Phytosphere Research - Horticulture / Urban Forestry / Plant Resources / Agriculture
Management of Phytophthora ramorum (sudden oak death) in tanoak and oak stands
Ted Swiecki and
Matteo Garbelotto, Forest Pathology and Mycology Extension Specialist
Yana Valachovic - Forest Advisor
Project funding provided by:
USDA Forest Service, Pacific Southwest Research Station
USDA Forest Service, State and Private Forestry, Forest Health Protection
Landowners and managers have been seeking ways to protect coast live oak (Quercus agrifolia), California black oak (Q. kelloggii), and tanoak (Notholithocarpus [=Lithocarpus] densiflorus) from Phytophthora ramorum, the pathogen that causes sudden oak death (SOD), both in newly-infested areas and areas that have been impacted by this disease for many years. Recent research has been used to formulate disease management strategies for minimizing the impacts of P. ramorum canker in susceptible stands of oaks and tanoak. However, data are needed to determine whether these management techniques will be effective when applied in the field at a practical scale.
In this collaborative project, we have established a network of long-term disease management plots to test the efficacy of the most promising techniques for managing P. ramorum canker in forests containing tanoak, coast live oak, and California black oak. Because disease epidemiology differs between different canker hosts, we are testing different control strategies in tanoaks and susceptible oaks, as described below. Results of this project will be used to improve disease management recommendations and will provide additional information on the epidemiology of the disease in treated and untreated stands.
|Application of phosphite to stem of a tanoak. A long spray wand is used so that the spray can be applied higher on the stem, where bark is thinner, to help increase uptake.|
Disease management in tanoak stands using potassium phosphite (Agrifos)
Managing SOD in tanoak stands is difficult because P. ramorum can complete its entire disease cycle on this host alone. P. ramorum causes leaf and twig infections in tanoak that lead to dieback of the fine twigs. UC Davis researchers in Dr. David Rizzo's lab have shown that P. ramorum also produces spores on infected tanoak twigs. These spores cause additional twig infections and, in sufficient numbers, can initiate bark cankers on the main stems of tanoak. These cankers can girdle and kill entire trees.
Potassium phosphite (also known as potassium phosphonate; trade name Agri-fos) is a selective, systemic fungicide with a high level of environmental safety and very low non-target toxicity (see box below). It has shown good levels of efficacy against P. ramorum canker in various trials. However, it has not been used widely enough in tanoak to determine the range of conditions under which it is effective. Furthermore, other questions remain as to the most effective way to utilize this material to manage P. ramorum canker in tanoak stands. Lab studies indicate that phosphite-treated tanoaks show resistance to artificial inoculations in the laboratory. Tanoaks that are treated with phosphite before being exposed to P. ramorum are less likely to develop stem cankers. Phosphite-treated tanoaks should also be less likely to develop the twig infections that produce spores. Treating blocks of tanoaks should therefore be more effective than treating scattered individual trees because the combination of these two effects (increased resistance to disease in plant tissues and reduced spore production) should provide a greater level of disease protection. In general, fungicidal materials such as phosphite typically work best when they are not exposed to very high disease pressure.
This study is testing whether phosphite is effective at reducing disease in tanoak when applied to a contiguous block of tanoaks. To account for possible regional differences, tanoak plots are distributed through much of the north to south range of P. ramorum in California’s Coast Ranges.
Study progress to date (Phytosphere Research plots)
Plots treated in 2005 were established in cooperation with the Kashia Band of Pomo Indians of Stewarts Point Rancheria under a project funded by USDA Forest Service, State and Private Forestry. We collected baseline observations on tree health and are reevaluating the trees periodically so that they can be compared with other plots that are part of this multi-location study.
All plots are close to or within areas where P. ramorum was present at the time plots were established. However, since the treatment is primarily preventative in nature, we selected study plot areas where all or almost all tanoaks were apparently free of trunk cankers. One difficulty in establishing this study was finding plot locations where trees were noninfected at the time of the original treatment but where trees were likely to be exposed to P. ramorum inoculum within a fairly short time after treatments had been initiated.
