Open Access
How to translate text using browser tools
15 September 2017 Reply to Lee & Holyoak: how definite are 20th-century reports of Chattering Kingfisher Todiramphus tutus from Tahiti?
Roland E. van der Vliet, Justin J. F. J. Jansen
Author Affiliations +
Abstract

Lee & Holyoak (2017) focused on Lesson as a source that we had neglected in our discussion of Chattering Kingfisher Todiramphus tutus on Tahiti. They are apparently confident in the accuracy of specimen labels from Lesson's era despite that the labelling of even Lesson's own specimens is poor. Based on meticulous notes taken during the Whitney South Sea Expedition by Beck and Quayle in the early 1920s, as well as their specimen material, we demonstrate that they never collected T. tutus on Tahiti, where they collected only Society (Tahitian) Kingfisher T. veneratus. Lee & Holyoak's suggestion that both species occurred in the Society Islands but became extinct in either the western Leeward Islands (veneratus) or eastern Windward Islands (tutus) seems to be a case of selective extinction following an established biogeographical divide. We believe that the observed pattern is best explained by the fact that veneratus was never present on the Leeward Islands and tutus never occurred on Tahiti: this represents the most parsimonious interpretation of the available data.

Lee & Holyoak's (2017) commentary on our papers concerning the occurrence of Chattering Kingfisher Todiramphus tutus raises many interesting points. Let us first summarise our original findings. For 115 specimens of Chattering Kingfisher T. t. tutus (hereafter tutus) in museums worldwide, we compiled data on collection locality, collector and date. For at least eight specimens reportedly taken on Tahiti (of 13 specimens labelled such), we identified problems of provenance. For the remaining five, no collector was mentioned, preventing our researching their precise locality. Problems also arose with the provenance of the only two specimens reported from the atoll of Tupai. We concluded that tutus never occurred on Tahiti or Tupai (Jansen & van der Vliet 2015, van der Vliet & Jansen 2015). Another important conclusion was that the oldest two specimens of tutus were probably collected by George Bass, who visited French Polynesia, including Tahiti, in 1802 (Jansen 2014). It is unfortunate that Lee & Holyoak (2017) neglect this point because he appears to have been an important source of bird specimens from this region in the period between Cook and Lesson. This brings us to Lee & Holyoak's (2017) arguments. Some of these appear to represent long-standing misconceptions (for example, concerning the use of label data on old specimens), while others relate to the situation in French Polynesia (e.g. biogeography of the Society Islands).

Poor labelling: Lesson's specimens as an example

Lee & Holyoak (2017) are apparently confident in the accuracy of specimen labels in the early era of collecting. This is strange because, for specimens of tutus, even Holyoak himself (in Thibault & Holyoak 1984: 138) alluded to the possibility that ‘beaucoup de vieux specimens libelles <<Otahiti>> ont pu être collectes ailleurs dans les Iles de la Société’ (many old specimens labelled << Otahiti >> could have been collected elsewhere in the Society Islands), without providing details. In that sense, our papers can be considered a follow-up to his statement. In them, we referred to, for example Rasmussen & Prŷs-Jones (2003), who demonstrated that poor labelling was almost common practice in the early collecting era. Many cases of simply inaccurate labelling, rather than fraudulent activity, are known, even in the modern era (e.g. Peterson et al. 2004, Boessenkool et al. 2009).

As Lee & Holyoak (2017) discuss Lesson, his specimens in Muséum national d'Histoire naturelle, Paris (MNHN) well illustrate this point. The voyage of La Coquille took Lesson around the world between 8 November 1822 and 24 March 1825, visiting amongst others the Falklands, Chile, Peru, Tuamotu, Tahiti, Bora Bora, several islands in New Guinea and Indonesia, Australia (Sydney), New Zealand, Mauritius, Réunion, St. Helena and Ascension (Cretella 2010). From our research at MNHN, we have concluded that Lesson twice donated specimens from the La Coquille expedition to the museum: in April 1825 (168 specimens of 139 species) and on 24 August 1825 (416 specimens of 252 species) (Ms in MNHN Lab, Catalogue 1823 à 1829), i.e. 584 specimens arrived at MNHN, of which many were used for exchange. None of Lesson's specimens has an original label. The only information available, for some, is on the base of their pedestals, but this was added later by someone else, in some instances years after the specimen was collected. It is easy to imagine that mistakes were made during the process. It is also difficult to interpret specimen dates from acquisition books as these were commenced only in c.1854 (Jansen 2014), i.e. Lesson's specimens had already been present in excess of 25 years.

