Multiannual effects of induced plant defenses: Are defended plants good or bad neighbors?

Defenses induced by herbivore feeding or phytohormones such as methyl jasmonate (MeJA) can affect growth, reproduction, and herbivory, not only on the affected individual but also in its neighboring plants. Here, we report multiannual defense, growth, and reproductive responses of MeJA‐treated bilberry (Vaccinium myrtillus) and neighboring ramets. In a boreal forest in western Norway, we treated bilberry ramets with MeJA and water (control) and measured responses over three consecutive years. We observed the treatment effects on variables associated with herbivory, growth, and reproduction in the MeJA‐treated and untreated ramet and neighboring ramets distanced from 10 to 500 cm. MeJA‐treated ramets had fewer grazed leaves and browsed shoots compared to control, with higher effects in 2014 and 2015, respectively. In 2013, growth of control ramets was greater than MeJA‐treated ramets. However, MeJA‐treated ramets had more flowers and berries than control ramets 2 years after the treatment. The level of insect and mammalian herbivory was also lower in untreated neighboring ramets distanced 10–150 cm and, consistent with responses of MeJA‐treated ramets, the stronger effect was also one and 2 years delayed, respectively. The same neighboring ramets had fewer flowers and berries than untreated ramets, indicating a trade‐off between defense and reproduction. Although plant–plant effects were observed across all years, the strength varied by the distance between the MeJA‐treated ramets and its untreated neighbors. We document that induced defense in bilberry reduces both insect and mammalian herbivory, as well as growth, over multiple seasons. The defense responses occurred in a delayed manner with strongest effects one and 2 years after the induction. Additionally, our results indicate defense signaling between MeJA‐treated ramets and untreated neighbors. In summary, this study shows that induced defenses are important ecological strategies not only for the induced individual plant but also for neighboring plants across multiple years in boreal forests.     

Male sterility in flowering plants: are plant growth substances involved?

Male sterility in flowering plants is of tremendous importance not only in molecular and developmental studies of stamen and pollen grains and evolutionary studies on the origin of dioecy, but also in its commercial application in hybrid seed production. This paper reviews the literature on the possible involvement of plant growth substances (PGSs) in male sterility, and in normal stamen and pollen development. Different experimental approaches on a number of male sterile systems and normal plants have shown that nearly all PGSs, i.e., gibberellins, cytokinins, auxin, abscisic acid, and ethylene, directly or indirectly influence the expression of male sterility. Analyses of endogenous PGSs have revealed that in male sterile plants the level and/or metabolism of more than one PGS is affected. These studies support the suggestion that it is the relative ratio of various PGSs, rather than any one substance, that is critical for normal stamen and pollen development. It is also proposed that gene-regulated male sterility is likely mediated through an altered balance of endogenous PGSs in developing flowers and stamens.     

Do plants have rhodopsin after all? A mystery of plant G protein-coupled signalling

Considerable physiological and biochemical evidence suggests that plants, like animals, widely use intracellular signalling coupled to heterotrimeric G proteins. Yet, the molecular components of this machinery remained elusive until recently. We overview the work carried out during the last two decades, aimed at identification of the plant proteins involved in G protein-coupled signalling. The completion of the sequencing of the Arabidopsis genome now permits to assess whether plants possess signalling and regulatory components of this machinery corresponding to those known from animals.     

Competition and facilitation among plants for pollination: can pollinator abundance shift the plant–plant interactions?

We hypothesize interactions among plants for pollination may depend on pollinator abundance, which always varies among years and habitats and has different effects on plant reproductive success. Honeybee-pollinated plants, Lotus corniculatus, and its commonly coflowering neighbor, Potentilla reptans var. sericophylla, were used in a two-year project. We designed six types of plant combinations with different conspecific and interspecific flower densities in 2011 and repeated this in the same site in 2012. Meanwhile, we artificially increased pollinator abundance by hiring beehives only in 2011. Pollinator abundance as well as flower density significantly affected pollination of L. corniculatus plants from both the conspecific and interspecific plots. Total number of bees visiting a plot was enhanced by an increase in both the conspecific and interspecific flower densities regardless of high or low pollinator abundance. However, changes in visitation rates and fruit sets in the focal plants when flower densities were increased depended on pollinator abundance. Under high pollinator abundance, an increase in both the conspecific and interspecific flower densities significantly enhanced pollinator visits to L. corniculatus. However, under low pollinator abundance, the pollinator visitation rate remained unchanged as conspecific flower density increased, but decreased when there was an increase in interspecific flower density. Coflowering plants enhanced fruit sets of L. corniculatus only when the pollinator abundance was high. The findings suggest that the interactions among plants for pollination are influenced not only by a plant density threshold, but also by a pollinator abundance threshold.     

