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The theory of the fall factor and two different tree climbing scenarios involving (A) a safe versus (B) an extremely dangerous condition. Note that the fall factor theory applies to ascents when (and only when) the tree climber is located above the last anchor. The black line represents the climbing rope, the arrow: the attachment of the researcher to the rope, the hand: one end of the rope attached to a solid trunk on the ground (the belay), the upper black-and-white circle: the last anchor which would support a fall, and the lower circle: an additional anchor, should the upper one fail because of the shock provided by a fall. The length of rope absorbing the fall is the amount of rope between the climber and the next knot. Assuming the amount of rope between the last anchor and the belay is 15 m in both scenarios, the length of rope that would absorb a fall in Condition A is 18 m (3 m of rope between the researcher and the last anchor, plus 15 m between the last anchor and the belay). However, the climber in Condition B has made a knot with the climbing rope at the last anchor before moving above it, dangerously shortening the amount of rope which could absorb the energy of a fall (3 m).
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Primate ecological studies can benefit from accessing the canopy to estimate intra-tree and inter-tree variation in food availability and nutrient value, patch and subpatch depletion, foraging efficiency, as well as nest structure and nesting behaviors, parasitic transmission and predator detectability. We compare several ways to access the canopy...
Contexts in source publication
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... II. Variation in the fall factor of 28 individual trees climbed during a 1-yr primate field study. Trees divided as main canopy tree (m) versus emergent tree (e) to compare which of the 2 categories presents a higher climbing risk. Height and length in m Length of rope Climber’s height Length of which would have Fall Tree species above last anchor potential fall absorbed the fall factor (m) 10 20 22 0.91 (m) 5 10 19 0.53 (m) 5 10 24 0.42 (m) 6 12 21 0.57 (m) 4 8 25 0.32 (m) 7 14 26 0.54 (m) 7 14 25 0.56 (m) 6 12 26 0.46 (e) 6 12 30 0.40 (e) 9 18 25 0.72 (e) 2 4 26 0.15 (e) 4 8 28 0.29 (e) 4.5 9 31 0.29 (e) 6 12 35 0.34 (e) 6 12 25 0.48 (e) 4.5 9 34 0.26 (e) 2.5 5 26 0.19 (e) 11.5 23 32 0.72 (e) 7 14 29 0.48 (e) 4.5 9 31 0.29 (e) 5 10 30 0.33 (e) 4 8 30 0.27 (e) 6 12 30 0.40 (e) 6 12 29 0.41 (e) 3 6 24 0.25 (m) 4 8 30 0.27 (e) 1 2 21.5 0.09 (m) 1.5 3 16 0.19 Mean 5.3 10.6 26.8 0.40 Note. Fall factors calculated as length of potential fall divided by length of rope which would have absorbed the fall (Fig. 2). No knot has been tied at the last anchor (equivalent of Figure 2, condition A). Climber’s height above last anchor was measured with a 50-m tape. The use of a second independent safety device (like a daisy chain, Fig. 1e and text) has not been considered in calculations because there is the real possibility for a climber to fall before the additional safety device could be properly installed. All trees located in Kanyawara (Kibale N.P., Uganda), UTM: N36, 2 km of radius from 0.56567 North 30.35684 ...
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... II. Variation in the fall factor of 28 individual trees climbed during a 1-yr primate field study. Trees divided as main canopy tree (m) versus emergent tree (e) to compare which of the 2 categories presents a higher climbing risk. Height and length in m Length of rope Climber’s height Length of which would have Fall Tree species above last anchor potential fall absorbed the fall factor (m) 10 20 22 0.91 (m) 5 10 19 0.53 (m) 5 10 24 0.42 (m) 6 12 21 0.57 (m) 4 8 25 0.32 (m) 7 14 26 0.54 (m) 7 14 25 0.56 (m) 6 12 26 0.46 (e) 6 12 30 0.40 (e) 9 18 25 0.72 (e) 2 4 26 0.15 (e) 4 8 28 0.29 (e) 4.5 9 31 0.29 (e) 6 12 35 0.34 (e) 6 12 25 0.48 (e) 4.5 9 34 0.26 (e) 2.5 5 26 0.19 (e) 11.5 23 32 0.72 (e) 7 14 29 0.48 (e) 4.5 9 31 0.29 (e) 5 10 30 0.33 (e) 4 8 30 0.27 (e) 6 12 30 0.40 (e) 6 12 29 0.41 (e) 3 6 24 0.25 (m) 4 8 30 0.27 (e) 1 2 21.5 0.09 (m) 1.5 3 16 0.19 Mean 5.3 10.6 26.8 0.40 Note. Fall factors calculated as length of potential fall divided by length of rope which would have absorbed the fall (Fig. 2). No knot has been tied at the last anchor (equivalent of Figure 2, condition A). Climber’s height above last anchor was measured with a 50-m tape. The use of a second independent safety device (like a daisy chain, Fig. 1e and text) has not been considered in calculations because there is the real possibility for a climber to fall before the additional safety device could be properly installed. All trees located in Kanyawara (Kibale N.P., Uganda), UTM: N36, 2 km of radius from 0.56567 North 30.35684 ...
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... the Single Rope Technique, though one might compensate by rappelling rather than climbing down with the spurs. If the same tree must be climbed many times, this method is not recommended as it may have long-term effect on tree survival. To determine how much damage could be done to trees accessed with the climbing spurs, we noted whether spur holes were later infested by insects, losing sap, par- asitized by mushrooms, or whether bark formed again and recovered the original hole. For the 26 species of trees monitored, 20 exhibited no sign of insect or mushroom invasion and were not bleeding. Since local employment is a critical issue for conservation, we recommend that primate researchers hire local climbers who master the use of spurs to climb trees (contra Moffett and Lowman, 1995) but only on those trees that are known not to be spur- sensitive. How dangerous is tree climbing? For the Single Rope Technique, one way to answer this question is to consider whether the tree climber is located above or below the last anchor. An anchor is a support over which the climbing rope is free to move, like a branch in a tree. The last anchor is the highest point of support over which the rope has been passed. When the climber is located below the last anchor, the risk of falling is practically nil because there is no slack in the rope: the latter is attached on the ground at the belay, goes up until it passes over the branch and comes back down to the climber. However, when the climber moves above the last anchor, the risk of falling is real, because loose rope accumulates between the climber and the last point of support, i.e., the last anchor. In such a case, the length of the fall is twice the distance between the climber and the last anchor, a kind of pendulum effect. Therefore, the risk of collecting data in a tree largely depends on whether the climber must work above or below the last anchor. In any tree, a risky solution for the climber is obviously to set the last anchor over a branch located in the lowest part of a tree crown, forcing the climber to work above the last anchor, with a constant risk of falling. The safest strategy is to position the climbing rope over the highest solid branch in the tree. Then, the climber can work most of the time below the last anchor, thus minimizing the risk of falling. Sometimes it is not possible to work below the last anchor because of tree structure, or because the highest part of the canopy must be accessed for scientific purposes, such as collecting