High temperature affects olive fruit fly populations in California's Central Valley
Kent M. Daane, UC Berkeley
Marshall W. Johnson, UC Riverside
Kris Lynn-Patterson, UC Kearney Agricultural Center
Hannah Nadel, U. S. Department of Agriculture
Susan B. Opp, California State University
Judy Stewart-Leslie, Consolidated Central Valley Table Grape Pest and Disease Control District
Xin-Geng Wang, UC Berkeley
California Agriculture 65(1):29-33. DOI: 10.3733/ca.v065n01p29.
K. M. Daane is Cooperative Extension Specialist, Department of Environmental Science, Policy and Management, UC Berkeley; M. W. Johnson is Cooperative Extension Specialist and Entomologist, Department of Entomology, UC Riverside; K. Lynn-Patterson is GIS Academic Coordinator, UC Kearney Agricultural Center, Parlier; H. Nadel is Supervisory Entomologist, U. S. Department of Agriculture Animal and Plant Health Inspection Service, Plant Protection and Quarantine program, Buzzards Bay, MA; S. B. Opp is Associate Vice President, Academic Programs and Graduate Studies, California State University, East Bay; J. Stewart-Leslie is Manager, Consolidated Central Valley Table Grape Pest and Disease Control District, Exeter, CA; X.-G. Wang is Associate Specialist, Department of Environmental Science, Policy and Management, UC Berkeley;
Olive fruit fly commonly infests olives in California's Central Valley. Field studies indicate that trap counts for olive fruit fly adults in pesticide-free sites decrease in mid-and late summer and then rebound from September to November. Part of this decline is associated with heat stress that the flies experience in mid-July and August. Studies have shown that adult flies will die within a few days if they cannot access adequate amounts of water and carbohydrates. Flight ability is dramatically reduced when resources are unavailable. Olive fruit fly adults may use black scale honeydew as a carbohydrate source to help them survive hot periods. Heat also affects the fly's reproduction and immature stages within olive fruit. Geographic information system (GIS) maps may be useful for predicting the risk of olive fruit fly infestation.
The discovery in 1998 and subsequent spread of the olive fruit fly throughout the major olive-producing areas of California dramatically affected the pest management activities practiced by growers. Prior to its introduction, the major arthropod pests targeted for control in California olives were olive scale (Parlatoria oleae Colvée) (Hempitera: Diaspididae) and black scale (Saissetia oleae [Olivier]) (Hempitera: Coccidae) (Daane et al. 2005). Olive scale is well managed with biological control due to the introduction and establishment of the parasitoids Aphytis paramaculicornis DeBach and Rosen, and Coccophagoides utilis Doutt (Daane et al. 2005). Black scale is mainly controlled in the Central Valley by pruning infested trees to facilitate greater air movement in the summer, which results in significant desiccation of first-instar crawlers (Daane and Caltagirone 1989).
An adult female olive fruit fly deposits an egg into olive fruit.
However, the establishment of olive fruit fly (Bactrocera oleae [Rossi]) (Diptera: Tephritidae) forced many growers onto a weekly treatment regime that runs from mid-June through harvest (September to December), using the spinosad product GF-120 NF Naturalyte Fruit Fly Bait (Dow AgroSciences) (Johnson et al. 2006). This management protocol enables growers to deliver fruit with near-zero infestation levels to the table olive processors. Olives destined for oil pressing may have significant levels of infestation without an appreciable decline in quality, as long as the time between harvest and pressing is minimal (Pereira et al. 2004; Torres-Villa et al. 2003).
Olive fruit fly adults may be monitored with flat-panel sticky traps or McPhail traps (Johnson et al. 2006). The numbers of adults captured in the Central Valley decline during the hottest periods of July and August and increase in September as temperatures decrease (Rice et al. 2003; Yokoyama et al. 2006) (fig. 1). For most insect species, a decline in trap counts suggests a reduction in adult densities in an area. This is not initially the case with olive fruit fly, whose behavior changes as daily temperatures rise.
