Bosque Ecosystem Monitoring Program Tamarisk Leaf Beetle Monitoring May-August 2013 Introduction The tamarisk leaf beetle (Diorhabda spp.) was released by the U.S. Department of Agriculture as a biological control agent for Tamarix spp. (often referred to tamarisk or saltcedar) in Nevada, Utah, Colorado and Wyoming in 2001 and in Texas in 2004 (Knutson et al., 2009). Tamarisk is a nonnative tree introduced to the U.S. in the 1800’s (Sher, 2013). The initial cause of concern about tamarisk was the amount of water it was thought to consume (Cleverly, 2013). However, its risk as a fire hazard and regrowth after fires at the expense of native species have become more of a concern. Tamarisk serves as a ladder fuel (Steuver, 2000), burns intensely, and resprouts well after fires (Glenn and Nagler, 2005). In 2007, the Tamarisk Coalition partnered with other agencies to track the expansion of the beetles, which were thought not to survive below the 38th parallel (Minard, 2011). This location, which includes the bottom third of Colorado and Utah and south, is significant because in this area, tamarisk is potential habitat for the endangered Southwestern Willow Flycatcher (Sogge et al., 2008). Thus, agencies are tracking tamarisk leaf beetle migration in this area, their impacts on tamarisk trees and Southwestern Willow Flycatcher numbers. The beetle migrated to Arizona in 2009 and New Mexico in 2010 (Tamarisk Coalition, 2012). In May 2013, the Bosque Ecosystem Monitoring Program (BEMP) partnered with the Tamarisk Coalition, Northern Arizona University and the U.S. Army Corps of Engineers to track tamarisk leaf beetle populations at 22 of its 27 sites, ranging from Santo Domingo Pueblo in the north to Lemitar (near Socorro) in the south (Figure 1). Four of the five sites not sampled contain no tamarisk; Mesilla, the southernmost site, was not monitored. Figure 1: Tamarisk leaf beetle presence at BEMP sites from May to August 2013 Goals of this monitoring were to determine how fast the beetles are spreading, the change in its population, its effect on tamarisk and the effect of these beetles on the Rio Grande riparian ecosystem. A longer-term goal was to see what happens after tamarisk dies or tamarisk cover is reduced. For instance, will native willows (preferred historical habitat of the Southwestern Willow Flycatcher) grow inside tamarisk skeletons as they did in Colorado (A. Sher, Associate Professor at University of Denver, personal communication); or will other invasive exotic species take advantage of the available habitat? 1 Methods The week of the third Tuesday in May, June, July and August 2013, BEMP sites were surveyed for tamarisk leaf beetles using methods based on Tamarisk Coalition protocols. Five tamarisk trees at least five meters apart were sampled using sweep nets (Photo 1). Five sweeps were taken from each tree. After sampling each tree, net contents were emptied into labeled plastic bags (Photo 2), and photographs were taken of the trees to track defoliation over time. The same trees and photo points were visited each month. BEMP staff and University of New Mexico (UNM) interns, in addition to some middle and high school students, collected field samples. Contents of the plastic bags were processed in the lab by BEMP staff and UNM interns using a dissecting scope. Quantities of adults, early larvae and late larvae tamarisk leaf beetles were counted, as were splendid tamarisk weevils (Coniatus splendidulus), tamarisk leafhoppers (Opsius stactogalus), spiders and ants. Other arthropods present were counted and identified to order. We paid specific attention to the weevils because they were also considered as a biological control agent but were not deliberately released because of concern over the impact to “sensitive and endangered species” (Eckberg and Foster, 2011). Leafhoppers play an important role because they are competitors of the tamarisk leaf beetle (Gould, 2008). Finally, spiders and ants are predators of the tamarisk leaf beetle (Gould, 2008). Photo 2: UNM interns empty contents of the net into a plastic bag Photo 1: BEMP staff samples for tamarisk leaf beetles Results In May, tamarisk leaf beetles were present at seven of the 20 sites monitored, including Santo Domingo and six sites in Albuquerque between Alameda Blvd and Rio Bravo (Figure 2). Santo Domingo had the highest number of beetles, with 11 adults. Albuquerque sites only had one to two 2 beetles present; all were adults except for one larva. Little to no impact was seen on any tamarisk monitored, even at Santo Domingo (Photo 3), which had the greatest number of beetles. Figure 2: Tamarisk leaf beetles were present at seven BEMP sites in May 2013. In June, tamarisk leaf beetles were present at 11 of the 22 sites1 monitored, including Santo Domingo, Santa Ana, seven sites in Albuquerque between Alameda Blvd and I-40 and two sites in Belen (Figure 3). Again, Santo Domingo had the highest number of beetles, at 179. Dominance shifted from mostly adults in May to mostly larvae in June. There was little defoliation to the trees at Santo Domingo (Photo 4) or any other site. In July, tamarisk leaf beetles were present at 13 of the 22 sites monitored, including Santo Domingo, eight sites in Albuquerque between Alameda Blvd and I-40, Bosque Farms, Los Lunas and Belen (Figure 4). Two sites in central Albuquerque had the highest number of beetles; Montaño had 362, and Savannah had 223. Adults dominated the population, but a number of larvae were present. There was defoliation to tamarisk at Santo Domingo (Photo 5), Diversion, Minnow, Montaño, Savannah, Route 66, RGNC and Reynolds Forest and Reynolds Clear. 