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Journal ArticleDOI

Drove roads: keystone structures that promote ant diversity in Mediterranean forest landscapes

TL;DR: In this article, Ant communities were studied on four active drove roads, two in forests (submediterranean and conifer) and two in open environments (croplands and rangelands).
Abstract: Drove roads are the traditional corridors used by pastoralists for seasonal movements of livestock (transhumance). They cover a considerable land area in Mediterranean countries and, although they are an obvious source of landscape diversity, their influence on the diversity and composition of animal assemblages has not been documented. Ant communities were studied on four active drove roads, two in forests (submediterranean and conifer) and two in open environments (croplands and rangelands). They were compared with the respective matrix communities and their contribution to local species richness was evaluated. The effects were heavily dependent on the open or closed nature of the matrix. In forest environments, drove roads increased ant species richness at the local scale, acting as clear keystone structures. Their species richness and functional diversity were highest on the fine scale, species composition was different, and a slight edge effect in the matrix was detected. In contrast, drove roads had little or even a negative effect in open environment locations. We conclude that drove roads have a high conservation value for ants in Mediterranean forest environments, in addition to their importance as reservoirs of plant biodiversity and generators of ecological goods and services.

Summary (1 min read)

1. Introduction 38 39

  • Drove roads are at least 51 several centuries old, and may have originally been based on the migratory 52 routes of wild ungulates (Manzano and Casas, 2010) .
  • Because of their 53 enormous area, long-term persistence, impact on the landscape structure and 54 capacity to host herbivore migrations, drove roads can have played a major 55 ecological role in the Mediterranean Basin.
  • Their influence on 59 populations and communities may thus disappear before they are identified and 60.

studied. 61

  • The few published ecological studies of drove roads have focused on their 63 effects on plant communities.
  • More recently, the effects of drove roads on landscape patterns, 68 species composition and functional diversity of plant communities have been 69 measured (Azcárate et al, 2012) , showing that drove roads are a source of 70 spatial heterogeneity and a reservoir for many plant species in non-or 71 moderately-grazed habitats.
  • Examples of keystone structures at different spatial 84 scales are tree cavities in forests (for insects, birds and mammals), trees in 85 African savannas (for arboreal rodents, ungulates, raptors and other species 86 groups) and temporary wetlands in agricultural fields (for carabid beetles) (Tews 5 et al., 2004; Remm and Lohmus, 2011) .
  • Drove roads might then function 90 as keystone structures by favouring rich groups of terrestrial species with 91 relevant roles on ecosystem functioning, such as ants.

2.3. Distributional status of the ant species 159 160

  • To take into account that these maps could be biased by several factors 164 (geographic distribution of myrmecologists, detectability of the different 165 species), and could underestimate the distribution range of many species, the authors 166 have considered that those species present in more than 25% of the Iberian 167 1ºx1º cells are widespread species.
  • The rest of species were considered 168 uncommon.

2.4. Functional traits and functional diversity 171 172

  • The aspect of the curves does not suggest increases in richness at the location 354 scale on the sole basis of the inclusion of a drove road.
  • The composition of the 355 drove road communities also showed no substantial differences from the 356 cropland and rangeland matrices.
  • It is important to note that although the study 357 locations are still managed extensively, they are increasingly being replaced by 358 more common intensive schemes, and also that ants are sensitive to 359 agricultural and grazing intensification (Wilson et al., 1999; Andersen et al., 360 2002; Philpott and Armbrecht, 2006) .
  • Thus, drove roads within these intensively 361 managed open landscapes may indeed have higher richness values.

