Secondary insects and diseases contribute to sudden aspen decline in southwestern Colorado, USA

2011 ◽  
Vol 41 (12) ◽  
pp. 2315-2325 ◽  
Author(s):  
Suzanne Bethers Marchetti ◽  
James J. Worrall ◽  
Thomas Eager

Reports of drought-associated forest mortality have increased around the world, but the mechanisms of mortality are rarely direct in nature. Biotic agents may kill trees that could otherwise recover and can perpetuate and expand mortality after the stress is relieved. Sudden aspen decline (SAD) has caused rapid, widespread branch dieback and mortality of quaking aspen ( Populus tremuloides Michx.). We compared insects and diseases in 162 damaged and neighboring healthy plots to determine contributing factors and their ecological roles. Cytospora canker, bronze poplar borer, and aspen bark beetles were the most common agents in damaged plots and correlated with crown loss and other factors related to SAD. This was the first documented outbreak of Trypophloeus populi , an aspen bark beetle. As bark beetles and bronze poplar borer increased in damaged stands, they tended to attack trees with healthier crowns. Environmental stress may have directly affected the success of these agents by increasing host susceptibility followed by a density-dependent increase in the insects’ invasive ability. In contrast, Cytospora canker had an identical relationship to crown loss in healthy versus damaged plots, suggesting that it was not limited by inoculum but responded to host susceptibility. Most other pathogens and insects contributed little to SAD and appear to be primary or weakening agents. The biotic agents of mortality in a decline differ greatly from primary agents and play complex and varied roles in healthy versus declining stands.

2014 ◽  
Vol 44 (8) ◽  
pp. 914-921 ◽  
Author(s):  
J.E. Korb ◽  
S. Bombaci ◽  
R. Siegel

Sudden aspen decline (SAD), present in many parts of North America, is the sudden dieback of branches, crown loss, and rapid mortality of aspen (Populus tremuloides Michx.). We surveyed 21 plots in southwestern Colorado and categorized each plot by the mean percentage of recent crown loss (RCL) into three SAD levels: low SAD (0%–25% RCL), moderate SAD (25.1%–50% RCL), and high SAD (50.1%–100% RCL). Our research quantified the effects of SAD on microclimate and understory vegetation at the individual species and community level. Mean day surface, day subsurface, and night subsurface temperatures were warmer in high SAD stands than in low ones. High SAD stands had lower soil moisture, lower litter and duff depth, higher bare soil cover, higher photosynthetically active radiation, higher arbuscular mycorrhizal propagule densities, and higher grass biomass. Indicator plant species were uniquely associated with low and high SAD. Our study illustrates that SAD has multiple ecological effects on aspen understories, including a potential positive feedback in which warmer temperatures and decreased soil moisture, consequences of SAD, may lead to increased branch dieback and tree mortality, which would alter microclimate-making conditions more favorable to SAD and escalate the effects of SAD on understory vegetation.


Forests ◽  
2019 ◽  
Vol 10 (8) ◽  
pp. 671 ◽  
Author(s):  
Jack Singer ◽  
Rob Turnbull ◽  
Mark Foster ◽  
Charles Bettigole ◽  
Brent Frey ◽  
...  

