Sandra Nogué’s research while affiliated with Autonomous University of Barcelona and other places

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Publications (88)


Location of studied lakes in the context of the North Hemispheric temperature anomaly and the Island of São Miguel, Azores
a Annual Northern Hemisphere surface temperature anomaly (NHSTA) averaged from 1982 to 2011 compared to the 1901–1981 average, the black rectangle indicates the Azores archipelago. b Location of the studied lakes in São Miguel Island. c Studied lakes 1 Azul, 2 Santiago, 3 Empadadas Norte, 4 Fogo, and 5 Furnas.
Hypothetical island and lake-scale regime shifts in response to environmental change
a Lakes responding coherently to climate warming at both local and island-wide scales; b lakes showing divergent lake-specific (local) responses yet aligning at the island scale; or c lakes diverging at the local scale without a shared response at the island scale. Lake-scale responses indicate changes in diatom community turnover over time. Lake-scale shifts (thicker coloured bands) indicate significant rates of change for each lake. Island-scale responses represent the island-fitted trend of diatom community turnover for all lakes (the shared regional response). An increase or decrease in the y-axis is reflected in the “average” predicted value of community turnover at the island scale. Island-scale shifts (thicker red band) indicate significant rates of change that are common in all lakes.
Abrupt changes in diatom communities recorded in lake sediments
a HGAM-fitted trends of DCA axis 1 values for the five studied lakes in São Miguel Island. The shaded band represents the 95% credible interval (Lake Furnas shows the shortest record). The relationship between changes in DCA axis 1 score and time is an estimation of the turnover rate. b Rate of change as measured by the response first derivative for each lake. The thickening of the curve indicates statistically significant changes in community turnover. The shaded band is the 95% simultaneous confidence interval of the HGAM fitted to DCA trends. c Island-scale trends of HGAM adjusted to the five DCA axis 1 records, showing the shared response among all lakes studied. The partial effect plot is centred on the overall mean of the response variable (i.e., DCA axis 1 scores), and the shaded band is a 95% credible interval. An increase or decrease shown in the y-axis is reflected in the average predicted value of community turnover. d The island-scale response derivative shows statistically significant changes in community turnover trend shared for all studied lakes (thicker dark red line) and 95% simultaneous confidence intervals of the HGAM fitted to DCA trends. e Northern Hemisphere surface temperature anomaly (i.e., NHSTA based on the average temperature between 1901 and 2000) since 1850.
Shifts in the dominance of key diatom functional groups over time
Diatom species were grouped into plankton (i.e., small free-floating species), benthos (i.e., bottom substrates or floating debris), Aulacoseira spp. (planktonic), and small tychoplanktonic fragilarioids (i.e., often benthic but known to proliferate in the plankton), reflecting their taxonomy, morphology and habitat preferences. Dashed horizontal lines indicate main clusters (time-constrained cluster -CONISS-) using all diatom species (see Supplementary Fig. 1 for the stratigraphy of each lake’s most abundant diatom species). Values inside brackets after the lake name indicate the community turnover in DCA standard deviation units (SD) using only the data from the last 50 years.
Changes in diatom communities across NHSAT anomaly at the island scale
An island-scale HGAM-based model of NHSAT anomaly fitted to DCA (diatom community turnover; R²adj = 0.76; deviance explained = 77.8%). Data were divided into six 30-year intervals for visualisation (see plot legend). This division corresponds to periods used in the standardisation procedure for calculating diversity metrics (see “Methods” section). Partial effect of NHSAT anomaly on community turnover, the shaded area represents the 95% credible interval. An increase or decrease shown in the y-axis is reflected in the average predicted value of community turnover. The histogram on the y-axis shows the bimodality in the community turnover response to recognise an ecological threshold. The inset plot shows statistically significant changes in the regional response (thicker dark red line) in community turnover and a 95% simultaneous interval for the common smoothing function of the HGAM fitted to DCA axis 1 score. See Supplementary Fig. 3 for an HGAM model based on the São Miguel air temperature instrumental record anomalies since 1874.