Why are higher plants green? Evolution of the higher plant photosynthetic pigment complement

The physiological reason that higher plants are green is unknown. Other photosynthetic organisms utilize pigments that strongly absorb green light; therefore, there must have been natural forces that ‘selected’ the photosynthetic pigments found in higher plants. Based on previously published data and our recent findings about green light and photosynthesis within leaves (Sun et al.), a specific functional role is described for the primary photosynthetic pigments of higher plants, that were derived from green algal progenitors. The particular absorptive characteristics of chlorophylls a and b appear to perform two contradictory, but necessary functions in higher plants. Firstly, chlorophylls a and b absorb light for maximum utilization under non‐saturating conditions, a function that is well understood. Secondly, they can act as protective pigments under over‐saturating light conditions, when absorbed light is dissipated as heat. Under such conditions, a significant portion of light can also be efficiently utilized, especially in the bottom portion of the leaf, that is mainly illuminated by green light and not down‐regulated. The second function may have been the selective force that gave rise to the extremely successful terrestrial plants, that evolved from green algae.     

Hallmarks of cancer: of all cancer cells,all the time?

In two landmark articles, Hanahan and Weinberg synthesized into one conceptual framework 'the hallmarks of cancer', a massive amount of information describing the characteristics of a cancer cell. Although this is neither the intention nor the belief of the authors, hallmarks are often interpreted as applying to a canonic cancer cell, or equally to all cells within a cancer. In this article, we clarify the separate concepts of causes, oncogenic events, signal transduction programs, and hallmarks to show that there is no unimodal relation between these concepts but a complex network of interrelations that vary in different cells, between cells, and at different times in any given cell. We consider cancer as an evolving, dynamic, and heterogeneous system, explaining, at least in part, the difficulty of treating cancer and supporting the use of simultaneous, multitarget therapies.     

Native parasitic plants: Biological control for plant invasions?

Plant invasions cause biodiversity loss and degradation in ecosystems worldwide. The invasive species involved may be introduced, or native invaders, and controlling them is a major global challenge. Here, we highlight an emerging role for native parasitic plants in suppressing invasive species, thus aiding in restoration of affected habitats. Compelling empirical evidence is provided by three study systems located in Central Europe, southern Australia and eastern China. Further cases of parasitism of invasive plants have been recorded across five continents. We propose including the interactions between parasitic and invasive plants into the theoretical framework of the biotic resistance hypothesis concerning generalist interactions between invaders and native biota. Among parasitic plants, numerous root hemiparasites, mistletoes and parasitic vines show low host specificity and exert substantial negative effects on their hosts. These parasitic plants may interfere with key traits of invaders such as symbiotic nitrogen fixation or clonal propagation which provide them with competitive advantage over native species. We contend that some parasitic plants may present a cost‐effective environmentally sustainable component of invasion management schemes. Therefore, we encourage exploration of this potential and the development of methods for practical applications in ecological restoration and nature conservation.     

How many species of flowering plants are there?

We estimate the probable number of flowering plants. First, we apply a model that explicitly incorporates taxonomic effort over time to estimate the number of as-yet-unknown species. Second, we ask taxonomic experts their opinions on how many species are likely to be missing, on a family-by-family basis. The results are broadly comparable. We show that the current number of species should grow by between 10 and 20 per cent. There are, however, interesting discrepancies between expert and model estimates for some families, suggesting that our model does not always completely capture patterns of taxonomic activity. The as-yet-unknown species are probably similar to those taxonomists have described recently—overwhelmingly rare and local, and disproportionately in biodiversity hotspots, where there are high levels of habitat destruction.     

Endozoochorous dispersal of aquatic plants: does seed gut passage affect plant performance?

The ingestion of seeds by vertebrates can affect the germinability and/or germination rate of seeds. It is, however, unclear if an earlier germination as a result of ingestion affects later plant performance. For sago pondweed, Potamogeton pectinatus, the effects of seed ingestion by ducks on both germinability and germination rate have been previously reported from laboratory experiments. We performed an experiment to determine the effects of seed ingestion by ducks on germination, seedling survival, plant growth and asexual multiplication. Both at the start and end of the winter, seeds were fed to three captive shovelers (Anas clypeata) and planted outdoors in water-filled containers. Plant biomass and its allocation to vegetative parts (shoot and roots), tubers, and seeds were determined in autumn. More duck-ingested seeds than control (uningested) seeds germinated in early winter, but this difference disappeared for seeds planted in late winter, when the treatments were first stratified for 3 mo. None of the variables for measuring seedling survival and plant performance varied between treatments. Under our experimental conditions (no herbivory or competition), ingestion by ducks in early winter resulted in increased performance for seeds surviving gut passage due to enhanced seed germinability, without other costs or benefits for the seedlings.     

