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240 results for “Plant reproduction”
Data from: Nitrogen fertilizer decreases survival and reproduction of female locusts by increasing plant protein to carbohydrate ratio
<p>1. Nitrogen limitation theory predicts that terrestrial plants should benefit from nitrogen inputs and that herbivores should benefit from subsequent higher plant protein contents. While this pattern has generally been supported, some herbivorous insects have shown preference and higher performance on low protein (p), high carbohydrate (c) diets as juveniles.</p> <p>2. However, little is known about the effects on reproduction in adults. Using nitrogen fertilizer, we demonstrate that high plant p:c has negative effects on Senegalese locust (Orthoptera: Oedaeleus senegalensis) reproduction and survival in an agroecological setting.</p> <p>3. For this, we measured p:c in millet plants (Pennisetum glaucum) that received two levels of fertilizer (high and moderate) and a control, then we caged locusts on these plants for two weeks. In the laboratory, we gave locusts the choice between untreated millet leaves and leaves that received one of the two fertilization treatment.</p> <p>4. We found that fertilization increased p:c ratio in a concentration dependent fashion. We counted the number of locusts alive over the course of two weeks and showed that fewer females survived on fertilized plants than on control plants. Females that ate plants from the high fertilization treatment laid lighter eggs. Finally, we showed that female locusts prefer unfertilized plants to plants with a high p:c.</p> <p>5. We hypothesize that this pattern will apply broadly to species that have extensive carbohydrate needs, such as long-distance migrators. Because many ecological studies focus primarily on nitrogen or protein, and fail to consider carbohydrates, this study has important implications for how ecologists consider nutrient limitation of primary consumers in ecosystems globally. </p>
Non-continuous reproductive phenology of animal-dispersed species in young forest restoration plantings
<p class="MsoNoSpacing">Tree species that produce resources for fauna are recommended for forest restoration plantings to attract pollinators and seed dispersers; however, information regarding the flowering and fruiting of these species during early growth stages is scarce. We evaluated the reproductive phenology of animal-dispersed tree species widely used in Atlantic Forest restoration. We marked 16 animal-dispersed tree species in 3- to 8-year-old forest restoration plantings in Itu-São Paulo, southeast Brazil. We noted the age of the first reproductive event, flowering and fruiting seasonality, percentage of trees that reached reproductive stages, and intensity of bud, flower, and fruit production for each species. Flowering and fruiting are seasonal for most species; only two, <i>Cecropia pachystachya</i> and <i>Ficus guaranitica,</i> exhibited continuous flowering and fruiting throughout the year; we also identified <i>Schinus terebinthifolia </i>and<i> Dendropanax cuneatus </i>fruiting in the dry season during resource scarcity. Therefore, we recommend all as framework species, that is, species that are animal-dispersed with early flowering and fruiting potential, for forest restoration. Further, we recommend identifying and planting similar animal-dispersed tree species that produce fruits constantly or in the dry season to maximize fauna resource availability throughout the year in tropical forest restoration plantings.</p>
Data from: Strategies for a successful plant invasion: the reproduction of Phragmites australis in northeastern North America
1. Knowing the relative contribution of vegetative propagation and sexual reproduction to the dispersal and establishment of exotic plants is crucial for devising efficient control strategies. This is particularly true for the common reed (Phragmites australis), one of the most invasive species in North America. 2. For the first time we combined in situ field observations and genetic evidence, based on two genotyping techniques, i.e., microsatellite markers (SSR) and genotyping-by-sequencing (GBS), to determine the propagation strategies of this invader at its northern distribution limit in North America, and especially in roadside ditches. 3. Field observations revealed that, in a region where the common reed is already abundant, both seeds and plant fragments contributed to the establishment of new populations. Newly established individuals originated mostly (84%) from seeds rather than fragments, but a larger proportion of individuals originating from fragments survived the second year compared to seedlings. 4. High genetic diversity among marsh and roadside common reed stands indicated the prime role of sexual reproduction for dispersal. The vast majority of genotypes were found in only one stand; such high genetic variability can only be explained by sexual reproduction. Half the surveyed stands comprised a single clone, suggesting that local expansion mainly occurred vegetatively. As the small proportion of SSR genotypes initially thought to be common between distant stands proved to be distinct (as revealed by GBS data), it is likely that all the stands examined were initially founded by genetically distinct individuals. 5. Synthesis. Our study suggests that long-distance dispersal by seeds is important for the common reed, in marshes and roadsides, while both seeds and plant fragments contribute to short-distance dispersal along roads, at least in regions where the species is already abundant. The success of this invader in North America seems to be attributable to a reproduction strategy combining the advantages of sexuality with those of vegetative propagation. Moreover, this study shows that the GBS approach strongly reduces uncertainties associated with the use of a limited number of markers. This approach is especially valuable for ecologists dealing with an ever increasing number of invaders, of which few have identified microsatellite markers.