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Global warming triggers abrupt regime shifts in island lake ecosystems in the Azores Archipelago
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October 2024

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Global warming significantly alters lake ecosystems worldwide. However, the effects of warming at a regional scale are often overlooked due to the scarcity of multidecadal to centennial regional studies. Here, we examined diatom sedimentary records from five lakes on São Miguel Island (Azores archipelago) over the last 170 years. Our analysis using hierarchical generalised additive models revealed an abrupt shift in the island-wide diatom community around 1982 CE, when the Northern Hemisphere temperature exceeded 0.35 °C above the 20th-century mean. This community regime shift resulted in a 27% loss in regional diatom diversity across the Island. Furthermore, previous anthropogenic impacts may have enhanced lakes’ rapid response to warming. These findings highlight the vulnerability of freshwater island ecosystems to climate warming and emphasise the importance of transitioning from local to regional assessments to preserve regional resilience and prevent irreversible damage to these essential freshwater resources and their biodiversity.

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First paleoenvironmental and archaeological investigations in the Gulf of Guinea Islands and their potential to reveal land use change and human impacts

September 2024

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13 Reads

The Gulf of Guinea Islands (Fig. 1) present diverse natural and historical contexts but remain a blind spot in archaeological and paleoenvironmental research. Written documents starting in the 15th century describe the landscapes encountered by Europeans, but rarely mention the deep changes caused by such encounters. The earliest and most detailed account of São Tomé and its settlement, for example, comes from the mid-16th century and describes an island covered by a thick forest of unfamiliar tree species that “seemed to touch the sky” and how Europeans cut and burned trees and vegetation to make way for a town and sugar plantations (Loureiro 1989: 29). This account is a small window into human impacts driven by colonial encounters; however, prior to the initiation of our research efforts, one could only speculate about the full scope of environmental changes in the Gulf of Guinea Islands. Our research highlights the potential of multi-disciplinary collaborations - in this case, integrating archaeological and paleoenvironmental (coring-based) research - to shed light on changes through time, generate new data, and bring this area to the attention of the scientific community, while fostering local participation through capacity-building.


Climate outweighs human effects on vegetation properties during the early-to-mid Holocene

July 2024

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722 Reads

Controversies exist regarding the extent of past human influence on terrestrial ecosystems and the relative importance of human versus climatic factors in shaping Holocene vegetation. However, there has been no systematic examination of these issues at a global scale. Here we integrate palaeoecological, archaeological, and palaeoclimate data to assess the influence of humans and climate in driving patterns of past vegetation during the early and middle Holocene (8500 - 2000 years before present) as recorded by pollen-assemblage properties. We quantify and summarise the patterns of change in different properties from individual records to a global scale and assess the relative importance of humans and/or climate in influencing them. Additionally, we assess whether the internal relationships among these properties changed through time. While we find evidence that humans have high localized impact on vegetation dynamics in various regions and times periods, when considered globally, humans appear to be a secondary factor, during the early-to-mid Holocene. Our results underscore the value of merging multidisciplinary palaeodata to provide a holistic understanding of millennia-spanning relationships between humans, climate, and vegetation across different spatial scales.


Assessing the potential of bacterial and archaeal membrane lipids (GDGTs) to reconstruct Late Pleistocene and Holocene climatic changes in the Canary Islands

