Forestry Advance Access originally published online on January 27, 2009
Forestry 2009 82(2):185-198; doi:10.1093/forestry/cpn053
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Seedling height and the impact of harvesting operations on advance regeneration of conifer species in upland Britain
1 Forest Research, Alice Holt Lodge, Wrecclesham, Farnham, Surrey GU10 4LH, England
2 Forest Research, Technical Development, Ae Village, Dumfries DG1 1QB, Scotland
* Corresponding author. E-mail: victoria.stokes{at}forestry.gsi.gov.uk
| Summary |
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Extensive damage to and mortality of understorey seedlings during overstorey thinning could prevent the use of natural regeneration as a method of restocking. Experiments carried out on three upland conifer sites in Britain assessed the short-term impact of thinning operations on survival and damage to advance regeneration seedlings of different heights. At two sites dominated by Sitka spruce, the number of small-sized (<50 cm) and medium-sized (50–200 cm) seedlings lost during harvesting was significantly higher than the number of large seedlings (>200 cm) which tended to be damaged rather than lost. At the Scots pine/Japanese larch site, damage and loss were not related to seedling size. Survival or damage was significantly related to the distance from the nearest extraction rack (striproad). At two of the sites, survival or damage was related to distance to the nearest felled tree stumps. The seedlings in 25–30 per cent of the area were lost due to clearing the extraction racks prior to harvesting. In the stand matrix, 40–80 per cent of the regeneration survived and was not severely damaged; the remaining regeneration was likely to be sufficient to restock at all three sites, although distributions were clumped. There were no marked differences between motor-manual and harvester felling.
| Introduction |
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In some British upland (>250 m above sea level), conifer plantations that have been thinned or felled, extensive natural regeneration has been observed with seedling densities as high as 300 000 ha–1 (Clarke, 1992
Although factors influencing the regeneration and survival of coniferous seedlings in Britain have been studied (e.g. McNeill and Thomson, 1982; Mason and Quine, 1995
; Malcolm et al., 2001
), little work has been done on the effects of felling and extraction of the overstorey on survival of advance regeneration (seedlings and saplings already present on the site). Managers implementing alternative silvicultural systems such as Continuous Cover Forestry (CCF) have expressed concern that damage to regeneration may hinder their attempts at transformation, i.e. the process of increasing within-stand structural diversity in even-aged forests (Mason and Kerr, 2004
).
Vorob et al. (1994)
found that overstorey thinning using harvesters killed 52–56 per cent of coniferous advance regeneration. These concerns are also partially supported by work in other countries using other felling and extraction methods, such as manual or motor-manual felling (Andersson and Fries, 1979
), the Kostroma method (in which trees are felled in a fan pattern onto a lying tree before being de-limbed and skidded root-end first as described by Jeansson and Laestadius, 1981
) and narrow-strip methods (trees are felled with their crowns towards the extraction rack, or striproad, before being skidded top-end first as described by Jeansson and Laestadius, 1981
). Glöde and Sikström (2001)
reported on a method of felling known as tossing the caber in which trees are felled top-end first into an extraction rack with the lower end then lifted over the regeneration. Tesch et al. (1986)
and Youngblood (1990)
reported the effects of skyline logging and of ground skidding and cable yarding, respectively, on regeneration. However, with all of these, overstorey thinning and particularly final overstorey removal has been found to kill or damage a large proportion of coniferous advance regeneration, e.g. 48–54 per cent (Westerberg and Berg, 1994
), 38–65 per cent (Sikström and Glöde, 2000
) and 17–76 per cent (Granhus and Fjeld, 2001
). Work in the US has shown that overstorey thinning caused up to 83 per cent mortality in under-planted red oak (Quercus rubra L.) seedlings but that the thinning intensity had no significant effect on mortality (Olson et al., 2003
). Coniferous seedlings planted under Douglas-fir (Pseudotsuga menziesii (Mirbel) Franco) before thinning of the overstorey to different densities also showed severe harvesting damage (Newton and Cole, 2006
). Overall 40 per cent of the seedlings were damaged with up to 30 per cent being removed or buried under debris. A further 16 per cent had significant damage, such as broken or dead tops or severe lean, and 2 years after the thinning, these damaged seedlings had grown 10 cm less than undamaged seedlings (Newton and Cole, 2006
). Conversely, Douglas-fir seedlings and saplings were found to recover from most types of harvesting damage within 6 years (Tesch et al., 1993
) although taller trees at the time of thinning showed the poorest recovery.
