New Phytologist
○ Wiley
All preprints, ranked by how well they match New Phytologist's content profile, based on 346 papers previously published here. The average preprint has a 0.34% match score for this journal, so anything above that is already an above-average fit. Older preprints may already have been published elsewhere.
Williams, A.; Sinanaj, B.; Rodriguez-Morelos, V.; Prout, J.; Howard, N. O. A.; Durant, E.; Pressel, S.; Field, K.
Show abstract
Most plants form mutualistic symbioses with soil fungi, including arbuscular mycorrhizal (AM) fungi. These fungi usually transfer soil nutrients to plants and assimilate carbon from host plant photosynthesis. Recently, Mucoromycotina fine root endophytes (MFRE) were identified as nutritionally mutualistic and widespread fungal symbionts of plants, establishing MFRE as a new class of mycorrhizal fungi. However, the regulatory mechanisms for MFRE symbioses are completely unknown. Other symbionts, like AM fungi, use the Common Symbiotic Signalling Pathway (CSSP) to establish symbiosis. To explore whether MFRE interactions also involve this pathway, we cultured MFRE with CSSP mutants of Medicago truncatula which show impaired AM symbioses and tracked carbon and nutrient transfers using isotope tracers. Results show no differences in root colonization or nutrient exchange, suggesting MFRE symbioses are regulated by different molecular mechanisms. This finding highlights the unique nature of MFRE symbiosis, broadening our understanding of diverse fungal symbioses and their evolutionary significance.
Ferreras-Garrucho, G.; Hull, R.; Rubens, D.; Bates, R.; Hope, M. S.; Bowden, S.; Wallington, E.; Paszkowski, U.
Show abstract
Arbuscular mycorrhizal (AM) symbiosis is conserved across land plants and is the default nutrient uptake strategy in nature. Within roots, AM colonisation is tightly patterned and dynamically tuned by nutritional cues. Multiple genetic modules contribute to this regulation, including the phosphate starvation response, DWARF14-LIKE (D14L) karrikin signalling, and the common symbiosis signalling pathway (CSSP). Transcriptional overlap among these has led to the hypothesis that phosphate starvation and D14L signalling act upstream of the CSSP. Here, we examined the epistatic relationship between D14L and CSSP in rice. Overexpression of an autoactive gain-of-function CCaMK (gofCCaMKox) restored AM colonisation and symbiosis marker gene expression in d14l mutants to wild-type levels or above, whereas overexpression of wild-type CCaMK did not, confirming that CSSP operates downstream of D14L signalling. However, gofCCaMKox did not rescue the d14l mesocotyl elongation phenotype, supporting a bifurcation of D14L into developmental and symbiotic outputs. Unexpectedly, gofCCaMKox also expanded fungal access to normally restrictive tissue domains (the meristematic zone and endodermis) assigning a role for CCaMK activation in defining root zone and cell-type competence for AM colonisation. Despite restored colonisation, introduction of gofCCaMKox into d14l produced arbuscules, which however were less developed and had increased hyphal septation, revealing a CCaMK-independent role for D14L in intraradical colonisation and arbuscule development. Transcriptome profiling resolved AM-relevant genes into modules controlled by CCaMK activation alone, in combination with D14L, or requiring additional colonisation-associated cues, and further suggested CCaMK primarily acts through AP2 transcription factors. Together, these findings reinforce CCaMK as a master regulator of AM symbiosis at the genetic, transcriptomic and anatomical levels while uncovering CCaMK-independent functions of D14L in arbuscule development.
Qiao, T.; Wang, L.; Zhao, Y.; Li, Y.; Yang, G.; Zhu, B.; Pan, K.