The American quaking aspen (Populus tremuloides Michx.) and its close relative, the Eurasian quaking aspen (Populus tremula L.), cover a realm that is perhaps the most expansive of all tree species in the world. In North America, sudden aspen decline (SAD) is a growing concern that marks the rapid decline of quaking aspen trees leading to mortality at the stand and landscape scale. Research suggests that drought and water stress are the primary causes of SAD. Predisposing factors (age, structure, and landscape position), as well as associated stressors (i.e., pests and pathogens), have been linked to mortality in affected stands. The conflation of multiple interacting factors across the aspen’s broad geographic range in North America has produced significant debate over the classification of SAD as a disease and the proper management of affected stands. Interestingly, no such effects have been reported for the Eurasian aspen. We here review and synthesize the growing body of literature for North America and suggest that SAD is a novel decline disease resulting from multiple inciting and interacting factors related to climate, land-use history, and successional dynamics. We suggest that the range of aspen observed at the onset of the 21st Century was bolstered by a wet period in western North America that coincided with widespread regional cutting and clearing of late-successional forests for timber and grazing. No comparable land-use history, successional status, or age-class structure is apparent or linked for Eurasian forests. Eurasian aspen is either absent or young in managed forests, or old and decadent in parks in Fenno-Scandinavia, or it grows more intimately with a more diverse mixture of tree species that have arisen from a longer period of frequent timber cutting in Russia. Based on these insights we provide recommendations for practical management techniques that can promote stand resilience and recovery across a range of stand conditions in North America. Managers should attempt to identify SAD-prone stands using the presence of predisposing conditions and focus treatments such as coppice or prescribed fire on stands with suitable topographies, elevations, and climates. We conclude that SAD will persist throughout the coming decades, given the enormity of past cutting history, fire exclusion, and current changes in climate until a more active restoration agenda is implemented.


2017 ◽  
Vol 38 (4) ◽  
pp. 630-640 ◽  
Author(s):  
Burke T Greer ◽  
Christopher Still ◽  
Grace L Cullinan ◽  
J Renée Brooks ◽  
Frederick C Meinzer

2012 ◽  
Vol 90 (7) ◽  
pp. 798-807 ◽  
Author(s):  
T.W. Pettit ◽  
K.T. Wilkins

Characteristics of edges affect the behavior of species that are active in and near edges. Forest canopies may provide edge-like habitat for bats, though bat response to edge orientation has not been well examined. We sampled bat activity in quaking aspen ( Populus tremuloides Michx.) forest canopies and edges in Heber Valley, Utah, during summer 2009 using Anabat detectors. Categorization and regression tree (CART) analysis of echolocation characteristics (e.g., frequency, duration) identified two guilds based on characteristic frequency (i.e., high- and low-frequency guilds). We used linear regression to compare characteristics of canopy and edge vegetation (e.g., tree height, diameter at breast height) to bat activity levels. Activity levels of high-frequency bats did not respond differentially to edge vegetation; low-frequency bat activity seemed to respond to canopy height. Activity levels of high-frequency bats were significantly greater than low-frequency bats in both edges and canopies. We detected significantly more bat activity in forest edges than in forest canopies, indicating the importance of edges to bats in forests.


2015 ◽  
Vol 148 (1) ◽  
pp. 36-42 ◽  
Author(s):  
Jonathon R. Newman ◽  
Diane Wagner ◽  
Patricia Doak

AbstractFor quaking aspen (Populus tremuloides Michaux; Salicaceae) the rate of extrafloral (EF) sugar secretion is increased by defoliation and decreased by drought. Although wholesale blocking of EF nectar has been shown to reduce ant (Hymenoptera: Formicidae) visitation to aspen, the effect of more subtle and realistic variations in nectar availability on ant recruitment is unknown. Working in Alaskan boreal forest (United States of America), we reduced and supplemented EF nectar availability on potted aspen ramets of three genotypes and surveyed visitation by free-living Formica fusca (Linnaeus) (Hymenoptera: Formicidae). Ants were more responsive to a subtle increase in sugar availability than to a decrease. While nectar reduction had no effect on ant visitation, nectar supplementation increased ant visitation to one aspen genotype by 70% during an early summer trial. Average ant visitation to different aspen genotypes varied during the late summer, indicating that aspen genotype can influence attractiveness to ants. We conclude that natural induction of EF secretion in response to herbivory may benefit aspen through improved ant recruitment, though the response is dependent on aspen genotype and time of year. Differences among aspen genets in attractiveness to ants could influence the relative success of genotypes, especially in settings in which aspen regenerates from seed.