Sedimentary records covering the Late Pleistocene show glacial-interglacial and millennial temperature changes accompanied with, for instance, rainfall and vegetation changes at the global and regional scales. However, such records are missing for the islands of Macaronesia. Here we generate three sedimentary records over the last 10,000 to 45,000 years from the islands of Tenerife, Gran Canaria, and La Gomera using glycerol dialkyl glycerol tetraethers (GDGTs). At the global scale, air temperature and soil pH influence GDGT distributions in soils, although these biomarkers also react to other environmental factors (e.g., land use, vegetation, and soil moisture and chemistry) and shifts in bacterial and archaeal communities. Accordingly, we examined several GDGT-based proxies, notably those using bacterial branched GDGTs (brGDGTs), to assess their applicability in the Canary Islands. Our preliminary results show drastic downcore and inter-site changes in GDGT distributions, with brGDGT-based air temperature ranges larger than 10°C over the last 10,000 to 45,000 years when applying global calibrations at the three study sites. Air temperatures and soil pH inferred from brGDGTs decrease in Tenerife and La Gomera over the end of the African Humid Period, which suggests an effect of reduced rainfall on brGDGTs, possibly accompanied with a shift in bacterial communities. Air temperatures inferred from brGDGTs show a general increase over the last 27,000 years in Gran Canaria, whereas cyclization and isomerization indices of brGDGTs suggest typically opposite changes in soil pH, in disagreement with global-scale patterns from surficial soils. Our GDGT-based records also show a few drastic increases in archaeal GDGT abundances relative to the full GDGT pool after the Last Glacial Maximum, notably in Gran Canaria and La Gomera, partly related to the rainfall increase during the African Humid Period.



