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Woodland NOTES - Vol. 15, No. 1 - Fall/Winter, 2003-2004

In this issue:


 

 

 

 

 


Woodland NOTES Celebrates 15th Year in Production

Woodland NOTES, which began as a one-page mimeographed handout, is now an award winning peer-reviewed publication enjoyed by over 10,000 readers per issue. Over the years we have written about all aspects of forestry and forest management, stewardship, wildlife, soils, and water. We have given you information on how and when to plant a tree, fertilize, thin, prune, or burn your forest, keep fish or birds alive over the winter, measure a log, control weeds, wildlife, and water quality, sell your forest products, and identify, prevent, and control insect and disease problems. And we still haven’t told it all!

This year we will continue to address a wide variety of topics, from fire to fungi. We thank you for readership and hope you continue to enjoy Woodland NOTES for another 15 years!


Mycorrhizae – the friendly forest fungi
Chris Schnepf

Many forest owners do not immediately see fungi as a beneficial organism. If you have seen patches of fir dying cancerously from root disease or learned about the profound effect white pine blister rust has had on north Idaho’s forest ecology, it may be easy to forget that the majority of forest fungi do not kill trees.

You probably know that microbes inhabit your stomach and other parts of your body, performing beneficial roles (e.g., helping you to digest food). Most of us could not name any of these if asked. There are also a whole host of relatively unknown microbes and fungi that help trees by recycling forest nutrients, decomposing slash, and improving soil, to list a few of their positive functions. Some suggest that even tree-killing fungi (the native ones, at least) perform a positive role by taking out trees that are poorly adapted to a forest site.

One of the groups of fungi that most directly benefit tree growth is called mycorrhizal fungi. Mycorrhiza is translated from Latin as "fungus root". These fungi enter the roots of trees and other plants and form a symbiotic relationship (a relationship in which both the host and the fungi benefit). Mycorrhizal fungi get carbon (the product of photosynthesis) from trees and the trees get a larger effective absorbing root surface (more nutrients and moisture) from the hyphae (the fungus equivalent to roots) and mycelia (matted hyphae) of mycorrhizal fungi. In addition to rooting capacity, mycorrhizae can also:

  • provide reservoirs for nutrients that might otherwise be leached from the soil;

  • physically block pathogenic fungi access to tree roots;

  • help "unlock" soil nutrients (convert them into forms that can be used by plants);

  • exude or decay into substances that act as "organic glues", helping to aggregate soil particles and improve soil structure;

  • move nutrients and photosynthate (carbon) between trees (they can even move materials between different tree species, where the same fungus is capable of associating with multiple tree and shrub species);

  • exude antibiotic substances that deter root pathogens; and

  • provide food for "fungivores", organisms ranging from ants to deer, that feed on mycelia or fruiting bodies of forest fungi.

Mycorrhizae are essential for good growth on many tree species, particularly on nutrient-poor or droughty sites.

Mycorrhizal fungi form relationships with over 95% of the plants on earth, and there are many, many different species. Over 2,000 fungi have been reported to form mycorrhizal relationships with Douglas-fir alone! Mycorrhizae are separated into two general types. Ectomycorrhizae cover the outside of rootlets, just penetrating the rootlets’ outer cells. Endomycorrhizae do not form a sheath over rootlets. Instead their filaments grow deeper into the rootlets and out into the soil.

 

Ectomycorrhizal fungi are the most common. If you have ever seen plants grown hydroponically, you may have been struck by the many small root hairs. If you dig up seedlings in the forest, you may notice that the roots look a little thicker than those hydroponic roots – that is because they are covered, to some degree, by ectomycorrhizal fungi.

Mycorrhizal fungi produce many different kinds of fruiting bodies. Some are above-ground mushrooms. For example, golden chanterelles (Cantharellus cibarius) are the fruiting body of a mycorrhizal fungus. Other fruiting bodies are underground (e.g., truffles).

There has been a large amount of research on forest fungi that kill trees. There has been much less research on forest mycorrhizal fungi (even less on fungi that decay downed logs, etc). The amorphous nature of forest fungi often makes them difficult to pin down and do precise experimental research in a forest setting. So, with the standard academic caveat of "we need more research", here are a few general principles you can apply on your forest regarding mycorrhizal fungi:

  • There is usually no need to add mycorrhizae to well-established forest sites. Native forests are usually well-stocked with native mycorrhizal species. However, trees planted to non-forested areas such as agricultural fields or dramatically altered sites (e.g., a reclaimed mining area) may very well benefit from mycorrhizal inoculation. Some hardwood nurseries in the eastern U.S. have actually inoculated seedlings with mycorrhizae in anticipation of their being planted in farm fields.

