Epizootic of Acalitus vaccinii (Acari: eriophyidea) caused by Hirsutella thompsonii on southern highbush blueberry in north-central Florida.
Hirsutella thompsonii (Fisher) is a mesothermic mycopathogen of various invertebrates including insects, mites, and nematodes (Boucias et al. 2007). The fungus requires an optimal temperature of 25 to 30[degrees]C and a RH of 98% for growth and sporulation (Boucias et al. 2007; Gerson et al 1979; Kenneth et al. 1979; McCoy 1996). As a parasite it has been reported to cause epizootics of several eriophyoid mites including Calacarus heueae on rubber trees (Tanzini et al. 2000), Phyllocoptruta oleivora, citrus rust mite (Fisher et al. 1949), and Aceria guerreronis on coconut (Gopal & Gupta 2001).
In Apr 2007, the presence of H. thompsonii became apparent during a population study conducted in a commercial southern highbush blueberry planting in Windsor, FL (Fig. 1). Hirsutella thompsonii, has previously been found in association with the BBM in North Carolina (Baker & Neunzig 1968, 1970) but an epizootic has not been observed in Florida.
[FIGURE 1 OMITTED]
The objective of this study was to determine the seasonal development of a well-established BBM population and its mycopathogen, H. thompsonii, in a commercial planting of southern highbush blueberries under north-central Florida conditions.
MATERIALS AND METHODS
The selected study site was a 1.2-ha commercial southern highbush blueberry (Vaccinium corymbosum L. X V darrowi Camp.) planting, infested with high populations of BBM. Bushes were 1.6-2 m high (approximately 10 years old) and consisted of a mixed planting of Windsor and Star cultivars. Blueberry bushes were spaced about 1 m apart. No insecticide or acaricide was applied to the field prior to field survey. However, foliar fungal pathogens were controlled with Cabrio[R], Switch[R], Pristine[R], Bravo[R], Indar[R], and Elevate[R]. The fungicides were applied according to the recommended calendar spray technique (Krewer et al. 2008). With the first appearance of the fungal infection, distorted BBM were plated on sterilized water agar, incubated at 27[degrees]C (Boucias et al. 2007), and sporulating fungal structures were submitted for expert identification. The fungus was identified by Dr. Drion Boucias in the insect pathology laboratory at the University of Florida.
In order to determine the population dynamics of BBM, 10 terminal flower buds were collected randomly from the cultivar 'Windsor' in the following developmental stages: (1) tightly closed buds, (2) symptomatically swollen and reddened buds, and (3) separating or opened buds. Buds were collected bi-weekly from two, 10-m sections of the planting from Mar until Jun 2007. After Jun, when BBM populations are known to decline to low numbers (Barker & Neunzig 1970), samples were collected every 8 weeks from the same two 10-m sections. At each sampling date, the percent of symptomatic buds was estimated visually by examining bushes for at least 1 min, and counting and recording the number of buds that appeared reddened and rosetted, as well as the number of buds with healthy appearance. The percentages of 10 plants were averaged for each section at each sampling date.
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Buds were placed in a cooler, brought to the Small Fruit and Vegetable IPM Laboratory at the University of Florida, and stained with red food coloring (McCormick & Co., Hunt Valley, MD) by a slightly modified technique commonly used to stain phyto-parasitic nematodes in or on roots (Thies et al. 2002). The number of mites per bud was determined by dissecting the stained buds and counting individual mites of all life stages (excluding the eggs) on the inside of the bud scales with the aid of a dissecting microscope at X63. Based on their appearance, blueberry bud mites were differentiated into healthy, oblong to cigar-shaped individuals of reddish color, and other distorted and grayish individuals.
A sub-sample of symptomatic buds was preserved in 1% glutharaldehyde and prepared for scanning via electron microscopy (SEM) applying the critical point drying technique commonly used for soft bodied specimen. Samples were observed on a Hitachi S-400 FE-SEM (Hitachi High Tech America). Average relative humidity and temperature data were recorded by the Florida Automated Weather Network station in Citra, FL, with a CSI 107 temperature probe and a CSI CS215 temperature and humidity probe (Anonymous 2009b).
The total population density was determined by pooling the data from healthy and distorted BBM. The population health (healthy versus distorted) was determined by subtracting the number of distorted BBM from the number of healthy BBM. We used paired t-tests to compare symptomatic and opened buds for the period of 5 Mar-5 May 2007 to determine statistical differences (SAS Institute 2003).
