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RYAN, B.F., JOtNER, B.L., and RYAN, T.A., Jr. t992. Minitab Handbook. Second edition. Boston: PWS-KENT Publ. Comp. SCHOENEWEISS, D.F. t986. Water stress predisposition to disease - an overview, p. 157-174. In Ayres, EG. and Boddy, L., eds. Water, fungi and plants. Cambridge University Press. SCHROEDER, M. 1990. Duct resin flow in Scots pine in relation to attack of the bark beetle, Tomicus piniperda (L.) (Col., Scolytidae). J. Appl. Ent. 109:t05-112. SOLHEIM, H. 1986. Species of Ophiostornataceae isolated from Picea abies infested by the bark beetle, Ips O'pographus. Nord. J. Bot. 6: 19%207. SOLHEIM, H. 1988. Pathogenicity of some Ips 07)ographt_s-associated blue-stain fungi to Norway spruce. Medd. Nor. inst. skogforsk. 40(14): 1-11. SOLHEIM, H. t992. The early stages of fungal invasion in Norway spruce infested by the bark beetle, Ips O'pographus. Can. J. Bot. 70: 1-5. THALENHORST, W. t958. Grundztige der Populationdynamik desgrossen Fichtenborkenk_ifers Ips typographus L. SchrReiheforstl. Fak. Univ. G6ttingen 21: 1-126. 199
A[ PROACHES TO STUDYING ENVIRONMENTAL EFFECTS ON RESISTANCE OF PINUS 7AEDA L. TO DENDROCTONUS FRONTALIS Z IMM.ERMANN ..... ._ , PETER L. LORIO, JR. USDA Forest Service, Southern Forest Experiment Station, 2500 Shreveport Highway, Pineville, Louisiana 7 t360, USA INTRODUCTION E_vh>n_nental conditions and the genetic potential of loblolly pines, Pinus taeda L., affect or determine tree resista_ce to ;:mackby the southern pine beetle, DendroctonusJ?ontalis Zimmermann, by operating on physiological processes (Fig_ _). Er_vironment and genetic potential must operate through physiological processes to determine the quantity and quality of growdu as well as to express resistance to invasion by pathogens and bark beetles (Kramer t986). Only in this way can eiflaer e,_vironment or genetics affect growth and development at the cell or the whole tree level. Itere, I would like to focus primarily cm one major aspect of the environment that commonly affects the growth and development of lobtolly pines gradtheir _etative resistance to attack by the southern pine beetle; that is, the water regimes under which they may grow. It is important _:_consider the eft_ectsof environment across a range of time fi'ames, from very short (diurnal or even hourly) to very h:m_(litk:time). For example, trees growing on wet sites and in humid environments may grow rapidly and reach large size over king time frames because of prolonged wet conditions; however, in short time frames of days or weeks they may be su}:_icctedto severe water deficits not evident when data are summed over long periods. ROLE OF PHYSIOLOGY IN FORESTRY GENETIC POTENTIAL ENVIRONMENTAL FACTORS Tree Improvement Atmospheric, soil, programs and biotic Silvicultural treatments PHYSIOLOGICAL PROCESSES At whole plant level At cellular level QUANTITY AND QUALITY OF GROWTH (Usually far below the possible maximum) Figure I.o--Diagram illustrating the role of physiology in forestry. Genetic potential and environment operate through physiological processes in determining the quantity and quality of growth. Expression of resistance mechanisms of conifers to invasion by patho,,ense. _ and bark beetles is likewise governed by, these relationships (From Kramer, 1986). Ma{tson, W,J., Niemel_i, E, and Rousi, M., eds. 1996. Dynamics of forest herbivory: quest tbr pattern and principle. USDA For Serv. Gen. Tech. Rep. NC-t83, N.C. For. Exp. Sta., St. Paul, MN 55108. 2{X}
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DYNAMICS OF FOREST HERBIVORY: QUEST
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TABLE OF CONTENTS Seeking The Rules
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32. Companion planting of the nitro
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GRIMALSKY, ¥.I., Research Institut
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POUTTU, ANTTI, Finnish Forest Resea
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persist in mature leaves and affect
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THE SINK-SOURCE HYPOTHESIS: TYPE AN
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late season defoliation decreases t
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BLANCHE, C.A., LORIO, EL., Jr., SOM
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NIEMELA, R, TUOMI, J,, and LOJANDER
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induced reactions have been studied
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summer, but the other sawfly specie
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LARSSON, S., BJ(_RKMAN, C., and GRE
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STAND AND LANDSCAPE DIVERSITY AS A