  • Leave more coarse woody debris distributed across the site. Coarse woody debris (wood larger than 3 inches in diameter) helps mycorrhizae because as it decays into the soil it provides better soil moisture for the fungi, particularly during drought periods. Ideally, woody debris from Douglas-fir, pines and larch is best because it decays with ‘brown rots", leaving debris products that last longer than those left by "white rots" which typically decay true firs or hemlock. You don’t have to leave a lot of material — typically 1-2 cull logs left per acre are adequate (to estimate how many tons of coarse woody debris you have, see a previous Woodland Notes article entitled Tons of Slash, available online at www.cnr.uidaho.edu/extforest/Vol14,No1.htm.)

  • Minimize compaction and soil disturbance. Compaction reduces pore space in soils. Pore space provides the air that tree roots need to draw the moisture out of the soil. Many scientists also believe that compaction and excessive soil disturbance impairs the growth of beneficial forest fungi, including mycorrhizal fungi. Soil compaction can be quite variable by the type of soil, time of the year, type of equipment, and care of the operator using the equipment. Operating on snow or when soils are dry and limiting equipment to designated trails will help minimize soil compaction. For more information, see an Oregon State University Extension publication titled Soil compaction on woodland properties (OSU EC 1109).

  • Mycorrhizal fungi play a fascinating role in our forests. If you would like to learn more about these fungi and research being conducted on them, check the web site of the USFS mycological research team at http://www.fs.fed.us/pnw/mycology. In addition to useful links to ongoing research on mycorrhizal fungi, the web site also includes photos of mycorrhizal fungi and their fruiting bodies, publications on mycorrhizal fungi, and links to other sites on these fungi.


    Do I still believe in landscaping for fire prevention?
    Ron Mahoney

    On July 30, 2003, our Moscow Mountain home, shop, and 5-acre forest property burned to the ground in a human-caused wildfire that covered 200 acres and consumed 4 other homes. It was 98 degrees that day, with about 5% humidity and a 10 mph wind when the fire started. We had done many of the things we advise in our popular publication Landscaping for Fire Prevention. We had a large area of gravel and grass around the home, a circular turnaround that could accommodate large trucks and fire engines, and had thinned and maintained most of our timbered 5-acres. Since the fire, I have been asked many times if I still believed in these practices. My answer is an absolute YES. Here is why.

    It gave us a chance. Initially, the fire approached our property burning into the wind. We were able to stop and hold it at the line along the lawn and gravel areas, using only a garden hose. Likely, the fire would have stopped on its own at those boundaries, as there was no additional fuel for over 100 feet and the light winds were blowing the heat back into the fire. At this point, a rural fire truck was also on site and the driver told me he would come back because he had adequate space to turn around quickly and escape if necessary.

    It helped slow down the fire and gave firefighters and our neighbors a chance to save other homes and properties. When the fire stopped at the edge of our defensible space, we thought we were safe. Then, just as the fire truck ran out of water, we heard a roar. The fire had jumped the road below us, and now came charging up the slope, this time with the wind. Trees, including some large pines pruned up to 30 feet, were exploding into flame eighty feet or so in front of the rapidly advancing fire. The heat was so intense that the fire ignited our buildings without any flame reaching them first. As this happened, I could see the fire-retardant tanker planes and helicopters suspending large bags of water approaching on the horizon. We were defensible, but the conditions that day didn’t give the defenders enough time to save our home. However, our open spaces, thinned and pruned trees, and ability to halt the fire on its initial front, may have helped save our neighbor’s home. I also believe that it gave the superb group of firefighters the small edge they needed to stop the fire at only 200 acres. We all feared it would consume all of Moscow Mountain and perhaps thousands of additional acres east of our area.

    Under less severe conditions, I believe the fire hazard reduction measures we took would have saved our home. Under the conditions that day, the potential fire damage was only thwarted by the well-trained and equipped firefighters from local and state agencies, private forest industry, and logging companies that responded with incredible courage and skill.


    Wildfire and Wildlife: Living in Fire-Based Ecosystems
    Yvonne Barkley

    Many people believe that all wildlife flee before the flames of a fire like the animated characters in the movie Bambi. Contrary to this belief, during the 1988 burns around Yellowstone Park, animal behavioral scientists didn’t observe large animals fleeing the fire; to the contrary, most seemed completely indifferent even to crowning fires. Bison, elk, and other ungulates grazed and rested within sight of flames, often 100 yards or less from burning trees. Smaller mammals and most birds that left their habitat while it was burning returned within hours or days.

    An animals ability to survive a fire depends on their mobility and on the fire’s uniformity, severity, size, and duration. Large animals die most often in very large, active fires with wide flaming fronts, active crown fires, and thick ground smoke. For example, most of the large animals killed in the Yellowstone fires of 1988 died of smoke inhalation. Animals with limited mobility living above ground are most vulnerable to fire-caused injury and mortality. Animals that live in moist habitats, such as amphibians, are least likely to be affected. Season is also important with burning during the nesting season being the most damaging.

