Embracing Unpredictability in Prairie Management

Much of what determines the outcome of prairie management treatments is out of our control.  Sure, we can decide when to burn a prairie or set the timing and stocking rate for grazing treatments, but cascades of interactions between countless factors such as weather, insect population cycles, and many others can easily overwhelm any decisions we make.  Over the holiday season, I found time to analyze some plant community data for one of our Platte River Prairies.  The results provide a thought-provoking look at the unpredictable ways prairies respond to management.

Cattle

The results of grazing treatments are always a little unpredictable because while they tend to follow certain patterns, cattle can still make their own decisions about what to graze and what not to.  However, variability in management results goes much beyond just the way cattle choose to act in a certain year.  Burning, haying, and other management treatments can also have very different results from year to year.  High-diversity restored prairie – The Nature Conservancy’s Platte River Prairies, Nebraska.

The following data are from a prairie that was managed with variant of patch-burn grazing, in which a different portion of the prairie was burned each year (in the spring) and cattle had access to both burned and unburned portions of the prairie during most of the growing season.  As typically happens, cattle grazed the most recently burned patch pretty heavily and lightly grazed the remainder of the pasture.  Details about the fire and grazing treatments can be found at the end of this post.

If you look at the two graphs below, you can see that there was a significant increase in the average number of plant species (species richness) per square meter between 2012 and 2013 in the portion of prairie that was burned in 2012.  There was no significant change in species density in the unburned areas of the prairie – which were also grazed, but much less intensively.  Data were collected during June in both years.

Two graphs

Two graphs showing the average number (Mean N) of plant species per square meter in one of our Platte River Prairies.  The left graph shows an increase from about 9 spp/m to 11 spp/m in a patch of prairie burned in 2012, and the right graph shows data from the remainder of the prairie, which was not burned in either 2012 or 2013 and had about the same species richness/meter in both years.  The entire site was grazed in both years, with the 2012 burned patch getting much more intensive grazing than the unburned areas.  The error bars show 95% confidence intervals.

We see this pattern of higher species richness after fire/grazing treatments over and over in our prairies.  My explanation of the phenomenon is two-fold, and was covered in more detail in a previous post.  First, the burn exposes soil (and seeds) to light, allowing relatively high germination rates of seeds waiting for an opportunity.  Second, the concentrated heavy grazing in those burned areas weakens the dominant grasses, prolonging the light exposure of the soil/seeds and also reducing the root masses of those grazed grasses, thereby opening up space belowground for new plants to gain a foothold.  Those new plants start both from seed germination and from the rhizomes and buds of existing perennial plants.

The color-coded table below shows some species-level data from the same site that help explain the above graphs.  The numbers indicate the frequency of occurrence (the percentage of sample plots each species was found in) each year.  Some plant species appear to have responded positively or negatively to the burn and subsequent grazing intensity, while others seem unaffected by those management treatments.

Table 1

Plant species frequency (% of occurrence within sample plots) between 2012 and 2013 in a portion of the prairie that was burned in 2012 and the remainder of the prairie that was not burned.  The entire prairie was exposed to livestock grazing in both years.  An * indicates species with particularly high abundance, for which frequency is shown at the 1/10 m scale.  The remainder of the data are from 1  m square plots.

So far, so easy.  Fire and grazing are having positive effects on the vigor and occurrence of some species, negative effects on others, and no effect on still others.  Cumulatively, the effects add up to an increase in the number of plant species per square meter in the year following the burn.  Simple and clean.  The next two graphs (below) seem to fit the same pattern, showing similar increases in small-scale species richness in burned patches back in 2007 and 2008, respectively.

Two other graphs

Two more graphs, showing results from burned patches from 2007 and 2008, respectively, and an increase in the number of plant species per square meter in the year following each burn.  Again, cattle grazing was much more intensive in these burned patches than in the unburned remainder of the prairie each year.  Error bars indicate 95% confidence intervals.

Here’s where it gets interesting…  The next table (below) shows how individual plant species responded within the three burn patches (2007, 2008, and 2012) between the year of the burn and the subsequent year.  Of the 29 most abundant species, only THREE showed the same response to fire/grazing in each of the three years, and another two were consistent in that they didn’t appear to respond at all to management in any of the three years.  The remaining 24 species were inconsistent in their responses – some wildly so.  Look, for example at indiangrass (Sorghastrum nutans), rough dropseed – aka tall dropseed – (Sporobolus compositus), and blue prairie violet (Viola pratincola, aka Viola sororia).  Each of those three species showed a strong increase in frequency of occurrence in the burn patch one year, but a strong decrease in another.

Table 2

Plant species frequency (% of occurrence within sample plots) between the year of burn and the subsequent year in prairie patches burned in 2007, 2008, and 2012.  The entire prairie was grazed in each of the years, with higher grazing intensity in the more recently burned patches.  An * indicates species for which the frequency is shown at the 1/10 m scale – the remainder of the data are from 1 m square plots.