Show abstract
Diatoms synthesize silica cell walls (frustules) with genetically encoded morphologies, ranging from nanopatterns to micropatterns, that far exceed current synthetic chemistry. Silaffins, a family of phosphoproteins undergoing complex post-translational modifications, have been isolated from frustules and shown to facilitate and regulate biosilica formation in vitro with long-chain polyamines. However, their particular role in frustule morphogenesis and functionality remains unclear. In this study, functions of two representative silaffins, TpSil1 and TpSil3, were investigated in the model organism Thalassiosira pseudonana using gene overexpression and CRISPR/Cas9-mediated knockout approaches. Due to high sequence homology, TpSil2 was concurrently disrupted in TpSil1 knockout strains, while the homozygous knockout of TpSil3 proved to be lethal. Quantitative morphological analysis revealed distinct yet complementary roles: TpSil3 governs both microscale overall size and mesoscale features, including macropore (fultoportula) density and mesopore (cribrum pore) pattern, whereas TpSil1/2 exclusively contribute to macropore morphogenesis and mesopore density. Overexpression of silaffins increased silica deposition, while knockouts exhibited reduced silicification but enhanced cell growth and photosynthetic efficiency. Furthermore, these genetic modifications significantly influenced the physicochemical and optical properties of bulk frustules, potentially enhancing the hemostatic, catalytic and photonic performances, thereby positioning them as versatile candidates for a wide range of biotechnological and industrial applications. Collectively, our findings elucidate the distinct roles of TpSil1/2 and TpSil3 in diatom physiology and frustule morphology, highlighting a promising pathway for engineering nanostructured silica materials with tailored properties through synthetic biology.
Rana, S. K.; Rana, H. K.; Landis, J.; Chen, J.; Deng, T.; Sun, H.
Show abstract
O_LIFloral polymorphisms frequently persist across heterogeneous environments despite ongoing gene flow, yet the regulatory mechanisms maintaining discrete phenotypes remain unclear. We tested whether alternative flower-colour morphs in Stellera chamaejasme L. are maintained by canalized gene regulatory architectures that stabilize expression around morph-specific optima. C_LIO_LIWe used a pan-transcriptomic and eco-evolutionary framework integrating genome-wide gene expression profiling, co-expression network analysis, functional enrichment, ortholog-based phylogenomics, and variance-based modeling of regulatory canalization and transgressive expression to quantify regulatory variation across morphs. C_LIO_LITranscriptomic variation was structured primarily by morph identity rather than geography, indicating consistent morph-associated regulatory programs. Parental morphs showed reduced within-morph variance in gene co-expression modules, consistent with strong regulatory constraint at the network level. In contrast, a naturally occurring mosaic morph exhibited extensive non-additive and predominantly transgressive expression, with most genes falling outside the parental range. This transgressive signal was modular, with most networks remaining stable while a subset showed elevated variance and disrupted inheritance. Functional analyses further reveal that floral pigmentation is embedded within broader metabolic and stress-response pathways, linking color polymorphism to coordinated physiological states and ecological differentiation. C_LI
Ray, R.; Maloof, J.; Magney, T.
Show abstract
Leaf reflectance spectra are emerging as a viable substitute for gas-exchange measurements of photosynthetic capacity, with a community benchmark reporting that a spectrum accurately recovers most Farquhar-von Caemmerer-Berry (FvCB) parameters. This study re-scores the recovery under dataset-blocked, species-blocked, and leave-one-dataset-out designs, measuring the split-half reliability of each curated parameter. We constructed a convolutional encoder that maps a spectrum to the four parameters through a fixed, differentiable FvCB decoder trained on measured assimilation. A conspecific of 97.4% of held-out leaves were present in the training set, and accuracy is lost along the dataset axis but not along the species axis. Under blocked evaluation, a spectrum constrains a single capacity axis. Jmax25 retains only 17% of its recovery when Vcmax25 is held constant, and the Jmax25:Vcmax25 ratio is not predicted above a median null. The curated values of TPU25 are not reproducible, whereas those of Rday25 are well determined, but its recovery fails due to the loss. The published study measures interpolation rather than transfer, and spectra constrain less of the FvCB parameter space than assumed, including the carboxylation to electron transport balance. Routing predictions through explicit biochemistry makes identifiability measurable, although it does not improve prediction accuracy.
Guo, H.; Zhao, Y.; Zheng, B.; Huang, Y.; Chen, X.; Wang, L.
