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Ines Ibanez

Publications and source records attributed to Ines Ibanez.

15 recordsLinked to original sources

Why are non-native plants successful? Consistently fast economic traits and novel origin jointly explain abundance across US ecoregions

Are non-native plants abundant because they are non-native, and have advantages over native plants, or because they possess ‘fast’ resource strategies, and have advantages in disturbed environments? This question is central to invasion biology but remains unanswered. We quantified the relative importance of resource strategy and biogeographic origin in 69 441 plots across the conterminous United States containing 11 280 plant species. Non-native species had faster economic traits than native species in most plant communities (77%, 86% and 82% of plots for leaf nitrogen concentration, specific leaf area, and leaf dry matter content). Non-native species also had distinct patterns of abundance, but these were not explained by their fast traits. Compared with functionally similar native species, non-native species were (1) more abundant in plains and deserts, indicating the importance of biogeographic origin, and less abundant in forested ecoregions, (2) were more abundant where co-occurring species had fast traits, for example due to disturbance, and (3) showed weaker signals of local environmental filtering. These results clarify the nature of plant invasion: Although non-native plants have consistently fast economic traits, other novel characteristics and processes likely explain their abundance and, therefore, impacts.

conterminous United States

A quantitative classification of the geography of non-native flora in the United States

Aim Non-native plants have the potential to harm ecosystems. Harm is classically related to their distribution and abundance, but this geographical information is often unknown. Here, we assess geographical commonness as a potential indicator of invasive status for non-native flora in the United States. Geographical commonness could inform invasion risk assessments across species and ecoregions. Location Conterminous United States. Time Period Through 2022. Major Taxa Studied Plants. Methods We compiled and standardised occurrence and abundance data from 14 spatial datasets and used this information to categorise non-native species as uncommon or common based on three dimensions of commonness: area of occupancy, habitat breadth and local abundance. To assess consistency in existing categorizations, we compared commonness to invasive status in the United States. We identified species with higher-than-expected abundance relative to their occupancy, habitat breadth or residence time. We calculated non-native plant richness within United States ecoregions and estimated unreported species based on rarefaction/extrapolation curves. Results This comprehensive database identified 1874 non-native plant species recorded in 4,844,963 locations. Of these, 1221 species were locally abundant (> 10% cover) in 797,759 unique locations. One thousand one hundred one non-native species (59%) achieved at least one dimension of commonness, including 565 species that achieved all three. Species with longer residence times tended to meet more dimensions of commonness. We identified 132 species with higher-than-expected abundance. Ecoregions in the central United States have the largest estimated numbers of unreported, abundant non-native plants. Main Conclusions A high proportion of non-native species have become common in the United States. However, existing categorizations of invasive species are not always consistent with species' abundance and distribution, even after considering residence time. Considering geographical commonness and higher-than-expected abundance revealed in this new dataset could support more consistent and proactive identification of invasive plants and lead to more efficient management practices.

Conterminous United States

Using plant invasions to compare occurrence- and abundance-based calculations of biotic homogenisation: Are results complementary or contradictory?

Aim Beta diversity quantifies the similarity of ecological assemblages. Its increase, known as biotic homogenisation, can be a consequence of biological invasions. However, species occurrence (presence/absence) and abundance-based analyses can produce contradictory assessments of the magnitude and direction of changes in beta diversity. Previous work indicates these contradictions should be less frequent in nature than in theory, but a growing number of empirical studies report discrepancies between occurrence- and abundance-based approaches. Understanding if these discrepancies represent a few isolated cases or are systematic across a diversity of ecosystems would allow us to better understand the general patterns, mechanisms and impacts of biotic homogenisation. Location United States. Time Period 1963–2020. Major Taxa Studied Vascular plants. Methods We used a dataset of more than 70,000 vegetation survey plots to assess differences in biotic homogenisation with and without invasion using both occurrence- and abundance-based metrics of beta diversity. We estimated taxonomic biotic homogenisation by comparing beta diversity of invaded and uninvaded plots with both classes of metrics and investigated the characteristics of the non-native species pool that influenced the likelihood that these metrics disagree. Results In 78% of plot comparisons, occurrence- and abundance-based calculations agreed in direction, and the two metrics were generally well correlated. Our empirical results are consistent with previous theory. Discrepancies between the metrics were more likely when the same non-native species was at high cover at both plots compared for beta diversity, and when these plots were spatially distant. Main Conclusions In about 20% of cases, our calculations revealed differences in direction (homogenisation vs. differentiation) when comparing occurrence- and abundance-based metrics, indicating that the metrics are not interchangeable, especially when distances between plots are high and invader diversity is low. When data permit, combining the two approaches can offer insights into the role of invasions and extirpations in driving biotic homogenisation/differentiation.