Of the kingfishers among these 584 specimens, in the MNHN archives we have located three documents relating to the first batches (varying in content and with different numbering) and an incomplete manuscript, drafted by Lesson in 1824. The latter excludes the Pacific section of the voyage (Bibliothèque centrale, MNHN, Ms 354). Table 1 shows that Lesson sent 26 kingfisher specimens to MNHN of which 14 were mounted for the galleries (leaving 12 for exchange). Nine of these (cat. nos. 73–78) arrived with the first donation, and the rest (cat. nos. 135–142) with the second. From Table 1, it is clear that four kingfishers from Tahiti and Bourbon (Réunion) were registered under one entry, probably meaning that they concerned similar-coloured species like Collared T. chloris or Sacred Kingfishers T. sanctus. In Table 1 note also the mention of both the Malouines (Falkland Islands) and Bourbon (Réunion) where no kingfishers occur, although both localities were visited by Lesson on La Coquille, illustrating just one way in which errors of location can find their way into history.

TABLE 1

Details of kingfisher specimens in the Catalogue 1823 à 1829, collected by Lesson and which arrived at the Muséum national d'Histoire naturelle (Paris) in either April 1825 (pp. 100–101) or 24 August 1825 (p. 132). Presented are page number, catalogue number, name, original collection location as drafted, the number of individuals and any additional information.

t01_218.gif

TABLE 2

The number of kingfisher specimens collected during the La Coquille voyage (1822–25), with the current scientific name, acquisition book number or recent renumbered registration number, collection location based on the acquisition book and the type catalogue in which the specimens were published in.

t02_218.gif

At present (June 2017) only eight of these kingfishers are present at MNHN (Table 2). Note that both Todiramphus albicilla and Alcedo meninting do not occur in New Ireland and New Guinea, respectively, contrary to what is mentioned in the acquisition books.

Lee & Holyoak (2017) appear surprised that we did not refer to Lesson (1827), wherein he described the genus Todiramphus. We did, of course, read this paper but, as our concern was not taxonomic, there was no reason to cite it. Furthermore, the descriptions Lesson gave of both species are not type descriptions as is abundantly clear from our papers. However, we might note that Lesson's paper appeared in 1827, four years after his visit to the Society Islands and two years after his return to Europe. Given all of the problems with Lesson's labelling, we are less certain than Lee & Holyoak (2017) that Lesson had his collection localities right for each specimen. For the same reason, we do not believe that much can be inferred from Lesson's texts quoted by Lee & Holyoak.

Arrival of rats (Rattus spp.) in the Pacific

Lee & Holyoak (2017) afford extra significance to Lesson's specimens from French Polynesia because, according to them, they were collected in an environment free of Black Rats Rattus rattus. They state that Lesson's ‘timing was critical because it took place just a few years (c.10) before the invasion of Black Rat’. Lee & Holyoak (2017) rightly state that the arrival of this invasive species had ‘a devastating impact on the avifauna of eastern Polynesia’. Whether Brown Rat R. norvegicus or Black Rat arrived first is potentially important because predation of landbirds by Brown Rats is much less severe than by Black Rats.