Data from: Divergence before the host shift? Prezygotic reproductive isolation among three varieties of a specialist fly on a single host plant
1. Although divergence via host-plant shifting is a common theme in the speciation of some phytophagous insects, it is not clear whether host shifts are typically initiators of speciation or if they instead contribute to divergence events already in progress. While host shifts appear to be generally associated with speciation events for flies in the genus Strauzia, three sympatric varieties of the sunflower fly [Strauzia longipennis (Wiedemann)] co-occur on the same host plant in the Midwestern United States and may have evolved reproductive barriers without a host shift. 2. The strength of two prezygotic reproductive barriers was compared among the three S. longipennis varieties: one barrier that is often associated with divergent ecological selection (allochronic isolation), and another that is more likely to be independent of ecological selection (pre-copulatory sexual isolation). The presence and relative strength of each barrier between fly varieties were evaluated using microsatellites, no choice mating experiments, studies of allochronic isolation, and field collection data. 3. Evidence for both allochronic isolation and pre-copulatory sexual isolation was detected between the three varieties of S. longipennis. The measure of isolation calculated for each barrier between the three varieties was lower than measures calculated between different species of Strauzia found on different hosts, suggesting that subsequent host shifts may increase the degree of reproductive isolation. For Strauzia and other specialist insects, some reproductive isolation may evolve prior to, and indeed may facilitate, host shifts.
Data from: Suppression of reproductive characteristics of the invasive plant Mikania micrantha by sweet potato competition
Background: As a means of biologically controlling Mikania micrantha H.B.K. in Yunnan, China, the influence of sweet potato [Ipomoea batatas (L.) Lam.] on its reproductive characteristics was studied. The trial utilized a de Wit replacement series incorporating six ratios of sweet potato and M. micrantha plants in 25 m2 plots over two years. Results: Budding of M. micrantha occurred at the end of September; flowering and fruiting occurred from October to February. Flowering phenology of M. micrantha was delayed (P<0.05), duration of flowering and fruiting was reduced (P<0.05) and duration of bud formation was increased (P<0.05) with increasing proportions of sweet potato. Reproductive allocation, reproductive investment and reproductive index of M. micrantha were significantly reduced (P<0.05) with increasing sweet potato densities. Apidae bees, and Calliphoridae or Syrphidae flies were the most abundant visitors to M. micrantha flowers. Overall flower visits decreased (P<0.05) as sweet potato increased. Thus the mechanism by which sweet potato suppressed sexual reproduction in M. micrantha was essentially two-fold: causing a delay in flowering phenology and reducing pollinator visits. The number, biomass, length, set rate, germination rate, and 1000-grain dry weight of M. micrantha seeds were suppressed (P<0.05) by sweet potato competition. With proportional increases in sweet potato, sexual and asexual seedling populations of M. micrantha were significantly reduced (P<0.05). The mortality of both seedling types increased (P<0.05) with proportional increases in sweet potato. Conclusions: These results suggest that sweet potato significantly suppresses the reproductive ability of the invasive species M. micrantha, and is a promising alternative to traditional biological control and other methods of control. Planting sweet potato in conjunction with other control methods could provide a comprehensive strategy for managing M. micrantha. The scenario of controlling M. micrantha by utilizing a crop with a similar growth form may provide a useful model for similar management strategies in other systems.
Data from: Geographic variation of reproductive traits and competition for pollinators in a bird-pollinated plant
Geographic variation in the reproductive traits of animal-pollinated plants can be shaped by spatially variable selection imposed by differences in the local pollination environment. We investigated this in Babiana ringens (Iridaceae), an enigmatic species from the Western Cape region of South Africa. B. ringens has evolved a specialized perch facilitating cross-pollination by sunbirds and displays striking geographic variation in perch size and floral traits. Here, we investigate whether this variation can be explained by geographic differences in the pollinator communities. We measured floral and inflorescence traits, abiotic variables (N, P, C and rainfall) and made observations of sunbirds in populations spanning the range of B. ringens. In each population, we recorded sunbird species identity and measured visitation rates, inter-floral pollen transfer and whether the seed set of flowers was pollen limited. To evaluate whether competition from co-occurring sunbird-pollinated species might reduce visitation, we quantified nectar rewards in B. ringens and of other co-flowering bird-pollinated species in local communities in which populations occurred. Variation in abiotic variables was not associated with geographical variation of traits in B. ringens. Malachite sunbirds were the dominant visitor (97% of visits) and populations with larger-sized traits exhibited higher visitation rates, more between-flower pollen transfer and set more seed. No sunbirds were observed in four populations, all with smaller-sized traits. Sunbird visitation to B. ringens was not associated with local sunbird activity in communities, but sunbird visitation was negatively associated with the amount of B. ringens sugar relative to the availability of alternative nectar sources. Our study provides evidence that B. ringens populations with larger floral traits are visited more frequently by sunbirds and we propose that visitation rates to B. ringens may be influenced, in part, by competition with other sunbird pollinated species.