The Phytosphere tanoak plots are all dominated by tanoak, but most plots contain some conifers (Douglas-fir and/or coast redwood) and/or some madrone trees. California bay trees are not present in the plots. In a few plots, we removed small diameter bay trees at the onset of the study. P. ramorum spores are produced abundantly on infected bay leaves, and field studies and observations by various researchers have indicated that tanoaks adjacent to California bay trees have a very high risk of being infected and killed by P. ramorum. Since bay trees are not present in our plots, we are testing the efficacy of phosphite under conditions where it is most likely to be effective - in plots where tanoak is the primary source of P. ramorum spores and where all tanoaks in the plot have been treated with phosphite.
Although phosphite can be injected directly into tanoak trunks, in this study we are applying phosphite as a spray to the trunk. For this application, the phosphite solution is combined with a relatively high amount (2.5% by volume) of an organosilicate surfactant (trade name Pentrabark), as specified by the Agri-fos label. The trunk spray application allows one to treat a larger number of trees in a shorter time compared to trunk injection, so the spray method is more suited to treating large numbers of trees. We have used both an ATV-mounted sprayer and an electric backpack sprayer mounted on a custom cargo bicycle to apply calibrated amounts of spray solution to the treated trees.
For both types of sprayers, we used custom-made telescoping spray booms that allowed us to apply the spray high on the trunk - up to a height of about 20 ft (6 m) (top photo; details of the construction of the high reach spray wand are available from this link). Applying the spray high on the trunk provides two main advantages that should increase phosphite uptake:
We use TeeJet air induction nozzles to provide relatively large spray droplets and minimize drift. Nonetheless, some overspray and drift is inevitable. One disadvantage of the trunk application method is that the spray solution is quite phytotoxic to tanoak foliage (photo), and leaves that are wetted by the spray solution become scorched or are completely killed. Hence, stem application is impractical for small understory tanoaks because the overspray will kill much of the foliage.
While it is impractical to treat very small understory tanoaks, these seedlings and saplings may still serve as a source of P. ramorum spores. Therefore, in our treatment protocol, small understory tanoaks (less than about about 3 inch diameter), if present, are cut down and removed from the phosphite-treated and control plots. In the two locations where we removed a significant amount of understory tanoak, we set up a second control plot with no understory tanoak removal. The plots without understory tanoak removal are included as a check to determine whether removal of understory tanoaks alone can affect disease development within the plot.
We are currently using a spray program that includes two applications the first year (winter and spring), followed by annual reapplication. The reapplication interval may be extended later in the study if the one-year reapplication interval is shown to be effective.
Spore monitoring in plots. During the spring of 2007, we monitored spore production within the plots using buckets containing bay leaf baits. In spring 2008 and 2009 we monitored spore production by collecting soil samples and using rhododendron leaf disks to bait the samples for P. ramorum. In June 2008, we also collected leaf samples that were assayed for disease resistance by the Garbelotto lab. In 2009, we began testing a new type of spore trap that we have devloped. These spore traps were tested in one location (FE) in 2009 and two locations (FE and PC) in 2010.
Results and observations through 12/2010
Efficacy. Monitoring disease development on tanoaks within the study plots is our main method for determining whether the Agri-fos treatment is effective. We assessed the disease status of each tanoak stem in the plots prior to the start of the study and are periodically reassessing the stems to detect evidence of disease. The plots that were established in the winter of 2005/2006 have the now been observed for 4 years since the start of the experiment. Likely symptoms of P. ramorum canker were noted in the plots at location SF within the first 6 months of the study, and trees killed by P. ramorum were present by 1.5 years after the start of the study. At the other location (BL), likely P. ramorum cankers were not noted until 1.5 years after the start of the study. Levels of disease in these two locations are summarized in the table below.
