scholarly journals Novel Predators and Naïve Prey: How Introduced Mammals Shape Behaviours and Populations of New Zealand Lizards

2021 ◽  
Author(s):  
◽  
Joanne Marie Hoare
Keyword(s):  
New Zealand ◽  
Synergistic Effects ◽  
Activity Patterns ◽  
Major Influence ◽  
Population Declines ◽  
Lizard Species ◽  
Predator Detection ◽  
Term Survival ◽  
Mammalian Predators ◽  
Invasive Mammals

<p>Biotas that evolved in isolation from mammalian predators are susceptible to degradation due to recent human-mediated introductions of mammals. However, behavioural, morphological and life historical adaptations of prey to novel mammalian predators can allow prey to persist in mammal-invaded areas. Lizards in New Zealand are an ideal group for exploring the effects of invasive mammals on vertebrate prey because: (1) the ca. 80 endemic species evolved without mammals as a major influence for 80 my, (2) mammalian introductions during the past 2000 y have differentially affected lizard species, and (3) some species coexist with mammals on the mainland as well as occurring on mammal-free offshore islands. I tested three hypotheses: (1) lizard populations that have persisted on New Zealand’s mainland are no longer declining in the presence of introduced mammalian predators, (2) introduced mammals induce behavioural shifts in native lizards, and (3) lizard behavioural patterns and chemosensory predator detection abilities vary according to exposure to introduced mammals. Trends in capture rates of five sympatric native lizard populations over a 23 year (1984-2006) period demonstrate that not all lizard populations that have persisted thus far on New Zealand’s mainland have stabilised in numbers. Large, nocturnal and terrestrial species remain highly vulnerable at mainland sites. Introduced kiore, Rattus exulans, induce behavioural changes in Duvaucel’s geckos, Hoplodactylus duvaucelii. A radio telemetric study demonstrated that geckos start reverting to natural use of habitats within six months of kiore eradication. Activity patterns of common geckos, H. maculatus, and common skinks, Oligosoma nigriplantare polychroma, in laboratory trials are also correlated with their exposure to mammalian predators. Lizard activity (time spent moving) increases relative to freeze behaviour with greater exposure to mammals. However, specific antipredator behaviours are not elicited by chemical cues of either native (tuatara, Sphenodon spp) or introduced (ship rat, R. rattus) predators. Lizard populations may persist by changing their behaviours in the presence of invasive mammals. However, the continued declines of particularly vulnerable mainland lizard taxa suggest that mammal-induced behavioural shifts may only slow population declines rather than enabling long-term survival. Eradicating pest mammals from offshore islands has proven effective at restoring both populations and behaviours of native lizards, but lizard populations on the mainland also deserve conservation priority. Research directed at understanding the synergistic effects of invasive species that are causing continued lizard population declines and mammal-proof fencing to protect the most vulnerable mainland populations from extinction are both urgently required.</p>

scholarly journals Novel Predators and Naïve Prey: How Introduced Mammals Shape Behaviours and Populations of New Zealand Lizards

2021 ◽  
Author(s):  
◽  
Joanne Marie Hoare
Keyword(s):  
New Zealand ◽  
Synergistic Effects ◽  
Activity Patterns ◽  
Major Influence ◽  
Population Declines ◽  
Lizard Species ◽  
Predator Detection ◽  
Term Survival ◽  
Mammalian Predators ◽  
Invasive Mammals

