An Inordinate Fondness? The Number, Distributions, and Origins of Diatom Species

The number of extant species of diatoms is estimated here to be at least 30,000 and probably ca. 100,000, by extrapolation from an eclectic sample of genera and species complexes. Available data, although few, indicate that the pseudocryptic species being discovered in many genera are not functionally equivalent. Molecular sequence data show that some diatom species are ubiquitously dispersed. A good case can be made that at least some diatom species and even a few genera are endemics, but many such claims are still weak. The combination of very large species numbers and relatively rapid dispersal in diatoms is inconsistent with some versions of the “ubiquity hypothesis” of protist biogeography, and appears paradoxical. However, population genetic data indicate geographical structure in all the (few) marine and freshwater species that have been examined in detail, sometimes over distances of a few tens of kilometres. The mode of speciation may often be parapatric, in the context of a constantly shifting mosaic of temporarily isolated (meta) populations, but if our “intermediate dispersal hypothesis” is true (that long‐distance dispersal is rare, but not extremely rare), allopatric speciation could also be maximized.

[1]  David G. Mann,et al.  A proposed protocol for nomenclaturally effective DNA barcoding of microalgae , 2009 .

[2]  D. Wujek,et al.  Catalog of the Fossil and Recent Genera and Species of Diatoms and Their Synonyms , 1968 .

[3]  D. Mann Discovering diatom species: is a long history of disagreements about species-level taxonomy now at an end? , 2010 .

[4]  David G. Mann,et al.  The use of partial cox1, rbcL and LSU rDNA sequences for phylogenetics and species identification within the Nitzschia palea species complex (Bacillariophyceae) , 2010 .

[5]  S. Bates,et al.  Pseudo-nitzschia physiological ecology, phylogeny, toxicity, monitoring and impacts on ecosystem health , 2012 .

[6]  F. Hustedt Systematische und ökologische Untersuchungen über die Diatomeen-Flora von Java, Bali und Sumatra, nach dem Material der Deutschen Limnologischen Sunda-Expedition , 1980 .

[7]  E. Theriot Clusters, species concepts, and Morphological Evolution of Diatoms , 1992 .

[8]  K. Evans,et al.  HIGH LEVELS OF GENETIC DIVERSITY AND LOW LEVELS OF GENETIC DIFFERENTIATION IN NORTH SEA PSEUDO‐NITZSCHIA PUNGENS (BACILLARIOPHYCEAE) POPULATIONS 1 , 2005 .

[9]  W. Vyverman,et al.  USING QUANTITATIVE PCR TO DETERMINE THE DISTRIBUTION OF A SEMICRYPTIC BENTHIC DIATOM, NAVICULA PHYLLEPTA (BACILLARIOPHYCEAE) 1 , 2006 .

[10]  W. Vyverman,et al.  The diversity and distribution of diatoms: from cosmopolitanism to narrow endemism , 2008, Biodiversity and Conservation.

[11]  W. Vyverman,et al.  Limits to gene flow in a cosmopolitan marine planktonic diatom , 2010, Proceedings of the National Academy of Sciences.

[12]  J. Neustupa,et al.  Pseudocryptic diversity versus cosmopolitanism in diatoms: a case study on Navicula cryptocephala Kütz. (Bacillariophyceae) and morphologically similar taxa. , 2010, Protist.

[13]  J. Camp,et al.  Morphology, physiology, molecular phylogeny and sexual compatibility of the cryptic Pseudo-nitzschia delicatissima complex (Bacillariophyta), including the description of P. arenysensis sp. nov. , 2009 .

[14]  J. Neustupa,et al.  Ecological variation within traditional diatom morphospecies: diversity of Frustulia rhomboides sensu lato (Bacillariophyceae) in European freshwater habitats , 2012 .

[15]  David G. Mann,et al.  Morphology and identity of some ecologically important small Nitzschia species , 2013 .