It may be possible to minimize harvesting damage to regeneration by carrying out operations when seedlings are at their most resilient size. However, reviewing the published literature relating harvesting damage to seedling and sapling height does not reveal a clear relationship between the two. Table 1 summarizes the results of nine papers reporting on different conifer species and harvesting methods from which we have drawn tentative optimum harvesting heights. In some situations, smaller seedlings were more resilient to harvesting damage (e.g. Andersson and Fries, 1979
, Preuhsler and Jakobi, 1996
, Eliasson et al., 2003
), while in others, larger seedlings and saplings survived better (e.g. Gordon, 1973
, Tesch et al., 1993
). These differences may be partly due to the species being studied and the site conditions and partly due to the harvesting and extraction methods used. Granhus and Fjeld (2001)
reported that harvesting using a harvester and forwarder caused more injury to taller Norway spruce (Picea abies L.) H. Karst.) saplings while motor-manual felling and skidding with a farm tractor tended to damage smaller saplings, demonstrating the importance of the methods used. They hypothesized that this was due to a tendency to fell trees towards areas of shorter regeneration when using motor-manual felling, compared with harvester felling in which directional felling is less often practised. In Sweden, where the shelterwood system is commonly used to regenerate Norway spruce (Westerberg, 1995
), tall saplings have been found to suffer more damage than short saplings and damage can be reduced by manually felling trees away from densely regenerating areas (Eliasson et al., 2003
).
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The lack of information on the impact of harvesting on differently sized regeneration in British conditions has lead to an understandable reluctance on the part of forest managers to intervene. There is no clear guidance on whether smaller seedlings, with their lower chance of being hit, or taller seedlings, with larger inflexible stems, are more at risk. Recent work (S.E. Hale and G. Kerr, unpublished data) has shown that there is also very little guidance on acceptable stocking densities for coniferous natural regeneration. The target density for British restock or new planting sites is 2500 plants per hectare 5 years after planting (Anonymous, 2004
Work is needed to determine how and when to plan interventions in order to minimize damage and to establish whether the remaining regeneration is likely to be sufficient to restock the site. In this study, we examined the hypotheses that:
- 1 Smaller seedlings would be more likely to survive harvesting operations than taller seedlings.
- 2 Taller seedlings would be more likely to be severely damaged by overstorey harvesting than smaller seedlings.
- 2 Taller seedlings would be more likely to be severely damaged by overstorey harvesting than smaller seedlings.
| Methods and materials |
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The experiment was carried out on three sites with similar management objectives, all situated within CCF pilot sites established by the Forestry Commission (McIntosh, 2000
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Stand parameters Basal Area (BA) per hectare and top height) were assessed using standard procedures as described by Matthews and Mackie (2006)
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All sites were being managed as a simple system, i.e. one in which there will be one or two canopy layers, and thinning was carried out according to Mason and Kerr (2004)
At Fernworthy, previously used extraction racks were still apparent. These were designated as permanent racks and cleared with chainsaws prior to harvesting. Where there was no previous rack and access was required, the areas with the lowest regeneration density were used. The spacing between racks was
20 m, although there were some areas where the spacing increased to 30 m. Due to the large tree size, trees were felled with chainsaws using feller selection, i.e. trees were not marked and operators selected trees according to a felling prescription as they worked. Trees were felled towards the racks and then the first one or two timber lengths were cut before processing the remainder of the stem with a CAT-318 excavator base and Logset harvesting head, reducing the need to drag long timber lengths out. The bulk of the top (harvesting residue) was processed in the rack and was used as a brash (slash) mat. The weather had been dry in the preceding weeks but was cold and wet during felling, although not below freezing.
