Cryptic biodiversity in a changing world
© BioMed Central Ltd 2007
Published: 21 December 2007
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© BioMed Central Ltd 2007
Published: 21 December 2007
DNA studies are revealing the extent of hidden, or cryptic, biodiversity. Two new studies challenge paradigms about cryptic biodiversity and highlight the importance of adding a historical and biogeographic dimension to biodiversity research.
Biodiversity, the variety of life, is one of nature's most exuberant manifestations. Scientists have long struggled to understand the evolutionary and ecological processes underlying the origin, distribution and maintenance of biodiversity. This dilemma is faced not only by researchers working in undersampled regions such as tropical rainforests and marine habitats, but also by those studying densely sampled and well characterized temperate systems. The problem is partly generated by the difficulty of detecting and measuring biodiversity solely on the basis of morphological information. Despite the central and unrivalled position of morphology-based taxonomy in biodiversity research, human visual perception will probably never quite suffice to capture natural complexity. A good example of this is the escalating number of DNA-based studies reporting cryptic species [1, 2]. Cryptic, or sibling, species are discrete species that are difficult, or sometimes impossible, to distinguish morphologically and thus have been incorrectly classified as a single taxon. Cryptic species are found from the poles to the Equator and in all major terrestrial and aquatic taxonomic groups [2, 3]. For example, a recent meta-analysis yielded 2,207 articles reporting cryptic species in all metazoan phyla and classes, including 996 new species in insects, 267 in mammals, 151 in fishes and 94 in birds . Similarly, a recent report shows that global biodiversity in protozoa is often cryptic and significantly higher than previously considered .
Analysis of the genetic diversity distributed within 'species' provides a powerful framework for recognizing cryptic species. In this context, historical considerations are important, as the current genetic architectures of many species have been shaped by global climatic fluctuations, environmental gradients and the separation of populations by geographic barriers during the past 3 million years and, to a lesser extent, by more ancient physical processes [5, 6].
Here we discuss two recent studies on cryptic species that take a historical biogeographical perspective on the distribution of genetic diversity in populations, and discuss how such perspectives can inform our knowledge of cryptic biodiversity. In one, published in BMC Biology, a team led by Robert Wayne  details the discovery of at least six cryptic species in the giraffe (Giraffa camelopardalis) based on the geographic distribution of genetic diversity in the giraffe population today, and discusses how conditions in the mid to late Pleistocene might have led to such speciation. In the other, in BMC Evolutionary Biology, Elmer et al.  report previously unsuspected cryptic species within the upper Amazonian leaflitter frog (Eleutherodactylus ockendeni).
Any biogeographic scenario, recent or historical, begins with the process of population differentiation and speciation. Phylogeography, the study of the geographic distribution of genealogical lineages , adds an essential component – time – to the understanding of population structure, reproductive isolation and speciation. Changes over time in the physical and biotic environment of a population lead to demographic variations that are correlated with the structure of population genealogies . As a consequence, phylogeographic studies have the potential for describing the chronology of demographic variation and the reproductive isolation of population units. This is particularly true for surveys that also incorporate intraspecific analyses of migration using sophisticated analytical developments based on the coalescent [9, 10], a theory on the evolutionary history of alleles at genetic loci that allows inferences to be made about the timing and demographic events linked to genealogical processes. This combination of phylogeographic and population-genetic approaches offers an important framework for delineating morphologically cryptic species and for appreciating the processes that have shaped speciation. A valuable extension of this framework is to compare phylogeographic data for multiple co-distributed species to test for historical contingencies and processes that have shaped the diversification of entire biotas. These comparative assessments of regional evolutionary subdivision are important in informing biodiversity discovery and management as they can potentially identify hotspots of biodiversity – regions within which entire communities have been affected by events in Earth's history [6, 11, 12].
The two articles by Brown et al.  and Elmer et al.  highlight important DNA-based discoveries of multiple evolutionary diversifications that challenge paradigms about cryptic biodiversity. The first paradigm is that cryptic species are expected to be rare in megafauna, such as large mammals. This is because many large-bodied mammals can disperse over large distances, a life-history attribute expected to prevent local genetic differentiation and reproductive isolation. In an exemplary study, Brown et al. present a phylogeographic and population genetic analysis in one such mammal, the giraffe . Giraffes are capable of long-distance dispersal and have an extensive range in sub-Saharan Africa. Based on adequate sampling and mitochondrial DNA (mtDNA) and nuclear microsatellite DNA data, Brown et al.  convincingly show that giraffes are composed of at least six distinct lineages. These lineages show levels of evolutionary and genetic distinctiveness consistent with speciation events during the Pleistocene (divergences estimated at between 1.6 million years and 113,000 years ago). In addition, marked genetic subdivision is also apparent within five of the six lineages, yielding a minimum of 11 independent biological units. The authors propose that a combination of increasing aridity, periodic oscillations in wet and dry conditions and regional changes in habitat (for example, the expansion of the 'Mega Kalahari' desert, an area much larger than the present-day Kalahari desert) may have caused fragmentation of giraffe populations during the Pleistocene and divergence within habitat refugia. This agrees with patterns of phylogeographic structure observed in other large African mammals (for example, hartebeest  and zebra ) and illustrates the influence of large-scale climatic fluctuations in the diversification of Africa's biodiversity.
