Published alkenone  p records spanning known glacial pCO 2 cycles show considerably less variability than predicted by the diffusive model for cellular carbon acquisition and isotope fractionation. We suggest this pattern is consistent with a systematic cellular enhancement of the carbon supply to photosynthesis via carbon concentrating mechanisms under the case of carbon limitation during low pCO 2 glacial time periods, an effect also manifest under carbon limitation in experimental cultures of coccolithophores as well as diatoms. While the low-amplitude  p signal over glacial pCO 2 cycles has led some to question the reliability of  p for reconstructing long-term pCO 2 , the [CO 2 ] aq in the tropical oceans during glacial pCO 2 minima represents the most extreme low CO 2 conditions likely experienced by phytoplankton in the Cenozoic, and the strongest upregulation of carbon concentrating mechanisms. Using a statistical multilinear regression model, we quantitatively parse out the factors (namely light, growth rate, and [CO 2 ] aq ), that contribute to variation in  p in alkenone-producing algae, which confirms a much smaller dependence of  p on [CO 2 ] aq in the low [CO 2 ] aq range, than inferred from the hyperbolic form of the diffusive model. Application of the new statistical model to two published tropical  p records spanning the late Neogene produces much more dynamic pCO 2 estimates than the conventional diffusive model and reveals a significant pCO 2 decline over the last 15 Ma, which is broadly consistent with recent results from boron isotopes of foraminifera. The stable isotopic fractionation between coccolith calcite and seawater dissolved inorganic carbon (here ∆ coccolith-DIC ) also shows systematic variations over glacial-interglacial cycles which may, following future experimental constraints, help estimate the degree of upregulation of parts of the algal carbon concentrating mechanism over glacial cycles.This simplified formulation clarifies the dependence of b on variation in the cellular C content and surface area, which scale with cell size; as well as variation in the growth rate and the effective permeability to CO 2 . When the effects of these factors are considered in aggregate, e.g. by empirical derivations of b from photic zone or culture samples, it must be remembered that the covariation and relative weight of each of these factors spatially in the modern ocean, or in culture experiments, may differ from past temporal significance and covariation of these factors. In practice, however, most previous work has interpreted variation in b to reflect either changes only in the growth rate parameter (Bidigare et al., 1997;Seki et al., 2010), or over long timescales also changes in the cell size and consequently in /S (Henderiks and Pagani, 2008;Seki et al., 2010). Potential variations in P have not been evaluated for glacial samples or the full range of published experiments with  p determinations in experimental culture, although some previous studies have acknowledged that the b...

Summary1. Knowledge of the spatial scale of the dispersal service provided by important seed dispersers (i.e. common and/or keystone species) is essential to our understanding of their role on plant ecology, ecosystem functioning and, ultimately, biodiversity conservation. 2. Carnivores are the main mammalian frugivores and seed dispersers in temperate climate regions. However, information on the seed dispersal distances they generate is still very limited. We focused on two common temperate carnivores differing in body size and spatial ecology -red fox (Vulpes vulpes) and European pine marten (Martes martes) -for evaluating possible functional diversity in their seed dispersal kernels. 3. We measured dispersal distances using colour-coded seed mimics embedded in experimental fruits that were offered to the carnivores in feeding stations (simulating source trees). The exclusive colour code of each simulated tree allowed us to assign the exact origin of seed mimics found later in carnivore faeces. We further designed an explicit sampling strategy aiming to detect the longest dispersal events; as far we know, the most robust sampling scheme followed for tracking carnivore-dispersed seeds. 4. We found a marked functional heterogeneity among both species in their seed dispersal kernels according to their home range size: multimodality and long-distance dispersal in the case of the fox and unimodality and short-distance dispersal in the case of the marten (maximum distances = 2846 and 1233 m, respectively). As a consequence, emergent kernels at the guild level (overall and in two different years) were highly dependent on the relative contribution of each carnivore species. 5. Our results provide the first empirical evidence of functional diversity among seed dispersal kernels generated by carnivorous mammals. Moreover, they illustrate for the first time how seed dispersal kernels strongly depend on the relative contribution of different disperser species, thus on the composition of local disperser assemblages. These findings provide a key starting point for understanding and modelling plant population processes that include mammal-mediated seed dispersal, such as connectivity, range expansion and colonization.

We examine the hierarchical geographic structure of the interaction between a plant, Helleborus foetidus, and its floral herbivores and pollinators (interactors). Six populations from three distant regions of the Iberian Peninsula were used to examine intra‐ and inter‐regional variation in plant traits, interactors and plant fecundity, and to compare, through selection gradient and path analyses, which traits were under selection, and which interactors were responsible for differential selection. Geographic and temporal congruency in interactor‐mediated selection was further tested using a recent analytical approach based on multi‐group comparison in Structural Equation Models. Most plant traits, interactors and fecundity differed among regions but not between populations. Similarly, the identity of the traits under selection, the selection gradients (strength and/or the direction of the selection) and the path coefficients (identifying the ecological basis for selection) varied inter‐ but not intra‐regionally. Results show a selection mosaic at the broad scale and, for some traits, a link of differential selection to trait differentiation.

