Abstract:Social life is usually associated with enhanced propagule pressure, which increases the chance of introducing several individuals during a single introduction event. Social insects are therefore among the most successful invasive species, benefiting from rapid establishment and increased foundation success in new habitats. In termites, propagule pressure may also be increased by the development of reproductive individuals from a small group of foraging workers. This suggests that enhanced exploration activity … Show more
“…Reticulitermes flavipes is a successful invasive species, introduced to many regions worldwide, such as France, Chile, and Uruguay (Clément et al 2001; Austin et al 2005; Su et al 2006; Eyer et al 2021), while A. parvulus has not been reported as introduced outside of its endemic range. The spatially expansive foraging range of A. parvulus is a potential characteristic enhancing invasiveness, as it increases the chance of being inadvertently picked up and transported abroad (Evans et al 2011, 2013; Pailler et al 2022); however, this species was mostly found tunneling in mulch areas but not inhabiting substantial pieces of wood. The absence of dense colony fragments within large pieces of wood may have restricted the opportunity for large fragments of colonies to be transported.…”
Section: Discussionmentioning
confidence: 99%
“…Some lower termites nest and feed on a single piece of wood (one-piece nesters), while others (both in lower and higher termites) feed on several pieces of wood connected by networks of galleries (multiple-piece nesters), or build large nests separate from their food sources (separate-piece nesters; Abe 1987; Eggleton and Tayasu 2001). Variation in foraging patterns can also be found among species of the same genus (Mizumoto et al 2020; Janowiecki and Vargo 2022; Pailler et al 2022), and sometimes even among colonies within species (Mizumoto and Matsuura 2013). Different tunneling patterns have been reported in subterranean termites of the genus Coptotermes (Mizumoto et al 2020), where colonies of C. formosanus construct a small number of long tunnels, while C. gestroi colonies usually make a large number of short tunnels (Grace et al 2004, Lee et al 2007; Hapukotuwa and Grace 2014).…”
In insects, ecological competition has often resulted in phenotypic changes and modifications to foraging areas. In termites - and social insects as a whole - colonies cannot easily escape competition through the relocation of their colony. In these species, the outcomes of inter and intra-specific competition are influenced by different life history traits, such as colony size, breeding system (number and types of reproductives), food preference, tunneling patterns, nest site selection, and antagonism between colonies. Here, we investigated variation in breeding system and spatial distribution among colonies of a higher termite Amitermes parvulus and a subterranean termite Reticulitermes flavipes within an urban landscape. We first developed microsatellite markers as a tool to study these life history traits in A. parvulus. Second, we assessed competitive exclusion or tolerance of A. parvulus and R. flavipes colonies by determining their fine-scale distribution using monitoring stations on a grid site, and their large-scale distribution across an urban landscape. Third, we investigated the breeding system of A. parvulus colonies. We showed that the numerous colonies of R. flavipes inhabiting a restricted area contrast with the few, but spatially expansive colonies of A. parvulus, suggesting these species face different degrees of intra-specific competition. We showed that colonies of A. parvulus frequently merged together, and all of them were headed by inbred neotenic reproductives, two characteristics rarely observed in higher termites. Overall, our study revealed drastic differences in colony structure, breeding systems and foraging ranges between the two species. These differences may reflect differences in food preference and food availability between the two species allowing their co-existence within the same urban environment.
“…Reticulitermes flavipes is a successful invasive species, introduced to many regions worldwide, such as France, Chile, and Uruguay (Clément et al 2001; Austin et al 2005; Su et al 2006; Eyer et al 2021), while A. parvulus has not been reported as introduced outside of its endemic range. The spatially expansive foraging range of A. parvulus is a potential characteristic enhancing invasiveness, as it increases the chance of being inadvertently picked up and transported abroad (Evans et al 2011, 2013; Pailler et al 2022); however, this species was mostly found tunneling in mulch areas but not inhabiting substantial pieces of wood. The absence of dense colony fragments within large pieces of wood may have restricted the opportunity for large fragments of colonies to be transported.…”
Section: Discussionmentioning
confidence: 99%
“…Some lower termites nest and feed on a single piece of wood (one-piece nesters), while others (both in lower and higher termites) feed on several pieces of wood connected by networks of galleries (multiple-piece nesters), or build large nests separate from their food sources (separate-piece nesters; Abe 1987; Eggleton and Tayasu 2001). Variation in foraging patterns can also be found among species of the same genus (Mizumoto et al 2020; Janowiecki and Vargo 2022; Pailler et al 2022), and sometimes even among colonies within species (Mizumoto and Matsuura 2013). Different tunneling patterns have been reported in subterranean termites of the genus Coptotermes (Mizumoto et al 2020), where colonies of C. formosanus construct a small number of long tunnels, while C. gestroi colonies usually make a large number of short tunnels (Grace et al 2004, Lee et al 2007; Hapukotuwa and Grace 2014).…”
In insects, ecological competition has often resulted in phenotypic changes and modifications to foraging areas. In termites - and social insects as a whole - colonies cannot easily escape competition through the relocation of their colony. In these species, the outcomes of inter and intra-specific competition are influenced by different life history traits, such as colony size, breeding system (number and types of reproductives), food preference, tunneling patterns, nest site selection, and antagonism between colonies. Here, we investigated variation in breeding system and spatial distribution among colonies of a higher termite Amitermes parvulus and a subterranean termite Reticulitermes flavipes within an urban landscape. We first developed microsatellite markers as a tool to study these life history traits in A. parvulus. Second, we assessed competitive exclusion or tolerance of A. parvulus and R. flavipes colonies by determining their fine-scale distribution using monitoring stations on a grid site, and their large-scale distribution across an urban landscape. Third, we investigated the breeding system of A. parvulus colonies. We showed that the numerous colonies of R. flavipes inhabiting a restricted area contrast with the few, but spatially expansive colonies of A. parvulus, suggesting these species face different degrees of intra-specific competition. We showed that colonies of A. parvulus frequently merged together, and all of them were headed by inbred neotenic reproductives, two characteristics rarely observed in higher termites. Overall, our study revealed drastic differences in colony structure, breeding systems and foraging ranges between the two species. These differences may reflect differences in food preference and food availability between the two species allowing their co-existence within the same urban environment.
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