How perennial are perennial plants?

Trade-offs involving life span are important in the molding of plant life histories. However, the empirical examination of such patterns has so far been limited by the fact that information on life span is mainly available in terms of discrete categories; annuals, semelparous perennials and iteroparous perennials. We used transition matrix models to project continuous estimates of conditional life spans from published information on size- or stage-structured demography for 71 perennial plant species. The projected life span ranged from 4.3 to 988.6 years and more than half of the species had a life span of more than 35 years. Woody plants had on average a projected life span more than four times as long as non-woody plants. Life spans were higher in forests than in open habitats and individuals of non-clonal species tended to have a longer life span than ramets of clonal species. Self-incompatible plants on average lived longer than self-compatible plants. There were no clear relations between life span and geographical region, dispersal syndrome, pollination mode, seed size or the presence of a seed bank. We conclude that accurate estimates of life span are central to understand how longevity is correlated to other traits within the group of perennial plants.     

What proportion of declared QTL in plants are false?

The false discovery rate (FDR) is the probability that a quantitative trait locus (QTL) is false, given that a QTL has been declared. A misconception in QTL mapping is that the FDR is equal to the comparison-wise significance level, _C. The objective of this simulation study was to determine the FDR in an F₂ mapping population, given different numbers of QTL, population sizes, and trait heritabilities. Markers linked to QTL were detected by multiple regression of phenotype on marker genotype. Phenotypic selection and marker-based recurrent selection were compared. The FDR increased as _C increased. Notably, the FDR was often 10–30 times higher than the _C level used. Regardless of the number of QTL, heritability, or size of the genome, the FDR was 0.01 when _C was 0.0001. The FDR increased to 0.82 when _C was 0.05, heritability was low, and only one QTL controlled the trait. An _C of 0.05 led to a low FDR when many QTL (30 or 100) controlled the trait, but this lower FDR was accompanied by a diminished power to detect QTL. Larger mapping populations led to both lower a FDR and increased power. Relaxed significance levels of _C=0.1 or 0.2 led to the largest responses to marker-based recurrent selection, despite the high FDR. To prevent false QTL from confusing the literature and databases, a detected QTL should, in general, be reported as a QTL only if it was identified at a stringent significance level, e.g., _C0.0001.Communicated by H.C. Becker     

Paradoxical oncogenesis: are all BRAF inhibitors equal?

Cutaneous squamous cell carcinoma (cSCC) is a concerning toxicity with BRAF inhibitors in the treatment for melanoma. While the two drugs shown to improve survival, vemurafenib, and dabrafenib, have similar efficacy, the reported rates of cSCC are quite different. Drawing upon preclinical and clinical trial data, this article discusses the potential factors behind the different cSCC incidences reported with the two BRAF inhibitors and provides a strategic approach to understand this issue further.     

The evolution of plant reproductive systems: how often are transitions irreversible?

Flowering plants are characterized by striking variation in reproductive systems, and the evolutionary lability of their sexual traits is often considered a major driver of lineage diversification. But, evolutionary transitions in reproductive form and function are never entirely unconstrained and many changes exhibit strong directionality. Here, I consider why this occurs by examining transitions in pollination, mating and sexual systems, some of which have been considered irreversible. Among pollination systems, shifts from bee to hummingbird pollination are rarely reversible, whereas transitions from animal to wind pollination are occasionally reversed. Specialized pollination systems can become destabilized through a loss of pollinator service resulting in a return to generalized pollination, or more commonly a reliance on self-pollination. Homomorphic and heteromorphic self-incompatibility systems have multiple origins but breakdown to self-compatibility occurs much more frequently with little evidence for subsequent gains, at least over short time-spans. Similarly, numerous examples of the shift from outcrossing to predominant self-fertilization are known, but cases of reversal are very limited supporting the view that autogamy usually represents an evolutionary dead-end. The evolution of dioecy from hermaphroditism has also been considered irreversible, although recent evidence indicates that the occurrence of sex inconstancy and hybridization can lead to the origin of derived sexual systems from dioecy. The directionality of many transitions clearly refutes the notion of unconstrained reproductive flexibility, but novel adaptive solutions generally do not retrace earlier patterns of trait evolution.     

Geographic variability of ecological niches of plant species: are competition and stress relevant?

