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Carolyn F. Scagel

Seven highbush blueberry cultivars were inoculated with one of three different isolates of ericoid mycorrhizal fungi (EMF) and grown in pots for 2 years with either inorganic or organic fertilizer. Root colonization of noninoculated plants was low (<15%) regardless of fertilizer source. Root colonization on inoculated plants was 15-30%. Colonization was typically higher when plants were grown with organic fertilizer. Inoculation generally increased plant growth but decreased root:shoot biomass ratios regardless of the type of fertilizer used. Inoculation also increased nutrient uptake and/or nutrient use efficiency in several cultivars, particularly when plants were fertilizer with organic fertilizer. Without inoculum, however, some cultivars fertilized with organic fertilizer had less growth and lower concentrations of N, K, S, and Cu than those fertilized with inorganic fertilizer. Cultivars that were genetically close in ancestry showed a high degree of variability in response to mycorrhizal fungi, while responses to fertilizer type were similar in closely related cultivars. Results suggest that nutrient availability may influence colonization and growth responses to EMF; however aspects of fungus–host specificity and inoculum availability also play a role in EMF colonization of roots in container production.

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Carolyn F. Scagel

Using several different ericaceous ornamental species, we compared the growth, mineral nutrition, and composition of plants in response to growing media amended with varying proportions of sphagnum moss peat (peat) or coir dust (coir). Plants were grown for 16 weeks in media consisting of 80% composted Douglas fir bark with 20% peat, 20% coir, or 10% peat and 10% coir. Sixteen weeks after planting, decreases in extractable P were larger in peat-amended medium than the coir-amended medium, while decreases in extractable NH4-N and NO3-N were larger in the coir-amended medium. In general, leaf and stem dry weight, the number of leaves and stems, and total stem length increased with increasing proportion of coir in the medium while root dry weight either increased (Kalmia latifolia), decreased (Rhododendron, Gaultheria), or was not influenced by increasing the proportion of coir in the medium. The composition of the growing medium also influenced aspects of plant marketability and quality including: leaf greenness (SPAD), plant form (e.g., number of leaves per length of stem), and partitioning of biomass (e.g., root to shoot ratio). Nutrient uptake and fertilizer use was significantly different between the media types. Depending on the cultivar, we found that the coir-amended medium resulted in higher uptake or availability of several nutrients than peat-amended medium. Up take or availability of N, P, K, Ca, and S was enhanced for several cultivars, while uptake or availability of Mg, Fe, and B was similar between media types. Most cultivars/species growing in the coir-amended medium had higher production or accumulation of proteins and amino acids in stems than plants growing in peat-amended medium, while the production of proteins and amino acids in roots was lower in plants growing in coir-amended than in peat-amended medium. For the cultivars/species we tested, coir is a suitable media amendment for growing ericaceous plants and may have beneficial effects on plant quality.

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Carolyn F. Scagel and Jungmin Lee

Four cultivars of basil (Ocimum basilicum L. ‘Cinnamon’, ‘Siam Queen’, ‘Sweet Dani’, and ‘Red Rubin’) were inoculated or not with the arbuscular mycorrhizal fungus (AMF), Rhizophagus (formerly Glomus) intraradices (Schenck & Smith) Walker & Schüßler and grown with a fertilizer containing either 64 mg·L−1 phosphorus (P) (low P) or 128 mg·L−1 P (high P) to assess whether 1) P availability and inoculation with AMF influences the phenolic composition of basil; and 2) treatment effects on phenolic composition are related to plant nutrient status. Growth, root colonization by AMF, anthocyanins, total phenolics, specific polyphenolics, and mineral nutrients were measured after 16 weeks of growth. Non-inoculated plants were not colonized by AMF. AMF colonization of inoculated plants was not influenced by P rate. Increased P rate and AMF inoculation increased biomass. Increased P rate enhanced (increased concentration and content) P and calcium (Ca) uptake and AMF inoculation enhanced nitrogen (N), potassium (K), sulfur (S), boron (B), iron (Fe), and zinc (Zn) uptake. Increased or decreased uptake (content) of other nutrients between P rates and AMF treatments were related to differences in biomass (e.g., similar or lower concentration). Treatment effects on phenolic accumulation were related to the effects of P rate and AMF on 1) plant growth; 2) nutrient uptake; and 3) other factors not directly related to measured differences in nutrient uptake or plant growth. Differences between treatments in rosmarinic acid, the predominant polyphenolic produced by all cultivars, were related to the effects of P rate and AMF on plant growth. Both increased P rate and AMF inoculation enhanced production (increased concentration and content) of chicoric acid and caffeic acid derivative. Increased P rate and inoculation with AMF differentially enhanced production of several other minor polyphenolics resulting in plants with different polyphenolic profiles. Results indicate that AMF inoculation may be an additional strategy for optimizing basil quality in terms of polyphenolic production and composition beyond benefits obtained from just altering plant nutrient status or selecting specific cultivars.

