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84 results for “flower associations”
How early does the selfing syndrome arise? Associations between selfing ability and flower size within populations of the mixed mater Collinsia verna
<p>Widespread associations between selfing rate and floral size within and among taxa suggest that these traits may evolve in concert. Does this association develop immediately, because of shared genetic/developmental control, or stepwise with selection shaping the evolution of one trait following the other? If the former, then association ought to appear within and across populations. We explore this fundamental question in three populations of the mixed-mater Collinsia verna where autonomous selfing (AS) ability has been shown to be under selection by the pollination environment. We grew clonal replicates of C. verna in a controlled environment to characterize broad-sense genetic correlations among traits within populations and to assess whether divergence in mating system and floral traits among these populations is consistent with their previously observed selection pressures. As predicted by their respective pollination environments, we demonstrate significant genetic divergence among populations in AS ability. However, patterns of divergence in floral traits (petal, stamen, and style size, stigmatic receptivity, and stigma-anther distance) were not as expected. Within populations, genetic variation in AS appeared largely independent from floral traits, except for a single weak negative association in one population between flower size and AS rate. Together, these results suggest that associations between selfing rate and floral traits across Collinsia species are not reflected at microevolutionary scales. If C. verna were to continue evolving toward the selfing syndrome, floral trait evolution would likely follow stepwise from mating system evolution.</p>
Fig. 4. A–J in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 4. A–J. Habitus of males of Ebenacobius Haran gen. nov. in lateral view (part 1). A. E. curvisetis Haran gen. et sp. nov. B. E. thoracicus Haran gen. et sp. nov. C. E. rectirostris Haran gen. et sp. nov. D. E. xhosa Haran gen. et sp. nov. E. E. duplicatus Haran gen. et sp. nov. F. E. san Haran gen. et sp. nov. G. E. grobbelaarae Haran gen. et sp. nov. H. E. kuscheli Haran gen. et sp. nov. I. E. costalis (Fåhraeus, 1844) gen. et comb. nov. J. E. mulanjensis Haran gen. et sp. nov. A–J = not to scale.
Fig. 8 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 8. Best-fit ML tree of Ebenacobius Haran gen. nov. and Afrotropical Derelomini resulting from the partitioned analyses of the concatenated molecular dataset (the scale bar represents the estimated number of nucleotide substitutions per site). Support values (*) at nodes indicate SH-aLRT ≥ 80% and uBV ≥ 95% values, in that order.
Fig. 7 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 7. Habitus in natura, host plants and habitats of Ebenacobius Haran gen. nov. A. Habitus of adult of E. rectirostris Haran gen. et sp. nov. B. Inflorescence of Euclea natalensis A.DC. (Ebenaceae), host of E. rectirostris. C. Biotope of E. rectirostris in the Mpumalanga Province of South Africa. D. Habitus of adult of E. san Haran gen. et sp. nov. E. Inflorescence of Euclea racemosa L. (Ebenaceae), host of E. san. F. Biotope of E. san in the Western Cape Province of South Africa.
Fig. 2. A–I in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 2. A–I. Habitus of males of Ebenacobius Haran gen. nov. in dorsal view (part 1). A. E. curvisetis Haran gen. et sp. nov. B. E. rectirostris Haran gen. et sp. nov. C. E. duplicatus Haran gen. et sp. nov. D. E. grobbelaarae Haran gen. et sp. nov. E. E. costalis (Fåhraeus, 1844) gen. et comb. nov. F. E. thoracicus Haran gen. et sp. nov. G. E. xhosa Haran gen. et sp. nov. H. E. san Haran gen. et sp. nov. I. E. kuscheli Haran gen. et sp. nov. Scale bars = 1 mm.
Fig. 5. A–H in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 5. A–H. Habitus of males of Ebenacobius Haran gen. nov. in lateral view (part 2). A. E. hessei Haran gen. et sp. nov. B. E. incognitus (Hesse, 1929) gen. et comb. nov. C. E. pedi Haran gen. et sp. nov. D. E. oberprieleri Haran gen. et sp. nov. E. E. tsonga Haran gen. et sp. nov. F. E. turneri (Marshall, 1935) gen. et comb. nov. G. E. hippopotamorum Haran gen. et sp. nov. H. E. rhodesianus (Hesse, 1929) gen. et comb. nov. A–H = not to scale.
