Few studies have clearly linked long-term monitoring with in situ experiments to clarify potential drivers of observed change at a given site. This is especially necessary when findings from a site are applied to a much broader geographic area. Here, we document vegetation change at Barrow and Atqasuk, Alaska, occurring naturally and due to experimental warming over nearly two decades. An examination of plant cover, canopy height, and community indices showed more significant differences between years than due to experimental warming. However, changes with warming were more consistent than changes between years and were cumulative in many cases. Most cases of directional change observed in the control plots over time corresponded with a directional change in response to experimental warming. These included increases in canopy height and decreases in lichen cover. Experimental warming resulted in additional increases in evergreen shrub cover and decreases in diversity and bryophyte cover. This study suggests that the directional changes occurring at the sites are primarily due to warming and indicates that further changes are likely in the next two decades if the regional warming trend continues. These findings provide an example of the utility of coupling in situ experiments with long-term monitoring to accurately document vegetation change in response to global change and to identify the underlying mechanisms driving observed changes.
Extensive areas in the upper Midwest have been invaded by spotted knapweed, and effective management strategies are required to reestablish native plant communities. We examined effects of mowing, mowing plus clopyralid, or mowing plus glyphosate in factorial combination with hand pulling and burning on knapweed abundances on a knapweed-infested site in western Michigan. We applied mowing and herbicide treatments in summer 2008, and seeded all plots with native grasses and forbs in spring 2009. We conducted the knapweed pulling treatment from 2009 to 2012 in July. The prescribed burn was conducted in April 2012. By 2012, hand pulling reduced adult knapweed densities to 0.57 ± 0.12 m−2 (0.053 ± 0.011 ft−2) (mean ± SE), which was 5.8% of nonpulled treatments, juvenile densities to 0.29 ± 0.07 m−2 (2.1% of nonpulled treatments), and seedling densities to 0.07 ± 0.06 m−2 (2.6% of nonpulled treatments). After 3 yr, hand pulling reduced seed bank densities to 68 ± 26 m−2 as compared to 524 ± 254 m−2 in nonpulled treatments and 369 ± 66 m−2 in adjacent untreated areas of the study site. Without hand pulling, effects of mowing or mowing plus glyphosate were short-lived and allowed knapweed to rapidly resurge. In comparison, although a single mowing plus clopyralid treatment maintained significantly reduced densities of knapweed for 4 yr, by 2012 knapweed biomass in the nonpulled clopyralid treatment was approximately 60% of that in the other nonpulled treatments. Burning had minimal impacts on knapweed densities regardless of treatment combination, probably as a result of low fire intensity. Results demonstrated that persistent hand pulling used as a follow-up to single mowing or mowing plus herbicide treatments can be an effective practice for treating isolated spotted knapweed infestations or for removing small numbers of knapweed that survive herbicide applications.
The Arctic is experiencing rapid climate change. This research documents tundra vegetation changes near Atqasuk and Utqiaġvik, Alaska. At each location, 30 plots were sampled annually from 2010 to 2019 using a point frame. For every encounter, we recorded the height and classified it into eight groupings (deciduous shrubs, evergreen shrubs, forbs, graminoids, bryophytes, lichens, litter and standing dead vegetation); for vascular plants we also identified the species. We found an increase in plant stature and cover over time consistent with regional warming. Graminoid cover and height increased at both sites, with a fivefold increase in cover in Atqasuk. At Atqasuk shrub and forb cover and height increased. Species diversity decreased at both sites. Year was generally the strongest predictor of vegetation change suggesting a cumulative change over time; however, soil moisture and soil temperature were also predictors of vegetation change. We anticipate plants in the region will continue to grow taller as the region warms, resulting in greater plant cover, especially graminoids and shrubs. The increase of plant cover and accumulation of litter may impact nonvascular plants negatively. Continued changes in community structure will impact energy balance and carbon cycling and may result in regional and global consequences.
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