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Research ArticleArticles

Crown Density and its Correlation to Girdling Root Syndrome

Robert P. d’Ambrosio
Arboriculture & Urban Forestry (AUF) June 1990, 16 (6) 153-157; DOI: https://doi.org/10.48044/joa.1990.16.6.153
Robert P. d’Ambrosio
Landscape Consultant, Ambrose Laboratories Ltd., 235 Main St., Eastchester, NY 10707
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Abstract

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In 1983, 832 roadside trees, 690 Norway maples (Acer platanoìdes) and 142 sugar maples (A. saccharum) approximately 30 years old were surveyed in Eastchester and New Rochelle, N.Y. using 42 different entries per tree. Forty eight percent of these trees (400) did not exhibit any of the presently believed causes of girdling root syndrome (GRS), namely; planted too deeply or on raised grades, container grown or in restricted growing spaces. These trees were classified as atypical and divided into two groups; atypical with GRS 86% (343) trees and atypical without GRS 14% (57 trees). The 57 trees that had no GRS had four times the number of old wound-closure scars on their trunks and higher crowns. The results of this study suggest that early and periodical pruning of lower branches should be considered as a cultural control of GRS.

The normal pattern of tree roots is to grow horizontal to the ground surface and radially away from the trunk (5). The main framework of a tree’s root system is known as its lateral roots. Roots at their early stages of growth, grow down prior to growing radially and horizontally away from their trunk. The pattern of girdling roots (GR), however, is to grow tangent to the trunk, and in many cases, upwardly, prior to their radial and lateral growth. This condition has been termed girdling root syndrome (GRS) by the author. There are two types of girdling roots; those which occur below the root collar (Fig. 1) and those which occur at or above the root collar (Fig. 2) with the latter being the most serious. It is the tangential aspect of this abnormal root growth that causes physiological stress on the expanding tissues of the trunk that can cause partial or complete death of a tree (3, 6,9). When the expanding trunk is restricted by a girdling root it often causes sarcody (Figs. 2&3), an abnormal swelling of the trunk (7). Surgical removal of a girdling root (Fig. 4), prior to irreparable stem damage, will allow a tree to return to a normal healthy condition (Figs. 5&6).

Fig. 1.
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Fig. 1.

GRS below the root collar of an atypical European beech.

Fig. 2.
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Fig. 2.

GRS above the root collar of a Norway maple whose grade was raised by 15” approximately 15 years ago.

Fig. 3.
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Fig. 3.

Same tree as Fig. 2 after the girdling roots were removed to the depth of the original grade. Note the restricted stem and dying bark tissue. This tree died 5 years after surgery.

Fig. 4.
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Fig. 4.

Typical growth behavior of a girdling root of a sugar maple that was planted a little too deep. This tree responded favorably after the root was removed.

Fig. 5.
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Fig. 5.

Sugar maple exhibiting symptoms of a girdling root on its north side.

Fig. 6.
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Fig. 6.

Same tree as Fig. 5 ten years after girdling root was removed.

Bark tissue that has been restricted by girdling roots can be 1/30 the thickness of normal, unaffected bark (3). Some of the symptoms of girdling root syndrome are premature fall leaf color and/or premature leaf drop in part or whole, reduced leaf size, leaf scorch in part or whole, upper crown dieback, heavy seed production, lack of root buttress flare in part or whole, swelling of the trunk, patches of dying bark, reduced twig growth in part or whole and oozing areas on the trunk (6, 9).

Girdling roots have become more apparent in recent decades. One of the earliest records of girdling roots was reported in 1937 by Van Wormer (10). Girdling roots are found more often on plantation, nursery, park and lawn trees than on forest trees. Even self-seeded, open grown trees are more susceptible than forest trees. Transplanted maples, especially Norway maples, seem most prone to the problem. The history of GRS is unclear. We do not know if GRS has always been as serious a problem as it is today. Presently, there are three believed causes of GRS: 1) trees planted too deeply or on raised grade, 2) trees initially grown in containers, and 3) trees growing in very restricted growing spaces. These causes are considered typical. There are trees with GRS that did not originate from these 3 causes. These trees in this paper are called atypical and they became the target of this research.

Methods

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In 1983, 832 roadside maples (690 Norway maples and 142 sugar maples) of approximately 30 years of age were surveyed in both the Huntley Farms area of Eastchester, N.Y. and the Wilmot Woods area of New Rochelle, N.Y. (Table 1). Both of these areas were post World War II housing developments.

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Table 1. Girdling root survey, 1983 Huntley Farms, Eastchester, N.Y. Wilmot Woods. New Rochelle, N.Y.

Each tree was examined and the following data were collected: location (street address); species: girdling roots (yes or no); branch pattern (adaxial, abaxial or deliquescent); visual root buttress (yes or no); grade level (on or recessed); crown density (1, 2 or 3—3 being very dense); root restriction (0, 25, 50, 75 or 100%); nearest tree/feet (N, S, E, or W); height of trunk bifurcation (feet); sunlight on root flare (0, 25, 50, 75 or 100%); recent pruning scars (1—insignificant amount, 2—some, and 3—many and/or large); old pruning scars (1, 2 or 3—as above); planted too deeply (yes or no); percentage of root flare girdled; DBH; erosion (yes or no); crown height (low or high); and remarks.