food for nutritional analyses. Two strategies for the experienced climber can be used to minimize the risks related to gathering data above the last anchor: autoanchoring and dynamic belaying (Cox and Fulsaas, 2003). Autoanchoring is attaching oneself with a second set of climbing gear once positioned above the last anchor (Figure 1e). A shock-absorbing device like a daisy chain (Figure 1e) is recommended for autoanchoring. The expression dynamic belaying refers to the way the energy is absorbed during a fall. In dynamic belaying, the energy of the fall, instead of being absorbed in a small fraction of a second as during static belaying, is spread out and absorbed during a longer period of time, thus substantially increasing the climber’s safety. To understand how the notion of dynamic belaying applies to tree climbing, one can consider the fall factor (Cox and Fulsaas, 2003). Understanding the fall factor is critical if and only if the climber decides to move higher than the last anchor. It does not apply when the climber stays below that anchor. It is a dimensionless number that varies from 0 to 2, and is defined as the distance of the fall, divided by the length of the rope which absorbs the fall. Thus, a 5-m fall absorbed by 50 m of climbing rope results in a fall factor of 0.1 (5 divided by 50 = 0 . 1). The same fall factor value is obtained for a fall of 2 m if the rope which absorbs the energy of the fall is 20 m long (2 / 20 = 0 . 1). The resultant forces are the same because the energy of the longer fall is absorbed by a proportionally longer rope (Cox and Fulsaas, 2003). A fall factor < 0 . 5 is considered by experienced climbers to be safe, between 0.5 and 1.0 is risky, between 1.0 and 1.5 is dangerous, and between 1.5 and 2.0 is extremely dangerous. Extreme danger includes the real possibility that the weakest link in the safety system might break. Even if it does not, the climber can incur severe injuries, notably to the vertebral column. Paradoxically, a longer fall might be safer than a shorter fall. For instance, a free fall of 20 m absorbed by 50 m of rope in an emergent tree is safer for the climber than a free fall of only 2 m but absorbed by 1 m of rope in a small tree (fall factor of 0.4 versus 2, respectively). Although the fall factor assessments are arbitrary, they offer a rough safety guide. A safe climber not only considers the fall factor theory but also puts it in practice while in the tree. Figure 2 presents 2 additional scenarios to illustrate the importance of the fall factor concept, except that this time the length of the fall is identical in both conditions. The difference relates to the climber’s protection strategy. In condition A (Figure 2), the climber ties no knot with the climbing rope, so the latter can run freely at the last anchor and any backup anchors, then she or he moves above the last anchor. In condition B (Figure 2), the climber ties a solid knot at the last anchor, then she or he moves above it. The objective of this exercise is to calculate which of the 2 scenarios is safer. We set in both cases the distance of the climber above the last anchor to 3 m and the distance between the last anchor and the belay on the ground to 15 m. The fall factor in condition A is only 0.33: length of fall of 6 m divided by 18 m of rope which absorbs the energy of the fall, i.e. 3 m of rope between the climber and the last anchor, plus 15 m of rope between the last anchor and the belay. Condition A is thus a safe practice (fall factor < 0 . 5). However, if the tree climber ties a knot at the last anchor as in condition B then she or he moves 3 m above it, the fall factor reaches the maximum, 2: length of fall of 6 m divided by only 3 m of rope absorbing the fall. Only 3 m of rope can absorb the energy of the fall in condition B because the climber has tied a knot at the last anchor; indeed, the 15 m of rope below the last anchor is useless. Condition B is thus an extremely dangerous practice (fall factor > 1 . 5). When applied to tree climbing, the dynamic belaying and fall factor concepts urge tree climbers to let the rope running freely over branches or branch junctions, i.e., no knot using the climbing rope should be tied at these points. When the dynamic belaying principle is applied (Figure 2) and complemented with autoanchoring (Figure 1e), climbing above the last anchor is relatively safe though we recommend that apprentice climbers get experience below the last anchor before attempting an ascent above the last anchor. Appendix II presents the variation of the fall factor in 28 individual trees which were climbed during a 1-yr primate field study in Kibale. It illustrates how the fall factor varies as a function of the climber’s height above the last anchor and the amount of rope available to absorb a potential fall. All climbing conditions involved a fall factor lower than < 1, and were strictly complemented with autoanchoring. When trees are split as small versus emergent, small trees, with a mean fall factor of 0.48, were marginally more dangerous to climb than emergent trees, with a mean fall factor of 0.35 (Mann-Whitney, U = 53.0, p = 0.08). This is best explained by the shorter rope available to absorb a fall in small trees. Another strategy in tree climbing related to dynamic belaying is to increase shock absorption via a dynamic climbing rope versus a static climbing rope. A dynamic rope offers greater elasticity than a static rope. We recommend that inexperienced tree climbers use a dynamic rope. The rope is may be the most important piece of equipment related to the climber’s safety. Modern climbing ropes are composed of a core of braided or parallel nylon filaments encased in a smooth, woven sheath of nylon (Cox and Fulsaas, 2003). Kernmantle ropes are now the only climbing ropes approved by the UIAA. There are two kinds of climbing ropes: dynamic and static. For the same diameter, the dynamic rope offers more elasticity than a static rope and hence can endure higher impacts. Tree climbing rarely involves major falls, but the possibility is real, mostly when the climber moves horizontally in the tree or higher than the last anchor (Figure 2). The pro- tective sheath of a static rope is more abrasion resistant than the sheath of a dynamic rope, and therefore is more appropriate for primate field research. However, a static rope cannot endure severe falls and only experienced tree climbers should consider its purchase. Another factor to consider is the rope diameter. The larger the diameter of a rope, the greater is its energy- absorbing capacity. Descending gear requires a minimum diameter of 10 mm. It is also important to consider whether the rope will be used in a wet en- vironment. Wet ropes become difficult to manage, check fewer falls, and have ca. 30% less strength when they are wet (Cox and Fulsaas, 2003). Overall, we recommend that inexperienced tree climbers purchase a dynamic UIAA-approved 11 mm climbing rope, ideally water-repellent. For the advanced climber, a static 10 mm rope coupled with an explosive quickdraw—a kind a shock-absorbing device attached at the belay—is more appropriate: cheaper, long-lasting sheath, less annoying elasticity while ascending, and lighter. Stepping on a rope is a common form of abusive treatment that grinds cutting particles into and through the sheath (Cox and Fulsaas, 2003). Over time, the particles act like small knives that ...
