scholarly journals Foliage Removal Influences Sweetpotato Biomass Yields in Hydroponic Culture

HortScience ◽  
1995 ◽  
Vol 30 (5) ◽  
pp. 1000-1002 ◽  
Author(s):  
P.P. David ◽  
A.A. Trotman ◽  
D.G. Mortley ◽  
C.K. Bonsi ◽  
P.A. Loretan ◽  
...  
Keyword(s):  
Growth Rate ◽  
Ipomoea Batatas ◽  
Linear Growth ◽  
Canopy Cover ◽  
Linear Growth Rate ◽  
Shoot Biomass ◽  
Storage Root ◽  
Root Yield ◽  
Nutrient Film Technique ◽  
Half Strength

Greenhouse studies were conducted to determine the effect of harvesting sweetpotato [Ipomoea batatas L. (Lam.)] foliage tips (terminal 15 cm) on storage root yield, edible biomass index (EBI), and linear growth rate. Plants were grown hydroponically from 15-cm vine cuttings planted in 0.15 × 0.15 × 1.2-m growth channels using a recirculating nutrient film technique system. Nutrients were supplied from a modified half-strength Hoagland solution with a 1 N: 2.4 K ratio. Foliage tips were removed at 14-day intervals beginning 42 days after transplanting. Final harvest was at 120 days after planting. At the end of the growing season, harvested foliage tips totaled 225 g/plant (fresh mass). Foliage removal significantly reduced storage root yield, shoot biomass, and linear growth rate expressed on a canopy cover basis. The EBI was higher for plants with foliage removed than for the control.

scholarly journals Relative Humidity Influences Yield, Edible Biomass, and Linear Growth Rate of Sweetpotato

HortScience ◽  
1994 ◽  
Vol 29 (6) ◽  
pp. 609-610 ◽  
Author(s):  
D.G. Mortley ◽  
C.K. Bonsi ◽  
P.A. Loretan ◽  
W.A. Hill ◽  
C.E. Morris
Keyword(s):  
Growth Rate ◽  
Relative Humidity ◽  
Ipomoea Batatas ◽  
Linear Growth ◽  
Block Design ◽  
Dry Weight ◽  
Linear Growth Rate ◽  
Storage Root ◽  
Storage Roots ◽  
Temperature Regimes

Growth chamber experiments were conducted to study the physiological and growth response of sweetpotato [Ipomoea batatas (L.) Lam.] to either 50% or 85 % relative humidity (RH). Vine cuttings of T1-155 were grown using the nutrient film technique in a randomized complete-block design with two replications. Temperature regimes of 28/22C were maintained during the light/dark periods with irradiance at canopy level of 600 μmol·m-2·s-1 and a 14/10-hour photoperiod. High RH (85%) increased the number of storage roots per plant and significantly increased storage root fresh and dry weight, but produced lower foliage fresh and dry weight than plants grown at 50% RH. Edible biomass index and linear growth rate (in grams per square meter per day) were significantly higher for plants grown at 85 % than at 50% RH. Leaf photosynthesis and stomatal conductance were higher for plants at 85 % than at 50% RH. Thus, the principal effect of high RH on sweetpotato growth was the production of higher storage root yield, edible biomass, growth rate, and increased photosynthetic and stomatal activity.

scholarly journals Plant Spacing Influences Yield and Linear Growth Rate of Sweetpotatoes Grown Hydroponically

HortScience ◽  
1991 ◽  
Vol 26 (10) ◽  
pp. 1274-1275 ◽  
Author(s):  
D.G. Mortley ◽  
P.A. Loretan ◽  
C.K. Bonsi ◽  
W.A. Hill ◽  
C.E. Morris
Keyword(s):  
Growth Rate ◽  
Linear Growth ◽  
Linear Growth Rate ◽  
Plant Spacing ◽  
Storage Root ◽  
Root Area ◽  
Nutrient Film Technique ◽  
Canopy Area ◽  
Area Basis ◽  
Foliage Weight

The effects of within-channel spacings (WCS; 13, 18, 25 cm) and between-channel spacings (BCS; 13, 25,38 cm) on yield and linear growth rate of sweetpotatoes [Ipomoea batalas (L.) Lam.] grown by use of the nutrient film technique (NFT) were evaluated. Storage root count, fresh and dry weights, and linear growth rate, expressed as root area, declined linearly in response to decreased BCS, while fresh and dry foliage weight decreased linearly and quadratically as spacing was reduced within the growth channels. Neither linear growth rate on a canopy area basis nor the edible biomass index was significantly affected by WCS or BCS.

scholarly journals EFFECTS OF BIWEEKLY TOPPING ON NUTRIENT CONTENT OF SHOOT TIPS AND STORAGE ROOT YIELD OF SWEETPOTATO GROWN IN A NFT SYSTEM.