Quoting Sparrman, who accompanied Cook on his second circumnavigation, Atkinson & Atkinson (2000) reported that rats were already a great pest on Tahiti in 1773. These probably concerned Polynesian Rats R. exulans introduced by local Polynesians. Furthermore, Atkinson (1973) noted (quoting Cook 1785: 81 discussing his third voyage) that Cook let rats ashore on (at least) Raiatea and Moorea. Because Polynesian Rats did not occur in Cook's port(s) of departure and other ports of call, these must have been Brown or Black Rats. Black Rat had been established in Britain for centuries, while Brown Rat was a relative newcomer, with the first reliable reports in England in 1730 (Hedrich 2006). Being the more aggressive species, Brown Rats outcompeted Black Rats relatively quickly almost everywhere in Europe including Britain. However, how strong the resulting decline of Black Rat had been when Cook set sail in 1776 is unclear.

Based on interspecific competition and the start of intercontinental travel by ship, Atkinson (1985) concluded that Brown Rat would have been first to arrive on the Pacific islands. However, Atkinson & Atkinson (2000) noted that Brown Rats did not appear to reach the Pacific islands until the 19th century. It can be deduced that those rats that Cook introduced in the Society Islands, prior to Lesson's visit, may have been Black Rats, which therefore could have arrived much earlier in French Polynesia than Lee & Holyoak (2017) acknowledge. This means that assumptions by Lee & Holyoak (2017) regarding Lesson visiting islands not impacted by predatory rats, is not necessarily true. This furthermore indicates that their conclusions based on this assumption are not necessarily valid. In reality, however, it is impossible to be certain which species (Brown or Black Rat) was introduced first in the Society Islands.

Variation in Tahitian Kingfisher Todiramphus venerates

Lee & Holyoak (2017) provide a very brief description of the kingfisher that Holyoak claims to be tutus. It does not add much to those details provided by Holyoak (1974) and Holyoak & Thibault (1984). No photographs, videos or specimens are apparently available. The level of detail provided by Holyoak is in our view insufficient to claim these birds as tutus. That Holyoak does not doubt his own sightings is not necessarily sufficient for them to be accepted. He describes in Lee & Holyoak (2017) that ‘tutus was recognised [by him] by its white collar around the nape (lacking in T. veneratus), combined with brighter blue back and wing-coverts.’ In response to several recent claims of tutus in 2002–08, Cibois & Thibault (2009) already noted plumage similarities between tutus and veneratus. They emphasised, for example, that veneratus can show bluer upperparts than previously known. A study into kingfisher taxonomy led us to study 82 specimens of veneratus. Full details will be published elsewhere, but focusing on the important feature of the neck-band, most specimens of veneratus lack a neck-band or even an indication of one. However, a few show some white spots, a clear small white neck-band or, very rarely, a distinctly coloured neck-band (orange / green / white). That veneratus can show a white neck-band means that it can resemble tutus in this respect, as alluded to by Lee & Holyoak (2017). However, unlike Lee & Holyoak (2017), we believe this reflects variation within veneratus rather than hybridisation between veneratus and tutus as suggested by Lee & Holyoak (2017).

Biogeography of the Leeward and Windward Islands

Lee & Holyoak (2017) appear to dispute the different biogeographical histories of the western Leeward Islands and eastern Windward Islands. While it is difficult to draw firm conclusions from an impoverished biological class like birds, Hembry & Balukjian (2016) analysed a wide range of taxa. Their conclusion, that ‘the most common phylogeographical division seen in Societies taxa is between the Windward and Leeward Society Islands’, supports our assumptions based on a small number of bird species. They specifically mentioned Grey-green Fruit Dove Ptilinopus purpuratus as a probable example of this biogeographical pattern, while they considered Acrocephalus reed warblers to be also consistent with it. Both of these examples were also given by us (van der Vliet & Jansen 2015). We concur with Lee & Holyoak (2017) that not all landbird species on the Society Islands display this biogeographical pattern, as is evident from the genus Ducula. However, the example of Blue Lorikeet Vini peruviana to demonstrate their point is less fortunate because this species can cover relatively large distances over water (up to five km regularly recorded, but it is perhaps capable of larger distances; Ziembicki & Raust 2006).