A species’ niche position may differ strongly between geographic regions, for instance due to the effect of competitors or ecophysiological stress. However, it is unclear whether such strong geographic niche variation is the rule or the exception. We compared the niche positions of plant species between central England and eastern central Europe (as available from the literature), using phylogenetically independent contrasts. We found that most species occupied similar niche positions in both regions. More importantly, we found that niche variation was not higher in species susceptible to competitive displacement. Nor was niche variation higher in species that reach the edge of their range and thus suffer ecophysiological stress. We suggest that although these species might be easily displaced in their position along a niche axis, they may only be displaced over a short distance. Overall, ecological mechanisms that cause niche variation at the local scale may be much less relevant at the geographic scale.     

Flowering phenology of co-occurring Asteraceae: a matter of climate,ecological interactions,plant attributes or of evolutionary relationships among species?

We analyzed the flowering phenodynamics of 43 Asteraceae species co-occurring in natural populations of Chaco Serrano forests in central Argentina. We explored the potential influence of factors such as photoperiod and climate (variations in temperature, rainfall, and frost), animal-plant interactions (richness of floral visitors, frequency of visits), some plant attributes (plant growth form, seed dispersal mechanism), and evolutionary relationships among species on flowering phenodynamics. Cluster Analysis (CA) and Principal Component Analysis (PCA) were the multivariate statistical methods used to analyze emerging patterns associated with these co-occurring species. Null-model analyses were used to evaluate whether flowering times are aggregated, segregated, or random. Results showed that flowering phenology was significantly correlated with the seasonal variation in temperature, photoperiod, rainfall, and frost. The multivariate statistical methods separated all the species in three groups: 1) species with short flowering time, large plant floral display, high frequency of visits by a large number of species of floral visitors, anemochorous fruits, and shrubby growth form, with a tendency to a segregated flowering pattern; 2) species with long flowering time, small plant floral display, low frequency of visits by few insect species, anemochorous fruits, and herbaceous growth form; and 3) species with long flowering time, small plant floral display, intermediate values for frequency of visits and number of species of floral visitors, seed dispersal mechanisms other than anemochory, and herbaceous growth form. In addition, all but one species belonging to early-branching tribes (tribes phylogenetically close to the root of the Asteraceae tree) were grouped together and clustered in the same region of the two-dimensional PCA ordination. All species belonging to the late-branching tribes (Asteroideae subfamily tribes) included in group 1 were separated from the other Asteroideae species in the PCA. In conclusion, it seems that climatic factors restrict the phenological period of most species, and that plant attributes and taxonomic membership are strongly related to flowering phenodynamics in this group of Asteraceae studied.     

Jack of all trades,master of some? On the role of phenotypic plasticity in plant invasions

Invasion biologists often suggest that phenotypic plasticity plays an important role in successful plant invasions. Assuming that plasticity enhances ecological niche breadth and therefore confers a fitness advantage, recent studies have posed two main hypotheses: (1) invasive species are more plastic than non-invasive or native ones; (2) populations in the introduced range of an invasive species have evolved greater plasticity than populations in the native range. These two hypotheses largely reflect the disparate interests of ecologists and evolutionary biologists. Because these sciences are typically interested in different temporal and spatial scales, we describe what is required to assess phenotypic plasticity at different levels. We explore the inevitable tradeoffs of experiments conducted at the genotype vs. species level, outline components of experimental design required to identify plasticity at different levels, and review some examples from the recent literature. Moreover, we suggest that a successful invader may benefit from plasticity as either (1) a Jack-of-all-trades, better able to maintain fitness in unfavourable environments; (2) a Master-of-some, better able to increase fitness in favourable environments; or (3) a Jack-and-master that combines some level of both abilities. This new framework can be applied when testing both ecological or evolutionary oriented hypotheses, and therefore promises to bridge the gap between the two perspectives.     

Surfing, regulating and capturing: are all microtubule-tip-tracking proteins created equal?

A diverse group of microtubule-binding proteins has been linked through live-cell imaging of green fluorescent protein (GFP) fusion proteins. These proteins share the ability to associate with the plus ends of elongating microtubules and track with these tips as the microtubules grow, in a process known as "tip tracking". Several models have been proposed to explain the significance of this activity, including roles in delivering proteins to the cell periphery and in modulating microtubule dynamics. However, the recent observation that some of the tip trackers colocalize on structures undergoing search-capture suggests that tip tracking could be a fundamental aspect of the search-capture process. Focusing on the shared ability of these proteins to undergo tip tracking, this article is intended to place the search-capture model in the context of other proposed functions and to stimulate discussion in this area.