Nectria flute canker

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Forest Pathology in New Zealand No. 23 (Second Edition 2009) Nectria flute canker M.A. Dick (Revised by A.J.M Hopkins and M.A. Dick) Causal organism Neonectria fuckeliana (C. Booth) Castlebury & Rossman Fig. 1 Severe canker, or flute, associated with a pruned branch stub on the stem of Pinus radiata Type of injury Stem cankers or flutes range in size from minor depressions to flattened areas of the trunk to deep incisions. Flutes may extend up to several metres in length.

Diagnostic features Depressions or flutes on the stem, particularly associated with branch stubs in the years immediately after pruning (Fig. 1). Flutes are more severe above the pruned whorl than below. Malformed stems which may persist until the end of the rotation. Many diseased trees however appear to recover within the five years after pruning. In mature trees, flute cankers are sometimes still evident and these are often invaded by decay fungi and huhu (Prionoplus reticularis) beetles. Long, narrow bark cracks may also be present and usually indicate the presence of bark encased within the stem. Clusters of small red spherical fruit bodies that form on pruned branch stubs (Fig. 2) and on the cankers (Fig. 3) (fruit bodies do not form on all infected trees). Fig. 2 Fruit bodies of N. fuckeliana formed on a branch stub Fig. 3 Fruit bodies of N. fuckeliana on a stem canker Host Pinus radiata

Distribution Widespread and common in Dunedin, Southland and South Canterbury. Scattered locations in Otago Lakes, Central Otago, and Mid Canterbury (Banks Peninsula) (Fig. 4). Fig. 4 Distribution of N. fuckeliana in December 2009

Disease development Neonectria fuckeliana is a northern hemisphere fungus commonly recorded there as a saprophyte or weak pathogen of species of Picea and Abies. In contrast to the disease in P. radiata in New Zealand, stem cankers on these species are uncommon. Neonectria fuckeliana has been recognised in New Zealand since the 1990s but could have entered the country earlier. Neonectria fuckeliana cankers are generally associated with wounds such as the stubs of pruned branches. Death of the cambium, particularly on the stem above the infection point results in the characteristic depressed cankers which may extend to over a metre in length. Lateral extension is limited and girdling of the stem with consequent crown death is extremely rare. Sapwood colonised and killed by N. fuckeliana becomes a white-grey to pale brown colour (Fig. 5) but the structural integrity of the wood is not affected. Once dead however, the sapwood may be further invaded by other organisms including decay fungi which cause cellular breakdown (Fig. 6). Extensive huhu workings have also been found in the decayed segments of living trees. Typically, even trees that have severe stem cankers retain a healthy green crown, though stem breakage at an infected whorl may occur. Fig. 5 - Sapwood extensively stained by N. fuckeliana Fig. 6 Dead sapwood may be further colonised by decay fungi

Neonectria fuckeliana forms sexual and asexual spores but the sexual spores (ascospores) provide the primary inoculum in nature. Ascospores are produced in red to orange fruiting bodies which form in tight clusters on the branch stubs, around the stub collar and on the bark of cankered parts of the stem. Individual fruit bodies are approximately half a millimetre in diameter and clusters may reach several centimetres in diameter. With age the fruit bodies become a dull beige to dark brown colour, making them difficult to see. Fruit bodies do not begin to appear until at least nine months after initial infection has taken place. Clusters may continue to enlarge for several years as successive layers of new fruit bodies are produced around and on top of the existing group. Fruit bodies are not produced on all infected trees. Ascospores ooze out of the fruit bodies in droplets when adequate moisture is present and are primarily dispersed by water-splash or in wind-borne water droplets. Free water is also necessary for the ascospores to germinate. Germination can occur over a broad range of temperatures, (from 5 to 28 ºC) but at either end of the scale it is very slow or abnormal. The optimum temperature is between 18 and 25 ºC. Tree response to infection is variable. Cankers may continue to extend and elongate for several years after the initial infection has occurred and then persist, resulting in an extremely malformed stem. Many trees appear able to contain the infection. Depressions around the pruned whorl may form for up to a year after pruning, but then over several growing seasons they will occlude, leaving no residual damage. Economic importance Neonectria fuckeliana is currently confined to about 90,000 ha of P. radiata plantations in the southern half of the South Island. Forest companies in the affected region estimate that up to 15% of trees develop stem cankers after pruning. The development of new cankers not associated with silvicultural operations is thought to be rare. Although the actual volume loss of wood per tree may be low, N.fuckeliana affects the most valuable part of the tree and

stems with visible cankers at harvest will generally be culled. The disease is not as economically significant as first feared because on some trees cankers become occluded with time and consequently older stems may show no signs of the earlier infection. Studies of mature trees with Nectria flute canker defects identified three main external defect types: stem flattening, flute cankers and bark cracks. Results showed a clear relationship between the visible infection class and value recovery with stained and symptomatic wood usually associated with flute cankers and bark cracks only. An average loss in pruned log index (PLI) of 1.9 units was found across logs exhibiting defects from nectria flute canker. For logs with bark cracks, the average loss in PLI was 1.5 units, while for those exhibiting fluting, the average loss in PLI was a significant 2.9 units. Management and control Trials established to determine the effect of silviculture, stub treatment and environment on disease development showed that stubs less than 60 mm diameter were rarely associated with persistent fluting. Subsequent changes in operational silviculture have shown that managing for smaller pruned branch stub sizes appears to be the overwhelming key to control. Trial results also indicated that there is more infection after pruning in winter than in summer. The reason for this result is not yet clear but avoiding winter pruning should ensure that disease levels are reduced. A number of methods of exploiting this knowledge have been examined. These include pruning earlier, and more frequently, while branch diameter is small, and increasing stocking to limit branch growth. Currently flute canker levels appear to be markedly reduced by altering pruning regimes to take account of this information. There is preliminary evidence from field trials that some P. radiata genotypes do not develop severe flute canker disease. The identification of parents that may provide full or partial resistance is in the early stages but it is hoped that genotype selection will be a tool for the management of nectria flute canker in the future.

BIBLIOGRAPHY Dick, M A; Crane, P E; 2009. Neonectria fuckeliana is pathogenic to Pinus radiata in New Zealand. Australasian Plant Disease Notes 4(1): 12-14 (2009). http://www.publish.csiro.au/view/journals/dsp_journal_fulltext.cfm?nid=208&f= DN09005 Gadgil, P.D. 2005: Fungi on trees and shrubs in New Zealand. Fungi of New Zealand Volume 4. Fungal Diversity Research Series 16: 1-437 Ridley, G.S.; Dick, M.A. 2001: An introduction to the diseases of forest and amenity trees in New Zealand. Forest Research Bulletin 220. New Zealand Forest Research Institute, Rotorua.