Content uploaded by Spartaco Gippoliti
Author content
All content in this area was uploaded by Spartaco Gippoliti on Nov 10, 2020
Content may be subject to copyright.
COMMENT
Do biodiversity hotspots match with rodent conservation
hotspots?
Giovanni Amori •Spartaco Gippoliti •Luca Luiselli
Received: 12 January 2011 / Accepted: 24 July 2011 / Published online: 12 August 2011
ÓSpringer Science+Business Media B.V. 2011
Abstract Biodiversity hotspots are used widely to designate priority regions for
conservation efforts. It is unknown, however, whether the current network of hotspots
adequately represents globally threatened taxonomic diversity for whole plant and
animal groups. We used a mammalian group traditionally neglected in terms of con-
servation efforts, the rodents, in order to test whether biodiversity hotspots match the
current distribution of threatened taxa (genera and species). Significantly higher num-
bers of threatened rodent genera and species fell within biodiversity hotspots; none-
theless over 25% of the total threatened genera and species did not occur in any
biodiversity hotspot. This was particularly true for the Australian region, where 100%
of the threatened genera and species fell outside biodiversity hotspots, with many
threatened taxa found in Papua-New Guinea. We suggest to officially including Papua
New Guinea among biodiversity hotspots for rodents, and also the steppic/semidesert
areas of central Asia.
Keywords Biodiversity hotspots Rodentia Conservation Papua New Guinea
Introduction
In modern conservation biology, the concept of biodiversity hotspots has been used for
designating the biologically richest, most diverse in terms of endemic taxa, and most
threatened reservoirs of plant and animal life on earth (e.g., Myers 1998; Myers et al. 2000).
Indeed, primary natural habitats are reduced to 10% of their original coverage in the
G. Amori (&)
CNR, Institute of Ecosystem Studies, Viale dell’Universita
`32, 00185 Rome, Italy
e-mail: giovanni.amori@uniroma1.it
S. Gippoliti
Italian Institute of Anthropology, Piazzale Aldo Moro 5, 00185 Rome, Italy
L. Luiselli
Centre of Environmental Studies, Demetra s.r.l., via Olona 7, 00198 Rome, Italy
123
Biodivers Conserv (2011) 20:3693–3700
DOI 10.1007/s10531-011-0131-z
biodiversity hotspots (Myers et al. 2000). A total of 25 hotspots have been identified (Myers
et al. 2000), with their number subsequently revised by Stuart et al. (2004). These regions
include a majority of the threatened fauna and flora worldwide (Myers et al. 2000; Stuart
et al. 2004). The concept of biodiversity hotspots has become critical also for funding in
conservation biology research (for instance by such agencies as the World Bank;
see http://www.biodiversityhotspots.org/xp/hotspots/afromontane/pages/conservation.aspx;
accessed on 07 January 2011) (Bode et al. 2008; Bottrill et al. 2008; Carwardine et al. 2008).
Because biodiversity hotspots were selected on the basis of a few taxonomic groups (e.g.,
butterflies, 35% of all vertebrate species, 44% of vascular plants; see Myers 1998; Myers
et al. 2000), it is possible that, despite successive integrations (Stuart et al. 2004), some
groups are under-represented in terms of threatened genera/species within biodiversity
hotspots. This may be especially true for those taxa that traditionally have been overlooked
by conservation biology literature. Among mammals, rodents are the most numerous in
terms of species richness, but the least known in terms of conservation issues (Amori and
Gippoliti 2000,2001,2003).
In this study, we analyze whether the biodiversity hotspots defined as in Myers et al.
(2000) and Stuart et al. (2004) sufficiently encompass the whole of the threatened rodent
diversity of the world (Amori and Gippoliti 2001). We explore this issue both globally and
regionally.
Materials and methods
Biodiversity hotspots were selected according to Myers et al. (2000) and Stuart et al.
