Is the proportion of clonal species higher at higher latitudes in Australia?

We provide a large‐scale quantification of the relationship between latitude and the proportion of species with clonal reproduction. Parasite pressure is thought to be higher at low latitudes, while abiotic stress is thought to be higher at high latitudes. We therefore predicted that there would be a higher proportion of clonal species at high latitudes than at low latitudes. We collected data of 4386 native seed plant species from 446 genera and 99 families present in ABRSFlora of Australia. Species' occurrence records were taken from the Atlas of Living Australia, including 817 450 species‐site combinations spanning 34.5° of latitude. Logistic regression showed that the proportion of clonal species significantly increased with latitude, rising from 3.3% clonal species at 9.25°S to 26.7% clonal species at 43.75°S. The overall average proportion of clonal species in Australian seed plants was 9.4%. This study adds to our growing understanding of dramatic latitudinal gradients in the way plants grow and reproduce. It also reveals that Australian vegetation contains a relatively low proportion of clonally reproducing species.     

Can Epichloë endophytes enhance direct and indirect plant defence?

Induced or constitutive production of secondary metabolites is a successful plant defence strategy against herbivores which can be mediated by plant associated micro-organisms. Several grass species can be associated with an endophytic fungus of the genus Epichloë which produces herbivore toxic or deterring alkaloids. Besides these direct defences, herbivorous insects are controlled via indirect plant defence mechanisms by attracting predators. Recent studies indicate that Epichloë endophytes can improve the grass emitted volatile organic compounds towards herbivore deterrence. Due to their defensive mutualistic function, we hypothesize that Epichloë altered plant volatiles can attract aphid predators and contribute to an increased indirect plant defence. With a common garden study, we show that hoverfly (Syrphidae) larvae and pupae were more abundant on endophyte-infected plants compared to uninfected plants. Our results indicate that the Epichloë endophyte provides, besides direct defence (alkaloid), indirect plant defence by improving the plant odor attracting more olfactory foraging aphid predators. Future research is needed in order to understand: (I) whether endophyte-mediated changes in plant volatiles are induced herbivore specific, (II) whether there is a trade-off between endophyte-mediated direct and indirect plant defence, (III) whether the endophyte produces volatiles or induces a change in plant-derived volatiles, (IV) the role of plant signals in endophyte-mediated plant defence.     

Can the mass effect explain the mid-altitudinal peak in vascular plant species richness?

A mid-altitudinal peak in species richness is commonly observed and the mass effect (or source–sink effect) has been suggested as a possible cause. We test the importance of the mass effect for generating altitudinal patterns of plant species richness at two grain sizes using a simple estimate of sterility/fertility to indicate sinks and sources. To do this we identified species with fertile specimens (fertile species) and species with only sterile specimens (sterile species) in each sampling unit along altitudinal transects and assumed that the number of sterile species indicated the relative number of sink species, correspondingly that the number of fertile species indicated the relative number of source species when looking at the overall pattern of species richness along a transect. To evaluate this approach, we investigated the distribution of sterility and fertility of each species along the altitudinal transects. We found that sterile species are found more often at the edges and fertile species more often in the centre of the species altitudinal ranges than expected by chance. Using a fine grain, sterile species richness had a humped altitudinal pattern on all transects investigated at this scale, whereas using a coarse grain two of the three transects investigated had a humped pattern. At the fine grain, sterile species richness had a more pronounced peak than fertile species richness in two of the three transects investigated supporting the hypothesis of the mass effect, but this pattern did not persist at coarser grain. The observations at the fine grain are in accordance with the idea that the mass effect is important in shaping the mid-altitudinal peak in species richness, whereas the observations from the coarser grain are ambiguous.     

Does plant phylogenetic diversity increase invertebrate herbivory in managed grasslands?