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!"
"
Drove roads: keystone structures that promote ant diversity in !"
Mediterranean forest landscapes #"
$"
%"
Francisco M. Azcárate
a,*
, Javier Seoane
a
, Sara Castro
b
, Begoña Peco
a
&"
'"
a
TEG, Departamento de Ecología, Universidad Autónoma de Madrid. 28049, ("
Spain
)"
b
Unidad de Zoología, Departamento de Biología, Universidad Autónoma de *"
Madrid. 28049, Spain !+"
!!"
*
Corresponding author: Tel.: +34 91 497 3513; fax: +34 91 497 8001. E-mail !#"
address: fm.azcarate@uam.es !$"
!%"

#"
"
Abstract !&"
!'"
Drove roads are the traditional corridors used by pastoralists for seasonal !("
movements of livestock (transhumance). They cover a considerable land area !)"
in Mediterranean countries and, although they are an obvious source of !*"
landscape diversity, their influence on the diversity and composition of animal #+"
assemblages has not been documented. Ant communities were studied on four #!"
active drove roads, two in forests (submediterranean and conifer) and two in ##"
open environments (croplands and rangelands). They were compared with the #$"
respective matrix communities and their contribution to local species richness #%"
was evaluated. The effects were heavily dependent on the open or closed #&"
nature of the matrix. In forest environments, drove roads increased ant species #'"
richness at the local scale, acting as clear keystone structures. Their species #("
richness and functional diversity were highest on the fine scale, species #)"
composition was different, and a slight edge effect in the matrix was detected. #*"
In contrast, drove roads had little or even a negative effect in open environment $+"
locations. We conclude that drove roads have a high conservation value for $!"
ants in Mediterranean forest environments, in addition to their importance as $#"
reservoirs of plant biodiversity and generators of ecological goods and services. $$"
$%"
$&"
Keywords: Transhumance; Functional diversity; Spatial heterogeneity; $'"
Grasslands; Ant assemblages $("

$"
"
1. Introduction $)"
$*"
Drove roads, also known as stock routes, are one of the most characteristic %+"
components of traditional landscapes in Mediterranean countries (Ruiz and %!"
Ruiz, 1986; Mangas Navas, 1992; Merino García and Alier Gándaras, 2004). %#"
Active drove roads stand out in the landscape as well-defined strips up to 100 m %$"
in width with a savannah-like grassland appearance, in some cases running for %%"
several hundred kilometres. They are reserved for and ecologically modeled by %&"
transhumance, a traditional type of pastoralism consisting on the seasonal %'"
movement of livestock between summer and winter pastures. In Spain, drove %("
roads cover nearly 1% of the country's land area, with a total length of about %)"
125,000km (Mangas Navas, 1992; Merino García and Alier Gándaras, 2004). %*"
Due to their grid-like distribution, most of the country's land area is in contact &+"
with or near a drove road (Azcárate et al. 2012). Drove roads are at least &!"
several centuries old, and may have originally been based on the migratory &#"
routes of wild ungulates (Manzano and Casas, 2010). Because of their &$"
enormous area, long-term persistence, impact on the landscape structure and &%"
capacity to host herbivore migrations, drove roads can have played a major &&"
ecological role in the Mediterranean Basin. The current crisis in extensive &'"
grazing has led to the abandonment of transhumance and grazing uses of &("
drove roads (Ruiz and Ruiz, 1986; Ruiz, 2001), causing a loss of their &)"
differentiation from the surrounding ecological matrix. Their influence on &*"
populations and communities may thus disappear before they are identified and '+"
studied. '!"
'#"

%"
"
The few published ecological studies of drove roads have focused on their '$"
effects on plant communities. Drove roads have traditionally been regarded as a '%"
good example of ecological corridors for plant species (review in Bunce et al., '&"
2006), although no experimental evidence supported this view until Manzano ''"
and Malo (2006) detected epizoochorous seed dispersal over distances of up to '("
400 km. More recently, the effects of drove roads on landscape patterns, ')"
species composition and functional diversity of plant communities have been '*"
measured (Azcárate et al, 2012), showing that drove roads are a source of (+"
spatial heterogeneity and a reservoir for many plant species in non- or (!"
moderately-grazed habitats. (#"
($"
Drove roads could also have a noticeable effect on the diversity and (%"
composition of animal assemblages. Active drove roads maintain patches of (&"
open grassland in non-grazed environments such as forests, and hence ('"
increase spatial heterogeneity. Spatial heterogeneity and diversity of several (("
animal species groups are often (but not always) correlated (Duelli, 1997; Atauri ()"
and de Lucio, 2001; Szczepko et al., 2012). It has been argued that each (*"
animal species group depends on a specific structural aspect of the vegetation )+"
whose presence or quality can be detected at a certain spatial scale (Tews et )!"
al, 2004). At that scale, biodiversity is favoured by the occurrence of “keystone )#"
structures”, characterized by their ability to provide resources, shelter or nesting )$"
sites to that species group. Examples of keystone structures at different spatial )%"
scales are tree cavities in forests (for insects, birds and mammals), trees in )&"
African savannas (for arboreal rodents, ungulates, raptors and other species )'"
groups) and temporary wetlands in agricultural fields (for carabid beetles) (Tews )("