<p>Biotas that evolved in isolation from mammalian predators are susceptible to degradation due to recent human-mediated introductions of mammals. However, behavioural, morphological and life historical adaptations of prey to novel mammalian predators can allow prey to persist in mammal-invaded areas. Lizards in New Zealand are an ideal group for exploring the effects of invasive mammals on vertebrate prey because: (1) the ca. 80 endemic species evolved without mammals as a major influence for 80 my, (2) mammalian introductions during the past 2000 y have differentially affected lizard species, and (3) some species coexist with mammals on the mainland as well as occurring on mammal-free offshore islands. I tested three hypotheses: (1) lizard populations that have persisted on New Zealand’s mainland are no longer declining in the presence of introduced mammalian predators, (2) introduced mammals induce behavioural shifts in native lizards, and (3) lizard behavioural patterns and chemosensory predator detection abilities vary according to exposure to introduced mammals. Trends in capture rates of five sympatric native lizard populations over a 23 year (1984-2006) period demonstrate that not all lizard populations that have persisted thus far on New Zealand’s mainland have stabilised in numbers. Large, nocturnal and terrestrial species remain highly vulnerable at mainland sites. Introduced kiore, Rattus exulans, induce behavioural changes in Duvaucel’s geckos, Hoplodactylus duvaucelii. A radio telemetric study demonstrated that geckos start reverting to natural use of habitats within six months of kiore eradication. Activity patterns of common geckos, H. maculatus, and common skinks, Oligosoma nigriplantare polychroma, in laboratory trials are also correlated with their exposure to mammalian predators. Lizard activity (time spent moving) increases relative to freeze behaviour with greater exposure to mammals. However, specific antipredator behaviours are not elicited by chemical cues of either native (tuatara, Sphenodon spp) or introduced (ship rat, R. rattus) predators. Lizard populations may persist by changing their behaviours in the presence of invasive mammals. However, the continued declines of particularly vulnerable mainland lizard taxa suggest that mammal-induced behavioural shifts may only slow population declines rather than enabling long-term survival. Eradicating pest mammals from offshore islands has proven effective at restoring both populations and behaviours of native lizards, but lizard populations on the mainland also deserve conservation priority. Research directed at understanding the synergistic effects of invasive species that are causing continued lizard population declines and mammal-proof fencing to protect the most vulnerable mainland populations from extinction are both urgently required.</p>

scholarly journals Assessing bird predation on New Zealand’s lizard fauna using lizard-mimicking replicas

2021 ◽  
Author(s):  
◽  
Brittany Florence-Bennett
Keyword(s):  
New Zealand ◽  
Predation Risk ◽  
Bird Species ◽  
Canopy Cover ◽  
Daily Rainfall ◽  
Small Range ◽  
Lizard Species ◽  
Avian Predation ◽  
Top Predators ◽  
Mammalian Predators

<p>Wildlife management is fraught with challenges due to the complexities of community ecology. Interventions aimed at restoring ecosystems, or managing species, can have unintended negative outcomes for target species. The effect of avian predation on native lizard fauna in New Zealand is not clearly understood, despite birds being regarded as top predators within mammal-free ecosystems. At least thirty-one species of bird have been recorded preying on native lizards, but few studies have directly addressed avian predation on lizards, with the majority of evidence sourced from published anecdotes. New Zealand’s herpetofauna are already vulnerable due to range contractions resulting from mammalian predation and habitat loss, with 87% of New Zealand lizard species considered ‘At Risk’ or ‘Threatened’. Understanding the risks posed to lizards will help to inform successful management of vulnerable populations.  I used lizard-mimicking replicas to identify and assess predation rates exerted by bird species on lizard populations within the Wellington region of New Zealand. I examined the use of lizard replicas as a tool to quantify predation by examining how birds interacted with replicas and comparing attack rates with novel items simultaneously placed in the field. I determined which bird species were preying on replicas, the extent of such predation, and whether site vegetation or daily weather influenced the probability of avian attack on replicas. Although attack frequency did not differ between novel items and lizard replicas, birds exhibited a realistic predatory response by preferentially attacking the head of lizard replicas. Interactions by birds with lizard-mimicking replicas cannot be confirmed as true predation attempts, but lizard replicas can nevertheless be used to quantify predation pressures exerted on lizard populations by opportunistic bird species.   Seven ground-foraging bird species were found to attack lizard replicas. Two species, the pūkeko (Porphyrio melanotus melanotus) and southern black-backed gull (Larus dominicanus dominicanus), were identified as high impact species. The average predation risk experienced by lizard replicas varied greatly across environments, with 0 – 25% of replicas attacked daily at sites. Canopy cover and daily rainfall were not significant predictors, but potentially decreased the likelihood of replica attack. Predation risk varied for lizard replicas as a result of differing assemblages of bird predators at sites, and the presence and foraging behaviour of specific predatory birds.   Predation by birds is likely to be an issue where predation pressure is high, or lizard populations are small, range restricted, or recovering from the presence of mammalian predators. When managing vulnerable lizard populations, managers should take into account the threats posed by avian predators so that lizard communities can recover successfully following the same trajectory as native birds.</p>

scholarly journals Is habitat enhancement a viable strategy for conserving New Zealand's endemic lizards?