(2004); threatened rodent diversity was evaluated at both genus and species levels, using
the database in Amori and Gippoliti (2001). According to this database, we considered
‘threatened’ each genus having all extant species listed as Critically Endangered, Endan-
gered or Vulnerable level by IUCN (2010). Rodent nomenclature follows Wilson and
Reeder (2005).
For each zoogeographical region (i.e., Nearctic, Neotropical, Palearctic, Afrotropical,
Oriental, and Australian (=Australasian)), we considered whether the distribution range of
each threatened genus coincided, at least partially, with one or more of the biodiversity
hotspots. If so, we considered that a given threatened genus was covered by at least one
biodiversity hotspot; otherwise, that threatened genus was considered disjunct from hot-
spots. Chi-squared tests were used to explore whether, either globally or regionally, the
frequency of threatened genera inside and outside biodiversity hotspots differed signifi-
cantly. Alpha was assessed at 5%.
Results
The list of threatened genera falling within biodiversity hotspots is given in Table 1,
whereas the list of those falling outside biodiversity hotspots is given in Table 2. Despite a
statistically greater number of threatened genera within biodiversity hotspots (v
2
=11.57,
df =1, P\0.00067), 28.6% of the total threatened genera (n=63) did not co-occur with
any biodiversity hotspot (Fig. 1a). Similar trends were observed for threatened species:
significantly more species were covered by biodiversity hotspots (v
2
=15.69, df =1,
3694 Biodivers Conserv (2011) 20:3693–3700
123
Table 1 List of threatened rodent genera included inside biodiversity hotspots as defined by Myers et al.
(2000) and Stuart et al. (2004)
Region Hotspot Threatened
genera
List of the
threatened
genera
Number of
species in
each genus
Family
Nearctic California floristic province 0 0
Neotropical MesoAmerica 1 Zygogeomys 1 Geomyidae
Caribbean Podomys 5 Muridae
Mesocapromys 4 Capromyidae
Isolobodon 1 Capromyidae
Plagiodontia 1 Capromyidae
Geocapromys 2 Capromyidae
513
Choco/Darien west Equador Anotomys 1 Muridae
Scolomys 2 Cricetidae
23
Tropical Andes 1 Dinomys 1 Dinomyidae
Brazil’s Cerrado 0 0
Brazil’s Atlantic Forest Abrawayaomys 1 Muridae
Chaetomys 1 Echimyidae
Phaenomys 1 Muridae
Rhagomys 1 Muridae
44
Central Chile 1 Chinchilla 2 Chinchillidae
Palearctic Mediterranean Basin 1 Myomimus 3 Gliridae
Caucasus 1 Selevinia 1 Gliridae
Afrotropical West African forests Leimacomys 1 Muridae
Lamottemys 1 Muridae
Myosciurus 1 Sciuridae
33
Eastern Arc 1 Pedetes 2 Pedetidae
Madagascar Gymnuromys 1 Nesomyidae
Hypogeomys 1 Nesomyidae
22
Succulent Karoo 0 0 0
Cape Florisitc province 1 Mystromys 1 Nesomyidae
Horn of Africa Muriculus 1 Muridae
Horn of Africa Megadendromus 1 Muridae
Horn of Africa Ammodillus 1 Muridae
Horn of Africa Nilopegamys 1 Muridae
Oriental Western Ghats and
Sri Lanka
000
Indo-Burma Biswamoyopterus 1 Sciuridae
Biodivers Conserv (2011) 20:3693–3700 3695
123
P\0.0001), but a considerable portion of the total (29.3%, n=92) did not coincide with
any biodiversity hotspot (Fig. 1b).
Exploring these issues by zoogeographical region, a complex pattern appears for
both threatened genera (Fig. 2a) and species (Fig. 2b). Significantly more threatened
genera (v
2
=31.5, df =5, P\0.0001) and more species (v
2
=46.00, df =5,
P\0.0001) were covered by biodiversity hotspots. However, closer inspection of the
data revealed that for both genera and species the biodiversity hotspots included the
great majority of threatened rodent taxa in four zoogeographical region, but not in
the Australian region where 100% of threatened taxa were outside biodiversity hotspots
(Fig. 2).