1 Two sites in Albuquerque (Calabacillas and BioPark) were not sampled in May but were sampled in June and July. Four trees were added to the Los Lunas sample in June and July; only one tree was sampled in May. 3 Figure 3: Tamarisk leaf beetles were present at 11 BEMP sites in June 2013. Note shift in scale of y-axis. Figure 4: Tamarisk leaf beetles were present at 13 BEMP sites in July 2013. Note shift in scale of y-axis. 4 Photo 3: Santo Domingo tamarisk #5 May 2013 Photo 4: Santo Domingo tamarisk #5 June 2013 Photo 5: Santo Domingo tamarisk #5 July 2013 Photo 6: Santo Domingo tamarisk #5 August 2013 In August, tamarisk leaf beetles were present at 15 of the 22 sites monitored, including Santo Domingo, Santa Ana, nine sites in Albuquerque between Alameda Blvd and Rio Bravo, Los Lunas, two sites in Belen and Lemitar, just north of Socorro, NM (Figure 5). Santa Ana had the greatest number of beetles, at 558 – the highest number for the season. There were mostly adults, with a few larvae present. Tamarisk trees were highly defoliated at Santo Domingo, Santa Ana, Diversion, Minnow, Montaño, Savannah, Route 66, RGNC and Reynolds Forest and Reynolds Clear (e.g., Santo Domingo, Photo 6). 5 Figure 5: Tamarisk leaf beetles were present at 15 BEMP sites in August 2013. Note shift in scale of y-axis. For the entire sampling season (May to August), tamarisk leaf beetles were present at 19 of the 22 sites sampled (Figure 6). At two of the three sites where the beetles were not obtained through sampling (Reynolds Forest and Reynolds Clear), tamarisk trees were visibly defoliated (Photo 7); our sampling did not determine whether the defoliation was caused by tamarisk leaf beetles or tamarisk leafhoppers. The abundance of splendid tamarisk weevils (Figure 7), tamarisk leafhoppers (Figure 8), spiders (Figure 9) and ants (Figure 10) varied across sites during the sampling period. No significant correlation, positive or negative, existed among the abundance of tamarisk leaf beetles and abundance of weevils, leafhoppers, spiders or ants. Photo 7: Tamarisk defoliation at the Reynolds Forest site in July 2013. 6 Figure 6: Tamarisk leaf beetles were found at 19 of the 22 BEMP sites sampled from May to August 2013. Figure 7: Abundance of splendid tamarisk weevils varied across sites from May to August 2013. 7 Figure 8: Abundance of tamarisk leafhoppers varied across sites from May to August 2013. Figure 9: Abundance of spiders varied across sites from May to August 2013. 8 Figure 10: Abundance of ants varied among sites from May to August 2013. Discussion We were informed that tamarisk leaf beetles were present at the Pueblo of Santa Ana in 2010 (Nathan Schroeder, Restoration Division Manager at the Pueblo of Santa Ana, personal communication) and in Albuquerque in 2012 (Ondrea Hummel, Ecologist at the U.S. Army Corps of Engineers, personal communication). Our monitoring officially documented the beetle in 2013 at BEMP sites where tamarisk is present; these data are being used by the U.S. Army Corps of Engineers in collaboration with Northern Arizona University via the Tamarisk Coalition. We will continue monitoring to determine the change in beetle, weevil and leafhopper abundance; impact to tamarisk, both short- and long-term; tamarisk recovery time; tamarisk mortality; and potential impacts to Southwestern Willow Flycatcher habitat. In addition, BEMP will monitor reestablishing vegetation and thus track changes in native and exotic cover. References Cleverly, J.R. 2013. Water Use by Tamarix. In Tamarix: A Case Study of Ecological Change in the American West. A. Sher and M.F. Quigley (eds). Oxford University Press: New York, NY. Eckberg, J.R. and M.E. Foster. 2011. First Account of the Splendid Tamarisk Weevil, Coniatus splendidulus Fabricus, 1781 (Coleoptera: Curculionidae) in Nevada. The Pan-Pacific Entomologist 87(1):51-53. 9 Glenn, E.P. and P.L. Nagler. 2005. Comparative Ecophysiology of Tamarix ramosissima and Native Trees in Western U.S. Riparian Zones. Journal of Arid Environments 61:419-446. Gould, J. 2008. Life-History of Diorhabda elongata in Secure Field Cages: Results of Research during Stage A of Research Releases in 1999. U.S. Department of Agriculture – Agricultural Research Service. Last edited June 4, 2008. http://www.ars.usda.gov/Research/docs.htm?docid=6937 Knutson, A, M. Muegge and Jack DeLoach. 2009. Biological Control of Tamarix in Texas. A presentation at the Weed Science Society of America Symposium, Orlando, FL. http://www.wsweedscience.org/Slides/2009/Biocontrol%20Symposium/10%20Biological%20Contr ol%20of%20Tamarix%20in%20Texas%20-%20Knutson.pdf Minard, A. 2011. Concern over the Spread of Tamarisk Beetles. Four Corners Free Press. May issue. http://fourcornersfreepress.com/news/2011/051101.htm Sher, A. 2013. Introduction to the Paradox Plant. In Tamarix: A Case Study of Ecological Change in the American West. A. Sher and M.F. Quigley (eds). Oxford University Press: New York, NY. Sogge, M.K., S.J. Sferra and E.H. Paxton. 2008. Tamarix as Habitat for Birds: Implications for Riparian Restoration in the United States. Restoration Ecology 16(1):14-154. Stuever, M.C. 2000. Bosque Fires and Fire Mortality of Cottonwood. A presentation at the Bosque Consortium Conference on Fire in the Bosque. 8 p. Tamarisk Coalition. 2012. Yearly Distribution (2007-2012) of Tamarisk Leaf Beetle (Diorhabda spp.). Published November 8, 2012. http://allaboutwatersheds.org/library/inbox/2012_TLB_Distribution_Map.pdf 10
© Copyright 2024 Paperzz