scholarly journals Ammonium and Nitrate Accumulation in Containerized Southern Highbush Blueberry Plants

HortScience ◽  
1995 ◽  
Vol 30 (7) ◽  
pp. 1378-1381 ◽  
Author(s):  
Donald J. Merhaut ◽  
Rebecca L. Darnell

Ammonium and \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NO}_{3}^{-}\) \end{document} uptake and partitioning were monitored in `Sharpblue' southern highbush blueberry plants (Vaccinium corymbosum L. interspecific hybrid) using 10% 15N-enriched N. Shoots and roots were harvested at 0, 6, 12, 24, and 48 hours after labeling. The rate of \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NH}_{4}^{+}\mathrm{-}\mathrm{N}\) \end{document} uptake was higher than that of \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NO}_{3}^{-}\mathrm{-}\mathrm{N}\) \end{document} uptake, averaging 17.1 vs. 8.6 g N/g plant dry weight per hour during the 48-hour period for \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NH}_{4}^{+}\mathrm{-}\) \end{document} and \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NO}_{3}^{-}\mathrm{-treated}\) \end{document} plants, respectively. At the end of the 48 hours, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NH}_{4}^{+}\mathrm{-}\mathrm{N}\) \end{document} accumulation averaged 79 mg N/plant compared to 40 mg accumulated by the \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NO}_{3}^{-}\mathrm{-}\mathrm{N}\mathrm{-treated}\) \end{document} plants. Similarly, the translocation rate of \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NH}_{4}^{+}\mathrm{-}\mathrm{N}\) \end{document} to shoots was higher than translocation of \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NO}_{3}^{-}\mathrm{-}\mathrm{N}\) \end{document} to shoots (7.7 vs. 1.9 g N/g shoot dry weight per hour, respectively) during the 48 hours. Shoot accumulation of \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NH}_{4}^{+}\mathrm{-}\mathrm{N}\) \end{document} averaged 40 mg N/plant at the end of 48 hours, while accumulation in shoots of \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NO}_{3}^{-}\mathrm{-}\mathrm{N}\mathrm{-treated}\) \end{document} plants averaged 10 mg N/plant. Short-term \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NO}_{3}^{-}\) \end{document} uptake and translocation to shoots appears to be limited relative to \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{NH}_{4}^{+}\) \end{document} uptake and translocation in southern highbush blueberry when plants are previously fertilized with NH4NO3.

HortScience ◽  
2019 ◽  
Vol 54 (6) ◽  
pp. 1067-1076 ◽  
Author(s):  
Ryan C. Costello ◽  
Dan M. Sullivan ◽  
David R. Bryla ◽  
Bernadine C. Strik ◽  
James S. Owen

New markets for organic northern highbush blueberry (Vaccinium corymbosum L.) have stimulated interest in using composts specifically tailored to the plant’s edaphic requirements. Because composts are typically neutral to alkaline in pH (pH 7 to 8), and blueberry requires acidic soil (pH 4.2 to 5.5), we investigated elemental sulfur (S0) addition as a methodology for reducing compost pH. The objectives were to 1) characterize initial compost chemistry, including the pH buffering capacity of compost (acidity required to reduce pH to 5.0), 2) measure changes in compost chemistry accompanying acidification, and 3) evaluate plant growth and mineral nutrition of blueberry in soil amended with an untreated or acidified compost. Ten composts prepared from diverse feedstocks were obtained from municipalities and farms. Addition of finely ground S0 reduced compost pH from 7.2 to 5.3, on average, after 70 d at 22 °C, and increased the solubility of nutrients, including K (from 22 to 36 mmol(+)/L), Ca (from 5 to 19 mmol(+)/L), Mg (from 5 to 20 mmol(+)/L), and Na (from 6 to 9 mmol(+)/L). Sulfate-S, a product of S0 oxidation, also increased from 5 to 45 mmol(−)/L. The composts were incorporated into soil at a high rate (30% v/v) in a greenhouse trial to evaluate their suitability for use in blueberry production. Shoot and root growth were strongly affected by compost chemical characteristics, including pH and electrical conductivity (EC). Potassium in compost was highly variable (2–32 g·kg−1). Concentration of K in the leaves increased positively in response to compost K, whereas shoot dry weight and root growth declined. Leaf Mg also declined in response to compost K, suggesting that elevated K concentrations in compost may cause Mg deficiency. Composts with the highest K were also high in total N, pH, and EC. Compost acidification to pH ≤ 6 improved growth and increased leaf Mg concentration. On the basis of these results, composts derived from animal manures or young plant tissues (e.g., green leaves) appear to be unsuitable for high-rate applications to blueberry because they usually require high amounts of S0 for acidification and are often high in EC and K, whereas those derived from woody materials, such as local yard debris, appear promising based on their C:N ratio, compost acidification requirement, and EC.