The Whitney South Sea Expedition in the Society Islands

One important point of reference is the visit by the Whitney South Sea Expedition (WSSE) to the south Pacific (including the Society Islands) in the early 1920s, collecting birds for the American Museum of Natural History (AMNH), New York, in the process discovering many taxa described as new to science. The expedition was not without its controversy though, and the number of specimens taken by WSSE sparked outrage even at the time, with New Zealand denying the expedition collecting permits in the Cook Islands (Collar 2000). Rigorous collecting by WSSE in areas they visited, combined with their equally detailed record-taking (see below), means that we attach high value to their results.

At AMNH, the kingfishers that WSSE collected on the Society Islands numbered 71 veneratus from Tahiti (6 October 1920–13 January 1923), 30 youngi on Moorea (13 June 1921–5 November 1921) and 14 tutus on Raiatea (10 December 1921–10 January 1922) and Bora Bora (12–13 January 1922). Due to their efficient labelling, we can deduce that all of their veneratus were assigned to Tahiti, all youngi to Moorea and all tutus to Raiatea or Bora Bora. The principal collectors were Rollo Beck and Ernest Quayle. The diaries of both men are available.

From Beck's diaries, it is evident that both he and Quayle visited highland areas on Tahiti up to 1,220 m, i.e. the elevation where Holyoak sighted his kingfishers. This is reinforced by Quayle's diaries as detailed by Monnet et al. (1993). Lee & Holyoak (2017), emphasising the broadly circular shape of Tahiti Nui, note that the sites of Holyoak's observations and those of unverified sightings in 2002–08, would have been ‘at similar altitude and approximately similar distances inland’. Due to the size of the island, Lee & Holyoak (2017) conclude that the locations would have been close together. Because Beck and Quayle visited sites at similar elevations, these were probably also close to those of Holyoak's sightings. If tutus was really that readily encountered at that elevation in that region of Tahiti (as seems to have been the case based on the numbers observed by Holyoak), it is very surprising that WSSE did not collect it there. Despite staying c.9 months on Tahiti spread over several visits between September 1920 and April 1923, WSSE did not collect a single specimen of tutus on Tahiti.

Quayle's diaries reveal that he ‘was primarily engaged in collecting, but he evidently noted all of the land and freshwater bird species he encountered’ (Monnet et al. 1993). Again, according to Monnet et al. (1993), Quayle ‘... explored the island more intensively than the other members of the expedition, and in his journal, he noted ecological observations as few naturalists did at this time. […] He mentioned 19 localities where he collected (or observed) birds.’ Monnet et al. (1993) identified 15 of Quayle's collecting sites, with four being impossible to determine, and investigated 14 of the known localities between 1986 and 1991, but not the 15th, Vaiote. Because this site is in the smaller, eastern part of Tahiti (Tahiti Iti), where Holyoak did not observe kingfishers, it is of no concern here. Like WSSE, Monnet et al. (1993) failed to observe tutus on Tahiti.

Overall, we still find it difficult to credit that WSSE would not have collected tutus on Tahiti, had it occurred there, given their intensive collecting and visits to appropriate elevations, especially as WSSE worked on Tahiti 50 years earlier than Holyoak. The field work and collecting practice of WSSE reinforces a point discussed earlier: if collectors record data precisely during field work, few (if any) errors occur during subsequent labelling with respect to, for example, date and locality. Because data for specimens collected during WSSE can be checked against the diaries of Beck and Quayle, in our opinion they can be deemed trustworthy.

A case of selective extinction?

Lee & Holyoak (2017) mention three implicit or explicit hypotheses in our papers. Foremost, we propose that (1) tutus never occurred on Tahiti or (2) on Tupai. Lee & Holyoak (2017) furthermore state that (3) veneratus never occurred on the Leeward Islands should be considered a further conclusion. In contrast, they advance a scenario where veneratus and tutus occurred in sympatry on both the Windward and Leeward Islands (except perhaps for tutus occurring on Moorea). They rightly state that this occurs elsewhere in Oceania, despite that kingfishers are territorial predators. While we obviously agree that this trait does not exclude sympatry, it also means that kingfishers are often clearly detectable by all observers.