Global Ecology and Biogeography

The relationship between maturation size and maximum tree size from tropical to boreal climates

The fundamental trade-off between current and future reproduction has long been considered to result in a tendency for species that can grow large to begin reproduction at a proportionately larger size. Due to the prolonged time required to reach maturity, estimates of tree maturation size remain unavailable and we lack a global view on the generality and the shape of this trade-off. Using seed production from five continents, we estimate tree maturation sizes for 486 tree pecies spanning tropical to boreal climates. Results show that a species’ maturation size increases with maximum size, but in a non-proportional way: the largest species begin reproduction at smaller sizes than would be expected if maturation size were simply proportional to maximum size. Furthermore, the decrease in relative maturation size is steepest in cold climates. These findings on maturation size drivers are key to accurately represent forests’ responses to disturbance and climate change.

Ecology Letters

Macroscale analyses suggest invasive plant impacts depend more on the composition of invading plants than on environmental context

Aim Native biodiversity is threatened by the spread of non-native invasive species. Many studies demonstrate that invasions reduce local biodiversity but we lack an understanding of how impacts vary across environments at the macroscale. Using ~11,500 vegetation surveys from ecosystems across the United States, we quantified how the relationship between non-native plant cover and native plant diversity varied across different compositions of invading plants (measured by non-native plant richness and evenness) and environmental contexts (measured by productivity and human activity). Location Continental United States. Time Period Surveys from 1990s-present. Major Taxa Studied Terrestrial plant communities. Methods We fit mixed effects models to understand how native plant richness, diversity and evenness varied with non-native cover. We tested how this relationship varied when non-native cover interacted with non-native plant richness and evenness, and with productivity and human activity. Results Across the United States, communities with greater cover of non-native plants had lower native plant richness and diversity but higher evenness, suggesting rare native plants can be lost while dominant plants decline in abundance. The relationship between non-native cover and native community diversity varied with non-native plant richness and evenness but was not associated with productivity and human activity. Negative associations were strongest in areas with low non-native richness and evenness, characterizing plant communities that were invaded by a dominant non-native plant. Main Conclusions Non-native plant cover provides a first approximation of invasion impacts on native community diversity, but the magnitude of impact depended on non-native plant richness and evenness. Relationships between non-native cover and native diversity were consistent in strength across continental scale gradients of productivity and human activity. Therefore, at the macroscale, invasive plant impacts on native plant communities likely depend more on the characteristics of the invading plants, that is the presence of a dominant invader, than on the environmental context.

Global Ecology and Biogeography

Masting is uncommon in trees that depend on mutualist dispersers in the context of global climate and fertility gradients

The benefits of masting (volatile, quasi-synchronous seed production at lagged intervals) include satiation of seed predators, but these benefits come with a cost to mutualist pollen and seed dispersers. If the evolution of masting represents a balance between these benefits and costs, we expect mast avoidance in species that are heavily reliant on mutualist dispersers. These effects play out in the context of variable climate and site fertility among species that vary widely in nutrient demand. Meta-analyses of published data have focused on variation at the population scale, thus omitting periodicity within trees and synchronicity between trees. From raw data on 12 million tree-years worldwide, we quantified three components of masting that have not previously been analysed together: (i) volatility, defined as the frequency-weighted year-to-year variation; (ii) periodicity, representing the lag between high-seed years; and (iii) synchronicity, indicating the tree-to-tree correlation. Results show that mast avoidance (low volatility and low synchronicity) by species dependent on mutualist dispersers explains more variation than any other effect. Nutrient-demanding species have low volatility, and species that are most common on nutrient-rich and warm/wet sites exhibit short periods. The prevalence of masting in cold/dry sites coincides with climatic conditions where dependence on vertebrate dispersers is less common than in the wet tropics. Mutualist dispersers neutralize the benefits of masting for predator satiation, further balancing the effects of climate, site fertility and nutrient demands.