Methodological framework used to critically evaluate 30 contemporary plant traits (from Pérez‐Harguindeguy et al., 2013) for their potential application to the plant fossil record as paleo‐functional traits. Four traits (leaf water potential, leaf dry matter content, leaf and litter PH, and seedling functional morphology, see Supporting Information Notes S1–S7) were deemed to have low potential applicability to fossil plants and were not evaluated beyond the initial assessment step. The 26 remaining traits were reviewed (Sections V–VII) and semi‐quantitatively evaluated by the authors to produce an initial list of paleo‐functional traits (Table S1), which we then ranked according to taphonomic bias (i, ii), ease and robustness of trait measurement in fossil plants (iii, iv), strength of the trait's impact on the Earth system (v) and capacity to quantify the impact of the trait on an Earth system process within paleo‐ecosystem models (vi; Figs 3, 4).
Examples of fossil plant functional traits. (a) Vein density trait illustrated for Permian Glossopteris from Esperança Júnior et al. (2023, reused with permission) Bar, 5 mm. (b) Leaf gmax trait (a function of stomatal density and pore geometry) illustrated on Cretaceous aged Podocarpaceae compression fossils (Pole & Philippe, 2010, reused with permission) Bar, 50 μm. (c) Spinescence trait (SI) illustrated for Eocene fossil twigs from Tibet (Zhang et al., 2022, reused under the terms of a CC‐BY 4.0 license) Bar, 10 mm. (d) Leaf mass per area (LMA) trait illustrated on cross‐section of Jurassic fossil Ginkgo leaf estimated from measurements of cuticle thickness (Soh et al., 2017, reused with permission) Bar, 10 μm. (e) Salinity trait illustrated by the ghost presence of CaOx globules (interpreted as druses) on late Oligocene aged Quercus neriifolia impression fossils (Malekhosseini et al., 2022, reused under the terms of a CC‐BY 4.0 license) Bar, 200 μm, inset = 40 μm. (f) Plant height trait can be estimated from fossil trunk diameter on in situ fossil tree stumps such as illustrated from the Triassic of Antarctica (Cúneo et al., 2003, reused with permission) pen Bar, 14 cm. (g) Bark thickness trait illustrated on Early Carboniferous fossil tree from Australia (Decombeix, 2013, reused with permission) showing successive zones of periderm layers, Bar, 2 mm. (h) Palatability trait measured from the ratio of presence of feeding damage as illustrated by large circular hole feeding on fossil dicot leaf species (Currano et al., 2008, reused with permission, copyright (2008) National Academy of Sciences) Bar, 11 mm. (i) Xylem conductivity trait measured from xylem pit membrane (arrow), pit orientation, and abundance shown here on longitudinal sections of polished pyritized Eocene fossil twigs of Pityoxylon (Grimes et al., 2002, reused with permission). (j) Cuticle trait illustrated using auto‐fluorescent properties of Cretaceous aged Angiosperm cuticles (LK‐B‐55) from West Greenland highlighting secretory trichomes (pellucid dots; C Fay, JC McElwain, & S Robinson, unpublished) Bar, 100 μm. (k) Pollen trait indicating resistance to drought by the presence of furrows illustrated here for recent Citrus lanatus (Franchi et al., 2011, reused with permission) Bar, 10 μm . (l) Dispersal syndrome illustrated in winged fossil fruits of Eocene aged Bridgesia bovayensis (Manchester & O'Leary, 2010, reused with permission) scale bar in mm. (m) LMA trait based on petiole thickness illustrated for Eocene Alnus parvifolia from Royer et al. (2007), reused with permission) Bar, 1 cm. (n) Life history and maximum plant lifespan can be indirectly inferred from fossil ring width measurements illustrated here in Jurassic permineralized fossil wood Protophyllocladoxylon from Vajda et al. (2016, reused under the terms of a CC‐BY 3.0 license) Bar, 100 μm; (o) Photosynthetic pathway is a syndrome of traits, one of which, cuticle pegs (spandrels) are observed here on the inner surface of the adaxial leaf epidermis of Cretaceous Frenelopsis teixeirae compression fossils (Mendes et al., 2010; reused with permission) Bar, 200 μm. (p) Mesophyll conductance (gm) trait can be inferred from mesophyll cell wall thickness within anatomically preserved fossil leaves as illustrated here in a permineralized conifer scale leaf of Cunninghamia lanceolata from Brink et al. (2009), reused with permission) Bar, 0.5 mm.
Comparison of paleo‐functional trait scores according to different weighting criteria. (a) Paleo‐functional trait (PT in Fig. 1; Supporting Information Table S1) score plots the consensus results of the author team's semi‐quantitative evaluation (Fig. 1; Table S1) of how taphonomic bias and methodology of trait measurement influence trait values in fossil plants. Higher PT scores indicate less taphonomic bias and more robust methods of trait estimation. (b) Earth System effect (ESE in Fig. 1; Table S1; ESE = PT × v) score plots the results of the PT score weighted by the author team's semi‐quantitative evaluation of the strength of effect of the paleo‐trait on the Earth system, with higher scores indicating greater impact. (c) Earth system implementation (Earth system implementation (ESI) in Fig. 1; Table S1; ESI = ESE × vi) score adjusts the results of the ESE score according to the current capacity to parameterize the paleo‐trait and its impact on the Earth system within paleo‐ecosystem models. Higher ESI scores indicate greater potential application of the paleo‐trait to address questions in relation to Earth system processes.
A ranked list of paleo‐functional traits that can be applied to fossil plants. (a) Ranked list of paleo‐functional traits based on Earth system implementation (ESI) scores illustrating the rank order of traits with the highest (photosynthetic rate) to lowest (salinity tolerance) potential application to the plant fossil record as evaluated by the author team. (b) Bi‐plot illustrating the breakdown of components within the final trait ranking shown in panel a, where the horizontal axis shows the Earth system effect (ESE) score (in Fig. 1; Supporting Information Table S1; ESE = PT × v) and the vertical axis is the implementation multiplier (vi in Fig. 1; Table S1).
Functional traits of fossil plants

February 2024

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996 Reads

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8 Citations

A minuscule fraction of the Earth's paleobiological diversity is preserved in the geological record as fossils. What plant remnants have withstood taphonomic filtering, fragmentation, and alteration in their journey to become part of the fossil record provide unique information on how plants functioned in paleo‐ecosystems through their traits. Plant traits are measurable morphological, anatomical, physiological, biochemical, or phenological characteristics that potentially affect their environment and fitness. Here, we review the rich literature of paleobotany, through the lens of contemporary trait‐based ecology, to evaluate which well‐established extant plant traits hold the greatest promise for application to fossils. In particular, we focus on fossil plant functional traits, those measurable properties of leaf, stem, reproductive, or whole plant fossils that offer insights into the functioning of the plant when alive. The limitations of a trait‐based approach in paleobotany are considerable. However, in our critical assessment of over 30 extant traits we present an initial, semi‐quantitative ranking of 26 paleo‐functional traits based on taphonomic and methodological criteria on the potential of those traits to impact Earth system processes, and for that impact to be quantifiable. We demonstrate how valuable inferences on paleo‐ecosystem processes (pollination biology, herbivory), past nutrient cycles, paleobiogeography, paleo‐demography (life history), and Earth system history can be derived through the application of paleo‐functional traits to fossil plants.


