Papers of the Week: 25.03 – 01.04.2013

1 04 2013

Another week, another batch of new papers. [OA] indicates open access. Feel free to request a detailed look at any of these.

Important, General Interest:

Near the end of my post on tracheae, I mentioned that it would be interesting to use terrestrial isopods as models for investigating the convergent evolution of tracheal systems in all terrestrial arthropods. This paper echoes my thoughts exactly, and goes on to review what we know of their evolutionary history from their fossil record, relationships, and biogeography.

One of the more influential geologists of the 20th century, Dieter Meischner died last year. This great eulogy gives a glimpse of what he was like as a person and researcher.

Those who know me would know that such a paper title hits all of my muttons:deep animal phylogeny has always been one of my major research interests, and the uncritical acceptance of molecular phylogenetics is one of my major pet peeves. Luckily, I’m not the only one with such tastes. This paper is one of several by Gert Wörheide examining the various inconsistencies present in current deep metazoan molecular phylogenetics, and how to fix them. I heard a lecture by him where he explained all of this, and his work is pretty exciting. This paper is an excellent showcase of how critical it is to properly sample your genes: every gene has a different history, and all those genetic stories do not match up to the species history – which is what we want to elucidate.

Some cyanobacteria are already commonly grown for biotechnological purposes. Spirulina platensis is used to produce phycocyanins used in health foods and cosmetics, while Lingbya majuscule is used to produce immune modulators for pharmaceuticals. Nostoc commune and Aphanizomenon flos-aquae are also important species. The review goes through the classification of Cyanobacteria – a bit of a muddled mess – and explains their potential for all sorts of biotechnological and environmental applications.

If you’ve ever wondered about how widespread venoms are in the animal kingdom, how this hunting style evolves, and how we use this knowledge for medicine, then you want to read this review.

If you’ve ever wondered how advanced the science of analysing trace fossils (ichnology) is, go through this paper.

Placodonts were one of the groups of marine reptiles that radiated in the Triassic, before disappearing at the end of the Triassic. They were most notable for having convergently achieved a turtle-like body plan with a bony covering on their underside. Their teeth were large, flat, and heavily-enameled, hinting at an animal that fed by crushing shells (molluscs, brachiopods). The excellent new fossil described in this paper is of a stem placodont, and shows the transition between the ancestral dentition and the specialised placodont shell-crushing teeth.

I don’t usually care much for these genome-sequencing projects because they don’t tend to target species I consider important – basal ones that hold important clues to decoding phylogenetic history (the giant panda genome may be cool, but it’s useless to all but people who study pandas). This is an example of a good species to sequence: a lamprey, a basal vertebrate, a vestige of the era before vertebrate jaws evolved. Sequencing its genome holds a lot of promise in the quest to flesh out the events that led to the vertebrate radiation that we can’t tell from the fossil record and developmental biology. This paper already dishes out some answers, underlining the importance of innovations in the nervous system.

I can’t say much about the actual results and their implications, I’m just putting this here so you can see just how advanced aDNA research and the associated technology has come. I was very (pleasantly) surprised when I read the title.

Some (me included) say that Chengjiang and other Chinese localities have eclipsed the Burgess Shale by now, but the old quarry still has treasures to yield, as this paper proves. You can find numerous mentions of an undescribed Burgess Shale enteropneust in Simon Conway Morris’s papers (e.g. 1, 2), and I presume this is its long-overdue description.

Another awesome bit of exceptional preservation, also from this week’s Nature, this time from the Chinese Jehol biota: Preservation of ovarian follicles reveals early evolution of avian reproductive behaviour.

Evolutionary medicine, using evolutionary theory to understand the mechanisms behind diseases, is a pretty exciting field, especially in its potential applications to studying cancers (see here, [OA]). This paper argues for investigating cancers with the tools of experimental evolution – putting cancer cells through the rigours of artificial selection to determine how they evolve, adapt, and their ecological limitations, which would then give us insights into how we can curb their proliferation in the body. I support this kind of framework. Read the rest of this entry »





Picocyanobacteria

22 07 2012

This is a guest post by Sophie, written in response to a reader request I am unqualified to fulfil.

