New PhytologistPub Date : 2026-11-01Epub Date: 2026-09-04DOI: 10.1111/nph.71562
Xiong He, Spencer C H Barrett, Ze-Yu Tong, Yu Peng, Ling-Yun Wu
{"title":"Morphological fit promotes pollen segregation and disassortative pollination in an open-flowered, nontubular heterostylous species.","authors":"Xiong He, Spencer C H Barrett, Ze-Yu Tong, Yu Peng, Ling-Yun Wu","doi":"10.1111/nph.71562","DOIUrl":"10.1111/nph.71562","url":null,"abstract":"<p><p>Heterostyly is a classic Darwinian adaptation promoting disassortative pollination. The polymorphism usually depends on floral tubes to enforce spatial segregation of pollen deposited on pollinators. How this is achieved in species with bowl-shaped flowers and generalised pollinators remains less well-understood. We investigated the mechanistic basis of Darwin's cross-promotion hypothesis in distylous Persicaria jucunda, which lacks a floral tube and is fly-pollinated. We integrated morphological measurements of flowers and flies with high-definition video analysis of foraging behaviour. Exploiting pollen-size dimorphism, we quantified morph-specific pollen placement on pollinator body parts and the composition of naturally pollinated stigmatic pollen loads. A 'morphological fit' was evident with fly proboscis length matching lower-level sex organs and upper-level organs matching the position of the head. This morphological congruence caused L-morph pollen to be deposited primarily on proboscides (76.6%) and S-morph pollen on heads (85.7%), resulting in a significantly higher proficiency of intermorph than intramorph pollen transfer. Despite the absence of a floral tube in P. jucunda, our findings of a morphological fit between flower and pollinator structures and consistent foraging behaviour by flies provide mechanistic support for Darwin's cross-promotion hypothesis and resolve the puzzle of how disassortative pollination occurs in open-flowered heterostylous systems.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":"1283-1295"},"PeriodicalIF":8.1,"publicationDate":"2026-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148892702","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
New PhytologistPub Date : 2026-11-01Epub Date: 2026-09-16DOI: 10.1111/nph.71589
Min-Soo Choi, Dale L Forrister, Guillaume J Dury, Kyo Bin Kang, Brian E Sedio, Youngsung Joo
{"title":"eCOMET: an R package for evaluating metabolic diversity and enrichment from LC-MS/MS data to test ecological hypotheses from individuals to ecosystems.","authors":"Min-Soo Choi, Dale L Forrister, Guillaume J Dury, Kyo Bin Kang, Brian E Sedio, Youngsung Joo","doi":"10.1111/nph.71589","DOIUrl":"10.1111/nph.71589","url":null,"abstract":"<p><p>Methods in metabolomics have grown exponentially in recent years, providing new insight into the ecological function and evolutionary impact of diverse plant metabolites. Metabolomics requires a command of numerous tools, the outputs of which are typically integrated through in-house custom code that presents a workflow bottleneck and a barrier to entry for researchers in ecology, evolution, and behavior who may benefit from adding a metabolomics perspective to their research. We introduce eCOMET, an R package for integrating and harmonizing the outputs of common metabolomics bioinformatics tools and conducting statistical analyses and data visualization methods useful for ecological metabolomics. Our package combines metabolome feature metadata with quantification tables (e.g. mzmine), feature dissimilarity matrices (e.g. modified cosine and DreaMS), and feature annotations (e.g. SIRIUS) into a cohesive R data object to facilitate downstream analyses, including the calculation of diversity and disparity metrics and differential accumulation analysis. We provide two tutorials, each explores herbivore-induced Arabidopsis thaliana metabolome and 10 co-occurring tropical trees species metabolomes. Our goal is to make metabolomics accessible to a wider range of researchers in ecology, evolution, and behavior to unlock the potential of ecological metabolomics to generate novel insight into these fields.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":"1675-1687"},"PeriodicalIF":8.1,"publicationDate":"2026-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13669803/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148983901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ellen J Quinlan, James B Pease, Jhonatan Sallo Bravo, Alfredo F Fuentes, William Farfan-Rios, Miles R Silman
{"title":"Diversification and coexistence amid widespread and persistent gene flow in Andean trees.","authors":"Ellen J Quinlan, James B Pease, Jhonatan Sallo Bravo, Alfredo F Fuentes, William Farfan-Rios, Miles R Silman","doi":"10.1111/nph.71657","DOIUrl":"https://doi.org/10.1111/nph.71657","url":null,"abstract":"<p><p>Hybridization and introgression are increasingly recognized as important in plant evolution, yet their prevalence and consequences remain poorly understood in tropical Andean trees, where species coexist at low densities and turn over rapidly across elevation gradients. Here, we investigate whether species boundaries are maintained among 10 congeneric Andean Prunus L. species distributed across the Andes-Amazon elevational gradient by reconstructing phylogenetic relationships, divergence times, and patterns of historical and recent gene flow. We find that Andean Prunus diversified during the Miocene, likely in response to novel habitat opportunities resulting from mountain uplift, combined with allopatric processes. Despite this evolutionary divergence, these species show extensive ancient introgression and recent admixture, indicating that species boundaries remain permeable across both ecological and phylogenetic distance. Together, these results suggest that Andean Prunus comprise distinct but evolutionarily connected lineages that retain morphological identity while potentially functioning as a long-lived syngameon, with implications for understanding the origin and maintenance of tropical tree diversity and future response to global change.