So what are we to make of all this?  How can we manage prairies effectively if the impacts of very similar management treatments are so different from year to year?

As far as the first question, it’s clear that other variables – particularly weather – interact strongly with management treatments to influence the response of plant species.  Every species has a different optimum range of temperature and moisture conditions, so the timing and intensity of rains and warm/cool spells affects the competitive balance between species differently each season.  Many other factors and interactions are also in play.  Year-to-year changes in population size of various seed-eating species can influence the seed bank, for example. In addition, the success of a particular plant species in one year catalyzes or suppresses other species (plant, insect, mammal, etc.) in the following year.  All of those interactions are signs of healthy prairies, but make it very difficult to predict how those prairies will respond to our management.

As to the question of how we’re supposed to manage prairies in light of all this variability, there are at least two ways to respond.  The first is to throw our hands up in disgust because we can’t seem to predict results well enough to make useful decisions.  The second option is to relax, embrace the variability, and roll with it.

prairies

Healthy prairies have a great diversity of plant and animal species, but also a great diversity of responses to year-to-year stresses imposed by both managers and the environment.  Tallgrass prairie in Richardson County, Nebraska.

Our human nature makes us want (need?) control over our environment.  In agriculture, landscape architecture, engineering and many other fields, the objective is to manipulate the world to our benefit – often by reducing the variables and controlling the remaining ones.  However, when managing ecosystems in order to conserve the diversity of species and their functional roles, that approach simply doesn’t fit.  Instead,we need to think differently about both short-term objectives and long-term goals.

To help me deal with unpredictability, I tend to consider prairie management objectives in terms of ecological resilience, rather than in terms of desired responses from particular species.  (See this earlier post on ecological resilience for background.)  I think of a prairie as a ball in a bowl.  The bowl represents a range of conditions, within which the prairie (the ball) maintains its integrity as a prairie – even if it rolls around quite a bit.  Some disturbances, such as plowing or broadcast herbicide can quickly push a prairie out of its bowl and into another state, from which it is tremendously difficult to recover.  Other disturbances, such as drought, tree encroachment, or intensive grazing may push the ball toward the edge, but as long as those disturbances don’t continue for too many years in a row, the ball doesn’t leave the bowl.

My management objective is not to prevent the metaphorical ball from moving, or to push it toward some optimal part of the bowl.  Rather, I have two big objectives:

1.)   Make sure the ball can move freely around the bowl in response to disturbances, but nudge it back from the edge when necessary.  I celebrate the fact that our Platte River Prairies change in appearance from year to year.  That tells me they are rolling around that bowl as they need to do.  In order to prevent an exit from the bowl, I make sure that we’re suppressing tree encroachment before a prairie becomes a woodland, and that we’re avoiding the kind of chronic intensive grazing that can push some prairie species to local extinction.  During extended droughts, we modify our management to avoid imposing too much additional stress on prairie communities.

2.)  Keep the bowl as large as possible by maintaining a high diversity of prairie species, along with the functional roles each contributes.  That diversity of function allows the prairie to absorb stress and respond to adversity without leaving the bowl.  Maintaining that diversity means manipulating the field of competition between prairie species so that every species can win now and then (by reproducing) and maintain itself within the community.  We create an annual patchwork of various fire, grazing and rest treatments and shift the location of those patches from year to year to provide for the needs of as many plant and animal species as possible.

Prairies are dynamic, and thank goodness for that.  Their ability to flex and respond to various stresses is a key characteristic that has allowed them to survive for thousands of years.  As prairie managers, we need to facilitate that flexibility instead of becoming frustrated with our inability to predict how prairies will respond to our management.  After all, our job is to keep prairies healthy, not turn them into something they’re not just to help ourselves feel more in control.

Management Details

For those of you who might be interested, here is some additional information about the management treatments applied to the prairie in the above example.  The pasture the burns were conducted in is often grazed in conjunction with adjacent prairies, so the total grazed area varies in size from year to year.  In each year, the overall management was patch-burn grazing, in which cattle had access to the entire grazing area, but did most of their grazing in the most recently burned patch.  The stocking rate shown (AUMs/ac) is calculated for the entire pasture and entire season.

2007 Burn (North 1/2 burned on Apr 16, South 1/2 on May 2)

240 acres grazed overall in 2007.  27 pairs from 4/1 – 10/31 (Approx. 1 AUMs/ac)

 

2008 Burn  (Burned on March 18)

171 acres grazed overall in 2008.  27 pairs from 4/1-5/20, 15 pairs till 9/15 (Approx. 0.7 AUMs/ac)

 

2012 Burn (Burned on March 30)

300 acres grazed overall in 2012.  75 pairs 4/20-Jun 1, 50 pairs till 10/1  (Approx. 1.3 AUMs/ac)

Looking for Ecological Impacts? Urine Luck!