Show abstract
Global nitrogen (N) deposition has fundamentally reshaped plant nutrient acquisition by altering mechanistic trade-offs between root exploration-exploitation strategies and mycorrhizal symbiosis. Through a meta-analysis of 135 studies spanning 153 sites, we demonstrate that N deposition stimulates root exploration (+84.6% root length density) and exploitation (+13.2% nitrogen content and +8.5% root biomass) while suppressing mycorrhizal dependence (-32.8% biomass, -18.73% colonized root length, -7.55% hyphal length), indicating a systemic shift toward root-autonomous nutrient acquisition. Divergent responses emerged between plant lifeforms: woody plants prioritize exploitation (+13.2% nitrogen content) over exploration capacity (-7.9% root length density), whereas herbaceous species exhibit synergistic enhancement of both strategies (+88% root length density, +13.2% nitrogen content and +71.3% root biomass). In contrast to N-only effects, Combined nitrogen and phosphorus additions reversed mycorrhizal suppression (+41.9% biomass), highlighting their persistent role in phosphorus acquisition under elevated nutrient conditions. The root economics space framework demonstrates predictive power, with plants possessing lower specific root length (SRL) and higher nitrogen content exhibiting stronger positive responses to N deposition, while those possessing higher SRL and lower nitrogen content showed reduced investment in root systems. These trait-mediated thresholds in carbon-nutrient tradeoffs refine our capacity to model belowground ecological responses to anthropogenic nitrogen perturbation, establishing a mechanistic basis for projecting ecosystem trajectories under global change.
Zaharescu, D. G.
Show abstract
The emergence of vascular plants on land is one of evolution greatest triumphs. This success was contingent on the capacity of roots and their symbionts to acquire resources from exposed geology. However, how rock chemistry shapes plant root architectural strategies, and their return on investment during early ecosystem colonization remains poorly understood. Here we use a two-year mesocosm experiment with Bouteloua dactyloides grass and an arbuscular mycorrhizal symbiont, grown on four mineral substrates of contrasting composition, to show that rock geochemistry predictably determines root topological strategy, from herringbone architecture on nutrient-poor granite to dichotomous-like branching on nutrient-rich basalt. Substrate identity governed investment allocation between root complexity and biomass, with plants consolidating existing transport pathways as weathering-derived nutrients subsided. Traits associated with exploratory effort were generally decoupled from those related to biomass buildup. In basalt and rhyolite plants preferentially invested in complexity, generating the largest numbers of prospective tips for mining and biomass buildup; in granite, plants chose a surviving strategy, limiting branching to preserve biomass; while in schist, plants balanced biomass with complexity, extending growth on low investment, which increased tissue density. Surprisingly, mycorrhizal fungi did not alter the whole root system size, but reallocated investment between specific root orders, discouraging investment in embryonic roots in some substrates, and stimulating lateral expansion of the rooting system in others. This extends the functional balance mechanism from plant to the plant-fungus system. The extensive phenotypic plasticity of the root-mycorrhiza system shown here provides an evolutionary space for natural selection, which must have played a crucial role in the success of plants on land in the past, and is crucial for understanding plant ecological dynamics today.
Yuan, J.; Xu, T.; Hiltbrunner, A.
Show abstract
O_LIPhytochromes are photoreceptors enabling plants to respond to various light conditions. Independent gene duplication events resulted in small phytochrome gene families in mosses, ferns, and seed plants. This phytochrome diversity is hypothesised to be critical for sensing and adapting to different light conditions, but experimental evidence for this idea is lacking for mosses and ferns. C_LIO_LIThe model moss species Physcomitrium patens contains seven phytochromes grouped into three clades, PHY1/3, PHY2/4, and PHY5. Here, we used CRISPR/Cas9 generated single and higher order mutants to investigate their role in light-regulation of protonema and gametophore growth, protonema branching, and induction of gametophores. C_LIO_LIWe found both specific and partially overlapping roles for the three clades of moss phytochromes in regulating these responses in different light conditions, and we identified a mechanism for sensing simulated canopy shade different from the mechanism in seed plants. PHY1/3 clade phytochromes act as primary far-red light receptors, while PHY5 clade phytochromes are the primary red light receptors. PHY2/4 clade phytochromes have functions in both red and far-red light. C_LIO_LISimilar to seed plants, gene duplication events in the phytochrome lineage in mosses were followed by functional diversification into red and far-red light sensing phytochromes. C_LI
Anokye, M.; Hellwig, T.; Haraldsson, E. B.; Schüller, R.; Döring, N.; Westhoff, P.; Bucharova, A.; von Korff, M.
