Aim To provide the first global quantification of the slope and shape of the latitudinal gradient in seed mass, and to determine whether global patterns in seed mass are best explained by growth form, vegetation type, seed dispersal syndrome, or net primary productivity (NPP). Location Global.Methods We collected seed mass data for 11,481 species × site combinations from around the world. We used regression to describe the latitudinal gradient in seed mass, then applied general linear models to quantify the relative explanatory power of each of the variables hypothesized to underlie the latitudinal gradient in seed size. ResultsThere is a 320-fold decline in geometric mean seed mass between the equator and 60 ° . This decline is not linear. At the edge of the tropics, there is a sudden 7-fold drop in mean seed mass. The strongest correlates of the latitudinal gradient in seed mass are plant growth form, and vegetation type, followed by dispersal syndrome and NPP. A model including growth form, vegetation type, dispersal syndrome and NPP explains 51% of the variation in seed mass. Latitude explains just 0.2% of the residual variation from this model. Main conclusionsThis is the first demonstration of a major decrease in seed size at the edge of the tropics. This drop in seed mass is most closely correlated with changes in plant growth form and vegetation type. This suggests that the drop in seed mass might be part of a sudden change in plant strategy at the edge of the tropics.

Aim To provide the first global quantification of the slope and shape of the latitudinal gradient in seed mass, and to determine whether global patterns in seed mass are best explained by growth form, vegetation type, seed dispersal syndrome, or net primary productivity (NPP).Location Global. MethodsWe collected seed mass data for 11,481 species × site combinations from around the world. We used regression to describe the latitudinal gradient in seed mass, then applied general linear models to quantify the relative explanatory power of each of the variables hypothesized to underlie the latitudinal gradient in seed size. ResultsThere is a 320-fold decline in geometric mean seed mass between the equator and 60 ° . This decline is not linear. At the edge of the tropics, there is a sudden 7-fold drop in mean seed mass. The strongest correlates of the latitudinal gradient in seed mass are plant growth form, and vegetation type, followed by dispersal syndrome and NPP. A model including growth form, vegetation type, dispersal syndrome and NPP explains 51% of the variation in seed mass. Latitude explains just 0.2% of the residual variation from this model. Main conclusionsThis is the first demonstration of a major decrease in seed size at the edge of the tropics. This drop in seed mass is most closely correlated with changes in plant growth form and vegetation type. This suggests that the drop in seed mass might be part of a sudden change in plant strategy at the edge of the tropics.

† Background and Aims Most priming studies have been conducted on commercial seed lots of unspecified uniformity and maturity, and subsequent seed longevity has been reported to both increase and decrease. Here a seed lot of Digitalis purpurea L. with relatively uniform maturity and known history was used to analyse the effects of priming on seed longevity in air-dry storage. † Methods Seeds collected close to natural dispersal and dried at 15 % relative humidity (RH), 15 8C, were placed into experimental storage (60 % RH, 45 8C) for 14 or 28 d, primed for 48 h at 0, 21, 22, 25, 210 or 215 MPa, re-equilibrated (47 % RH, 20 8C) and then returned to storage. Further seed samples were primed for 2 or 48 h at 21 MPa and either dried at 15 % RH, 15 8C or immediately re-equilibrated for experimental storage. Finally, some seeds were given up to three cycles of experimental storage and priming (48 h at 21 MPa). † Key Results Priming at 21 MPa had a variable effect on subsequent survival during experimental storage. The shortest lived seeds in the control population showed slightly increased life spans; the longer lived seeds showed reduced life spans. In contrast, seeds first stored for 14 or 28 d before priming had substantially increased life spans. The increase tended to be greatest in the shortest lived fraction of the seed population. Both the period of rehydration and the subsequent drying conditions had significant effects on longevity. Interrupting air-dry storage with additional cycles of priming also increased longevity. † Conclusions The extent of prior deterioration and the post-priming desiccation environment affect the benefits of priming to the subsequent survival of mature seeds. Rehydration-dehydration treatments may have potential as an adjunct or alternative to the regeneration of seed accessions maintained in gene banks for plant biodiversity conservation or plant breeding.

The zebrafish genome contains at least five msx homeobox genes, msxA, msxB, msxC, msxD, and the newly isolated msxE. Although these genes share structural features common to all Msx genes, phylogenetic analyses of protein sequences indicate that the msx genes from zebrafish are not orthologous to the Msx1 and Msx2 genes of mammals, birds, and amphibians. The zebrafish msxB and msxC are more closely related to each other and to the mouse Msx3. Similarly, although the combinatorial expression of the zebrafish msx genes in the embryonic dorsal neuroectoderm, visceral arches, fins, and sensory organs suggests functional similarities with the Msx genes of other vertebrates, differences in the expression patterns preclude precise assignment of orthological relationships. Distinct duplication events may have given rise to the msx genes of modern fish and other vertebrate lineages whereas many aspects of msx gene functions during embryonic development have been preserved.

Variation in individual seed behaviours within a developing population is inherent and inevitable. In this outbreeder, there is significant variation in seed longevity which appears dependent on embryo genotype with little effect of maternal genotype or architectural factors.