At Wykeham, existing racks with a spacing of
20 m were cleared and used. Trees were felled using operator selection with a Valmet 921 harvester with tracks and steel rollers. Logs were extracted using a Valmet 840.1 forwarder with a 6 m reach and 10 tonne bunk capacity. No tracks or chains were used and conditions were mainly dry during the operations.
At Clocaenog, the intention was to use the existing rack system, but the machine operator found that in the dense regeneration and low light conditions these were not visible from the cab and therefore a new rack system was established. Racks were not pre-cleared as the harvester was large enough to drive over the regeneration. Trees were felled using a John Deere 1270D with standard metal feed rollers and Clarke tracks were fitted to the front bogie of the six-wheeled machine. Extraction was using a John Deere 1110D with CF585 loader and 0.35 m2 grab. The bunk capacity was 12 000 kg with Clarke tracks on the rear bogie. The thinning was carried out up and down the slope using operator selection. Weather conditions were sunny and dry during the work and snow on the ground was thawing.
The operators were all highly experienced in the harvesting methods used on each site and had many years experience of working in the local site conditions. They were aware that the intention was to utilize the regeneration to restock the site but were not informed that the sites were being used for a harvesting damage study. No special precautions were taken to protect the regeneration in the experiment plots which were marked as discretely as possible.
Approximately 70 regeneration assessment plots were laid out across each study area prior to thinning, positioned systematically on a grid, as described by Kerr et al. (2002)
. Plots were 2 x 2 m quadrats with the distance between plot centres calculated as described by Kerr et al. (2002)
, see Table 3. Quadrats were aligned north–south and were permanently marked with discrete wooden marker pegs with 5 cm above ground in opposite corners. The distance and bearing from the nearest canopy tree was recorded to aid relocation, and the plot number was painted discretely on the tree.
Prior to harvesting, the regeneration in each quadrat was counted by species and it was noted whether they were alive or dead. Seedlings with no green leaf or needle tissues (and for broadleaves, no fresh, healthy buds) were assumed to be dead. For the purposes of this study, all regenerating stems have been termed seedlings, recorded on the basis of height as small (<50 cm), medium (50–200 cm) or large (>200 cm). Presence or absence of deer browsing damage was also recorded for each seedling.
The second assessment of the plots took place within 2 months of completion of the thinning. The plots were relocated and number of seedlings by species, height class and whether they were alive or dead was recorded. An assessment of harvesting damage to each seedling was also made using the scale: no damage, low damage (central axis not snapped and likely to recover) and high damage (central axis snapped and unlikely to recover). At Clocaenog, the level of damage was not recorded; seedlings were recorded as damaged or undamaged. The number of seedlings lost from each quadrat was calculated by subtracting the number after harvesting from the number before harvesting for each height class. The distance from the centre of each plot to the closest edge of the two nearest extraction racks and to the two nearest recently felled stumps was also recorded.
Statistical analyses
The pre-harvest seedling numbers were first tested for a random distribution by testing the goodness of fit of a Poisson distribution (the distribution that would be observed if the seedlings were randomly distributed). Then a negative binomial distribution was fitted to give a measure of aggregation, 1/k, where k is the exponent parameter of the negative binomial distribution (GenStat, 2005
).
Pearsons chi-squared tests were applied to tables of before and after counts in order to determine whether seedling fate was related to height.
The principal model used to relate the damage to the explanatory variables of the distance to the nearest racks and nearest stumps was an ordinal logistic model for the three classes: undamaged, low damage and high damage. Data were pooled across size classes when numbers of seedlings were too low for analysis. In some cases, the numbers in the three damage classes were too low for a successful fit with an ordinal logistic model and a simpler logistic regression model regression (binomial generalized linear model (GLM) with logit link) was fitted (GenStat, 2005
). For this model, the numbers in a particular damage category were the response and the initial numbers of seedlings were the binomial denominator.
For the Fernworthy data, occasional increases in post-harvesting numbers of seedlings occurred which could be due to misclassification. This precluded the use of the logistic type models and instead a Poisson GLM was used with the log of the pre-harvesting number of seedlings included as an offset (GenStat, 2005
).
| Results |
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Regeneration characteristics before harvesting
The regeneration at the three sites was markedly different before the harvesting took place (Table 4).