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Guihong Bi and Carolyn F. Scagel

Rooted liners of Hydrangea macrophylla (Thunb.) Ser. ‘Berlin’ were fertigated with different rates of nitrogen (N) from July to Sept. 2007 and leaves were sprayed with 15N-labeled urea in late October to evaluate urea uptake and 15N translocation by hydrangea leaves in relation to plant N status. Four plants from each N fertigation rate were harvested before they were sprayed with urea and 2, 5, 10, and 15 days after urea spray. Increasing rate of N fertigation increased plant N content in October before being sprayed with urea. Leaves rapidly absorbed 15N from urea spray. The highest rate of 15N uptake occurred during the first 2 days after urea spray and then decreased. Export of 15N from leaves occurred rapidly after uptake and the highest rate of 15N export occurred during the first 2 days after urea spray and then decreased. During the first 5 days after urea spray, the rate of 15N uptake by leaves and export from leaves decreased with increasing rate of N fertigation. On a whole plant basis, the total amount of 15N from foliar 15N–urea spray increased with increasing rate of N fertigation; however, the percentage of 15N exported from leaves and the percentage of N that derived from foliar 15N–urea spray decreased with increasing rate of N fertigation. Results suggest that hydrangea plants with lower N status in the fall are more efficient in absorbing and translocating N from foliar urea than plants with higher N status.

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R. Paul Schreiner and Carolyn F. Scagel

Grape growers rely on tissue tests of leaf blades or petioles for routine monitoring of vine nutritional health and for diagnosing potential nutrient deficiency or toxicity. There has been a long-standing debate as to which tissue better reflects the nutrient status of vines. A comparison of leaf blade and petiole nutrient concentrations was carried out to investigate which tissue better relates to vine growth, yield, and must nutrient responses of ‘Pinot noir’ grapevines to varying levels of nitrogen (N), phosphorus (P), and potassium (K) supply using data from a pot-in-pot vineyard over 4 years. Leaf blades and petioles were collected at 50% bloom and 50% veraison in each year and N, P, and K concentrations were assessed as predictors of leaf area at veraison, pruning mass at dormancy, yield, and must nutrient concentrations at fruit maturity. Data from commercial ‘Pinot noir’ vineyards were also used to investigate the relationship between leaf blade and petiole N concentrations with must N levels. Results indicated that leaf blades were superior to petioles in predicting vine growth, yield, and must yeast assimilable nitrogen (YAN) responses across a wide range of vine N status at both sampling times. Leaf blade N was a better predictor than petiole N in predicting YAN using data sets from both the pot-in-pot vineyard and commercial vineyards. Relationships between leaf blade and petiole concentrations of P and K and vine response variables generally did not differ and both tissues appeared to be equally effective in predicting P and K effects on growth, yield, and must P or K levels. Although petiole P was slightly better than leaf blade P at bloom in predicting must P levels, and models including both leaf and petiole K simultaneously as predictors relied only on leaf K. For all three nutrients, sampling at bloom and veraison had a similar predictive strength for response variables. Based on these findings, we recommend using leaf blades as opposed to petioles for diagnosing the N, P, and K status of ‘Pinot noir’.