Show abstract
O_LIThere is growing interest in developing perennial cereal crops for sustainable production, yet key differences in trait syndromes between annual and perennial grasses and their influence on environmental adaptation remain poorly understood. C_LIO_LIWe measured 25 traits in 16 annual and perennial Hordeum species (45 accessions), including barley, grown over three seasons in a common garden. Using a phylogenetic framework and repeated transitions between annual and perennial forms, we (i) identified traits distinguishing these life strategies and (ii) tested how they relate to climate at the accessions origins. C_LIO_LIWild and cultivated barley are distinguished within the Hordeum clade by high growth rates and large organs, which may have predisposed wild barley to domestication. Annual and perennial accessions differed in resource allocation: annuals had higher harvest index and leaf and grain nitrogen, while perennials produced carbon-rich tissues and sustained vegetative growth. Seasonal temperature variation shaped trait syndromes: annual traits aligned with temperature in the driest quarter, reflecting selection under terminal stress, while perennial traits correlated with temperature in the wettest quarter, the main growth phase shaping long-term performance and survival. C_LIO_LIWe provide important information on traits and climate adaptations underlying perennial persistence and annual resource strategies, relevant for developing perennial cereal crops. C_LI
Tumber-Davila, S. J.; Andraczek, K.; Laughlin, D. C.; Bruelheide, H.; Bombo, A. B.; Fan, Y.; Fidelis, A.; Freschet, G. T.; Hartmann, L.; Hennecke, J.; Howard, C. C.; Jimoh, S. O.; Klimesova, J.; Mommer, L.; Ramalevha, T.; Siebert, F.; Weigelt, A.; Bergmann, J.
Show abstract
Belowground plant trait research has predominantly focused on trade-offs in fine root traits via the root economics space. Yet, this fine root framework captures only a fraction of the functional strategies plants employ beneath the soil surface. Here, we broaden the perspective on belowground plant functioning by integrating traits related to root system extent, clonality and bud banks, using data from the new UNDERPLOT database. This integration links measurable traits to key belowground functions: resource acquisition, spatial exploration, and persistence. Our analysis shows that the fine root economics space explains less than 5% of the variation in traits related to root system extent, clonality, and bud banks. Instead, an expanded trait analysis reveals three significant dimensions, explaining 62% of total trait variation. The third dimension, represents an independent, persistence-related gradient, not captured by existing root economics frameworks. We propose that understanding belowground plant strategies requires embracing additional functional gradients. The strategy of persistence, in particular, varies significantly across growth forms and is a critical dimension of plant response to resource limitation and stress, becoming increasingly important as global change shifts disturbance regimes.
Parry, C.; Turnbull, C. J.; Barter, L.; Smith, M.; Barmpoutis, P.; Skirlo, K.; Florence, H.; Gill, R. J.
Show abstract
O_LIPollination is essential for plant reproduction, ecosystem resilience and human health. Yet, our capability to map pollination service delivery in real-time across large areas remains poor. Determining where and when flowers are pollinated is vital to mitigate widespread pollination deficits, increase plant health and yield, and support pollinator management. Hence, innovative approaches are urgently needed for establishing scalable predictive bioindicators of plant pollination status with the goal of achieving real-time landscape-scale monitoring. C_LIO_LIHere we present two parallel controlled pollination assays in which we characterise the post-pollination petal physiology of a world leading flowering crop, Brassica napus, using in-situ close-range hyperspectral reflectance and semi-untargeted metabolomics. C_LIO_LIThis multiomics approach coupled with supervised machine learning and biomarker detection reveals cryptic changes in the UV petal reflectance spectrum which are predictive of pollination status, representing a novel set of candidate pollination bioindicators ( polli-markers), and our high-resolution time series enables prediction of when this pollination event occurred. It also reveals an associated set of candidate metabolites, including flavonoids and senescence markers, shedding light on the functional pathways related to our polli-markers. C_LIO_LIThis study provides key insights into floral development, enabling a transformative step towards predicting, mapping and quantifying pollination service delivery at the landscape scale. C_LI
Authier, E.; Frachon, L.; Friedrichs, J.; Brokate, L.; Junker, R. R.; Müller, C.; Dussarrat, T.
