PE EIE[R-Rg RESEARCH ON - HJ Andrews Experimental Forest

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60-80 m tall, 1-1 .5-m dbh, with their lowest branches 12-25 m above the ground . Climbing trees of this height is dangerous . A fall would probably be fatal . But probably there is greater danger of injury to personnel under the tree in the event equipment or part s of branch systems are accidentally dropped upon them . We have worked through two sea - sons without injury . The climbing techniques are described in detail to permit others to adopt them . Th e rock-climbing techniques on which they are based are described in books on mountaineering (Blackshaw 1970 ; Manning 1967) but may be unfamiliar to biologists . The access technique, the methods o f description and measurement, and one application of the data, a diagramatic reconstruction of a tree, are treated in this paper . Another paper in this symposium (Pike et al . 1972) describes the estimation of tree surfac e area and epiphyte biomass . Riggin g Rigging involves an initial ascent and preparation of the tree for subsequent climbing . The ascent is slow, and requires exceptiona l agility and endurance . A team of three experienced climbers should rig the tallest trees i n a day and a half . The procedure used in ascending the tre e and placing climbing and belay ropes is outlined in figures 1-4 . 1 Figure 1 . A lag screw is used to fasten a steel hanger to the tree . The Access Techniques Access to the tree involves three steps : rigging, climbing, and use of the spar, eac h described below. Rigging and climbing techniques are modified from direct-aid rock - climbing techniques . Basic safety procedures , equipment, terminology, and philosophy hav e been adopted from mountaineering . Anyone without prior mountaineering experience who expects to adopt these techniques should consult one of the standard texts (Blackshaw 1970; Manning 1967) . The specialized rope and hardware may be obtained from either mountaineering or yachting suppliers . Basic equipment for all climbers includes : hard hat, heavy climbing shoes, and a harnes s of nylon webbing to which a belay rope i s attached. The climber is always belayed-tha t is, she is protected by a safety rope held b y another experienced climber . Climbing an d belay ropes are 11 mm nylon "goldline" an d the webbing used in making slings, stirrups , etc . is of nylon and 40-50 mm wide . Figure 2 . A carabiner is clipped into the hanger . 148
Figure 3. Two additional carabiners are used to faste n two climbing stirrups to the first carabiner. (Only the upper ends of the webbing stirrups are shown . ) The belay rope is clipped through the carabiner . 5 Figure 4 . The climber ascends the climbing stirrup s until the first carabiner is at her waist . Tension on the belay rope holds her in position while sh e drives the next lag screw . 6 Figure 5 . The climbing rope is fastened to the tree b y four lag screws, hangers, and carabiners . A loop, Figure 6 . The belay rope runs through a block hun g tied near the end of the rope, is connected to the by heavy chain with welded links. The chain i s carabiners by two loops of webbing. The free end fastened around the tree above a limb and secure d of the rope is tied around the tree using a bowline . by two 1-cm bolts with washers and lock nuts . 149
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PE EIE[R-Rg RESEARC H O N CONIFEROU
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Research on Coniferous Forest Ecosy
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Contents SOME BROADER VIEWS OF BIOM
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Page AQUATIC PROCESS STUDIES 279 St
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Proceedings-Research on Coniferous
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directly, to solution of major natu
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4. Nutritional adaptation to enviro
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where validation studies could be c
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have been developed . Prior to thei
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of gross production and respiration
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Figure 1 . Aerial photo of Findley
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Nutrient levels in stream and lake
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Acknowledgments The work reported i
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inputs into the lakes . Recent stud
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was slightly raised in 1902, the la
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climate, surrounding terrestrial en
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more similar than between the diffe
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The net rate of primary production
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community structure and energy flo
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est adapted organism vacillates bet
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U .S . Analysis of Ecosystems, Inte
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successful . Thus we can see modeli
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of the external quantities of S wou
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Figure 2 . The major subsystems of
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subsystems as objects . In addition
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several models together to form the
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The study areas are located at seve
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K m Figure 1 . Watershed 2, H . J.