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Guihong Bi, Carolyn F. Scagel and Richard Harkess

Plants of Hydrangea macrophylla ‘Merritt's Supreme’ were fertigated with 0, 70, 140, 210, or 280 mg·L−1 nitrogen (N) from July to Sept. 2005 and sprayed with 0% or 3% urea in late October to evaluate whether plant N status during vegetative growth influences plant performance during forcing. In late November, plants were manually defoliated, moved into a dark cooler (4.4 to 5.5 °C) for 8 weeks, and then placed into a greenhouse for forcing. After budbreak, plants were supplied with either 0 N or 140 mg·L−1 N for 9 weeks. Plant growth and N content were evaluated in Nov. 2005 before cold storage and plant growth, flowering, and leaf quality parameters were measured in late Apr. 2006. Increasing N fertigation rate in 2005 significantly increased plant biomass by ≈14 g (26%) and plant N content by ≈615 mg (67%). Spray applications of urea (urea sprays) in the fall had no influence on plant biomass but significantly increased plant N content by ≈520 mg (54%). In general, plants grown with 210 and 280 mg·L−1 N during 2005 had the greatest growth (total plant biomass, height), flowering (number of flowers, flower size), and leaf quality (leaf area, chlorophyll content) during forcing in 2006. Urea sprays before defoliation increased plant growth, flowering, and leaf quality characteristics during forcing in 2006. Providing plants with N during the forcing period also increased plant growth, flowering, and leaf quality characteristics. Urea sprays in the fall were as effective as N fertilizer in the spring on improving growth and flowering. We conclude that both vegetative growth and flowering during forcing of ‘Merritt's Supreme’ hydrangea are influenced by both the N status before forcing and N supply from fertilizer during forcing. A combination of optimum rates of N fertigation during the vegetative stage of production with urea sprays before defoliation could be a useful management strategy to control excessive vegetative growth, increase N storage, reduce the total N input, and optimize growth and flowering of container-grown florists’ hydrangeas.

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R. Paul Schreiner and Carolyn F. Scagel

An interplay between carbon and phosphorus is known to regulate root colonization by arbuscular mycorrhizal fungi (AMF); however, it is unclear whether plant C or plant P status plays a bigger role in controlling the abundance of arbuscules (the primary site of nutrient exchange in AMF symbiosis) in roots. In this study, ‘Pinot noir’ grapevine (Vitis vinifera) was grown in an unsterilized vineyard soil and colonized by indigenous AMF in two experiments, where photosynthetic capacity (defoliation or shading) and shoot nutrition (foliar fertilizer) were manipulated. Temporal changes in root colonization by AMF and plant growth and nutrition were determined. Foliar fertilizer application increased P and K uptake, but reduced Cu uptake in both experiments. Decreasing the photosynthetic capacity of shoots due to defoliation or shading rapidly reduced arbuscules in fine roots (within 7 to 14 days). In contrast a 3-fold increase in shoot P status from foliar fertilizer only reduced arbuscules after a more prolonged time (28 to 56 days). The combination of shading (15% of full sun) and foliar P application reduced arbuscules more than shading alone within the first month, whereas foliar P use in full sun had no influence on arbuscules within a month. Returning plants to full sun after 28 days in shade resulted in a resurgence of arbuscules in roots regardless of plant P status. Arbuscules in grapevine roots are regulated by the interaction between plant C and P status, such that high shoot P reduces arbuscule formation or maintenance more when combined with reduced plant photosynthesis. This indicates that grapevines do not reduce AMF nutrient transfer as an immediate response to elevated shoot P as long as plants are maintained in a high light environment.

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Carolyn F. Scagel, David R. Bryla and Jungmin Lee