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At Fernworthy, the vast majority (94.5 per cent) of the regeneration was Sitka spruce while the remainder (all species pooled) were 82 per cent rowan (Sorbus aucuparia L.), 15 per cent holly (Ilex aquifolium L.) and 3 per cent western hemlock (Tsuga heterophylla (Raf.) Sarg.). Of the total number of Sitka spruce seedlings, 25 per cent were dead and a further 5 per cent were browsed. The majority of live, unbrowsed Sitka spruce seedlings were in the medium size class, although there were also many small seedlings; fewer unbrowsed Sitka spruce seedlings had reached the large class.
At Wykeham, there was a wider range of species regenerating, reflecting the mixed overstorey, but the overall density of seedlings was much lower. The commonest seedlings were Sitka spruce and birch (Betula pendula L.), with similar numbers, but while there were few dead birch, more than half of the Sitka spruce seedlings recorded were dead. The numbers of Japanese larch and other seedlings were lower. Other seedlings were 34 per cent western hemlock, 22 per cent rowan, 18 per cent lodgepole pine (Pinus contorta Dougl. ex. Loud), 11 per cent Norway spruce, 10 per cent Scots pine, 4 per cent holly and 1 per cent grand fir (Abies grandis Dougl. ex. D. Don). Despite a large number of small dead Sitka seedlings, there were a few small live Sitka; the most common size class was the largest. The opposite was true for birch with the majority of live seedlings being small and a high number of dead seedlings in the medium class. Most live Japanese larch seedlings were large.
At Clocaenog, the total regeneration density was intermediate between the other sites. As at Fernworthy, the large majority (>99 per cent) of the seedlings were Sitka spruce, due to the single species overstorey. The two other species present were rowan (90 per cent of the remainder) and larch (10 per cent of the remainder) and were all small. The proportion of dead Sitka seedlings was 6 per cent (much lower than at Fernworthy) and these were exclusively in the medium class. This was also the most common height class for the live seedlings at Clocaenog with only 10 per cent being large. At all sites, the distribution of the seedlings among the quadrats was not random, with high Poisson indices (Table 4) due to the occurrence of quadrats with zero seedlings, showing the distributions to be clumped.
Harvesting damage
Regeneration in the plots positioned on extraction racks was usually completely destroyed; in many cases, the plot could not be located due to heavy brash or wheel ruts (data not shown). At Fernworthy, 14 of 70 plots fell on a rack and a further three were less than 1 m from the rack and lost all regeneration, totalling 24 per cent of the plots. At Clocaenog, 15 of 63 plots were on racks and suffered very severe or complete seedling loss, again representing 24 per cent of the plots. At Wykeham, the number was slightly higher, as 20 of 70 plots were on racks, representing 29 per cent of the plots.
Within the matrix plots, the percentage of seedlings surviving the thinning with no damage or low damage (i.e. still potential canopy trees) was variable. The highest percentages were seen at Wykeham, where 81.9 per cent of Sitka spruce seedlings (Figure 2) and 69.4 per cent of birch seedlings (data not shown) were not severely damaged, compared with 44.6 per cent of Sitka spruce seedlings at Fernworthy (Figure 2). At Clocaenog (where level of damage was not recorded), 40.6 per cent of the Sitka spruce seedlings in the matrix survived with no damage and a further 23.4 per cent survived with damage (Figure 2). The fate of matrix Sitka spruce seedlings is summarized in Figure 2.
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There was no indication that harvesting method significantly affected survival; at the two similar sites, Fernworthy and Clocaenog, motor-manual felling and harvester felling both resulted in heavy loss of small seedlings and heavy damage to tall seedlings (Table 5). The percentage of undamaged Sitka spruce seedlings at these two sites was almost identical (Figure 2) indicating that the harvesting method used had little influence.