Knowledge of both species in the Society Islands in the 1800s was scant to say the least. Most if not all contemporary literature considered that veneratus occurred on the Society Islands, and tutus (or taxa with which tutus was synonymised) also on Tahiti (e.g. Gray 1859, Finsch & Hartlaub 1867, Sharpe 1868, 1892, 1906, Wiglesworth 1891). These sources often referred to the less precisely delineated ‘Society Islands’ among which, for biogeographical reasons outlined above, it is important to distinguish the Leeward and Windward groups. Confusion in that era was exaggerated because several influential works disagreed as to the specific status of tutus, sometimes considering veneratus and tutus as conspecific; hence our quotation of Sharpe (1868), repeated by Lee & Holyoak (2017). This was still true in 1904 when S. B. Wilson visited the Society Islands (Wilson 1907). Wilson (1907) described both veneratus and tutus as (fairly) common in the Society Islands, noting that veneratus was ‘fairly common, especially on the island of Bora-Bora’. As noted above, even WSSE was unable to collect any veneratus on Bora Bora or the other Leeward Islands, only 20 years later.

Considering the present-day distribution of both taxa, the scenario outlined by Lee & Holyoak (2017) represents a case of selective extinction, wherein veneratus must have died out quite rapidly between Wilson's visit in 1904 and that by WSSE in 1921–22 to Raiatea and Bora Bora. Furthermore, according to their scenario, tutus must have become extinct on Tahiti alone (given the lack of credible reports since Holyoak's in 1972) whereas it still thrives in the Leeward group. Yet, this selective extinction occurred in the presence of the same predators (rats) on both groups and coincidentally followed an established biogeographical divide between the archipelagos. We consider this to be an unrealistic scenario not supported by facts, and we do not agree with Lee & Holyoak (2017) to consider the current distribution of veneratus as a working hypothesis. We believe that the available facts support only one plausible hypothesis, namely that (1) veneratus never occurred on the Leeward Islands, while (2) tutus was never present on Tahiti. Reaching this conclusion we cannot help wondering how Lee & Holyoak believe that tutus became extinct on Tahiti so soon after Holyoak's sightings, but also how veneratus on Bora Bora slipped to extinction so swiftly after Wilson's sightings, despite being considered common?

Our conclusions are supported by the WSSE results. As stated, we believe their data are trustworthy and therefore that accurate distributions can be inferred from their specimens. In this case, based on their data concerning kingfishers collected in the Society Islands, we conclude that veneratus occurs only on Tahiti, youngi only on Moorea, and tutus does not occur on Tahiti and Moorea, but in the Leeward group. From van der Vliet & Jansen (2015) we contend that nominate tutus not only occurs on Raiatea and Bora Bora (where WSSE collected it) but also on Huahine, Maupiti and Tahaa. For veneratus, this follows all modern world checklists (e.g. Peters 1955, Dickinson & van Remsen 2013, del Hoyo & Collar 2014, Clements et al. 2016, Gill & Donsker 2017) and other literature (e.g. Pratt et al. 1987, Fry et al. 1992). That tutus never occurred on Tahiti is the most logical explanation for the observed distributional pattern, and represents the most parsimonious interpretation of the available data.

Acknowledgements

Jérôme Fuchs and Patrick Boussès, both at MNHN, are thanked for their help during the preparation of this reply. Paul Sweet at AMNH was of great assistance in supplying photographs of tutus and veneratus. Laurent Raty helped us to decipher the French word tamatioïde.

References:

1.

Atkinson, I. A. E. 1973. Spread of the ship rat (Rattus r. rattus L.) in New Zealand. J. Roy. Soc. New Zealand 3: 457–472. Google Scholar

2.