Plant diversity and land-use intensity have been shown to affect invertebrate herbivory. Several hypotheses predict positive (e.g. associational susceptibility) or negative (e.g. associational resistance) relationships of herbivory with plant species richness. Also, the strength and direction of reported relationships vary greatly between studies leading to the conclusion that relationships either depend on the specific system studied or that other unconsidered factors are more important. Here, we hypothesized that plant phylogenetic diversity is a stronger predictor of invertebrate herbivory than plant species richness because it integrates additional information about the phenotypical and functional composition of communities. We assessed the community-wide invertebrate herbivory, plant species richness and phylogenetic diversity across a range of land-use intensities including a total of 145 managed grasslands in three regions in Germany. Increasing land-use intensity decreased plant species richness and phylogenetic diversity. Plant species richness did not predict invertebrate herbivory. By contrast herbivory moderately increased with increasing plant phylogenetic diversity even after accounting for the effects of region and land use. The strength of direct effects of land-use intensity and indirect effects via altered phylogenetic diversity on herbivory, however, varied among regions. Our results suggest that increasing phylogenetic diversity of plant communities increases invertebrate herbivory probably by providing higher resource diversity. Differences between regions underline the need to account for regional peculiarities when attempting to generalize land-use effects on invertebrate herbivory.     

Jasmonate in plant defence: sentinel or double agent?

Plants and their biotic enemies, such as microbial pathogens and herbivorous insects, are engaged in a desperate battle which would determine their survival–death fate. Plants have evolved efficient and sophisticated systems to defend against such attackers. In recent years, significant progress has been made towards a comprehensive understanding of inducible defence system mediated by jasmonate (JA), a vital plant hormone essential for plant defence responses and developmental processes. This review presents an overview of JA action in plant defences and discusses how microbial pathogens evade plant defence system through hijacking the JA pathway.     

Are there general patterns in plant defence against megaherbivores?

Field surveys were conducted to test whether plants deploy structural defences in ways that match the distribution of megaherbivores. In Western Australian scrublands, where adult plants are within the reach of megaherbivores, structural defences increased vertically and were deployed preferentially by adult plants. Conversely, in woodlands of Eastern Australia and California, where adult plants grow above the reach of megaherbivores, structural defences decreased vertically. Populations of closely‐related taxa on offshore islands exhibited significant reductions in defence in the absence of megaherbivores. The results also demonstrate that island plant taxa can evolve vertical changes in defence after colonizing continents, where they are exposed to megaherbivores. Overall, the results of the present study illustrate a complex array of spatial patterns in plant defence that match the distribution and foraging behaviour of large mammals. When interpreted alongside previous work demonstrating similar spatial patterns in other types of plant defence, the results may help to unify our understanding of how megaherbivores have shaped the evolution of plant form and function. © 2013 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 111 , 38–48.     

Do nutrients and invertebrate herbivory interact in an artificial plant community?

The addition of nutrients has been shown to decrease the species richness of plant communities. Herbivores feed on dominant plant species and should release subdominant species from competitive exclusion at high levels of nutrient availability with a severe competitive regime. Therefore, the effects of nutrients and invertebrate herbivory on the structure and diversity of plant communities should interact. To test this hypothesis, we used artificial plant communities in microcosms with different levels of productivity (applying fertilizer) and herbivory (adding different numbers of the snail, Cepaea hortensis, and the grasshopper, Chorthippus parallelus). For analyses, we assigned species to three functional groups: grasses, legumes and (non-leguminous) herbs. With the addition of nutrients aboveground biomass increased and species richness of plants decreased. Along the nutrient gradient, species composition shifted from a legume-dominated community to a community dominated by fast-growing annuals. But only legumes showed a consistent negative response to nutrients, while species of grasses and herbs showed idiosyncratic patterns. Herbivory had only minor effects, and bottom–up control was more important than top–down control. With increasing herbivory the biomass of the dominant plant species decreased and evenness increased. We found no interaction between nutrient availability and invertebrate herbivory. Again, species within functional groups showed no consistent responses to herbivory. Overall, the use of the functional groups grasses, legumes and non-leguminous herbs was of limited value to interpret the effects of nutrients and herbivory during our experiments.     