Picocyanobateria are cyanobacteria that are less than 3 µm in diameter. Their tiny size makes them significant parts of nutrient cycles: their surface area:volume ratios make them very efficient at nutrient uptake, much more so than larger cells. In lakes, they can contribute up to 80% of the primary production when conditions are suitable (Stockner et al., 2000). In ultraoligotrophic environments, picocyanobacteria dominate, as seen in Lake Superior where picocyanobacteria have radiated in the offshore part of the lake (Ivanikova et al., 2007). Their success in this type of environment is due to advantages in phosphorus use: they can make membranes with less phosphorus than other bacteria (Dyhrman et al., 2009) and they have higher uptake rates of phosphorus due to their ability to hydrolyse dissolved organic phosphorus (Moore et al., 2005).

Picocyanobacteria can be individuals (rods and coccoids) or they can be colonial. Colonies have more than 50 individuals; microcolonies of less than 50 individuals also form. Colonial picocyanobacteria are chroococcal ovoids, rods and cones. The colony can be loose, dense, stalked or filamentous. The arrangement is species-specific, used for identification.

Our knowledge of individual picocyanobacteria is limited. They are in a clade called the Syn/Pro clade with three genera, Synechococcus, Prochlorococcus and Cyanobium. They have higher diversity in marine environments: most strains belong to one lineage and are collected in two genera, Synechococcus and Prochlorococcus (Sánchez-Baracaldo et al., 2005). Freshwater strains are similar to Synechococcus (Weisse, 1993). This summary is not satisfactory because Synechoccus is polyphyletic (Robertson et al., 2001), but this is the state of the art at the moment.

Picocyanobacteria are classified in two types according to the light-harvesting pigment, visible with epifluorescence microscopy: yellow autofluorescing phycoerythrin or red autofluorescing phycocyanin (Wood et al., 1985). The first absorb green light (560 nm), the second absorb orange-red light (625 nm).

Their phylogeny is investigated only with molecular sequences (Steglich et al., 2003). Morphology is useless (Ernst et al., 2003) but molecular sequences are also problematic. Ssu rDNA is not reliable for broad phylogenetic study (Litvaitis, 2002) because it is too conserved. ITS-1 (the spacer between 16S and 23S rDNA) is useful for fingerprinting (Becker et al., 2002) because of its variability, but not good for phylogeny. Pigment genes are tricky because of lateral gene transfer (Dufresne et al., 2008).

Sánchez-Baracaldo et al. (2005) is the largest and most reliable study of cyanobacterial phylogeny, including picocyanobacteria. It is a total evidence analysis with phylogenomics, individual sequences and some morphology. Picocyanobacteria are the second most ancient lineage. By parsimony character reconstruction, the study concludes that the habitus of picocyanobacteria is representative of the first cyanobacteria. It also concludes that cyanobacteria evolved on land or in freshwater, not in the oceans. All together this means that studying freshwater picocyanobacteria is an exciting avenue for future research.

Picocyanobacteria can be health hazards. Their small size allows them to pass through all filters used in water treatment. Toxin-producing (microcystin) picocyanobacteria have been found (Bláha and Marsálek, 1999) and are a potential risk if they bloom in drinking water, as shown by deaths of people in Brazil getting treated with contaminated water (Domingos et al., 1999).

References:

Becker S, Fahrbach M, Börger P & Ernst A. 2002. Quantitative tracing, by Taq nuclease assays, of a Synechococcus ecotype in a highly diversified natural population. Applied Environmental Microbiology 68, 4486-4494.