Atkinson, I. A. E. 1985. The spread of commensal species of Rattus to oceanic islands and their effects on island avifaunas. Pp. 35–81 in Moors, P. J. (ed.) Conservation of island birds. International Council for Bird Preservation, Cambridge, UK. Google Scholar

3.

Atkinson, I. A. E. & Atkinson, T. J. 2000. Land vertebrates as invasive species on islands served by the South Pacific Regional Environment Programme. Pp. 19–84 in Sherley, G. (ed.) Invasive species in the Pacific: a technical review and draft regional strategy. South Pacific Regional Environment Programme (SPREP), Apia, Samoa. Google Scholar

4.

Boessenkool, S., Star, B., Scofield, R. P., Seddon, P. J. & Waters, J. M. 2009. Lost in translation or deliberate falsification? Genetic analyses reveal erroneous museum data for historic penguin specimens. Proc. Roy. Soc. Lond. Ser. B 277: 1057–1064. Google Scholar

5.

Cibois, A. & Thibault, J.-C. 2009. Combien d'espèces de martins-chasseurs existe-t-il à Tahiti? Te Manu 65: 16–18. Google Scholar

6.

Clements, J. F., Schulenberg, T. S., Iliff, M. J., Roberson, D., Fredericks, T. A., Sullivan, B. L. & Wood, C. L. 2016. The eBird / Clements checklist of birds of the world: v. 2016.  www.birds.cornell.edu/ clementschecklist/download/Google Scholar

7.

Collar, N. J. 2000. Collecting and conservation: cause and effect. Bird Conserv. Intern. 10: 1–15. Google Scholar

8.

Cretella, M. 2010. The complete collation and dating of the section Zoologie of the Coquille voyage. Boll. Malacologico 46: 83–103. Google Scholar

9.

Dickinson, E. C. & Remsen, J. V. (eds.) 2013. The Howard & Moore complete checklist of the birds of the world , vol. 1. Fourth edn. Aves Press, Eastbourne. Google Scholar

10.

Finsch, O. & Hartlaub, G. 1867. Beitrag zur Fauna Centralpolynesiens. Ornithologie der Viti-, Samoa- und Tonga-Inseln. H. W. Schmidt, Halle. Google Scholar

11.

Fry, C. H., Fry, K. & Harris, A. 1992. Kingfishers, bee-eaters and rollers. Christopher Helm, London. Google Scholar

12.

Gill, F. & Donsker, D. 2017. IOC world bird list (v. 7.2). https://doi.org/10.14344/ioc.ml.7.2. Google Scholar

13.

Gray, G. R. 1859. Catalogue of the birds of the tropical islands of the Pacific. Trustees of the Brit. Mus., London. Google Scholar

14.

Hedrich, H. J. 2006. Taxonomy and stocks and strains. Pp. 71–92 in Suckow, M. A., Weisbroth, S. H. & Franklin, C. L. (eds.) The laboratory rat. Second edn. Academic Press, Toronto. Google Scholar

15.

Hembry, D. H. & Balukjian, B. 2016. Molecular phylogeography of the Society Islands (Tahiti; South Pacific) reveals departures from hotspot archipelago models. J. Biogeogr. 43: 1372–1387. Google Scholar

16.

Holyoak, D. T. 1974. Les oiseaux des îles de la Société. Part 2. L'Oiseau et R.F.O. 44: 153–184. Google Scholar

17.

Holyoak, D. T. & Thibault, J.-C. 1984. Contribution à l'étude des oiseaux de Polynésie orientale. Mém. Mus. Natl. Hist. Nat. Paris 127: 1–209. Google Scholar

18.

del Hoyo, J. & Collar, N. J. 2014. HBW and BirdLife International illustrated checklist of the birds of the world , vol. 1. Lynx Edicions, Barcelona. Google Scholar

19.

Jansen, J. J. F. J. 2014. Towards the resolution of long-standing issues regarding the birds collected during the Baudin expedition to Australia and Timor (1800–1804): a review of original documents reveals new details about collectors, donors, numbers and disbursement. J. Natl. Mus. (Prague), Nat. Hist. Ser. 183: 5–18. Google Scholar

20.

