No plant is an island Renner, Susanne S.
CB/Current biology,
06/2023, Letnik:
33, Številka:
11
Journal Article
Recenzirano
Odprti dostop
Most of the world’s ecosystems are dominated by plants, and preserving the natural and agricultural landscapes that we depend on therefore requires understanding plants and their interactions at ...local and global scales. This is challenging because plants’ ways of perceiving each other and communicating with each other and with animals are so fundamentally different from the ways we animals communicate with, and manipulate, each other. The collection of articles in the present issue of Current Biology illustrates the progress being made in deciphering some of the processes and mechanisms involved in plant interactions at different scales. While the topic of interactions with plants is very broad, any overview will require covering chemical signals and their reception; mutualisms and symbioses; interactions with pathogens; and interactions in communities. Approaches taken in these fields range from molecular biology and physiology to ecology.
Susanne Renner introduces the special issue and highlights the many ways in which plants interact with other organisms (and with each other).
Melastomataceae are among the most abundant and diversified groups of plants throughout the tropics, but their intrafamily relationships and morphological evolution are poorly understood. Here we ...report the results of parsimony and maximum likelihood (ML) analyses of cpDNA sequences from the rbcL and ndhF genes and the rpl16 intron, generated for eight outgroups (Crypteroniaceae, Alzateaceae, Rhynchocalycaceae, Oliniaceae, Penaeaceae, Myrtaceae, and Onagraceae) and 54 species of melastomes. The sample represents 42 of the family's currently recognized ∼150 genera, the 13 traditional tribes, and the three subfamilies, Astronioideae, Melastomatoideae, and Memecyloideae (= Memecylaceae DC.). Parsimony and ML yield congruent topologies that place Memecylaceae as sister to Melastomataceae. Pternandra, a Southeast Asian genus of 15 species of which five were sampled, is the first-branching Melastomataceae. This placement has low bootstrap support (72%), but agrees with morphological treatments that placed Pternandra in Melastomatacaeae because of its acrodromal leaf venation, usually ranked as a tribe or subfamily. The interxylary phloem islands found in Memecylaceae and Pternandra, but not most other Melastomataceae, likely evolved in parallel because Pternandra resembles Melastomataceae in its other wood characters. A newly discovered plesiomorphic character in Pternandra, also present in Memecylaceae, is a fibrous anther endothecium. Higher Melastomataceae lack an endothecium as do the closest relatives of Melastomataceae and Memecylaceae. The next deepest split is between Astronieae, with anthers opening by slits, and all remaining Melastomataceae, which have anthers opening by pores. Within the latter, several generic groups, corresponding to traditional tribes, receive solid statistical support, but relationships among them, with one exception, are different from anything predicted on the basis of morphological data. Thus, Miconieae and Merianieae are sister groups, and both are sister to a trichotomy of Bertolonieae, Microlicieae + Melastomeae, and Dissochaeteae + Blakeeae. Sonerileae/Oxysporeae are nested within Dissochaeteae, Rhexieae within Melastomeae, and African and Asian Melastomeae within neotropical Melastomeae. These findings have profound implications for our understanding of melastome morphological evolution (and biogeography), implying, for example, that berries evolved from capsules minimally four times, stamen connectives went from dorsally enlarged to basal/ventrally enlarged, and loss of an endothecium preceded poricidal dehiscence.
Phylogenetic and phylogenomic analyses require multi-gene input files in different formats, but there are few user-friendly programs facilitating the workflow of combining, concatenating or ...separating, aligning and exploring multi-gene datasets.
We present Concatenator, a user-friendly GUI-driven program that accepts single-marker and multi-marker DNA sequences in different input formats, including Fasta, Phylip and Nexus, and that outputs concatenated sequences as single-marker or multi-marker Fasta, interleaved nexus or Phylip files, including command files for downstream model selection in IQ-TREE. It includes the option to (re)align markers with MAFFT and produces exploratory trees with FastTree. Although tailored for medium-sized phylogenetic projects, Concatenator is able to process phylogenomic datasets of up to 30 000 markers.
Concatenator is written in Python, with C extensions for MAFFT and FastTree. Compiled stand-alone executables of Concatenator for MS Windows and Mac OS along with a detailed manual can be downloaded from www.itaxotools.org; the source code is openly available on GitHub (https://github.com/iTaxoTools/ConcatenatorGui).