HortScience ◽  
1992 ◽  
Vol 27 (11) ◽  
pp. 1170f-1170
Author(s):  
P.P. David ◽  
A. Almazan ◽  
C.K. Bonsi ◽  
D.G. Mortley ◽  
A.A. Trotman ◽  
...  
Keyword(s):  
Nutrient Content ◽  
Shoot Tips ◽  
Shoot Biomass ◽  
Storage Root ◽  
Root Yield ◽  
Storage Roots ◽  
Ipomea Batatas ◽  
Half Strength ◽  
And Storage ◽  
Final Harvest

Studies were conducted in a greenhouse to determine the effects of harvesting sweetpotato (Ipomea batatas L. (Lam.) cv. “TI-82-155”) shoot tips (top 10 cm) at biweekly intervals beginning 42 days after transplanting on yield of storage root and nutrient content of harvested shoot tips. Plants were grown hydroponically from vine cuttings of 15 cm length, planted in 0.15 × 0.15 × 0.12 m growth channels using a closed NFT system. Nutrient was supplied in a modified half-strength Hoagland's solution with a N:K ratio of 1:2.4. Final harvest was at 120 days when shoot biomass and yield of storage roots were measured. Biweekly topping did not affect storage root yield or shoot biomass. However, harvesting time had a significant effect on dry matter and nutrient content of shoot tips.

scholarly journals Growth Responses of Hydroponically Grown Sweetpotato Tolerant and Intolerant of a Continuous Daily Light Period

HortScience ◽  
1996 ◽  
Vol 31 (2) ◽  
pp. 209-212 ◽  
Author(s):  
D.G. Mortley ◽  
P.A. Loretan ◽  
W.A. Hill ◽  
C.K. Bonsi ◽  
C.E. Morris
Keyword(s):  
Ipomoea Batatas ◽  
Production Efficiency ◽  
Elemental Concentration ◽  
Light Period ◽  
Photon Flux ◽  
Storage Root ◽  
Growth Responses ◽  
Area Index ◽  
Nutrient Film Technique ◽  
Half Strength

Two sweetpotato [Ipomoea batatas (L.) Lam] genotypes (`Georgia Jet' and the breeding clone TI-155) were grown at 12-, 15-, 18-, and 21-h light/12-, 9-, 6-, 3-h dark cycles, respectively, to evaluate their growth and elemental concentration responses to duration and amount of daily lighting. Vine cuttings (15 cm long) of both genotypes were grown in rectangular nutrient film technique channels for 120 days. Conditions were as follows: photosynthetic photon flux (PPF) mean 427 μmol·m–2·s–1, 28C day/22C night air cycle, and 70% ± 5% relative humidity. The nutrient solution used was a modified half-strength Hoagland's solution. Storage root count per plant and per unit area, yield (in grams per square meters per day), and harvest index increased, while production efficiency (in grams per mole) decreased with increased daily PPF. Stomatal conductance for both genotypes declined with increased daily PPF. Leaves were smallest for both genotypes at the 21-h light period, while storage root yield declined as leaf area index increased. Except for a linear decrease in leaf N and K with increased light period, elemental concentration was not significantly influenced.

scholarly journals Potassium Fertilization Stimulates Sucrose-to-Starch Conversion and Root Formation in Sweet Potato (Ipomoea batatas (L.) Lam.)

2021 ◽  
Vol 22 (9) ◽  
pp. 4826
Author(s):  
Yang Gao ◽  
Zhonghou Tang ◽  
Houqiang Xia ◽  
Minfei Sheng ◽  
Ming Liu ◽  
...  
Keyword(s):  
Sweet Potato ◽  
Ipomoea Batatas ◽  
Intercellular Co2 Concentration ◽  
Biomass Accumulation ◽  
Starch Accumulation ◽  
Storage Root ◽  
Root Yield ◽  
Starch Conversion ◽  
And Storage ◽  
Low K