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... tree largely depends on whether the climber must work above or below the last anchor. In any tree, a risky solution for the climber is obviously to set the last anchor over a branch located in the lowest part of a tree crown, forcing the climber to work above the last anchor, with a constant risk of falling. The safest strategy is to position the climbing rope over the highest solid branch in the tree. Then, the climber can work most of the time below the last anchor, thus minimizing the risk of falling. Sometimes it is not possible to work below the last anchor because of tree structure, or because the highest part of the canopy must be accessed for scientific purposes, such as collecting food for nutritional analyses. Two strategies for the experienced climber can be used to minimize the risks related to gathering data above the last anchor: autoanchoring and dynamic belaying (Cox and Fulsaas, 2003). Autoanchoring is attaching oneself with a second set of climbing gear once positioned above the last anchor (Figure 1e). A shock-absorbing device like a daisy chain (Figure 1e) is recommended for autoanchoring. The expression dynamic belaying refers to the way the energy is absorbed during a fall. In dynamic belaying, the energy of the fall, instead of being absorbed in a small fraction of a second as during static belaying, is spread out and absorbed during a longer period of time, thus substantially increasing the climber’s safety. To understand how the notion of dynamic belaying applies to tree climbing, one can consider the fall factor (Cox and Fulsaas, 2003). Understanding the fall factor is critical if and only if the climber decides to move higher than the last anchor. It does not apply when the climber stays below that anchor. It is a dimensionless number that varies from 0 to 2, and is defined as the distance of the fall, divided by the length of the rope which absorbs the fall. Thus, a 5-m fall absorbed by 50 m of climbing rope results in a fall factor of 0.1 (5 divided by 50 = 0 . 1). The same fall factor value is obtained for a fall of 2 m if the rope which absorbs the energy of the fall is 20 m long (2 / 20 = 0 . 1). The resultant forces are the same because the energy of the longer fall is absorbed by a proportionally longer rope (Cox and Fulsaas, 2003). A fall factor < 0 . 5 is considered by experienced climbers to be safe, between 0.5 and 1.0 is risky, between 1.0 and 1.5 is dangerous, and between 1.5 and 2.0 is extremely dangerous. Extreme danger includes the real possibility that the weakest link in the safety system might break. Even if it does not, the climber can incur severe injuries, notably to the vertebral column. Paradoxically, a longer fall might be safer than a shorter fall. For instance, a free fall of 20 m absorbed by 50 m of rope in an emergent tree is safer for the climber than a free fall of only 2 m but absorbed by 1 m of rope in a small tree (fall factor of 0.4 versus 2, respectively). Although the fall factor assessments are arbitrary, they offer a rough safety guide. A safe climber not only considers the fall factor theory but also puts it in practice while in the tree. Figure 2 presents 2 additional scenarios to illustrate the importance of the fall factor concept, except that this time the length of the fall is identical in both conditions. The difference relates to the climber’s protection strategy. In condition A (Figure 2), the climber ties no knot with the climbing rope, so the latter can run freely at the last anchor and any backup anchors, then she or he moves above the last anchor. In condition B (Figure 2), the climber ties a solid knot at the last anchor, then she or he moves above it. The objective of this exercise is to calculate which of the 2 scenarios is safer. We set in both cases the distance of the climber above the last anchor to 3 m and the distance between the last anchor and the belay on the ground to 15 m. The fall factor in condition A is only 0.33: length of fall of 6 m divided by 18 m of rope which absorbs the energy of the fall, i.e. 3 m of rope between the climber and the last anchor, plus 15 m of rope between the last anchor and the belay. Condition A is thus a safe practice (fall factor < 0 . 5). However, if the tree climber ties a knot at the last anchor as in condition B then she or he moves 3 m above it, the fall factor reaches the maximum, 2: length of fall of 6 m divided by only 3 m of rope absorbing the fall. Only 3 m of rope can absorb the energy of the fall in condition B because the climber has tied a knot at the last anchor; indeed, the 15 m of rope below the last anchor is useless. Condition B is thus an extremely dangerous practice (fall factor > 1 . 5). When applied to tree climbing, the dynamic belaying and fall factor concepts urge tree climbers to let the rope running freely over branches or branch junctions, i.e., no knot using the climbing rope should be tied at these points. When the dynamic belaying principle is applied (Figure 2) and complemented with autoanchoring (Figure 1e), climbing above the last anchor is relatively safe though we recommend that apprentice climbers get experience below the last anchor before attempting an ascent above the last anchor. Appendix II presents the variation of the fall factor in 28 individual trees which were climbed during a 1-yr primate field study in Kibale. It illustrates how the fall factor varies as a function of the climber’s height above the last anchor and the amount of rope available to absorb a potential fall. All climbing conditions involved a fall factor lower than < 1, and were strictly complemented with autoanchoring. When trees are split as small versus emergent, small trees, with a mean fall factor of 0.48, were marginally more dangerous to climb than emergent trees, with a mean fall factor of 0.35 (Mann-Whitney, U = 53.0, p = 0.08). This is best explained by the shorter rope available to absorb a fall in small trees. Another strategy in tree climbing related to dynamic belaying is to increase shock absorption via a dynamic climbing rope versus a static climbing rope. A dynamic rope offers greater elasticity than a static rope. We recommend that inexperienced tree climbers use a dynamic rope. The rope is may be the most important piece of equipment related to the climber’s safety. Modern climbing ropes are composed of a core of braided or parallel nylon filaments encased in a smooth, woven sheath of nylon (Cox and Fulsaas, 2003). Kernmantle ropes are now the only climbing ropes approved by the UIAA. There are two kinds of climbing ropes: dynamic and static. For the same diameter, the dynamic rope offers more elasticity than a static rope and hence can endure higher impacts. Tree climbing rarely involves major falls, but the possibility is real, mostly when the climber moves horizontally in the tree or higher than the last anchor (Figure 2). The pro- tective sheath of a static rope is more abrasion resistant than the sheath of a dynamic rope, and therefore is more appropriate for primate field research. However, a static rope cannot endure severe falls and only experienced tree climbers should consider its purchase. Another factor to consider is the rope diameter. The larger the diameter of a rope, the greater is its energy- absorbing capacity. Descending gear requires a minimum diameter of 10 mm. It is also important to consider whether the rope will be used in a wet en- vironment. Wet ropes become difficult to manage, check fewer falls, and have ca. 30% less strength when they are wet (Cox and Fulsaas, 2003). Overall, we recommend that inexperienced tree climbers purchase a dynamic UIAA-approved 11 mm climbing rope, ideally water-repellent. For the advanced climber, a static 10 mm rope coupled with an explosive quickdraw—a kind a shock-absorbing device attached at the belay—is more appropriate: cheaper, long-lasting sheath, less annoying elasticity while ascending, and lighter. Stepping on a rope is a common form of abusive treatment that grinds cutting particles into and through the sheath (Cox and Fulsaas, 2003). Over time, the particles act like small knives that slice the rope’s nylon filaments. It is hard to decide when to retire a rope. Its condition depends on many factors including frequency of use, the care it has received, its age, and the number of falls it has endured. As a general guideline, a dynamic rope used daily should be retired within a year, while a rope used 2–3 days per week should offer about 2 years of service (Cox and Fulsaas, 2003). A static rope can last twice the time of a dynamic rope. After one very severe fall with fall factor 1.5, any rope should be replaced immediately. The climbing rope is the most important and sensitive equipment, and a safe climber takes great care of it. Knots allow the climber to use the rope for many special purposes: to tie into the rope, to temporarily anchor to a branch, to tie 2 ropes together, to use slings to climb the rope itself, and much more. Climbers rely most heavily on 12 different knots (Cox and Fulsaas, 2003; Vines and Hudson, 1992). A tree climber should practice them until tying them is second nature, including in the dark at cold temperatures. The novice climber should master at least, eyes closed, the following set of tested knots: Figure 8 Follow-through (also called the Flemish Bend), Figure 8 on a Bight, Double or Triple Fisherman’s Knot (also called Grapevine), and one self-rescue knot like the Prusik or Bachman or Klemheist Knot. For intermediate and advanced climbers, there are the Butterfly Knot, Equalizing Figure 8, Water Knot (Ring Bend), Girth Hitch, Stopper Knot, Munter Hitch or Clove Hitch, and for rescuing an injured colleague, the Munter Mule. Contrary to common belief, knots are weaker than the rope used to tie them. Moreover, they do not all offer the same strength. In case of a sudden shock, any chain of safety will break up at the weakest link, most often at the weakest ...