Author(s):  
Monica Turner ◽  
Rebecca Reed ◽  
William Romme ◽  
Gerald Tuskan

An unexpected consequence of the 1988 Yellowstone fires was the widespread establishment of seedlings of quaking aspen (Populus tremuloides) in the burned forests, including areas outside the previous range of aspen (Kay 1993; Romme et al. 1997). Although aspen is the most widely distributed tree species in North America (Powells 1965), it is relatively uncommon and localized in distribution within Yellowstone National Park (Despain 1991). Most aspen stands in Yellowstone are found in the lower elevation landscapes in the northern portion of the park, and the species was absent - prior to 1988 -- across most of the high plateaus that dominate the southern and central park area. Aspen in the Rocky Mountain region reproduces primarily by means of vegetative root sprouting. Although viable seeds are regularly produced, establishment of seedlings in the wild is apparently a rare event due to the limited tolerance of aspen seedlings for desiccation or competition (e.g., Pearson 1914; McDonough 1985). In the immediate aftermath of the 1988 Yellowstone fires, there was a brief "window of opportunity" for aspen seedling establishment, as a result of abundant aspen seed production, moist weather conditions in spring and summer, and bare mineral soil and reduced plant competition within extensive burned areas (Jelinski and Cheliak 1992; Romme et al. 1997). We initiated this 3-year study in 1996 to address four questions about the aspen seedlings now growing in burned areas across the Yellowstone Plateau: (1) What are the broad-scale patterns of distribution and abundance of aspen seedlings across the subalpine plateaus of Yellowstone National Park? (2) What is the morphology and population structure -- e.g., proportions of genets (genetic individuals that developed from a single seed) and ramets (vegetative root sprouts produced by a genet) of various ages - in aspen seedling populations? (3) What are the mechanisms leading to eventual persistence or extirpation of seedling populations along an elevational gradient, particularly with respect to ungulate browsing and plant competition? (4) What is the genetic diversity and relatedness of the seedling populations along gradients of elevation and substrate?


Author(s):  
Kathryn Brown ◽  
Andrew Hansen ◽  
Robert Keane ◽  
Lisa Graumlich

Considerable debate surrounds the persistence of quaking aspen (Populus tremuloides) communities in western North America. Loss of aspen cover has been documented in several studies in various Rocky Mountain ecosystems (Loope and Gruel 1973; Romme et al. 1995; Renkin and Despain 1996; Wirth et al. 1996; Baker et al. 1997; Kay 1997; Bartos and Campbell 1998; White et al. 1998; Gallant et al. 2003). Explanations for loss of aspen include conifer encroachment, fire exclusion, herbivory, and climatic fluctuations (Loope and Gruell 1973; Mueggler 1985; Bartos et al. 1994; Romme et al. 1995; Kay 1997; White et al. 1998). However, many studies documenting aspen decline have been geographically limited or based on a small sample of subjectively chosen stands (Barnett and Stohlgren 2001; Hessl 2002; Kaye et al. 2003).


2017 ◽  
Vol 35 (1) ◽  
pp. 35-40 ◽  
Author(s):  
Darby McGrath ◽  
Jason Henry ◽  
Ryan Munroe ◽  
Erin Agro

Abstract This experiment investigated the effect of different plug-tray cell designs on root development of red maple (Acer rubrum), red oak (Quercus rubra), and quaking aspen (Populus tremuloides) seedlings. In April of 2015, seeds of each species were sown into three plug trays with different substrate volumes and grown for 17 weeks. Two trays had permeable walls for air-pruning, one with vertical ribs and one without. The third tray had impermeable plastic cell walls. Harvested seedlings were analyzed for root dry weight, length, volume, surface area and number of deflected roots. Root length per volume was highest in the impermeable-walled tray for red maple and quaking aspen. The total numbers of deflected root systems were higher for all species in the impermeable-walled tray. Seedlings grown in the air-pruning trays had smaller proportions of deflected root masses. Greater substrate volume did not influence root deflection development. The air-pruning tray without vertical ribs had the lowest total number of root masses with misdirected roots and lower proportions of root masses with misdirected roots for all species. These results indicate that improved root architecture in root-air pruning tray designs is achievable in tree propagation; however, vertical plastic structures in air-pruning trays can still cause root deflections. Index words: Deflected roots, air-pruning, seedling, propagation, plugs, root architecture. Species used in the study: red maple (Acer rubrum L.); red oak (Quercus rubra L.); quaking aspen (Populus tremuloides Michx.).


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