    Fire most commonly affects wildlife by modifying the proportions and arrangements of habitats across a landscape. Wildlife habitats are not static, but evolve in response to fire and the subsequent changes in vegetation and structure that follow a fire. Immediately after a fire food and shelter are temporarily lost. Hidden runways and burrow openings become exposed and predation increases.

    Particular successional stages or structures are important to many wildlife species when looking for a place to hide, escape to, or reproduce in. Species will immigrate to new areas when the food and cover they require are not available after a burn. The time it takes for a particular species to return to an area will depend on how much fire altered the habitat structure and food supply. Wildlife populations can shift from species that require cool, moist conditions, such as warblers and wood mice, to species that require warm, dry conditions, such as ground squirrels and quail. Unburned areas adjacent to burned areas create a mosaic, increasing wildlife choices from a range of habitat structures and conditions. Herbivores and species that prefer herbaceous vegetation for cover prefer early successional, grass/forb habitats or broad-leafed seedlings that establish after a burn. Depending on the vegetation type, burning often increases or improves wildlife forage from a few years to as long as 100 years. Sometimes, the nutritional content and digestibility of plants increases for a few years. Dead wildlife becomes food for scavengers, including grizzly and black bears, wolves, coyotes, bald and golden eagles, crows, and ravens, and fire-killed trees become food for millions of insect larvae (and the animals that feed on them) and provide perches for raptors.

    As succession continues, conifers succeed broad-leafed trees, which become snags and add to dead wood accumulating on the ground. Snags and downed logs provide important habitat for cavity nesters, small mammals, and even large mammals like bears. Openings created by downed and dead trees are invaded by shrubs and saplings. When interspersed with dense patches of shrubs and trees in long-unburned areas, openings provide excellent food and cover for deer and elk. By suppressing fire, this mosaic of disturbance-born habitats succeed to forests, and wildlife species dependent on early and mid-successional stages move away.

    Invertebrate populations tend to decrease after a fire because eggs, food supplies, and/or shelter are destroyed. Flying insects are especially vulnerable because they are attracted to fire by heat or smoke and are incinerated in great numbers. Surface insect populations, such as grasshoppers, also tend to decrease. Other insect populations, especially bark beetles and wood borers, increase after a fire, as trees damaged or killed provide large amounts of suitable habitat. Ants also tend to increase after fires and can eat large amounts of seed. Soil dwelling and aquatic invertebrates generally suffer little immediate damage, though indirect and long term effects are less understood or unknown. Earthworms generally live 4-8 inches under the soil surface and are probably protected from the direct effects of heating. Amphibians and reptiles avoid direct effects of fire by either moving away from it or burrowing into the soil.

    Wetlands are less likely to burn, and when they do, are burned less severely than upland sites. Wetlands provide a refuge from fires for many wildlife species and activities such as breeding by aquatic species may be carried out with little interruption. Although fire in wetland areas usually increases open water and stimulates vegetation favored by many aquatic and semiaquatic species, removing adjacent riparian habitat can cause problems. Riparian vegetation shades wetland habitats and vegetative root systems hold the soil and prevent or decrease deposition of sediment into the water. When riparian plants are removed, water temperatures usually increase and dissolved oxygen content decreases, which can increase fish diseases and reduce spawning efficiency. Fine sediment can also clog fish gills, suffocate eggs and aquatic larvae on the bottom of the stream, fill in the spaces between bottom cobbles where fish lay eggs.

    From the elk browsing in the meadows to the trout swimming in the streams, western wildlife has evolved and adapted to living with fire.


    Cultural Methods to Stimulate Conifer Seed Production
    Randy Brooks

    Private forest owners rarely have access to genetically superior tree seedlings. Tree seed for reforestation of private lands is frequently collected with inadequate attention to seed tree quality, particularly if the focus is in getting cones.

    Once a forest owner has identified superior trees based on phenotype (observable characteristics) these trees can be cultured in several different ways to help stimulate seed cone production. Cultural methods are typically practices that will improve tree growth or stimulate flowering and subsequent growth of flowers and fruits/cones. Cultural methods can be very effective for promoting seed cone production, but there are many external and internal factors that can affect results. Some external factors include climate and pests. Internal factors can include seed cone cycles (one good crop every few years) and genetics (how a tree will respond to cultural practices).

    Forest owners can use plant growth regulators, fertilizers, root raking, pruning and/or thinning, irrigation and/or moisture stress, girdling, or some combination of the above methods to improve conifer seed production.