Can differences in salinity tolerance explain the distribution of four genetically distinct lineages of Phragmites australis in the Mississippi River Delta?

In the Mississippi River Delta, the common wetland grass, Phragmites australis, displays high genetic diversity, as several genetically distinct populations are co-occurring. Differences in salinity tolerance may be an important factor determining these populations’ distribution in the delta. Our study investigated the salt tolerance of four genotypes exposed to 0, 10, 20, 30, and 40 ppt salinity. The growth rate, biomass, and the light-saturated photosynthetic rate were stimulated at 10 ppt salinity and inhibited at salinities higher than 20 ppt, compared to controls. Increased concentrations of Cl^? and Na⁺ were found in the roots and older leaves of plants exposed to high salinities. Salt tolerance levels differed between genotypes. High salinity tolerance was mainly achieved by reduced water uptake and vacuole compartmentalization of toxic ions. The most tolerant genotype sustained biomass and photosynthesis even at 40 ppt, whereas the most sensitive genotype did not survive salinities higher than 20 ppt. Our findings show that the observed occurrence of different genotypes in the Mississippi River Delta is correlated to genetically determined differences in salinity tolerance. Further investigations are needed to better understand the role that salinity tolerance plays in the invasion of certain introduced P. australis genotypes.     

Can Simpson's paradox explain co-operation in Pseudomonas aeruginosa biofilms?

Co-operative behaviours, such as the production of public goods, are commonly displayed by bacteria in biofilms and can enhance their ability to survive in environmental or clinical settings. Non-co-operative cheats commonly arise and should, theoretically, disrupt co-operative behaviour. Its stability therefore requires explanation, but no mechanisms to suppress cheating within biofilms have yet been demonstrated experimentally. Theoretically, repeated aggregation into groups, interleaved with dispersal and remixing, can increase co-operation via a 'Simpson's paradox'. That is, an increase in the global proportion of co-operators despite a decrease in within-group proportions, via differential growth of groups. We investigate the hypothesis that microcolony formation and dispersal produces a Simpson's paradox that explains bacterial co-operation in biofilms. Using the production of siderophores in Pseudomonas aeruginosa as our model system for co-operation, we use well-documented co-operator and siderophore-deficient cheat strains to measure the frequency of co-operating and cheating individuals, in-situ within-microcolony structures. We detected significant within-type negative density-dependant effects that vary over microcolony development. However, we find no evidence of Simpson's paradox. Instead, we see clear within-microcolony spatial structure (cheats occupying the interior portions of microcolonies) that may violate the assumption required for Simpson's paradox that group members share equally in the public good.     

Can changes in fishery landings explain long-term population trends in gulls?

Capsule: Long-term population trends of gulls on the Isle of Canna, Scotland, showed a correlation to fish tonnage landed in a nearby port.

Aims: To assess whether gull numbers and breeding success at Canna have been influenced by the amount of fish discarded in the area.

Methods: We examined data on gull breeding numbers, breeding success and diet studied at Canna from 1969 to 2014, and data on fish landings at the nearby port of Mallaig for 1985 to 2014. We examined correlations between gull and fishery data, and performed a detrended analysis of Herring Gull Larus argentatus numbers in relation to demersal fish catch (the latter as a proxy for discard volumes).

Results: Gulls fed extensively on discards. Gull breeding numbers declined at Canna, especially between 2000 and 2006, the decline being more pronounced than seen in national totals. Gull breeding numbers correlated with demersal landings, even after detrending for long-term decreases in both.

Conclusions: Correlation between detrended Herring Gull breeding numbers and detrended demersal fish landings provided strong evidence for a causal link between fishery discarding and gull breeding numbers.     

Can wind help explain seasonal differences in avian migration speed?