Nature Plants

Combining local, landscape, and regional geographies to assess plant community vulnerability to invasion impact

Invasive species science has focused heavily on the invasive agent. However, management to protect native species also requires a proactive approach focused on resident communities and the features affecting their vulnerability to invasion impacts. Vulnerability is likely the result of factors acting across spatial scales, from local to regional, and it is the combined effects of these factors that will determine the magnitude of vulnerability. Here, we introduce an analytical framework that quantifies the scale-dependent impact of biological invasions on native richness from the shape of the native species–area relationship (SAR). We leveraged newly available, biogeographically extensive vegetation data from the U.S. National Ecological Observatory Network to assess plant community vulnerability to invasion impact as a function of factors acting across scales. We analyzed more than 1000 SARs widely distributed across the USA along environmental gradients and under different levels of non-native plant cover. Decreases in native richness were consistently associated with non-native species cover, but native richness was compromised only at relatively high levels of non-native cover. After accounting for variation in baseline ecosystem diversity, net primary productivity, and human modification, ecoregions that were colder and wetter were most vulnerable to losses of native plant species at the local level, while warmer and wetter areas were most susceptible at the landscape level. We also document how the combined effects of cross-scale factors result in a heterogeneous spatial pattern of vulnerability. This pattern could not be predicted by analyses at any single scale, underscoring the importance of accounting for factors acting across scales. Simultaneously assessing differences in vulnerability between distinct plant communities at local, landscape, and regional scales provided outputs that can be used to inform policy and management aimed at reducing vulnerability to the impact of plant invasions.

Ecological Applications

Linking seed size and number to trait syndromes in trees

Aim Our understanding of the mechanisms that maintain forest diversity under changing climate can benefit from knowledge about traits that are closely linked to fitness. We tested whether the link between traits and seed number and seed size is consistent with two hypotheses, termed the leaf economics spectrum and the plant size syndrome, or whether reproduction represents an independent dimension related to a seed size–seed number trade-off. Location Most of the data come from Europe, North and Central America and East Asia. A minority of the data come from South America, Africa and Australia. Time period 1960–2022. Major taxa studied Trees. Methods We gathered 12 million observations of the number of seeds produced in 784 tree species. We estimated the number of seeds produced by individual trees and scaled it up to the species level. Next, we used principal components analysis and generalized joint attribute modelling (GJAM) to map seed number and size on the tree traits spectrum. Results Incorporating seed size and number into trait analysis while controlling for environment and phylogeny with GJAM exposes relationships in trees that might otherwise remain hidden. Production of the large total biomass of seeds [product of seed number and seed size; hereafter, species seed productivity (SSP)] is associated with high leaf area, low foliar nitrogen, low specific leaf area (SLA) and dense wood. Production of high seed numbers is associated with small seeds produced by nutrient-demanding species with softwood, small leaves and high SLA. Trait covariation is consistent with opposing strategies: one fast-growing, early successional, with high dispersal, and the other slow-growing, stress-tolerant, that recruit in shaded conditions. Main conclusions Earth system models currently assume that reproductive allocation is indifferent among plant functional types. Easily measurable seed size is a strong predictor of the seed number and species seed productivity. The connection of SSP with the functional traits can form the first basis of improved fecundity prediction across global forests.

Global Ecology and Biogeography

Limits to reproduction and seed size-number trade-offs that shape forest dominance and future recovery

The relationships that control seed production in trees are fundamental to understanding the evolution of forest species and their capacity to recover from increasing losses to drought, fire, and harvest. A synthesis of fecundity data from 714 species worldwide allowed us to examine hypotheses that are central to quantifying reproduction, a foundation for assessing fitness in forest trees. Four major findings emerged. First, seed production is not constrained by a strict trade-off between seed size and numbers. Instead, seed numbers vary over ten orders of magnitude, with species that invest in large seeds producing more seeds than expected from the 1:1 trade-off. Second, gymnosperms have lower seed production than angiosperms, potentially due to their extra investments in protective woody cones. Third, nutrient-demanding species, indicated by high foliar phosphorus concentrations, have low seed production. Finally, sensitivity of individual species to soil fertility varies widely, limiting the response of community seed production to fertility gradients. In combination, these findings can inform models of forest response that need to incorporate reproductive potential.

Nature Communications

Globally, tree fecundity exceeds productivity gradients

Lack of tree fecundity data across climatic gradients precludes the analysis of how seed supply contributes to global variation in forest regeneration and biotic interactions responsible for biodiversity. A global synthesis of raw seedproduction data shows a 250-fold increase in seed abundance from cold-dry to warm-wet climates, driven primarily by a 100-fold increase in seed production for a given tree size. The modest (threefold) increase in forest productivity across the same climate gradient cannot explain the magnitudes of these trends. The increase in seeds per tree can arise from adaptive evolution driven by intense species interactions or from the direct effects of a warm, moist climate on tree fecundity. Either way, the massive differences in seed supply ramify through food webs potentially explaining a disproportionate role for species interactions in the wet tropics.