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not related to resistance to the se
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In contrast to the situation in eas
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ROOT, R.B. 1973. Organization of a
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We tlhus neglect two potential sour
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c__ c__ 1T1 Ill a) a) 0 0 0 e 1 o e
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c_ >l.s S S S m N < DN DN < D c DN
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:hen k > 0 suggest that the cue or
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oth as protective weapons and as po
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DEFENSE THEORIES AND BIRCH RESISTAN
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P 45 A L 40 A T 35 A B 30 I L 25 I
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However, hares showed strong prefer
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DUGLE, J.A. 1966. A taxonomic study
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accommodate findings related to mic
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Table l.--Mean ±S.E. area eaten by
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Sulfhydryl-Disulfide Mechanisms In
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Iraa prior experimental analysis of
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FRAZIER, J.L. and HEITZ, J.R. 1975.
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REICHARD, R 1993. From RNA to DNA,
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; trees, and between and within ind
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Encapsulated objects are data struc
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_re3.--The Lignum model can be cont
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SEVERE DEFOLIATION Tree Fine Root +
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RUMBAUGH, J., BLAHA, M., PREMERLANI
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oo0 a b ol ¢' _achiman_i ()® 1,eA
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1000 Conspicuous Defo i at ion 100
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2.oo 2.oo o t 4 t ¢._ e'- 1.80 1.8
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Qualitative Changes in [,eaves and
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t00 2 Yr 1 Yr o_ 80 Treatment Treat
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Table 2.--Body size of Q. purzctate
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06 b AddedBSA < 04 _ 2rag -'=' i:3
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Severe Defol iat ion Site-A 1993 _
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KAMATA, N. and IGARASHI, M. 1995b.
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enclosure %r 20 post-diapausing sec
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2,500 F 000 F NF NF b _7 a _;_ a _7
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8O D 09 i 4,'.) F AS4L a Z___7 2o !
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2,500 _ st2-st4 El st5 0 st6 [_ pup
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96 SLANSKY, E, Jr. 1990. Insect nut
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later, we selected one more floweri
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Table 2.---Mean spruce budworm perf
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Table 3..--Mean spruce budworm perf
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FOLIVORE FEEDING ON MALE CONIFER FL
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Table 3.--Lymantria monacha prefere
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500- 400- i 300 v ¢ m a 200- I00 L
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From the point of view of trees, th
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THE BLACKMARGINED APHID AS A KEYSTO
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Wood et al. (1987) report that M. c
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MIZELL, R.E 1991. Pesticides and be
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METHODS Study Site The study took p
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the samples. Fertilization had subs
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Table 2.--Percent nutrient content
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Some tree responses to fertilizatio
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PHYTOCHEMICAL PROTECTION AND NATURA
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Indirect effects of abiotic factors
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HUNTER, M.D. and PRICE, P.W. 1992.
