scholarly journals Effectiveness of movement-based animal signals is a function of display structure and habitat characteristics: simulations of Australian dragons

Author(s):  
Xue Bian ◽  
Angela Pinilla ◽  
Tom Chandler ◽  
Richard Peters

Abstract Habitat-specific characteristics can affect signal transmission such that different habitats dictate the optimal signal. One way to examine how the environment influences signals is by comparing changes in signal efficacy in different habitats. Examinations of signal efficacy between different habitats has helped to explain signal divergence/convergence between populations and species utilising acoustic and colour signals. Although previous research has provided evidence for local adaptations and signal divergence in many species of lizards, comparative studies in movement-based signals are rare due to technical difficulties in quantifying movements in nature and ethical restrictions in translocating animals between habitats. We demonstrate herein that these issues can be addressed using 3D animations, and compared the relative performance of the displays of four Australian lizard species in the habitats of each species under varying environmental conditions. Our simulations show that habitats differentially affect signal performance, and an interaction between display and habitat structure. Interestingly, the signal adapted to the noisier environment did not show an advantage in signal efficacy, but the noisy habitat was detrimental to the performance of all displays. Our study is one of the first studies for movement-based signals that directly compares signal performance in multiple habitats, and our approach has laid the foundation for future investigations in motion ecology that have been intractable to conventional research methods.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Xue Bian ◽  
Angela Pinilla ◽  
Tom Chandler ◽  
Richard Peters

AbstractHabitat-specific characteristics can affect signal transmission such that different habitats dictate the optimal signal. One way to examine how the environment influences signals is by comparing changes in signal effectiveness in different habitats. Examinations of signal effectiveness between different habitats has helped to explain signal divergence/convergence between populations and species using acoustic and colour signals. Although previous research has provided evidence for local adaptations and signal divergence in many species of lizards, comparative studies in movement-based signals are rare due to technical difficulties in quantifying movements in nature and ethical restrictions in translocating animals between habitats. We demonstrate herein that these issues can be addressed using 3D animations, and compared the relative performance of the displays of four Australian lizard species in the habitats of each species under varying environmental conditions. Our simulations show that habitats differentially affect signal performance, and an interaction between display and habitat structure. Interestingly, our results are consistent with the hypothesis that the signal adapted to the noisier environment does not show an advantage in signal effectiveness, but the noisy habitat was detrimental to the performance of all displays. Our study is one of the first studies for movement-based signals that directly compares signal performance in multiple habitats, and our approach has laid the foundation for future investigations in motion ecology that have been intractable to conventional research methods.


2021 ◽  
Vol 9 ◽  
Author(s):  
Jose A. Ramos ◽  
Richard A. Peters

Closely related species make for interesting model systems to study the evolution of signaling behavior because they share evolutionary history but have also diverged to the point of reproductive isolation. This means that while they may have some behavioral traits in common, courtesy of a common ancestor, they are also likely to show local adaptations. The Ctenophorus decresii complex is such a system, and comprises six closely related agamid lizard species from Australia: C. decresii, C. fionni, C. mirrityana, C. modestus, C. tjanjalka, and C. vadnappa. In this study, we analyze the motion displays of five members of the C. decresii complex in the context of their respective habitats by comparing signal structure, habitat characteristics and signal contrast between all species. Motor pattern use and the temporal sequence of motor patterns did not differ greatly, but the motion speed distributions generated during the displays were different for all species. There was also variation in the extent to which signals contrasted with plant motion, with C. vadnappa performing better than the other species at all habitats. Overall, this study provides evidence that members of the C. decresii complex exhibit local adaptations in signaling behavior to their respective habitat, but they also maintain some morphological and behavioral traits in common, which is likely a consequence from the ancestral state.


2016 ◽  
Vol 14 (1) ◽  
Author(s):  
Mariela Domiciano Ribeiro ◽  
Fabrício Barreto Teresa ◽  
Lilian Casatti

Abstract Functional traits are important for understanding the links between species occurrence and environmental conditions. Identifying these links makes it possible to predict changes in species composition within communities under specific environmental conditions. We used functional traits related to habitat use and trophic ecology in order to assess the changes in fish community composition between streams with varying habitat structure. The relationship between the species traits and habitat characteristics was analyzed using an RLQ ordination analysis. Although species were widely distributed in habitats with different structures, physical conditions did favor some species based on their functional characteristics. Eight functional traits were found to be associated with stream habitat structure, allowing us to identify traits that may predict the susceptibility of fish species to physical habitat degradation.


