tubers (%). Making use of the Clausius-Clapeyron's equation with the masses of CO 2 equal to 44 g·mol −1

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Guohai Xia, Lailiang Cheng, Alan Lakso, and Martin Goffinet

harvest was calculated as the difference between total tree dry weight at fruit harvest and at budbreak. Harvest index was calculated as percent of the net dry matter gain from budbreak to fruit harvest partitioned into fruit. Data analysis

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Harbans L. Bhardwaj and Anwar A. Hamama

narrow rows with similar plant density may be conducive to higher mungbean seed yields. We speculate that narrow row spacings might also be conducive to better weed control in mungbean fields. Mungbean Seed Yield and Harvest Index Harvest index (ratio of