ABSTRACT We present numerically derived orbits and mass estimates for the inner Saturnian satellites, Atlas, Prometheus, Pandora, Janus, and Epimetheus from a fit to 2580 new Cassini Imaging Science ...Subsystem astrometric observations spanning 2004 February to 2013 August. The observations are provided as machine-readable and Virtual Observatory tables. We estimate = (0.384 0.001) × 10−3 km3 s−2, a value 13 smaller than the previously published estimate but with an order of magnitude reduction in the uncertainty. We also find = (10.677 0.006) × 10−3 km3 s−2, = (9.133 0.009) × 10−3 km3 s−2, = (126.51 0.03) × 10−3 km3 s−2, and = (35.110 0.009) × 10−3 km3 s−2, consistent with previously published values, but also with significant reductions in uncertainties. We show that Atlas is currently librating in both the 54:53 co-rotation-eccentricity resonance (CER) and the 54:53 inner Lindblad (ILR) resonance with Prometheus, making it the latest example of a coupled CER-ILR system, in common with the Saturnian satellites Anthe, Aegaeon, and Methone, and possibly Neptuneʼs ring arcs. We further demonstrate that Atlasʼs orbit is chaotic, with a Lyapunov time of ∼10 years, and show that its chaotic behavior is a direct consequence of the coupled resonant interaction with Prometheus, rather than being an indirect effect of the known chaotic interaction between Prometheus and Pandora. We provide an updated analysis of the second-order resonant perturbations involving Prometheus, Pandora, and Epimetheus based on the new observations, showing that these resonant arguments are librating only when Epimetheus is the innermost of the co-orbital pair, Janus and Epimetheus. We also find evidence that the known chaotic changes in the orbits of Prometheus and Pandora are not confined to times of apse anti-alignment.
Herbarium specimens deposited in publicly accessible collections are the basis for all scientific names because only permanent specimens can be re-studied by independent researchers, the very essence ...of science. Re-investigations may be done with morphological, chemical, genomic, computer-tomographic, or other methods. Based on new herbarium material, I here provide a name for the Xishuangbanna gourd, a plant long cultivated in Yunnan because of its large non-bitter fruits, rich in β-carotene. Genome re-sequencing of numerous accessions has shown that this cucumber mutant is closer to Cucumis sativus var. sativus than is the wild bitter-fruited progenitor
var. hardwickii, and two dozen studies have further clarified the genetics of key traits, including pulp color, fruit shape, and flowering times. Morphological and molecular diagnoses of the new variety are provided and museum-quality specimens have been distributed to the World's major herbaria.
The order Laurales comprises a few indisputed core constituents, namely Gomortegaceae, Hernandiaceae, Lauraceae, and Monimiaceae sensu lato, and an equal number of families that have recently been ...included in, or excluded from, the order, namely Amborellaceae, Calycanthaceae, Chloranthaceae, Idiospermaceae, and Trimeniaceae. In addition, the circumscription of the second largest family in the order, the Monimiaceae, has been problematic. I conducted two analyses, one on 82 rbcL sequences representing all putative Laurales and major lineages of basal angiosperms to clarify the composition of the order and to determine the relationships of the controversal families, and the other on a concatenated matrix of sequences from 28 taxa and six plastid genome regions (rbcL, rpl16, trnT-trnL, trnL-trnF, atpB-rbcL, and psbA-trnH) that together yielded 898 parsimony-informative characters. Fifteen morphological characters that play a key role in the evolution and classification of Laurales were analyzed on the most parsimonious molecular trees as well as being included directly in the analysis in a total evidence approach. The resulting trees strongly support the monophyly of the core Laurales (as listed above) plus Calycanthaceae and Idiospermaceae. Trimeniaceae form a clade with Illiciaceae, Schisandraceae, and Austrobaileyaceae, whereas Amborellaceae and Chloranthaceae represent isolated clades that cannot be placed securely based on rbcL alone. Within Laurales, the deepest split is between Calycanthaceae (including Idiospermaceae) and the remaining six families, which in turn form two clades, the Siparunaceae (Atherospermataceae-Gomortegaceae) and the Hernandiaceae (Monimiaceae s.str. sensu stricto-Lauraceae). Monimiaceae clearly are polyphyletic as long as they include Atherospermataceae and Siparunaceae. Several morphological character state changes are congruent with the molecular tree: (1) Calycanthaceae have disulculate tectate-columellate pollen, while their sister clade has inaperturate thin-exined pollen, with the exception of Atherospermataceae, which have columellate but meridionosulcate or disulcate pollen. (2) Calycanthaceae have two ventral ovules while their sister clade has solitary ovules. Within this sister clade, the Hernandiaceae (Lauraceae-Monimiaceae) have apical ovules, while the Siparunaceae (Atherospermataceae-Gomortegaceae) are inferred to ancestrally have basal ovules, a condition lost in Gomortega, the only lauralean genus with a syncarpous ovary. (3) Calycanthaceae lack floral nectaries (except for isolated nectarogeneous fields on the inner tepals), while their sister clade ancestrally has paired nectar glands on the filaments. Filament glands were independently lost in higher Monimiaceae and in Siparunaceae concomitant with pollinator changes away from nectar-foraging flies and bees to non-nectar feeding beetles and gall midges. (4) Disporangiate stamens with anthers dehiscing by two apically hinged valves are ancestral in Siparunaceae-(Atherospermataceae-Gomortegaceae) and evolved independently within Hernandiaceae and Lauraceae. Depending on the correct placement of Calycanthaceae-like fossil flowers, tetrasporangiate anthers with valvate dehiscence (with the valves laterally hinged) may be ancestral in Laurales and lost in modern Calycanthaceae and Monimiaceae.