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A° ADDITIVE C. HYBRID SUSCEPTIBILI
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Galls, leaf miners, or leaf folds w
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Table 2.--Summary of the hypotheses
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the inheritance patterns of seconda
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FLOATE, K.D. and WHITHAM, T.G. 1993
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Elements of the Suitability/Defense
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Table l.--Comparing the mean number
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ACKNOWLEDGEMENTS The authors sincer
Page 158 and 159: SINGH, D.R 1986_ Breeding for resis
Page 160 and 161: The objectives of this presentation
Page 162 and 163: Table 1.--Average weevil attack on
Page 164 and 165: 1977, Kline and Mitchell 1979, Wood
Page 166 and 167: Further research is underway to cla
Page 168 and 169: A SUGI CLONE HIGHLY PALATABLE TO HA
Page 170 and 171: RESULTS Seasonal Stability of Palat
Page 172 and 173: -
Page 174 and 175: OGAWA, A., NAGATA, Y., and SUKENO,
Page 176 and 177: MATERIALS AND METHODS Field Work In
Page 178 and 179: Laboratory Procedures The week afte
Page 180 and 181: E 120 Nogent-sur-Vernisson Remnings
Page 182 and 183: Interdependence Between Reaction Zo
Page 184 and 185: alance hypothesis (Lorio 1986) cann
Page 186 and 187: SOLHEIM, H., LANGSTROM, B., and HEL
Page 188 and 189: In a second experiment, three 30-ye
Page 190 and 191: Considering biochemical pathways, i
Page 192 and 193: - = 120 N /'_" =40 1/ _ j Days 0 _
Page 194 and 195: BIGGS, A.R. 1985. Suberized boundar
Page 196 and 197: DIFFERENTIAL SUSCEPTIBILITY OF WHIT
Page 198 and 199: Table 2.--Mortality of white fir pr
Page 200 and 201: Results from the geographic range p
Page 202 and 203: esulting seedlings were then rooted
Page 204 and 205: -0.2 0 5 82. _j -0,4 e a a a D4 E I
Page 206 and 207: 1960, Kalkstein 1976). Increased su
Page 210 and 211: It is seldom feasible to control wa
Page 212 and 213: 15 15 u. 10 |O O N tal 5 5 g ao o 4
Page 214 and 215: Only recently have we conducted stu
Page 216 and 217: esistance to beetle attack. Another
Page 218 and 219: LORIO, EL., Jr'. and HODGES, J.D. 1
Page 220 and 221: EFFECTS OF ROOT INHABITING INSECT-F
Page 222 and 223: OCCURRENCE OF ROOT AND STEM SUBCORT
Page 224 and 225: ]Predisposition of Root-infected Tr
Page 226 and 227: chemistry associated with root colo
Page 228 and 229: Implications to Natural Resource Ma
Page 230 and 231: KLEPZIG, K.D., RAFFA, K.F., and SMA
Page 232 and 233: RAFFA, K.F., PHILLIPS, T., and SALO
Page 234 and 235: METHODS The study was installed in
Page 236 and 237: FURNISS, M.M., LIVINGSTON, R.L., an
Page 238 and 239: METHODS In the spring and summer of
Page 240 and 241: The importance of a compound as a r
Page 242 and 243: WERNER, R.A. 1995. Toxicity and rep
Page 244 and 245: 41 40 42 \ 4t 42 41 42 ",,,\ 42 40
Page 246 and 247: Table 1.--Summary data for the 26 p
Page 248 and 249: One weakness of using data from gen
Page 250 and 251: Lower Peninsula (populations 14-26)
Page 252 and 253: AUCLAIR, A.ND., WORREST, R.C., LACH
Page 254 and 255: KELLOMAKI, S., HANNINEN, H., and KO
Page 256 and 257: WARGO, RM. and HAACK, R.A. 1991. Un
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investigation. Sampling was done on
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Figure 2.--Changes in protein preci
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q) J 400 T J ! i i i i o control tr
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attacked trees than in control tree
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ACIDIC DEPOSITION, DROUGHT, AND INS
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Table 1.--Impact of acidic fog upon
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MENGEL, K., BREININGER, T., and LUT
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THE RESISTANCE OF SCOTCH PINE TO DE
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EXPERIMENTAL METHODS Experiments we
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C w Q. 1,200 1,000 o 800 C_ --- 600
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0 .................................
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FONTAtNE, R.G. 1985. Forty years of
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Host Defenses An important componen
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Functional Heterogeneity of Forest
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The Connectivity Index (CI). The CI
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FUNCTIONAL HETEROGENEITYANALYSIS :
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The Modified Hazard Map. The next l
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systems facilitate mapping of fores
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KOLASA, J. and ROLLO, C.D. 1991. In
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) i,i_i)i_)i_i_ U.S. Departme_]t of
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