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Damage related to seedling size
Throughout the stand as a whole (matrix and racks) at Fernworthy and Clocaenog, high numbers of small and medium Sitka spruce seedlings were lost (Pearsons chi-square, P < 0.001 for both sites) while much lower numbers of large seedlings were lost, as the large seedlings tended to sustain high levels of damage instead (Table 5). At both of these sites, there were too few seedlings of other species to carry out statistical analysis.
No significant difference in damage or loss was found between size classes for birch, Sitka spruce or other seedlings (analysed together) at Wykeham (Table 5). For the large height class, a comparison of numbers of undamaged Sitka spruce and birch seedlings at Wykeham was significant (Sitka spruce 70 per cent undamaged, birch 42 per cent, P < 0.01). At Wykeham, large birch were more likely to be damaged than large Sitka spruce.
Seedling fate and proximity to harvesting disturbance
At Fernworthy, both the number of Sitka spruce seedlings remaining and the number undamaged were related to the distance to the closest rack (Table 6, both P = 0.002). No distance variables were significantly related to the number of seedlings recorded as damaged. For the other species at Fernworthy, there were no significant relationships between distance variables and the numbers of seedlings damaged, undamaged or total surviving.
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At Clocaenog, the ordinal logistic model showed significant relationships between damage and distance parameters for all three size classes for Sitka spruce. For all classes, the distance to the closest rack was significant (Table 6, P = 0.035, P < 0.001 and P = 0.022 for small, medium and large classes, respectively). For the middle height class, the distances to the two nearest stumps were also significant (P = 0.024 and P = 0.008 for the first and second stump, respectively). The alternative binomial GLM showed that for medium seedlings only the distance to the closest rack significantly influenced the numbers of seedlings surviving (P < 0.001). The numbers of other species were too low to analyse.
At Wykeham, the binomial GLM showed a weak relationship between the number of undamaged, medium-sized Sitka spruce seedlings and the distance to the closest rack but there was no relationship for small or large seedlings. Combining the lost and heavily damaged categories and using the ordinal logistic model, the distance to the first and second closest cut stumps were significant (P = 0.03 and P = 0.021, respectively). For birch, no significant distance effects were found for the small- or medium-sized seedlings but for large seedlings the ordinal logistic model showed a significant relationship between damage and distance to the closest rack (P = 0.020). There were too few seedlings of other species to analyse.
| Discussion and practical implications |
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The first hypothesis that smaller seedlings would be more likely to survive harvesting than taller seedlings was not supported for the species, harvesting methods and sites studied; despite the lower likelihood of being hit, smaller seedlings tended to be lost on all three of the sites. The second hypothesis that taller seedlings would be more likely to be severely damaged than smaller seedlings was supported. This agrees with some of the literature, e.g. Gordon (1973)
Despite the high losses, seedling density is likely to be sufficient to restock all three sites. At Fernworthy and Clocaenog, the two similar Sitka-dominated sites, the percentage of initial seedlings surviving undamaged was remarkably similar; 27–43 per cent across the three size classes, despite the different harvesting techniques used on the two sites. The high density of the regeneration at these two sites means that even at the lowest survival rates seedling densities would be close to 10 000 ha–1. At Wykeham, although the seedling densities were lower, they were still clumped and the operator was able to protect the regeneration better while carrying out the work; between 51 and 70 per cent of the Sitka seedlings and between 41 and 54 per cent of birch seedlings were undamaged. As the survival of smaller seedlings can be unpredictable (as demonstrated by the large number of small and medium seedlings that were dead before harvesting, Table 4), Kerr et al. (2002)
recommend >2000 saplings per hectare (>1.3 m tall; broadly comparable with our large seedling size class) as being sufficient to restock a site. Post-harvesting numbers of undamaged or slightly damaged large seedlings were in excess of this at 2214 Sitka spruce per hectare at Fernworthy and 2090 Sitka spruce and Japanese larch per hectare at Wykeham. At Clocaenog, where damage scores were not differentiated, there were 4444 surviving large Sitka spruce per hectare after harvesting, 1825 ha–1 of which were undamaged. The quality of trees developing from damaged seedlings may be poor; hence, it may be preferable to base assessment of sufficient seedling density on the number of undamaged seedlings. However, Tesch et al. (1993)
reported that surviving Douglas-fir seedlings and saplings recovered from almost all logging damage within 6 years of overstorey removal, to the extent that 62 per cent of those initially classified as non-crop trees were reclassified as crop trees, indicating that some of the severely damaged regeneration on our sites may also recover.