In tropical rainforests, 30-65% of tree species grow at densities of less than one individual per hectare. At these low population densities, successful cross-pollination relies on synchronous ...flowering. In rainforests with low climatic seasonality, photoperiodic control is the only reliable mechanism for inducing synchronous flowering. This poses a problem because there is no variation in day length at the Equator. Here we propose a new mechanism of photoperiodic timekeeping based on the perception of variation in sunrise or sunset time, which explains and predicts the annually repeated, staggered, synchronous and bimodal flowering of many tree species in Amazonian rainforests near the Equator.
Celotno besedilo
Dostopno za:
DOBA, IJS, IZUM, KILJ, NUK, PILJ, PNG, SAZU, SIK, UILJ, UKNU, UL, UM, UPUK
We used next-generation sequencing to characterize the genomes of nine species of Orobanchaceae of known phylogenetic relationships, different life forms, and including a polyploid species. The study ...species are the autotrophic, nonparasitic Lindenbergia philippensis, the hemiparasitic Schwalbea americana, and seven nonphotosynthetic parasitic species of Orobanche (Orobanche crenata, Orobanche cumana, Orobanche gracilis (tetraploid), and Orobanche pancicii) and Phelipanche (Phelipanche lavandulacea, Phelipanche purpurea, and Phelipanche ramosa). Ty3/Gypsy elements comprise 1.93%-28.34% of the nine genomes and Ty1/Copia elements comprise 8.09%-22.83%. When compared with L. philippensis and S. americana, the nonphotosynthetic species contain higher proportions of repetitive DNA sequences, perhaps reflecting relaxed selection on genome size in parasitic organisms. Among the parasitic species, those in the genus Orobanche have smaller genomes but higher proportions of repetitive DNA than those in Phelipanche, mostly due to a diversification of repeats and an accumulation of Ty3/Gypsy elements. Genome downsizing in the tetraploid O. gracilis probably led to sequence loss across most repeat types.
To combat the loss of flower-rich meadows, many cities are supporting greening measures, including the creation of flower strips. To assess the effectiveness of these measures in supporting ...flower-visiting insects, their faunas need to be compared to the background fauna at various distances from the flower strips. To meet this goal, we quantified the bee faunas of nine 1000 m
2
-large and newly established flower strips in the city of Munich, all planted with a regional seed mix, and compared them to the fauna recorded between 1997 and 2017 within 500, 1000, and 1500 m from the respective strip. The 68 species recorded during the flower strips’ first season represent 21% of the 324 species recorded for Munich since 1795 and 29% of the 232 species recorded between 1997 and 2017. Non-threatened species are statistically over-represented in the strips, but pollen generalists are not. These findings illustrate the conservation value of urban flower strips for common species that apparently quickly discover this food source. To our knowledge, this is the first quantitative assessment of the speed and distance over which urban flower strips attract wild bees.
We explain the recent excess seen by ATLAS and CMS experiments at around 750 GeV in the diphoton invariant mass as a narrow-width sneutrino decaying to diphotons via a stau loop in R-parity violating ...supersymmetry. The stau mass is predicted to be somewhere between half the resonant sneutrino mass and half the sneutrino mass plus 14 GeV. The scenario also predicts further signal channels at an invariant mass of 750 GeV, the most promising being into dijets and WW. We also predict a left-handed charged slepton decaying into WZ and Wgamma at a mass 750-754 GeV.
PDF
