61 research outputs found

    Ready for change: seed traits contribute to the high adaptability of mudflat species to their unpredictable habitat

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    Question A better understanding of species distribution and establishment requires in-depth information on their seed ecology. We hypothesised that seed traits of mudflat species may indicate a strong environmental adaptation in their highly specialised habitat. Furthermore, we asked the question, do seeds of mudflat species have a specific trait value to contribute high adaptability to small-scale variation in their unpredictable habitat? Location Central Europe. Methods Seeds of 30 typical mudflat species were used to measure 15 traits that govern seed dispersal (buoyancy and production), persistence (seed desiccation, mass and persistence in soil), and germination and establishment (germination response to different light, temperature and oxygen conditions). Cluster analysis and phylogenetic principal components analysis (pPCA) were conducted to define potential mudflat species functional groups as per their ecological optima. Results Seed production and seed mass displayed extremely high variation while seed buoyancy, desiccation and persistence in soil showed almost no variation. All study species produced buoyant, desiccation-tolerant and long-term persistent seeds. Germination and establishment traits also displayed similarity in their responses to different germination treatments as the majority (73%) of species has a moderate seed germination niche width. They germinated well under light/aerobic conditions irrespective to temperature fluctuations. The cluster analysis and pPCA separated species into three potential plant functional groups as 'true', 'flood-resistant' and 'facultative', mudflat species. Conclusion Moderate variation in the seed traits of mudflat plants suggests they employ different ecological strategies that seem highly predictive to the peculiarity of their specific micro-habitats, which are largely controlled by the hydroperiod gradient. It implies that seed trait information, which further needs to be tested for their adaptability, can advance our understanding of how community composition at the micro-habitat level depends on trait values of participating species

    Perianth colour dimorphism is related to germination properties and salinity tolerance in Salsola vermiculata in the Arabian deserts

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    © 2017 The Authors We investigated the dimorphic perianth colour of Salsola vermiculata and its association with seed germination percentage, interactions with temperature, light, salinity and recovery from prior salinity exposure. Seeds with and without pink and yellow perianth were incubated at three thermal regimes, two photoperiods, and five salinity levels. Germination recovery after salinity exposure was observed on seeds that failed to germinate during the salinity study. The germination percentage and rate were significantly related to the perianth colour, the presence of perianth wings, thermal regimes and photoperiod. The presence of a perianth wing significantly reduced germination percentage and germination rate in both the pink and the yellow morph, but the yellow morph exhibited a higher germination percentage. Perianth wing removal increased germination in saline conditions. With the perianth removed, germination recovery was higher for the pink morph than for the yellow one. We suggest that by providing two different strategies for balancing germination with dormancy during favourable conditions, the presence of two morphs makes S. vermiculata more successful in highly unpredictable desert environments

    Inferring community assembly processes from functional seed trait variation along elevation gradient

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    Assembly of plant communities has long been scrutinized through the lens of trait-based ecology. Studies generally analyse functional traits related to the vegetative growth, survival and resource acquisition and thus ignore how assembly rules may affect plants at other stages of their life cycle, particularly when seeds disperse, persist in soil and germinate. Here, we analysed an extensive dataset of 16 traits for 167 species measured in-situ in 36 grasslands located along an elevation gradient and studied the impact of abiotic filtering, biotic interactions and dispersal on traits reflecting different trait categories: plant vegetative growth, germination, dispersal and seed morphology. For each community, we quantified community-weighted means (CWMs) and functional diversity (FD) for all traits and established their relationships to mean annual temperature. The seed traits were weakly correlated with vegetative traits. Therefore, these traits constituted independent axes of plant phenotypical variation that could be affected differently by community assembly rules. Abiotic filtering impacted mostly vegetative traits and to a lesser extent seed germination and morphological traits. Increasing low-temperature stress in upland sites selected for short-stature, slow-growing and frost-tolerant species that produce small quantities of small seeds with high degree of dormancy, high temperature requirements for germination and low germination speed. Biotic interactions, specifically competition in the lowlands and facilitation in uplands, also filtered some functional traits in the studied communities. The benign climate in lowlands seems to promote plant with competitive strategies that include fast growth and resource acquisition (vegetative growth traits) and early and fast germination (germination traits), whereas the effects of facilitation on the vegetative and germination traits were cancelled out by the strong abiotic filtering. The changes in the main dispersal vector from zoochory to anemochory along the elevation gradient strongly affected the dispersal and the seed morphological trait structure of the communities. This may be explained by stronger vertical turbulence and moderate warm upwinds and low grazing intensity in the uplands that select for light and non-round shaped seeds with lower terminal velocity and endozoochorous potential. Synthesis. We demonstrate that, in addition to vegetative traits, seed traits can substantially contribute to functional structuring of plant communities along environmental gradients. Thus, the ‘hard’ seed traits related to germination and dispersal are critical to detect multiple, complex community assembly rules. Consequently, such traits should be included in core lists of plant traits and, when applicable, be incorporated into the analysis of community assembly