Avidov (1954) reported that below 62°F the adults are inactive. As temperatures increase above the threshold temperature, adult activity increases. Normal activity, flight and egg laying occur between 73°F and 84°F. As temperatures surpass 84°F, adult flies become increasingly agitated and egg laying is halted, and above 95°F they are motionless. Laboratory observations (M. W. Johnson, unpublished) also suggest that adults seek and remain near moisture sources as temperatures approach and surpass 95°F.
Reduced adult fly activity can result in lower trap counts in the field while maximum daily temperatures remain around 95°F to 99°F and the flies have access to adequate water and carbohydrate sources (Wang et al. 2009a). However, as the frequency at which daily maximum temperatures equal or surpass 100°F increases, greater numbers of adults will die due to heat stress, especially when they cannot access adequate quantities of water and food (Wang et al. 2009a, b) (fig. 2). Although adult females may ingest liquid from punctures they make in olive fruit, this secretion does not provide the needed carbohydrates to help them survive heat-induced stress (Johnson and Nadel, unpublished data).
Fig. 1. Average olive fruit fly populations at nine untreated sites (e. g., urban, landscape and abandoned commercial plantings) and five treated (with GF-120) commercial sites in Fresno and Tulare counties during the 2003 growing season (Johnson, Nadel and Stewart-Leslie, unpublished data).
Fig. 2. Mortality of olive fruit fly adults subjected to 1 to 3 days exposure to 95°F and 100°F, in the absence of food and with and without access to water (Wang et al. 2009b). Different letters above columns representing the same temperature/resource treatment indicate significant differences (P < 0.05; Tukey's HSD test) within the exposure duration.
Fig. 3. Mean distances flown by olive fruit fly adults exposed to various temperatures and resources. Flies (A-E) were preconditioned for 7 days at 75°F with ample food and water prior to treatment. Treatments were: (A) no treatment (control); (B) preconditioned at 95°F, then 24 hours of water only; (C) preconditioned at 100°F, then 24 hours of water only; (D) preconditioned at 95°F, then 24 hours with no resources; (E) preconditioned at 100°F, then 24 hours with no resources; (F) no preconditioning, held from 1 to 2 days at 95°F with no resources; and (G) no preconditioning, held from 1 to 2 days at 100°F with no resources (Wang et al. 2009b). Different letters above columns indicate significant differences (P < 0.05; Tukey's HSD test).
One might assume that acquisition of adequate amounts of food and water would be easy for olive fruit fly adults, which are strong flyers. Using a custom-designed flight mill, Wang et al. (2009b) reported that adults of both sexes held for 7 days at 75°F (constant temperature) and provided with ample food (honey and hydrolyzed yeast) and water, were able to fly uninterrupted for an average of 2,164.8 ± 228.8 yards during a mean period of 1.54 ± 0.16 hours (fig. 3).
Nonetheless, heat stress and lack of water and food can affect flight ability. Olive fruit fly adults that were subject to the same conditions as described for 7 days and then to water only or no food and water in diurnal temperature regimes (65°F at night; 95°F or 100°F during the day) for 24 hours before the flight test did not perform as well as the control group (fig. 3). All stressed groups of tested flies flew significantly shorter distances (≥ 42%) than the control (F6,252 = 62.7, P < 0.01). Additionally, individual flies that were denied food and water from the time that they emerged as adults and were held at either 65°F at night and 95°F, or 100°F, during the day for 1 to 2 days, flew significantly shorter distances (≥ 92%) than the flies provided no food and water for 24 hours after having access to food and water for 7 days (fig. 3).
In a worst-case scenario, an adult fly that emerges in mid-August in the Central Valley may commonly experience maximum daily temperatures over 100°F for 3 consecutive days (Lynn-Patterson 2006). Without food or water immediately available, an adult will only be able to fly an average of 16.4 ± 4.4 yards to locate these resources in a dry and unexplored landscape. Such a fly would have an 84% chance of dying in the first 24 hours, and of those that did survive only about 25% would be able to fly (Wang et al. 2009b). Additionally, when olive fruit fly adults were held at 65°F at night and 95°F or 100°F during the day over a 3-day period with either water alone or no food or water, those flies that survived one day could fly significantly farther than those that survived 3 days (F2,407 = 18.7, P < 0.01) (fig. 4).