In comparison to Fernworthy, the proportion of Sitka spruce seedlings lost was much lower at Wykeham, although a higher proportion was damaged (Figure 2). The high Poisson index of Sitka spruce at Wykeham (4.138, compared with 0.325 at Fernworthy) indicates that the seedlings were highly aggregated or clumped, perhaps enabling operators to avoid crushing the Wykeham seedlings during felling. However, it is surprising that the proportion of seedlings receiving damage was higher at Wykeham than at Fernworthy. The practice used at Fernworthy, of cutting the first one or two timber lengths from the felled tree before processing the remainder, may have minimized damage rates by reducing the need to drag long timber lengths out of the stand.
The distribution and species composition of the seedlings should be considered. Both before and after harvesting, distributions at all sites were clumped with areas of no regeneration and areas with very dense regeneration. Virtually all of the seedlings at Fernworthy and Clocaenog were Sitka spruce, reflecting the overstorey composition, while at Wykeham, although there had been successful regeneration of Japanese larch at some point in the past, there was little new larch regeneration and very little Scots pine regeneration on the site. Therefore, if only the existing seedlings are used to restock these sites, the future stands at all three will remain clumped and at Wykeham, the stand will become more heavily dominated by Sitka spruce and birch, as these species tended to be more resilient.
Although the relationship varied between the sites, species and size classes, there was considerable evidence that loss and damage to seedlings were related to proximity to extraction racks. Granhus and Fjeld (2001)
also reported that distance to the extraction rack had a significant effect on sapling damage. They noted that although the rack spacing was at the maximum allowing the harvester access to all trees, increasing the rack spacing when using motor-manual felling could potentially reduce damage rates as a large proportion of damage was in the rack plots. As it is now the intention at all three sites to maintain and reuse the existing racks, it is unlikely that a similar level of damage would be sustained in subsequent thinnings or final overstorey removal. Distance to the nearest stump was less commonly related to the damage or losses, regardless of the harvesting method used. This indicates that once a good rack system is in place, the harvesting disturbance caused by the felling of the tree is unlikely to cause much further regeneration to be lost. This probably partly reflected the skill of the operators in directing the tree away from particularly dense areas of regeneration but also suggests that the seedlings were more resilient than expected.
The high numbers of seedlings lost on racks highlights the importance of maintaining a strict rack system while working and using the same racks in subsequent operations as this will result in very little impact of the thinning on the rest of the matrix. The racks should be well protected with brash (Moffat et al., 2006
) to protect them for future operations. Rack spacing should be optimized to minimize the destruction of seedlings in the racks while allowing the large majority of the matrix to be accessed without leaving the rack. If new racks are created in each operation, the regeneration will be lost over a larger area. However, the operators at Clocaenog commented that the previously existing racks were difficult to see due to dense regeneration, particularly when working in low light. Investing some time in motor-manual clearing of the racks prior to the harvesting (as was done at Fernworthy) or marking the rack position with painted arrows beforehand may be beneficial in the long run and reduce wandering in the stand. However, it should be noted that higher disturbance rates in the extraction racks may cause a change in vegetation type, possibly promoting vigorous or woody weed growth, as was reported by Harvey and Brais (2002)
. This could potentially increase time and cost, particularly for motor-manual operations, and may result in the need for costly control of invasive woody weeds.