A bird's ground speed is influenced by the wind conditions it encounters. Wind conditions, although variable, are not entirely random. Instead, wind exhibits persistent spatial and temporal dynamics described by the general circulation of the atmosphere. As such, in certain geographical areas wind's assistance (or hindrance) on migratory flight is also persistent, being dependent upon the bird's migratory direction in relation to prevailing wind conditions. We propose that, considering the western migration route of nocturnal migrants through Europe, winds should be more supportive in spring than in autumn. Thus, we expect higher ground speeds, contributing to higher overall migration speeds, in spring. To test whether winds were more supportive in spring than autumn, we quantified monthly wind conditions within western Europe relative to the seasonal direction of migration using 30 years (1978–2008) of wind data from the NCEP/NCAR Reanalysis dataset. We found that supporting winds were significantly more frequent for spring migration compared to autumn and up to twice as frequent at higher altitudes. We then analyzed three years (2006–2008) of nocturnal migratory ground speeds measured with radar in the Netherlands which confirmed higher ground speeds in spring than autumn. This seasonal difference in ground speed suggests a 16.9% increase in migration speed from autumn to spring. These results stress the importance of considering the specific wind conditions experienced by birds when interpreting migration speed. We provide a simple methodological approach enabling researchers to quantify regional wind conditions for any geographic area and time period of interest.     

Can imperfect host discrimination explain partial patch exploitation in parasitoids?

1. Host discrimination by Aphidius rhopalosiphi (De Stefani Perez) (Hymenoptera: Braconidae) was first studied on the grain aphid Sitobion avenae (Fabricius) (Homoptera: Aphididae). Females tended to avoid oviposition in hosts parasitised 3 h earlier. No evidence of host discrimination ability on freshly parasitised hosts was suggested, however, and ovipositional experience had no effect on host discrimination. 2. The effects of host discrimination ability on the exploitation strategy of patches containing different proportions of unparasitised hosts and hosts parasitised for 3 h were studied. Females spent less time on patches with a higher proportion of parasitised hosts, reflecting the females' ability to perceive the potential profitability of the patch. This ability may be based on the nature of the hosts encountered (unparasitised or parasitised). 3. Incomplete exploitation of unparasitised hosts was also observed. It seems that this partial exploitation is related to the inability of A. rhopalosiphi to recognise freshly parasitised hosts. As a female may experience a risk of self‐superparasitism during patch depletion, this could promote early departure from incompletely exploited patches. 4. The effect of previous experience on the patch exploitation strategy was also assessed. Females were tested twice on two patches of the same quality. Results suggested that the experience acquired during a previous visit led the females to leave the patch sooner and to lay fewer eggs in parasitised hosts. 5. Patch exploitation strategy may therefore be the result of different factors such as host discrimination and experience. The evolutionary consequences of the results are discussed.     

Does anti‐parasitoid defense explain host‐plant selection by a polyphagous caterpillar?

While studies of tri-trophic interactions have uncovered a variety of mechanisms influencing the dietary specialization of insect herbivores, such studies have neglected host-plant selection by generalists. Here, we report an initial investigation on how host-plant quality and a tachinid parasitoid interact to affect the survival and host-plant selection by a polyphagous herbivore. This herbivore, Grammia geneura (Strecker) (Lepidoptera: Arctiidae), is a food-mixing caterpillar that feeds preferentially on forbs. A previous study suggested that G. geneura might eat certain host species for reasons other than benefits of physiological utilization. We hypothesized that host-plant mediated defenses could act against parasitoids, the major mortality agents of late instar G. geneura . Field observations indicated that caterpillars sometimes survived an attack by the parasitoid Exorista mella Walker (Diptera: Tachinidae) in nature. Laboratory experiments showed that the survival of parasitized caterpillars increased on acceptable but nutritionally inferior host-plant species, indicating that anti-parasitoid defense may explain host-plant selection in this dietary generalist. We found no indication that host-plant selection changed according to the parasitism status of individual caterpillars.     