Experimental setup shows (A) the typical distribution of five olive fruit fly adults (circled) within an observation chamber, with cotton wicks and water (W) and honey (H) at a cool temperature (80°F) and 20% relative humidity, and (B) the congregation of olive fruit fly adults (circled) around a water wick (W) when the temperature is hot (99. 5°F) and 37% relative humidity.
Fig. 4. Mean distances flown by olive fruit fly adults subjected to 1 to 3 days exposure to 95°F and 100°F, in the absence of food and with and without access to water (Wang et al. 2009b). Different letters above columns representing the same temperature/resource treatment indicate significant differences (P < 0. 05; Tukey's HSD test) within the exposure duration.
Fly flight is measured using (A) a custom-designed flight mill setup with computer; (B) an individual flight mill unit; (C) a beam that rotates during insect flight; and (D) a tethered fly fastened to a rotating beam.
Reproductive dormancy in olive fruit fly subsides as greater numbers of mature fruit appear within the orchard, commonly in late July and early August in California (Burrack and Zalom 2008; Wang et al. 2009a). During periods of high maximum daily temperatures (3 consecutive days at 100°F or above in July and August) (Lynn-Patterson 2006), mated adult females may lay their eggs in developing olives prior to morning temperatures reaching 95°F. No eggs are deposited during the night, even when temperatures are cool enough for normal activity (Avidov 1954; Wang et al. 2009a). Eggs are deposited just beneath the fruit epidermis and may be exposed to high temperatures, depending on where an individual fruit is located on the tree (Wang et al. 2009a).
Laboratory studies showed that adult females held under different diurnal temperature regimes (65°F at night and 75°F, 95°F or 100°F during the day) laid similar numbers of eggs when the temperature was 65°F and the experimental chamber was illuminated (F2,55 = 0. 2, P = 0.852). However, under illumination and higher temperatures, females laid significantly fewer eggs at 95°F (about four per female) than at 75°F (about 12 per female) (F1,38 = 8.4, P = 0.006), and no eggs were laid at 100°F (Wang et al. 2009a).
Even after eggs are deposited within olive fruit, they are still susceptible to the high temperatures common in Central Valley orchards. Eggs within fruit held at 65°F (night) and 75°F (day) developed into first-instar larvae after 6 days (Wang et al. 2009a). In contrast, eggs within fruit subjected to 65°F (night) and 95°F (day) had a 49% mortality rate, and of the first-instar larvae that did develop, none became second instars. When subjected to 65°F (night) and 100°F (day), no eggs hatched after 10 days exposure and all died. The overall finding was that egg (F3,57 = 2472, P < 0.001) and first-instar (F3,57 = 2472, P < 0.001) mortality increased as exposure time increased (Wang et al. 2009a).
Later field studies showed that maximum daily temperatures in olive trees in the Central Valley (Parlier) varied depending on whether measurements were taken within the canopy interior or the east or west perimeter. Mean temperatures recorded on the west side of the tree canopy in August 2007 were 108°F (and over 104°F for 26 days) compared to 101°F (and over 104°F for 13 days) on the east side, and 96°F (and never over 104°F) within the canopy interior (F2,90 = 52.7, P < 0.001). All of these temperatures are high enough to impose some level of mortality on olive fruit fly eggs and larvae. Field studies in the same locality in mid-and late summer 2007 and 2008 showed that less than 2% of offspring from eggs laid in olives completed development to the adult stage (Wang et al. 2009a).
Fig. 5. Survival of olive fruit fly adults when held at 65°F (night) and 97. 5°F (day) with access to various combinations of water, honey and black scale honeydew, or no food or water.
This information suggests that it is difficult for olive fruit fly adults to survive the high summer temperatures in the Central Valley. Water may commonly be found within or near most orchards from a variety of sources, such as morning dew, creeks, ponds, irrigation water (ditches and canals), sprinklers, drip tape and fan jets. However, fly adults also need carbohydrates to survive heat stress. Honeydew (fresh or dry) produced by black scale is a common carbohydrate source in olive orchards. Our laboratory tests have shown that fly adults provided with honey and water, or black scale honeydew and water, survive temperatures of 65°F (night) and 97.5°F (day) with minimal mortality compared to adults only provided honey alone, honeydew alone, or no food and water over 5 days (F4,36 = 189.9, P < 0.0001) (fig. 5) (M. W. Johnson and H. Nadel, unpublished data).