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... again and recovered the original hole. For the 26 species of trees monitored, 20 exhibited no sign of insect or mushroom invasion and were not bleeding. Since local employment is a critical issue for conservation, we recommend that primate researchers hire local climbers who master the use of spurs to climb trees (contra Moffett and Lowman, 1995) but only on those trees that are known not to be spur- sensitive. How dangerous is tree climbing? For the Single Rope Technique, one way to answer this question is to consider whether the tree climber is located above or below the last anchor. An anchor is a support over which the climbing rope is free to move, like a branch in a tree. The last anchor is the highest point of support over which the rope has been passed. When the climber is located below the last anchor, the risk of falling is practically nil because there is no slack in the rope: the latter is attached on the ground at the belay, goes up until it passes over the branch and comes back down to the climber. However, when the climber moves above the last anchor, the risk of falling is real, because loose rope accumulates between the climber and the last point of support, i.e., the last anchor. In such a case, the length of the fall is twice the distance between the climber and the last anchor, a kind of pendulum effect. Therefore, the risk of collecting data in a tree largely depends on whether the climber must work above or below the last anchor. In any tree, a risky solution for the climber is obviously to set the last anchor over a branch located in the lowest part of a tree crown, forcing the climber to work above the last anchor, with a constant risk of falling. The safest strategy is to position the climbing rope over the highest solid branch in the tree. Then, the climber can work most of the time below the last anchor, thus minimizing the risk of falling. Sometimes it is not possible to work below the last anchor because of tree structure, or because the highest part of the canopy must be accessed for scientific purposes, such as collecting food for nutritional analyses. Two strategies for the experienced climber can be used to minimize the risks related to gathering data above the last anchor: autoanchoring and dynamic belaying (Cox and Fulsaas, 2003). Autoanchoring is attaching oneself with a second set of climbing gear once positioned above the last anchor (Figure 1e). A shock-absorbing device like a daisy chain (Figure 1e) is recommended for autoanchoring. The expression dynamic belaying refers to the way the energy is absorbed during a fall. In dynamic belaying, the energy of the fall, instead of being absorbed in a small fraction of a second as during static belaying, is spread out and absorbed during a longer period of time, thus substantially increasing the climber’s safety. To understand how the notion of dynamic belaying applies to tree climbing, one can consider the fall factor (Cox and Fulsaas, 2003). Understanding the fall factor is critical if and only if the climber decides to move higher than the last anchor. It does not apply when the climber stays below that anchor. It is a dimensionless number that varies from 0 to 2, and is defined as the distance of the fall, divided by the length of the rope which absorbs the fall. Thus, a 5-m fall absorbed by 50 m of climbing rope results in a fall factor of 0.1 (5 divided by 50 = 0 . 1). The same fall factor value is obtained for a fall of 2 m if the rope which absorbs the energy of the fall is 20 m long (2 / 20 = 0 . 1). The resultant forces are the same because the energy of the longer fall is absorbed by a proportionally longer rope (Cox and Fulsaas, 2003). A fall factor < 0 . 5 is considered by experienced climbers to be safe, between 0.5 and 1.0 is risky, between 1.0 and 1.5 is dangerous, and between 1.5 and 2.0 is extremely dangerous. Extreme danger includes the real possibility that the weakest link in the safety system might break. Even if it does not, the climber can incur severe injuries, notably to the vertebral column. Paradoxically, a longer fall might be safer than a shorter fall. For instance, a free fall of 20 m absorbed by 50 m of rope in an emergent tree is safer for the climber than a free fall of only 2 m but absorbed by 1 m of rope in a small tree (fall factor of 0.4 versus 2, respectively). Although the fall factor assessments are arbitrary, they offer a rough safety guide. A safe climber not only considers the fall factor theory but also puts it in practice while in the tree. Figure 2 presents 2 additional scenarios to illustrate the importance of the fall factor concept, except that this time the length of the fall is identical in both conditions. The difference relates to the climber’s protection strategy. In condition A (Figure 2), the climber ties no knot with the climbing rope, so the latter can run freely at the last anchor and any backup anchors, then she or he moves above the last anchor. In condition B (Figure 2), the climber ties a solid knot at the last anchor, then she or he moves above it. The objective of this exercise is to calculate which of the 2 scenarios is safer. We set in both cases the distance of the climber above the last anchor to 3 m and the distance between the last anchor and the belay on the ground to 15 m. The fall factor in condition A is only 0.33: length of fall of 6 m divided by 18 m of rope which absorbs the energy of the fall, i.e. 3 m of rope between the climber and the last anchor, plus 15 m of rope between the last anchor and the belay. Condition A is thus a safe practice (fall factor < 0 . 5). However, if the tree climber ties a knot at the last anchor as in condition B then she or he moves 3 m above it, the fall factor reaches the maximum, 2: length of fall of 6 m divided by only 3 m of rope absorbing the fall. Only 3 m of rope can absorb the energy of the fall in condition B because the climber has tied a knot at the last anchor; indeed, the 15 m of rope below the last anchor is useless. Condition B is thus an extremely dangerous practice (fall factor > 1 . 5). When applied to tree climbing, the dynamic belaying and fall factor concepts urge tree climbers to let the rope running freely over branches or branch junctions, i.e., no knot using the climbing rope should be tied at these points. When the dynamic belaying principle is applied (Figure 2) and complemented with autoanchoring (Figure 1e), climbing above the last anchor is relatively safe though we recommend that apprentice climbers get experience below the last anchor before attempting an ascent above the last anchor. Appendix II presents the variation of the fall factor in 28 individual trees which were climbed during a 1-yr primate field study in Kibale. It illustrates how the fall factor varies as a function of the climber’s height above the last anchor and the amount of rope available to absorb a potential fall. All climbing conditions involved a fall factor lower than < 1, and were strictly complemented with autoanchoring. When trees are split as small versus emergent, small trees, with a mean fall factor of 0.48, were marginally more dangerous to climb than emergent trees, with a mean fall factor of 0.35 (Mann-Whitney, U = 53.0, p = 0.08). This is best explained by the shorter rope available to absorb a fall in small trees. Another strategy in tree climbing related to dynamic belaying is to increase shock absorption via a dynamic climbing rope versus a static climbing rope. A dynamic rope offers greater elasticity than a static rope. We recommend that inexperienced tree climbers use a dynamic rope. The rope is may be the most important piece of equipment related to the climber’s safety. Modern climbing ropes are composed of a core of braided or parallel nylon filaments encased in a smooth, woven sheath of nylon (Cox and Fulsaas, 2003). Kernmantle ropes are now the only climbing ropes approved by the UIAA. There are two kinds of climbing ropes: dynamic and static. For the same diameter, the dynamic rope offers more elasticity than a static rope and hence can endure higher impacts. Tree climbing rarely involves major falls, but the possibility is real, mostly when the climber moves horizontally in the tree or higher than the last anchor (Figure 2). The pro- tective sheath of a static rope is more abrasion resistant than the sheath of a dynamic rope, and therefore is more appropriate for primate field research. However, a static rope cannot endure severe falls and only experienced tree climbers should consider its purchase. Another factor to consider is the rope diameter. The larger the diameter of a rope, the greater is its energy- absorbing capacity. Descending gear requires a minimum diameter of 10 mm. It is also important to consider whether the rope will be used in a wet en- vironment. Wet ropes become difficult to manage, check fewer falls, and have ca. 30% less strength when they are wet (Cox and Fulsaas, 2003). Overall, we recommend that inexperienced tree climbers purchase a dynamic UIAA-approved 11 mm climbing rope, ideally water-repellent. For the advanced climber, a static 10 mm rope coupled with an explosive quickdraw—a kind a shock-absorbing device attached at the belay—is more appropriate: cheaper, long-lasting sheath, less annoying elasticity while ascending, and lighter. Stepping on a rope is a common form of abusive treatment that grinds cutting particles into and through the sheath (Cox and Fulsaas, 2003). Over time, the particles act like small knives that slice the rope’s nylon filaments. It is hard to decide when to retire a rope. Its condition depends on many factors including frequency of use, the care it has received, its age, and the number of falls it has endured. As a general guideline, a dynamic rope used daily should be retired within a year, while a rope used 2–3 days per week should offer about 2 years of service (Cox and Fulsaas, 2003). A static rope can last twice the time of a ...
