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Notes: SUMMARY 1. Negative effects of zooplankton on the availability of phosphorus (P) for phytoplankton as a result of the retention of nutrients in zooplankton biomass and the sedimentation of exoskeletal remains after moulting, have been recently proposed.2. In a mesocosm study, the relative importance of these mechanisms was tested for the freshwater cladoceran Daphnia hyalina×galeata. A total of 13 mesocosm bags was suspended in a mesotrophic German lake during summer 2000 and fertilised with inorganic P in order to obtain a total nitrogen to total P ratio closer to the Redfield ratio. D. hyalina×galeata was then added at a logarithmically scaled density gradient of up to 40 ind. L−1. Zooplankton densities, dissolved inorganic, particulate organic (seston 〈100 μm), as well as total nutrient concentrations were monitored. Additionally, nutrient concentrations of sediment water removed from the bottom of the mesocosm bags via a manual pump were determined.3. Seston carbon (C), seston P and total P were significantly negatively correlated with Daphnia densities. The amount of particulate P (∼5–6 μg P L−1) sequestered from the seston compartment by Daphnia corresponded roughly to the increase of zooplankton biomass (population growth). Soluble reactive phosphorous (SRP) was at all times high (∼25–35 μg P L−1) and possibly unavailable to phytoplankton as a result of P adsorption to calcite during a calcite precipitation event (whiting). P concentrations determined in sediment water were generally 〈60 μg P m−2 and thus never exceeded 1% of the total amount of P bound in particulate matter of the overlying water column.4. Seston C : P ratios followed a polynomial second-order function: At Daphnia densities 〈40 ind. L−1 a positive linear relationship was evident, which is explained by the stronger reduction of P compared with C in seston, and transfer of seston P to zooplankton. Highest seston C : P ratios of ∼300 : 1 were observed at Daphnia densities of ∼30–50 ind. L−1, which is in agreement with proposed threshold values limiting Daphnia reproductive growth. At Daphnia densities 〉40–50 ind. L−1 C : P ratios were decreased because of the strong reduction of seston C at close to constantly low seston P-values of ∼3–4 μg P L−1.5. At least for Daphnia, it may be concluded that – unlike population growth – the sedimentation of faecal pellets and carapaces after moulting seem negligible processes in pelagic phosphorus dynamics.

Notes: 1. Density gradients of cladocerans and copepods were generated in an enclosure experiment to compare the impact on the plankton of a filter feeder (Daphnia hyalina × galeata) with that of more selective feeders (calanoid and cyclopoid copepods). The experiment was conducted in situ over 25 days during spring in a mesotrophic lake, Schöhsee, Germany.2. The plankton community was monitored regularly. Daphniids were able to graze on the phytoplankton present, which mainly consisted of small (〈1000 μm3) species, whereas copepods did not show any impact on algae.3. At the end of the experiment, Daphnia and remaining cyclopoid copepods were harvested and sorted manually, prior to analyses for stable isotopes of carbon and nitrogen. Daphniids from mesocosms stocked purely with differing densities of Daphnia showed little variability in stable isotope values, whereas those that thrived in enclosure bags together with copepods exhibited lower δ13C values.4. The change in Daphniaδ13C indicates a change of food sources, modified by the presence of the copepods: the higher the mean abundance of copepods in the enclosures, the more 13C-depleted the daphniids. Increasing abundance of high nucleic acid (HNA) bacteria in the copepod bags may account for the trend in Daphniaδ13C via increased grazing on the bacteria themselves, or via grazing on phytoplankton utilising isotopically light CO2 from respiratory release.5. Cyclopoid copepod stable isotope signatures were related to Daphnia and copepod abundances in copepod bags, suggesting that cyclopoids preyed on the available zooplankton.

Notes: The differentiation of the surface mucous-cell lineage during physiological cell renewal was investigated using light and electron microscopy in the abomasal mucosa of adult cattle. The surface mucous cells constitute a morphologically and functionally heterogeneous population, whose members correspond to different developmental stages, arranged in a distoproximal gradient from the depth of the pit towards the free luminal surface. The cell lineage comprises immature pre-pit cells near the proliferative isthmus, mature pit cells within the foveola, and older interfoveolar cells lining the free surface. Ultrastructurally, differentiation can be traced towards a predominantly mucus-producing cell type and finally towards a surface-protective cell variant, which degenerates in situ and is extruded into the lumen without affecting epithelial integrity.

Notes: The structure and occurrence of nerve fibres and nerve terminals in the lingual marginal papillae of newborn piglets are investigated by means of the osmium-zinc-iodate method and by transmission-electron microscopy. Subepithelial nerve fibres primarily accompany the blood vessels. They cross the epithelium with an almost vertical course to terminate in the stratum superficiale or the stratum corneum. Due to rows of varicosities, the axons look like a ‘string of pearls’. As a result of the superficial localization and the typical ultrastructure, they seem to have a sensory function. Therefore, the papillae marginales are considered to function as mechanoreceptors.

Notes: The spermathecal epithelium of the honey bee queen (Apis mellifera): ultrastructure, age-dependent alterations, and cellular junctionsThe spermatheca of the honey bee queen is covered by a single-layered, uniform, polarised epithelium. The apical cell surface is greatly enlarged by protrusions and plasma membrane infoldings, the basal cell surface by numerous inter-digitating, long, small processes. Cytoplasmic organelles are chiefly represented by mitochondria. Numerous microtubuli extend throughout the cytoplasm. Golgi and endoplasmic profiles are rare. The cells are subject to senile degeneration: with increasing age, a variety of cytoplasmic inclusions appear, among which are myelinated membranes, dense bodies and dense filamentous aggregates. The spermathecal epithelium does not seem to be involved in exocrine secretion related to nutrition of the long-term stored spermatozoa. The ultra-structure points, however, to ion transport functions and to an engagement in the maintenance of an adequate physicochemical environment ensuring the viability of the spermatozoa. Cellular junctions are represented by luminal zonulae adherentes, focal cell–cell adhering junctions and hemi-adhering junctions along the basal plasmalemma. Desmosomal contacts and cytoskeletal intermediate filaments are missing. Along the lateral plasmalemma, gap junctions and septate junctions are found.