Jansen, J. J. F. J. & van der Vliet, R. E. 2015. The chequered history of the Chattering Kingfisher Todiramphus tutus in Tahiti. I: type specimens. Bull. Brit. Orn. Cl. 135: 108–120. Google Scholar

21.

Lee, M. & Holyoak, D. T. 2017. ‘The chequered history of Chattering Kingfisher Todiramphus tutus on Tahiti’: a response. Bull. Brit. Orn. Cl. 137: 211–217. Google Scholar

22.

Lesson, R. P. 1827. Description du genre Todiramphe et de deux espèces d'oiseaux qui le composent. Mém. Soc. Hist. Nat. Paris (2)3: 419–421, pl. 11–12. Google Scholar

23.

Monnet, C., Thibault, J.-C. & Varney, A. 1993. Stability and changes during the twentieth century in the breeding landbirds of Tahiti (Polynesia). Bird Conserv. Intern. 3: 261–280. Google Scholar

24.

Peters, J. L. 1955. Check-list of the birds of the world , vol. 5. Mus. Comp. Zool., Harvard Univ., Cambridge, MA. Google Scholar

25.

Peterson, A. T., Navarro-Sigüenza, A. G. & Pereira, R. S. 2004. Detecting errors in biodiversity data based on collectors’ itineraries. Bull. Brit. Orn. Cl. 124: 143–151. Google Scholar

26.

Pratt, H. D., Bruner, P. L. & Berrett, D. G. 1987. The birds of Hawaii and the tropical Pacific. Princeton Univ. Press. Google Scholar

27.

Rasmussen, P. C. & Prŷs-Jones, R. P. 2003. History vs mystery: the reliability of museum specimen data. Bull. Brit. Orn. Cl. 123A: 66–94. Google Scholar

28.

Sharpe, R. B. 1868. A monograph of the Alcenididae. Privately published, London. Google Scholar

29.

Sharpe, R. B. 1892. Catalogue of the birds in the British Museum , vol. 17. Trustees of the Brit. Mus., London. Google Scholar

30.

Sharpe, R. B. 1906. The history of the collections of the natural history departments of the British Museum. Birds. Trustees of the Brit. Mus., London. Google Scholar

31.

van der Vliet, R. E. & Jansen, J. J. F. J. 2015. The chequered history of the Chattering Kingfisher Todiramphus tutus Tahiti. II: present status. Bull. Brit. Orn. Cl. 135: 121–130. Google Scholar

32.

Voisin, C. & Voisin, J.-F. 2008. List of type specimens of birds in the collection of the Muséum National d'Histoire naturelle (Paris, France). 18. Coraciiformes. J. Natl. Mus. (Prague), Nat. Hist. Ser. 177: 1–25. Google Scholar

33.

Wiglesworth, L. K. 1891. Aves polynesiae: a catalogue of the birds of the Polynesian subregion. R. Friedländer & Sohn, Berlin. Google Scholar

34.

Wilson, S. B. 1907. XVIII — Notes on birds of Tahiti and the Society group. Ibis 49: 373–379. Google Scholar

35.

Ziembicki, M. & Raust, P. 2006. Status and conservation of the Vini lorikeets of French Polynesia. Rep. to Loro Parque Foundation and Conservation des espèces et des populations animales (CEPA). Société d'Ornithologique de Polynésie, Papeete. Google Scholar
© 2017 The Authors; Journal compilation © 2017 British Ornithologists' Club
Roland E. van der Vliet and Justin J. F. J. Jansen "Reply to Lee & Holyoak: how definite are 20th-century reports of Chattering Kingfisher Todiramphus tutus from Tahiti?," Bulletin of the British Ornithologists’ Club 137(3), 218-225, (15 September 2017). https://doi.org/10.25226/bboc.v137i3.2017.a6
Received: 9 June 2017; Published: 15 September 2017
Back to Top