Ecology Letters

North American tree migration paced by climate in the West, lagging in the East

Tree fecundity and recruitment have not yet been quantified at scales needed to anticipate biogeographic shifts in response to climate change. By separating their responses, this study shows coherence across species and communities, offering the strongest support to date that migration is in progress with regional limitations on rates. The southeastern continent emerges as a fecundity hotspot, but it is situated south of population centers where high seed production could contribute to poleward population spread. By contrast, seedling success is highest in the West and North, serving to partially offset limited seed production near poleward frontiers. The evidence of fecundity and recruitment control on tree migration can inform conservation planning for the expected long-term disequilibrium between climate and forest distribution.

PNAS

Is there tree senescence? The fecundity evidence

Despite its importance for forest regeneration, food webs, and human economies, changes in tree fecundity with tree size and age remain largely unknown. The allometric increase with tree diameter assumed in ecological models would substantially overestimate seed contributions from large trees if fecundity eventually declines with size. Current estimates are dominated by overrepresentation of small trees in regression models. We combined global fecundity data, including a substantial representation of large trees. We compared size–fecundity relationships against traditional allometric scaling with diameter and two models based on crown architecture. All allometric models fail to describe the declining rate of increase in fecundity with diameter found for 80% of 597 species in our analysis. The strong evidence of declining fecundity, beyond what can be explained by crown architectural change, is consistent with physiological decline. A downward revision of projected fecundity of large trees can improve the next generation of forest dynamic models.

Proceedings of the National Academy of Sciences

Continent-wide tree fecundity driven by indirect climate effects

Indirect climate effects on tree fecundity that come through variation in size and growth (climate-condition interactions) are not currently part of models used to predict future forests. Trends in species abundances predicted from meta-analyses and species distribution models will be misleading if they depend on the conditions of individuals. Here we find from a synthesis of tree species in North America that climate-condition interactions dominate responses through two pathways, i) effects of growth that depend on climate, and ii) effects of climate that depend on tree size. Because tree fecundity first increases and then declines with size, climate change that stimulates growth promotes a shift of small trees to more fecund sizes, but the opposite can be true for large sizes. Change the depresses growth also affects fecundity. We find a biogeographic divide, with these interactions reducing fecundity in the West and increasing it in the East. Continental-scale responses of these forests are thus driven largely by indirect effects, recommending management for climate change that considers multiple demographic rates.

Nature Communications

Tools and technologies for quantifying spread and impacts of invasive species

The need for tools and technologies for understanding and quantifying invasive species has never been greater. Rates of infestation vary on the species or organism being examined across the United States, and notable examples can be found. For example, from 2001 to 2003 alone, ash ( Fraxinus spp.) mortality progressed at a rate of 12.97 km year −1 (Siegert et al. 2014), and cheatgrass ( Bromus tectorum ) is expected to increase dominance on 14% of Great Basin rangelands (Boyte et al. 2016). The magnitude and scope of problems that invasive species present suggest novel approaches for detection and management are needed, especially those that enable more cost-effective solutions. The advantages of using technologically advanced approaches and tools are numerous, and the quality and quantity of available information can be significantly enhanced by their use. They can also play a key role in development of decision-support systems; they are meant to be integrated with other systems, such as inventory and monitoring, because often the tools are applied after a species of interest has been detected and a threat has been identified. In addition, the inventory systems mentioned in Chap. 10 are regularly used in calibrating and validating models and decision-support systems. For forested areas, Forest Inventory and Analysis (FIA) data are most commonly used (e.g., Václavík et al. 2015) given the long history of the program. In non-forested systems, national inventory datasets have not been around as long (see Chap. 10), but use of these data to calibrate and validate spatial models is growing. These inventory datasets include the National Resources Inventory (NRI) (e.g., Duniway et al. 2012) and the Assessment Inventory and Monitoring program (AIM) (e.g., McCord et al. 2017). Similarly, use of the Nonindigenous Aquatic Species (NAS) database is growing as well (e.g., Evangelista et al. 2017). The consistent protocols employed by these programs prove valuable for developing better tools, but the data they afford are generally limited for some tools because the sampling intensity is too low.

Book chapter

Adjusting the lens of invasion biology to focus on the impacts of climate-driven range shifts

As Earth’s climate rapidly changes, species range shifts are considered key to species persistence. However, some range-shifting species will alter community structure and ecosystem processes. By adapting existing invasion risk assessment frameworks, we can identify characteristics shared with high-impact introductions and thus predict potential impacts. There are fundamental differences between introduced and range-shifting species, primarily shared evolutionary histories between range shifters and their new community. Nevertheless, impacts can occur via analogous mechanisms, such as wide dispersal, community disturbance and low biotic resistance. As ranges shift in response to climate change, we have an opportunity to develop plans to facilitate advantageous movements and limit those that are problematic.

Nature Climate Change