scholarly journals Trade-offs among plant reproductive traits determine interactions with floral visitors

2021 ◽  
Author(s):  
Jose B. Lanuza ◽  
Romina Rader ◽  
Jamie Stavert ◽  
Liam K. Kendall ◽  
Manu E. Saunders ◽  
...  

Plant life-history strategies are constrained by cost-benefit trade-offs that determine plant form and function. However, despite recent advances in the understanding of trade-offs for vegetative and physiological traits, little is known about plant reproductive economics and how they constrain plant life-history strategies and shape interactions with floral visitors. Here, we investigate plant reproductive trade-offs and how these drive interactions with floral visitors using a dataset of 17 reproductive traits for 1,506 plant species from 28 plant-pollinator studies across 18 countries. We tested whether a plant's reproductive strategy predicts its interactions with floral visitors and if the different reproductive traits predict the plant's role within the pollination network. We found that over half of all plant reproductive trait variation was explained by two independent axes that encompassed plant form and function. Specifically, the first axis indicated the presence of a trade-off between flower number and flower size, while the second axis indicated a pollinator dependency trade-off. Plant reproductive trade-offs helped explain partly the presence or absence of interactions with floral visitors, but not differences in visitation rate. However, we did find important differences in the interaction level among floral visitor guilds on the different axes of trait variation. Finally, we found that plant size and floral rewards were the most important traits in the understanding of the plant species network role. Our results highlight the importance of plant reproductive trade-offs in determining plant life-history strategies and plant-pollinator interactions in a global context.

2010 ◽  
Vol 88 (10) ◽  
pp. 995-1002 ◽  
Author(s):  
A. Nicolai ◽  
J. Filser ◽  
V. Briand ◽  
M. Charrier

When a life history is characterized by both seasonality in reproduction and seasonality in offspring fitness, trade-offs in reproductive traits might be adjustments to seasonal time constraints to optimize reproductive success. Therefore, we compared in the laboratory the trade-offs in reproductive traits between early (after maturity) and delayed (after dormancy) reproduction in young land snails Cornu aspersum (Müller, 1774) (syn. Helix aspersa ), depending on food energy content. We also investigated the maternal investment in reproductive output in both breeding periods. After attaining maturity, snails produced single clutches with many small eggs, which resulted, in contrast to previous studies, in large offspring with a low hatching rate owing to high within-clutch cannibalism. The young cannibals may have a higher survival probability in the following hibernation. Snails starting to reproduce after hibernation had smaller clutches of larger eggs, resulting in high quantity of lighter offspring. The clutch mass was positively correlated with maternal mass in snails reproducing after having attained maturity and negatively correlated in snails reproducing after hibernation. Multiple oviposition occurred only after hibernation, thereby enhancing reproductive success. An energy-rich diet did not affect reproductive strategies. Further studies should focus on seasonal plasticity of reproductive strategies in natural populations of C. aspersum and investigate survival probabilities of breeders and juveniles in an evolutionary context.


2020 ◽  
Vol 126 (1) ◽  
pp. 1-23 ◽  
Author(s):  
Igor Cesarino ◽  
Raffaele Dello Ioio ◽  
Gwendolyn K Kirschner ◽  
Michael S Ogden ◽  
Kelsey L Picard ◽  
...  

Abstract Background Model organisms are at the core of life science research. Notable examples include the mouse as a model for humans, baker’s yeast for eukaryotic unicellular life and simple genetics, or the enterobacteria phage λ in virology. Plant research was an exception to this rule, with researchers relying on a variety of non-model plants until the eventual adoption of Arabidopsis thaliana as primary plant model in the 1980s. This proved to be an unprecedented success, and several secondary plant models have since been established. Currently, we are experiencing another wave of expansion in the set of plant models. Scope Since the 2000s, new model plants have been established to study numerous aspects of plant biology, such as the evolution of land plants, grasses, invasive and parasitic plant life, adaptation to environmental challenges, and the development of morphological diversity. Concurrent with the establishment of new plant models, the advent of the ‘omics’ era in biology has led to a resurgence of the more complex non-model plants. With this review, we introduce some of the new and fascinating plant models, outline why they are interesting subjects to study, the questions they will help to answer, and the molecular tools that have been established and are available to researchers. Conclusions Understanding the molecular mechanisms underlying all aspects of plant biology can only be achieved with the adoption of a comprehensive set of models, each of which allows the assessment of at least one aspect of plant life. The model plants described here represent a step forward towards our goal to explore and comprehend the diversity of plant form and function. Still, several questions remain unanswered, but the constant development of novel technologies in molecular biology and bioinformatics is already paving the way for the next generation of plant models.


