Theoretical mechanisms describing species abundance distributions should also underpin geographic variation in life-history traits. However, recent studies suggest that abundance and trait patterns may not co-vary and may respond differently to abiotic conditions acting at different spatial scales. We examined patterns in abundance and body size of 2 estuarine molluscs, the arkshell Anadara trapezia and the mudsnail Batillaria australis, across their wide distributions in eastern Australia. We related abundance and body size patterns to abiotic variables including water temperature, pH, salinity, sediment redox and dissolved oxygen content at multiple spatial scales. Two hypotheses were tested: (1) geographic patterns in abundance and body size do not co-vary, and (2) patterns in abundance are more strongly influenced by abiotic conditions occurring at a large spatial scale (e.g. across latitudinal gradients) whereas body size is more strongly influenced by variation in abiotic conditions occurring at smaller scales. The influence of spatial scale and associated abiotic variables on abundance and body size distributions was determined using multiple linear regression, ANOVA and variance component analyses. Geographic variation in abundance and body size were independent of each other in both species. Abiotic variation across latitudinal gradients was the strongest predictor of abundance, but factors that varied substantially at local scales (e.g. dissolved oxygen and sediment redox) were the strongest predictors of body size. Our data indicate that geographic patterns in body size and abundance can be disconnected from each other, most likely due to differential responses to abiotic variation acting at different spatial scales.KEY WORDS: Biogeography · Spatial scale · Abiotic variation · Abundance · Body size · Anadara trapezia · Batillaria australis 463: 205-214, 2012 Recent studies that have simultaneously determined trait and abundance patterns indicate that each may respond differently to spatially distributed abiotic variables. This contrasts with theory suggesting that the factors underlying species abundance distributions should also influence geographic variation in life-history traits (Rivadeneira et al. 2010). For example, for 3 mussel species on the northwest Atlantic coast of the USA, there is a negative relationship between abundance and abiotic stress acting at large spatial scales (Tam & Scrosati 2011). In contrast, traits of the mussels such as body size and age are regulated more by local conditions. The size of the limpet Collisella scabra is more strongly influenced by microhabitat and is less variable at large spatial scales, in contrast to patterns of abundance (Gilman 2005). We therefore make 2 predictions: (1) patterns of abundance and traits are disconnected and (2) the geographic distribution of abundance is more strongly influenced by large-scale abiotic processes, while life-history traits are influenced more by abiotic processes acting at small spatial scales. We suggest ...