I came across a copy of one of my all-time favorite research articles the other day.  The paper tells a great story about the kinds of complex interactions that occur between the biotic and abiotic components of an ecosystem, including feedback loops and ecological hierarchies.  But more importantly, it’s a story about a guy who dumps bison urine on the prairie to see what happens.

The research paper, written by Ernie Steinauer and Scott Collins was actually a report from the second of two projects they conducted on bison urine impacts at the Konza Prairie Biological Station in Kansas.  Both projects were interesting, but I like the second one best because it focused on how bison urine can affect the prairie community at multiple scales.

Bison and cattle urine creates patches of high nitrogen concentration in the soil.  You can identify those patches in a pasture because they look like dinner plate-sized areas of extra dark green grass that, if left ungrazed, are taller than the surrounding vegetation.  Previous studies had shown that livestock urine increased the aboveground production of plants and altered plant species composition.  Other researchers had also found that herbivores preferentially graze urine-treated areas because of increased plant production and higher N concentration in leaves.  Steinauer and Collins fully expected to see the same patterns, but they also wanted to see whether or not those urine patches acted as initiation points for grazing lawns.

If you were to walk around a pasture being grazed at a moderate stocking rate, you’d see patches of uniformly short vegetation (often bathtub to bathroom-sized or so) surrounded by a matrix of somewhat taller vegetation.  Those short-cropped areas are called “grazing lawns”, and often consist of a single species of grass such as smooth brome (Bromus inermis) or big bluestem (Andropogon gerardii) that is particularly favored by grazers.  Grazing lawns are a result of livestock repeatedly feeding from the same plants all season long while ignoring others.  They do this because the regrowth from plants that have already been grazed tends to be more nutritious than more mature leaves of plants that haven’t. 

In their study, Steinauer and Collins wanted to see whether small deposits of bison urine would stimulate much larger grazing lawns around them.  If so, a small fertilization event by a bison would actually lead to a much larger disturbance to the prairie community.  In order to test their idea, they first needed some bison urine.  (How would you like to be handed that task?)  Fortunately, the great wealth of scientific literature includes a publication from 1978 that has a recipe for simulated bison urine.  Don’t you love science?  Steinauer and Collins helpfully reprinted the recipe in their research paper so the rest of us could join in the fun.

 (“…Excuse me, I’d like to buy a big batch of urea so I can mix me up some artificial bison urine.  Yes, I can wait a moment.  Oh, hello officer, where’d you come from?  You’d like me to step that way?  Sure.  Hey! Where are we going??”)

I’ve included links to both bison urine research papers by Steinauer and Collins at the bottom of this post, but in summary, they confirmed that bison preferentially grazed patches treated with urine (65% of urine-treated plots were grazed, compared to only 18% of untreated plots).  However, the bigger story is that those urine patches also acted as initiation points for larger grazing lawns.  In fact, many fewer untreated plots would have been grazed if they hadn’t been enveloped by grazing lawns that started in nearby treated plots.

What do we learn from this?  We learn that when a bison (or cow) decides to relieve itself in a particular place, it’s very likely starting a cascade of impacts…

  1. Urine fertilization increases the growth rate and nitrogen content of the plants in a small area.
  2. Those particularly nutritious plants attract a hungry bison, which after devouring the vegetation in that little spot, keeps its head down and eats a lot more of the same plants in the vicinity.
  3. The competitive balance between the plant species within the grazing lawn temporarily changes as grazed grasses lose root mass, opening up space for other plants that couldn’t otherwise compete with them.
  4. Grazing lawns improves habitat for a number of wildlife species, including insects and reptiles, that depend upon the availability of open sunny areas adjacent to taller shady vegetation.

A cow selflessly initiates a cascade of ecological processes in a prairie. This one happens to be within the burned patch of one of our patch-burn grazed prairies - thus, the uniformly short vegetation.

While Steinauer and Collins studied changes in plant composition within their urine patches, they only followed those plants for a single season, and found some conflicting results between their two studies.  Some of those may have come from the fact that their two studies took place on somewhat different soil types.  However, my own grazing research has shown that many of the effects of grazing are most evident in the year following the grazing event, after colonizing plants have had time to move into areas left open by weakened grasses.  It would have been very interesting to have followed the urine patches through several seasons to see how plant composition changed over that time period.

I’ve never met Ernie Steinauer but I bet I’d like him.  I say this because in addition to being crazy enough to mix up and dump bison urine on the prairie just to see what happened, Ernie also kept track of other interesting things that happened within his urine-treated patches.  One thing he noticed was that insect herbivory – especially on switchgrass (Panicum virgatum) – seemed to be influenced by urine treatments as well.  Now there’s the beginning to a great follow up project for someone!  After you try it, let me know what you find.

Here are the links to the two articles.

1995 article

2001 article