Show abstract
Phytochemistry is a core player in shaping plant-pollinator networks and pollination services. Yet, little is known about the dynamic evolution of phytochemical traits in response to limited pollinator access, especially concerning chemical diversity. We combined an evolutionary experiment manipulating pollinator access with predictive metabolomics to uncover evolutionary changes in phytochemical traits of Brassica rapa. Our results unveiled chemical changes in both leaf and flower chemistry. Moreover, plants under selection by limited pollinator access showed a decreased chemical richness and diversity and a modulated primary and specialised metabolism, which could be used to predict pollinator access with 88% accuracy. Chemical indices and metabolites responding to pollinator access were associated with variation in flowering time and performance of outcrossing flowers. Our findings provide key insights into the influence of pollinator access on plant chemistry and indicate a risk of pollinator decline and losses of chemical diversity for plant-pollinator network structure and ecosystem dynamics.
Sanaei, A.; Andraczek, K.; Kretz, L.; Schnabel, F.; Richter, R.; Kahl, A.; Nabel, N.; von_Sivers, L.; Künne, T.; Leonore.van_braak, J.; Felicitas Hofmann, R.; Sophie Hensel, C.; Mora, K.; Feilhauer, H.; Wirth, C.; Weigelt, A.
Show abstract
Quantifying the variation in plant traits reveals the trade-offs involved in plant ecological strategies and is fundamental to understanding underlying plant fitness mechanisms. Thus, the ecological success of plant species in a certain habitat may depend on the coordinated performance of both leaves and roots. However, despite the growing interest in trait variation, it is still uncertain i) to what extent the leaf economics spectrum (LES) and root economics space (RES) hold across locally coexisting tree species and ii) whether leaf and fine-root traits are correlated. In a research arboretum, we simultaneously measured eight key traits in leaves and fine-roots on 270 individuals belonging to 90 tree species, encompassing both angiosperm and gymnosperm species. We find varied plant resource strategies associated with leaves and fine-roots for angiosperms and gymnosperms. We observe a clear LES for gymnosperms and a clear RES for angiosperms. Our results support the existence of a correlation between analogous leaf and fine-root traits across all species. However, varying trait coordination across clades indicates varying resource acquisition strategies above- and belowground, highlighting the need to consider large-scale phylogenetic relatedness to better understand plant fitness.
Hellwig, T.; Doering, N.; Haraldsson, E. B.; von Korff, M.
Show abstract
Annual and perennial life-history strategies have evolved repeatedly across angiosperms, yet the genomic and environmental underpinnings of these transitions remain poorly understood, particularly in grasses. We generated de novo transcriptomes from 82 accessions representing 22 Hordeum species, including barley, and identified 257 single-copy orthologs present in all accessions to infer a robust phylogeny of the genus. By combining phylogenetic network inference with ABBA-BABA tests, we detected four cases of interspecific hybridization, three coinciding with major long-distance dispersal events across continents. Comparative climatic niche analysis indicated annual Hordeum species inhabit environments with higher temperatures, greater interannual variability, and increased human disturbance, compared to perennials, although no consistent precipitation differences were observed. Using our phylogeny as a framework, we analyzed selection and gene expression to uncover genomic changes associated with life-history strategy while accounting for phylogenetic non-independence. Additionally, we analysed gene copy number variations associated with life-history strategy. These analyses yielded 174 candidate genes across diverse biological functions, suggesting the genetic architecture underlying life-history evolution is more complex than assumed. Candidate genes grouped into six major functional categories, the most prominent being signal transduction and development, including regulators of flowering, dormancy, and meristem activity, metabolic and biosynthetic processes related to carbon allocation and storage, and stress response and defense, reflecting the resilience of perennials compared to the accelerated growth strategies of annuals. Our study reconstructs the evolutionary history and climatic niche differentiation of Hordeum species and demonstrates that convergent life-history evolution is driven by multifaceted, functionally diverse genetic mechanisms.
Tyszka, A. S.; Chia, K.-S.; Bretz, E. C.; Mansour, L.; Larson, D. A.; Carella, P.; Walker, J. F.