2021 ◽  
Author(s):  
◽  
Sarah Herbert
Keyword(s):  
New Zealand ◽  
Habitat Loss ◽  
The Other ◽  
Habitat Characteristics ◽  
Lizard Species ◽  
Apparent Survival ◽  
Stage 4 ◽  
Invasive Mammals ◽  
Habitat Enhancement

<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>

scholarly journals Is habitat enhancement a viable strategy for conserving New Zealand's endemic lizards?

2021 ◽  
Author(s):  
◽  
Sarah Herbert
Keyword(s):  
New Zealand ◽  
Habitat Loss ◽  
The Other ◽  
Habitat Characteristics ◽  
Lizard Species ◽  
Apparent Survival ◽  
Stage 4 ◽  
Invasive Mammals ◽  
Habitat Enhancement

<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>

scholarly journals Evaluation of remote cameras for monitoring multiple invasive mammals in New Zealand

2020 ◽  
Author(s):  
V Anton ◽  
Stephen Hartley ◽  
Heiko Wittmer
Keyword(s):  
New Zealand ◽  
Native Species ◽  
Detection Rates ◽  
Remote Cameras ◽  
Ecological Society ◽  
Mammalian Predators ◽  
Invasive Mammals ◽  
Conservation Projects ◽  
Multiple Species ◽  
Tracking Tunnels

© New Zealand Ecological Society. Numerous conservation projects in New Zealand aim to reduce populations of invasive mammalian predators to facilitate the recovery of native species. However, results of control efforts are often uncertain due to insufficient monitoring. Remote cameras have the potential to monitor multiple species of invasive mammals. To determine the efficiency of cameras as a multi-species monitoring tool, we compared the detection rates of remote cameras and tracking tunnels over 4 non-consecutive days across 40 sites in Wellington. On average, cameras detected significantly more hedgehogs (Erinaceus europaeus) and rats (Rattus spp.) than tracking tunnels, and their images could be used to identify rats to the species level in 50% of detections. Cameras also detected more possums (Trichosurus vulpecula) but missed recording mice (Mus musculus) on some occasions where tracking tunnels detected them, and vice-versa. We conclude that remote cameras are well-suited for simultaneously monitoring multiple species of invasive mammals in New Zealand.

scholarly journals Assessing bird predation on New Zealand’s lizard fauna using lizard-mimicking replicas

2021 ◽  
Author(s):  
◽  
Brittany Florence-Bennett
Keyword(s):  
New Zealand ◽  
Predation Risk ◽  
Bird Species ◽  
Canopy Cover ◽  
Daily Rainfall ◽  
Small Range ◽  
Lizard Species ◽  
Avian Predation ◽  
Top Predators ◽  
Mammalian Predators

<p>Wildlife management is fraught with challenges due to the complexities of community ecology. Interventions aimed at restoring ecosystems, or managing species, can have unintended negative outcomes for target species. The effect of avian predation on native lizard fauna in New Zealand is not clearly understood, despite birds being regarded as top predators within mammal-free ecosystems. At least thirty-one species of bird have been recorded preying on native lizards, but few studies have directly addressed avian predation on lizards, with the majority of evidence sourced from published anecdotes. New Zealand’s herpetofauna are already vulnerable due to range contractions resulting from mammalian predation and habitat loss, with 87% of New Zealand lizard species considered ‘At Risk’ or ‘Threatened’. Understanding the risks posed to lizards will help to inform successful management of vulnerable populations.  I used lizard-mimicking replicas to identify and assess predation rates exerted by bird species on lizard populations within the Wellington region of New Zealand. I examined the use of lizard replicas as a tool to quantify predation by examining how birds interacted with replicas and comparing attack rates with novel items simultaneously placed in the field. I determined which bird species were preying on replicas, the extent of such predation, and whether site vegetation or daily weather influenced the probability of avian attack on replicas. Although attack frequency did not differ between novel items and lizard replicas, birds exhibited a realistic predatory response by preferentially attacking the head of lizard replicas. Interactions by birds with lizard-mimicking replicas cannot be confirmed as true predation attempts, but lizard replicas can nevertheless be used to quantify predation pressures exerted on lizard populations by opportunistic bird species.   Seven ground-foraging bird species were found to attack lizard replicas. Two species, the pūkeko (Porphyrio melanotus melanotus) and southern black-backed gull (Larus dominicanus dominicanus), were identified as high impact species. The average predation risk experienced by lizard replicas varied greatly across environments, with 0 – 25% of replicas attacked daily at sites. Canopy cover and daily rainfall were not significant predictors, but potentially decreased the likelihood of replica attack. Predation risk varied for lizard replicas as a result of differing assemblages of bird predators at sites, and the presence and foraging behaviour of specific predatory birds.   Predation by birds is likely to be an issue where predation pressure is high, or lizard populations are small, range restricted, or recovering from the presence of mammalian predators. When managing vulnerable lizard populations, managers should take into account the threats posed by avian predators so that lizard communities can recover successfully following the same trajectory as native birds.</p>