[16]  Paul J. Harrison,et al.  Effects of temperature and irradiance on growth of strains belonging to seven Skeletonema species isolated from Dokai Bay, southern Japan , 2011 .

[17]  D. Mann,et al.  Highly differentiated populations of the freshwater diatom Sellaphora capitata suggest limited dispersal and opportunities for allopatric speciation. , 2009, Protist.

[18]  D. Mann,et al.  An assessment of potential diatom "barcode" genes (cox1, rbcL, 18S and ITS rDNA) and their effectiveness in determining relationships in Sellaphora (Bacillariophyta). , 2007, Protist.

[19]  David G. Mann,et al.  The Sellaphora pupula species complex (Bacillariophyceae): morphometric analysis, ultrastructure and mating data provide evidence for five new species , 2004 .

[20]  D. Sarno,et al.  Effects of salinity on the growth rate and morphology of ten Skeletonema strains , 2011 .

[21]  Adriana Zingone,et al.  Global diversity and biogeography of Skeletonema species (bacillariophyta). , 2008, Protist.

[22]  W. Vyverman,et al.  Heterothallic sexual reproduction in the model diatom Cylindrotheca , 2013 .

[23]  G. Ledyard Stebbins,et al.  Variation and Evolution in Plants , 1951 .

[24]  David G. Mann,et al.  Biodiversity, biogeography and conservation of diatoms , 1996 .

[25]  D. Mann,et al.  Morphology and formal description of Sellaphora bisexualis sp. nov. (Bacillariophyta). , 2009 .

[26]  D. Mann,et al.  Ecological variation within Sellaphora species complexes (Bacillariophyceae): specialists or generalists? , 2008, Hydrobiologia.

[27]  Kimon K. Moschandreou,et al.  Inter- and intra-specific diversity of Pseudo-nitzschia (Bacillariophyceae) in the northeastern Mediterranean , 2012 .

[28]  H. LANGE-BERTALOT,et al.  Eunotia and some related genera , 2011 .

[29]  D. Mann,et al.  13 Molecular genetics and the neglected art of diatomics , 2007 .

[30]  D. Mann,et al.  Congruence of morphological, reproductive and ITS rDNA sequence data in some Australasian Eunotia bilunaris (Bacillariophyta) , 2007 .

[31]  W. Vyverman,et al.  Molecular evidence for distinct Antarctic lineages in the cosmopolitan terrestrial diatoms Pinnularia borealis and Hantzschia amphioxys. , 2013, Protist.

[32]  F. Leliaert,et al.  Tetraselmis indica (Chlorodendrophyceae, Chlorophyta), a new species isolated from salt pans in Goa, India , 2013 .

[33]  D. Mann,et al.  Molecular species discovery in the diatom Sellaphora and its congruence with mating trials , 2013 .

[34]  W. Vyverman,et al.  Tolerance of benthic diatoms from temperate aquatic and terrestrial habitats to experimental desiccation and temperature stress , 2010 .

[35]  William F. Gregory XXXI.—On New Forms of Marine Diatomaceæ, found in the Firth of Clyde and in Loch Fine , 1857, Transactions of the Royal Society of Edinburgh.

[36]  Koen Sabbe,et al.  Morphological, genetic and mating diversity within the widespread bioindicator Nitzschia palea (Bacillariophyceae) , 2009 .

[37]  D. Mann,et al.  Genetic divergence and reproductive barriers among morphologically heterogeneous sympatric clones of Eunotia bilunaris sensu lato (Bacillariophyta). , 2008, Protist.

[38]  M. Guiry,et al.  HOW MANY SPECIES OF ALGAE ARE THERE? , 2012, Journal of phycology.

[39]  David G. Mann,et al.  The species concept in diatoms , 1999 .

[40]  K. J. Clarke,et al.  Ubiquitous dispersal of microbial species , 1999, Nature.