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... much damage could be done to trees accessed with the climbing spurs, we noted whether spur holes were later infested by insects, losing sap, par- asitized by mushrooms, or whether bark formed again and recovered the original hole. For the 26 species of trees monitored, 20 exhibited no sign of insect or mushroom invasion and were not bleeding. Since local employment is a critical issue for conservation, we recommend that primate researchers hire local climbers who master the use of spurs to climb trees (contra Moffett and Lowman, 1995) but only on those trees that are known not to be spur- sensitive. How dangerous is tree climbing? For the Single Rope Technique, one way to answer this question is to consider whether the tree climber is located above or below the last anchor. An anchor is a support over which the climbing rope is free to move, like a branch in a tree. The last anchor is the highest point of support over which the rope has been passed. When the climber is located below the last anchor, the risk of falling is practically nil because there is no slack in the rope: the latter is attached on the ground at the belay, goes up until it passes over the branch and comes back down to the climber. However, when the climber moves above the last anchor, the risk of falling is real, because loose rope accumulates between the climber and the last point of support, i.e., the last anchor. In such a case, the length of the fall is twice the distance between the climber and the last anchor, a kind of pendulum effect. Therefore, the risk of collecting data in a tree largely depends on whether the climber must work above or below the last anchor. In any tree, a risky solution for the climber is obviously to set the last anchor over a branch located in the lowest part of a tree crown, forcing the climber to work above the last anchor, with a constant risk of falling. The safest strategy is to position the climbing rope over the highest solid branch in the tree. Then, the climber can work most of the time below the last anchor, thus minimizing the risk of falling. Sometimes it is not possible to work below the last anchor because of tree structure, or because the highest part of the canopy must be accessed for scientific purposes, such as collecting food for nutritional analyses. Two strategies for the experienced climber can be used to minimize the risks related to gathering data above the last anchor: autoanchoring and dynamic belaying (Cox and Fulsaas, 2003). Autoanchoring is attaching oneself with a second set of climbing gear once positioned above the last anchor (Figure 1e). A shock-absorbing device like a daisy chain (Figure 1e) is recommended for autoanchoring. The expression dynamic belaying refers to the way the energy is absorbed during a fall. In dynamic belaying, the energy of the fall, instead of being absorbed in a small fraction of a second as during static belaying, is spread out and absorbed during a longer period of time, thus substantially increasing the climber’s safety. To understand how the notion of dynamic belaying applies to tree climbing, one can consider the fall factor (Cox and Fulsaas, 2003). Understanding the fall factor is critical if and only if the climber decides to move higher than the last anchor. It does not apply when the climber stays below that anchor. It is a dimensionless number that varies from 0 to 2, and is defined as the distance of the fall, divided by the length of the rope which absorbs the fall. Thus, a 5-m fall absorbed by 50 m of climbing rope results in a fall factor of 0.1 (5 divided by 50 = 0 . 1). The same fall factor value is obtained for a fall of 2 m if the rope which absorbs the energy of the fall is 20 m long (2 / 20 = 0 . 1). The resultant forces are the same because the energy of the longer fall is absorbed by a proportionally longer rope (Cox and Fulsaas, 2003). A fall factor < 0 . 5 is considered by experienced climbers to be safe, between 0.5 and 1.0 is risky, between 1.0 and 1.5 is dangerous, and between 1.5 and 2.0 is extremely dangerous. Extreme danger includes the real possibility that the weakest link in the safety system might break. Even if it does not, the climber can incur severe injuries, notably to the vertebral column. Paradoxically, a longer fall might be safer than a shorter fall. For instance, a free fall of 20 m absorbed by 50 m of rope in an emergent tree is safer for the climber than a free fall of only 2 m but absorbed by 1 m of rope in a small tree (fall factor of 0.4 versus 2, respectively). Although the fall factor assessments are arbitrary, they offer a rough safety guide. A safe climber not only considers the fall factor theory but also puts it in practice while in the tree. Figure 2 presents 2 additional scenarios to illustrate the importance of the fall factor concept, except that this time the length of the fall is identical in both conditions. The difference relates to the climber’s protection strategy. In condition A (Figure 2), the climber ties no knot with the climbing rope, so the latter can run freely at the last anchor and any backup anchors, then she or he moves above the last anchor. In condition B (Figure 2), the climber ties a solid knot at the last anchor, then she or he moves above it. The objective of this exercise is to calculate which of the 2 scenarios is safer. We set in both cases the distance of the climber above the last anchor to 3 m and the distance between the last anchor and the belay on the ground to 15 m. The fall factor in condition A is only 0.33: length of fall of 6 m divided by 18 m of rope which absorbs the energy of the fall, i.e. 3 m of rope between the climber and the last anchor, plus 15 m of rope between the last anchor and the belay. Condition A is thus a safe practice (fall factor < 0 . 5). However, if the tree climber ties a knot at the last anchor as in condition B then she or he moves 3 m above it, the fall factor reaches the maximum, 2: length of fall of 6 m divided by only 3 m of rope absorbing the fall. Only 3 m of rope can absorb the energy of the fall in condition B because the climber has tied a knot at the last anchor; indeed, the 15 m of rope below the last anchor is useless. Condition B is thus an extremely dangerous practice (fall factor > 1 . 5). When applied to tree climbing, the dynamic belaying and fall factor concepts urge tree climbers to let the rope running freely over branches or branch junctions, i.e., no knot using the climbing rope should be tied at these points. When the dynamic belaying principle is applied (Figure 2) and complemented with autoanchoring (Figure 1e), climbing above the last anchor is relatively safe though we recommend that apprentice climbers get experience below the last anchor before attempting an ascent above the last anchor. Appendix II presents the variation of the fall factor in 28 individual trees which were climbed during a 1-yr primate field study in Kibale. It illustrates how the fall factor varies as a function of the climber’s height above the last anchor and the amount of rope available to absorb a potential fall. All climbing conditions involved a fall factor lower than < 1, and were strictly complemented with autoanchoring. When trees are split as small versus emergent, small trees, with a mean fall factor of 0.48, were marginally more dangerous to climb than emergent trees, with a mean fall factor of 0.35 (Mann-Whitney, U = 53.0, p = 0.08). This is best explained by the shorter rope available to absorb a fall in small trees. Another strategy in tree climbing related to dynamic belaying is to increase shock absorption via a dynamic climbing rope versus a static climbing rope. A dynamic rope offers greater elasticity than a static rope. We recommend that inexperienced tree climbers use a dynamic rope. The rope is may be the most important piece of equipment related to the climber’s safety. Modern climbing ropes are composed of a core of braided or parallel nylon filaments encased in a smooth, woven sheath of nylon (Cox and Fulsaas, 2003). Kernmantle ropes are now the only climbing ropes approved by the UIAA. There are two kinds of climbing ropes: dynamic and static. For the same diameter, the dynamic rope offers more elasticity than a static rope and hence can endure higher impacts. Tree climbing rarely involves major falls, but the possibility is real, mostly when the climber moves horizontally in the tree or higher than the last anchor (Figure 2). The pro- tective sheath of a static rope is more abrasion resistant than the sheath of a dynamic rope, and therefore is more appropriate for primate field research. However, a static rope cannot endure severe falls and only experienced tree climbers should consider its purchase. Another factor to consider is the rope diameter. The larger the diameter of a rope, the greater is its energy- absorbing capacity. Descending gear requires a minimum diameter of 10 mm. It is also important to consider whether the rope will be used in a wet en- vironment. Wet ropes become difficult to manage, check fewer falls, and have ca. 30% less strength when they are wet (Cox and Fulsaas, 2003). Overall, we recommend that inexperienced tree climbers purchase a dynamic UIAA-approved 11 mm climbing rope, ideally water-repellent. For the advanced climber, a static 10 mm rope coupled with an explosive quickdraw—a kind a shock-absorbing device attached at the belay—is more appropriate: cheaper, long-lasting sheath, less annoying elasticity while ascending, and lighter. Stepping on a rope is a common form of abusive treatment that grinds cutting particles into and through the sheath (Cox and Fulsaas, 2003). Over time, the particles act like small knives that slice the rope’s nylon filaments. It is hard to decide when to retire a rope. Its condition depends on many factors including frequency of use, the care it has received, its age, and the number of falls it has endured. As a general guideline, a dynamic ...