Table 1 continued
Region Hotspot Threatened
genera
List of the
threatened
genera
Number of
species in
each genus
Family
Trogopterus 1 Sciuridae
Vernaya 1 Muridae
33
South-Central China Cardiocranius 1 Dipodidae
Eozapus 1 Dipodidae
Euchoreutes 1 Dipodidae
Chetocauda 1 Gliridae
44
Sundaland 0 0 0
Wallacea Eropeplus 1 Muridae
Hyosciurus 2 Sciuridae
Melasmothrix 1 Muridae
Tateomys 2 Muridae
Komodomys 1 Muridae
Paulamys 1 Muridae
Papagomys 3 Muridae
711
Philippines Abditomys 1 Muridae
Anonymomys 1 Muridae
Archboldomys 2 Muridae
Crateromys 4 Muridae
Limnomys 1 Muridae
Palawanomys 1 Muridae
Triphomys 1 Muridae
711
Australian Polynesia/Micronesia 0 0 0
New Caledonia 0 0 0
South-west Australia 0 0 0
New Zealand 0 0 0
3696 Biodivers Conserv (2011) 20:3693–3700
123
Discussion
Our study provides evidence that biodiversity hotspots fail to capture all of the threa-
tened rodent diversity throughout the world, and that, although this is a somewhat minor
point for Neotropical, Palearctic, Afrotropical and Oriental regions (because indeed the
great majority of threatened taxa fall into biodiversity hotspots), the same is not true as
for the Australian region. Surprisingly, all threatened taxa of this region fell outside
biodiversity hotspots, thus showing that the current designation of Australian region
hotspots is totally inadequate for highlighting threatened rodent diversity. This is due to
the fact that most of the Australian-region threatened rodents inhabit the Papua-New
Guinea forests (e.g., Macruromys, Mayermys, Microhydromys, Neohydromys, and
Pseudohydromys; see Amori and Gippoliti, 2001), which are not listed among the
Table 2 List of threatened rodent genera with range falling outside the biodiversity hotspots as defined by
Myers et al. (2000) and Stuart et al. (2004)
Region Outside hotspots Threatened
genera
List of the
threatened
genera
Number of
species in
each genus
Family
Nearctic 0 0 0 0 0
Neotropical NE Argentina, Brazil,
Bolivia
Kunsia 2 Muridae
Argentina (Mendoza
province)
Tympanoctomys 1 Octodontidae
Galapagos islands Nesoryzomys 2 Muridae
35
Palearctic Japan 1 Glirulus 1 Gliridae
Afrotropical Senegambia, Mali,
Mauritania
1Felovia 1 Ctenodactyilidae
11
Oriental Pakistan, India Eupetaurus 1 Sciuridae
Okinawa, Amami,
Tokuno-shima
islands
Tokudaia 3 Muridae
24
Australian Papua-New Guinea Macruromys 1 Muridae
Papua-New Guinea Mayermys 1 Muridae
Papua-New Guinea Microhydromys 2 Muridae
Papua-New Guinea Neohydromys 1 Muridae
Papua-New Guinea Pseudohydromys 2 Muridae
Solomon Islands Solomys 4 Muridae
North and Eastern
Australia
Xeromys 1 Muridae
Franklin Islands Leporillus 1 Muridae
813
Biodivers Conserv (2011) 20:3693–3700 3697
123
biodiversity hotspots (Myers et al. 2000; Stuart et al. 2004). Recent overviews of
worldwide distribution of threatened mammals (Schipper et al. 2008) and even of
threatened vertebrates (Hoffmann et al. 2010) showed a better match with designated
biodiversity hotspots (Schipper et al. 2008) than in our rodent case. Thus, rodents seem
to represent a peculiar case for conservation biologists, especially because of the
unusually high number of endemic genera on islands of the Australian region, particu-
larly New Guinean islands (Amori et al. 2008). We therefore suggest officially including
Papua New Guinea among biodiversity hotspots at least for rodent conservation research.
