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 | Biological Journal of the Linnean Society 2002, Vol 75 |
| BH Jordal, RA Beaver, BB Normark, BD Farrell | Extraordinary sex ratios and the evolution of male neoteny in sib-mating Ozopemon beetles | 353-360 |
| C Abegg, B Thierry | Macaque evolution and dispersal in insular south-east Asia | 555-576 |
| C CameronBeaumont, SE Lowe, JWS Bradshaw | Evidence suggesting preadaptation to domestication throughout the small Felidae | 361-366 |
| C Garma, N HenriquesGil | Egg yolk polypeptide variation in acridids (Orthoptera) | 281-290 |
| CD Wilga | A functional analysis of jaw suspension in elasmobranchs | 483-502 |
| CG Williams, KL Joyner, LD Auckland, S Johnston, HJ Price | Genomic consequences of interspecific Pinus spp. hybridization | 503-508 |
| D Adriaens, S Devaere, GG Teugels, B Dekegel, W Verraes | Intraspecific variation in limblessness in vertebrates: a unique example of microevolution | 367-377 |
| DC Morris, MP Schwarz, BJ Crespi | Pleometrosis in phyllode-glueing thrips (Thysanoptera : Phlaeothripidae) on Australian Acacia | 467-474 |
| FJ GathorneHardy, Syaukani, RG Davies, P Eggleton, DT Jones | Quaternary rainforest refugia in south-east Asia: using termites (Isoptera) as indicators | 453-466 |
| J Sueur | Cicada acoustic communication: potential sound partitioning in a multispecies community from Mexico (Hemiptera : Cicadomorpha : Cicadidae) | 379-394 |
| JF Martin, A Gilles, M Lortscher, H Descimon | Phylogenetics and differentiation among the western taxa of the Erebia tyndarus group (Lepidoptera : Nymphalidae) | 319-332 |
| JM Shephard, JM Hughes, MP Zalucki | Genetic differentiation between Australian and North American populations of the monarch butterfly Danaus plexippus (L.) (Lepidoptera : Nymphalidae): an exploration using allozyme electrophoresis | 437-452 |
| JWH Ferguson | On the use of genetic divergence for identifying species | 509-516 |
| K Jordaens, S VanDongen, P VanRiel, S Geenen, R Verhagen, T Backeljau | Multivariate morphometrics of soft body parts in terrestrial slugs: comparison between two datasets, error assessment and taxonomic implications | 533-542 |
| 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 | 291-300 |
| LM Cook, AM Riley, IP Woiwod | Melanic frequencies in three species of moths in post industrial Britain | 475-482 |
| M Nogales, V Quilis, FM Medina, JL Mora, LS Trigo | Are predatory birds effective secondary seed dispersers? | 345-352 |
| MG Filippucci, M Macholan, JR Michaux | Genetic variation and evolution in the genus Apodemus (Muridae : Rodentia) | 395-419 |
| P Bouchet, P Lozouet, P Maestrati, V Heros | Assessing the magnitude of species richness in tropical marine environments: exceptionally high numbers of molluscs at a New Caledonia site | 421-436 |
| S Pekar, J Kral | Mimicry complex in two central European zodariid spiders (Araneae : Zodariidae): how Zodarion deceives ants | 517-532 |
| S Volis, S Mendlinger, D Ward | Differentiation in populations of Hordeum spontaneum Koch along a gradient of environmental productivity and predictability: plasticity in response to water and nutrient stress | 301-312 |
| S Volis, S Mendlinger, D Ward | Differentiation along a gradient of environmental productivity and predictability in populations of Hordeum spontaneum Koch: multilevel selection analysis | 313-318 |
| TJ Abatzopoulos, I Kappas, P Bossier, P Sorgeloos, JA Beardmore | Genetic characterization of Artemia tibetiana (Crustacea : Anostraca) | 333-344 |
| YQ Lu | Why is cleistogamy a selected reproductive strategy in Impatiens capensis (Balsaminaceae)? | 543-553 |