Homogenizing and differentiating trends in floristic similarity for each site
Proportions for each site of Bray–Curtis similarity homogenizing trends (<0 slope coefficients) in blue and differentiating trends (>0 slope coefficients) in yellow over time based on the standardization-1 dataset. The Andesite Line is shown as a green dashed line. Circles with solid leader lines indicate sites settled ∼3,000 cal years BP, and squares with dashed leader lines indicate sites settled ∼700 cal years BP. Island names follow site names in parentheses. The x axis and y axis represent longitude and latitude, respectively.
Floristic similarity trends for each site ordered by elevation
The direction and steepness of the floristic similarity trends is based on the standardization-1 dataset between sites (n = 14 site comparisons as we exclude comparisons within a given site) based on pairwise Bray–Curtis similarity slope coefficients. Sites are organized by elevation with the lowest (sea level) on the left to the highest on the right (760 m a.s.l.). Data points above the grey horizontal dashed line are differentiating trends and below this line are homogenizing trends. The black horizonal lines indicate the medians of the data for each site, and the blue bars encompass the first and third quantiles of the data. Whiskers extend to the maximum and minimum of the data.
Floristic similarity trends over time and grouped by human occupancy for all sites
a, Non-parametric regressions were fitted using smoothing splines deploying package npreg⁹² with function ss (fit a smoothing spline). Smoothing splines showing pairwise Bray–Curtis similarity scores among all 15 sites on 13 islands, over the past 5,000 cal years BP. 1, greatest similarity; 0, lowest similarity. The dark blue line represents the standardization-1 dataset, and the lighter blue line represents the standardization-2 dataset. The grey shaded areas represent 95% confidence intervals. Open circles represent standardization-1 datapoints, and open triangles represent standardization-2 datapoints. b, Pairwise Bray–Curtis comparisons for the standardization-1 dataset grouped according to whether neither (n = 223), one (n = 430) or both (n = 157) islands were settled during a time interval. n, number of individual pairwise comparisons. The black horizonal lines represent the medians, and the box areas represent the first and third quantiles. The whiskers of the boxplot extend to the last data points within 1.5 times the range from first quantile to third quantile (interquartile range of the box).
Floristic homogenization of South Pacific islands commenced with human arrival

January 2024

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1 Citation

Nature Ecology & Evolution

The increasing similarity of plant species composition among distinct areas is leading to the homogenization of ecosystems globally. Human actions such as ecosystem modification, the introduction of non-native plant species and the extinction or extirpation of endemic and native plant species are considered the main drivers of this trend. However, little is known about when floristic homogenization began or about pre-human patterns of floristic similarity. Here we investigate vegetation trends during the past 5,000 years across the tropical, sub-tropical and warm temperate South Pacific using fossil pollen records from 15 sites on 13 islands within the biogeographical realm of Oceania. The site comparisons show that floristic homogenization has increased over the past 5,000 years. Pairwise Bray–Curtis similarity results also show that when two islands were settled by people in a given time interval, their floristic similarity is greater than when one or neither of the islands were settled. Importantly, higher elevation sites, which are less likely to have experienced human impacts, tended to show less floristic homogenization. While biotic homogenization is often referred to as a contemporary issue, we have identified a much earlier trend, likely driven by human colonization of the islands and subsequent impacts.