&"
"
et al., 2004; Remm and Lohmus, 2011). If a key structure affects several ))"
species groups, or groups with a strong influence on ecosystem functioning, )*"
then its conservation is of crucial importance. Drove roads might then function *+"
as keystone structures by favouring rich groups of terrestrial species with *!"
relevant roles on ecosystem functioning, such as ants. *#"
*$"
Ants are considered to be a focal group for the monitoring of terrestrial *%"
ecosystems (Underwood and Fisher, 2006; Crist, 2009). This is not surprising, *&"
given their ability to stockpile a considerable amount of primary and secondary *'"
production, interact with several organisms and act as ecosystem engineers *("
(Folgarait, 1998; MacMahon et al., 2000; Crist, 2009). Literature shows that *)"
ants respond strongly to land management (Bestelmeyer and Wiens, 1996; **"
Chen et al., 2011), and are sensitive to different levels of grazing (Read and !++"
Andersen, 2000; Boulton et al. 2005; Azcárate and Peco, 2011). Moreover, ants !+!"
are widespread, moderately diverse and easy to sample (Alonso and Agosti, !+#"
2000; Andersen et al., 2004). Their role as indicators has improved with the !+$"
development of the concept of functional groups to classify ants within species !+%"
assemblages, as first proposed in Australia (Andersen, 1995), and then !+&"
extended worldwide (Brown, 2000). More recently, the role of ants in ecosystem !+'"
functioning has been studied by measuring their functional diversity (Bihn et al., !+("
2010; Silva and Brandao, 2010) although this approach has still been little !+)"
addressed, in contrast to other taxa. !+*"
!!+"
The present study evaluates the role of drove roads as keystone structures. !!!"
Specifically, our work analyzes the effects of drove roads on ant assemblages !!#"

Citations
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Journal ArticleDOI
TL;DR: The relationship of land use with taxonomic diversity and functional diversity is highly complex and context-dependent and it is found that TD and FD did not vary consistently, but rather followed different trajectories that largely depended on the biotic group and the intensity of land-use transformation.
Abstract: Land-use change is the major driver of biodiversity loss. However, taxonomic diversity (TD) and functional diversity (FD) might respond differently to land-use change, and this response might also vary depending on the biotic group being analysed. In this study, we compare the TD and FD of four biotic groups (ants, birds, herbaceous, woody vegetation) among four land-use types that represent a gradient of land-use intensity in a Mediterranean landscape (Mediterranean shrublands, dehesas, mixed-pine forests, olive groves). Analyses were performed separately at two different spatial scales: the sampling unit scale and the site scale. Land-use intensity effects on TD and FD were quite different and highly varied among the four biotic groups, with no single clear pattern emerging that could be considered general for all organisms. Additive partitioning of species diversity revealed clear contrasting patterns between TD and FD in the percentage of variability observed at each spatial scale. While most variability in TD was found at the larger scales, irregardless of organism group and land-use type, most variability in FD was found at the smallest scale, indicating that species turnover among communities is much greater than functional trait turnover. Finally, we found that TD and FD did not vary consistently, but rather followed different trajectories that largely depended on the biotic group and the intensity of land-use transformation. Our results highlight that the relationship of land use with TD and FD is highly complex and context-dependent.

