PubMed · 12979218
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J EYME. 1952-02-04. [Spermatogenesis in mosses].. https://pubmed.ncbi.nlm.nih.gov/12979218/
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Bryophytes dominate the carbon and nitrogen cycling of many poorly drained terrestrial ecosystems and are important in the vegetation-atmosphere exchange of carbon and water, yet few studies have estimated their leaf area at the stand scale. This study quantified the bryophyte-specific leaf area (SLA) and leaf area index (LAI) in a group of different-aged boreal forest stands in well and poorly drained soils. Species-specific SLA (for three feather mosses, four Sphagnum spp. and Aulacomnium palustre mixed with Tomentypnum nitens) was assessed by determining the projected area using a flatbed scanner and cross-sectional geometry using a dissecting microscope. The hemisurface leaf area was computed as the product of SLA and live biomass and was scaled by coverage data collected at all stands. Pleurozium schreberi dominated the spatial coverage, biomass and leaf area in the well-drained stands, particularly the oldest, while S. fuscum and A. palustre were important in the poorly drained stands. Live moss biomass ranged from 47 to 230 g m(-2) in the well-drained stands dominated by feather mosses and from 102 to 228 g m(-2) in the poorly drained stands. Bryophyte SLA varied between 135 and 473 cm(2) g(-1), for A. palustre and S. capillifolium, respectively. SLA was strongly and significantly affected by bryophyte species, but did not vary between stands; in general, there was no significant difference between the SLA of non-Sphagnum mosses. Bryophyte LAI increased with stand age, peaking at 3.1 and 3.7 in the well and poorly drained stands, respectively; this represented approximately 40% of the overstory LAI in the well-drained stands and 100-1,000% in the poorly drained stands, underscoring the important role bryophytes play in the water and carbon budgets of these boreal forests.
Twenty samples of the moss species Hylocomium splendens and Pleurozium schreberi were collected at 10 sites of the Holy Cross Mountains (south-central Poland) and analyzed for 16 polycyclic aromatic hydrocarbons and 33 elements. The ring sequence of PAHs in the moss samples is: 4 (92-1040 ng x g(-1))>3 and 5 (21-272 ng x g(-1))>6 (<5-131 ng x g(-1)). H. splendens accumulates PAHs more effectively than P. schreberi, and therefore the former may be regarded as a better bioindicator of PAHs. No correlation was found between concentrations of PAHs and elements. However, both H. splendens and P. schreberi shows different bioaccumulative capabilities depending on the plant communities. The mosses growing in the dry pine forest Cladonio-Pinetum reveal higher levels of Fe, Na, Sr, Ti, Cr, Mo, Ni, V and higher mean concentrations of summation operator16 PAHs, whereas those from the continental coniferous forest Querco roboris-Pinetum are highlighted by elevated levels of B, Ca, K, Mg, Mn, P, Rb and Sb and lower mean concentrations of summation operator16 PAHs. These differences seem to be brought about by a higher biodiversity of the second forest type and its higher productivity that favors more effective cycling of elements.
A sensitive method for the determination of long-chain fatty acids (LCFAs) (>C20) using 1-[2-(p-toluenesulfonate)-ethyl]-2-phenylimidazole-[4,5-f]-9,10-phenanthrene (TSPP) as tagging reagent with fluorescence detection and identification with post-column APCI/MS has been developed. The LCFAs in bryophyte plant samples were obtained based on distillation extraction with 1:1 (v/v) chloroform/methanol as extracting solvent. TSPP could easily and quickly label LCFAs at 90 degrees C in the presence of K2CO3 catalyst in DMF. Eleven free LCFAs from the extracts of bryophyte plants were sensitively determined. Maximal labeling yields close to 100% were observed with a five-fold excess of molar reagent. Separation of the derivatized fatty acids exhibited a good baseline resolution in combination with a gradient elution on a reversed-phase Eclipse XDB-C8 column. Calculated detection limits from 1.0 pmol injection, at a signal-to-noise ratio of 3, were 26.19-76.67 fmol. Excellent linear responses were observed with coefficients of >0.9996. Good compositional data were obtained from the analysis of the extracted LCFAs containing as little as 0.2g of bryophyte plant samples. Therefore, the facile TSPP derivatization coupled with HPLC/APCI/MS analysis allowed the development of a highly sensitive method for the quantitation of trace levels of LCFAs from biological and natural environmental samples.