Proefschrift Maastricht. / Met lit. opg. - Met samenvattingen in het Nederlands en Turks.

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The ultrastructure of spermatozoa from six crayfish species were described. The acrosome complex and nucleus are located at the anterior and posterior of the spermatozoon, respectively. The acrosome complex organelle is divided into two main parts: the main body of the acrosome that is a dense inverted cup-shaped structure and organized into three layers of differing electron densities and extended parallel filaments, and the sub-acrosome zone occupying the central part of the acrosome complex, which is divided into two electron dense areas. The spermatozoon of Orconectes limosus is described for the first time. In addition, an acrosome spike in the spermatozoon of Procambarus clarkii is described. Despite a well conserved general structure and similarity of pattern among these spermatozoa, differences in the dimensions of the acrosome within the studied species may be useful to help distinguish the different crayfish. The ultrastructure of the spermatozoon and spermatophore wall of the narrow clawed crayfish Astacus leptodactylus during three stages including freshly ejaculated, post-mating, and after release of the spermatozoon were described and compared. The crayfish spermatophore consists of a sperm mass enveloped by a three layered spermatophore wall. After mating, the thickness of the outer layer of the spermatophore is increased. The matrix in the middle layer of the spermatophore becomes reticulated, and granules inside this layer release their contents. Fibers in the inner layer degrade to small particles. The spermatozoon capsule swells and space between the capsule and the spermatozoon appears. The area of the plasma membrane is increased by wrinkling of the surface and alteration from a single to a multilayered structure at the anterior part of the acrosome. The density of the subacrosome zone increases in the vicinity of the main body of the acrosome. With the onset of fertilization, the layers of the spermatophore are dissolved by female glair glands secretions. The capsule, plasma membrane, and membranous lamellae are eliminated, and bundles of filaments are released. The subacrosome zone loses electron density and retracts. The electron-dense material of the innermost layer of the acrosome is discharged and, together with filaments, forms a filament/droplet structure at the anterior part of the spermatozoon. The most important change is observed in the subacrosome zone, which may play a key role in the fertilization. Also, morphological changes of the spermatozoon after release from the capsule, especially formation of the filament/droplet structure, may contribute to the mechanism of egg-spermatozoon binding in the crayfish.

Genus Frustulia was chosen for this work due to the continuity of the previous research of our phycological group. Using molecular techniques, it was found that a number of morphologically defined species of diatoms is cryptic species complex, which may have limited dispersal. The aim of this study was to: 1) evaluate the diversity of the genus Frustulia in northern Europe by molecular methods and classify found species in the phylogenetic context of related species; 2) find out if it possible to identify the isolated species in natural samples by using morphological characters. There have been analyzed 234 strains by molecular methods. Isolated ones were in four clades. 86 % of the strains belonged to a generic complex F. crassinervia-saxonica. Two strains were identified as species F. gaertnerae and F. septentrionalis. The last line was not described yet so it was labeled as F. sp. This line is closely related to the species F. maoriana, which is considered to be endemic in New Zealand. Phylogeny of the genus was created based on a dataset of four molecular markers. Published morphometric data were then compared with 264 cells photos taken by scanning electron microscope. There was done surveillance comparison of the results of the analysis of quantitative and qualitative characters with...

P. magnifica is an invasive freshwater bryozoan species which is native to the North America. The aim of this thesis is to ascertain the pace of the colonies' growth. The survey was carried out in three locations during twenty-one days in July 2018.

Inaug.-diss.--Greifswald. / Vita. Bibliography: p. 7.

Proefschrift Universiteit van Amsterdam. / Met lit. opg. - Met samenvatting in het Nederlands.