This article is about a group of very similar species. For "species-group names" in zoological nomenclature, see ICZN Code, for individuals of different species grouping together, see Mutualism (biology).
"Cryptic species" redirects here. For the principles of hiding, see Crypsis, and for a supposed creature whose existence is not scientifically recognized, see Cryptid.
In biology, a species complex is a group of two or more species very similar in appearance, where exact boundaries between them are often unclear. More narrow terms sometimes used synonymously are cryptic species, sibling species, or species flock. As informal taxonomic ranks, species group, species aggregate, and superspecies are in use.
A species complex is typically considered as a group of close, but distinct species. Obviously, the concept is closely tied to the definition of a species, and thus to the species concept one adheres to. Following a morphological species concept, the members of a species complex although being very similar overall, will show some slight differences in appearance, while the biological species concept requires reproductive isolation to accept species as distinct.
A more restricted use applies the term to close species between which hybridisation occurred or is occurring, leading to intermediate forms and blurred species boundaries.
The following terms are sometimes used as synonyms for a species complex, but apply in general to more narrow concepts:
Cryptic species: This describes "distinct species that are erroneously classified (and hidden) under one species name". More generally, the term is often applied when species, even if known to be distinct, cannot be reliably distinguished based on their morphology.
Sibling species: Also "aphanic species", this term was initially used with the same meaning as cryptic species, but later authors emphasized the common phylogenetic origin. A recent article defines sibling species as "cryptic sister species", meaning "two species that are the closest relative of each other and have not been distinguished from one another taxonomically".
Species flock: Also "species swarm", this refers to "a monophyletic group of closely related species all living in the same ecosystem". Conversely, the term has also been applied very broadly to a group of closely related species than can be variable and widespread.
In the nomenclature codes of botany, zoology, and bacteriology, no taxonomic ranks are defined at the level between subgenera and species, although additional ranks are allowed in the botanical code as long as confusion is avoided. Defining species groups is sometimes a convenient, informal way of subdividing well-defined genera with a large number of species.
The term superspecies has sometimes been used as an informal rank to refer to a species complex around one "representative" species. It was popularized by Bernhard Rensch and later Ernst Mayr, with the initial requirement that species forming a superspecies must have allopatric distributions. For the component species of a superspecies, allospecies was proposed.
Species aggregate has likewise been used, with the previous species collectiva introduced by Adolf Engler at the beginning of the 20th century, and alternative terms including conspecies and grex. This has been applied especially to plant taxa in which polyploidy and apomixis are prevalent. The components of a species aggregate have been called segregates or microspecies.
When a species is assumed to actually represent a species complex, this is often indicated by the abbreviation "agg." (for "aggregate") after the binomial species name. Another possibility is the use of sensu lato, abbreviated as "s.l."
Distinguishing close species within a complex requires the study of often very small differences. Morphological differences may be minute and only visible using adapted methods, such as microscopy. However, distinct species may sometimes have no morphological differences. In these cases, other characters, e.g. in the species' life history, behavior, physiology, or karyology can be explored. As an example, territorial songs are indicative of species in the treecreepers, a bird genus with little morphological differences. Mating tests are common in some groups such as fungi to confirm the reproductive isolation of two species.
A species complex typically forms a monophyletic group that has diversified rather recently, as shown by the short branches between the species A-E (blue box) in this phylogenetic tree.
Species forming a complex have typically diverged very recently from each other, allowing in some cases to retrace the process of speciation. Species with differentiated populations such as ring species are sometimes seen as an example of early, ongoing speciation, i.e. a species complex in formation. Nevertheless, similar but distinct species have sometimes been isolated for a long time without evolving differences, a phenomenon called "morphological stasis".
Stabilizing selection has been invoked as a force maintaining similarity in species complexes, especially when adaptation to special environments, such as a host in the case of symbionts, or extreme environments, constrains possible directions of evolution: In such cases, strongly divergent selection is not to be expected. Also, asexual reproduction, such as through apomixis in plants, may separate lineages without producing a great degree of morphological differentiation.
In regards to whether or not members of a species group share a range, sources differ. A source from Iowa State University Department of Agronomy says that members of a species group usually have partially overlapping ranges but do not interbreed with each other.A Dictionary of Zoology (Oxford University Press 1999) describes a species group as complex of related species that exist allopatrically and explains that this "grouping can often be supported by experimental crosses in which only certain pairs of species will produce hybrids." The examples given below may support both uses of the term "species group."
Often such complexes only become evident when a new species is introduced into the system, breaking down existing species barriers. An example is the introduction of the Spanish slug in Northern Europe, where interbreeding with the local black slug and red slug, traditionally considered clearly separate species that did not interbreed, shows they may be actually just subspecies of the same species.
Where closely related species coexist in sympatry, it is often a particular challenge to understand how these similar species persist without outcompeting each other. Niche partitioning is one mechanism invoked to explain this. Studies in some species complexes indeed suggest that species divergence went in par with ecological differentiation, with species now preferring different microhabitats.
The fly agaric comprises several cryptic species with different ranges and habitats.
It has been suggested that cryptic species complexes are very common in the marine environment. Although this suggestion came before the detailed analysis of many systems using DNA sequence data, it has been proven correct. The increased use of DNA sequence in the investigation of organismal diversity (also called Phylogeography and DNA barcoding) has led to the discovery of a great many cryptic species complexes in all habitats. In the marine bryozoan Celleporella hyalina, detailed morphological analyses and mating compatibility tests between the isolates identified by DNA sequence analysis were used to confirm that these groups consisted of more than 10 ecologically distinct species that had been diverging for many million years.
Evidence from the identification of cryptic species has led some[who?] to conclude that current estimates of global species richness are too low. For example, mitochondrial DNA research published in January 2008 suggests that there are at least 11 genetically distinct populations of giraffes. Similar methods also found that the Amazonian frog Eleutherodactylus ockendeni is actually at least 3 different species that diverged over 5 million years ago.
Species complexes as vectors and pathogens: The A. gambiae mosquito complex contains malaria vector and non-vector species;wilt-causing bacteria in the R. solanacearum complex have distinct geographic ranges.
Pests, species causing diseases, and their vectors, have direct importance for humans. When they are found to be cryptic species complexes, the ecology and virulence of each of these species needs to be reevaluated to devise appopriate control strategies. An example are cryptic species in the malaria vector Anopheles, or the fungi causing cryptococcosis.
When a species is found to comprise in fact several phylogenetically distinct species, each of these typically have smaller distribution ranges and population sizes than reckoned before. These different species can also differ in their ecology, e.g. having different breeding strategies or habitat requirements, which has to be taken into account for appropriate management.
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