Show abstract
While DNA has built the framework for molecular insights from museum collections, the utility of archival RNA remains largely unexplored. Likely a consequence of the known instability of RNA relative to DNA, this has effectively precluded the use of herbaria for transcriptomics. Here, we challenge the assumption that herbaria cannot be used for transcriptomics by assembling transcriptomes from RNA extracted from herbarium specimens. Through systematic comparison of transcriptomes from fresh-collected, silica-dried, and archival specimens, we demonstrate the suitability of herbarium-derived RNA for transcriptomics. We show the practical applicability of archival mRNA by functionally validating a plant immune receptor synthesized from a specimen collected in 1956. These results contradict the community consensus regarding archival RNA and open the door to subsequent transcriptomic explorations of rare and extinct plant species. Our findings highlight the importance of preserving and utilizing the diversity embedded within herbarium collections.
Nichodemus, C. O.; Meireles, J. E.
Show abstract
O_LIPlant functional traits vary across leaf ontogeny and phenology, yet most trait data are snapshots from narrow time windows that miss this temporal dimension. Leaf spectra are increasingly used with empirical models to predict traits, but whether such models accurately capture phenological variation remains unclear. C_LIO_LIWe monitored leaf traits and spectra weekly across a full growing season, generating 7,515 spectra from seven temperate species. Using partial least squares regression, we built three models --all-season and week-as-covariate models (both trained on full-phenology data), and a peak-season model -- and evaluated them alongside a widely used model against directly measured traits. C_LIO_LIFull-phenology models predicted LMA and equivalent water thickness (EWT) with high accuracy (R{superscript 2} > 0.85) and nitrogen with intermediate accuracy (R{superscript 2} = 0.64); carbon accuracy was low across all models (R{superscript 2} < 0.26), likely due to a small sample size. Peak-season trained models performed poorly when evaluated across the full season, often producing biologically unrealistic predictions. Traits and spectra varied significantly across phenological stages both within and among species. C_LIO_LIIgnoring phenological variation systematically biases trait estimates and ecological inference. Coupled with phenologically representative training data, spectra can capture the temporal dynamics of plant function, enabling novel research in ecology and evolution. C_LI
Oren, E.; Zhai, J.; Rooney, T. E.; Angelovici, R.; Hale, C. O.; Brindisi, L. J.; Hsu, S.-K.; Gault, C. M.; Hua, J.; La, T.; Lepak, N.; Fu, Q.; Buckler, E. S.; Romay, M. C.
Show abstract
O_LIGrasses in the PACMAD clade independently colonized cold environments from warm-climate ancestors, but whether their molecular responses to freezing reflect shared evolutionary solutions or lineage-specific innovations remains unknown. We used comparative proteomics to test whether protein-level cold responses show stronger cross-species conservation than previously observed at the transcript level. C_LIO_LIWe quantified seasonal rhizome proteomes (winter vs summer) from five PACMAD species grown in a common garden exposed to sustained sub-zero temperatures, identified differentially abundant proteins, and compared fold-change magnitudes across species using orthogroup-based correlation analyses. We further examined LEA3 protein structure through hydropathy profiling and motif analysis. C_LIO_LIShared cold-responsive proteins showed higher cross-species fold-change correlation ({rho} = 0.80) than background proteins ({rho} = 0.45), despite greater divergence in baseline abundance. LEA3 was the only ortholog elevated across all five species. Cold-tolerant species contained more tandem 11-mer repeats than the cold-sensitive maize, and two species accumulated multiple LEA3 paralogs, increasing total LEA3 abundance. C_LIO_LIIndependent evolution of freezing tolerance in PACMAD grasses is governed by evolutionary constraints on protein-level response magnitude, reflecting the retention of an ancestral protective capacity. Structural divergence of LEA3 in maize suggests that transcriptional induction alone does not ensure freezing tolerance; functional protection likely requires intact motif architecture. C_LI
Bhadra, S.; Leitch, I.; Bellot, S.; Baker, W. J.; Onstein, R.