Fig. 1 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 1 (see preceding page). A–M. Details of morphology and measurements of Ebenacobius Haran gen. nov. and Derelomus Schoenherr, 1825. A. Ebenacobius rhodesianus (Hesse, 1929) gen. et comb. nov. in dorsal view, with the white arrows showing where the measurements of width (w) and length (L) are made for the prothorax (top) and elytra (bottom). Black arrow showing the narrowing of prothorax near apical margin. B. Head in lateral view of E. rhodesianus with white arrow showing the groove on forehead and the black arrow showing the convexity of the eyes, exceeding the lateral curve of head. C. Head and apex of prothorax in dorsal view of Derelomus chamaeropsis Fabricius, 1798 with the white arrow showing flat forehead, lacking groove and black arrow showing the constriction on the prothorax near apical margin. D. Detail of the top-left part of the right elytron in E. rhodesianus showing the white scales on interstriae and with the well aligned punctures at base of stria 1 highlighted in white. E. Detail of the top-left part of the right elytron in E. costalis (Fåhraeus, 1844) gen. et comb. nov. showing the setae on interstriae and with the misaligned punctures at base of stria 1 highlighted in white. F. Protibia of males of E. rhodesianus, showing the apical acute mucro and the ante-apical brush of setae. G. Head and prothorax of E. rhodesianus in lateral view with the arrows showing where measurements of rostrum and prothorax length are made. H. Right maxilla of E. rhodesianus in dorsal view. I. Penis of E. costalis in dorsal view showing were measurements are made for the body of penis (white arrows: width; top right black arrows: length) and the length of apodemes (bottom right black arrows). J. Stridulatory plate (tergite VII) in male of E. rhodesianus in dorsal view, with the cuticular tubercles used for stridulation highlighted in white. K–M. Female genitalia. K. Ovipositor in E. rhodesianus. L. Sternite VIII, same species. M. Spermatheca, same species. N. Right mandible, same species. O. Labial prementum, same species. A–O: not to scale.
Fig. 6 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 6 (part 1). A–I. Male genitalia of Ebenacobius Haran gen. nov., penis in dorsal (left) and lateral (right) view.A. E. curvisetis Haran gen. et sp. nov. B. E. rectirostris Haran gen. et sp. nov. C. E. duplicatus Haran gen. et sp. nov. D. E. grobbelaarae Haran gen. et sp. nov. E. E. costalis (Fåhraeus, 1844) gen. et comb. nov. F. E. thoracicus Haran gen. et sp. nov. G. E. xhosa Haran gen. et sp. nov. H. E. san Haran gen. et sp. nov. I. E. kuscheli Haran gen. et sp. nov. A–I = not to scale.
Fig. 6 in Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants
Fig. 6 (part 2). J–R. Male genitalia of Ebenacobius Haran gen. nov.. penis in dorsal (left) and lateral (right) view. J. E. mulanjensis Haran gen. et sp. nov. K. E. hessei Haran gen. et sp. nov. L. E. pedi Haran gen. et sp. nov. M. E. tsonga Haran gen. et sp. nov. N. E. hippopotamorum Haran gen. et sp. nov. O. E. incognitus (Hesse, 1929) gen. et comb. nov. P. E. oberprieleri Haran gen. et sp. nov. Q. E. turneri (Marshall, 1935) gen. et comb. nov. R. E. rhodesianus (Hesse, 1929) gen. et comb. nov. J–R = not to scale.
Selection against early flowering in geothermally heated soils is associated with pollen but not prey availability in a carnivorous plant
<p>This data set includes data on flowering phenology, rosette diameters and fitness of the perennial herb Pinguicula vulgaris, as well as data on soil temperature and experimental treatment applied. The data was collected during the summer of 2020 in 287 plant individuals located in a sub-arctic geothermal area in Ölfus municipality in SW-Iceland, Hengill (64°03’N; 21°18’W, ~360 m.a.s.l.).</p>
Text-fig. 8. SEM (a, b) and SRXTM (c, d) images of fruit associated with Miranthus elegans and Miranthus kvacekii; Mira locality, Portugal. a: Apical view of capsular fruit with five, partly open valves revealing the enclosed reticulate seeds (arrows). b: Detail of fruit wall showing an enclosed seed (arrow). c: Transverse section (orthoslice xy1200) of fruit showing central column (cc) of placenta and numerous angular and bitegmic seeds; note that the outer integument (black arrow) is thicker than inner integument (white arrow). d: Longitudinal section (orthoslice yz1239) of fruit showing perigynous attachment of calyx, central column (cc) of the placenta and sections through seeds. Specimen, Mira 99-S156331 (a–d). Scale bars = 600 µm (a, c, d), 200 µm (b). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications
Text-fig. 8. SEM (a, b) and SRXTM (c, d) images of fruit associated with Miranthus elegans and Miranthus kvacekii; Mira locality, Portugal. a: Apical view of capsular fruit with five, partly open valves revealing the enclosed reticulate seeds (arrows). b: Detail of fruit wall showing an enclosed seed (arrow). c: Transverse section (orthoslice xy1200) of fruit showing central column (cc) of placenta and numerous angular and bitegmic seeds; note that the outer integument (black arrow) is thicker than inner integument (white arrow). d: Longitudinal section (orthoslice yz1239) of fruit showing perigynous attachment of calyx, central column (cc) of the placenta and sections through seeds. Specimen, Mira 99-S156331 (a–d). Scale bars = 600 µm (a, c, d), 200 µm (b).