The Auk ◽  
1984 ◽  
Vol 101 (3) ◽  
pp. 487-498 ◽  
Author(s):  
Gerald J. Niemi ◽  
JoAnn M. Hanowski

Abstract The effects of a 500-kV transmission line on bird populations were assessed by comparing paired treatment areas [which included a transmission line and right-of-way (ROW)] with similar control areas in six different habitat types during the breeding and migration seasons. Habitat structure was measured to examine the inherent differences between control and treatment areas. Using two census methods, territorial mapping and transect counts, we determined that Sedge Wrens and LeConte's Sparrows had lower breeding-population densities in treatment areas than in control areas. LeConte's Sparrows and Connecticut Warblers occurred at greater mean distances from the transmission line in treatment areas than from a similarly positioned line in control areas. Fifteen paired t-tests (five habitats in 3 yr), in which territorial mapping data were used, revealed that community densities were lower in one treatment habitat (high shrub) in 1 of 3 yr (P < 0.05). A two-way analysis of variance with transect counts, however, was not confirmatory when yearly variation was included. Transect counts revealed lower population densities in one treatment habitat (low shrub) in 2 of 3 yr (P < 0.05). In contrast, we observed greater species richness (P < 0.05) in two treatment habitats (closed spruce and sedge fen) than in controls. Treatment habitats were most similar in habitat structure to their paired control habitats, but each habitat of the pair was significantly different (P < 0.05) from the other in at least 2 of 10 habitat characteristics analyzed. We suggest that the avian differences observed between paired areas were primarily attributable to (1) the inherent habitat differences between control and treatment areas, and (2) the new habitat created under the transmission line. Our data indicated negligible effects of this transmission line on bird populations, but interpretations are difficult, because the effects varied with (1) habitat, (2) season, and (3) method considered. Postimpact studies, which compare control and treatment areas, are less effective than before-and-after studies, because differences in habitat structure exist between any two areas.


2019 ◽  
Vol 70 (10) ◽  
pp. 1445 ◽  
Author(s):  
Ana María Torres-Huerta ◽  
Ramón Andrés López-Pérez ◽  
Margarito Tapia-García ◽  
Adolfo Gracía

Information on the relationship between batoid demersal assemblages and environmental factors is scarce. We captured a total of 23414 batoids belonging to 16 species with bottom trawls at 243 sampling stations in the Gulf of Tehuantepec, Mexico. The species Urotrygon rogersi, Urotrygon chilensis and Narcine vermiculatus represented 70.1% of the abundance and 46.3% of the biomass. Five batoid assemblages were identified using hierarchical cluster and similarity profile analyses. Four assemblages were located at depths less than 40m and one assemblage was located at depths between 40 and 62m. The main batoid group was located in front of the most important lagoon complexes. The abundance biomass comparison method indicated that small species were dominant in terms of abundance in most assemblages. The set of environmental conditions and habitat characteristics (longitude, depth and sea surface temperature) present in the Gulf of Tehuantepec predicted important changes in the batoid community and affected its spatiotemporal distribution pattern.


2021 ◽  
Vol 21 (5) ◽  
Author(s):  
Jordan P Cuff ◽  
Fredric M Windsor ◽  
Emma C Gilmartin ◽  
Lynne Boddy ◽  
T Hefin Jones

Abstract Hollows of veteran trees (i.e., rot holes) provide habitat for many rare and threatened saproxylic invertebrates. Rot holes are highly heterogeneous, particularly in terms of substrate and microclimate conditions. There is, however, a dearth of information regarding the differences in biological communities inhabiting rot holes with different environmental conditions. Invertebrates were sampled from European beech (Fagus sylvatica) rot holes in Windsor, Savernake, and Epping Forests (United Kingdom). For each rot hole, physical and environmental conditions were measured, including tree diameter, rot hole dimensions, rot hole height, substrate density, water content, and water potential. These parameters were used to assess the influence of environmental conditions and habitat characteristics on invertebrate communities. Rot hole invertebrate communities were extremely diverse, containing both woodland generalist and saproxylic specialist taxa. Large variation in community structure was observed between rot holes and across woodlands; all sites supported threatened and endangered taxa. Environmental conditions in rot holes were highly variable within and between woodland sites, and communities were predominantly structured by these environmental conditions. In particular, turnover between invertebrate communities was linked to high β-diversity. The linked heterogeneity of environmental conditions and invertebrate communities in rot holes suggests that management of deadwood habitats in woodlands should strive to generate environmental heterogeneity to promote invertebrate diversity. Additional research is required to define how management and conservation activities can further promote enhanced biodiversity across rot holes.