A field experiment was established to study sweet potato growth, starch dynamic accumulation, key enzymes and gene transcription in the sucrose-to-starch conversion and their relationships under six K2O rates using Ningzishu 1 (sensitive to low-K) and Xushu 32 (tolerant to low-K). The results indicated that K application significantly improved the biomass accumulation of plant and storage root, although treatments at high levels of K, i.e., 300–375 kg K2O ha−1, significantly decreased plant biomass and storage root yield. Compared with the no-K treatment, K application enhanced the biomass accumulation of plant and storage root by 3–47% and 13–45%, respectively, through promoting the biomass accumulation rate. Additionally, K application also enhanced the photosynthetic capacity of sweet potato. In this study, low stomatal conductance and net photosynthetic rate (Pn) accompanied with decreased intercellular CO2 concentration were observed in the no-K treatment at 35 DAT, indicating that Pn was reduced mainly due to stomatal limitation; at 55 DAT, reduced Pn in the no-K treatment was caused by non-stomatal factors. Compared with the no-K treatment, the content of sucrose, amylose and amylopectin decreased by 9–34%, 9–23% and 6–19%, respectively, but starch accumulation increased by 11–21% under K supply. The activities of sucrose synthetase (SuSy), adenosine-diphosphate-glucose pyrophosphorylase (AGPase), starch synthase (SSS) and the transcription of Susy, AGP, SSS34 and SSS67 were enhanced by K application and had positive relationships with starch accumulation. Therefore, K application promoted starch accumulation and storage root yield through regulating the activities and genes transcription of SuSy, AGPase and SSS in the sucrose-to-starch conversion.

Microborings and growth in Late Ordovician halysitids and other corals

1993 ◽  
Vol 67 (6) ◽  
pp. 922-934 ◽  
Author(s):  
Robert J. Elias ◽  
Dong-Jin Lee
Keyword(s):  
Growth Rate ◽  
Linear Growth ◽  
Inverse Correlation ◽  
Weight Percent ◽  
Late Ordovician ◽  
Coral Growth ◽  
Linear Growth Rate ◽  
Skeletal Density ◽  
Rugose Coral ◽  
Endolithic Algae

Microborings in the Late Ordovician tabulate corals Catenipora rubra (a halysitid) and Manipora amicarum (a cateniform nonhalysitid) and in an epizoic solitary rugose coral differ from nearly all of those previously reported in Paleozoic corals. These microborings were formed within the coralla by endolithic algae and fungi located beneath living polyps. Comparable structures in the Late Ordovician tabulate Quepora ?agglomeratiformis (a halysitid) represent algal microborings, not spicules, and halysitids are corals, not sponges as suggested by Kaźmierczak (1989).Endolithic algae in cateniform tabulates relied primarily on light entering through the outer walls of the ranks rather than through the polyps; lacunae within coralla permitted appropriate levels of light to reach many corallites. The direction of boring was determined by corallum microstructure and possibly also by the distribution of organic matter within the skeleton. There is an apparent inverse correlation between boring activity and coral growth rate.The location and relative abundance of pyritized microborings within calcareous coralla can be established quantitatively and objectively from electron microprobe determinations of weight percent sulfur along appropriate traverses of the coral skeleton. The distribution of such microborings in Catenipora rubra and Manipora amicarum is comparable to algal banding in modern corals; this is the first report of such banding in the interiors of Paleozoic corals. Change in the intensity of boring within each corallum was evidently a response to variation in the linear growth rate of the coral, or to fluctuation in an environmental factor (perhaps light intensity) that could control both algal activity and growth rate in these corals. Change in the algal boring intensity and linear growth rate of the coral was generally but not always seasonal and usually but not invariably associated with change in the density of coral skeletal deposition.Cyclic bands of boring abundance maxima within fossil colonial corals provide a measure of annual linear growth comparable to the widely accepted method based on skeletal density bands. Algal bands are more sporadically developed than density bands within and among coralla, thus increasing the difficulty of interpretation. Fluctuations in the abundance of algal microborings apparently provide a detailed record of changes in the linear growth rate of colonies and of individuals within colonies. Combined analyses of microboring abundance and skeletal density will contribute significantly to our understanding of the biological and environmental factors involved in endolithic activity and coral growth.

scholarly journals <sup>210</sup>Pb-<sup>226</sup>Ra chronology reveals rapid growth rate of <i>Madrepora oculata</I> and <i>Lophelia pertusa</i> on world's largest cold-water coral reef

2011 ◽  
Vol 8 (6) ◽  
pp. 12247-12283
Author(s):  
P. Sabatier ◽  
J.-L. Reyss ◽  
J. M. Hall-Spencer ◽  
C. Colin ◽  
N. Frank ◽  
...  
Keyword(s):  
Growth Rate ◽  
Coral Reef ◽  
Linear Growth ◽  
Cold Water ◽  
Optimal Growth ◽  
Growth Conditions ◽  
Age And Growth ◽  
Linear Growth Rate ◽  
Lophelia Pertusa ◽  
Water Coral