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":""},"PeriodicalIF":8.1,"publicationDate":"2026-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149196455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Engineering root development with high precision.","authors":"Roza D Bilas, Sarah Guiziou","doi":"10.1111/nph.71583","DOIUrl":"https://doi.org/10.1111/nph.71583","url":null,"abstract":"<p><p>Root development is controlled by dynamic interactions between gene regulation, hormonal signalling, developmental history and environmental inputs, creating multiple layers of control that can be harnessed for engineering. Recent advances in single-cell technologies, spatial transcriptomics and synthetic biology are beginning to resolve root development at the cellular level and enable increasingly precise manipulation of developmental programmes. Here, we discuss how lineage tracing, genetic recording of developmental history, cell-type-specific engineering and programmable genetic circuits can be integrated to understand and control root architecture. We highlight emerging strategies for engineering adaptive and context-dependent developmental behaviours, including history-dependent and reversible response programmes and rewired root-environment interactions. Together, these approaches establish a foundation for programmable and adaptive root system engineering in plants.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":""},"PeriodicalIF":8.1,"publicationDate":"2026-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149196755","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The homologous GRAS transcription factors RAM1 and RAD1 coordinate shared and separate gene networks to regulate arbuscular mycorrhiza symbiosis.","authors":"Tian Zeng, Jessica Alpers, Fabio Boniolo, Regine Huettl, Florian Berger, Carlos Hernandez Cortes, Caroline Gutjahr","doi":"10.1111/nph.71662","DOIUrl":"https://doi.org/10.1111/nph.71662","url":null,"abstract":"<p><p>Arbuscular mycorrhiza (AM), a symbiosis between plants and Glomeromycotan fungi is based on the exchange of nutrients, which majorly occurs between fungal tree-shaped arbuscules and root cortex cells. Two homologous plant GRAS transcription factors, RAM1 and RAD1, were previously reported to interact, and both were implicated in regulating arbuscule branching in Lotus japonicus. We revisited the role of L. japonicus RAM1 and RAD1 and asked whether they act together in mediating arbuscule development and gene expression, or whether they act additively. We performed comprehensive genetic, phenotypic, and transcriptome analyses of two allelic Lotus ram1, rad1, and ram1 rad1 mutants; and of roots ectopically expressing RAM1 and/or RAD1. We found that RAD1 is required for full root colonization in a RAM1-dependent manner, but in our growth conditions, RAD1 is not required for arbuscule branching. In addition, RAM1 and RAD1 are required for activation of partially common and partially distinct sets of downstream genes. Thus, in contrast to RAM1, Lotus RAD1 is not essential for arbuscule branching. Furthermore, RAM1 and RAD1 seem to act partially synergistically but seem to participate in additional alternative transcription factor complexes to regulate AM-induced gene expression and AM development.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":""},"PeriodicalIF":8.1,"publicationDate":"2026-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149196721","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lindsay A McCulloch, A Elizabeth Arnold, James W Dalling, Adam S Davis, Carolina Sarmiento, Paul-Camilo Zalamea
{"title":"Dormancy type, seed traits, and species identity shape seed-associated fungal community composition in tropical pioneer trees.","authors":"Lindsay A McCulloch, A Elizabeth Arnold, James W Dalling, Adam S Davis, Carolina Sarmiento, Paul-Camilo Zalamea","doi":"10.1111/nph.71601","DOIUrl":"https://doi.org/10.1111/nph.71601","url":null,"abstract":"<p><p>Seed germination is regulated in many plants by seed dormancy, while postdispersal survival is often determined by soilborne fungi that infect seeds. In tropical forests, seeds in each of three dormancy types (physical, physiologically dormant, or quiescent) often share similar physical and chemical traits. We hypothesized that variation in seed traits aligned with seed dormancy should shape seed-associated fungal communities, linking dormancy to seed survival. Seeds of 18 pioneer tree species were buried in each of five common garden plots in a lowland tropical forest in Panama for up to 36 months. Seeds were screened for viability and fungal infection at intervals throughout the experiment. Plant species with different dormancy types harbored distinct fungal communities. Dormancy type explained 6.5% of variation in fungal community composition after accounting for the far stronger signature of plant species identity (34%). Within dormancy types, differences in seed traits among species explained 49-56% of the variation in fungal communities, suggesting that seed traits drive niche partitioning beyond what is imposed by dormancy type alone. This study shows that variation in seed traits within a dormancy type filters seed-associated fungal communities, which likely shapes the demography of tropical forest trees by influencing seed survival and germination.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":""},"PeriodicalIF":8.1,"publicationDate":"2026-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149196762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Meng-Di Wang, Frédéric Choulet, Fan Zhang, Fu-Hao Lu
