Effects of Japanese Barberry (Ranunculales: Berberidaceae)

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Effects of Japanese Barberry (Ranunculales: Berberidaceae) Effects of Japanese Barberry (Ranunculales: Berberidaceae) Removal and Resulting Microclimatic Changes on Ixodes scapularis (Acari: Ixodidae) Abundances in Connecticut, USA Author(s): Scott C. Williams and Jeffrey S. Ward Source: Environmental Entomology, 39(6):1911-1921. 2010. Published By: Entomological Society of America DOI: 10.1603/EN10131 URL: http://www.bioone.org/doi/full/10.1603/EN10131 BioOne (www.bioone.org) is an electronic aggregator of bioscience research content, and the online home to over 160 journals and books published by not-for-profit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. PLANT-INSECT INTERACTIONS Effects of Japanese Barberry (Ranunculales: Berberidaceae) Removal and Resulting Microclimatic Changes on Ixodes scapularis (Acari: Ixodidae) Abundances in Connecticut, USA 1 SCOTT C. WILLIAMS AND JEFFREY S. WARD The Connecticut Agricultural Experiment Station, Department of Forestry and Horticulture, PO Box 1106, New Haven, CT 06504 Environ. Entomol. 39(6): 1911Ð1921 (2010); DOI: 10.1603/EN10131 ABSTRACT Japanese barberry (Berberis thunbergii de Candolle) is a thorny, perennial, exotic, invasive shrub that is well established throughout much of the eastern United States. It can form dense thickets that limit native herbaceous and woody regeneration, alter soil structure and function, and harbor increased blacklegged tick (Ixodes scapularis Say) populations. This study examined a potential causal mechanism for the link between Japanese barberry and blacklegged ticks to determine if eliminating Japanese barberry could reduce tick abundance and associated prevalence of Borrelia burgdorferi (Johnson, Schmid, Hyde, Steigerwalt, and Brenner). Japanese barberry was controlled at Þve study areas throughout Connecticut; adult ticks were sampled over three years. Each area had three habitat plots: areas where barberry was controlled, areas where barberry remained intact, and areas where barberry was minimal or absent. Sampled ticks were retained and tested for B. burgdorferi presence. At two study areas, temperature and relative humidity data loggers were deployed in each of the three habitat plots over two growing seasons. Intact barberry stands had 280 Ϯ 51 B. burgdorferi- infected adult ticks/ha, which was signiÞcantly higher than for controlled (121 Ϯ 17/ha) and no barberry (30 Ϯ 10/ha) areas. Microclimatic conditions where Japanese barberry was controlled were similar to areas without barberry. Japanese barberry infestations are favorable habitat for ticks, as they provide a buffered microclimate that limits desiccation-induced tick mortality. Control of Japanese barberry reduced the number of ticks infected with B. burgdorferi by nearly 60% by reverting microclimatic conditions to those more typical of native northeastern forests. KEY WORDS Berberis thunbergii, Borrelia burgdorferi, Ixodes scapularis, microclimate, vapor pres- sure deÞcit Japanese barberry (Berberis thunbergii de Candolle) is several agents that cause Lyme disease, human gran- a thorny, perennial shrub native to southern and cen- ulocytic anaplasmosis, and human babesiosis (Mag- tral Japan (Ohwi 1965) that was Þrst planted in North narelli et al. 2006). Japanese barberry management America in the late 1800s (Harrington et al. 2003). It was documented to reduce both blacklegged tick has since escaped from landscape plantings and is now abundance and infection prevalence with Borrelia established in 31 states in the United States, the Dis- burgdorferi (Johnson, Schmid, Hyde, Steigerwalt, and trict of Columbia, and Þve Canadian provinces [U.S. Brenner) in Connecticut (Williams et al. 2009). As a Department of Agriculture (USDA), NRCS 2010]. result, Japanese barberry infestations can have an in- Dense barberry stands are associated with a lack of direct, adverse effect on human health. desirable tree and herbaceous plant regeneration Temperature and relative humidity (RH) are de- (Harrington et al. 2003). Barberry may alter nitrogen termining factors in the survival of blacklegged ticks cycling, affecting soil biota (Kourtev et al. 1999, because of their high surface area to volume ratio and Ehrenfeld et al. 2001), as well as soil structure and resulting susceptibility to desiccation. Stafford (1994) function (Kourtev et al. 2003). Two Maine studies maintained immature blacklegged ticks at constant reported blacklegged tick (Ixodes scapularis