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... absorbs the fall. Thus, a 5-m fall absorbed by 50 m of climbing rope results in a fall factor of 0.1 (5 divided by 50 = 0 . 1). The same fall factor value is obtained for a fall of 2 m if the rope which absorbs the energy of the fall is 20 m long (2 / 20 = 0 . 1). The resultant forces are the same because the energy of the longer fall is absorbed by a proportionally longer rope (Cox and Fulsaas, 2003). A fall factor < 0 . 5 is considered by experienced climbers to be safe, between 0.5 and 1.0 is risky, between 1.0 and 1.5 is dangerous, and between 1.5 and 2.0 is extremely dangerous. Extreme danger includes the real possibility that the weakest link in the safety system might break. Even if it does not, the climber can incur severe injuries, notably to the vertebral column. Paradoxically, a longer fall might be safer than a shorter fall. For instance, a free fall of 20 m absorbed by 50 m of rope in an emergent tree is safer for the climber than a free fall of only 2 m but absorbed by 1 m of rope in a small tree (fall factor of 0.4 versus 2, respectively). Although the fall factor assessments are arbitrary, they offer a rough safety guide. A safe climber not only considers the fall factor theory but also puts it in practice while in the tree. Figure 2 presents 2 additional scenarios to illustrate the importance of the fall factor concept, except that this time the length of the fall is identical in both conditions. The difference relates to the climber’s protection strategy. In condition A (Figure 2), the climber ties no knot with the climbing rope, so the latter can run freely at the last anchor and any backup anchors, then she or he moves above the last anchor. In condition B (Figure 2), the climber ties a solid knot at the last anchor, then she or he moves above it. The objective of this exercise is to calculate which of the 2 scenarios is safer. We set in both cases the distance of the climber above the last anchor to 3 m and the distance between the last anchor and the belay on the ground to 15 m. The fall factor in condition A is only 0.33: length of fall of 6 m divided by 18 m of rope which absorbs the energy of the fall, i.e. 3 m of rope between the climber and the last anchor, plus 15 m of rope between the last anchor and the belay. Condition A is thus a safe practice (fall factor < 0 . 5). However, if the tree climber ties a knot at the last anchor as in condition B then she or he moves 3 m above it, the fall factor reaches the maximum, 2: length of fall of 6 m divided by only 3 m of rope absorbing the fall. Only 3 m of rope can absorb the energy of the fall in condition B because the climber has tied a knot at the last anchor; indeed, the 15 m of rope below the last anchor is useless. Condition B is thus an extremely dangerous practice (fall factor > 1 . 5). When applied to tree climbing, the dynamic belaying and fall factor concepts urge tree climbers to let the rope running freely over branches or branch junctions, i.e., no knot using the climbing rope should be tied at these points. When the dynamic belaying principle is applied (Figure 2) and complemented with autoanchoring (Figure 1e), climbing above the last anchor is relatively safe though we recommend that apprentice climbers get experience below the last anchor before attempting an ascent above the last anchor. Appendix II presents the variation of the fall factor in 28 individual trees which were climbed during a 1-yr primate field study in Kibale. It illustrates how the fall factor varies as a function of the climber’s height above the last anchor and the amount of rope available to absorb a potential fall. All climbing conditions involved a fall factor lower than < 1, and were strictly complemented with autoanchoring. When trees are split as small versus emergent, small trees, with a mean fall factor of 0.48, were marginally more dangerous to climb than emergent trees, with a mean fall factor of 0.35 (Mann-Whitney, U = 53.0, p = 0.08). This is best explained by the shorter rope available to absorb a fall in small trees. Another strategy in tree climbing related to dynamic belaying is to increase shock absorption via a dynamic climbing rope versus a static climbing rope. A dynamic rope offers greater elasticity than a static rope. We recommend that inexperienced tree climbers use a dynamic rope. The rope is may be the most important piece of equipment related to the climber’s safety. Modern climbing ropes are composed of a core of braided or parallel nylon filaments encased in a smooth, woven sheath of nylon (Cox and Fulsaas, 2003). Kernmantle ropes are now the only climbing ropes approved by the UIAA. There are two kinds of climbing ropes: dynamic and static. For the same diameter, the dynamic rope offers more elasticity than a static rope and hence can endure higher impacts. Tree climbing rarely involves major falls, but the possibility is real, mostly when the climber moves horizontally in the tree or higher than the last anchor (Figure 2). The pro- tective sheath of a static rope is more abrasion resistant than the sheath of a dynamic rope, and therefore is more appropriate for primate field research. However, a static rope cannot endure severe falls and only experienced tree climbers should consider its purchase. Another factor to consider is the rope diameter. The larger the diameter of a rope, the greater is its energy- absorbing capacity. Descending gear requires a minimum diameter of 10 mm. It is also important to consider whether the rope will be used in a wet en- vironment. Wet ropes become difficult to manage, check fewer falls, and have ca. 30% less strength when they are wet (Cox and Fulsaas, 2003). Overall, we recommend that inexperienced tree climbers purchase a dynamic UIAA-approved 11 mm climbing rope, ideally water-repellent. For the advanced climber, a static 10 mm rope coupled with an explosive quickdraw—a kind a shock-absorbing device attached at the belay—is more appropriate: cheaper, long-lasting sheath, less annoying elasticity while ascending, and lighter. Stepping on a rope is a common form of abusive treatment that grinds cutting particles into and through the sheath (Cox and Fulsaas, 2003). Over time, the particles act like small knives that slice the rope’s nylon filaments. It is hard to decide when to retire a rope. Its condition depends on many factors including frequency of use, the care it has received, its age, and the number of falls it has endured. As a general guideline, a dynamic rope used daily should be retired within a year, while a rope used 2–3 days per week should offer about 2 years of service (Cox and Fulsaas, 2003). A static rope can last twice the time of a dynamic rope. After one very severe fall with fall factor 1.5, any rope should be replaced immediately. The climbing rope is the most important and sensitive equipment, and a safe climber takes great care of it. Knots allow the climber to use the rope for many special purposes: to tie into the rope, to temporarily anchor to a branch, to tie 2 ropes together, to use slings to climb the rope itself, and much more. Climbers rely most heavily on 12 different knots (Cox and Fulsaas, 2003; Vines and Hudson, 1992). A tree climber should practice them until tying them is second nature, including in the dark at cold temperatures. The novice climber should master at least, eyes closed, the following set of tested knots: Figure 8 Follow-through (also called the Flemish Bend), Figure 8 on a Bight, Double or Triple Fisherman’s Knot (also called Grapevine), and one self-rescue knot like the Prusik or Bachman or Klemheist Knot. For intermediate and advanced climbers, there are the Butterfly Knot, Equalizing Figure 8, Water Knot (Ring Bend), Girth Hitch, Stopper Knot, Munter Hitch or Clove Hitch, and for rescuing an injured colleague, the Munter Mule. Contrary to common belief, knots are weaker than the rope used to tie them. Moreover, they do not all offer the same strength. In case of a sudden shock, any chain of safety will break up at the weakest link, most often at the weakest knot. The different types of Figure 8 Knots are known to break at 75–80% of rope strength, the Double Fisherman’s Knot at 65– 70%, Water Knot at 60–70%, Overhand Knot and Clove Hitch at 60–65%, and the Square Fisherman’s Knot at a very poor 45% (Luebben, 1993). An 11-mm climbing rope can support 3,000 kg. In this case, if the weakest link is a Square Fisherman’s Knot, then the rope theoretically can break up at 1,300 kg of pressure (45% of 3,000). Regardless of the knot, one should tie it neatly, keeping the separate strands of the knot parallel and free of twists. Figures 1a to 1g present the most important gear necessary to climb trees with the Single Rope Technique. With properly fitted leg loops, the seat harness transfers the force of a fall over the entire pelvis (Cox and Fulsaas, 2003). Hardware loops are desirable to carry descending gear, carabiners, runners of different length, binoculars, field book and other equipment. A chest harness is needed for additional comfort and additional safety. One mechanical ascender—the handle or the Jumar TM (Figures 1a and 1b)—is locked to the seat harness through a runner. A second mechanical ascender— the chest ascender or the Croll TM (Figures 1a to 1b)—is independently locked to the chest harness. Once in the tree crown, the climber uses a daisy chain (Figure 1e) to autoanchor to a branch or a branch junction, independently of the climbing rope. Very short runners or quickdraws like the one on the right of Figure 1g have little value in tree climbing, except for the rappelling system (Fig. 1c and 1d). One should purchase long or very long webbings (120 cm in length), because the climber is often far from suitable branches. Carabiners are another versatile and indispensable tree climbing tool. These ingenious snap-links are used for belaying, rappelling, prusiking, clipping to safety anchors like branches, securing the ...