Biologia ◽  
2009 ◽  
Vol 64 (2) ◽  
Author(s):  
Adalbert Balog ◽  
Viktor Markó ◽  
Attila Imre

AbstractIn field experiments over a period of five years the effects of farming systems and habitat structure were investigated on staphylinid assembly in Central European apple and pear orchards. The investigated farms were placed in three different geographical regions with different environmental conditions (agricultural lowland environment, regularly flooded area and woodland area of medium height mountains). During the survey, a total number of 6,706 individuals belonging to 247 species were collected with pitfall traps. The most common species were: Dinaraea angustula, Omalium caesum, Drusilla canaliculata, Oxypoda abdominale, Philonthus nitidulus, Dexiogya corticina, Xantholinus linearis, X. longiventris, Aleochara bipustulata, Mocyta orbata, Oligota pumilio, Platydracus stercorarius, Olophrum assimile, Tachyporus hypnorum, T. nitidulus and Ocypus olens. The most characteristic species in conventionally treated orchards with sandy soil were: Philonthuss nitidulus, Tachyporus hypnorum, and Mocyta orbata, while species to be found in the same regions, but frequent in abandoned orchards as well were: Omalium caesum, Oxypoda abdominale, Xantholinus linearis and Drusilla canaliculata. The species Dinaraea angustula, Oligota pumilio, Dexiogya corticina, Xantholinus longiventris, Tachyporus nitidulus and Ocypus olens have a different level of preferences towards the conventionally treated orchards in clay soil. The species composition of the staphylinid fauna in apple and pear orchards could not be considered uniform. The environmental conditions and the soil together have a significant influence upon the richness of species, and the cumulative effects of these factors can modify even the dominance structures of the communities.


2007 ◽  
Vol 58 (5) ◽  
pp. 419 ◽  
Author(s):  
Thien T. Mai ◽  
Kevin A. Hovel

For many marine systems, little is known about the effects of habitat structure on ecological processes that dictate population dynamics. This study focused on the effects of habitat structure on behaviour, abundance, and survival of California spiny lobster (Panulirus interruptus Randall) in the Point Loma kelp forest, San Diego, California. Habitat characteristics were quantified in 400-m2 landscapes to determine the role of shelter and understorey kelp characteristics at local (shelter) scales and landscape scales on lobster habitat use. A tethering experiment determined the effects of the presence of understorey kelp on lobster survival. At the shelter scale, lobsters preferred permanent shelters to ephemeral shelters, but did not respond to shelter size. At the landscape scale, lobster density increased with Pterygophora californica (stipitate kelp) density and decreased with Laminaria farlowii (prostrate kelp) density, but lobster density did not vary with shelter density or dispersion. Lobster size increased with P. californica density in two of three surveys, while lobster size did not vary with L. farlowii density. Lobster relative survival was higher in the presence of understorey kelp than when kelp was absent. We conclude that lobsters respond to habitat characteristics at local and landscape scales, and that understorey kelp has strong effects on lobster habitat use and survival.