Evidence for contemporary reproductive isolation in the wild comes from comparisons between adjacently distributed giraffe lineages, which share essentially no gene flow despite the absence of dispersal barriers. It is suggested that reproductive isolation might be maintained by climatically driven differences in reproductive timing or by sexually imprinted assortative mating due to differences in coat patterns . According to current taxonomy, giraffes are considered to represent a single species and as such are listed as "Lower Risk" on the IUCN Red List (downloaded 22 October 2007) . Given the endangered status of several of the lineages reported by Brown et al. , giraffes represent another unfortunate example of the negative consequences of neglected taxonomy on conservation management [16, 17].
The other paradigm often mentioned in the literature is that most cryptic species are the product of recent speciation events. Hence, recent speciation would account for the apparent morphological stasis observed in many cryptic species. In a phylogeographic study across eastern Ecuador, Elmer et al.  report previously unsuspected cryptic species within the upper Amazonian leaflitter frog (Eleutherodactylus ockendeni). They used comparison of mtDNA to uncover three highly divergent clades and non-overlapping microsatellite allele sizes as further evidence for reproductive isolation among clades. These clades occur together in some geographic regions without interbreeding, providing strong support that they represent distinct species. Elmer et al.  estimate divergence times between the three clades that date back to late Oligocene and late Miocene (around 24–9 million years ago). These estimates are inconsistent with the idea that climatic cycles of the Quaternary and associated isolation in refugia promoted speciation in this Amazonian frog. In fact, the ancient events of diversification coincide with periods of major and complex geotectonics in the northern Andes during the Miocene . The reports of ancient species in this frog and in other tropical species (for example [18, 19]) imply that species richness in tropical regions has been grossly underdocumented by inventories based on morphology. Notwithstanding a recent suggestion that the proportion of cryptic species in nature is similar across different biogeographic regions , efforts to increase systematic population sampling in tropical rainforests, especially in developing countries, are urgently needed to better document species richness.
Despite its usefulness, the phylogeographic method has serious shortcomings as seems to be the case for any discipline with a historical dimension. Generally, direct genetic evidence about phylogeographic divergence can be gathered only where populations currently exist. Even then, the evidence is temporally fragmented as the result of past population extinctions. These factors can obscure inferences about the prevalence and the spatial scale of cryptic speciation. Obtaining genealogical signal from genetic markers is also challenging if speciation occurred very rapidly, as is often the case in Quaternary biological radiations. Partial solutions to these shortcomings exist, but their effectiveness is dictated by the peculiarities of each biogeographic scenario. Solutions include combining traditional tree-based phylogenetic methods with estimates of demographic parameters that take into account uncertainties in phylogeographic inference [9, 10, 20–22], adding data from extinct populations , adding temporal samples from the same populations [24–27] and adding data from a large number of individuals, localities and fast-evolving genetic markers [21, 26–28].
Justifiably or not, species as established in the current taxonomy are often used as units in biodiversity research and in conservation policy. Thus, investment towards a better resourced morphology-based taxonomy is urgently needed to implement a modern and integrated system to ensure that newly reported cryptic species will be described following their discovery . Human activity has had a greater impact on biodiversity in the past 50 years than at any time in human history, and the rate of change is predicted to continue or to increase . Some of the key drivers affecting the loss of biodiversity worldwide are habitat alteration, climate change, overexploitation and invasive alien species. By improving the way we discover, document and measure biodiversity, we will move towards understanding the consequences of changes in these drivers for biodiversity. For this to become a reality, biodiversity programs need to bring a spatial and temporal perspective to the forefront of their research agenda. Biologists need to dedicate more time to fieldwork (for example, the giraffe study) and expand their intellectual 'confidence zone' to better address temporal axes of diversification (for example, the frog study). The prevalence of cryptic species, even in charismatic and well studied animals like the giraffe, highlights the importance of combining multidisciplinary approaches in order to capture nature's complexity.
We thank the participants of the 'Phylogeography and Coalescence Workshop' (Melbourne, 2007) for constructive discussions and David Briscoe, Rob Fleischer and Rus Hoelzel for comments on the manuscript.