Say) temperature (27ЊC) while manipulating RH levels. abundances were twice as numerous in exotic-inva- Half of all ticks kept at 100, 93, 85, 75, and 65% RH died sive infested forests, particularly Japanese barberry, after 67.1, 26.6, 8.3, 1.3, and 1.1 d, respectively, sug- than in adjacent forests dominated by native shrubs gesting that the critical threshold for tick survival is (Lubelczyk et al. 2004, Elias et al. 2006). This is of Ϸ80% RH. While these experimental variables were concern as blacklegged ticks are the major vector for held constant in the laboratory, both temperature and RH exhibit daily ßuctuations in the Þeld. Bertrand and 1 Corresponding author, e-mail: [email protected]. Wilson (1996) reported that blacklegged ticks in open 0046-225X/10/1911Ð1921$04.00/0 ᭧ 2010 Entomological Society of America 1912 ENVIRONMENTAL ENTOMOLOGY Vol. 39, no. 6 Þelds suffered higher mortality rates than those in (Tsuga canadensis Linnaeus (Carrie`re)) in the early edge or forested habitats and that tick survival was 1990s. The remaining upper canopy in North Branford negatively related to air temperature, vapor pressure was primarily sugar maple (Acer saccharum Marshall) deÞcit, and the coefÞcient of variation of RH. How- with mixed oak (Quercus spp.), white ash (Fraxinus ever, precipitation and temperature were reported to americana Linnaeus), American beech (Fagus gran- be poor predictors of annual abundances of nymphal difolia Ehrhart), and scattered yellow poplar (Liri- blacklegged ticks (Schultze et al. 2009). Ostfeld et al. odendron tulipifera Linnaeus). Upper canopies in (2006) suggested that because ticks spend Ͼ95% of Storrs and Redding were characterized by a predom- their lives on the forest ßoor digesting a blood meal, inance of white ash, red maple (Acer rubrum Lin- undergoing diapause, or questing, temperature and naeus), oak, yellow poplar, and some cherry (Prunus RH could have an impact on survival. serotina Ehrhart). Our previous research documented that Japanese Because of low light conditions under intact upper barberry is favorable habitat for blacklegged ticks, canopies and browse damage caused by exceedingly particularly where white-tailed deer (Odocoileus vir- high white-tailed deer populations (upwards of 40 ginianus Zimmermann) populations are high and na- deer/km2), there were virtually no native shrub spe- tive shrubs are scarce, and that barberry management cies on study sites except northern spicebush (Lindera can reduce blacklegged tick density in such areas benzoin Linnaeus) (Williams et al. 2009). In addition, (Williams et al. 2009). In Williams et al. (2009), we there was little regeneration of native tree species and speculated that the causal mechanism of this linkage as a result, sightlines extended several hundred meters was that the closed canopy growth form of Japanese through the forest (Fig. 1). However, the invasive barberry may better retain humidity, thus creating a wine raspberry (Rubus phoenicolasius Maximowicz), more favorable microclimate for blacklegged ticks. multißora rose (Rosa multiflora Thunberg), and burn- We also noted that another contributing factor to the ingbush (Euonymus alatus Thunberg) were also decline in tick abundance could have been the elim- present in the understory. All study areas had medium ination of suitable questing habitat after the removal to dense stands of mature Japanese barberry that dom- of Japanese barberry stems. inated the understory and excluded desirable forest Our overall objectives of this research were to: (1) regeneration and native herbaceous vegetation (Fig. provide additional and longer-term data to further 1). Further details on stand histories, forest composi- document the relationship between blacklegged tick tion, soil types, and local climate can be found in Ward abundance and Japanese barberry cover, (2) provide et al. (2009). additional and longer-term data to show that Japanese Plot Design and Japanese Barberry Control. The barberry is a public health threat by harboring B. research consisted of two parallel studies. The Þrst burgdorferi-infected blacklegged ticks, and whether study was established in the winter of 2007, and all controlling barberry would again reduce B. burgdor- aboveground portions of Japanese barberry were feri prevalence, and (3) determine if Japanese bar- mulched. Treatment details are given below. There berry provides suitable questing habitat and/or ideal were three study areas in this study: Egypt, Storrs, and microclimatic
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