Overall disease levels in all plots are higher at the SF location than at the BL location. Plot SF1 (Agri-Fos treated) had the highest incidence of disease overall. However, plot SF1 is also closest to the original P. ramorum disease center at this location, and it appears likely that many of the trees that have developed sypmptoms to date were already infected at the start of the study. Cankers on tanoak are often cryptic and may not produce visible external symptoms (such as bleeding) until the disease is very advanced. Small-diameter tanoaks may actually be killed by SOD without developing bleeding cankers. Our data indicate that spore production was negligible in the plots in spring 2007, 2008, and 2009. It is likely that most disease symptoms in the SF plots resulted from infections initiated in the wet springs of 2006 or 2005.
From these observations, we infer that phosphite application was ineffective at preventing disease progress in tanoaks that were already infected in plot SF1. Various researchers have noted that phosphite is most likely to be effective when applied as a protectant to uninfected plants. It is generally much less successful at limiting established infections.
For all of the SF plots, the mean diameter of trees with P. ramorum symptoms in June 2008 was significantly greater than the diameter of asymptomatic trees. Furthermore, 5 of the 7 stems killed by P. ramorum in the Agri-Fos plot SF1 had stem diameters greater than 15 inches (38 cm). This raises the possibility that the lack of efficacy in plot SF1 could also be related to phosphite concentrations in the treated trees. The larger-diameter stems might not have received a high enough dose of phosphite to prevent established cankers from expanding. In general, high doses of phosphite are needed to show any post-infection activity.
Although the surface area of the trunk increases in a linear fashion with increasing stem radius or diameter, the volume of bark and sapwood tissue increases as a function of the square of the radius. Hence, large-diameter trees receive proportionately less phosphite per unit stem volume than do small diameter trees when sprayed according to the standard label recommendation. In our plots, we have been using a spray volume that has been calculated to reduce this disparity (see graph below), but it is not possible to completely correct for this effect in large-diameter trees because only a limited amount of spray volume can be adsorbed onto the bark surface. See our Dec 2007 progress report for a full discussion about stem diameter and application rate. A key question that we are examining in this study is whether Agri-fos is effective across the range of tree diameters at the rates we are testing.
The plots at the BL location were further from an active P. ramorum disease center at the time that the study was started. Disease levels at this location are still very low. To date, SOD incidence has been lower in the Agri-fos treated plot, but it is still too early to tell whether this is due to the treatment or simply due to uneven disease distribution. Average trunk diameter is smaller at the BL location than at the SF location, so a treatment effect may be more likely to be seen at BL.
At locations that were initially treated in Jan/Feb 2007 (table below), levels of SOD have been low since the start of the study. Spore monitoing results indicate that Disease pressure has been low since the plots were established. As disease pressure increases, these plots should provide a good test of how well Agri-fos protects against SOD. A range of trunk diameters is present in these plots.
Phytotoxicity. As expected, Agri-fos / Pentrabark caused phytotoxicity on foliage that received overspray. We have seen necrosis (tissue death) on tanoak and redwood foliage as well as on mosses growing on the stem surfaces that were thoroughly wetted by the spray solution. In most cases, exposed woody twigs were not killed. New shoots have formed from buds on twigs that were defoliated due to phytotoxicity. However, some small diameter understory stems that were retained in some plots appear to have been killed as the result of Agri-fos phytotoxicity. These trees have had severe phytotoxicity affecting the majority of their foliage in successive years. This result supports our study design concept of removing rather than spraying small understory tanoaks.
Spore monitoring in plots. If phosphite is absorbed by Agri-fos treated tanoaks, it should be translocated throughout the trees. Phosphite in leaves and twigs should prevent P. ramorum infection and sporulation. Therefore there should be fewer spores produced in treated plots than in nontreated control plots. Monitoring for spore production in treated and control plots could provide an early indication of Agri-fos efficacy.