Host-plant choices determined by reproductive interference between closely related butterflies
<p>A number of empirical studies have concluded that reproductive interference, RI, contributes to parapatric species distributions or sexual exclusion. However, the possibility that divergent host-plant use in phytophagous insects is due to sexual exclusion has seldom been considered. Here we present evidence that RI is responsible for different host-plant use by two Pierid butterfly species, Pieris napi and P. melete . When a novel host species was introduced about 50 years ago, two Pierid butterfly species at first used both the ancestral host species and the novel one. Subsequently, P. napi shifted to use only the novel host, while P. melete shifted to specialize on the ancestral host. To explain these patterns, we investigated whether the two host species differ in suitability for larval growth and survival. Additionally, we tested whether RI occurred between the two species using large outdoor field cages. Courtship of females by conspecific and heterospecific males reduces the number of eggs laid by approximately half. However, RI is asymmetric and would generate selection on P. melete females to evolve to avoid the more suitable host species preferred by P. napi . Thus, our study suggests that sexual exclusion can explain the shift in host use by these two butterfly species.</p>
Data from: Evolution of the selfing syndrome: anther orientation and herkogamy together determine reproductive assurance in a self-compatible plant
Capacity for autonomous self-fertilization provides reproductive assurance, has evolved repeatedly in the plant kingdom, and typically involves several changes in flower morphology and development (the selfing syndrome). Yet, the relative importance of different traits and trait combinations for efficient selfing and reproductive success in pollinator-poor environments is poorly known. In a series of experiments, we tested the importance of anther-stigma distance and the less studied trait anther orientation for efficiency of selfing in the perennial herb Arabis alpina. Variation in flower morphology among eight self-compatible European populations was correlated with efficiency of self-pollination and with pollen limitation in a common-garden experiment. To examine whether anther-stigma distance and anther orientation are subject to directional and/or correlational selection, and whether this is because these traits affect pollination success, we planted a segregating F2 population at two native field sites. Selection strongly favored a combination of introrse anthers and reduced anther-stigma distance at a site where pollinator activity was low, and supplemental hand-pollination demonstrated that this was largely because of their effect on securing self-pollination. The results suggest that concurrent shifts in more than one trait can be crucial for the evolution of efficient self-pollination and reproductive assurance in pollinator-poor habitats.
Data from: Fungal symbionts as manipulators of plant reproductive biology
Symbioses have shaped the evolution of life, most notably through the fixation of heritable symbionts into organelles. The inheritance of symbionts promotes mutualism and fixation by coupling partner fitness. However, conflicts arise if symbionts are transmitted through only one sex and can shift host resources toward the sex through which they propagate. Such reproductive manipulators have been documented in animals with separate sexes but not in other phyla or sexual systems. Here we investigated whether the investment in male relative to female reproduction differed between hermaphroditic host plants with versus without a maternally inherited fungal symbiont. Plants with the fungus produced more seeds and less pollen than plants lacking the fungus, resulting in an ∼40% shift in functional gender and a switch from male-biased to female-biased sex allocation. Given the ubiquity of endophytes in plants, reproductive manipulators of hermaphrodites may be widespread in nature.