Although not tested on sufficient sites to draw firm conclusions, there was no indication that motor-manual felling resulted in higher survival than harvester felling. Despite the similar species composition of the Clocaenog and Fernworthy sites in this study, both the motor-manual felling method used at Fernworthy and the harvester felling at Clocaenog resulted in heavy loss of small seedlings and heavy damage to tall seedlings. This is in contrast to Granhus and Fjeld (2001)
who showed that motor-manual felling reduced injury rates to tall regeneration while harvester felling caused lower injury rates to small regeneration. As our data indicate that smaller seedlings are less likely to survive the operation, use of motor-manual felling may enable operators to increase survival rates by felling trees into the areas of smaller regeneration, rather than into areas of less-dense, but larger regeneration. However, further studies designed to examine the effects of different operational methods would be required to confirm this. Across all three sites, the damage rates sustained were comparable with those quoted in other studies on the impact of overstorey thinning on coniferous advance regeneration (Vorob et al., 1994
; Westerberg and Berg, 1994
; Sikström and Glöde, 2000
).
In summary, the recommendations are as follows:
- 1 Create and maintain a permanent rack system, with distance between racks appropriate to the intended harvesting method. This is likely to kill
25–30 per cent of the regeneration on the site as a whole.
- 2 Allow for a further loss of 20–60 per cent of the regeneration in the stand matrix due to damage caused by thinning operations.
- 3 Clear and/or mark the racks before harvesting to ensure machinery stays on the rack.
- 4 Protect the taller regeneration, e.g. by felling trees away from these areas. Taller regeneration is more likely to survive undamaged and develop to become a future crop tree.
- 2 Allow for a further loss of 20–60 per cent of the regeneration in the stand matrix due to damage caused by thinning operations.
| Conflict of Interest Statement |
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None declared.
| Acknowledgements |
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The authors would like to thank the Forest Research Technical Support staff at each of the sites for carrying out the assessments, Geoff Morgan for advising on and carrying out statistical analyses and Ewan Mackie and two anonymous reviewers for helpful comments on an earlier draft.
| References |
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Andersson O, Fries J. Pilot study on plant damage in a seed tree cutting. Sver. Skogsvårdsförb. Tidskr. (1979) 2:123–129. (in Swedish, English summary).
Anonymous. Plant Density: Right First Time (2004) Edinburgh: Forestry Commission. Operational Guidance Booklet No. 4.
Clarke GC. The natural regeneration of spruce. Scott. For. (1992) 46:107–129.
Eliasson L, Lageson H, Valinger E. Influence of sapling height and temperature on damage to advance regeneration. For. Ecol. Manage. (2003) 175:217–222.[CrossRef]
Payne RW. GenStat. The Guide to GenStat Release 8.1. Part 2: Statistics. In: Lawes Agricultural Trust (Rothamsted Experimental Station) (2005) Oxford: VSN International.
Glöde D, Sikström U. Two felling methods in final cutting of shelterwood, single-grip harvester productivity, and damage to the regeneration. Silva Fenn. (2001) 35:71–83.
Gordon DT. Released Advance Reproduction of White and Red Fir: Growth, Damage, Mortality (1973) USDA Forest Service Research Paper PSW-95. US Department of Agriculture, Berkley, CA.
Granhus A, Fjeld D. Spatial distribution of injuries to Norway spruce advance growth after selection harvesting. Can. J. For. Res. (2001) 31:1903–1913.[CrossRef]
Harvey B, Brais S. Effects of mechanized careful logging on natural regeneration and vegetation competition in the southeastern Canadian boreal forest. Can. J. For. Res. (2002) 32:653–666.[CrossRef]
Jeansson E, Laestadius L. Reforestation by Site Preparation, Natural Regeneration and Understorey Regeneration in the Soviet Union (1981) Umeå: Department of Silviculture, The Swedish University of Agricultural Sciences. Rapporter 6:65 p. (in Swedish, English summary).
Kerr G, Mason B, Boswel R, Pommerening A. Monitoring the Transformation to Continuous Cover Management (2002) Edinburgh: Forestry Commission. Forestry Commission Information Note 45.
Malcolm DC, Mason WL, Clarke GC. The transformation of conifer forests in Britain—Regeneration, gap size and silvicultural systems. For. Ecol. Manage. (2001) 151:7–23.[CrossRef]
Mason WL. Natural regeneration of Sitka spruce in the forest of Ae: development over 25 years. Scott. For. (2008) 62:2–8.