2021 ◽  
Author(s):  
◽  
Sarah Herbert

<p>In our current era, the Anthropocene, species are disappearing at an unprecedented rate due to the impact of humans on Earth’s environments. Of the many causes of these extinctions, habitat loss is thought to be the most severe. Three habitat management strategies are available for halting habitat loss: reservation, restoration and reconciliation. The latter two of these strategies actively seek to improve the ability of degraded or lost habitats to support species. If successful on a large enough scale, use of restoration and reconciliation (hereafter referred to collectively as ‘habitat enhancement’) could reverse the effects of habitat loss.  I evaluated the viability of habitat enhancement for the conservation of New Zealand’s lizard fauna. 83% of New Zealand’s 106+ endemic species are threatened or at risk of extinction. While habitat loss is one key driver of declines, predation by invasive mammals is the other. Neither of these processes are well understood. Habitat enhancement is increasingly being employed in New Zealand by landowners, community groups, conservationists, and businesses as a strategy for mitigating lizard declines, but outcomes are rarely investigated comprehensively. This is concerning because habitat manipulation potentially affects both exotic and native species, which has led to unexpected negative effects on threatened fauna in New Zealand and overseas. I posed four questions to help address this knowledge gap. (1) What habitat enhancement strategies are available for reptiles, and have they produced successful conservation outcomes? (2) How do habitat characteristics affect populations and communities of endemic New Zealand lizards? (3) How does the presence of invasive mammals affect populations and communities of endemic New Zealand lizards over intermediate to long-term time frames? (4) Can habitat enhancement produce positive conservation outcomes in the presence of invasive mammals?  A review of the global literature on habitat enhancement for reptiles identified 75 studies documenting 577 responses of 251 reptile species. For outcome evaluation, I adapted an existing stage-based framework for assessment of translocation success. High levels of success (84-85%) at Stages 1 (use of enhanced habitat) and 2 (evidence of reproduction in enhanced habitat) suggested that enhancement could be useful for creating areas that can be inhabited, and reproduced in, by reptiles. Fewer cases were successful at Stage 3 (30%; improvement of at least one demographic parameter demonstrated in enhanced habitat) or Stage 4 (43%; self-sustaining or source population established in enhanced habitat). Additionally, only 1% of the 577 cases sufficiently examined or modelled long-term population trends to allow evaluation against the Stage 4 criterion. Thus, there was a lack of evidence indicating that enhancement could result in higher population growth rates, or reduced extinction risk, of reptiles.  I conducted field work in the Wellington region to investigate the effects of habitat characteristics and mammals on terrestrial lizards inhabiting coastal environments. Surveys conducted in two mammal-invaded mainland areas and on two mammal-free offshore islands showed that presence or absence of invasive mammals had a stronger effect on lizard community structure than habitat variables. However, occupancy probabilities of northern grass skinks Oligosoma polychroma and Raukawa geckos Woodworthia maculata were positively correlated with increasing cover of divaricating shrubs. O. polychroma were also more likely to occupy patches with increasing cover by non-Muehlenbeckia vines. Mark-recapture studies were conducted at two mammal-invaded mainland sites to investigate the current abundance of lizard species: Turakirae Head and Pukerua Bay. Estimated densities of O. polychroma ranged between 3,980 and 4,078 individuals / ha and W. maculata between 4,067 and 38,372 individuals / ha. Other species known to occur, at least historically, at each site were either not detected or comprised only a small proportion of total lizard captures. Analysis of longitudinal lizard monitoring data available for Pukerua Bay, Turakirae Head, and an additional mammal-invaded site, Baring Head, did not reveal a significant decline in abundance, occupancy, or catch rates of O. polychroma over time periods ranging between six and 34 years, nor of W. maculata over six to 49 years. Habitat information available for Baring Head showed that the probability of local extinction of W. maculata was significantly lower at rocky sites.  Finally, I conducted a before-after-control-impact habitat enhancement experiment on lizard communities inhabiting 100 m2 plots on the mammal-invaded Miramar Peninsula. After a six-month pre-enhancement monitoring period, native plants and gravel piles were added to enhancement plots and lizard monitoring continued for a further nine months. Enhancement did not significantly affect plot use, body condition, or evidence of reproduction in Oligosoma aeneum, O. polychroma or W. maculata, but were considered successful at Stages 1 and 2 due to the absence of a negative effect. Neither the abundance, probability of entry into plots by birth or immigration, nor apparent survival of O. aeneum was significantly affected by enhancement (Stage 3). Apparent survival of O. polychroma increased significantly in response to enhancement, but this did not result in increased abundance.   Adding gravel and native vegetation (especially divaricating shrubs and vines) may be a suitable strategy for creating habitat in invaded coastal landscapes for O. polychroma and W. maculata. However, most of the other lizard species that would have historically occurred in mammal-invaded coastal areas of Wellington appeared to be sensitive to sustained mammal presence, even with low-to-moderate levels of control in operation. Therefore, habitat enhancement without intensive mammal control or eradication is not expected to benefit these species, nor be capable of restoring coastal lizard communities. In invaded landscapes it is, at best, a reconciliation measure that could allow co-existence of an endemic lizard community comprised of common species with invasive mammals. However, habitat enhancement could still be useful for restoring lizard communities in mammal-free sanctuaries.</p>