    Plant growth regulators are hormone-like substances that have a chemical-like control over plant growth processes. Gibberellins are naturally occurring hormones that affect cell enlargement and cell division. Gibberellic acid (GA 4/7) has been used successfully to promote flowering and seed production in conifers (specifically larch). Gibberellic acid is mixed in a 95% solution of ethanol (ethyl alcohol) and then injected into the tree when lateral shoot elongation reaches about 70%, but before bud differentiation begins. Trees less than 12 inches DBH receive a 50 cc injection, while trees greater than 12 inches DBH receive a 100 cc injection of the mixture. A hole can be drilled about ¼ inch into the tree and the mixture poured into the hole, or the mixture can be applied with a hypo-hatchet.

    Mineral requirements of reproductive tissues are high. Limited nutrients can effect conifer seed cone production. Nitrogen (N) and phosphorous (P) promotes flowering in conifers. Specifically, N produces vegetative growth while P produces flower buds, fruit, and root development. Potassium (K) helps build strong healthy plants. Fertilizer application timing is critical. It must be applied before initiation of floral buds if immediate increased flowering is to result. For pines that require 2 years for cones to mature, spring application influences flowering in the subsequent year, and cones in the 2nd year. Application rates vary, but the average is about 100 pounds actual N per acre (typically ammonium nitrate), and about 250 pounds P (as P2O5) and 100 pounds per acre K (as K2O).

    Fertilization can keep trees healthy while maximizing growth and vigor. However, it is recommended that a soil test be taken first to assess nutrient levels and perhaps take foliar samples as well to assess tree nutritional status. If adequate nutrient levels exist, the money spent on fertilizers may be wasted. Fertilizer applications in north Idaho can be difficult, depending on terrain and accessibility. If you are only interested in seed production, consider choosing a few phenotypically superior trees and fertilize those trees. Fertilization can have other benefits such as increased tree health, growth, and vigor. When used with a combination of crown release or irrigation, the results are often better than when fertilizers are used alone.

    Traumatic stress often induces heavier flowering and cone production. Increased flowering of woody plants has been stimulated by root raking (or root pruning). This is accomplished by dragging sharp tines through the soil and cutting/severing the roots. This process can be accomplished on one or two sides of the tree, not necessarily all the way around a tree. The drawbacks are that heavy equipment is needed, and terrain may be limiting. Root raking can also kill smaller trees if damage is severe enough. Another drawback is that soil disturbance can lead to other problems such as soil erosion. The Idaho Forest Practices Act says that sediment must be kept out of streams.

    Vigorous, dominant trees produce more seed than intermediate or suppressed trees, and when competition is severe, suppressed trees fail to produce any seed. Residual trees left after thinning generally show increased flower and seed crops. Reasons for the increase are thought to be from more exposure to sunlight and less competition for resources such as moisture and nutrients.

    Suppressed basal branches with only a few leaves/needles often consume more carbohydrates in respiration than they produce in photosynthesis for stem or fruit growth. Research has shown that within a tree crown the vigor of individual branches also influences fruit and cone development. Larger cones containing more seed tend to be produced on branches in the upper one-third of a tree.

    When used in conjunction with each other, thinning and pruning select trees should be a cultural practice that is practical for any landowner looking to produce more seed.

    Girdling involves removing, excising, or cutting a small, thin strip of bark containing the cambium and phloem from the around the stem, branch, limb, or scaffold of a tree. Doing so often stimulates reproductive growth because it impedes the translocation of carbohydrates and growth regulators in the phloem. Phloem transports materials down, while the xylem transports materials upwards. When downward transport of carbohydrates is blocked, they tend to diffuse back into the xylem and are translocated back up to, and concentrate in the leaves and tissues involved in reproduction. Girdling trees in years when cone production is high does not increase overall numbers of cones. Girdling can increase cone production on individually treated branches. However, one must gain access to the upper third of the tree and this is often times difficult to do.

    Girdling can be accomplished with a variety of tools, ranging from chainsaws, pruning saws, handsaws, or knives. Larger saws make it more difficult to control the cut, and care must be exercised in order to avoid cutting into the xylem, which would disrupt the flow of water upward, thus killing the tree. Special girdling knives are available that allow cutting between the bark and the xylem. Smaller wounds heal much faster than larger wounds.

    Girdle the tree at breast height as the needles emerge. Only girdle about 60% around the tree, and on the opposite side as high as the diameter is wide. In other words, you will have two girdles on each side of the tree, one higher than the other, and barely overlapping. Do not girdle around the entire bole or the tree will be killed.

    There are a number of effects of different cultural practices to stimulate conifer reproductive growth. Some measures are more destructive than others, and may be better served on trees that are intended for harvest. A combination of practices may work better than an individual practice. Economics (cost/benefit ratio) must be examined, as well as damage to the tree.

    Applied Forest Tree Improvement, Zobel, Bruce and John Talbert. 1984. John Wiley and Sons, Inc., Publishers. 505 pages. ISBN 0-471-09682-2