14,000 years of climatic and anthropogenic change in the Afromontane forest of São Tomé Island, Gulf of Guinea

December 2023

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3 Citations

Quaternary Science Reviews

São Tomé (Gulf of Guinea, Central Africa) is a 854 km2 tropical island that had a pivotal role in early European colonial expansion through the Atlantic between the 15th and 16th centuries. Historical sources suggest that native vegetation has been heavily impacted since human arrival (1470 CE) due to monoculture economies and the introduction of mammals and plants, some of which now have established wild populations. The Afromontane forest of São Tomé, located above 800 m.a.sl., is particularly rich in endemic plant species and has remained relatively unaffected by direct human impacts. Here, we explore how environmental change influenced this forest through the study of a sedimentary sequence from the volcanic crater of Lagoa Amélia (1340 m a.s.l.), a palustrine system located at the boundary between submontane (800–1400 m a.s.l.) and mist forest (above 1400 m a.s.l.). We used fossil pollen, non-pollen palynomorphs, sedimentology and charcoal to determine forest dynamics from the Late Pleistocene to the present. From 14,000 to 12,500 cal yr BP the forest was dominated by taxa from higher altitudes, adapted to cooler and drier climates (e.g. Afrocarpus mannii trees and Psychotria nubicola). After 12,500 cal yr BP, a potential uphill migration was identified by an increase in taxa like the trees Symphonia globulifera and Craterispermum cerinanthum. From 11,200 cal yr BP through the rest of the Holocene taxa from lower altitudes became dominant (e.g. Prunus africana, Polyscias, and Sabicea), except at c. 8500 cal yr BP when rapid cooling led to forest opening. Charcoal showed that fires were frequent during the Late Pleistocene (14,000 to 11,200 cal yr BP), becoming rare during the Holocene until anthropogenic fires started at c. 220 cal yr BP. Other recent anthropogenic impacts detected in Lagoa Amélia included the appearance of pollen of introduced plant species (e.g., Cestrum), and the increase in pollen of economically important species (Elaeis guineensis, Zea mays) and in fungal spores related to introduced herbivores. Our results reveal that climate changed the altitudinal distribution of the Afromontane forest in São Tomé during the Late Pleistocene, as observed on the African continent, and that this ecosystem was also strongly impacted by human arrival, through fire, farming, and introduced species.


Citations (61)


... One question that arises from the widespread occurrence of wildfire through the Carboniferous is to what extent has this affected the evolution of plant traits to cope with wildfire (other aspects such as atmospheric compositionsee Beerling et al. (1998) and climate have been consideredsee Boyce and Lee, 2017;Clark et al., 2023;Fluck et al., 2007;Matthaeus et al., 2023;McElwain et al., 2024). Such a topic is more easily considered in Cretaceous and later plants where we have some clues from modern plants and from molecular data (He et al., 2016). ...

Reference:

Fire in the Carboniferous Earth System
Functional traits of fossil plants

... This is separate from the IPPD, but related, and contains many of the same sites, though with a focus on pre-European samples. Examples of other important work in this region that used their own pollen sample compilations include a floristic diversity study of South Pacific islands (Strandberg et al., 2024) and a study of human impact on the biodiversity of islands (Nogué et al., 2021). ...

Floristic homogenization of South Pacific islands commenced with human arrival

Nature Ecology & Evolution

... Around 4,000 cal BP, the relative sea-level (RSL) in the region was higher than the present state resulting in a different mangrove forest area of occupancy. Analysis of organic matter beneath mangrove stands in New With similar scenarios of sea-level change in the province, high soil carbon sequestration is expected in mangrove ecosystems on other islands such as Tonga or Vanuatu after their seaward migration or reestablishment (Ellison, 2006, Combettes et al., 2015, Strandberg et al., 2023. Despite variations in structural complexity and carbon stocks among mangrove sites in Fiji, all assessed areas were significant carbon reservoirs, with carbon storage corresponding to 73% of carbon stock of the archipelago, while representing only 7% of total forest area (Cameron et al., 2021b). ...