In 2007 we did not detect any P. ramorum on bay leaf baits in any of the tanoak plots. Rainfall measured in plots was low during April and May. Results are consistent with those of other researchers sampling in northern California during this period. Rainfall amounts in the first 3 weeks of April were about 1 to 2 inches (2.5-5.8 cm) in the plots, but in the following three week period, less than 0.5 inch (0.13-0.4 cm) was recorded. Spring 2007 was unfavorable for spore production by P. ramorum due to low rainfall. The overall lack of P. ramorum spore production in the plots does not allow us to determine whether spore production was affected by the Agri-fos treatment. However, it does suggest very few or no new infections in the plots would have been likely to occur in spring 2007. Hence, trees that have shown trunk symptoms for the first time in 2007 were almost certainly infected in previous years. Monitoring by researchers in Dr. David Rizzo's lab (UC Davis) has indicated that the rainy springs of 2005 and especially 2006 were favorable for P. ramorum spore production.
Rainfall in spring 2008 and 2009 was also very low; little or no measurable precipitation fell in the study areas over the intended baiting period. We used soil baiting rather than the floating bay leaf baits to monitor spore production in the plots in these years. Soil baiting detects P. ramorum inoculum that has been washed into the soil, and has the potential to detect inoculum deposited earlier in the rainy season. These tests were conducted by Dr. Elizabeth Fitchner in Dr. Dave Rizzo's lab at UC Davis. No P. ramorum was detected in any of the soil samples. This indicates that very few spores were produced in the plots in early 2008 and 2009 irrespective of the treatment (Agrifos or control). Dry soil and warm temperatures through most of the spring of 2008 and 2009 may also have reduced the survival of any inoculum that washed into the soil during the short rainy season.
Rainfall in spring 2010 was higher than in the previous four years. We used sand spore traps to filter out spores from canopy throughfall of rainwater in the plots at two locations. Three traps were set up in both Agri-Fos treated and control plots at both locations. At the FE location, traps were left in place from 26 March to 22 April 2010. During this interval, 4.4 inches of rain fell in the plots. At the PC location, traps were in place for just over a week, from 24 May to 1 June 2010. We measured 1 inch of rain in the plots during this interval. We did not detect any P. ramorum in any of the spore traps. These results suggest that overall P. ramorum infection levels in the canopies of trees in these plots was still low. After three dry years, it appears that the 2010 spring rain was insufficient to develop a strong infection event in the plots.
Bioassay to test for phosphite activity in leaves. In June 2008, we collected leaf samples from Agrifos-treated and control tanoaks for a bioassay conducted by the Garbelotto lab. In the assay, P. ramorum inoculum is applied to the petiole end of detached leaves, and the length of the resulting lesion is measured. This assay has been used previously to show effects of phosphite application, and we had hoped to use it to get an early indication of whether the Agrifos treatments were having an effect in treated plots and to look at relationships between phosphite activity and stem diameter. Results from the assay failed to show any average difference in lesion development between trees from treated and control plots. In fact, the only significant relationship in the data was a correlation between leaf size and lesion development. Data from the assay were also highly variable. At this point, it appears that the assay did not perform this year as it had in the past and appears to be sensitive to leaf size and/or maturity.
Application amount and cost. To treat the original 256 live stems in the 5 sprayed plots described above required 39 gal (148 L) of spray solution. This volume of spray solution contains about 19 gallons (72 L) of Agrifos and 1 gallon (3.7 L) of Pentrabark. The average diameter (DBH) of all stems in the treated plots was 6.75 inches (17 cm), with a range from about 3 inches (8 cm) to about 35 inches (89 cm). The spray volume used per stem was modest for small diameter trees (e.g., about 1 pint [473 ml] for a 6 inch [15 cm] diameter stem). However, for larger stems, the spray volume was much more substantial because the spray volume curve we used (graph) was calculated by averaging the linear rate based on stem surface area and the power curve rate based on stem volume. For a 30 inch diameter stem, the spray volume applied would be 1.3 gal (4.9 L). This is more than 10 times the volume applied to the 6 inch stem, even though the diameter is only 5 times that of the smaller stem.