scholarly journals The responses of New Zealand's arboreal forest birds to invasive mammal control

2021 ◽  
Author(s):  
◽  
Iona Fea
Keyword(s):  
New Zealand ◽  
Endemic Species ◽  
Bird Species ◽  
Control Operation ◽  
Forest Bird ◽  
Bird Populations ◽  
The North ◽  
Ship Rat ◽  
Mammalian Predators ◽  
Invasive Mammals

<p>Introduced mammalian predators are responsible for over half of contemporary extinctions and declines of birds. Endemic bird species on islands are particularly vulnerable to invasions of mammalian predators. The native bird species that remain in New Zealand forests continue to be threatened by predation from invasive mammals, with brushtail possums (Trichosurus vulpecula) ship rats (Rattus rattus) and stoats (Mustela erminea) identified as the primary agents responsible for their ongoing decline. Extensive efforts to suppress these pests across New Zealand’s forests have created "management experiments" with potential to provide insights into the ecological forces structuring forest bird communities. To understand the effects of invasive mammals on birds, I studied responses of New Zealand bird species at different temporal and spatial scales to different intensities of control and residual densities of mammals.  In my first empirical chapter (Chapter 2), I present two meta-analyses of bird responses to invasive mammal control. I collate data from biodiversity projects across New Zealand where long-term monitoring of arboreal bird species was undertaken. The projects cover a range of treatments including fenced sanctuaries, offshore islands, forests treated periodically and sites lacking significant mammal control. I found that New Zealand bird species exhibit complex responses to the varied and sustained management effort that has occurred across New Zealand’s landscape in the last fifty years. Some species show significant positive outcomes to control, notably the larger endemic species, while others, including highly endemic species, consistently decline after control.  In Chapter 3, I estimate the responses of bird populations in the central New Zealand region to changes in ship rat densities. I collaborated with scientists from the Department of Conservation (DOC) and Greater Wellington Regional Council and collated biodiversity data from four restoration projects located across the central New Zealand region. I constructed multiple density impact functions (DIFs), where the effect of a change in density of a pest on a valued resource is quantified, to describe the impacts of ship rat population dynamics on native bird populations. These responses were then modelled in a meta-analysis to provide overall effects for bird populations when rat abundance increases. I identified two taxa that exhibit significant negative responses across the region: the native parakeet species (Cyanoramphus spp.) and the tomtit (Petroica macrocephala). Evidence from single projects also showed that two other species were negatively affected by increases in rats: the South Island kaka (Nestor meridionalis) and the North Island rifleman (Acanthisitta chloris). Conversely, populations of the recently introduced silvereye (Zosterops lateralis) were resilient to rat population recovery as silvereye counts significantly increased the year after an increase in ship rat populations was observed.  In Chapter 4, I monitored bird species through a 1080 mammal-control operation in the southern Wairarapa. This operation coincided with a heavy beech mast, an irruptive event that occurs every 2-6 years. Most likely because of the abundance of seed, suppression of ship rats and possums appeared to be short-lived, and detections of these two mammals returned to pre-control levels within one and two years, respectively. Short-term responses of native birds to the control operation were positive: initially, for the small-medium sized bird species (i.e. the bellbird (Anthornis melanura), rifleman, tomtit, and tui (Prosthemadera novaeseelandiae) with a delayed positive response of the largest species 2.5 years after control (the New Zealand pigeon (Hemiphaga novaeseelandiae).  In my final data chapter, I focus on the nesting outcomes of a common endemic species, the North Island fantail (Rhipidura fuliginosa placabilis), to different densities of ship rats. Through intensive monitoring of over 100 fantail nests, I estimated the outcomes of nesting attempts and formulated a DIF where nesting success was modelled as a function of the abundance of ship rats at the nest micro-site. Nesting attempts suffered higher failure rates at sites with higher rat abundance however, in this study I also identified a feature of nest placement that apparently limits predation from mammals. Nests placed on thinner branches were more likely to survive rat predation, a neat trick that perhaps only the smallest of birds can manage.  My thesis identifies some species as particularly vulnerable to invasive mammalian predation while others are more resilient. Understanding resilience and vulnerability in New Zealand’s bird species sheds light on historical extinctions and the processes that continue to mould New Zealand's avifauna. I quantified responses of New Zealand forest bird species, to different levels of invasive mammal management and residual densities of mammals, with consideration of climate and forest productivity. These estimates could be applied by conservation managers to more effectively gauge future threats to native avifauna according to the attributes of bird species and present and future management scenarios.</p>