{"title":"A St-derived genome contributes to the formation of the wheat BB genome.","authors":"Meng-Di Wang, Frédéric Choulet, Fan Zhang, Fu-Hao Lu","doi":"10.1111/nph.71664","DOIUrl":"https://doi.org/10.1111/nph.71664","url":null,"abstract":"<p><p>Although substantial efforts have been made to identify the progenitor of the wheat BB genome, the precise donor remains elusive. In this study, we first investigated the origin of the BB genome using a BB-specific atp6 gene harboring unique 5'-end sequences, which is present in multiple copies and partially pseudogenized in the BB genome. BLAST searches revealed that multi-copied atp6 (pseudo)genes occur exclusively in polyploid St-genome species. An ultrametric phylogeny constructed from genome-wide single-copy genes resolved the divergence of Aegilops speltoides (SS genome) and the St genome c. 4 million years ago, coinciding with the estimated origin of the BB genome. Furthermore, genome-wide single-nucleotide polymorphism (SNP)-based allele matching showed that the St genome best explains BB alleles after SS, with an SS : St SNP ratio of 3 : 1, suggesting that the St genome likely contributed to the BB formation via two independent hybridization events with the SS ancestor. Finally, we identified 52 BB-specific genes to facilitate the search for the true BB donor or the transitional hybrid. This study provides compelling evidence for the St genome's critical contribution to the BB genome and advances our understanding of how the complex hexaploid genome of bread wheat was formed and reshaped over evolutionary time.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":""},"PeriodicalIF":8.1,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149196460","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Preparing, pairing and recovering: how angiosperms coordinate double fertilization.","authors":"Yaxiao Liu, Sheng Zhong","doi":"10.1111/nph.71663","DOIUrl":"https://doi.org/10.1111/nph.71663","url":null,"abstract":"<p><p>Double fertilization is a defining reproductive characteristic of angiosperms. During this process, two sperm cells fuse separately with the egg cell and the central cell to generate the embryo and endosperm, the two core components of the seed. Recent studies have revealed that male and female gametes are maintained in tightly regulated prefusion states and that their subsequent interaction proceeds through a series of precisely controlled steps. In angiosperms, gamete interaction also raises distinctive biological questions because it involves two fertilization events. Elucidating the molecular basis of male-female gamete interaction will not only deepen our understanding of double fertilization but also provide a conceptual foundation for improving crop-breeding strategies.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":""},"PeriodicalIF":8.1,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149196773","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Anis Meschichi, Marinela Dukić, Lars C Schmid, Andreas L Bachmann, Tadeas J Priklopil, Hui San Tan, Kirsten Bomblies
{"title":"Excess endopolyploidy associated with cellular defects in neo-autotetraploid Arabidopsis arenosa is in part corrected by a naturally evolved allele of CYCD3;2.","authors":"Anis Meschichi, Marinela Dukić, Lars C Schmid, Andreas L Bachmann, Tadeas J Priklopil, Hui San Tan, Kirsten Bomblies","doi":"10.1111/nph.71647","DOIUrl":"https://doi.org/10.1111/nph.71647","url":null,"abstract":"<p><p>Endopolyploidy (within-organism polyploidy) is an often-beneficial aspect of development. But polyploids, which have a higher baseline genome content, have been reported to have less endoreduplication than diploid relatives. Why has remained unclear; we explored this in Arabidopsis arenosa. We measured endopolyploidy levels and phenotyped cellular traits, comparing diploids, neo-autotetraploids, and established autotetraploids of A. arenosa. We used a genetic approach to ask whether CYCD3;2, a polyploidy regulator with evidence of selection in tetraploids, might be responsible for endopolyploidy-related phenotypic differences between neo- and established polyploids, and whether there are associated costs. Neo-tetraploids had the most 16C and 32C cells, whereas established tetraploids have proportions of 16C and 32C cells comparable to diploids. Tetraploid plants homozygous for a novel allele of CYCD3;2 have reduced endopolyploidy compared to homozygotes for the diploid allele and, surprisingly, also show cellular defects seen in neo-tetraploids. Suggesting this link is specific, we find that A. thaliana cycd3;2 mutants have not only increased endopolyploidy but also root hair defects like neo-tetraploids. Our results suggest reverting endopolyploidy in polyploids to diploid-like levels could be advantageous, and that one driver might be cellular defects that arise with excess high-ploidy cells.</p>","PeriodicalId":48887,"journal":{"name":"New Phytologist","volume":" ","pages":""},"PeriodicalIF":8.1,"publicationDate":"2026-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149170543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}