[41]  Koen Sabbe,et al.  ECOLOGICAL DIFFERENTIATION BETWEEN SYMPATRIC PSEUDOCRYPTIC SPECIES IN THE ESTUARINE BENTHIC DIATOM NAVICULA PHYLLEPTA (BACILLARIOPHYCEAE) 1 , 2009, Journal of phycology.

[42]  J. Brodie,et al.  Unravelling the algae: the past, present, and future of algal systematics , 2007 .

[43]  D. Mann,et al.  TAXONOMY, LIFE CYCLE, AND AUXOSPORULATION OF NITZSCHIA FONTICOLA (BACILLARIOPHYTA) 1 , 2006 .

[44]  F. Hustedt Süßwasser-Diatomeen des indomalayischen Archipels und der Hawaii-Inseln. Nach dem Material der Wallacea-Expedition , 1942 .

[45]  G. E. Hutchinson,et al.  Homage to Santa Rosalia or Why Are There So Many Kinds of Animals? , 1959, The American Naturalist.

[46]  M. Kelly,et al.  THE UNMASKING OF A SUB-ANTARCTIC ENDEMIC: PSAMMOTHIDIUM ABUNDANS (MANGUIN) BUKHTIYAROVA ET ROUND IN EUROPEAN RIVERS , 2008 .

[47]  R. Flower,et al.  Historical processes constrain patterns in global diatom diversity. , 2007, Ecology.

[48]  S. Droop Morphological variation in Diploneis smithii and D. fusca (Bacillariophyceae) , 1994 .

[49]  W. Vyverman,et al.  Lack of population genetic structuring in the marine planktonic diatom Pseudo-nitzschia pungens (Bacillariophyceae) in a heterogeneous area in the Southern Bight of the North Sea , 2009 .

[50]  D. Mann,et al.  DNA barcoding for species identification and discovery in diatoms , 2010 .

[51]  Kevin de Queiroz,et al.  Species Concepts and Species Delimitation , 2007 .

[52]  Dietrich Werner,et al.  The Biology of diatoms , 1977 .

[53]  S. Maberly,et al.  Hypothesis: the rate and scale of dispersal of freshwater diatom species is a function of their global abundance. , 2002, Protist.

[54]  D. Mann,et al.  Paedogamy and auxosporulation in Nitzschia sect. Lanceolatae (Bacillariophyta) , 2013 .

[55]  S. Droop Diploneis sejuncta (Bacillariophyta ) and some new species from an ancient lineage , 1998 .

[56]  D. Mann,et al.  Experimental studies on sexual reproduction in diatoms. , 2004, International review of cytology.

[57]  D. Sarno,et al.  Functional diversity in cryptic species of Chaetoceros socialis Lauder (Bacillariophyceae) , 2012 .

[58]  W. Vyverman,et al.  Tolerance of resting cells of freshwater and terrestrial benthic diatoms to experimental desiccation and freezing is habitat-dependent , 2013 .

[59]  K. de Queiroz,et al.  Species concepts and species delimitation. , 2007, Systematic biology.

[60]  T. Fenchel,et al.  Protist diversity is different? , 2004, Protist.

[61]  Victor A Chepurnov,et al.  A MOLECULAR SYSTEMATIC APPROACH TO EXPLORE DIVERSITY WITHIN THE SELLAPHORA PUPULA SPECIES COMPLEX (BACILLARIOPHYTA) 1 , 2008, Journal of phycology.

[62]  A. Zingone,et al.  Metabolic fingerprinting reveals differences between northern and southern strains of the cryptic diatom Chaetoceros socialis , 2012 .

[63]  K. Karino,et al.  Developmental plasticity and genotype–environment interactions influence valve morphology in the Cyclotella meneghiniana species complex (Bacillariophyceae) , 2012 .

[64]  D. Mann,et al.  Effects of salinity on growth and on valve morphology of five estuarine diatoms , 2011 .