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Biological Invasions

, Volume 21, Issue 10, pp 3101–3108 | Cite as

Assessing gaps in reporting non-target mortality in island rodent eradication operations

  • Simon Ward
  • Auriel M. V. Fournier
  • Alexander L. BondEmail author
Open Access
Original Paper
First Online:

Abstract

Eradicating invasive species is a key part of island restoration, and can reverse the devastating impacts on native biota. Rodents are one of the most widespread invasive species, found on 80% of oceanic island systems, but have been removed from hundreds of islands through the application of anticoagulant-treated cereal bait. While such eradication operations are often net positive events for island ecosystems over the long-term, some native biota are also susceptible, resulting in short-term non-target mortality. One of the most widely distributed groups of birds, rails and allies (Rallidae) are highly adaptable, often endemic, and are known often to suffer mortality during rodent eradication operations, to varying degrees. Our goal was determine if the year of eradication or the size of the island predicted whether non-target mortalities were reported, including those that were true absences of mortality. We examined 122 eradication operations on 81 islands with rails present from 1983 to 2015, and found 78% with no reported information on non-target mortality using our search criteria. We found non-target mortality reporting has decreased over time, and there was no relationship with island size. Post-operational monitoring of eradication operations should thoroughly record non-target mortality to improve our understanding of factors affecting non-target mortality, and the efficacy of mitigation measures.

Keywords

Invasive species Island restoration Non-target Rallidae Rodent 

Introduction

The removal of invasive, alien, or introduced species has become a frequently used tool in the restoration of island ecosystems (Atkinson 2001; Bellingham et al. 2010; Rauzon 2007; Russell and Holmes 2015). Introduced mammals, in particular cats (Felis catus), house mice (Mus musculus) and rats (Rattus exulans, R. norvegicus, and R. rattus), are among the most detrimental (Angel et al. 2009; Jones et al. 2008; Medina et al. 2011), and have been the subject of hundreds of eradication operations in the last 50 years (DIISE 2016; Howald et al. 2007; Russell and Broome 2016).

Rodents in particular have invaded more than 1000 islands, and are now a globally-distributed invasive species and found on many oceanic and coastal islands (Atkinson 1985). Introduced rodents can have destructive effects on native biota, and can alter the ecosystem structure and function of islands (Blackburn et al. 2004; Croll et al. 2005; Jones et al. 2008; Towns et al. 2006). Because of islands’ importance for biodiversity, and the devastating effects of introduced rodents (Holmes et al. 2019), conservationists have undertaken hundreds of eradication operations worldwide to remove introduced rodents from islands, and implemented biosecurity measures to prevent reinvasion (Harris et al. 2012; Howald et al. 2007; Russell and Broome 2016; Springer 2011; Towns and Broome 2003).

The most common eradication method is the use of pelletized cereal bait. Pelletizied bait contains an anticoagulant rodenticide and is distributed in a variety of manners dependant on the size and structure of the island, and government regulations (Russell et al. 2016). These methods include bait distributed in bait stations laid out on a grid pattern, or broadcast by hand or aerial application techniques. This approach has been effective in temperate zones at removing invasive rodents from hundreds of islands across the world (Howald et al. 2007; Russell and Holmes 2015) resulting in significant benefits to native biodiversity (Brooke et al. 2018; Jones 2010; Jones et al. 2016; Lavers et al. 2010). Such eradication operations, however, often incur non-target mortality, in which animals not considered the target species are killed unintentionally (Eason et al. 2002; Hoare and Hare 2006). This involves either the direct consumption of the bait (primary poisoning) or through secondary poisoning by eating contaminated prey. In some cases, this can be mitigated by keeping a population of susceptible individuals in captivity, or translocating individuals to another island, for the duration of bait availability (Oppel et al. 2016a). A fundamental element in such restoration efforts is that the ecological benefits must exceed the costs, which includes the risks to non-target species, and of the mitigation measures themselves (Bomford and O’Brien 1995; Broome et al. 2014).

Rails (Gruiformes: Rallidae) consist of approximately 140 extant species distributed globally, that range in body size from ~ 30 to > 3000 g (Ripley 1977; Taylor and van Perlo 1998). They occupy a wide range of habitats including wetlands, freshwater and saltwater marshes, mangroves, tropical forests, and grasslands, as well as small oceanic islands, where they have evolved into distinct lineages (Livezey 1998; Taylor and van Perlo 1998). These species are often flightless, and have adapted to be generalist forest species due to the lack of mammal predators and in order to balance energy costs (Olson 1973; Ripley and Beehler 1985). More than 60 rail species have gone extinct since 1000 CE (Hume and Walters 2012), often because of anthropogenic factors (Ripley 1977).

The combination of a highly plastic and adaptable diet, and the frequent evolution of flightlessness, particularly on islands formerly free of native predators, makes rails susceptible to non-target mortality during rodent eradiation operations. Primary and secondary poisoning can result in population level non-target mortality and possibly local extirpation or extinction (e.g., Dowding et al. 1999; Oppel et al. 2016a, b; Vyas 2017; Wanless et al. 2010). Despite this, there is little information on the susceptibility of rails, or other non-target taxa, during rodent eradication operations, which limits our ability to assess tradeoffs of future eradication efforts.

