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Table 2.--_ummary statistics for genetic diversity in populations ofAndricus lignicola. HDCis the mean heterozygosity per locus through direct count from the data, while HHwis mean heterozygosity calculated under the assumption of Hardy-Weinberg equilibrium. N is the sample size, and all errors are standard errors. N = northern, and S = southern. o 286 Population n Mean n Mean alleles % loci Htxz Hnw Total Regionally - per locus per locus poly- (%+_SE) (%+_SE) alleles private alleles (__.SE) (+_SE) morphic Hungary 108 107.6 (.3) 3.9 (.3) 100 25_+7 33_+8 35 6 N. France 23 23.0 (.0) 2.2 (.3) 66.7 27_+8 30!-_8 20 0 S. UK 41 40.9 (. 1) 2.0 (.3) 66.7 20+-7 22+_7 18 0 N.UK 147 146.4 (.2) 3.0 (.4) 88.9 26+-8 30+-7 27 2 Ireland 163 162.9 (. 1) 2.8 (.4) 88.9 28+_9 27+_8 25 0 TOTAL 482 . Ir J 0 1
Table 3.--Summary statistics for genetic diversity in populations ofAndricus kollari. HDc is the mean heterozygosity per locus through direct count from the data, while HHve is mean heterozygosity calculated under the assumption of Hardy-Weinberg equilibrium. N is the sample size, and all errors are standard errors. Population Mean n Meanalleles % loci HDc HFrW per locus per locus poly- (%+_SE) (%+SE) . .- (_+SE) (+_SE) morphic ., Spain •Madrid SP 20.0 (0) 1.5 (0.2) 45.5 14.5+7 14.2+6 Orense & Potes S 19.0 (0) 2.0 (0.3) 54.5 17.7+7 19.2___7 Salamanca SP 35.0 (0) 2.4 (0.3) 72.7 12.5+5 17.2+6.5 Quintanilla SP 23.0 (0) 1.8 (0.4) 45.5 14.2+6 15.4+6 Gudina SP 66.7 (0.2) 2.5 (0.2) 72.7 16.7+6 17.5+6 " _ Eastern Native Range Rest of Hungary 29.8 (0.2) 2.6 (0.5) 72.7 23.4+_9 25.9+_ 10 Matrafured HU 34.2 (0.3) 2.6 (0.5) 72.7 25.3+_9 26.6+_9 Italy Appenines IT 59.4 (2.7) 2.7 (0.5) 63.6 22.7_+9 24.9+_9 Florence IT 15.8 (0.2) 2.4 (0.4) 63.6 25.510 25.4+_10 Germany North Germany 37.0 (0.0) 2.0 (0.4) 54.5 15.2+_6 17.0+7 South Germany 7.6 (0.2) 1.9 (0.4) 45.5 19.7+_8 23.0+_9.5 France Saumur N.FR 31.9 (0.1) 2.1 (0.4) 54.5 23.4+_9 20.3+_7 Cherbourg N.FR 16.6 (0.2) 2.0 (0.4) 54.5 15.5+_8 21.8___9 Bordeaux W.FR 8.9 (0.7) 1.8 (0.3) 54.5 18.5+_8 20.9+8 Agen S. FR 29.1 (0.8) 2.2 (0.4) 63.6 22.9+_9 24.8+_9 Nouvion N. FR 10.9 (1.0) 1.6 (0.3) 36.4 18.2_+10 18.0+_9 Auch S. FR 20.0 (1.0) 2.2 (0.4) 54.5 23.7+_9 23.2_+9 Low Countries Utrecht HOL 10.9 (0.1) 1.5 (0.2) 36.4 14.5_+7 15.1 +_7.5 Belgium 13.5 (0.5) 1.7 (0.3) 36.4 19.3+9 18.0+_9 UK Oxford ENG 33.0 (0.0) 1.9 (0.4) 45.5 18.2+8 18.1 +8 Dunrobin SCOT 42.7 ( 1.5) 2.3 (0.4) 54.5 20.1 +9 20.5+8.5 Pul_tenham ENG 22.0 (0.0) 2.0 (0.4) 45.5 15.3+6 19.6+8.5 Ireland J Muckross IR 29.0 (0.0) 1.9 (0.4) 36.4 18.8_+8 19.1 +_8 Rest of Ireland 7.0 (0.0) 1.5 (0.2) 27.3 9.1+_5 12.6+_7 u 0 287 A
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LJSDA United States i Department Ag
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• , THE BIOLOGY OF GALL-INDUCING
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. TABLE OF CONTENTS - BIOGEOGRAPHY
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Genetic and environmental contribut
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.. GALL INDUCING AND OTHER GALL MID
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Table l. -,Gall midge species assoc
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C e. f. . Figure i'.--Galls of gall
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species and several inquilines may
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XYLOPHILOUS GALL MIDGE SPECIES from
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Rtibsaamen, E.H. 1899. Ueber die Le
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Table ° 1.--A summary of studies o
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• 3 ]5
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Skuhrava, • M.; .. Skuhravy, V. 1
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midge sPecies, several hosts yieldi
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Fedotoval Z,A. 1991. Gall midges (D
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known, nol_having been noted except
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Actilasioptera tumidifoHum GAGNE, N
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° _._. _. ..._..... _._:..--._...,
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Figures 13-16, Postabdomens ofActil
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-7"-% 25 i'.., 27 26 28 30 31 32 I
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Thorax. Wing length, 2.1-2.3 mm (n
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I' . McAlpine, J.F. 1981.2. Morphol
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Table 1.---Comparison between Tephr
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Table 3.raThe Afrotropical Myopitin
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........ _"i!_; _ 2,:_::;_ :L I,_ ,
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anthracina (Doane) (Diptera: Tephri
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o Host Plants Gall-forming insects
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, ENCLOSED 63% Figure 3.--A pie cha
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80% 70% 60% ° 50% - 40% 30% ' 20%
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Table 3. Major galling plant famili
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Appendix 1. Data Sheet for Galls Co