Data from: Bumble bee nest abundance, foraging distance, and host-plant reproduction: implications for management and conservation
Recent reports of global declines in pollinator species imply an urgent need to assess the abundance of native pollinators and density-dependent benefits for linked plants. In this study, we investigated (1) pollinator nest distributions and estimated colony abundances, (2) the relationship between abundances of foraging workers and the number of nests they represent, (3) pollinator foraging ranges, and (4) the relationship between pollinator abundance and plant reproduction. We examined these questions in an alpine ecosystem in the Colorado Rocky Mountains, focusing on four alpine bumble bee species (Bombus balteatus, B. flavifrons, B. bifarius, and B. sylvicola), and two host plants that differ in their degrees of pollinator specialization (Trifolium dasyphyllum and T. parryi). Using microsatellites, we found that estimated colony abundances among Bombus species ranged from ~18 to 78 colonies/0.01 km2. The long-tongued species B. balteatus was most common, especially high above treeline, but the subalpine species B. bifarius was unexpectedly abundant for this elevation range. Nests detected among sampled foragers of each species were correlated with the number of foragers caught. Foraging ranges were smaller than expected for all Bombus species, ranging from 25 to 110 m. Fruit set for the specialized plant, Trifolium parryi, was positively related to the abundance of its Bombus pollinator. In contrast, fruit set for the generalized plant, T. dasyphyllum, was related to abundance of all Bombus species. Because forager abundance was related to nest abundance of each Bombus species and was an equally effective predictor of plant fecundity, forager inventories are probably suitable for assessing the health of outcrossing plant populations. However, nest abundance, rather than forager abundance, better reflects demographic and genetic health in populations of eusocial pollinators such as bumble bees. Development of models incorporating the parameters we have measured here (nest abundance, forager abundance, and foraging distance) could increase the usefulness of foraging worker inventories in monitoring, managing, and conserving pollinator populations.
Data from: Facilitation consequences for reproduction of the benefactor cushion plant Laretia acaulis along an elevational gradient: costs or benefits?
Environmental stress may favour facilitative interactions among plants but whether these interactions are positive for the benefactor and how this depends on stress factors, remains to be determined. We studied the effect of beneficiary cover and biomass on reproduction of the benefactor cushion plant Laretia acaulis (Apiaceae) in the central Chilean Andes during three years. Study sites were situated along an elevational gradient at 2600, 2800, 3000 and 3150 m a.s.l. This range comprises a cold- and a drought-stress gradient, with moisture increasing and temperature decreasing with elevation. We studied the effect of natural gradients in beneficiary cover and of experimental cover removal on cushion flower and fruit production. Beneficiary cover had a negative effect on flower production but not on infructescence and fruit densities or fruit weights. A positive effect of beneficiaries on the fraction of flowers converted into fruits was detected for hermaphrodite cushions. The effect of beneficiary cover on flowering was independent of elevation or cushion gender, although these latter factors explained most of the variation. Removing the aboveground parts of the beneficiaries positively affected flowering at 2800 m a.s.l. but not at the other elevations. Our results suggest negative effects of facilitation on L. acaulis flowering, but these are neutralized in fruit production. Surprisingly, this conclusion holds along the entire elevational or stress gradient. This suggests that this system of facilitation is evolutionarily stable and not very sensitive to environmental change. It remains to be tested, however, whether facilitation affects fitness via growth and long-term survival in these slow-growing alpine cushions.
Data from: When spring ephemerals fail to meet pollinators: mechanism of phenological mismatch and its impact on plant reproduction
The flowering phenology of early-blooming plants is largely determined by snowmelt timing in high-latitude and high-altitude ecosystems. When the synchrony of flowering and pollinator emergence is disturbed by climate change, seed production may be restricted due to insufficient pollination success. We revealed the mechanism of phenological mismatch between a spring ephemeral (Corydalis ambigua) and its pollinator (overwintered bumble bees), and its impact on plant reproduction, based on 19 years of monitoring and a snow removal experiment in a cool-temperate forest in northern Japan. Early snowmelt increased the risk of phenological mismatch under natural conditions. Seed production was limited by pollination success over the three years of pollination experiment and decreased when flowering occurred prior to bee emergence. Similar trends were detected on modification of flowering phenology through snow removal. Following snowmelt, the length of the pre-flowering period strongly depended on the ambient surface temperature, ranging from 4 days (at >7ºC) to 26 days (at 2.5ºC). Flowering onset was explained with an accumulated surface degree-day model. Bumble bees emerged when soil temperature reached 6ºC, which was predictable by an accumulated soil degree-day model, although foraging activity after emergence might depend on air temperature. These results indicate that phenological mismatch tends to occur when snow melts early but subsequent soil warming progresses slowly. Thus, modification of the snowmelt regime could be a major driver disturbing spring phenology in northern ecosystems.
