9 research outputs found
Beyond the water column: aquatic hyphomycetes outside their preferred habitat
Aquatic hyphomycetes have adapted to running waters by their uncommon conidial shape, which facilitates dispersal as well as adherence to plant substrata. However, they have been early and regularly reported to occur in a variety of environments other than their preferred habitat (e.g., in lentic freshwaters, brackish and marine environments, in terrestrial niches such as stream banks, dew, canopy waters and tree holes). In addition, several aquatic hyphomycetes have adapted to a mutualistic lifestyle which may involve plant defence, as endophytes in leaves, gymnosperm needles, orchids and terrestrial roots. There are several lines of evidence suggesting that aquatic hyphomycetes survive under terrestrial conditions due to their sexual states. Although exhibiting higher diversity in pristine streams, aquatic hyphomycetes can survive environmental stress, e.g., pollution or river intermittency. They also inhabit ground and hyporheic waters, where they appear to be subjected to both physical and physiological selection. Appropriate methods including molecular ones should provide a more comprehensive view of the occurrence and ecological roles of aquatic hyphomycetes outside their preferred habitat
Microbial Decomposition of Elm and Oak Leaves in a Karst Aquifer
Dry Chinquapin oak (
Quercus macrocarpa
) and American elm (
Ulmus americana
) leaves were placed in four microcosms fed by groundwater springs to monitor changes in dry mass, ash-free dry mass, and microbial activity over a 35-day period. Oxygen microelectrodes were used to measure microbial activity and to estimate millimeter-scale heterogeneity in that activity. Oak leaves lost mass more slowly than elm leaves. Generally, there was a decrease in total dry weight over the first 14 days, after which total dry weight began to increase. However, there were consistent decreases in ash-free dry mass over the entire incubation period, suggesting that the material remaining after initial leaf decomposition trapped inorganic particles. Microbial activity was higher on elm leaves than on oak leaves, with peak activity occurring at 6 and 27 days, respectively. The level of oxygen saturation on the bottom surface of an elm leaf ranged between 0 and 75% within a 30-mm
2
area. This spatial heterogeneity in O
2
saturation disappeared when the water velocity increased from 0 to 6 cm s
-1
. Our results suggest that as leaves enter the groundwater, they decompose and provide substrate for microorganisms. The rate of decomposition depends on leaf type, small-scale variations in microbial activity, water velocity, and the length of submersion time. During the initial stages of decomposition, anoxic microzones are formed that could potentially be important to the biogeochemistry of the otherwise oxic aquifer.
</jats:p
Heterogeneity and scaling of photosynthesis, respiration, and nitrogen uptake in three Atlantic Rainforest streams
The external micro-anatomy of the cephalon of the asellotan isopod Craseriella anops
The micro-anatomy of the cephalon is described in the troglobic asellotan isopod Craseriella anops from the Nohoch Nah Chich anchialine cave system in southeast Mexico. The cephalon is entirely covered by cuticular scales bordered by marginal spines. The anterior end of the cephalon is bordered by a carina that is wider medially. The isopod is eyeless. The distal seventh portion of the cephalon is characterized by the presence of two sutures and six setae. A suture is found on each side of the distal margin of the cephalon. Each suture is bordered by microtrichs. Two simple setae with a sensory hair, articulated on the base by a socket, are found one on each side of each of the sutures. Two additional setae, similar in shape and size, occur medially on the cephalon. A terminal pore is absent on the sensory hairs of all setae. These setae are suggested to be mechanoreceptors that provide directional sensitivity and enhance the sensibility of turbulent motion, viscosity and changes of hydrostatic pressure