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... Over three breeding seasons from 2014 to 2016, we located and monitored 45 Northern Mealy Amazon nests to obtain reproductive parameters and determine nest success. As nests were located in cavities high-up tall trees (De Labra-Hernández and Renton, 2016), we used single-rope ascending techniques (Perry and Williams, 1981;Houle et al., 2004) to determine nest contents. Where possible, each nest was visited weekly to obtain reproductive parameters of clutch size, hatching success, number of hatchlings, and nestling survival to 50 days of age when nestlings were fully-feathered and close to fledging. ...
Anthropogenic activities are the major drivers of biodiversity loss, and human pressure of capture for trade is closely associated with decreasing population trends of Psittaciformes. We evaluated reproductive output and daily survival rate of 45 nests of the threatened Northern Mealy Amazon (Amazona guatemalae) in tropical moist forest of southern Mexico to determine the influence of anthropogenic and natural factors on nest survival. We applied GLMM to determine which variables, at three scales of: nest-site; habitat; and landscape level, influenced daily survival of nests when failure was due to anthropogenic factors or animal predation. Northern Mealy Amazons had a high 74 % loss of initial reproductive investment of 2.6 ± 0.6 eggs/female, resulting in a low reproductive output of 0.6 ± 1.1 nestlings >50 days old/female, mainly due to human poaching of nests. GLMM determined that human impacts on nest survival were influenced by the landscape feature of distance from the nearest village, with nests located >2.3 km from a human settlement having greater probability of survival. However, the risk of animal predation of nests was influenced by nest-site features, with higher, smaller, and deeper nest-cavities having increased daily survival. Our results suggest that while parrots may have evolved nest-site selection criteria to reduce the risks of animal predation, these may have less influence over survival when faced with anthropogenic threats. The increasing human pressures on wild populations require landscape level and socially-focused conservation strategies for threatened species.
... The use of tree-climbing techniques can both: (1) double the costs associated with any ecological study using arboreal equipment -given that this method requires complex logistics to transport the equipment and human-resource climbing training (Haysom et al. 2021) -and (2) increase of potential risks to people associated with climbing trees, especially in remote tracks of forest remnants . Furthermore, even after all these efforts, this method still requires several hours whereby the equipment is placed in the correct position for the arboreal biomonitoring (Houle et al. 2004;Bowler et al. 2017). An alternative that has been used to deal with the problems of accessing forest canopies has been the use of folding ladders, but this technique also represents many difficulties in terms of fieldwork logistics and transport, failing to access the forest canopy embracing tall trees (40-50 m) (Zhu et al. 2021). ...
Recent studies in forest canopies have revealed new findings on species interactions and diversity; hitherto poorly understood. This glaring gap results from the challenges of recording arboreal and scansorial species and their interactions in the vertical strata. We present a new methodology that allows installing camera-traps at multiple forest strata to detect species and record ecological interactions. We have developed wooden support to place the environmental monitoring equipment at the forest canopy, evaluating and testing its cost-effectiveness by monitoring six fruiting plant species across a triple ecotone of the Cerrado, Amazon, and Pantanal biomes. Our structure to install camera-traps in the forest canopy had a total cost of US 1,248.00. After 11 months of using camera-traps coupled with our wood structure, we recorded 137 mammal-plant interaction events and identified 11 mammal species. Our approach recorded 47.8% of mammal species that potentially can both occur in the area and use the forest canopy. Our findings indicate that our approach to documenting arboreal ecological dynamics is both efficient and innovative, offering researchers a cost-effective tool for future studies in several vegetation types.
... Standardized monitoring strategies are often recommended to generate the data necessary to evaluate changes in richness, abundance, and distribution of species, to increase the explanatory power of ecological drivers and threats, and to develop conservation strategies [4,5]. Standardized sampling techniques are used in many different fields, including canopy biology [6,7], entomology [8], mycology [9], ornithology [10], mammalogy [11,12], and parasitology [13]. However, an underlying assumption of all these standardized survey methods is that they provide comparable results in all ecosystems. ...
Standardized monitoring strategies are often used to study spatial and temporal ecological patterns and trends. Such approaches are applied for many study taxa, including bats (Mammalia, Chiroptera). However, local characteristics of individual field sites, including species assemblages, terrain, climatic factors, and presence or lack of landscape features, may affect the efficacy of these standardized surveys. In this paper, we completed mist-netting surveys for bats in two widely separated field sites, Calakmul Biosphere Reserve (CBR), a Mexican lowland tropical forest, and Krka National Park (KNP), a Mediterranean dry scrub forest in Croatia. Standardized surveys were conducted along predefined transects for six hours. We also completed targeted surveys in KNP that focused on the key bat activity period (the first two to three hours after sunset), with nets being deployed at sites of known or assumed value to bats (independent of predefined transects). We analyzed how survey success differed in standardized surveys between CBR and KNP and between standardized and targeted surveys in KNP. Survey success was measured through three parameters: capture rate = the number of individual bats captured per net hour, inventory rate = the number of unique bat species recorded per net hour, and inventory efficacy = the percentage of known species assemblage recorded per net hour across all surveys. Results for all three parameters indicate that standardized surveys in CBR were vastly more effective than those in KNP (e.g., mist-netting in CBR detected 69.8% of the species assemblage, compared to just 8.3% in KNP), and it was only by employing targeted mist-netting in KNP that meaningful capture rates could be achieved. This study contributes further evidence to discussions around how and when standardized survey methods should be employed, and the alternative approaches that can be taken in ecosystems where generally effective methods underperform.
... The first using tree climbing equipment to reach it, the second option is the use of a slingshot with a rope to gently shake the branch. In all circumstances a safety net (5 m × 5 m) must be positioned and held under the individual, to soften its fall and avoid it hitting the ground (Houle et al. 2004). Once the animal is in the safety net, the area should be set up for sample collection. ...
Restraint and threat of predation are possibly the most stressful events in wild animals' lives. Management techniques should, therefore, be improved to avoid or minimize suffering in such situations. Body mass and variation in behavior influence the techniques used during containment. Automatic traps are mostly used for small primates living in the lower canopy, while remotely delivered chemical immobilization is the recommended technique for larger primates, which live in the upper canopy. For both methods, careful physical restraint after the capture of the animal is essential. The use of equipment and materials that ensure biosecurity is imperative, as is choosing the most appropriate location for the collection of biological samples. Storage and transport must also be carried out in an adequate manner so as not to impair the samples. Here, therefore, we seek to describe capture, containment, and biological sample collection techniques with the intention of minimizing risks and increase success in the capture of Neotropical primates.
... In the case of multiple nests per tree, crown, height, and bearing from the tree trunk were recorded, and biodegradable tape with the name of the nest constructor was placed underneath each nest to avoid misidentification. Hair collection was carried out by V.M.O. and R. Martin Fernandez the following day(s) using rope-based tree access techniques (Houle et al., 2004;Anderson et al., 2015). From each nest, >20 hairs were collected for stable isotope analysis. ...
