Sagrario Gámez-Virués’s research while affiliated with Fujian Agriculture and Forestry University and other places

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Publications (9)


Broadening the scope of empirical studies to answer persistent questions in landscape-moderated effects on biodiversity and ecosystem functioning
  • Chapter

January 2022

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248 Reads

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10 Citations

Advances in Ecological Research

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Sagrario Gámez-Virués

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Despite a developing understanding of how landscape level processes moderate biodiversity patterns and ecosystem functioning, key questions remain unresolved, therefore limiting our ability to manage for biodiversity conservation and ecosystem functioning at the most appropriate scales. These questions have remained unanswered because studies in agricultural landscapes generally over-emphasize alpha diversity within managed land uses, and are focused at scales that are irrelevant to species studied. We argue that the key to resolving unanswered questions in landscape-moderated effects on biodiversity and ecosystem functioning lies in establishing the distribution of available species and functions across the landscape and between land uses, and in understanding how this distribution of species varies with changing landscape context. We emphasize the need for studies that empirically test the mechanisms underpinning landscape-moderated effects on biodiversity and ecosystem function and link these with ecosystem service delivery. We facilitate this approach by outlining the empirical investigations that will lead to a better understanding of biodiversity patterns and ecosystem functioning at the landscape scale, and we highlight statistical approaches to support these different approaches to sampling. Our paper is divided in four sections: (A) we identify where and why gaps exist in our mechanistic understanding of landscape level processes, by reviewing current hypotheses; (B) we outline why, and how, landscape level research would benefit from shifting the focus to the distribution and partitioning of species and functions within a landscape; (C) we outline why, and how, larger scale processes, such as dispersal and meta-population dynamics need to be addressed in a more interactive fashion; and finally, (D) we round out by highlighting the experimental settings where landscape effects most urgently need testing.


Figure 2. Schematic of the multi-trophic response-effect model adapted to biological control, showing how ecosystem service delivery is mediated through a series of filters. Environmental filters, such as local management intensity and landscape simplification, filter environmental response traits of plants and arthropods. Trophic effect traits of the plant community in-turn filter arthropod trophic response traits. Ecosystem effect traits of the resultant arthropod natural enemy community will determine the delivery of biological control services, but these traits are firstly determined by the series of filters described above. Traits in smaller solid boxes are linked across filters and may limit response diversity; traits in broken boxes are linked across trophic levels and drive trophic interactions.
Table 2. Arthropod traits identified to underpin response to environmental and trophic filters, and the ecological mechanisms that drive them
Managing biological control services through multi-trophic trait interactions: Review and guidelines for implementation at local and landscape scales

June 2017

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624 Reads

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171 Citations

Biological reviews of the Cambridge Philosophical Society

Ecological studies are increasingly moving towards trait-based approaches, as the evidence mounts that functions, as opposed to taxonomy, drive ecosystem service delivery. Among ecosystem services, biological control has been somewhat overlooked in functional ecological studies. This is surprising given that, over recent decades, much of biological control research has been focused on identifying the multiple characteristics (traits) of species that influence trophic interactions. These traits are especially well developed for interactions between arthropods and flowers – important for biological control, as floral resources can provide natural enemies with nutritional supplements, which can dramatically increase biological control efficiency. Traits that underpin the biological control potential of a community and that drive the response of arthropods to environmental filters, from local to landscape-level conditions, are also emerging from recent empirical studies. We present an overview of the traits that have been identified to (i) drive trophic interactions, especially between plants and biological control agents through determining access to floral resources and enhancing longevity and fecundity of natural enemies, (ii) affect the biological control services provided by arthropods, and (iii) limit the response of arthropods to environmental filters, ranging from local management practices to landscape-level simplification. We use this review as a platform to outline opportunities and guidelines for future trait-based studies focused on the enhancement of biological control services.