    Influence of aerial seed banks on germination response in three desert plant species

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    © The Author 2016. Aims To determine if the germination response of desert plant species to a period of aerial storage in field conditions (i.e. mature seeds that remain attached to the parent plant) is comparable to seeds harvested at maturity and stored in ambient laboratory conditions, to better understand the role of aerial seed bank in the germination ecology of desert plants, using one annual and two perennial species. Methods Seeds of three desert plants (Anastatica hierochuntica, Blepharis ciliaris and Scrophularia deserti) that matured in June 2014, were collected from wild plants in June and November 2014, and germinated under two photoperiods (0, 12 hours light) and three thermoperiods (night/day temperatures of 15/25, 20/30 and 25/35°C). Important Findings Seeds of B. ciliaris and S. deserti had significantly higher germination percentages when harvested and stored for five months, compared to being stored in the aerial seed bank. Germination percentages of these two species increased with decreasing temperature and in the presence of light. These results indicate that these species use a combination of aerial and soil seed banks to maintain a percentage of viable seeds through favourable germination periods. Germination percentages of A. hierochuntica were high under all tested circumstances, indicating that this species relies mainly on the aerial seed bank to maintain a percentage of viable seeds through favourable germination periods. This study shows that the population survival strategies of an aerial seed bank are species-specific. These results have practical implications for conservation and habitat restoration for these species, and also for their propagation since early collection of mature fruits and ex situ storage will result in greater germination percentages of some species

    Global maps of soil temperature

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    Research in global change ecology relies heavily on global climatic grids derived from estimates of air temperature in open areas at around 2 m above the ground. These climatic grids do not reflect conditions below vegetation canopies and near the ground surface, where critical ecosystem functions occur and most terrestrial species reside. Here, we provide global maps of soil temperature and bioclimatic variables at a 1-km2 resolution for 0\u20135 and 5\u201315 cm soil depth. These maps were created by calculating the difference (i.e. offset) between in situ soil temperature measurements, based on time series from over 1200 1-km2 pixels (summarized from 8519 unique temperature sensors) across all the world's major terrestrial biomes, and coarse-grained air temperature estimates from ERA5-Land (an atmospheric reanalysis by the European Centre for Medium-Range Weather Forecasts). We show that mean annual soil temperature differs markedly from the corresponding gridded air temperature, by up to 10\ub0C (mean = 3.0 \ub1 2.1\ub0C), with substantial variation across biomes and seasons. Over the year, soils in cold and/or dry biomes are substantially warmer (+3.6 \ub1 2.3\ub0C) than gridded air temperature, whereas soils in warm and humid environments are on average slightly cooler ( 120.7 \ub1 2.3\ub0C). The observed substantial and biome-specific offsets emphasize that the projected impacts of climate and climate change on near-surface biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments. The global soil-related bioclimatic variables provided here are an important step forward for any application in ecology and related disciplines. Nevertheless, we highlight the need to fill remaining geographic gaps by collecting more in situ measurements of microclimate conditions to further enhance the spatiotemporal resolution of global soil temperature products for ecological applications

    Global maps of soil temperature.

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    Research in global change ecology relies heavily on global climatic grids derived from estimates of air temperature in open areas at around 2 m above the ground. These climatic grids do not reflect conditions below vegetation canopies and near the ground surface, where critical ecosystem functions occur and most terrestrial species reside. Here, we provide global maps of soil temperature and bioclimatic variables at a 1-km <sup>2</sup> resolution for 0-5 and 5-15 cm soil depth. These maps were created by calculating the difference (i.e. offset) between in situ soil temperature measurements, based on time series from over 1200 1-km <sup>2</sup> pixels (summarized from 8519 unique temperature sensors) across all the world's major terrestrial biomes, and coarse-grained air temperature estimates from ERA5-Land (an atmospheric reanalysis by the European Centre for Medium-Range Weather Forecasts). We show that mean annual soil temperature differs markedly from the corresponding gridded air temperature, by up to 10°C (mean = 3.0 ± 2.1°C), with substantial variation across biomes and seasons. Over the year, soils in cold and/or dry biomes are substantially warmer (+3.6 ± 2.3°C) than gridded air temperature, whereas soils in warm and humid environments are on average slightly cooler (-0.7 ± 2.3°C). The observed substantial and biome-specific offsets emphasize that the projected impacts of climate and climate change on near-surface biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments. The global soil-related bioclimatic variables provided here are an important step forward for any application in ecology and related disciplines. Nevertheless, we highlight the need to fill remaining geographic gaps by collecting more in situ measurements of microclimate conditions to further enhance the spatiotemporal resolution of global soil temperature products for ecological applications