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An alternative way of considering i
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Snowmelt A flow chart of the snow a
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d Gs Gr = (1 - Ki) d t By integrati
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Calibration of Parameter s In gener
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model being developed under the Con
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Usually, we are interested in the o
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LINEAR Y~(T) 2nd ORDER Y2 (T) 3rd O
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the watershed. The hydrologic model
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considered as part of another food
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PRIMARY PRRODUCTIO N ■ FOLIAGE CO
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Graham, S. A. 1952. Forest entomolo
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ful in regions with relatively unif
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epresents the basic linkages betwee
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Cleary and Waring 1969, Reed 1971,
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vation that species such as Brewer
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Table 3.-Predicted plant response i
Page 93 and 94: Walker, Reed, Scott, and Webb are c
Page 95 and 96: Water and Nutrien t Movement Throug
Page 97 and 98: Here v is the volume of water cross
Page 99 and 100: 2 10 7100 .160 .220 .280 .340 .400
Page 101 and 102: .0500 .040 0 z .030 0 E L.) 0 .020
Page 103 and 104: Proceedings-Research on Coniferous
Page 105 and 106: ment of the flux of ions through th
Page 107 and 108: Table 2 .-Forest floor composition
Page 109 and 110: Table 5 .-Monthly amounts of litter
Page 111 and 112: Figure 2 illustrates how CO 2 produ
Page 113 and 114: Ballard, T. M. 1968 . Carbon dioxid
Page 115 and 116: 2. How effectively are these chemic
Page 117 and 118: Table 2 .-Nutrient budget for disso
Page 119 and 120: Figure 1 . Water content of the sur
Page 121 and 122: 0.12_ _30 rn z 0 Q z w 0 z 0 0 z Q
Page 123 and 124: _3 0 . Outflow Concentration _ __ R
Page 125 and 126: 0.10_ 0.08 _ Pea k 0.04_ Concentrat
Page 127 and 128: 8J Calciu m 0 I I I I 0.25 0.50 0.7
Page 129 and 130: water is dominant because flowing w
Page 133 and 134: Table 1.-Characteristics of study p
Page 135 and 136: Z w 2 w J w 3 0 Table 2. Average to
Page 137 and 138: of the nitrogen was not determined.
Page 139 and 140: Table 6. Total kg per hectare per y
Page 141 and 142: through litterfall . More amounts o
Page 143: Proceedings-Research on Coniferous
Page 147 and 148: 1 1 Figure 11 . The climber places
Page 149 and 150: Figure 16. The spar in use. The sus
Page 151 and 152: in our example) and the running tot
Page 153 and 154: Dashed lines are dead branches . Th
Page 157 and 158: Table 1.-Transpiration rates, mean
Page 159 and 160: this case the slopes of activity-ti
Page 161 and 162: solve equation 2 for Tm since the f
Page 165 and 166: ing methods . Every point in the sa
Page 167 and 168: Patterns in Point Displacemen t Mea
Page 169 and 170: trees indicates that the coordinate
Page 171 and 172: data; there is no obvious explanati
Page 175 and 176: where C is the percentage cover by
Page 177 and 178: Table 1.-Epiphyte biomass on the tr
Page 179 and 180: NZ. 4 50 100 150 EPIPHYTE IMPORTANC
Page 181 and 182: Table 4.-Biomass estimates (kg) for
Page 183 and 184: watershed 10 (C . T. Dyrness, perso
Page 185 and 186: Table 1 .-Some population character
Page 187 and 188: Table 2 .-Annual litter fall in Col
Page 189 and 190: Table 4. Biomass and growth increme
Page 191 and 192: Table 6.-Annual turnover from certa
Page 193 and 194: Kiil, A. D. 1968. Weight of the fue
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condition differ) ; the turnover ra
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proportionally about the same for e
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Bird Studies The forest birds were
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Further Studies The data provided f
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Terrestrial Process Studies 209
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from theses. The principal processe
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Table 1 .-Saturating light intensit
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at least 0 .06 percent CO 2 . Howev
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Pharis et al. 1967). Again Helms (1
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Effects of Leaf Temperature an d Le
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Literature Cited Baule, H., and C.
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Lopushinsky, W . 1969. Stomatal clo
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Von Bertalanffy (1969) calls nonsum
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which may be of importance in model
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The first three terms of equation 1
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P = F+ R where F = net assimilation
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This function is asymptotic to zero
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The important interaction between l
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(3 = H/AE=yo$/De (3 ) where y is th
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0.4 0.2 v 0 0 w IX -0.2 I- cr -0.4
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Table L-Diurnal energy budget compo
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4 8 10 12 14 16 18 20 22 24 TIME, H
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1970. Evapotranspiration an d meteo
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may bias the results . Meteorologic
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7.4 ppm . The lysimeters at Coshoct
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Acknowledgments The work reported i
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extracted was determined by the wei
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I - 5 -l o -1 5 HPV 1 10 . 0 I . 6
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Table 1 .- Tukey's w Multiple Compa
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studies in conifers-a review . In J
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permeable to both CO 2 and water va
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insolation (1 cal cm 2 min-1 ) and
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Aquatic Process Studies 279
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stream environments (Krygier and Ha
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S, - 4ydrolo9i c S2 = I¢rr¢strIa
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ingestion variation between individ
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contribute to detrital compartment
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volume measurement, realizing that
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fer of the indicated carbon-14 trac
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18L LAKE WATER LIGH T 50m1 HOURLY D
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a function of time and space, (b) c
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Table 1.-Suggested criteria for jud
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Table 4.-Average C, N, and P conten
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during 1963 to 1967 and from Lake S
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greater than 7 .2:1 (16:1 by atoms)
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2 .0 1 .0 0 Si P-N N-Si P-Si P-N-Si
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detectable increase in concentratio
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in lakes . J. Ecol . 29 : 280-329 .
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Woodey 1970 ; Thorne, Reeves, and M
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targets are insonified several time
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This program will automatically cal
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The FOREST SERVICE et ; U :' S D pa
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