Figure 1: Functional traits as ecological indicators of intensification. High levels of in-field management intensity and simplification at the landscape scale select for a functional community comprising mainly species with generalized traits (a). Reducing simplification at the landscape-scale (−) by creating more landscape heterogeneity (+), in terms of high diversity of land cover types and small patch size, selects for a functional community comprising species with generalized and specialized traits, despite high levels of in-field management intensity (b).
Figure 2: Conceptual overview of the RLQ analysis. RLQ is a co-inertia analysis that couples multiple data sets and identifies co-relationships between them. The multivariate RLQ analysis relates a species-traits table (Q) to a table of environmental variables at each site (R), using a species-abundances table (L) as a link (a). Correspondence analysis (CA) of the R variables against L (Plot 1) and Q variables against L (Plot 2) can be combined (Plot 3) to show the r-components (environmental variables from Table R) and q-components (species traits from Table Q) as vectors within a single bi-plot (b). Modified with kind permission from Dolédec et al., Figures 1 and 5 (ref. 19).
Figure 4: Trait responses to in-field management practices (IFM) and landscape variables (CNF=configurational landscape heterogeneity or patch size and CMP=compositional landscape heterogeneity or diversity of land cover types) within 2,000 m radius. RLQ biplot, showing the decomposition of co-correlations between environmental variables (R-Table 3 × 72) and trait attributes (Q-Table 598 × 4), constrained by abundance (L-Table 72 × 598). The size and direction of environmental effects are represented by red arrows (a). Clustered points identify trait syndrome groups and are represented with the same colour. Boxplots represent the distribution of trait attributes (mean, inner-quartile range (IQR) and outliers>1.5 × IQR) in cluster (b–e). The width of the bars represents relative abundance and the black component represents the proportion of generalist feeders within the whole community: the higher the bar, the greater the proportion (b,c). Note: a has been rescaled for display purposes.
Landscape simplification filters species traits and drives biotic homogenization
  • Article
  • Full-text available

October 2015

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9,467 Reads

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565 Citations

Biodiversity loss can affect the viability of ecosystems by decreasing the ability of communities to respond to environmental change and disturbances. Agricultural intensification is a major driver of biodiversity loss and has multiple components operating at different spatial scales: from in-field management intensity to landscape-scale simplification. Here we show that landscape-level effects dominate functional community composition and can even buffer the effects of in-field management intensification on functional homogenization, and that animal communities in real-world managed landscapes show a unified response (across orders and guilds) to both landscape-scale simplification and in-field intensification. Adults and larvae with specialized feeding habits, species with shorter activity periods and relatively small body sizes are selected against in simplified landscapes with intense in-field management. Our results demonstrate that the diversity of land cover types at the landscape scale is critical for maintaining communities, which are functionally diverse, even in landscapes where in-field management intensity is high.

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Configurational landscape heterogeneity shapes functional community composition of grassland butterflies

February 2015

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710 Reads

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178 Citations

Landscape heterogeneity represents two aspects of landscape simplification: (i) compositional heterogeneity (diversity of habitat types); and (ii) configurational heterogeneity (number, size and arrangement of habitat patches), both with different ecological implications for community composition. We examined how independent gradients of compositional and configurational landscape heterogeneity, at eight spatial scales, shape taxonomic and functional composition of butterfly communities in 91 managed grasslands across Germany. We used landscape metrics that were calculated from functional maps based on habitat preferences of individual species during different life stages. The relative effects of compositional and configurational landscape heterogeneity were compared with those of local land‐use intensity on butterfly taxonomic diversity, community composition and functional diversity of traits related to body size, feeding breadth and migratory tendency. As expected, compositional heterogeneity had strong positive effects on taxonomic diversity, while configurational heterogeneity had strong positive effects on trait dominance within the community. When landscapes had smaller mean patch size and greater boundary area, communities were dominated by species with more specialized larval feeding, decreased forewing length and limited migratory tendency. The positive effects of increased configurational landscape heterogeneity outweighed the negative effects of local land‐use intensity on larval‐feeding specialization, at all spatial scales, highlighting its importance for specialists of all dispersal capabilities. Synthesis and applications . We show that landscapes with high compositional heterogeneity support communities with greater taxonomic diversity, while landscapes with high configurational heterogeneity support communities that include vulnerable species (feeding specialists with larger body size, sedentary nature and more negatively affected by local management intensity). A decline in functional community composition can lead to functional homogenization, affecting the viability of the ecosystems by decreasing the variability in their responses to disturbance and altering their functioning. A landscape management for grasslands that promotes the maintenance of small patch sizes and a diversity of land uses in the surrounding landscape (within 250–1000 m) is recommended for the conservation of diverse butterfly communities. These strategies could also benefit government programmes such as the EU 2020 Biodiversity Strategy in their efforts to reduce the loss of biodiversity in agricultural landscapes.