Data from: Nectar robbing impacts pollinator behavior but not plant reproduction
Trait-mediated indirect effects (TMIEs) refer to interactions in which the effect of one species on another is mediated by the behavior of a third species. A mechanistic approach that identifies the direction and impact of TMIEs can shed light on why different net outcomes are observed in the same general phenomena across systems. Nectar robbing has variable net effects through TMIEs on animal-pollinated plants across systems, but the mechanistic steps underlying this range of outcomes are often unclear. To address this knowledge gap, we assessed linkages between nectar robbing, pollinator behavior and plant reproductive success in the Andean tree, Oreocallis grandiflora. We found that robbing in this system led to lower nectar volumes, higher nectar sucrose concentration, and higher nectar viscosity, which together negatively impact nectar quality. This drop in nectar quality was associated with decreased visitation rates by hummingbirds, which might be expected to impact plant reproduction negatively by pollen limitation. However, it was also associated with increased diversity (Shannon's) and evenness in the pollinator community due to reduced visitation by a territorial hummingbird, which might be expected to impact reproduction positively via enhanced genetic diversity of pollen as non-territorial pollinators forage over greater areas. We measured seed set and mass to distinguish the relative intensity of these two possible outcomes, but found no detectable effect. We tentatively conclude that these two consequences of TMIEs may have balanced each other out to yield a neutral net effect of nectar robbing on plant reproduction, though other explanations are also possible. This study highlights ways in which ecologically important TMIEs may act in opposing directions to mask important ecological forces, and underscores the continued need for detailed study of the mechanisms through which TMIEs operate.
Data from: Where consumers control plant reproduction in coastal wetlands: the environmental stress model in plants' versus consumers' perspectives
<p>This is the data set for the paper entitled "Where consumers control plant reproduction in coastal wetlands: the environmental stress model in plants’ versus consumers’ perspectives" upcoming in the Journal of Ecology.</p> <p>The metadata for interpreting the data set are included in the Excel file. </p>
Data from: Nectar robbing rather than pollinator availability constrains reproduction of a bee-flowered plant at high elevations
<p>The files contain data on the floral ecology of <em>Clinopodium alpinum</em> collected along an elevational gradient in the Berchtesgaden National Park in Germany in 2017. The data are presented in the work entitled "Nectar robbing rather than pollinator availability constrains reproduction of a bee-flowered plant at high elevations" by Patrick L. Kohl and Ingolf Steffan-Dewenter. Files include data on flower visitor observations (including raw data on the number of visits by individual specifmens), data on seed/ovule ratios (both open pollinated and bagged flowers), data on the incidence of nectar robbing by bumble bees (the frequency of corolla perforations) and of flower herbivory by Eulophidae, and data on basic flowering traits of <em>C. alpinum</em> (number of flowers per inflorescence, corolla tube length, display size).</p>
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Shift in reproductive strategies in the evolutionary trajectory of a plant lineage
<p>Target loci of The Angiosperms353 gene set (AGS) assembled on Easy353 pipeline for Saxifraga section Irregulares and related taxa.</p>
FIGURE 2. Lacomucinaea lineata vegetative and reproductive features. A. Plant habit. B in Lacomucinaea, a new monotypic genus in Thesiaceae (Santalales)
FIGURE 2. Lacomucinaea lineata vegetative and reproductive features. A. Plant habit. B. Base of stem showing bark features. C. Young branches bearing succulent leaves with petioles beginning to senesce. D. Older branches showing further senescence of leaves which eventually yellow and abscise leaving a peg-like petiolar stub. E. The flowers, here in bud stage, are borne singly in the axils of leaves. F. Inflorescences with flower buds and a flower in anthesis (photo by Nicky van Berkel, used with permission). G. Flower in longitudinal section, showing the two subtending bracteoles and the lobed hypanthial disk. H. Shoot with young and mature fruits. I. Closer view of fruits showing smooth surface and persistent corolla lobes at apex.
FIGURE 1. Trixis salina. A. Reproductive branch. B in A new species of Trixis (Nassauvieae, Asteraceae) from the Center of Plant Diversity of Cabo Frio, Brazil
FIGURE 1. Trixis salina. A. Reproductive branch. B. Detail of the abaxial side of the leaf. C. Detail of the capitulum. D. Detail of the receptaculum. E. Detail of the outer involucral bract. F. Detail of the intermediate involucral bract. G. Detail of the inner involucral bract. H. Flower. I. Detail of an open corolla with androecium and gynoecium. J. Detail of an open corolla. K. Detail of androecium and gynoecium. L. Anthers. M. Style. N. Cypsela. Drawing by Maria Alice Rezende.
FIGURE 3. Trixis salina. A. Reproductive branch. B. Shrubby restinga and habit. C in A new species of Trixis (Nassauvieae, Asteraceae) from the Center of Plant Diversity of Cabo Frio, Brazil
FIGURE 3. Trixis salina. A. Reproductive branch. B. Shrubby restinga and habit. C. Detail of the capitula. D. Lateral view of the capitula. E. Habit. F. Detail of vegetative structures. G. View of the ravine of the Foca's Beach. H. Rocky and sandy environment of the Prainha Beach populations of. I. Ravine environment. (Images A, G G.H.Shimizu; B–D C.N.Fraga; E, F, H, I M.Monge).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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OpenNeuro
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