43 citations


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Abstract: A high-altitude peat sequence from the heart of the Spanish Central System (Gredos range) was analysed through a multi-proxy approach to determine the sensitivity of high-mountain habitats to climate, fire and land use changes during the last seven hundred years, providing valuable insight into our understanding of the vegetation history and environmental changes in a mountain pass close to a traditional route of transhumance. The pollen data indicate that the vegetation was dominated by shrublands and grasslands with scattered pines in high-mountain areas, while in the valleys cereals, chestnut and olive trees were cultivated. Strong declines of high-mountain pines percentages are recorded at 1540, 1675, 1765, 1835 and 1925 cal AD, which may be related to increasing grazing activities and/or the occurrence of anthropogenic fires. The practice of mountain summer farming and transhumance deeply changed and redesigned the landscape of the high altitudes in central Spain (Gredos range) since the Middle Ages, although its dynamics was influenced in some way by climate variability of the past seven centuries.

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TL;DR: Ant taxonomic and functional diversity on a drove road that is still used by transhumant livestock (the Conquense Drove Road) versus an abandoned road (the Murciana Drove road) were compared in this paper, showing that the used drove road also had a positive edge effect on ant species diversity in adjacent croplands.
Abstract: Drove roads are a major feature of Mediterranean countries, where this live- stock management system has been practiced for centuries. In Spain, many drove roads have become completely or partially abandoned by herders, and transformed for other land uses. Yet, some major drove roads continue to be used for the passage of livestock, and might exert important effects on the conservation of biodiversity and ecosystem functions, particularly in highly transformed agricultural landscapes. In this study, we compare ant taxonomic and functional diversity on a drove road that is still used by transhumant livestock (the Conquense Drove Road) versus an abandoned road (the Murciana Drove Road). Ant species richness per trap and ant richness per sample unit were significantly higher on the used drove road compared to the abandoned drove road. The used drove road also had a positive edge effect on ant species diversity in adjacent croplands (both her- baceous crops and vineyards). Ant functional diversity was also higher on the used drove road. These results draw attention to the role of drove roads as ecologically unique systems and reservoirs of biodiversity, particularly within intensive agricultural landscapes. These effects, however, are largely dependent on maintaining livestock use.

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References
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Journal ArticleDOI
TL;DR: The results of this study highlight the role of adhesion in long-distance dispersal and support the inclusion of migrating ungulates among forces responsible rapid plant migrations (eg following glaciations, invasion events, or in a future global change scenario).
Abstract: Extremely long seed dispersal distances occur as a result of processes such as ocean drift and tornadoes. However, we have found that large numbers of seeds with different morphologies (Trifolium angustifolium, Daucus carota, Hordeum murinum, and Plantago lagopus) are frequently dispersed equivalent distances while attached to migrating ungulates. We determined experimentally that seeds attached to the fleece of traditional nomadic (“transhumant”) sheep are transported distances of up to several hundred kilometers in substantial numbers (ranging from 5–47% of the initial seed population). Given the current and historical importance of migrating herds of sheep (wild and domestic) on different continents, the results of this study highlight the role of adhesion in long-distance dispersal and support the inclusion of migrating ungulates among forces responsible rapid plant migrations (eg following glaciations, invasion events, or in a future global change scenario). Our results also highlight an unexplored ecological consequence of abandoning nomadism.

157 citations


"Drove roads: keystone structures th..." refers background in this paper

  • ...Drove roads have traditionally been regarded as a good example of ecological corridors for plant species (review in Bunce et al., 2006), although no experimental evidence supported this view until Manzano and Malo (2006) detected epizoochorous seed dispersal over distances of up to 400 km....

    [...]