Text-fig. 43. Synchrotron radiation X-ray tomographic microscopy SRXTM images of "Tricarpellate flower sp. 2"; Catefica locality, Portugal. a) Lateral view of floral structure (volume rendering) showing the apical projection of the carpels and the semiinferior organization; b) Apical view of floral structure (volume rendering) showing the triangular shape of the hypanthial rim, the tricarpellate ovary with a single apical style; note that one locule is fully developed while the other two are collapsed; note also slits of unknown nature in the corners of the triangular hypanthial rim (arrows); c) Transverse section (orthoslice xy0712) close to the floral apex showing the locule of the one fully developed carpel with ovules borne along ventral placentae; note amorphous substance (asterisk) associated with the developing ovules that fills part of the locule space; d) Longitudinal section (orthoslice xz0858) through the locule of the one fully developed carpel showing the semi-inferior organization and ovules arranged along the full length of the carpel; note amorphous substance (asterisk) associated with the developing ovules that fills part of the locule space; e) Tangential longitudinal section (orthoslice yz1019) through the one fully developed locule, showing the densely packed ovules and the amorphous substance (asterisk) with which they are associated. Specimen, Catefica 50-S174901 (a–e). Scale bars = 300 Μm (a–e). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 43. Synchrotron radiation X-ray tomographic microscopy SRXTM images of "Tricarpellate flower sp. 2"; Catefica locality, Portugal. a) Lateral view of floral structure (volume rendering) showing the apical projection of the carpels and the semiinferior organization; b) Apical view of floral structure (volume rendering) showing the triangular shape of the hypanthial rim, the tricarpellate ovary with a single apical style; note that one locule is fully developed while the other two are collapsed; note also slits of unknown nature in the corners of the triangular hypanthial rim (arrows); c) Transverse section (orthoslice xy0712) close to the floral apex showing the locule of the one fully developed carpel with ovules borne along ventral placentae; note amorphous substance (asterisk) associated with the developing ovules that fills part of the locule space; d) Longitudinal section (orthoslice xz0858) through the locule of the one fully developed carpel showing the semi-inferior organization and ovules arranged along the full length of the carpel; note amorphous substance (asterisk) associated with the developing ovules that fills part of the locule space; e) Tangential longitudinal section (orthoslice yz1019) through the one fully developed locule, showing the densely packed ovules and the amorphous substance (asterisk) with which they are associated. Specimen, Catefica 50-S174901 (a–e). Scale bars = 300 Μm (a–e).