HortScience ◽  
1999 ◽  
Vol 34 (4) ◽  
pp. 607-610 ◽  
Author(s):  
B.E. Maust ◽  
J.G. Williamson ◽  
R.L. Darnell

Floral budbreak and fruit set in many southern highbush blueberry (SHB) cultivars (hybrids of Vaccinium corymbosum L. with other species of Vaccinium) begin prior to vegetative budbreak. Experiments were conducted with two SHB cultivars, `Misty' and `Sharpblue', to test the hypothesis that initial flower bud density (flower buds/m cane length) affects vegetative budbreak and shoot development, which in turn affect fruit development. Flower bud density of field-grown plants was adjusted in two nonconsecutive years by removing none, one-third, or two-thirds of the flower buds during dormancy. Vegetative budbreak, new shoot dry weight, leaf area, and leaf area: fruit ratios decreased with increasing flower bud density in both cultivars. Average fruit fresh weight and fruit soluble solids decreased in both cultivars, and fruit ripening was delayed in `Misty' as leaf area: fruit ratios decreased. This study indicates that because of the inverse relationship between flower bud density and canopy establishment, decreasing the density of flower buds in SHB will increase fruit size and quality and hasten ripening.


Author(s):  
David R. Bryla ◽  
Carolyn F. Scagel ◽  
Scott B. Lukas ◽  
Dan M. Sullivan

Excess salinity is becoming a prevalent problem for production of highbush blueberry (Vaccinium L. section Cyanococcus Gray), but information on how and when it affects the plants is needed. Two experiments, including one on the northern highbush (Vaccinium corymbosum L.) cultivar, Bluecrop, and another on the southern highbush (V. corymbosum interspecific hybrid) cultivar, Springhigh, were conducted to investigate their response to salinity and assess whether any suppression in growth was ion specific or due primarily to osmotic stress. In both cases, the plants were grown in soilless media (calcined clay) and fertigated using a complete nutrient solution containing four levels of salinity [none (control), low (0.7–1.3 mmol·d−1), medium (1.4–3.4 mmol·d−1), and high (2.8–6.7 mmol·d−1)] from either NaCl or CaCl2. Drainage was minimized in each treatment except for periodic determination of electrical conductivity (EC) using the pour-through method, which, depending on the experiment, reached levels as high as 3.2 to 6.3 dS·m−1 with NaCl and 7.8 to 9.5 dS·m−1 with CaCl2. Total dry weight of the plants was negatively correlated to EC and, depending on source and duration of the salinity treatment, decreased linearly at a rate of 1.6 to 7.4 g·dS−1·m−1 in ‘Bluecrop’ and 0.4 to 12.5 g·dS−1·m−1 in ‘Springhigh’. Reductions in total dry weight were initially similar between the two salinity sources; however, by the end of the study, which occurred at 125 days in ‘Bluecrop’ and at 111 days in ‘Springhigh’, dry weight declined more so with NaCl than with CaCl2 in each part of the plant, including in the leaves, stems, and roots. The percentage of root length colonized by mycorrhizal fungi also declined with increasing levels of salinity in Bluecrop and was lower in both cultivars when the plants were treated with NaCl than with CaCl2. However, leaf damage, which included tip burn and marginal necrosis, was greater with CaCl2 than with NaCl. In general, CaCl2 had no effect on uptake or concentration of Na in the plant tissues, whereas NaCl reduced Ca uptake in both cultivars and reduced the concentration of Ca in the leaves and stems of Bluecrop and in each part of the plant in Springhigh. Salinity from NaCl also resulted in higher concentrations of Cl and lower concentrations of K in the plant tissues than CaCl2 in both cultivars. The concentration of other nutrients in the plants, including N, P, Mg, S, B, Cu, Fe, Mn, and Zn, was also affected by salinity, but in most cases, the response was similar between the two salts. These results point to ion-specific effects of different salts on the plants and indicate that source is an important consideration when managing salinity in highbush blueberry.


HortScience ◽  
2017 ◽  
Vol 52 (6) ◽  
pp. 905-909 ◽  
Author(s):  
Yang Fang ◽  
Jeffrey Williamson ◽  
Rebecca Darnell ◽  
Yuncong Li ◽  
Guodong Liu