A study was conducted to evaluate the effects of salinity on growth and nutrient uptake in basil (Ocimum basilicum L. ‘Siam Queen’). Plants were fertilized with a complete nutrient solution and exposed to no, low, or moderate levels of salinity using NaCl or CaCl2. The plants in control and moderate salinity treatments were also inoculated or not with the arbuscular mycorrhizal fungus (AMF), Rhizophagus irregularis (Blaszk., Wubet, Renker, & Buscot) C. Walker & A. Schler., to determine whether AMF mitigate the effects of salinity stress. Electrical conductivity (EC) of leachate collected from salinity treatments reached levels ≥8 dS·m−1 but had no effect on plant growth in the first 41 days of treatment. However, by 75 days, plants exposed to low and moderate levels of NaCl and CaCl2 had 20% to 38% less dry weight (DW) than controls. Reductions in DW were similar between NaCl and CaCl2 and was greater in roots than in shoots. Both NaCl and CaCl2 salinity reduced stomatal conductance (g S) within 25 days, but hastened flowering by 2–3 days, and nearly doubled the DW of flowers at 75 days. Salinity from NaCl increased uptake of Na and reduced uptake of Ca, whereas CaCl2 salinity increased uptake of Ca and reduced uptake of Mg and Mn. Both salts also increased relative uptake of N, Cu, and Zn, and reduced relative uptake of S and Fe. In general, Na was concentrated in roots and excluded from shoots, whereas Cl was concentrated primarily in leaves. Both salts reduced root colonization by AMF. However, AMF increased g S by 10% with NaCl and 22% with CaCl2, and increased shoot DW by 22% and 43%, respectively. Other than Ca and Cl, AMF did not enhance nutrient uptake under NaCl or CaCl2 salinity. ‘Siam Queen’ basil was moderately tolerant to salinity, due at least in part to exclusion of Na from the shoots, and inoculation with AMF increased tolerance to both NaCl and CaCl2 salinity. Differences in basil tolerance to NaCl and CaCl2 indicate plants may have different mechanisms for dealing with salinity and sensitivity is not solely a function of EC. This highlights the importance of understanding the source of salinity in irrigation waters and soil for predicting damage.

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Carolyn F. Scagel, Richard P. Regan and Guihong Bi

A study was conducted to determine whether the nitrogen (N) status of nursery-grown green ash (Fraxinus pennsylvanica ‘Summit’) trees in the autumn is related to bud necrosis during the following spring. In 2005, different rates of N from urea formaldehyde (UF) or a controlled-release fertilizer (CRF) containing ammonium nitrate were applied during the growing season to green ash trees and leaves were sprayed or not with urea in the autumn. Biomass and N content was determined in Autumn 2005 and Spring 2006, and stem biomass and bud necrosis were evaluated for necrosis in Spring 2006. Trees with low N content in Autumn 2005 grew less in Spring 2006 but bud necrosis was more prevalent on trees grown at the highest N rate. Compared with trees grown with a similar amount of N from UF, growing trees with CRF altered N allocation in 2005 and the relationship between carbon (C) and N dynamics (import, export, and metabolism) in stems in 2006. Additionally, trees grown with CRF had less total shoot biomass in Spring 2006 and more bud failure than trees grown with a similar N rate from UF. Significant relationships between bud failure and N status and C/N ratios in different tissues suggest that a combination of tree N status and the balance between N and C in certain tissues plays a role in the occurrence of bud failure of green ash trees in the spring.

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Carolyn F. Scagel, Richard P. Regan, Rita Hummel and Guihong Bi

A study was conducted to determine whether nitrogen (N) application rate and fertilizer form are related to cold tolerance of buds and stems using container-grown ‘Summit’ green ash (Fraxinus pennsylvanica) trees. Trees were grown with different rates of N from either urea formaldehyde (UF) or a controlled-release fertilizer (CRF) containing ammonium nitrate during the 2006 growing season; and growth, N and carbon (C) composition, and cold tolerance were evaluated in Oct. 2006, Dec. 2006, and Feb. 2007 by assessing the lowest survival temperature (LST) of stem and bud tissues on current season (2006) stems. Both fertilizer type and rate influenced the bud and stem LSTs. The influence of fertilizer rate was most evident on midwinter (December) stem LSTs and the influence of fertilizer type was observed in bud and stem LSTs during the deacclimation period in February. Higher LSTs were associated with higher N concentrations and lower C/N ratios; however, stems and buds of trees fertilized with UF were more cold-tolerant (had lower LSTs) than stems and buds on trees fertilized with CRF. Fertilizer type resulted in several differences in N and C translocation and metabolism during the fall and winter. Our results indicate trees with a similar N status are able to withstand different levels of cold depending on the rate of N and the type or form of fertilizer used during production. This may have to do with differences in how trees metabolize the different fertilizer forms, where and when the N is stored, and how it is remobilized in the spring, especially in relation to C metabolism.