scholarly journals Evaluation of remote cameras for monitoring multiple invasive mammals in New Zealand

2020 ◽  
Author(s):  
V Anton ◽  
Stephen Hartley ◽  
Heiko Wittmer
Keyword(s):  
New Zealand ◽  
Native Species ◽  
Detection Rates ◽  
Remote Cameras ◽  
Ecological Society ◽  
Mammalian Predators ◽  
Invasive Mammals ◽  
Conservation Projects ◽  
Multiple Species ◽  
Tracking Tunnels

© New Zealand Ecological Society. Numerous conservation projects in New Zealand aim to reduce populations of invasive mammalian predators to facilitate the recovery of native species. However, results of control efforts are often uncertain due to insufficient monitoring. Remote cameras have the potential to monitor multiple species of invasive mammals. To determine the efficiency of cameras as a multi-species monitoring tool, we compared the detection rates of remote cameras and tracking tunnels over 4 non-consecutive days across 40 sites in Wellington. On average, cameras detected significantly more hedgehogs (Erinaceus europaeus) and rats (Rattus spp.) than tracking tunnels, and their images could be used to identify rats to the species level in 50% of detections. Cameras also detected more possums (Trichosurus vulpecula) but missed recording mice (Mus musculus) on some occasions where tracking tunnels detected them, and vice-versa. We conclude that remote cameras are well-suited for simultaneously monitoring multiple species of invasive mammals in New Zealand.

scholarly journals The responses of New Zealand's arboreal forest birds to invasive mammal control

2021 ◽  
Author(s):  
◽  
Iona Fea
Keyword(s):  
New Zealand ◽  
Endemic Species ◽  
Bird Species ◽  
Control Operation ◽  
Forest Bird ◽  
Bird Populations ◽  
The North ◽  
Ship Rat ◽  
Mammalian Predators ◽  
Invasive Mammals