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TL;DR: It is argued that a general null model for the analysis of species association based on morphology can reveal objectively defined groups and may contribute to a robust theory to explain community structure in general and have important consequences on studies of litter ant community ecology in particular.
Abstract: We present a new approach to determine the number and composition of guilds, using the hyperdiverse leaf-litter ant fauna as a model, based on appropriate morphological variables and species co-occurrence null models to describe the complex assemblages of interacting species community structure at the 1-m2 scale. We obtained 18 linear morphometric measures from 949 workers of 171 leaf-litter ant species (18 762 measurements) surveyed in four Atlantic Forest localities to test whether the assemblages are morphologically structured; the morphological characters were selected to indicate diet and foraging habits. Principal components analysis was used to characterize the morphospace and to describe the guild structure (number of species and composition). The guild proportionality assembly rule (significant tendency toward constant proportion of species in guilds) was assessed at the 1-m2 scale. Our analysis indicates that the division of leaf-litter ants into guilds is based mainly on microhabitat distribution in the leaf-litter, body size and shape, eye size, and phylogeny. The same guild scheme applied to four more sites shows that different Atlantic Forest areas have the same leaf-litter ant guilds. The guild proportionality assembly rule was confirmed for most guilds, suggesting that there are guild-specific limitations on species coexistence within assemblages; on the other hand, in a few cases the variance in guild proportion was greater than expected under the null assumptions. Other studies on ant functional group classification are partially supported by our quantitative morphological analysis. Our results, however, imply that there are more compartments than indicated in previous models, particularly among cryptic species (confined to soil and litter) and tropical climate specialists. We argue that a general null model for the analysis of species association based on morphology can reveal objectively defined groups and may thus contribute to a robust theory to explain community structure in general and have important consequences on studies of litter ant community ecology in particular.

150 citations


"Drove roads: keystone structures th..." refers background or result in this paper

  • ...More recently, the role of ants in ecosystem functioning has been studied by measuring their functional diversity (Bihn et al., 2010; Silva and Brandao, 2010) although this approach has still been little addressed, in contrast to other taxa....

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  • ...Unfortunately, there is still little consensus about which and how many traits should be considered for this purpose (see, for example, differences between Bihn et al., 2010; Silva and Brandao, 2010)....

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TL;DR: Transhumance evolved a complex and widespread network of livestock routes in Spain, which were governed by livestock organisations benefiting from special legislation from the 13th century, and helped shape a characteristic landscape which has maintained one of the Mediterranean's most complex and interesting ecosystems.

117 citations


"Drove roads: keystone structures th..." refers background in this paper

  • ...Drove roads, also known as stock routes, are one of the most characteristic components of traditional landscapes in Mediterranean countries (Ruiz and Ruiz, 1986; Mangas Navas, 1992; Merino García and Alier Gándaras, 2004)....

    [...]

  • ...The current crisis in extensive grazing has led to the abandonment of transhumance and grazing uses of drove roads (Ruiz and Ruiz, 1986; Ruiz, 2001), causing a loss of their differentiation from the surrounding ecological matrix....

    [...]

