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 | Biological Journal of the Linnean Society 2002, Vol 76 |
A Berkov | The impact of redefined species limits in Palame (Coleoptera : Cerambycidae : Lamiinae : Acanthocinini) on assessments of host, seasonal, and stratum specificity | 195-209 |
A Simkova, M Ondrackova, M Gelnar, S Morand | Morphology and coexistence of congeneric ectoparasite species: reinforcement of reproductive isolation? | 125-135 |
AT Laugen, A Laurila, J Merila | Maternal and genetic contributions to geographical variation in Rana temporaria larval life-history traits | 61-70 |
BK Kristjansson, S Skulason, DLG Noakes | Morphological segregation of Icelandic threespine stickleback (Gasterosteus aculeatus L) | 247-257 |
BN Viguier | Is the morphological disparity of lemur skulls (Primates) controlled by phylogeny and/or environmental constraints? | 577-590 |
BR Grant, PR Grant | Simulating secondary contact in allopatric speciation: an empirical test of premating isolation | 545-556 |
DA Warner, RM Andrews | Laboratory and field experiments identify sources of variation in phenotypes and survival of hatchling lizards | 105-124 |
DAS Smith, IJ Gordon, G Lushai, D Goulson, JA Allen, N MacLean | Hybrid queen butterflies from the cross Danaus chrysippus (L.)xD. gilippus (Cramer): confirmation of species status for the parents and further support for Haldane's Rule | 535-544 |
EL Jockusch, DB Wake | Falling apart and merging: diversification of slender salamanders (Plethodontidae : Batrachoseps) in the American West | 361-391 |
FA Meier, S Scherrer, R Honegger | Faecal pellets of lichenivorous mites contain viable cells of the lichen-forming ascomycete Xanthoria parietina and its green algal photobiont, Trebouxia arboricola | 259-268 |
G Blanco, JA Davila, JAL Septiem, R Rodriguez, F Martinez | Sex-biased initial eggs favours sons in the slightly size-dimorphic Scops owl (Otus scops) | 1-7 |
G Garcia, F AlvarezValin, N Gomez | Mitochondrial genes: signals and noise in the phylogenetic reconstruction of the annual killifish genus Cynolebias (Cyprinodontiformes, Rivulidae) | 49-59 |
GM Barker | Phylogenetic diversity: a quantitative framework for measurement of priority and achievement in biodiversity conservation | 165-194 |
GY Rao, B Widen, S Andersson | Patterns of inbreeding depression in a population of Brassica cretica (Brassicaceae): evidence from family-level analyses | 317-325 |
H Ota, M Honda, SL Chen, T Hikida, S Panha, HS Oh, M Matsui | Phylogenetic relationships, taxonomy, character evolution and biogeography of the lacertid lizards of the genus Takydromus (Reptilia : Squamata): a molecular perspective | 493-509 |
J Johannesen, A Hennig, B Dommermuth, JM Schneider | Mitochondrial DNA distributions indicate colony propagation by single matri-lineages in the social spider Stegodyphus dumicola (Eresidae) | 591-600 |
J Ornborg, S Andersson, SC Griffith, BC Sheldon | Seasonal changes in a ultraviolet structural colour signal in blue tits, Parus caeruleus | 237-245 |
J PerezTris, R Carbonell, JL Telleria | Parasites and the blackcap's tail: implications for the evolution of feather ornaments | 481-492 |
JJ Day | Phylogenetic relationships of the Sparidae (Teleostei : Percoidei) and implications for convergent trophic evolution | 269-301 |
K Johannesson, A Ekendahl | Selective predation favouring cryptic individuals of marine snails (Littorina) | 137-144 |
K Schonrogge, B Barr, JC Wardlaw, E Napper, MG Gardner, J Breen, GW Elmes, JA Thomas | When rare species become endangered: cryptic speciation in myrmecophilous hoverflies (Vol 75, pg 291, 2002) | 315 |
L Kratochvil, D Frynta | Body size, male combat and the evolution of sexual dimorphism in eublepharid geckos (Squamata : Eublepharidae) | 303-314 |
L Monetti, RA SanchezGuillen, AC Rivera | Hybridization between Ischnura graellsii (Vander Linder) and I-elegans (Rambur) (Odonata : Coenagrionidae): are they different species? | 225-235 |
M Bosch, J Simon, AM Rovira, J Molero, C Blanche | Pollination ecology of the pre-Pyrenean endemic Petrocoptis montsicciana (Caryophyllaceae): effects of population size | 79-90 |
M Henriques, R Lourenco, F Almada, G Calado, D Goncalves, T Guillemaud, ML Cancela, VC Almada | A revision of the status of Lepadogaster lepadogaster (Teleostei : Gobiesocidae): sympatric subspecies or a long misunderstood blend of species? | 327-338 |
M Pfenninger | Relationship between microspatial population genetic structure and habitat heterogeneity in Pomatias elegans (OF Muller 1774) (Caenogastropoda, Pomatiasidae) | 565-575 |
MJ Voordouw, BR Anholt | Environmental sex determination in a splash pool copepod | 511-520 |
N Bouton, J DeVisser, CDN Barel | Correlating head shape with ecological variables in rock-dwelling haplochromines (Teleostei : Cichlidae) from Lake Victoria | 39-48 |
N Osawa | Sex-dependent effects of sibling cannibalism on life history traits of the ladybird beetle Harmonia axyridis (Coleoptera : Coccinellidae) | 349-360 |
OY Martin, DJ Hosken | Asymmetry and fitness in female yellow dung flies | 557-563 |
P Cassey | Life history and ecology influences establishment success of introduced land birds | 465-480 |
P Lenfant, S Planes | Temporal genetic changes between cohorts in a natural population of a marine fish, Diplodus sargus | 9-20 |
R Bickel, JB Losos | Patterns of morphological variation and correlates of habitat use in chameleons | 91-103 |
R Shine | Eggs in autumn: responses to declining incubation temperatures by the eggs of montane lizards | 71-77 |
R Shine, GP Brown | Effects of seasonally varying hydric conditions on hatchling phenotypes of keelback snakes (Tropidonophis mairii, Colubridae) from the Australian wet-dry tropics | 339-347 |
RM Brown, SI Guttman | Phylogenetic systematics of the Rana signata complex of Philippine and Bornean stream frogs: reconsideration of Huxley's modification of Wallace's Line at the Oriental-Australian faunal zone interface | 393-461 |
SM Tierney, MP Schwarz, T Neville, PM Schwarz | Sociality in the phylogenetically basal allodapine bee genus Macrogalea (Apidae : Xylocopinae): implications for social evolution in the tribe Allodapini | 211-224 |
TH Jorgensen | The importance of phylogeny and ecology in microgeographical variation in the morphology of four Canarian species of Aeonium (Crassulaceae) | 521-533 |
TJ Ord, DT Blumstein | Size constraints and the evolution of display complexity: why do large lizards have simple displays? | 145-161 |
V Schawaroch | Phylogeny of a paradigm lineage: the Drosophila melanogaster species group (Diptera : Drosophilidae) | 21-37 |
W Arthur, D Foddai, C Kettle, JGE Lewis, M Luczynski, A Minelli | Analysis of segment number and enzyme variation in a centipede reveals a cryptic species, Geophilus easoni sp. nov., and raises questions about speciation (Vol 74, pg 489, 2001) | 163 |
YQ Lu | Why is cleistogamy a selected reproductive strategy in Impatiens capensis (Balsaminaceae)? (Vol 4, pg 543, 2002) | 463 |