Results and Discussion

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There was no significant difference in the occurrence of GRS between Norway maples and sugar maples (Table 1). Restricted growing spaces were not associated with GRS. All of the typical GRS trees were associated with raised grades or were planted too deeply. Many of these trees had restricted growing spaces. Approximately 52% of the 832 trees had girdling roots of typical origin. Of the 400 atypical trees, 343 had girdling roots and 57 trees did not (Table 2).

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Table 2. Results of girdling root survey.

There appeared to be differences (not statistically determined) between the two latter groups of atypical trees in crown height, trunk height, and branching pattern. All of these characteristics could be related to the presence of old pruning wounds on the lower portion of the trunk. The early removal of lower branches allowed sunlight and wind movement to dry the soil surface area at the base of the tree trunk. The data on percent sunlight on the basal portion of the trees were extrapolated and related to GRS in (Fig. 7). They lead to the conclusion that atypical GRS was highest where soil conditions at the base of the tree remained cool and moist. Such conditions would favor the development of surface roots.

Fig. 7.
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Fig. 7.

Percentages of atypical maples expected to exhibit GRS under various levels of shading of their root collar zones. Estimated accuracy ±10%.

One other aspect of water or moisture concentration at the base of trees has seldom been considered. If we think of the tree trunk as a river and the branches as tributaries, it is obvious that during rainstorms there may be far more water running down the trunk than ever reaches the soil under the tree canopy 10 feet from the trunk. These “water trails” (Fig. 8) serve to keep the tree base cooler, moister, etc.

Fig. 8.
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Fig. 8.

The eroded soil was caused by a water trail which cascaded from a height of 15 feet. Note the girdling roots and their association with the water trail.

The hypothesis on the causal conditions of atypical girdling root syndrome deduced from this study needs further verification and experimentation, but, at the moment, appears to be worthy of consideration.

Acknowledgments

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The author wishes to thank Penny Fineburg for her assistance in collecting field data and data extrapolations, along with Dr. John Skelly, Penn State University, for his enlightenment on the subject of water trails.

Footnotes

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  • ↵1. Presented at the annual conference of the International Society of Arboriculture in San Antonio, Texas in August of 1986.

  • © 1990, International Society of Arboriculture. All rights reserved.

Literature Cited

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  1. 1.
    1. Hartig, R.
    1894. Textbook Of Diseased Trees. MacMillan & Co.
  2. 2.
    1. Holmes, Francis W.
    1984. Effects on maples of prolonged exposure by artifical girdling roots. J. Arboric. 10:40–44.
    OpenUrl
  3. 3.↵
    1. Hudler, G.W. and
    2. M.A. Beale
    . 1981. Anatomical features of girdling root injury. J. Arboric. 7:29–32.
    OpenUrl
  4. 4.
    1. Lyer, J.G.,
    2. R.B. Corey and
    3. S.A. Wilde
    1980. Mycohhrizae; facts and fallacies. J. Arboric. 6:215–220.
    OpenUrl
  5. 5.↵
    1. Perry, Thomas O
    . 1982. The ecology of tree roots and the practical significance thereof. J. Arboric. 8:197–211.
    OpenUrl
  6. 6.↵
    1. Pirone, P.P.
    1978. Tree Maintenance, pp. 219–222. Ed. 5. Oxford Univ. Press, N.Y.
  7. 7.↵
    1. Shaw, Kenneth
    . 1977. Girdling Roots. Arnoldia. 37:242–247.
    OpenUrl
  8. 8.
    1. Tate, Robert L
    . 1981. Characteristics of girdling roots on urban Norway maples. J. Arboric. 7:268–270.
    OpenUrl
  9. 9.↵
    1. Tattar, Terry A.
    1978. Diseases of Shade Trees, pp. 233–235. Academic Press, New York, San Francisco and London.
  10. 10.↵
    1. Van Wormer, H.M.
    1937. 13th Proceeding of the National Shade Tree Conference.
  11. 11.
    1. Wargo, Philip M.
    1983. Effects and consequences of stress on root physiology. J. Arboric. 9:173–176.
    OpenUrl
  12. 12.
    1. Zimmerman, M.H. and
    2. Brown, C.L.
    1971. Trees Structure and Form. Springer-Verlag, N.Y.
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Arboriculture & Urban Forestry (AUF)
Vol. 16, Issue 6
June 1990
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Crown Density and its Correlation to Girdling Root Syndrome
Robert P. d’Ambrosio
Arboriculture & Urban Forestry (AUF) Jun 1990, 16 (6) 153-157; DOI: 10.48044/joa.1990.16.6.153

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Crown Density and its Correlation to Girdling Root Syndrome
Robert P. d’Ambrosio
Arboriculture & Urban Forestry (AUF) Jun 1990, 16 (6) 153-157; DOI: 10.48044/joa.1990.16.6.153
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