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j " GALLS Ephedra nebrodensis Jt ?W
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IS THERE A COOL-WET TO HOT-DRY GRAD
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10 - These findings suggest that ho
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ROLE OF PERICLISTUS (HYMENOPTERA: C
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° tl A o "!. . I ' Ir Figure l.---
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f . It Figure 2.--Schematic represe
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, ° , ° 3 . _ _ "' . . " Figures
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Table 2._Number of Periclistus larv
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. ° . 12 13 B Figures 12.---Schema
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emain as does the circumscribing la
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. Table 3.--Incidence of inhabitant
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the previous two galls, Aprostocetu
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Periclistus apparently have many of
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O'Brien, T.E; McCully, M.E. 1981. T
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indicator trait for male fitness, a
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Table 1.---Initial analyses to esta
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., these cells, suggesting that fem
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o 8- 6- Krmnm 4- J _1) IP 2- '0- T
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Table 1. Mortality ofT. taxi expres
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kf) =_ i---. J i _ • i J _-" i i
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Table 2.---_-Correlationsfor number
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t Table 3. Mean values for total mo
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. 100 - ' / .r-! 0 i J0 - ,/O_OI 0
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(Figdre 5 continued) -. Tree 63 eve
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" Table 6.---Correlations (r) betwe
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Cameron,.R.A.D.; Redfem, M. 1978. P
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FurIhermore, Osten Sacken (1861 c)
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this letter, which was read at the
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9 WOLBA CHIA-INDUCED THELYTOKY IN C
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Lancieux Ile Besnard • Erquy / Sa
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I Table 3.-mFrequencies offemales h
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Table 7.---z-Frequency offemales in
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. DISCUSSION considered as independ
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Fulton, B.B. 1933. Notes on Habrocy
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• . (26,galls), Nassau (30.27S, 1
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with competition (Stewart 1996) and
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" GALL-FORMING APHIDS ON PISTA CIA:
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Although Geoica belongs in the Baiz
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THE LIFE-CYCLE OF THE BLACKCURRANT
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known" (1) Common form (E), which i
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Table 3._Average number of buds per
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Our prediction of a low cost of res
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- ? J Table 1.--Mean dry stem weigh
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stands; does the variation in resis
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Strong, D.R.; Larsson, S.; Gullberg
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The HR exhibited by the B. brevipes
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HR.is an important mechanism whereb
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q, J 10o • • O _80 • '= • O
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percent (n= 24) of the plants that
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REPROGRAMMING PLANT DEVELOPMENT: TW
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harvested and snap frozen. Protein
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Table 3.---Expected and observed fr
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whi.le it is not possible to discar
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. PLANT HORMONES AND GALL FORMATION
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As a follow up to Beck's (1947) fin
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Table 2.-_--Levels of extractable c
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.. J 0 0.16 m 0.14 - . 0.12 - 0.10
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probably occurs in the intact gall,
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Biddington, N.L.; Thomas, T.H. 1973
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.THE EFFECTS OF GALL FORMATION BY L