Southern highbush blueberry (SHB, Vaccinium corymbosum L. interspecific hybrid) is the major species planted in Florida because of the low-chilling requirement and early ripening. The growth pattern and nitrogen (N) demand of SHB may differ from those of northern highbush blueberry (NHB, V. corymbosum L.). Thus, the effect of plant growth stage on N uptake and allocation was studied with containerized 1-year-old SHB grown in pine-bark amended soil. Five ‘Emerald’ plants were each treated with 6 g 10% 15N labeled (NH4)2SO4 at each of 12 dates over 2 years. In the first year, plants were treated once in late winter, four times during the growing season, and once in the fall. In the second year, treatment dates were based on phenological stages. After a 14-day chase period following each 15N treatment, plants were destructively harvested for dry weight (DW) measurements, atom% of 15N, and N content of each of the plant tissues. Total DW increased continuously from mid-May 2015 to Oct. 2015 and from Mar. 2016 to late Sept. 2016. From August to October of both years, external N demand was the greatest and plants absorbed more N during the 2-week chase period, about 0.53 g/plant in year 1 and 0.67 g/plant in year 2, than in chase periods earlier in the season. During March and April, N uptake was as low as 0.03 g/plant/2 weeks in year 1 and 0.21 g/plant/2 weeks in year 2. Nitrogen allocation to each of the tissues varied throughout the season. About half of the N derived from the applied fertilizer was allocated to leaves at all labeling times except the early bloom stage in 2016. These results suggest that young SHB plants absorb greater amounts of N during summer and early fall than in spring.


2004 ◽  
Vol 129 (3) ◽  
pp. 294-298 ◽  
Author(s):  
Timothy M. Spann ◽  
Jeffrey G. Williamson ◽  
Rebecca L. Darnell

Experiments were conducted with `Misty' southern highbush blueberry (Vaccinium corymbosum L. interspecific hybrid) to test the effects of high temperature on flower bud initiation and carbohydrate accumulation and partitioning. Plants were grown under inductive short days (SDs = 8 hour photoperiod) or noninductive SDs with night interrupt (SD-NI = 8 hour photoperiod + 1 hour night interrupt), at either 21 or 28 °C for either 4 or 8 weeks. Flower bud initiation occurred only in the inductive SD treatments and was significantly reduced at 28 °C compared with 21 °C. The number of flower buds initiated was not significantly different between 4- and 8-week durations within the inductive SD, 21 °C treatment. However, floral differentiation appeared to be incomplete in the 4-week duration buds and bloom was delayed and reduced. Although plant carbohydrate status was not associated with differences in flower bud initiation between SD and SD-NI treatments, within SD plants, decreased flower bud initiation at high temperature was correlated with decreased whole-plant carbohydrate concentration. These data indicate that flower bud initiation in southern highbush blueberry is a SD/long night phytochrome-mediated response, and plant carbohydrate status plays little, if any, role in regulating initiation under these experimental conditions.


2021 ◽  
Vol 90 (2) ◽  
pp. 161-171
Author(s):  
Sakura Takahashi ◽  
Jingai Che ◽  
Naomi Horiuchi ◽  
Hnin Yin Cho ◽  
Siaw Onwona-Agyeman ◽  
...  

1992 ◽  
Vol 117 (5) ◽  
pp. 749-756 ◽  
Author(s):  
Glenn C. Wright ◽  
Kim D. Patten ◽  
Malcolm C. Drew

`Tifblue' and `Brightwell' rabbiteye blueberries (Vaccinium ashei Reade.) were subjected to 0, 25, or 100 mM Na+, as Na2SO4 or NaCl, and 0, 1, 3, or 10 mM supplemental Ca2+, primarily as CaSO4, in an irrigated sand culture in the greenhouse. Additionally, the effect of NaCl on `Sharpblue' southern highbush blueberry (primarily V. corymbosum L.) was examined. For unsalinized plants, fastest growth occurred in plants not receiving supplemental Ca2+. Root and shoot growth were depressed as salinity increased in plants lacking additional Ca2+. With 100 mM Na+ as Na2SO4. `Tifblue' root and shoot dry weight increases were only 37% and 25%, respectively, of the increase of unsalinized controls, while with 100 mM Na+ as NaCl, the corresponding shoot and root dry weight increases were only 38% and 43%, respectively. `Brightwell' plants reacted similarly to `Tifblue' in salinity treatments with Na2SO4 and NaCl, but `Sharpblue' plants were more severely affected by 100 mM NaCl than were the rabbiteye cultivars. In no case did addition of Ca2+ have any ameliorative effect on either the dry weight of roots of plants exposed to 25 or 100 mM NaCl or on the shoot growth of plants exposed to NaCl. The inability of Ca2+ to counter Cl- entry or toxicity may account for the lack of amelioration. In contrast, additional Ca2+ did improve shoot growth of plants exposed to Na2SO4. For `Tifblue' plants supplied with 25 mM Na+ as Na2SO4, growth increased by almost 25% in the presence of 10 mM Ca2+, while for `Tifblue' plants treated with 100 mM Na+ as Na2SO4, growth was more than three times greater in plants supplied with 1 mM Ca than in those not given any Ca2+. Growth increase was primarily due to increased leaf area and number. Low (1 mM) concentrations of Ca2+ were more effective in ameliorating the effects of 100 mM Na+ as Na2SO4 than were 3- and 10-mM Ca2+ supplements, possibly because higher Ca2+ additions lead to metabolic damage in these calcifuge Vaccinium species.


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