The carbohydrate source alone did not reduce the impact of heat on survival. Flies that had food resources (honeydew or pure honey) but no water suffered mortality similar to those flies without food or water. There was a significant interaction between carbohydrate source and days of exposure (F20,180 = 33.3, P < 0.0001). These results are similar to what we have observed in our laboratory and field studies on olive fruit fly when 50% honey water was used as a carbohydrate source. These findings are significant because they suggest that olive fruit fly adults could use black scale honeydew to help them survive periods of high temperature in the Central Valley. The management of black scale populations via cultural controls such as the pruning of interior canopies may also contribute to the management of olive fruit fly adults.
Geographic information systems (GIS) enable the examination of temperature trends over specific areas based on defined criteria, such as temperature levels for specific time intervals. The examination of temperature trends in olive-producing areas in the Central Valley over 10 years (1992–2001) revealed that it was quite common for temperatures to be greater than 100°F for 3 consecutive days during mid-July and August (fig. 6) (Lynn-Patterson 2006). On the California coast, these trends were rarely observed. Over this time period, temperatures greater than 100°F for 3 consecutive days were more common in the southern (San Joaquin Valley) than the northern (Sacramento Valley) Central Valley (see http://arcims.gis.uckac.edu/CIMIS ). By September, most of the Central Valley rarely had 3 consecutive days greater than 100°F (fig. 6).; in 2003, olive fruit fly surpassed one adult per trap per week at the end of August and continued to increase into November (fig. 1).
Growers and consultants may wish to use these maps to determine if they can temporarily halt insecticide treatments for olive fruit fly adults during July and August. However, there are many factors other than temperature that influence whether olive fruit fly will be a problem in a particular olive orchard. Olive fruit fly adults with access to adequate sources of water and carbohydrates can survive heat stress in large numbers and will be able to fly long distances (more than 1,000 yards) even when stressed. Growers who consider halting their control programs, especially in the San Joaquin Valley, should take under consideration the irrigation schedules and infestation levels of black scale and other insects that might produce honeydew within their own and neighboring orchards. Also important is the proximity of irrigation canals, creeks, ponds and rivers, as well as abandoned orchards or untreated olives trees used for landscaping, which can serve as an infestation source of olive fruit fly. Morning dew in the orchard may provide a moisture source for flies, and weedy undergrowth in the orchard or neighboring crops can afford some relief from the heat.
Perhaps the most useful information that one can obtain from the GIS maps is knowing when temperatures historically have dropped to low levels that would be conducive to olive fruit fly activity and survival in a particular area. As temperatures decline at the end of August, olive fruit are increasing in size and maturing (Martin and Sibbett 2005). Olive fruit fly adults prefer to lay their eggs in the largest olives available (Neuenschwander et al. 1985). As flies return to normal activity in late summer, the olives remaining on the trees are at greater risk of infestation than at anytime during the summer, and protecting the fruit then is of prime consideration.
Research on the ecology and management of olive fruit fly is continuing. A better understanding of the abilities of olive fruit fly adults to disperse among orchards in the summer would be helpful. Given that olive fruit fly adults need carbohydrate sources to survive heat stress, it may be best to continue treating with GF-120 in July and August. The adults are attracted to the sweet fruit fly bait in the GF-120. If stressed flies seek a carbohydrate source in summer, it may be assumed that they would then seek out available bait residues in GF-120. If this is true, the GF-120 may be having a greater impact than realized. This needs to be determined. Also of importance is the impact of summer heat either directly or indirectly on parasitoid natural enemies that are now being released as part of a classical biological control program for olive fruit fly control (see page 21).
Fig. 6. Mean temperature patterns in California over 10 years (1992–2001), showing number of years (occurrences) with maximum temperatures greater than or equal to 100°F for 3 consecutive days ending on July 15, Aug. 15 and Sept. 15 (Lynn-Patterson 2006).