Put another way, 5 gal of mixed spray solution would treat about 40 6-inch diameter stems, but would be a bit short of the amount needed to treat four 30-inch diameter stems. At current full retail prices for Agri-fos and Pentrabark (variable, but about $200 for 5 gal of mixed spray solution=2.5 gal Agri-fos and 1 pint Pentrabark) the cost of materials alone for each stem would range from about $5 (6 inch stem) to over $50 (30 inch stem) for each application. If the chemicals can be purchased at closer to wholesale cost, the cost per tree will be substantially lower.
Above graph shows the targeted amount of diluted Agri-fos spray solution used for treated stems by stem diameter at breast height (DBH). For trees less than 12 inches DBH, we use a linear function to calculate spray volume based on diameter. For stems 12 inches DBH or larger, a quadratic term is added to the equation, resulting in the curvilinear relationship seen in the graph. The quadratic formula helps keep the ratio of Agri-fos applied per unit stem volume relatively constant.
Disease management in coast live oak and California black oak using selective removal and/or pruning of California bay
The small understory bay to the left of this coast live oak was the source of the P. ramorum spores that killed the oak.
Disease epidemiology in coast live oaks and California black oaks differs from that in tanoaks because the pathogen, P. ramorum, has not been shown to sporulate to any significant degree on either oak. Several lines of research indicate infections on these oaks are usually initiated by spores that are produced on infected California bay leaves. Recent research indicates that most of the disease risk in oaks is associated with bay that are quite close to or actually overtopping the oak trunk. This study investigates whether selective removal of bay from this localized zone near the oak trunk is sufficient to reduce disease risk to an acceptably low level. To date, only Phytosphere Research has established plots for this portion of the study.
This study is based on matched pairs of SOD-susceptible oaks (coast live or California black oak). The trees within the pairs were matched to the degree possible for known factors that influence disease risk, especially the amount of bay in the immediate vicinity of the trunk. One tree of each pair was designated as the control and the bay surrounding it was not altered. For the other (treated) tree, we removed bay from the zone nearest to the trunk. For these trees, we attempted to achieve a minimum clearance of 8 ft (2.5 m) of horizontal distance between bay foliage and the oak trunk. Clearance is measured by projecting a vertical line down from the nearest bay foliage to the trunk and measuring the horizontal distance to the oak trunk from that line. Where it could be achieved without excessive effort, the clearance was increased up to about 16 ft (5 m), especially in the direction of the prevailing storm winds (generally south and west of the tree). Clearance was obtained by removing small-diameter bay stems close to the oak and/or bay branches from bays located farther from the oak. Oak trees were not pruned; the bay-oak clearance was obtained only through removal or pruning of bay. The box below summarizes lists the overall criteria that were used for clearing bay around treated trees .
Locations used in this study are in Sonoma, Napa, and Solano Counties in areas where P. ramorum is present and causing symptoms on bay and usually at least some oaks. Because localized bay removal is primarily a preventive treatment, oaks selected for the study were generally free of obvious stem cankers. However, we included nine trees with small cankers in the study to assess whether disease progress could be slowed by reducing the amount of additional inoculum that lands on already-infected trees.
Bay removal treatments were initiated in spring 2007. To date, 31 coast live oak pairs and 18 California black oak pairs have been established, each pair consisting of matched control and treated (bay removal) trees. Many trees in the study have multiple trunks, each of which is tracked separately for data collection anad analysis. Study trees are assessed annually for SOD symptoms. We are also evaluating the amount of regrowth that occurs from cut bay stumps. None of the bay stumps in this study were treated with herbicides to prevent resprouting.
To minimize the costs associated with felling/pruning and the handling of downed material, we generally selected oaks that required relatively little bay removal to make a large change in disease risk. Ideal oaks for treatment are those with only one to a few small diameter understory bays near the trunk. These situations commonly occur where bay is not the dominant tree in the stand. The largest diameter bay stem we removed was about 9 inches (23 cm) in diameter. However, bay stems typically flare widely at the base, so the basal cut is typically much larger than the DBH of the felled stem. Even small diameter bays are commonly quite tall. In dense stands, felled bay stems may hang up in the canopies of other trees and can be time consuming to drop.