The roots of human hunting and meat eating lie deep in our evolutionary past shared with chimpanzees (Pan troglodytes). From the few habituated wild populations, we know that there is considerable variation in the extent to which chimpanzees consume meat. Expanding our knowledge of meat eating frequencies to more, yet unhabituated, populations requires noninvasive, indirect quantitative techniques. We here evaluate the use of stable isotopes to reconstruct meat-eating behavior in wild chimpanzees. We present hair isotope data (n = 260) of two western chimpanzee (P. troglodytes verus) groups from Taï forest (Côte d’Ivoire) and relate them to directly observed amounts of meat consumed, sex/female reproductive state, and group, while controlling for differences between individuals, seasons, and observation efforts. Succeeding seven months of hunting observations, we collected hair of 25 individuals for sequential analysis of δ¹⁵N and δ¹³C. Hunting success in the 7-month study period varied between the groups, with 25 successful hunts in the East group and only 8 in the North group. However, our models only found a direct relationship between amounts of meat consumed and variation within individual hair δ¹⁵N values in the East group, but not in the North group and not when comparing between individuals or groups. Although on average East group individuals consumed more than double the amount of meat than North group individuals, their δ¹⁵N values were significantly lower, suggesting that differences in microhabitat are substantial between group territories. The effect of sex/female reproductive state was significant in δ¹⁵N and δ¹³C, suggesting it related to access to food or feeding preferences. We conclude that several factors additional to diet are influencing and thus obscuring the isotope ratios in wild chimpanzee hair, particularly when comparing between sexes and social groups.
... We also recorded defecation microsites of non-radio-tagged binturongs at their feeding and sleeping sites. We used the single-rope technique to access the defecation sites in the canopy [36]. The microsites were classified into five categories: tree fork, branch, epiphytic mat, foliage, and forest floor. ...
Ficus species are keystone plants in tropical rainforests, and hemi-epiphytic figs play a notably important role in forest ecosystems. Because hemi-epiphytic figs have strict germination requirements, germination and establishment stages regulate their populations. Despite the ecological importance of hemi-epiphytic figs in the rainforests, seed dispersal systems by fig-eating animals under natural conditions remain unknown because of the difficulty in tracing the destiny of dispersed seeds in the canopy. Therefore, seed dispersal effectiveness (SDE) has never been evaluated for hemi-epiphytic figs. We evaluated the SDE of hemi-epiphytic figs using qualitative and quantitative components by three relatively large-sized (> 3 kg) arboreal and volant animals in Bornean rainforests that largely depend on fig fruits in their diets: binturongs Arctictis binturong, Mueller’s gibbons Hylobates muelleri, and helmeted hornbills Rhinoplax vigil. The SDE values of binturongs was by far the highest among the three study animals. Meanwhile, successful seed dispersal of hemi-epiphytic figs by gibbons and helmeted hornbills is aleatory and rare. Given that seed deposition determines the fate of hemi-epiphytic figs, the defecatory habits of binturongs, depositing feces on specific microsites in the canopy, is the most reliable dispersal method, compared to scattering feces from the air or upper canopy. We showed that reliable directed dispersal of hemi-epiphytic figs occurs in high and uneven canopy of Bornean rainforests. This type of dispersal is limited to specific animal species, and therefore it may become one of the main factors regulating low-success hemi-epiphytic fig recruitment in Bornean rainforests.
... Technical tree climbing could enable access to wild nests to directly retrieve hair samples for examining stress history and for genetic analyses. Hair samples from nests could identify reintroduced orangutans, contributing to monitoring their ranging and survival and, as indicated by Houle et al. (2004;p.237), "primate ecological studies can benefit from accessing the canopy to estimate intra-tree and inter-tree variation in food availability and nutrient value, patch and subpatch depletion, foraging efficiency, as well as nest structure and nesting behaviors, parasitic transmission and predator detectability." ...
... Modern tree-climbing methodologies and reliable climbing gear are already available. Using climbing methods derived from those of arborists, rock climbers, and speleologists (Houle et al. 2004) allows for access to the tree canopy for scientific research and data collection (Lowman and Whittman 1996). We have given courses to orangutan caregivers during four trips to Indonesia and Malaysia-early 2016, early 2018, late 2018, and early 2019 (Fig 1). ...
Habitat loss, poaching and the pet trade have resulted in thousands of orangutans being rescued and taken to rehabilitation centers, many of them infant or juvenile orphans. Besides caring for them, the goal of these centers is to train them for release back into the wild, and critical to the success of post-release survival is their competence in moving through the forest canopy. Orphaned orangutans need regular practice at tree-climbing in order to prepare them for their future life in the wild. Training for this is lacking at rehabilitation centers, however, because caregivers engage with the orphaned orangutans largely on the ground. Orangutan rehabilitation can be greatly improved by training orangutan caregivers in a standardized and safe method of tree climbing so that they can encourage and accompany orangutans to spend more time in the trees. Caregivers trained in tree climbing can also help in wild orangutan rescues, in center maintenance and, through arboreal data collection, in scientific research. We discuss the practical solution of implementing a standardized tree climbing method to orangutan caregivers. Professional climbers have volunteered with the nonprofit Tree Monkey Project to teach orangutan caregivers in Bornean Indonesia and Malaysia. The tree-climbing training program has been successful in allowing caregivers to climb trees alongside orphaned orangutans, encouraging the orangutans to increase the time they spend in the trees and allowing them to hone their agility and skills in moving about in them.
... We climbed fruiting fig trees, using the single rope technique (Houle et al. 2004), to set 60 × 18 × 18 cm portable Havahart box traps (Woodstream Corp., PA, USA) on the branches. We used ripe bananas or chicken meat as baits. ...
We evaluated short-term movements of three radio-collared binturongs in relation to food distribution in Bornean rainforests, in addition to the basic ecological information on their home-range size and diet. Mean 95% fixed kernel and 95% MCP home-range size were 4.24 ± 0.79 km² and 1.54 ± 0.89 km², respectively (mean ± SD). We recorded 13 fig Ficus species and four non-fig species as their foods. Fig trees accounted for 87.5% of the feeding sites of the three collared binturongs, and 87.9% including uncollared individuals. Our results suggested that binturongs’ short-term movements were strongly affected by food distribution, especially figs. They feed on various fig species and may remember the location and fruiting periods of fig trees. They may use the biggest fig species, F. punctata, as a fallback food when other foods are scarce. Although this is the first systematic study to describe movement and feeding habits of binturongs, further studies are needed to understand their ecology so that proper measures can be designed for their conservation.
... double-rope technique (DRT) (Houle, Chapman, & Vickery, 2004;Stewart et al., 2011). ...
... We located nests of the Northern Mealy Amazon during the months of February to May over four consecutive breeding seasons in 2013 to 2016, by observation of the behavior of nesting pairs, and with the assistance of local guides. We used single-rope tree-ascending techniques (Houle, Chapman, & Vickery, 2004;Perry & Williams, 1981) to confirm nesting activity by the presence of eggs or chicks in the nest and take measurements of the nest cavity. For each nest-tree located, we recorded tree species, diameter at breast height (dbh), condition (live or dead), and GPS location. ...
The increasing conversion of primary tropical moist forest to secondary forest may have consequences for threatened, large-bodied cavity-nesters, such as the Northern Mealy Amazon (Amazona guatemalae). We determined availability and characteristics of tree-cavities in 24 1-ha survey plots in Los Chimalapas, southeast Mexico, with 9 plots in evergreen forest, 7 in riparian, and 8 in secondary forest. We compared these with 40 parrot nest-trees to determine whether parrots select cavities with specific characteristics for nesting. Over half of Northern Mealy Amazon nests occurred in live trees of Terminalia amazonia (32.5%) and Dialium guianense (20%). Compared with available cavities, the Northern Mealy Amazon selected nest-cavities in significantly larger trees, at a greater height above the ground, with larger internal diameter, and greater depth. In particular, internal diameter and cavity depth predicted whether a cavity was selected as a nest-site by parrots. We found a low density of 2.3 available cavities/ha in the study site, although only 1.6 cavities/ha had characteristics suitable for use as nest-sites by parrots. Cavities in secondary forest occurred in smaller trees, at a lower height, and with shallower depth, where only 0.75 cavities/ha were suitable for nesting by parrots. Our results demonstrate that the Northern Mealy Amazon requires nest-cavities in large, old trees able to form large cavities, the majority of which occur in primary forest. The low density of suitable nest-sites for parrots in secondary forest suggests that increased degradation of primary tropical moist forest may have long-term implications for reproduction of this threatened species.