Show abstract
O_LIThe importance of functional trait evolution and genome size on plant speciation are well established, but their interactive effects remain untested in a single comparative macroevolutionary framework. C_LIO_LIWe integrated phylogenetic, trait and genome size data for palms (Arecaceae) - a large pantropical family (>2600 species) with 167-fold variation in trait and 60-fold variation in genome size. We used structural equation modelling to test three key hypotheses: trait evolution promotes speciation (H1: trait flexibility hypothesis), and, speciation and trait evolution rates are constrained by allometry (H2: allometric constraint hypothesis) and genome size (H3: large genome constraint hypothesis). C_LIO_LIWe detected seven major speciation rate shifts during the ca. 110-million-year history of palms. Tip-derived speciation rates increased with faster evolution in leaves and plant height, supporting H1, whereas correlated evolution between trait evolution rates indirectly influenced speciation, supporting H2. Large genomes decreased plant height and stem diameter evolutionary rates, but increased leaf size evolution and speciation rates, thus partly supporting H3. C_LIO_LIOur findings illustrate how the complex interplay between genome size, allometry and trait evolvability affect speciation, emphasizing the importance of holistic approaches in macroevolution. Furthermore, our results point to potential general mechanisms driving speciation rates throughout the plant Tree of Life. C_LI
Jiang, G.-F.; Li, S.-Y.; Dinnage, R.; Cao, K.-F.; Simonin, K.; Roddy, A.
Show abstract
Background and AimsWhile genome size limits the minimum sizes and maximum numbers of cells that can be packed into a given leaf volume, mature cell sizes can be substantially larger than their meristematic precursors and vary in response to abiotic conditions. Mangroves are iconic examples of how abiotic conditions can influence the evolution of plant phenotypes. MethodsHere, we examined the coordination between genome size, leaf cell sizes, and cell packing densities, and leaf size in 13 mangrove species across four sites. Four of these species occurred at more than one site, allowing us to test the effect of climate on leaf anatomy. ResultsWe found that genome sizes of mangroves were very small compared to other angiosperms, and, like other angiosperms, mangrove cells were always larger than the minimum size defined by genome size. Increasing mean annual temperature of a growth site led to higher packing densities of veins (Dv) and stomata (Ds) and smaller epidermal cells but had no effect on stomatal size. Contrary to other angiosperms, mangroves exhibited (1) a negative relationship between guard cell size and genome size; (2) epidermal cells that were smaller than stomata, and (3) coordination between Dv and Ds that was not mediated by epidermal cell size. Furthermore, mangrove epidermal cell sizes and packing densities covaried with leaf size. ConclusionsWhile mangroves exhibited coordination between veins and stomata and attained a maximum theoretical stomatal conductance similar to other angiosperms, the tissue-level tradeoffs underlying these similar relationships across species and environments was markedly different, perhaps indicative of the unique structural and physiological adaptations of mangroves to their stressful environments.
Hernandez-Hernandez, T.; Vasquez-Cruz, M.; Israel, L.; DelAngel, M.; Nakamura, M.
Show abstract
Although distributed globally, plants possessing the succulent syndrome are thought to have evolved to adapt to arid climates, because they possess modifications that increase their water use efficiency. Here we study the evolution and the ecological nature of the succulent CAM syndrome at a global scale by analyzing the climatic niches of succulents within the Caryophyllales, testing the hypothesis of a climatic niche specialization by comparing them with their non-succulent, non-arid adapted relatives. We assembled and carefully curated a worldwide dataset of 5447 species in 28 families, and analyzed the current and evolutionary trajectories of climatic niches with an array of statistical methods including ecological niche modeling, phylogenetic regression and divergence dates estimation. Our results confirm the Core Caryophyllales tend to inhabit drylands probably since their origin in the Early Cretaceous. However, the succulent syndrome appeared later with some lineages diversifying profusely afterwards. The climatic niche of succulents is not differentiated from their non-succulent relatives, but narrower, and contained within the non-succulents, showing no relationship with extreme conditions such as high aridity or temperatures. Our results support alternative interpretations of the origin of the CAM syndrome and the ecological significance of succulence, as well as the prolific radiation of richest lineages. HighlightsThe climatic niche occupied by succulent CAM plants is not different from their non-succulent relatives. Estimated dates and character reconstruction suggest CO2 scarcity as the evolutionary pressure under these plants originated.