Landscape heterogeneity affects the functional diversity of grassland Lepidoptera

September 2013

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21 Reads

Biodiversity in agroecosystems is affected by human management practices at both the local and at the landscape‐levels (e.g., reduction of landscape heterogeneity via homogenisation of land‐uses). While local land use intensity is easier to measure in terms of fertiliser and pesticide application, grazing and mowing, landscape heterogeneity metrics are more difficult to obtain and are still at an early stage of development. To date, landscape heterogeneity has most‐commonly been defined as the diversity of human land uses within a landscape (structural heterogeneity) and not in terms of habitat‐ or resource‐requirements of animals (functional heterogeneity). While some species require quite specific resources or specific combinations of resources for different life‐stages, others are freed from such ecological constraints and can readily utilise a wide range of habitats. Thus, by considering land uses in terms of the functional value that they represent for species (and not simply from a human land use perspective) we can expect to have a more accurate understanding of effects of landscape heterogeneity on species, functional groups and communities. We examined the effects of landscape heterogeneity on community composition for Lepidoptera collected in the German Biodiversity Exploratories project. Further, we analysed the effects of landscape heterogeneity on the diversity of functional groups defined by traits representing habitat‐and feeding‐specialisation and dispersal ability. We report on how these different metrics of landscape heterogeneity relate to the functional diversity within the community. For example, preliminary results indicate that landscapes with decreased levels of structural heterogeneity select against smaller, less agile lepidopteran species. These findings may guide management practices for conservation of lepidopteran functional diversity in managed grasslands.



Plant diversity and habitat structure affect tree growth, herbivory and natural enemies in shelterbelts

September 2010

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27 Reads

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19 Citations

Basic and Applied Ecology

Shelterbelts have become a refuge and source of food for wildlife because of habitat loss in farmlands. However, effects of shelterbelt attributes such as plant diversity and habitat structure on different trophic levels within shelterbelts are unclear. Effects of shelterbelt woody plant diversity and habitat structure (lower vegetation strata, logs, litter and rocks) were measured on the growth and herbivory of Eucalyptus blakelyi saplings that were caged from birds, caged from birds and arthropods and un-caged. Arthropod diversity of E. blakelyi saplings and shelterbelts was evaluated. Height and stem diameter of saplings in all treatments was positively correlated with plant diversity. Habitat structure was negatively correlated with numbers of leaves on E. blakelyi saplings and positively correlated with herbivory, which was greater in saplings caged from birds. The overall abundance of arthropods inhabiting shelterbelts correlated positively with plant diversity, but negatively with habitat structure. Araneae and Formicidae were the most common taxa on E. blakelyi saplings and were more numerous on saplings caged from birds, suggesting an important role of these vertebrates as predators of shelterbelt arthropods.