Can variation in risk of nest predation explain altitudinal migration in tropical birds?

Migration is among the best studied of animal behaviors, yet few empirical studies have tested hypotheses explaining the ultimate causes of these cyclical annual movements. Fretwell’s (1980) hypothesis predicts that if nest predation explains why many tropical birds migrate uphill to breed, then predation risk must be negatively associated with elevation. Data from 385 artificial nests spanning 2,740 m of elevation on the Atlantic slope of Costa Rica show an overall decline in predation with increasing elevation. However, nest predation risk was highest at intermediate elevations (500–650 m), not at lowest elevations. The proportion of nests depredated by different types of predators differed among elevations. These results imply that over half of the altitudinal migrant bird species in this region migrate to safer breeding areas than their non-breeding areas, suggesting that variation in nest predation risk could be an important benefit of uphill migrations of many species. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Partial migration in expanding red deer populations at northern latitudes – a role for density dependence?

Partial migration is common in ungulates living in highly seasonal environments. Typically, at higher latitudes, this involves movement between high elevation summer areas used during breeding and lowland areas with less snow used during winter. Snow depth is regarded the main cause of migration to low elevation, but it is less clear why deer migrate to high elevation in spring. The forage maturation hypothesis explains the upward migration due to plant phenology. We here present also an alternative and non‐exclusive hypothesis, that deer migrate uphill in summer to escape competition due to the high density in winter areas (the competition avoidance hypothesis). We also suggest that social fences may play a role at high population density. Based on a unique study of 141 GPS‐marked red deer from seven regions covering the main distribution in Norway, we found that the proportion of migrants in the populations varied from 38% to 100%. Migration was more common in areas with a diverse topography, i.e. for areas with access to high elevation. Further, we found evidence that migration was negatively density dependent, and that fall migration was delayed at high density. We suggest that a combination of avoidance of competition in high density winter ranges, social fencing during summer in addition to the forage maturation and predation risk avoidance hypotheses, is needed to explain migration patterns of northern ungulates.     

Does host‐plant diversity explain species richness in insects? A test using Coccidae (Hemiptera)

1. The megadiverse herbivores and their host plants are a major component of biodiversity, and their interactions have been hypothesised to drive the diversification of both. 2. If plant diversity influences the diversity of insects, there is an expectation that insect species richness will be strongly correlated with host‐plant species richness. This should be observable at two levels (i) more diverse host‐plant groups should harbour more species of insects, and (ii) the species richness of a group of insects should correlate with the richness of the host groups it uses. However, such a correlation is also consistent with a hypothesis of random host use, in which insects encounter and use hosts in proportion to the diversity of host plants. Neither of these expectations has been widely tested. 3. These expectations were tested using data from a species‐rich group of insects – the Coccidae (Hemiptera). 4. Significant positive correlations were found between the species richness of coccid clades (genera) and the species richness of the host‐plant family or families upon which the clades occur. On a global scale, more closely related plant families have more similar communities of coccid genera but the correlation is weak. 5. Random host use could not be rejected for many coccids but randomisation tests and similarity of coccid communities on closely related plant families show that there is non‐random host use in some taxa. Overall, our results support the idea that plant diversity is a driver of species richness of herbivorous insects, probably via escape‐and‐radiate or oscillation‐type processes.     

Can telomere shortening explain sigmoidal growth curves?

A general branching process model is proposed to describe the shortening of telomeres in eukaryotic chromosomes. The model is flexible and incorporates many special cases to be found in the literature. In particular, we show how telomere shortening can give rise to sigmoidal growth curves, an idea first expressed by Portugal et al. [A computational model for telomere-dependent cell-replicative aging, BioSystems 91 (2008), pp. 262-267]. We also demonstrate how other types of growth curves arise if telomere shortening is mitigated by other cellular processes. We compare our results with published data sets from the biological literature.