<p>Introduced mammalian predators are responsible for over half of contemporary extinctions and declines of birds. Endemic bird species on islands are particularly vulnerable to invasions of mammalian predators. The native bird species that remain in New Zealand forests continue to be threatened by predation from invasive mammals, with brushtail possums (Trichosurus vulpecula) ship rats (Rattus rattus) and stoats (Mustela erminea) identified as the primary agents responsible for their ongoing decline. Extensive efforts to suppress these pests across New Zealand’s forests have created "management experiments" with potential to provide insights into the ecological forces structuring forest bird communities. To understand the effects of invasive mammals on birds, I studied responses of New Zealand bird species at different temporal and spatial scales to different intensities of control and residual densities of mammals.  In my first empirical chapter (Chapter 2), I present two meta-analyses of bird responses to invasive mammal control. I collate data from biodiversity projects across New Zealand where long-term monitoring of arboreal bird species was undertaken. The projects cover a range of treatments including fenced sanctuaries, offshore islands, forests treated periodically and sites lacking significant mammal control. I found that New Zealand bird species exhibit complex responses to the varied and sustained management effort that has occurred across New Zealand’s landscape in the last fifty years. Some species show significant positive outcomes to control, notably the larger endemic species, while others, including highly endemic species, consistently decline after control.  In Chapter 3, I estimate the responses of bird populations in the central New Zealand region to changes in ship rat densities. I collaborated with scientists from the Department of Conservation (DOC) and Greater Wellington Regional Council and collated biodiversity data from four restoration projects located across the central New Zealand region. I constructed multiple density impact functions (DIFs), where the effect of a change in density of a pest on a valued resource is quantified, to describe the impacts of ship rat population dynamics on native bird populations. These responses were then modelled in a meta-analysis to provide overall effects for bird populations when rat abundance increases. I identified two taxa that exhibit significant negative responses across the region: the native parakeet species (Cyanoramphus spp.) and the tomtit (Petroica macrocephala). Evidence from single projects also showed that two other species were negatively affected by increases in rats: the South Island kaka (Nestor meridionalis) and the North Island rifleman (Acanthisitta chloris). Conversely, populations of the recently introduced silvereye (Zosterops lateralis) were resilient to rat population recovery as silvereye counts significantly increased the year after an increase in ship rat populations was observed.  In Chapter 4, I monitored bird species through a 1080 mammal-control operation in the southern Wairarapa. This operation coincided with a heavy beech mast, an irruptive event that occurs every 2-6 years. Most likely because of the abundance of seed, suppression of ship rats and possums appeared to be short-lived, and detections of these two mammals returned to pre-control levels within one and two years, respectively. Short-term responses of native birds to the control operation were positive: initially, for the small-medium sized bird species (i.e. the bellbird (Anthornis melanura), rifleman, tomtit, and tui (Prosthemadera novaeseelandiae) with a delayed positive response of the largest species 2.5 years after control (the New Zealand pigeon (Hemiphaga novaeseelandiae).  In my final data chapter, I focus on the nesting outcomes of a common endemic species, the North Island fantail (Rhipidura fuliginosa placabilis), to different densities of ship rats. Through intensive monitoring of over 100 fantail nests, I estimated the outcomes of nesting attempts and formulated a DIF where nesting success was modelled as a function of the abundance of ship rats at the nest micro-site. Nesting attempts suffered higher failure rates at sites with higher rat abundance however, in this study I also identified a feature of nest placement that apparently limits predation from mammals. Nests placed on thinner branches were more likely to survive rat predation, a neat trick that perhaps only the smallest of birds can manage.  My thesis identifies some species as particularly vulnerable to invasive mammalian predation while others are more resilient. Understanding resilience and vulnerability in New Zealand’s bird species sheds light on historical extinctions and the processes that continue to mould New Zealand's avifauna. I quantified responses of New Zealand forest bird species, to different levels of invasive mammal management and residual densities of mammals, with consideration of climate and forest productivity. These estimates could be applied by conservation managers to more effectively gauge future threats to native avifauna according to the attributes of bird species and present and future management scenarios.</p>

scholarly journals Complete genomes of two extinct New Zealand passerines show responses to climate fluctuations but no evidence for genomic erosion prior to extinction

2019 ◽  
Vol 15 (9) ◽  
pp. 20190491 ◽  
Author(s):  
Nicolas Dussex ◽  
Johanna von Seth ◽  
Michael Knapp ◽  
Olga Kardailsky ◽  
Bruce C. Robertson ◽  
...  
Keyword(s):  
Climate Change ◽  
New Zealand ◽  
Human Impacts ◽  
Oceanic Islands ◽  
Genomic Diversity ◽  
Climate Fluctuations ◽  
Forest Clearing ◽  
Mammalian Predators ◽  
Demographic Trajectories ◽  
Human Climate

Human intervention, pre-human climate change (or a combination of both), as well as genetic effects, contribute to species extinctions. While many species from oceanic islands have gone extinct due to direct human impacts, the effects of pre-human climate change and human settlement on the genomic diversity of insular species and the role that loss of genomic diversity played in their extinctions remains largely unexplored. To address this question, we sequenced whole genomes of two extinct New Zealand passerines, the huia ( Heteralocha acutirostris ) and South Island kōkako ( Callaeas cinereus ). Both species showed similar demographic trajectories throughout the Pleistocene. However, the South Island kōkako continued to decline after the last glaciation, while the huia experienced some recovery. Moreover, there was no indication of inbreeding resulting from recent mating among closely related individuals in either species. This latter result indicates that population fragmentation associated with forest clearing by Maōri may not have been strong enough to lead to an increase in inbreeding and exposure to genomic erosion. While genomic erosion may not have directly contributed to their extinctions, further habitat fragmentation and the introduction of mammalian predators by Europeans may have been an important driver of extinction in huia and South Island kōkako.

Sign in / Sign up

Export Citation Format

Share Document