Table 1 Diversity of parasitoid and phytophagous wasps collected from the Lobularia maritima (Lm) treatment and control 
Fig. 1 Mean (±SE) abundance of the common parasitoid taxa: C, Cotesia sp.; P, Pteromalus sp.; A, Anagyrus sp.; E, Entedoninae sp., Ci, Cirrospilus sp., Eu1, Eulophidae sp. 1; and Eu2, Eulophidae sp. 2; and the common phytophagous taxa  
Effects of flowering groundcover vegetation on diversity and activity of wasps in a farm shelterbelt in temperate Australia

April 2009

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282 Reads

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25 Citations

BioControl

Significant worldwide interest in conservation biological control in agricultural systems currently exists but little information is available on the usefulness of this approach in farm forestry. In a field experiment conducted in a native vegetated shelterbelt in central-west New South Wales, we measured the diversity of wasps in plots comprising Eucalyptus blakelyi Maiden (Myrtaceae) trees with and without a groundcover of Lobularia maritima (L.) Desv. (Brassicaceae). Vacuum samples revealed a greater abundance and species richness of parasitic wasps in the plots comprising trees surrounded by the L. maritima groundcover. Cotesia sp. (Hymenoptera: Braconidae), Pteromalus sp. (Hymenoptera: Pteromalidae), Anagyrus sp. (Hymenoptera: Encyrtidae), Entedoninae sp. and Eulophidae sp. 1 (Hymenoptera: Eulophidae) were the most common taxa. These were more abundant also in the trees with the L. maritima groundcover. Ardozyga stratifera (Meyrick) (Lepidoptera: Gelechiidae) larvae, that were naturally infesting the E. blakelyi trees, were significantly more parasitized in the trees with the L. maritima groundcover. Results indicate that parasitic wasps associated with a native-tree shelterbelt in Australia were amenable to manipulation via groundcover vegetation.


Arthropod prey of shelterbelt-associated birds: Linking faecal samples with biological control of agricultural pests

November 2007

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183 Reads

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33 Citations

Australian Journal of Entomology

Abstract The value of insectivorous birds as agents for biological control of arthropod pests has been little studied, especially in Australia. This paper reports on the extent to which arthropods from various pest and non-pest taxa feature in the diets of birds captured in farm shelterbelts in central western New South Wales. The parameters examined were the types of arthropod fragments in bird faeces and percentage volume and frequency of occurrence of each component. The faecal data were compared with samples of the arthropod fauna trapped in shelterbelts during the period the birds were captured. In 26 of 29 faecal samples, arthropod fragments were the predominant components, the most common being from Coleoptera, Hymenoptera (especially Formicidae), Orthoptera and Araneae. The recognisable pest taxa in faecal samples were Scarabaeidae and wingless grasshopper Phaulacridium vittatum (Sjöstedt) (Orthoptera: Acrididae). The results indicate that the native bird species common in farm shelterbelts preyed on a range of arthropod taxa including several that are pests of crops and pastures. Accordingly, conservation of birds in farmlands could contribute to suppression of arthropod pests.

Citations (8)


... Floral resources offer nutrition to enhance longevity, reproductive capacity, and biological control impact of predators and parasitoids (Hatt et al. 2019;Lu et al. 2014;Wang et al. 2020;Xiong et al. 2021;Zhao et al. 2017). Because of these plants providing floral resources are often intercropped or planted on crop margins to improve biological control and reduce dependence on chemical pesticides in integrated pest management (IPM) programs worldwide, natural enemies easily get the floral resources (Parolin et al. 2012;Damien et al. 2017;Perovic et al. 2018Perovic et al. , 2021Gong et al. 2024;Gurr et al. 2016;Wang et al. 2022b). ...

Reference:

Ecological risks of cadmium-contaminated non-prey food on three Trichogramma egg parasitoids
Broadening the scope of empirical studies to answer persistent questions in landscape-moderated effects on biodiversity and ecosystem functioning
  • Citing Chapter
  • January 2022

Advances in Ecological Research

... For example, biological control impacts often even supersede those of plant quality (Asiimwe et al., 2013), while its relative contribution is greatly attenuated by 'full' host plant resistance (Kersch-Becker and Thaler, 2015). Habitat management through the establishment of intercrops, flower strips or hedgerows or a progressive phasedown of pesticide use might also enhance biological control agent abundance and diversity, which, in turn defines biological control outcomes (Landis et al., 2000;Perovic et al., 2018;Roudine et al., 2023). These approaches are slowly but surely being integrated in management toolkits for high-profile diseases such as citrus greening (Patt et al., 2020;Irvin et al., 2024;Cortez-Madrigal, 2024). ...