Our objectives were to: (1) assess the extent to which rail populations have been affected by rodent eradication operations, (2) examine the degree of reporting for non-target mortality using rails as exemplars, and (3) determine whether operation characteristics influence the probability of mortality being reported. We predicted that improved awareness around non-target mortality would result in greater reporting over time, and that smaller islands where a greater proportion of the island could be searched would be more likely to report the presence or absence of non-target mortality.

Methods

We collated available data on rodent eradications on islands, and the distribution of rails using publicly available sources, and expert opinion. Data on rodent eradication attempts were gathered from the Database of Island Invasive Species Eradication (DIISE 2016) through September 2015. This database provided a list of references for island rodent eradications which we consulted to obtain details on bait type, bait concentration, and delivery method, all of which can influence non-target mortality (Eason et al. 2002). We compiled distribution data of rail species on islands that have had rodent eradications from the Birdlife International Data Zone (http://www.birdlife.org/datazone/species), from eradication operational reports, and in-country experts. When range maps provided ambiguous information about rail diversity on islands, we consulted with in-country experts from an established network of island restoration scientists and practitioners. The combined list of eradication operations on islands with rails was then used to then gather detailed information of each operation, including the method of bait delivery (aerial, bait station, hand broadcast), and non-target rail mortalities from published papers, operational reports, and government documents. We excluded bait type, and bait concentration from analyses as many values were represented by only one or a few eradication operations. Data on rails’ predominant diet (herbivorous, omnivorous, insectivorous), and IUCN Red List status was collected from the literature (Birdlife International 2017; Ripley 1977; Ripley and Beehler 1985; Taylor and van Perlo 1998).

Statistical analyses

To determine whether the size of an island or the year in which the eradication took place could predict whether non-target mortality was reported (including when no mortality was observed, i.e., a true absence), we used logistic regression with a binomial error distribution and logit link function. We log-transformed island area as one island was several orders of magnitude larger than the others. Analyses were considered significant when p < 0.05, and we present parameter estimates with their associated standard errors (β ± SE). All analyses were conducted in R 3.4.4 (R Core Team 2018), and the script is provided in the Supplementary Information.

Results

We found 122 rodent eradication operations on 81 islands in 18 territories from 1983 to 2015 during which rail species were present during eradication operations (Fig. 1, Appendix 1 of electronic supplementary material). Mean island size was 15.4 km2 (0.01–1576.4 km2). These operations overlapped with the distribution of 1–3 rail species per site, and 18 species overall (Table 1). In total, 95 (78%) eradication operations included no information or no mention of non-target mortality generally, or rail mortality in particular, in any published paper, operational report, or available government document. More recent eradication operations were less likely to report non-target mortality, and island size was unrelated to whether mortality was reported (Table 2; Fig. 2). One species was listed as Endangered by IUCN, 3 as Vulnerable and the remainder (14) as least concern.
Fig. 1

Map of countries where rodent eradication operations occurred in the presence of rails

Table 1

Different rail species listed with various aspects of their biology and the number of instances of known and unknown mortality during rat eradications

Species

Scientific name

Average size (g)

Flight ability

Predominant diet

IUCN Red List status

Number of known mortality cases

Number of unknown mortality cases

Clapper rail

Rallus crepitans

160–400

Flight

Insectivorous

Least concern

0

1

Western water rail

Rallus aquaticus

92–164

Flight

Omnivorous

Least concern

0

10

Lewin’s rail

Lewinia pectoralis

63–112

Flight

Insectivorous

Least concern

1

1

Weka

Gallirallus australis

430–1400

Flightless

Omnivorous

Vulnerable

13

15

Buff-banded rail

Hypotaenidia philippensis

170

Flight

Insectivorous

Least concern

9

22

Corncrake

Crex crex

145–165

Flight

Insectivorous

Least concern

0

2

Henderson crake

Zapornia atra

66–88

Flightless

Insectivorous

Vulnerable

1

0

Spotless crake

Zapornia tabuensis

45

Flight

Omnivorous

Least concern

5

10

White-breasted waterhen

Amaurornis phoenicurus

166–328

Flight

Insectivorous

Least concern

0

6

White-browed crake

Amaurornis cinerea

40–63

Flight

Omnivorous

Least concern

0

4

Purple swamphen

Porphyrio porphyrio

880–1090

Flight

Omnivorous

Least concern

10

13

South Island takahe

Porphyrio hochstetteri

2000–3500

Flightless

Herbivorous

Endangered

3

6

Allen’s gallinule

Porphyrio alleni

82

Flight

Insectivorous

Least concern

0

2

Common moorhen

Gallinula chloropus

192–493

Flight

Insectivorous

Least concern

2

24

Common gallinule

Gallinula galeata

310–456

Flight

Herbivorous

Least concern

0

1

Common coot

Fulica atra

585–1100

Flight

Omnivorous

Least concern

0

11

Hawaiian coot

Fulica alai

450–900

Flight

Omnivorous

Vulnerable

0

1

American coot

Fulica americana

600–1000

Flight

Herbivorous

Least concern

0

1

Taxonomy sequence follows (del Hoyo and Collar 2014)