    Global maps of soil temperature

    Get PDF
    Research in global change ecology relies heavily on global climatic grids derived from estimates of air temperature in open areas at around 2 m above the ground. These climatic grids do not reflect conditions below vegetation canopies and near the ground surface, where critical ecosystem functions occur and most terrestrial species reside. Here, we provide global maps of soil temperature and bioclimatic variables at a 1-km2 resolution for 0–5 and 5–15 cm soil depth. These maps were created by calculating the difference (i.e. offset) between in situ soil temperature measurements, based on time series from over 1200 1-km2 pixels (summarized from 8519 unique temperature sensors) across all the world\u27s major terrestrial biomes, and coarse-grained air temperature estimates from ERA5-Land (an atmospheric reanalysis by the European Centre for Medium-Range Weather Forecasts). We show that mean annual soil temperature differs markedly from the corresponding gridded air temperature, by up to 10°C (mean = 3.0 ± 2.1°C), with substantial variation across biomes and seasons. Over the year, soils in cold and/or dry biomes are substantially warmer (+3.6 ± 2.3°C) than gridded air temperature, whereas soils in warm and humid environments are on average slightly cooler (−0.7 ± 2.3°C). The observed substantial and biome-specific offsets emphasize that the projected impacts of climate and climate change on near-surface biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments. The global soil-related bioclimatic variables provided here are an important step forward for any application in ecology and related disciplines. Nevertheless, we highlight the need to fill remaining geographic gaps by collecting more in situ measurements of microclimate conditions to further enhance the spatiotemporal resolution of global soil temperature products for ecological applications

    Global maps of soil temperature

    Get PDF
    Research in global change ecology relies heavily on global climatic grids derived from estimates of air temperature in open areas at around 2 m above the ground. These climatic grids do not reflect conditions below vegetation canopies and near the ground surface, where critical ecosystem functions occur and most terrestrial species reside. Here, we provide global maps of soil temperature and bioclimatic variables at a 1-km² resolution for 0–5 and 5–15 cm soil depth. These maps were created by calculating the difference (i.e., offset) between in-situ soil temperature measurements, based on time series from over 1200 1-km² pixels (summarized from 8500 unique temperature sensors) across all the world’s major terrestrial biomes, and coarse-grained air temperature estimates from ERA5-Land (an atmospheric reanalysis by the European Centre for Medium-Range Weather Forecasts). We show that mean annual soil temperature differs markedly from the corresponding gridded air temperature, by up to 10°C (mean = 3.0 ± 2.1°C), with substantial variation across biomes and seasons. Over the year, soils in cold and/or dry biomes are substantially warmer (+3.6 ± 2.3°C) than gridded air temperature, whereas soils in warm and humid environments are on average slightly cooler (-0.7 ± 2.3°C). The observed substantial and biome-specific offsets emphasize that the projected impacts of climate and climate change on near-surface biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments. The global soil-related bioclimatic variables provided here are an important step forward for any application in ecology and related disciplines. Nevertheless, we highlight the need to fill remaining geographic gaps by collecting more in-situ measurements of microclimate conditions to further enhance the spatiotemporal resolution of global soil temperature products for ecological applications

    How much leaf area do insects eat? A data set of insect herbivory sampled globally with a standardized protocol

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    Herbivory is ubiquitous. Despite being a potential driver of plant distribution and performance, herbivory remains largely undocumented. Some early attempts have been made to review, globally, how much leaf area is removed through insect feeding. Kozlov et al., in one of the most comprehensive reviews regarding global patterns of herbivory, have compiled published studies regarding foliar removal and sampled data on global herbivory levels using a standardized protocol. However, in the review by Kozlov et al., only 15 sampling sites, comprising 33 plant species, were evaluated in tropical areas around the globe. In Brazil, which ranks first in terms of plant biodiversity, with a total of 46,097 species, almost half (43%) being endemic, a single data point was sampled, covering only two plant species. In an attempt to increase knowledge regarding herbivory in tropical plant species and to provide the raw data needed to test general hypotheses related to plant–herbivore interactions across large spatial scales, we proposed a joint, collaborative network to evaluate tropical herbivory. This network allowed us to update and expand the data on insect herbivory in tropical and temperate plant species. Our data set, collected with a standardized protocol, covers 45 sampling sites from nine countries and includes leaf herbivory measurements of 57,239 leaves from 209 species of vascular plants belonging to 65 families from tropical and temperate regions. They expand previous data sets by including a total of 32 sampling sites from tropical areas around the globe, comprising 152 species, 146 of them being sampled in Brazil. For temperate areas, it includes 13 sampling sites, comprising 59 species
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