Andreas Ziegler

Thecideide brachiopods are an anomalous group of invertebrates. In this study, we discuss the evolution of thecideide brachiopods from the Triassic to the Holocene and base our results and conclusions on microstructure and texture measurements gained from electron backscatter diffraction (EBSD). In fossil and Recent thecideide shells, we observe the following mineral units: (1) nanometric to small granules; (2) acicles; (3) fibres; (4) polygonal crystals; and (5) large roundish crystals. We trace for thecideide shells the change of mineral unit characteristics such as morphology, size, orientation, arrangement and distribution pattern. Triassic thecideide shells contain extensive sections formed of fibres interspersed with large, roundish crystals. Upper Cretaceous to Pleistocene thecideide hard tissues consist of a matrix of minute to small grains reinforced by acicles and small polygonal crystals. Recent thecideide species form their shell of mineral units that show a wide range of shapes, sizes and arrangements. We find from Late Triassic to Recent a gradual decrease in mineral unit size, regularity of mineral unit morphology and orientation and the degree of calcite co‐orientation. While crystallite co‐orientation is the highest for fibrous microstructures, it is strikingly low for taxa that form their shell out of nanogranular to acicular mineral units. Our results indicate that Upper Jurassic species represent transitional forms between ancient taxa with fibrous shells and Recent forms that construct their shells of acicles and granules. We attribute the observed changes in microstructure and texture to be an adaptation to a different habitat and lifestyle associated with cementation to hard substrates.

The arthrodial membrane is a thin and flexible type of cuticle that inserts at the edge regions of neighbouring rigid skeletal elements creating a flexible connection. In the present study, we analyzed the structure, mineral composition, calcite organization and local stiffness and hardness of edge regions that form transitions to the arthrodial membranes in the tergites of the desert isopod Hemilepistus reaumuri. For the transitions to the arthrodial membrane, the results show an increase in the thickness of the epicuticle at cost of the distal exocuticle and a calcite layer, an increase in the ratio of phosphorus to calcium and a decrease in the local mechanical properties. The posterior edge region contains an unusually large stack of unidirectionally oriented parallel fibrils projecting to the lateral sides. At the edge, it turns down into a long ventral cuticle overlapping an anterior part of the neighbouring tergite. It forms a thin arched gap between the tergites that can help reducing water loss through the arthrodial membrane and protects the arthrodial membrane upon predation. A thick ventral ridge near the transition to the arthrodial membrane carrying bristles can prevent sand grains from access to the arthrodial membrane. From the dorsal cuticle to the transition to the arthrodial membrane, calcite units become larger and single crystalline turning their c-axes orientation perpendicular to the sagittal section plane. Comparison with edge regions of the beach isopod Tylos europaeus reveal common characteristics of the edge region, but also specific adaptations to the desert habitat of H. reaumuri.

We present results of bioaragonite to apatite conversion in bivalve, coral and cuttlebone skeletons, biological hard materials distinguished by specific microstructures, skeletal densities, original porosities and biopolymer contents. The most profound conversion occurs in the cuttlebone of the cephalopod Sepia officinalis, the least effect is observed for the nacreous shell portion of the bivalve Hyriopsis cumingii. The shell of the bivalve Arctica islandica consists of cross-lamellar aragonite, is dense at its innermost and porous at the seaward pointing shell layers. Increased porosity facilitates infiltration of the reaction fluid and renders large surface areas for the dissolution of aragonite and conversion to apatite. Skeletal microstructures of the coral Porites sp. and prismatic H. cumingii allow considerable conversion to apatite. Even though the surface area in Porites sp. is significantly larger in comparison to that of prismatic H. cumingii, the coral skeleton consists of clusters of dense, acicular aragonite. Conversion in the latter is sluggish at first as most apatite precipitates only onto its surface area. However, the process is accelerated when, in addition, fluids enter the hard tissue at centers of calcification. The prismatic shell portion of H. cumingii is readily transformed to apatite as we find here an increased porosity between prisms as well as within the membranes encasing the prisms. In conclusion, we observe distinct differences in bioaragonite to apatite conversion rates and kinetics depending on the feasibility of the reaction fluid to access aragonite crystallites. The latter is dependent on the content of biopolymers within the hard tissue, their feasibility to be decomposed, the extent of newly formed mineral surface area and the specific biogenic ultra- and microstructures.

The investigation of electrochemical processes at the interface of two immiscible electrolyte solutions (ITIES) is of great interest for sensing applications, and serves as a surrogate to the study of biological transport phenomena, e.g. ion channels. Alongside e-beam lithography, focused ion beam (FIB) milling is an attractive method to prototype and fabricate nanopore arrays that support nanoITIES. Within this contribution, we explore the capability of FIB/scanning electron microscopy (SEM) tomography to visualize the actual pore structure and interfaces at silica-modified nanoporous membranes. The nanopores were also characterized by atomic force microscopy (AFM) using ultra-sharp AFM probes to determine the pore diameter, and using scanning transmission electron microscopy (STEM) and energy dispersive X-ray (EDX) spectroscopy, providing additional information on the elemental composition of deposits within the pores. Si-rich particles could be identified within the pores as well as at the orifice that had faced the organic electrolyte solution during electrochemical deposition. The prospects of the used techniques for investigating the interface at or within FIB-milled nanopores will be discussed.