Abstract. Here we show the use of the 210Pb-226Ra excess method to determine the growth rate of corals from one of the world's largest known cold-water coral reef, the Røst Reef off Norway. Two large branching framework-forming cold-water coral specimens, one Lophelia pertusa and one Madrepora oculata were collected alive at 350 m water depth from the Røst Reef at ~67° N and ~9° E. Pb and Ra isotopes were measured along the major growth axis of both specimens using low level alpha and gamma spectrometry and the corals trace element compositions were studied using ICP-QMS. Due to the different chemical behaviors of Pb and Ra in the marine environment, 210Pb and 226Ra were not incorporated the same way into the aragonite skeleton of those two cold-water corals. Thus to assess of the growth rates of both specimens we have here taken in consideration the exponential decrease of initially incorporated 210Pb as well as the ingrowth of 210Pb from the decay of 226Ra. Moreover a~post-depositional 210Pb incorporation is found in relation to the Mn-Fe coatings that could not be entirely removed from the oldest parts of the skeletons. The 226Ra activities in both corals were fairly constant, then assuming constant uptake of 210Pb through time the 210Pb-226Ra chronology can be applied to calculate linear growth rate. The 45.5 cm long branch of M. oculata reveals an age of 31 yr and a~linear growth rate of 14.4 ± 1.1 mm yr−1, i.e. 2.6 polyps per year. However, a correction regarding a remaining post-depositional Mn-Fe oxide coating is needed for the base of the specimen. The corrected age tend to confirm the radiocarbon derived basal age of 40 yr (using 14C bomb peak) with a mean growth rate of 2 polyps yr−1. This rate is similar to the one obtained in Aquaria experiments under optimal growth conditions. For the 80 cm-long specimen of L. pertusa a remaining contamination of metal-oxides is observed for the middle and basal part of the coral skeleton, inhibiting similar accurate age and growth rate estimates. However, the youngest branch was free of Mn enrichment and this 15 cm section reveals a growth rate of 8 mm yr−1 (~1 polyp every two to three years). However, the 210Pb growth rate estimate is within the lowermost ranges of previous growth rate estimates and may thus reflect that the coral was not developing at optimal growth conditions. Overall, 210Pb-226Ra dating can be successfully applied to determine the age and growth rate of framework-forming cold-water corals, however, removal of post-depositional Mn-Fe oxide deposits is a prerequisite. If successful, large branching M. oculata and L. pertusa coral skeletons provide unique oceanographic archive for studies of intermediate water environmentals with an up to annual time resolution and spanning over many decades.

scholarly journals Generation of Wave Groups by Shear Layer Instability

Fluids ◽  
2019 ◽  
Vol 4 (1) ◽  
pp. 39 ◽  
Author(s):  
Roger Grimshaw
Keyword(s):  
Growth Rate ◽  
Group Velocity ◽  
Linear Growth ◽  
Linear Stability Theory ◽  
Linear Growth Rate ◽  
Wave Groups ◽  
Weakly Nonlinear ◽  
Complex Valued ◽  
Fundamental Requirement ◽  
Temporal Growth Rate

The linear stability theory of wind-wave generation is revisited with an emphasis on the generation of wave groups. The outcome is the fundamental requirement that the group move with a real-valued group velocity. This implies that both the wave frequency and the wavenumber should be complex-valued, and in turn this then leads to a growth rate in the reference frame moving with the group velocity which is in general different from the temporal growth rate. In the weakly nonlinear regime, the amplitude envelope of the wave group is governed by a forced nonlinear Schrödinger equation. The effect of the wind forcing term is to enhance modulation instability both in terms of the wave growth and in terms of the domain of instability in the modulation wavenumber space. Also, the soliton solution for the wave envelope grows in amplitude at twice the linear growth rate.

scholarly journals Wavelength dependence of the linear growth rate of the <I>E<sub>s</sub></I> layer instability

2007 ◽  
Vol 25 (6) ◽  
pp. 1311-1322 ◽  
Author(s):  
R. B. Cosgrove
Keyword(s):  
Growth Rate ◽  
Electric Fields ◽  
Large Scale ◽  
Linear Growth ◽  
Three Dimensional ◽  
Generalized Derivation ◽  
Wavelength Dependence ◽  
Meridional Wind ◽  
Linear Growth Rate ◽  
Significant Wavelength

Abstract. It has recently been shown, by computation of the linear growth rate, that midlatitude sporadic-E (Es) layers are subject to a large scale electrodynamic instability. This instability is a logical candidate to explain certain frontal structuring events, and polarization electric fields, which have been observed in Es layers by ionosondes, by coherent scatter radars, and by rockets. However, the original growth rate derivation assumed an infinitely thin Es layer, and therefore did not address the short wavelength cutoff. Also, the same derivation ignored the effects of F region loading, which is a significant wavelength dependent effect. Herein is given a generalized derivation that remedies both these short comings, and thereby allows a computation of the wavelength dependence of the linear growth rate, as well as computations of various threshold conditions. The wavelength dependence of the linear growth rate is compared with observed periodicities, and the role of the zeroth order meridional wind is explored. A three-dimensional paper model is used to explain the instability geometry, which has been defined formally in previous works.

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