Influences of sea level changes and volcanic eruptions on Holocene vegetation in Tonga
  • Citing Article
  • May 2023

Biotropica

... Mankind has been well aware of climate change in the last decades, due to atmosphere temperature increase caused by combustion gasses. The situation is so severe, it has been started to be called a climate catastrophe [1][2][3][4]. Consequently, humanity is impelled to reduce, or even halt, its green-house gases emission without delay, to circumvent an exacerbation of this climate catastrophe [1][2][3][4]. Concomitantly, the humanity's power consumption has been forewarned to increase to 30 TW by year 2050 [5,6]. ...

Catastrophic climate change and the collapse of human societies

National Science Review

... In oceanic islands, intensification of traditional land uses [2,3] and the growing expansion of human activities into the coastal areas originate habitat loss, changes in vegetation structure and the fragmentation of endemic plant populations [4], leading to biodiversity loss, plant extinctions [5,6] and to decreases in abundance and diversity [7]. Among these threats, the proliferation of non-indigenous taxa [8], biological invasions [4,7], and climate change are paramount. ...

Long‐term trajectories of non‐native vegetation on islands globally

Ecology Letters

... Pairwise comparisons in which neither site or one site or island was settled show that similarity was relatively low (Fig. 3b). Dynamics in pre-human settlement composition are likely related to natural drivers such as sea level change, hydroseral development of wetlands and lacustrine vegetation, volcanism and other disturbances (for example, cyclones and droughts) [34][35][36][37] . These drivers may have an impact on biotic similarity in numerous biotas and habitats as they can affect a given species and thus alter the species pool in similar ways across different communities (for example, ref. 38). ...

Island ecosystem responses to the Kuwae eruption and precipitation change over the last 1600 years, Efate, Vanuatu

... A high frequency and abundance of both natural and human-induced fires has occurred in southern Africa throughout the entire Holocene (Davies et al., 2022;Power et al., 2008), while no natural occurrence of fires on the Kerguelen Island is known in this same period. Local fires could possibly have been ignited by lightning or volcanic activity (Castilla-Beltrán et al., 2023) from the volcanic complexes in the southwest of the Kerguelen Islands (Gautier et al., 1990). However, the vegetation on the island provides relatively little fuel for burning and the oftentimes patchy vegetation cover could prevent fires from spreading over large areas. ...

Taming Fogo Island: Late-Holocene volcanism, natural fires and land use as recorded in a scoria-cone sediment sequence in Cabo Verde
  • Citing Article
  • January 2023

The Holocene

... The microscopic size of pollen and spores and their low taxonomic resolution create a challenge to their incorporation as functional traits into global trait analysis. However, potential methodologies have been proposed (reviewed in Reitalu & Nogué, 2023; Table 1). Taphonomic biases in the pollen and spore record are very well constrained compared with other fossilized plant parts, and there is a high likelihood of their fossilization. ...

Functional vegetation change over millennia

Nature Ecology & Evolution

... These proxies, however, come with various biases. First, many plants are insect pollinated, and their pollen production and dispersal are low (de Nascimento et al. 2015;Nogué et al. 2022). Second, the persistent northeasterly trade winds blowing in these latitudes may carry pollen to the islands from ecosystems on the mainland of the Maghreb, Sahara or the Iberian Peninsula, so that the pollen detected on the Canary Islands may include some extraregional components (Hooghiemstra et al. 2006). ...

The spatio‐temporal distribution of pollen traits related to dispersal and desiccation tolerance in Canarian laurel forest
  • Citing Article
  • August 2022

Journal of Vegetation Science

... The Madeira laurel pigeon is a close relative of the Bolle's pigeon and is largely confined to Madeira's relict forests or laurisilva on the island of Madeira; it was formerly found on the nearby island of Porto Santo (Cartwright, 2019;Florencio et al., 2021). ...

Macaronesia as a Fruitful Arena for Ecology, Evolution, and Conservation Biology