Mason WL, Kerr G. Transforming of even-aged conifer stands to continuous cover management. (2004) Edinburgh: Forestry Commission. Forestry Commission Information Note 40.
Mason WL, Quine CP. Silvicultural possibilities for increasing structural diversity in British spruce forests: the case of Kielder forest. For. Ecol. Manage. (1995) 79:13–28.[CrossRef]
Mason WL, Kerr G, Simpson JMS. What is continuous cover forestry? (1999) Edinburgh: Forestry Commission. Forestry Commission Information Note 29.
Matthews RW, Mackie ED. Forest Mensuration: A Handbook for Practitioners (2006) Edinburgh: Forestry Commission.
McIntosh B. Role of continuous cover silvicultural systems in the management of the Forestry Commission estate. CCFG Newsletter (2000) 16:5–9. Continuous Cover Forestry Group, Bellever, May Road, Turvey, Bedford, MK43 8DT.
McNeill JD, Thompson DA. Natural regeneration of Sitka spruce in the Forest of Ae. Scott. For. (1982) 36:269–282.
Moffat A, Jones BM, Mason B. Managing brash on conifer clearfell sites. (2006) Edinburgh: Forestry Commission. Forestry Commission Practice Note 13.
Nelson DG. Management of Sitka spruce natural regeneration. (1991) Edinburgh: Forestry Commission. Forestry Commission Research Information Note 204.
Newton M, Cole EC. Harvesting impacts on understory regeneration in two-storied Douglas-fir stands. West. J. Appl. For. (2006) 21:14–18.
O Hara KL. Silviculture for structural diversity: a new look at multi-aged stands. J. For. (1998) 96:4–10.
Olson MG, Clatterbuck WK, Schlarbaum SE. Mechanical damage incurred by underplanted northern red oak following six overstorey treatments: first-year results (2003) 554–551. General technical Report—Southern Research Station, USDA Forest Service (No. SRS-71).
Pommerening A, Murphy ST. A review of the history, definitions and methods of continuous cover forestry with special attention to afforestation and restocking. Forestry (2004) 77:27–44.
Preuhsler T, Jakobi K.-P. Effects of a shelterwood felling on the natural regeneration. Forst Holz (1996) 51:205–211. (in German, English summary).
Sikström U, Glöde D. Damage to Picea abies regeneration after final cutting of shelterwood with single- and double-grip harvester systems. Scand. J. For. Res. (2000) 15:274–283.[CrossRef]
Skoklefald S. Release of natural Norway spruce regeneration. Medd. Nor. Skogforsoksves. (1967) 23:381–409. (in Norwegian, English summary).
Tesch SD, Lysne DH, Mann JW, Helgerson OT. Mortality of regeneration during skyline logging of a shelterwood overstorey. J. For. (1986) 84:49–50.
Tesch SD, Baker-Katz K, Korpela EJ, Mann JW. Recovery of Douglas fir seedlings and saplings wounded during overstorey removal. Can. J. For. Res. (1993) 23:1684–1694.[CrossRef]
von Ow F, Joyce P, Keane M. Factors affecting the establishment of natural regeneration Sitka spruce (Picea sitchensis (Bong.) Carr.) in Ireland. Ir. For. (1996) 53:2–18.
Vorob VN, Danchenko AM, Bekh IA, Panevin VS, Burkov VP. Is it possible to preserve advance growth when using harvesters. Lesn. Khoz. (1994) 6:33–34. (in Russian, English abstract).
Westerberg D. Profitable forestry methods—maintaining biodiversity as an integral part of Swedish forestry. In: Innovative Silviculture Systems in Boreal Forests—Bamsey CR, ed. (1995) Edmonton, Alberta, Canada: Clear Lake Ltd. 61–65.
Westerberg D, Berg S. Felling of standards: trial method for determining productivity, costs and damage to advance growth. (1994) Uppsala: The Forestry Research Institute of Sweden. 10:26. Redogörelse.
Youngblood AP. Effects of shelterwood removal on established regeneration in an Alaska white spruce stand. Can. J. For. Res. (1990) 20:1378–1381.[CrossRef]
Received 2 April 2008.
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