Genome-wide association study of aphid abundance highlights a locus affecting plant growth and flowering in Arabidopsis thaliana
<div> <div>Plant life-history traits, such as size and flowering, contribute to shaping variation in herbivore abundance. Although plant genes involved in physical and chemical traits have been well studied, less is known about the loci linking plant life-history traits and herbivore abundance. Here, we conducted a genome-wide association study (GWAS) of aphid abundance in a field population of <em>Arabidopsis thaliana</em>. This GWAS of aphid abundance detected a relatively rare but significant variant on the third chromosome of <em>A. thaliana</em>, which was also suggestively but non-significantly associated with the presence or absence of inflorescence. Out of candidate genes near this significant variant, a mutant of a ribosomal gene (AT3G13882) exhibited slower growth and later flowering than a wild type under laboratory conditions. A no-choice assay with the turnip aphid, <em>Lipaphis erysimi</em>, found that aphids were unable to successfully establish on the mutant. Our genome-wide association study of aphid abundance unexpectedly found a locus affecting plant growth and flowering.</div> </div>
Sharing pollinators and pollen-associated viruses: understanding the diversity of the pollen virome within a co-flowering community
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Genome-wide association study of aphid abundance highlights a locus affecting plant growth and flowering in Arabidopsis thaliana
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Novel major loci shape habitat-associated flowering time variation in Yellowstone monkeyflowers
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How early does the selfing syndrome arise? Associations between selfing ability and flower size within populations of the mixed mater Collinsia verna
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Data from: Influence of range position on locally adaptive gene-environment associations in Populus flowering time genes
Local adaptation is pervasive in forest trees, which are characterized by large effective population sizes spanning broad climatic gradients. In addition to having relatively contiguous populations, many species also form isolated populations along the rear edge of their range. These rear-edge populations may contain unique adaptive diversity reflecting a history of selection in marginal environments. Thus, discovering genomic regions conferring local adaptation in rear edge populations is a key priority for landscape genomics to ensure conservation of genetic resources under climate change. Here, we report on adaptive gene-environment associations in SNPs from 27 genes in the Populus flowering time gene network, analyzed on a range-wide collection of >1000 balsam poplar trees, including dense sampling of the southern range edge. We use a combined approach of local adaptation scans to identify candidate SNPs, followed by modeling the compositional turnover of adaptive SNPs along multivariate climate gradients using Gradient Forests (GF). Flowering time candidate genes contained extensive evidence of climate adaptation, namely outlier population structure and gene-environment associations, along with allele frequency divergence between the core and edge of the range. GF showed strong allele frequency turnover along gradients of elevation and diurnal temperature variability, as well as threshold responses to summer temperature and precipitation, with turnover especially strong in edge populations that occur at high elevation but southerly latitudes. We discuss these results in light of how climate may disrupt locally adaptivegene-environment relationships, and suggest that rear edge populations hold climate-adaptive variants that should be targeted for conservation.
Bat-flower interaction networks in Caatinga reveal generalized associations and temporal stability
<p>Seasonal variation in precipitation regimes influences species composition and plant-animal interactions. Such temporal variation is especially relevant in the Brazilian Caatinga, the largest Seasonally Dry Tropical Forest in South America, where bat pollination is unusually frequent in comparison with other tropical plant communities. Here, we describe seasonal and annual variations of the interaction networks between nectarivorous bats and flower species in the Caatinga. Five species of nectar-feeding bats interacted with 30 plant species. Nectarivorous bats showed high levels of interaction overlap, which contributed to ecological generalization (low specialization and modularity) and lack of nestedness in the interaction networks. This pattern was consistent across seasons and years. Chiropterophilous and non-chiropterophilous plants were equally important components of the interaction network. The generalized interaction patterns found may be a necessary condition for the persistence of nectarivorous bats and their specialized plants in the environmentally harsh and variable Caatinga. The underappreciated generalized interactions of bats with plants calls for studies testing the effectiveness of bats in pollinating the plants they visit, including those not typically categorized as "bat-flowers".</p>
Data from: Fine-scale genetic structure in the orchid Gymnadenia conopsea is not associated with local density of flowering plants
<p><span><strong>Premise</strong>:</span><span> Density-dependent pollinator visitation can lead to density-dependent mating patterns and within-population genetic structure. In Gymnadenia conopsea, individuals in low-density patches receive more self-pollen than individuals in high-density patches, suggesting higher relatedness at low density. Ongoing fragmentation is also expected to cause more local matings, potentially leading to biparental inbreeding depression.</span></p> <p><span><strong>Methods</strong>: </span><span>To evaluate whether relatedness decreases with local density, we analysed 1315 SNP loci in 113 individuals within two large populations. We quantified within-population genetic structure in one of the populations, recorded potential habitat barriers, and visualized gene flow using estimated effective migration surfaces (EEMS). We further estimated the magnitude of biparental inbreeding depression that would result from matings restricted to within 5 m.</span></p> <p><span><strong>Results</strong>: </span><span>There was no significant relationship between local density and relatedness in any population. We detected significant fine-scale genetic structure consistent with isolation-by-distance, with positive kinship coefficients at distances below 10 m. Kinship coefficients were low, and predicted biparental inbreeding depression resulting from matings within the closest 5 m was a modest 1–3%.</span> <span>EEMS suggested that rocks and bushes may act as barriers to gene flow within a population.</span></p> <p><span><strong>Conclusions</strong>: </span><span>The results suggest that increased self-pollen deposition in sparse patches does not necessarily cause higher selfing rates, or that inbreeding depression results in low establishment success of inbred individuals. The modest relatedness suggests that biparental inbreeding depression is unlikely to be an immediate problem following fragmentation of large populations. The results further indicate that habitat structure may contribute to governing fine-scale genetic structure in <em>G. conopsea</em>.</span></p>
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