1997 ◽  
Vol 22 (3) ◽  
pp. 592
Author(s):  
Henrik Balslev ◽  
Philip W. Rundel ◽  
Alan P. Smith ◽  
F. C. Meinzer

2021 ◽  
Vol 11 (4) ◽  
pp. 1526-1534
Author(s):  
Jules Segrestin ◽  
Kevin Sartori ◽  
Marie‐Laure Navas ◽  
Jens Kattge ◽  
Sandra Díaz ◽  
...  

Author(s):  
Karl J Niklas ◽  
Frank W Telewski

Abstract Abiotic–biotic interactions have shaped organic evolution since life first began. Abiotic factors influence growth, survival, and reproductive success, whereas biotic responses to abiotic factors have changed the physical environment (and indeed created new environments). This reciprocity is well illustrated by land plants who begin and end their existence in the same location while growing in size over the course of years or even millennia, during which environment factors change over many orders of magnitude. A biomechanical, ecological, and evolutionary perspective reveals that plants are (i) composed of materials (cells and tissues) that function as cellular solids (i.e. materials composed of one or more solid and fluid phases); (ii) that have evolved greater rigidity (as a consequence of chemical and structural changes in their solid phases); (iii) allowing for increases in body size and (iv) permitting acclimation to more physiologically and ecologically diverse and challenging habitats; which (v) have profoundly altered biotic as well as abiotic environmental factors (e.g. the creation of soils, carbon sequestration, and water cycles). A critical component of this evolutionary innovation is the extent to which mechanical perturbations have shaped plant form and function and how form and function have shaped ecological dynamics over the course of evolution.


2009 ◽  
Vol 25 (1) ◽  
pp. 103-106 ◽  
Author(s):  
Nathan G. Swenson

Whole plant form and function vary spectacularly across the seed plants. In recent years, plant evolutionary ecologists have begun to document this diversity on large geographic scales by analysing ‘functional traits’ that are indicative of whole plant performance across environmental gradients (Swenson & Enquist 2007, Wright et al. 2004). Despite the high degree of functional diversity in tropical forests, convergence in function does occur locally along successional or light gradients (Bazzaz & Pickett 1980, Swaine & Whitmore 1988).


2021 ◽  
Vol 288 (1963) ◽  
Author(s):  
Iker Irisarri ◽  
Tatyana Darienko ◽  
Thomas Pröschold ◽  
Janine M. R. Fürst-Jansen ◽  
Mahwash Jamy ◽  
...  

Streptophytes are one of the major groups of the green lineage (Chloroplastida or Viridiplantae). During one billion years of evolution, streptophytes have radiated into an astounding diversity of uni- and multicellular green algae as well as land plants. Most divergent from land plants is a clade formed by Mesostigmatophyceae, Spirotaenia spp. and Chlorokybophyceae. All three lineages are species-poor and the Chlorokybophyceae consist of a single described species, Chlorokybus atmophyticus. In this study, we used phylogenomic analyses to shed light into the diversity within Chlorokybus using a sampling of isolates across its known distribution. We uncovered a consistent deep genetic structure within the Chlorokybus isolates, which prompted us to formally extend the Chlorokybophyceae by describing four new species. Gene expression differences among Chlorokybus species suggest certain constitutive variability that might influence their response to environmental factors. Failure to account for this diversity can hamper comparative genomic studies aiming to understand the evolution of stress response across streptophytes. Our data highlight that future studies on the evolution of plant form and function can tap into an unknown diversity at key deep branches of the streptophytes.


1995 ◽  
Vol 83 (3) ◽  
pp. 555
Author(s):  
J. C. Lovett ◽  
P. W. Rundel ◽  
A. P. Smith ◽  
F. C. Meinzer

Sign in / Sign up

Export Citation Format

Share Document