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three.larval instars (Mook 1967, Ru
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, + . 12 I I i i 4 .o • 1 10-- "
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, o Figure 5-1 to 5-6.----detailed
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Table 3.1Nutritional composition of
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gro.wing point, it is the latter th
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Byers, J.A+; Brewer, J.W.; Denna, D
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Skuhravy, V_1978. Invertebrates: de
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de.rivative spectra of pigment-prot
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Thylakoid Morphology CONCLUSION Ult
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.I THE DEVELOPMENT OF AN OVAL-SHAPE
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. LITERATURE CITED Rohfritsch, O. 1
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.PATTERNS IN GALL-INDUCING INSECTS
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fact, large Shrubs supported the hi
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We may conclude that the reduced ap
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Price, EW: 1997. Insect ecology. 3d
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of egg insertion. The galls of Euur
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species within each group. Close sp
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, According tO our present knowledg
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saying, that, according to A.K. Skv
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Benson, R.B. 1960a. Studies in Pont
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J Table 1. The Ranges of host plant
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(table 2 continued ) Host plant gen
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(table 4 continued) .. Host plant g
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Table 6.--List of host plants for P
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Table 9.--List of host plants for P
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(table o 9 continued) Host plant ge
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J America north of Mexico and addit
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Table 1.-,Host species and habitat
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this sampling and rearing of insect
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. Eastern USA Host Oaks White 0.8 g
Page 243 and 244: composed of Q. bicolor and Q. macro
Page 245 and 246: Q..rubraand Q. coccinea. Furthermor
Page 247 and 248: Fritz, R.S.; Nichols-Orians, C.M.;
Page 249 and 250: MOLECULAR PHYLOGENY OF NORTH AMERIC
Page 251 and 252: . RESULTS The heuristic search usin
Page 253 and 254: a few genera to consider evidence o
Page 255 and 256: . MOLECULAR PHYLOGENY OF THE GENUS
Page 257 and 258: . Table 1._Author names of the taxa
Page 259 and 260: 28 26 24 22 A 20 18 0 q_ 1.4 O. 0 !
Page 261 and 262: •" _ _ _ o ,. _ _ -.--_.,. _ Ii .
Page 263 and 264: Among species groups, the topology
Page 265 and 266: . D. ignota D. nebulosa _!I D. fusi
Page 267 and 268: . LITERATURE CITED Dalla Torre, K.W
Page 269 and 270: PATTERNS IN THE EVOLUTION OF GALL S
Page 271 and 272: Figure 1. Gallstructures induced by
Page 273 and 274: the s.ection Quercus, and the 'blac
Page 275 and 276: t SG AG Species Clade " _ _ Name 9a
Page 277 and 278: non-Andricus cynipine species (fig.
Page 279 and 280: SG AG Species Clade _ t Name 100 94
Page 281 and 282: .an asexual-only ancestor. The sexu
Page 283 and 284: .. "j V 6 '_ _!i..-".'='-,.. " •
Page 285 and 286: Abe, Y. 1997. Well-developed gall t
Page 287 and 288: Stone, G.N.; Schrnrogge, K.; Crawle
Page 289 and 290: Quercus cerris, while a parthenogen
Page 291 and 292: Table t.----Summary statistics for
Page 293: Distance from root . 0.00 0.04 0.08
Page 297 and 298: ° . A. 40- -, 30- _ w _ A. kollari
Page 299 and 300: the alleles they possess at specifi
Page 301 and 302: e!atively narrow water barrier to l
Page 303 and 304: . TESTS OF HYPOTHESES REGARDING HYB
Page 305 and 306: classifieati0nerrors for various ba
Page 307 and 308: Tabl.e 2. Canonical discriminantfun
Page 309 and 310: encourage hybrid zone workers to ab
Page 311 and 312: Strauss, S,Y. 1994. Level of herbiv
Page 313 and 314: sense heritability of resistance to
Page 315 and 316: 0.25 - Adelges abietis • 0.20 q)
Page 317 and 318: 0 a 1 . W ! 309 A
Page 319 and 320: " I I_)! o Io Io Io I__1o I I I I_)
Page 321 and 322: classes for A. abietis suggests tha
Page 323 and 324: 0 POSTER ABSTRACTS . W ! O ,l 315
Page 325 and 326: A . REFERENCES .. Huntley, B.H.; Bi
Page 327 and 328: CECIDOMYIID-INDUCED GALLS OF MA CHI
Page 329 and 330: . GALL MIDGE FAUNAS (DIPTERA: CECID
Page 331 and 332: GALL-INDUCER AND GALL-INQUILINE CYN
Page 333 and 334: " INDUCED RESISTANCE IN WILLOW AGAI
Page 335 and 336: .BROAD OVERVIEW OF A GALL-SYSTEM: F
Page 337 and 338: TWOSPECIES OF EURYTOMID GALL FORMER
Page 339 and 340: Csdka, Gyuri; Mattson, William J.;
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il ' ii - Northern Research Station - USDA Forest Service

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