Bláha L & Marsálek B. 1999. Microcystin production and toxicity of picocyanobacteria as a risk factor for drinking water treatment plants. Algological Studies 92, 95-108.

Domingos P, Rubim RK, Molica RJR, Azevedo SMFO & Carmichael WW. 1999. First report of microcystin production by picoplanktic cyanobacteria isolated from a Northeast Brazilian drinking water supply. Environmental Toxicology 14, 13-35.

Dufresne A, Ostrowski M, Scanlan DJ, Garczarek L, Mazard S, Palenik BP, Paulsen IT, Tandeau de Marsac N, Wincker P, Dossat C, Ferriera S, Johnson J, Post AP, Hess WR, Partensky F. 2008. Unraveling the genomic mosaic of a ubiquitous genus of marine cyanobacteria. Genome Biology 9, R90.

Dyhrman ST, Ammerman JW & van Mooy BAS. 2009. Microbes and the Marine Phosphorus Cycle. Oceanography 20, 110-116.

Ernst A, Becker S, Wollenzien UIA & Postius C. 2003. Ecosystem-dependent adaptive radiations of picocyanobacteria inferred from 16S rRNA and ITS-1 sequence analysis. Microbiology 149, 217-228.

Ivanikova NV, Popels LC, McKay RML & Bullerjahn G. 2007. Lake Superior supports novel clusters of cyanobacterial picoplankton. Applied Environmental Microbiology 73, 4055-4065.

Litvaitis MK. 2002. A molecular test of cyanobacterial phylogeny: inferences from constraint analyses. Hydrobiologia 468, 135-145.

Moore LR, Ostrowski M, Scanlan DJ, Feren K & Sweetsir T. 2005. Ecotypic variation in phosphorus-acquisition mechanisms within marine picocyanobacteria. Aquatic Microbial Ecology 39, 257-269.

Robertson BR, Tezuka N & Watanabe MM. 2001. Phylogenetic analyses of Synechococcus strains (Cyanobacteria) using sequences of 16S rDNA and part of the phycocyanin operon reveal multiple evolutionary lines and reflect phycobilin content. IJSEM 51, 861-871.

Sánchez-Baracaldo P, Hayes PK & Blank CE. 2005. Morphological and habitat evolution in the Cyanobacteria using a compartmentalization approach. Geobiology 3, 145-165.

Steglich C, Post AF & Hess WR. 2003. Analysis of natural populations of Prochlorococcus spp. in the northern Red Sea using phycoerythrin gene sequences. Environmental Microbiology 5, 681-690.

Stockner J, Callieri C & Cronberg G. 2000. Picoplankton and Other Non-Bloom-Forming Cyanobacteria in Lakes. In: Whitton B & Potts M (eds.). The Ecology of Cyanobacteria: Their Diversity in Time and Space.

Weisse T. 1993. Dynamics of autotrophic picoplankton in marine and freshwater ecosystems. Advances in Microbial Ecology 13, 327-370.

Wood AM, Horan PK, Muirhead K, Phinnea DA, Yentsch CM & Waterbury JB. 1985. Discrimination between types of pigments in marine Synechococcus spp. by scanning spectroscopy, epifluorescence microscopy and flow cytometry. Limnology and Oceanography 30, 1303-1315.

Research Blogging necessities :)

P. SÁNCHEZ-BARACALDO, P. K. HAYES, & C. E. BLANK (2005). Morphological and habitat evolution in the Cyanobacteria using a compartmentalization approach Geobiology DOI: 10.1111/j.1472-4669.2005.00050.x
Dufresne A, Ostrowski M, Scanlan DJ, Garczarek L, Mazard S, Palenik BP, Paulsen IT, de Marsac NT, Wincker P, Dossat C, Ferriera S, Johnson J, Post AF, Hess WR, & Partensky F (2008). Unraveling the genomic mosaic of a ubiquitous genus of marine cyanobacteria. Genome biology, 9 (5) PMID: 18507822








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