At most study locations, downed material was left on site. We disposed of cut material using "lop and scatter": material was cut into relatively short lengths and spread out to avoid forming piles. We kept cut bay foliage at least 3-6 ft (1-2 m) away from the trunks of susceptible oaks. Splash dispersal of most P. ramorum inoculum from bay foliage near the ground is generally likely to be limited to about 3 ft (1 m) or less. Depending on weather conditions and exposure to sunlight, cut bay foliage can dry out within a few days to weeks. In heavily shaded stands during cool, wet conditions, bay foliage can remain green (and potentially a source of P. ramorum inoculum) for at least a month. Hence, at least during the rainy season, we believe it is prudent to keep cut bay foliage away from susceptible oak trunks until the bay foliage has become completely desiccated.
We collected baseline observations on tree health prior to treatment and are reevaluating the trees periodically. We also measured the minimum oak trunk-bay foliage horizontal distance and assessed bay cover within concentric zones near the oaks prior to the study and after bay removal for the treated trees.
Spore monitoring in plots. During the spring of 2007, we monitored spore dispersal near the trunks of treated (bay removal) and control trees at two study locations using buckets containing bay leaf baits as noted for the tanoaks above. In 2010, we used the sand-based spore traps discussed above to sample spores at Annadel SP plots.
Results and observations through 12/2010
Spore monitoring in plots. As noted for the tanoak plots above, we did not detect any P. ramorum on bay leaf baits from any of the sampling buckets around control or treated trees in 2007 (photo). As with the tanoak plots, rainfall measured in plots was low during the monitoring period (beginning of April through mid May). Rainfall amounts in the first 3 weeks of April were 1.6 and 2.4 inches beneath tree canopy at the two locations. In the following three week period, we recorded 0.3 and 0.5 inch of rainfall through the canopy. The low rainfall in spring 2007 was generally unfavorable for P. ramorum sporulation in much of northern California. Because rainfall in spring 2008 and spring 2009 was even more sparse than in 2007, we did not repeat the P. ramorum monitoring in 2008 or 2009.
Phytophthora ramorum spores were detected using leaf baits floating in water in plastic buckets. Higher amounts of infection are seen in the leaf baits as the amount of P. ramorum spores falling in the bucket increases. However, no infected leaf baits were detected in the spring 2007 monitoring. For oaks, two buckets were placed near the north and south sides of the trunk. Note the sprouting bay stump behind the left bucket and dead bay foliage from the cut stems in the background.
In 2010, we used sand spore traps to assess inoculum deposition near study trees at Annadel State Park over two time intervals (3/26-4/22 and 4/22-6/3). Traps were set up adjacent to trunks of four trees from which bay had been removed and four control trees which had not had any bay removal. All control traps were located under bay canopy, whereas the traps near the bay removal trees were 3 to 5.8 m from bay canopy. The first time interval at Annadel was the same as used for the FE tanoak plots. At Annadel, 3.7 inches of rain fell during the first time increment. No P. ramorum inoculum was detected in this initial round of trapping. In addition, bay foliar symptoms were not observed in the vicinity of the traps when they were deployed (3/26/10) or picked up (4/22/10).
We set out four fresh spore traps on 22 April 2010 around two pairs of trees that were in a portion of the study area that had greater bay cover and more SOD overall. Over the interval from 4/22-6/3, we measured 2 inches of rainfall under the trees. When the traps were removed on 3 June 2010, bay leaves around one of the control trees had developed extensive foliar necrosis due to P. ramorum infection. We detected P. ramorum from the spore trap under this bay. The spore traps adjacent to oaks from which bay had been removed were negative, as was the spore trap adjacent to a noncleared oak in which the bay was nonsymptomatic. These results indicate that rainfall was sufficient for P. ramorum to initiate infections and produce spores on some bay trees, but weather conditions were not extreme enough to result in widespread infection of bays.