Blueberry bud mites and its fungal parasite, Hirsutella thompsonii, were present in all 3 developmental stages of the blueberry buds (Figs. 1-4). From the first sampling (5 Mar 2007) to the end of the observation period (3 Apr 2008), the BBM population declined drastically. The percentage of symptomatic buds recorded visually was reduced from over 50% to less than 5% (data not shown). Infection by H. thompsonii remained undetected until mid Apr 2007. By mid May 2007 and thereafter, the infection rate by H. thompsonii exceeded 50% in months with an average temperature higher than 25[degrees]C (Figs. 2-5). Voucher specimens of Acalitus vaccinii and H. thompsonii were saved and deposited in the Entomology and Nematology collection at the University of Florida.
[FIGURE 3 OMITTED]
With a population peaking at about 2,000 BBM per bud in Mar 2007, the population was significantly higher in symptomatic buds than in any other buds at any time during the spring 2007 observation period (t value = 8.51; P < 0.0001). Symptomatic buds opened or desiccated due to mite feeding by the end of May. In the newly formed closed buds, BBM numbers remained very low throughout the late summer, fall, and winter months only to increase slightly during spring 2008 (Figs. 2-4). Symptomatic buds were difficult to detect in Apr 2008, and were not present thereafter.
In early Mar 2007, the numbers of healthy BBM in symptomatic buds were significantly higher than numbers of distorted BBM (t value = 2.81; P < 0.0053). In mid Apr, infection rates in opened buds increased rapidly to exceed 50% until the winter months (Fig. 3). In symptomatic buds the same trend was observed with a two-week delay (Fig. 4). In all 3 bud types (closed, opened, and symptomatic), the BBM population and the mycopathogen were nearly undetectable during the months of Sep 2007 through Jan 2008. In 2008, the number of distorted BBM in symptomatic and opened buds started to increase at the end of Jan to exceed 50% in the beginning of Apr, and BBM numbers were suppressed to about 20 per bud.
During 2007/08 season, favorable temperature and humidity conditions supported an epizootic of BBM by H. thompsonii at our study site in north-central Florida. Although the average daily relative humidity (RH) did not exceed 75%, overhead irrigation contributed to the higher humidity ideal for fungal growth. However, from mid-Nov through mid-Mar the average temperature dropped below the optimum of 25[degrees]C, causing the frequency of the disease to decrease. During this time, the BBM population recovered only to be suppressed to below an average number of less than 20 BBM per bud in spring of 2008. The lack of symptomatic buds at this time suggests that the BBM population decreased to non-significant levels.
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By the end of May, as opened flower buds desiccated due to mite feeding, BBM appeared to have moved to tightly closed buds, which are newly formed on early summer growth. This observation agrees with Baker & Neunzig (1970), who reported that in North Carolina BBM moved to secondary growth starting in mid Jun. Throughout the observation period, the infection rate of BBM remained high in closed buds. McCoy & Lye (1995) demonstrated that copper sprays applied for foliar disease control in citrus reduced the magnitude of the epizootic of H. thompsonii on citrus rust mites, Phyllocoptruta oleivora. It is not clear whether the frequent application of fungicides had an effect on the population densities of either organism in blueberries.
The cryptic habits of BBM within the blueberry bud make them difficult to control with miticides, but they can be devastating if allowed to develop in the field. Our research is in agreement with McCoy (1981), who considered H. thompsonii a key biological control agent regulating mites. The fungus can play an important role in regulating populations of BBM in southern highbush blueberries in Florida. Although the full extent of the damage caused by BBM and the frequency of epizootics are still unknown, BBM management programs should consider possible effects on H. thompsonii when selecting fungicides for foliar disease control. With an increasing number of Florida blueberry farms installing micro jet irrigation systems to improve quality and quantity of the fruit (Williamson, pers. comm.), it remains to be seen if changing cultural practices will affect the frequency and population density of BBM.
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We thank the Florida Blueberry Growers Association for the financial support, Alto Straughn and his team for access to the blueberry farm and for technical assistance, and Dr. Drion Boucias and Marjorie Hoy for guidance in working with the fungus and mite. The authors acknowledge the help of the staff of the Small Fruit and Vegetable IPM lab.
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ELKS WEIBELZAHL AND OSCAR E. LIBURD
Entomology and Nematology Department, University of Florida/IFAS, 970 Natural Area Drive, Gainesville, FL 32611-0620
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|Author:||Weibelzahl, Elke; Liburd, Oscar E.|
|Date:||Dec 1, 2009|
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