Journal ArticleDOI
TL;DR: In populations of the same species in different types of environments, the seasonal variation of seed numbers was environment-dependent for the majority of the species and perennial grassland and its related low gaps availability appear to favour persistent seed banks.
Abstract: The size and dynamics of seed banks were studied in grazed and ungrazed Mediterranean pastures at different altitudes and topography positions. The soil samples were collected in autumn and spring and the seed banks composition was determined by greenhouse germination over a 9-month period. The percentage of bare ground and the presence of new seedlings were recorded monthly from October to July in the field. A fall in seed density and species richness in the banks and a tendency for seeds to remain in the banks were linked to a rise in altitude. Germination in lower pastures mainly occurred in October in the numerous gaps left by the summer drought. At higher altitudes, the scarcity of gaps and the harsh climate led to an autumn–spring segregation of germination. On a local scale, the low slope positions and the ungrazed plots had a larger number of persistent seed bank species and a lower percentage of bare ground where seeds could germinate than their respective plots in the upper positions and grazed plots. A higher seed density in ungrazed than grazed plots was only detected in the three highest plots. No seed bank species richness trend was detected. In populations of the same species in different types of environments, the seasonal variation of seed numbers was environment-dependent for the majority of the species. In general, perennial grassland and its related low gaps availability appear to favour persistent seed banks. Se estudian las diferencias en el tamano y dinamica de los bancos de semillas de pastizales Mediterraneos sometidos o no a consumo por herbivoros en diferentes altitudes y posiciones topograficas. Se determino el tamano y composicion de los bancos de semillas mediante la toma de muestras de suelo en otono y primavera y conteo de las germinaciones en invernadero por un periodo de 9 meses. Ademas se registro mensualmente en el campo el porcentaje de suelo desnudo y de germinaciones en el periodo de Octubre a Julio. El aumento de altitud esta asociado a una disminucion de la densidad de semillas y de la riqueza de especies de los bancos y a la tendencia de las semillas a persistir en los bancos. En los pastizales mas bajos la germinacion ocurre fundamentalmente en Octubre, en los numerosos huecos dejados por la sequia estival. A mayores altitudes se observa una segregacion de la germinacion entre los periodos de otono y primavera que esta relacionada probablemente con la baja disponibilidad de huecos y con la dureza climatica invernal. A escala local, las zonas bajas de las laderas y las privadas del consumo por herbivoros presentan un mayor nuAƒÂƒmero de especies con banco persistente y un menor porcentaje de suelo desnudo que sus respectivas zonas altas de ladera y zonas pastoreadas. A esta escala no se observa ninguna tendencia respecto a la riqueza de especies en los bancos de semillas y solo se detecta una mayor densidad de semillas en las zonas clausuradas frente a las pastoreadas en las tres posiciones mas altas del gradiente altitudinal. La variacion estacional en el nuAƒÂƒmero de semillas de poblaciones de diferentes ambientes resulto ser dependiente de estos para la mayoria de las especies. En general se observa que el aumento de herbaceas perennes, relacionado con la baja disponibilidad de huecos, parece favorecer la existencia de bancos persistentes.

114 citations


"Drove roads: keystone structures th..." refers background in this paper

  • ...Open Mediterranean grasslands are dominated by annual species producing large seed banks (Ortega et al., 1997), and not surprisingly both strict (e....

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  • ...Open Mediterranean grasslands are dominated by annual species producing large seed banks (Ortega et al., 1997), and not surprisingly both strict (e.g. Messor capitatus) and facultative (e.g. Aphaenogaster iberica) granivores (Azcarate and Peco, 2012) were found in drove roads but not in forests....

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Journal ArticleDOI
TL;DR: In general, soil chemistry and texture formed the most consistent associations with the ant community, and plants were less important than soil attributes in explaining variation in overall ant species richness and abundance, but the abundance of the three dominant ant species was significantly correlated with plant biomass or plant richness.
Abstract: We examined the role of cattle grazing, plants, and soil attributes on species richness, abundance, and composition of ground-dwelling ants in northern California serpentine and nonserpentine grasslands. In addition, we analyzed the relationship between three numerically dominant ant species and overall ant species richness and abundance. We used pitfall traps to collect worker ants at 80 sites over a 2-wk period in May 2002. Twenty species of ants were identified from a total of 5,149 worker ants; 80% of all individuals belonged to three dominant species: Messor andrei (Mayr), Pheidole californica Mayr, and Solenopsis xyloni McCook. Ant species richness was negatively affected by grazing on nonserpentine soils only. In general, soil chemistry and texture formed the most consistent associations with the ant community. Plants were less important than soil attributes in explaining variation in overall ant species richness and abundance, but the abundance of the three dominant ant species was significantly correlated with plant biomass or plant richness. Based on logistic regression analysis, the presence or absence of each dominant ant species was negatively correlated with the abundance of the other two dominants. However, the three numerically dominant ant species did not correlate with overall ant species richness or abundance.

109 citations


"Drove roads: keystone structures th..." refers background in this paper

  • ...Literature shows that ants respond strongly to land management (Bestelmeyer and Wiens, 1996; Chen et al., 2011), and are sensitive to different levels of grazing (Read and Andersen, 2000; Boulton et al., 2005; Azcarate and Peco, 2012)....

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