Sand spore trap (center) under bay foliage . Water that falls into the tray is channeled through a sand-filled column that retains P. ramorum spores. Note that bay canopy (bay trunk is next to bucket) overhangs the main stems of the oak (to left of spore trap).
Efficacy. Additional trees have become symptomatic over time, increasing the number of symptomatic trees from the original nine at the start of the study in 2007. At present, P. ramorum canker incidence does not differ by treatment. Based on spore monitoring data, it is likely that very few, if any, new stem cankers have been initiated since the start of the study. Infections that became visible in 2008 and 2009 were most likely initiated in the wet years of 2005 or 2006. In other field studies, we have seen that symptom development in coast live oak may not be visible for up to three years after an infection period. Given this long latent period, we will need to assess disease in these trees for at least several years after a significant infection period to determine whether the bay removal treatment is successful.
Many of the trees that had existing cankers at the start of the study showed an increase in symptom severity between 2007 to 2010. This disease progress was related to expansion of existing cankers rather than initiation of new cankers.
The table below shows P. ramorum infection status among individual oak trunks with and without nearby bay removed in 2007. No trees were dead in 2007. Early Pr=bleeding P. ramorum cankers only. Late Pr=bleeding cankers plus signs of beetle infestation and/or fruiting bodies of Annulohypoxylon thouarsianum.
Bay regrowth. Bay stumps can be treated with herbicides immediately after cutting to inhibit subsequent sprouting. In this study, cut bay stumps were not treated, which allows us to assess how fast sprouts regrowth and how often follow up treatments would be needed if herbicides are not used.
We first observed sprouts developing from cut stumps by mid-April (photos below), several months after trees were cut. Some of these new shoots were browsed by deer. Evaluations in June 2008 showed that browsing by deer and other animals was highly effective at reducing bay sprout growth. Browsers showed a clear preference for these young bay shoots, which are relatively succulent and not woody. Deer appeared to be the primary browsers at most locations, but cattle may also have browsed shoots at two locations (JT/GVR and Jacobs), and horses are present at Wall Rd.
More than a year after the initial bay removal, the tallest bay stump sprout was 53 inches (1.3 m), but shoots over 31 inches (0.8 m) were seen at only one of the study locations (SA) where browsing was limited. The remaining locations had average maximum bay sprouts heights of 14 inches (37 cm) or less. Basal diameters of sprouts averaged about 0.3 inch (0.78 cm) and were easily removed using loppers or an axe. In addition, very few of the pruning cuts made to remove bay branches from larger stems gave rise to epicormic sprouts. We removed all sprouts greater than about 10 inches (25 cm) in height in June 2008.
Browsing of bay sprouts was most intense at Annadel State Park, which is not grazed by livestock (photos below).
At the June 2009 and July 2010 evaluation (data shown below), we measured regrowth of sprouts from removed bay stems and trimmed off sprouts to suppress regrowth. None of the bay foliage on these new shoots showed symptoms of P. ramorum infection. Bay resprouts at all locations showed varying amounts of browsing. Due to browsing impacts and associated reduced vigor of the stumps, overall average sprout height was significantly less in 2009 and 2010 than in 2008.
Based on these early results, it does not appear that herbicide treatment of bay stumps to prevent resprouting is essential in areas with moderate to high levels of browsing pressure. Follow-up inspection of treated areas after 1 to 1.5 years should be conducted to determine whether browsing pressure is sufficient and to remove tall sprouts that have not been suppressed by browsers. At this stage, bay resprouts are easily removed with various types of hand tools. We will continue to monitor regrowth from these stumps to determine whether the combined effects of browsing and periodic removal of bay shoots effective for suppressing bay sprout growth. In particular, we would like to determine how long it is necessary to continue sprout monitoring and removal activities.