Otherwise, it is possible that conservation efforts may be overlooked for the threatened
rodent fauna of this region, with potentially negative consequences for the continued
survival of these animals in the coming decades. In addition, we suggest using the
threatened rodent genera currently excluded from biodiversity hotspots in order to
identify and designate new hotspots for conservation. In this regard, attention should be
paid also to the steppe/semidesert areas of central Asia, which in part enter only
Fig. 1 Comparison of number of genera (a) and number of species (b) of threatened rodents inside and
outside biodiversity hotspots as defined by Myers et al. (2000) and Stuart et al. (2004). For statistical details,
see the text
3698 Biodivers Conserv (2011) 20:3693–3700
123
currently designated hotspots but house important threatened rodent taxa (Amori and
Gippoliti 2001).
References
Amori G, Gippoliti S (2000) What do mammalogists want to save? Ten years of mammalian conservation
biology. Biodiv Conserv 9:785–793
Amori G, Gippoliti S (2001) Identifying priority ecoregions for rodent conservation at the genus level. Oryx
35:158–165
Amori G, Gippoliti S (2003) A higher-taxon approach to rodent conservation priorities for the 21st century.
Anim Biodiv Conserv 26(2):1–18
Amori G, Gippoliti S, Helgen KM (2008) Diversity, distribution, and conservation of endemic island
rodents. Quat Int 182:6–15
Fig. 2 Comparison of number of
genera (a) and number of species
(b) of threatened rodents inside
and outside biodiversity hotspots
as defined by Myers et al. (2000)
and Stuart et al. (2004) divided
by geographic region. For
statistical details, see the text
Biodivers Conserv (2011) 20:3693–3700 3699
123
Bode M, Wilson KA, Brooks TA, Turner WA, Mittermeier RA, McBride MF, Underwood EC, Possingham
HP (2008) Cost-effective global conservation spending is robust to taxonomic group. Proc Nat Acad
Sci USA 105:6498–6501
Bottrill MC, Joseph LN, Carwardine J, Bode M, Cook C, Game ET, Grantham E, Kark S, Linke S,
McDonald-Madden E, Pressey RL, Walker S, Wilson KA, Possingham HP (2008) Is conservation
triage just smart decision making? Trends Ecol Evol 23:649–654
Carwardine J, Wilson KA, Ceballos G, Ehrlich PR, Naidoo R, Iwamura T, Hajkowicz SA, Possingham HP
(2008) Cost-effective priorities for global mammal conservation. Proc Nat Acad Sci USA
105:11446–11450
Hoffmann M et al (2010) The impact of conservation on the status of the world’s vertebrates. Science
330:1503–1509
IUCN (2010) IUCN red list of threatened species. Version 2010.3. http://www.iucnredlist.org
Myers N (1998) Global biodiversity priorities and expanded conservation policies. In: Mace GM, Balmford
A, Ginsberg JR (eds) Conservation in a changing world. Cambridge University Press, Cambridge,
pp 273–285
Myers N, Mittermaier RA, Mittermaier CG, da Fonseca GAB, Kent J (2000) Biodiversity hotspots for
conservation priorities. Nature 403:853–858
Schipper J et al (2008) The status of the world’s land and marine mammals: diversity, threat, and knowl-
edge. Science 322:225–230
Stuart W, Vivero Po JL, Spawls S, Shimelis A, Kelbessa E (2004) Ethiopian highlands. In: Mittermeier RA,
Gil PR, Hoffmann M, Pilgrim J, Brooks T, Mittermeier CG, Lamoreux J, da Fonseca GAB (eds)
Hotspots revisited. CEMEX, Mexico, pp 262–273
Wilson DE, Reeder DR (2005) Mammal species of the world: a taxonomic and geographic reference, 3rd
edn. John Hopkins Univ. Press, Baltimore
3700 Biodivers Conserv (2011) 20:3693–3700
123