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 | Evolution 2003, Vol 57 |
AB Costello, TE Down, SM Pollard, CJ Pacas, EB Taylor | The influence of history and contemporary stream hydrology on the evolution of genetic diversity within species: An examination of microsatellite DNA variation in bull trout, Salvelinus confluentus (Pisces: Salmonidae) | 328-344 |
AK Eggert, K Reinhardt, SK Sakaluk | Linear models for assessing mechanisms of sperm competition: The trouble with transformations | 173-176 |
AS Kondrashov | Accumulation of Dobzhansky-Muller incompatibilities within a spatially structured population | 151-153 |
AV Badyaev, ML Beck, GE Hill, LA Whittingham | The evolution of sexual size dimorphism in the house finch. V. Maternal effects | 384-396 |
BC Sheldon, LEB Kruuk, J Merila | Natural selection and inheritance of breeding time and clutch size in the collared flycatcher | 406-420 |
C Biemont, C Nardon, G Deceliere, D Lepetit, C Loevenbruck, C Vieira | Worldwide distribution of transposable element copy number in natural populations of Drosophila simulans | 159-167 |
CP Klingenberg | Quantitative genetics of geometric shape: Heritability and the pitfalls of the univariate approach | 191-195 |
D Belotte, JB Curien, RC Maclean, G Bell | An experimental test of local adaptation in soil bacteria | 27-36 |
D Brem, A Leuchtmann | Molecular evidence for host-adapted races of the fungal endophyte Epichloe bromicola after presumed host shifts | 37-51 |
DC Marshall, JR Cooley, C Simon | Holocene climate shifts, life-cycle plasticity, and speciation in periodical cicadas: A reply to Cox and Carlton | 433-437 |
DE Starkey, HB Shaffer, RL Burke, MRJ Forstner, JB Iverson, FJ Janzen, AGJ Rhodin, GR Ultsch | Molecular systematics, phylogeography, and the effects of Pleistocene glaciation in the painted turtle (Chrysemys picta) complex | 119-128 |
F Vavre, P Fouillet, F Fleury | Between- and within-host species selection on cytoplasmic incompatibility-inducing Wolbachia in haplodiploids | 421-427 |
G Rowe, TJC Beebee | Population on the verge of a mutational meltdown? Fitness costs of genetic load for an amphibian in the wild | 177-181 |
J Bieri, TJ Kawecki | Genetic architecture of differences between populations of cowpea weevil (Callosobruchus maculatus) evolved in the same environment | 274-287 |
JF LeGalliard, R Ferriere, U Dieckmann | The adaptive dynamics of altruism in spatially heterogeneous populations | 1-17 |
JM Aparicio, R Bonal, PJ Cordero | Evolution of the structure of tail feathers: Implications for the theory of sexual selection | 397-405 |
JS Miller, DL Venable | Floral morphometrics and the evolution of sexual dimorphism in Lycium (Solanaceae) | 74-86 |
K McGuigan, CE Franklin, C Moritz, MW Blows | Adaptation of rainbow fish to lake and stream habitats | 104-118 |
K Rasanen, A Laurila, J Merila | Geographic variation in acid stress tolerance of the moor frog, Rana arvalis. I. Local adaptation | 352-362 |
K Rasanen, A Laurila, J Merila | Geographic variation in acid stress tolerance of the moor frog, Rana arvalis. II. Adaptive maternal effects | 363-371 |
KD McCoy, T Boulinier, C Tirard, Y Michalakis | Host-dependent genetic structure of parasite populations: Differential dispersal of seabird tick host races | 288-296 |
LF Delph, P Mutikainen | Testing why the sex of the maternal parent affects seedling survival in a gynodioecious species | 231-239 |
LR Monteiro, JAF Diniz, SF dosReis, ED Araujo | Shape distances in general linear models: Are they really at odds with the goals of morphometrics? A reply to Klingenberg | 196-199 |
M Capaul, D Ebert | Parasite-mediated selection in experimental Daphnia magna populations | 249-260 |
M GarciaParis, M Alcobendas, D Buclkey, DB Wake | Dispersal of viviparity across contact zones in Iberian populations of fire salamanders (Salamandra) inferred from discordance of genetic and morphological traits | 129-143 |
MB Routley, BC Husband | The effect of protandry on siring success in Chamerion angustifolium (Onagraceae) with different inflorescence sizes | 240-248 |
MD Eubanks, CP Blair, WG Abrahamson | One host shift leads to another? Evidence of host-race formation in a predaceous gall-boring beetle | 168-172 |
ME Hochberg, B Sinervo, SP Brown | Socially mediated speciation | 154-158 |
MY Chung, BK Epperson, MG Chung | Genetic structure of age classes in Camellia japonica (Theaceae) | 62-73 |
NJB Isaac, PM Agapow, PH Harvey, A Purvis | Phylogenetically nested comparisons for testing correlates of species richness: A simulation study of continuous variables | 18-26 |
P Andolfatto, JM Scriber, B Charlesworth | No association between mitochondrial DNA haplotypes and a female-limited mimicry phenotype in Papilio glaucus | 305-316 |
PS Fitze, M Kolliker, H Richner | Effects of common origin and common environment on nestling plumage coloration in the great tit (Parus major) | 144-150 |
RH Baker, GS Wilkinson | Phylogenetic analysis of correlation structure in stalk-eyed flies (Diasemopsis, Diopsidae) | 87-103 |
RR Hudson, M Turelli | Stochasticity overrules the ''three-times rule'': Genetic drift, genetic draft, and coalescence times for nuclear loci versus mitochondrial DNA | 182-190 |
RT Cox, CE Carlton | A comment on gene introgression versus en masse cycle switching in the evolution of 13-year and 17-year life cycles in periodical cicadas | 428-432 |
RT Kimball, DJ Crawford, EB Smith | Evolutionary processes in the genus Coreocarpus: Insights from molecular phylogenetics | 52-61 |
SA Church, JM Kraus, JC Mitchell, DR Church, DR Taylor | Evidence for multiple pleistocene refugia in the postglacial expansion of the eastern tiger salamander, Ambystoma tigrinum tigrinum | 372-383 |
SF McDaniel, AJ Shaw | Phylogeographic structure and cryptic speciation in the trans-antarctic moss Pyrrhobryum minoides | 205-215 |
SM Boback, C Guyer | Empirical evidence for an optimal body size in snakes | 345-351 |
T Tregenza, N Wedell, DJ Hosken, PI Wards | Maternal effects on offspring depend on female mating pattern and offspring environment in yellow dung flies | 297-304 |
TC Mendelson | Sexual isolation evolves faster than hybrid inviability in a diverse and sexually dimorphic genus of fish (Percidae: Etheostoma) | 317-327 |
WE Friedman, JH Williams | Modularity of the angiosperm female gametophyte and its bearing on the early evolution of endosperm in flowering plants | 216-230 |
Y Thomas, MT Bethenod, L Pelozuelo, B Frerot, D Bourguet | Genetic isolation between two sympatric host-plant races of the European corn borer, Ostrinia nubilalis Hubner. I. sex pheromone, moth emergence timing, and parasitism | 261-273 |