Seed-dispersing birds can be expected to optimize their energy intake through fruit selection and hence exert a positive selection on fruit pulp content, that is to say, favoring big fruits with small seeds. On the other hand they may select both, average fruit size and its variation. We addressed this issue by analyzing the phenotypic selection exerted by the dispersers of Crataegus monogyna on the fruit and seed size of this species. Fruit and seed size were analyzed at two ontogenic plant stages: the initial size of seeds (and their fruits) as future individuals and the mean size of fruits and seeds produced by adult plants. Fruit diameter and its within-individual variation are the actual targets of selection for maternal fruit traits, negatively affecting relative fitness, although total selection acts only on mean fruit size. For individual seeds, size selection is positive and directed at fruit diameter and seed length, while the remaining traits are subject to indirect selection. Birds exerted a correlational selection favoring big fruits with small seeds. Nevertheless the evolutionary consequences of this selection are expected to be limited by several factors. For example, the positive correlation between fruit and seed sizes, the existence of counteracting selective pressures exerted by other mutualistic or antagonist interactions and temporal or spatial changes in the environmental conditions that may alter the selective forces and even the optimum phenotype in each situation.

Flower color variation among plant populations might reflect adaptation to local conditions such as the interacting animal community. In the northwest Iberian Peninsula, flower color of Gentiana lutea varies longitudinally among populations, ranging from orange to yellow. We explored whether flower color is locally adapted and the role of pollinators and seed predators as agents of selection by analyzing the influence of flower color on (i) pollinator visitation rate and (ii) escape from seed predation and (iii) by testing whether differences in pollinator communities correlate with flower color variation across populations. Finally, (iv) we investigated whether variation in selective pressures explains flower color variation among 12 G. lutea populations. Flower color influenced pollinator visits and differences in flower color among populations were related to variation in pollinator communities. Selective pressures on flower color vary among populations and explain part of flower color differences among populations of G. lutea. We conclude that flower color in G. lutea is locally adapted and that pollinators play a role in this adaptation.

Individual plants produce repeated structures such as leaves, flowers or fruits, which, although belonging to the same genotype, are not phenotypically identical. Such subindividual variation reflects the potential of individual genotypes to vary with micro-environmental conditions. Furthermore, variation in organ traits imposes costs to foraging animals such as time, energy and increased predation risk. Therefore, animals that interact with plants may respond to this variation and affect plant fitness. Thus, phenotypic variation within an individual plant could be, in part, an adaptive trait. Here we investigated this idea and we found that subindividual variation of fruit size of Crataegus monogyna, in different populations throughout the latitudinal gradient in Europe, was explained at some extent by the selective pressures exerted by seed-dispersing birds. These findings support the hypothesis that within-individual variation in plants is an adaptive trait selected by interacting animals which may have important implications for plant evolution.

Animals which interact with plants often cause selective pressures on plant traits. Flower color variation within a species might be shaped by the action of animals feeding on the plant species. Pollinators might exert natural selection on color if flower color is related to their foraging efficiency. For example, some pollinator species might require more time to detect particular colors. If that is the case, flower color might have evolved as a pollination exploitation barrier-ensuring that flowers are more visited by the most efficient pollinators. In addition, non-pollinator agents such as predispersal seed predators may select on flower color, if color indicates food resources (seeds) or if color is related to deterrent compounds. We address selection on flower color in a population of Gentiana lutea where color varies among individuals from yellow to orange. We hypothesize that opposed selection from mutualists (pollinators) and antagonists (predispersal seed predators) maintains flower color variation in this population. By means of path analysis we addressed the role of both interactors in flower color selection. We found that selection acts on flower color, mediated by both pollinators and seed predators. Both agents favored yellow-flowered individuals, thus selection by pollinators and seed predators does not maintain flower color variation in this population.

Plants are shifting their ranges towards higher elevations in response to global warming, yet such shifts are occurring at a rate slower than is needed to keep pace with a rapidly changing climate. There is, however, an almost complete lack of knowledge on seed dispersal across altitude, a key process to understand what constrains climate-driven range shifts. Here, we report the first direct empirical evidence on altitudinal seed dispersal mediated by two common frugivorous mammals: the red fox Vulpes vulpes and the pine marten Martes martes. We conducted a three-year (bait-marking) experiment in a mountainous region of Spain. We offered experimental fruits containing colour-coded seed mimics at feeding stations that simulated source trees. The colour codes allowed us to identify the exact origin of seed mimics found later in mammal scats. Nearly half (47%) of the dispersal events occurred towards higher elevations, despite only ca 25% of the study area being above the average altitude of the feeding stations (1344 m). Seeds dispersed uphill gained an average of 106 m (median  111 m) and a maximum of 288 m, greatly exceeding the estimated requirements to escape warming (35.4 m per decade). Yet, foxes mediated much more uphill seed dispersal than martens (57% and 26% of dispersal events, respectively), which can be explained by between-disperser differences in home range size and habitat specificity. Dispersers with larger home ranges move farther and potentially disperse more seeds to higher altitudes, while habitat generalism is necessary to transport seeds above vegetation belts delimiting contrasting habitat types. We discuss how both traits (home range size and habitat specificity) can be used to infer altitudinal seed dispersal across disperser species and mountainous landscapes.