2021 ◽  
Author(s):  
◽  
Sarah Herbert

<p>In our current era, the Anthropocene, species are disappearing at an unprecedented rate due to the impact of humans on Earth’s environments. Of the many causes of these extinctions, habitat loss is thought to be the most severe. Three habitat management strategies are available for halting habitat loss: reservation, restoration and reconciliation. The latter two of these strategies actively seek to improve the ability of degraded or lost habitats to support species. If successful on a large enough scale, use of restoration and reconciliation (hereafter referred to collectively as ‘habitat enhancement’) could reverse the effects of habitat loss.  I evaluated the viability of habitat enhancement for the conservation of New Zealand’s lizard fauna. 83% of New Zealand’s 106+ endemic species are threatened or at risk of extinction. While habitat loss is one key driver of declines, predation by invasive mammals is the other. Neither of these processes are well understood. Habitat enhancement is increasingly being employed in New Zealand by landowners, community groups, conservationists, and businesses as a strategy for mitigating lizard declines, but outcomes are rarely investigated comprehensively. This is concerning because habitat manipulation potentially affects both exotic and native species, which has led to unexpected negative effects on threatened fauna in New Zealand and overseas. I posed four questions to help address this knowledge gap. (1) What habitat enhancement strategies are available for reptiles, and have they produced successful conservation outcomes? (2) How do habitat characteristics affect populations and communities of endemic New Zealand lizards? (3) How does the presence of invasive mammals affect populations and communities of endemic New Zealand lizards over intermediate to long-term time frames? (4) Can habitat enhancement produce positive conservation outcomes in the presence of invasive mammals?  A review of the global literature on habitat enhancement for reptiles identified 75 studies documenting 577 responses of 251 reptile species. For outcome evaluation, I adapted an existing stage-based framework for assessment of translocation success. High levels of success (84-85%) at Stages 1 (use of enhanced habitat) and 2 (evidence of reproduction in enhanced habitat) suggested that enhancement could be useful for creating areas that can be inhabited, and reproduced in, by reptiles. Fewer cases were successful at Stage 3 (30%; improvement of at least one demographic parameter demonstrated in enhanced habitat) or Stage 4 (43%; self-sustaining or source population established in enhanced habitat). Additionally, only 1% of the 577 cases sufficiently examined or modelled long-term population trends to allow evaluation against the Stage 4 criterion. Thus, there was a lack of evidence indicating that enhancement could result in higher population growth rates, or reduced extinction risk, of reptiles.  I conducted field work in the Wellington region to investigate the effects of habitat characteristics and mammals on terrestrial lizards inhabiting coastal environments. Surveys conducted in two mammal-invaded mainland areas and on two mammal-free offshore islands showed that presence or absence of invasive mammals had a stronger effect on lizard community structure than habitat variables. However, occupancy probabilities of northern grass skinks Oligosoma polychroma and Raukawa geckos Woodworthia maculata were positively correlated with increasing cover of divaricating shrubs. O. polychroma were also more likely to occupy patches with increasing cover by non-Muehlenbeckia vines. Mark-recapture studies were conducted at two mammal-invaded mainland sites to investigate the current abundance of lizard species: Turakirae Head and Pukerua Bay. Estimated densities of O. polychroma ranged between 3,980 and 4,078 individuals / ha and W. maculata between 4,067 and 38,372 individuals / ha. Other species known to occur, at least historically, at each site were either not detected or comprised only a small proportion of total lizard captures. Analysis of longitudinal lizard monitoring data available for Pukerua Bay, Turakirae Head, and an additional mammal-invaded site, Baring Head, did not reveal a significant decline in abundance, occupancy, or catch rates of O. polychroma over time periods ranging between six and 34 years, nor of W. maculata over six to 49 years. Habitat information available for Baring Head showed that the probability of local extinction of W. maculata was significantly lower at rocky sites.  Finally, I conducted a before-after-control-impact habitat enhancement experiment on lizard communities inhabiting 100 m2 plots on the mammal-invaded Miramar Peninsula. After a six-month pre-enhancement monitoring period, native plants and gravel piles were added to enhancement plots and lizard monitoring continued for a further nine months. Enhancement did not significantly affect plot use, body condition, or evidence of reproduction in Oligosoma aeneum, O. polychroma or W. maculata, but were considered successful at Stages 1 and 2 due to the absence of a negative effect. Neither the abundance, probability of entry into plots by birth or immigration, nor apparent survival of O. aeneum was significantly affected by enhancement (Stage 3). Apparent survival of O. polychroma increased significantly in response to enhancement, but this did not result in increased abundance.   Adding gravel and native vegetation (especially divaricating shrubs and vines) may be a suitable strategy for creating habitat in invaded coastal landscapes for O. polychroma and W. maculata. However, most of the other lizard species that would have historically occurred in mammal-invaded coastal areas of Wellington appeared to be sensitive to sustained mammal presence, even with low-to-moderate levels of control in operation. Therefore, habitat enhancement without intensive mammal control or eradication is not expected to benefit these species, nor be capable of restoring coastal lizard communities. In invaded landscapes it is, at best, a reconciliation measure that could allow co-existence of an endemic lizard community comprised of common species with invasive mammals. However, habitat enhancement could still be useful for restoring lizard communities in mammal-free sanctuaries.</p>


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