Managing biological control services through multi-trophic trait interactions: Review and guidelines for implementation at local and landscape scales
  • Citing Article
  • June 2017

Biological reviews of the Cambridge Philosophical Society

... The mining area under recovery with grassy shared more species with the Campo Rupestre field fragment, possibly due to the greater similarity in vegetation structure between these two habitats. Grassy revegetation is a limiting factor to resource availability, as the absence or low frequency of tree species, also characteristic of the rupestrian field, can reduce the diversity of ants in an area (Gámez-Virués et al., 2015;Prach and Walker, 2011). ...

Landscape simplification filters species traits and drives biotic homogenization

... Conservation corridors aim to provide healthy ecosystems, ideally through high levels of natural habitat heterogeneity, as these ecosystems harbour greater insect diversity through niche partitioning (Salas-López et al., 2022), reduced competition and predation (Palmer, 2003;Tokeshi, 1993), and increased resource availability and disturbance resilience (Cole et al., 2017;Dorrough et al., 2004). This is especially the case in grasslands, where compositional heterogeneity is an important predictor of increased taxonomic diversity (Öckinger and Smith, 2006;Perović et al., 2015). ...

Configurational landscape heterogeneity shapes functional community composition of grassland butterflies
  • Citing Article
  • February 2015

... The expansion of a monoculture at the expense of crop diversity decreases insect habitat diversity, which eventually affects the abundance and efficiency of natural enemies (Altieri et al., 1984). Complex landscapes often have a greater abundance and more diversity of natural enemies, than the ones already simplified by intensive agriculture (Virues et al., 2012). ...

The Ecology and Utility of Local and Landscape Scale Effects in Pest Management
  • Citing Chapter
  • May 2012

... It has also been shown that shelterbelts provide a habitat for diverse organisms inhabiting forests and grasslands, including threatened and endangered species (Hayamizu et al., 2019;Jobin et al., 1996;Kujawa & Kujawa, 2008;Marshall & Moonen, 2005;Workman et al., 2003). The biodiversity conservation impacts of shelterbelts have been studied for birds (Bonifacio et al., 2011;Hino, 1985), mammals (Yahner, 1983), and arthropods (G amez- Virués et al., 2010;Grabovska et al., 2021;Kajak, 2007). While many previous studies have been performed in Europe, North America, and Oceania, there are few examples of research in Japan or other parts of Far East Asia, and only a few taxa have been evaluated (Hino, 1985). ...

Plant diversity and habitat structure affect tree growth, herbivory and natural enemies in shelterbelts
  • Citing Article
  • September 2010

Basic and Applied Ecology

... Diets of woodland and ground-foraging insectivorous birds in Australia are typically dominated by a few prey groups including beetles, ants, spiders, bugs, flies, grasshoppers, caterpillars and lacewings (Major 1991;Gamez-Virues et al. 2007;Razeng and Watson 2012;Lindsay et al. 2014). ...

Arthropod prey of shelterbelt-associated birds: Linking faecal samples with biological control of agricultural pests
  • Citing Article
  • November 2007

Australian Journal of Entomology

... It has an extended, uninterrupted flowering period of around 10 months (Picó and Retana 2003) and establishes rapidly, making it competitive against weeds (Begum et al. 2006;Grasswitz 2013). Lobularia maritima was found to enhance the presence of beneficial insects including pollinators (Barbir et al. 2015;Scarlato et al. 2023), aphidophagous hoverflies (Pineda and Marcos-García 2008;Gillespie et al. 2011;Amorós-Jiménez et al. 2014;Harris-Cypher et al. 2023), various parasitoid wasps (Gámez-Virués et al. 2009;Aparicio et al. 2018;Arnó et al. 2018;Buchanan et al. 2018;Madeira et al. 2022) and predatory bugs (Haseeb et al. 2018). ...

Effects of flowering groundcover vegetation on diversity and activity of wasps in a farm shelterbelt in temperate Australia

BioControl