Table 2

Logistic regression of whether the island size, or the year in which an eradication took place predict whether non-target rail mortality was reported (including true absences)

Category

β estimate

SE

p value

Intercept

159.18

63.77

0.02

Log [area (km)]

0.12

0.12

0.30

Year

− 0.08

− 0.03

0.01

Fig. 2

Reporting the results of searches for non-target mortality was not a function of island size, but decreased over time

Discussion

The success of eradication operations worldwide is built on the shared knowledge of past experiences in the island restoration community (e.g., Veitch et al. 2019). This has included the development of best practices for operations (Broome et al. 2014; Keitt et al. 2015), and open discussions of the challenges associated with such complex projects. Better reporting of non-target mortality can only be beneficial as we collectively seek ways to reduce it in future eradication operations, which requires a strong evidence base. Curiously, more recent operations were less likely to report on the outcome of any searching for non-target mortality, regardless of island size (Table 2). Such information may well exist in permit reports that are not publicly available, or centralized, but the result is the same: the information is not available for practitioners, researchers, and managers. With a greater number of more complex eradication operations on the horizon (including Gough Island, Marion Island, Lord Howe Island, and the Auckland Islands), and greater scrutiny from the general public and statutory authorities around operations (Campbell et al. 2015; Santo et al. 2015; Wilkinson and Priddel 2011), transparency around non-target mortality is also essential to maintaining the integrity of eradications as a conservation tool.

To better support evidence-based decision making for future eradication operations, practitioners should better collect, report, and disseminate information about non-target mortality, including instances where no mortality was observed. We were surprised to find that reporting of non-target mortality has been decreasing over time. While the Database of Island Invasive Species Eradication gathers data about eradications, it does not go into the necessary detail regarding non-target mortalities. To gather non-target mortality information the individual eradication attempt reports had to be used. Reports varied greatly in their level of detail, from full reports of all species affected to no information in the report or no report found. To support our understanding of eradication impacts on non-target species eradication operations should endeavour to assess the pre- and post-operation abundance of non-target species. Not only will more complete documentation demonstrate the efficacy of the eradication in restoring native biota, but it will allow for an assessment of the potential non-target mortality incurred to inform future eradications efforts and necessary mitigation measures. The reporting of non-target mortality is often a condition of government permits for rodent eradication operations, but these documents are not necessarily publicly available, or easily found, thereby impeding analyses such as ours. Eradications that did report mortality often did so without giving a sense of search effort or area, which further complicates synthesis among studies. Reporting should include at least an indication of search effort, the species searched for, area searched (especially if the whole island was not searched for non-target mortality), and the duration of search effort following the eradication operation.

Given that only 22% of eradication operations reported on non-target rail mortality, we lacked sufficient data to understand which traits might predispose species to being particularly affected by rodent eradications. Equally, we were unable to assess which operational measures, such as bait type, concentration, spreading density, or application method might be associated with a greater probability of rail mortality.

Improved reporting would allow managers, practitioners, and other researchers to better predict the potential effects of rodent eradication operations, particularly when specific data for a given taxon or ecosystem may be lacking (Sutherland et al. 2004). While our work here highlights what is not known about rails, many other native or endemic species could also suffer non-target effects from eradications, and should also be monitored (Pitt et al. 2015). Several, but not all, mitigation measures, including captive holding, have been used successfully (e.g., Oppel et al. 2016a; Wilkinson and Priddel 2011), and the presence of rail populations does not necessarily imply that an eradication operation will encounter significant non-target mortality. Rodent eradications have a long collaborative history which would easily extend to the improved public accessibility of data on non-target impacts, and likely resulting in improved knowledge about the potential impacts of rodent eradications on rail populations, and informing mitigation measures to ensure eradication success while minimising impacts on non-target species.

Notes

Acknowledgements

We thank C. Miskelly for his help with gathering the distribution of New Zealand rails, and J. Russell for finding many reports pertaining to eradications on New Zealand islands. C. Eizaguirre provided guidance and statistical advice. Comments from N. Holmes, C. Stringer, and two anonymous reviewers improved this manuscript.

Supplementary material

10530_2019_2032_MOESM1_ESM.csv (54 kb)
Supplementary material 1 (CSV 53 kb)

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Copyright information

© The Author(s) 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.School of Biological and Chemical SciencesQueen Mary University of LondonLondonUK
  2. 2.Mississippi State UniversityBiloxiUSA
  3. 3.Forbes Biological Station–Bellrose Waterfowl Research Center, Illinois Natural History Survey, Prairie Research InstituteUniversity of Illinois at Urbana-ChampaignHavanaUSA
  4. 4.RSPB Centre for Conservation ScienceRoyal Society for the Protection of BirdsSandyUK
  5. 5.Bird Group, Department of Life SciencesThe Natural History MuseumTringUK

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