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To adapt to a wide range of physically demanding environmental conditions, biological systems have evolved a diverse variety of robust skeletal architectures. One such example, Euplectella aspergillum , is a sediment-dwelling marine sponge that is anchored into the sea floor by a flexible holdfast apparatus consisting of thousands of anchor spicules (long, hair-like glassy fibers). Each spicule is covered with recurved barbs and has an internal architecture consisting of a solid core of silica surrounded by an assembly of coaxial silica cylinders, each of which is separated by a thin organic layer. The thickness of each silica cylinder progressively decreases from the spicule’s core to its periphery, which we hypothesize is an adaptation for redistributing internal stresses, thus increasing the overall strength of each spicule. To evaluate this hypothesis, we created a spicule structural mechanics model, in which we fixed the radii of the silica cylinders such that the force transmitted from the surface barbs to the remainder of the skeletal system was maximized. Compared with measurements of these parameters in the native sponge spicules, our modeling results correlate remarkably well, highlighting the beneficial nature of this elastically heterogeneous lamellar design strategy. The structural principles obtained from this study thus provide potential design insights for the fabrication of high-strength beams for load-bearing applications through the modification of their internal architecture, rather than their external geometry. Significance The remarkable properties of biological structural materials can often be attributed to the composite arrangement of their constituents. This paper focuses on the high-aspect-ratio, load-bearing, glassy skeletal fibers (spicules) of the marine sponge Euplectella aspergillum . Considering that the spicules’ internal architecture cannot be repaired or remodeled, we hypothesize that there is a connection between their internal structure and their strength. Using a newly developed structural mechanics model for composite beams, we demonstrate that the unique internal geometry that maximizes a beam’s strength correlates well with the geometry observed in the native spicules. This bio-inspired design strategy for increasing a beam's strength has implications for a new generation of man-made structural materials.

Structural materials in nature exhibit remarkable designs with building blocks, often hierarchically arranged from the nanometer to the macroscopic length scales. We report on the structural properties of biosilica observed in the hexactinellid sponge Euplectella sp. Consolidated, nanometer-scaled silica spheres are arranged in well-defined microscopic concentric rings glued together by organic matrix to form laminated spicules. The assembly of these spicules into bundles, effected by the laminated silica-based cement, results in the formation of a macroscopic cylindrical square-lattice cagelike structure reinforced by diagonal ridges. The ensuing design overcomes the brittleness of its constituent material, glass, and shows outstanding mechanical rigidity and stability. The mechanical benefits of each of seven identified hierarchical levels and their comparison with common mechanical engineering strategies are discussed.

Hexactinellid sponges of the genus Euplectella produce highly ordered and mechanically robust skeletal systems of amorphous hydrated silica. The high damage tolerance of their constituent skeletal elements and the environmentally benign conditions under which these sponges form have prompted additional investigations into the characterization of the proteins driving the synthesis of these materials. In the present report, we describe a previously unidentified protein, named “glassin,” extracted from the demineralized skeletal elements of Euplectella . Glassin is a histidine-, aspartic acid-, threonine-, and proline-rich protein and directs silica polycondensation at neutral pH and room temperature. The hexactinellids are a diverse group of predominantly deep sea sponges that synthesize elaborate fibrous skeletal systems of amorphous hydrated silica. As a representative example, members of the genus Euplectella have proved to be useful model systems for investigating structure–function relationships in these hierarchically ordered siliceous network-like composites. Despite recent advances in understanding the mechanistic origins of damage tolerance in these complex skeletal systems, the details of their synthesis have remained largely unexplored. Here, we describe a previously unidentified protein, named “glassin,” the main constituent in the water-soluble fraction of the demineralized skeletal elements of Euplectella . When combined with silicic acid solutions, glassin rapidly accelerates silica polycondensation over a pH range of 6–8. Glassin is characterized by high histidine content, and cDNA sequence analysis reveals that glassin shares no significant similarity with any other known proteins. The deduced amino acid sequence reveals that glassin consists of two similar histidine-rich domains and a connecting domain. Each of the histidine-rich domains is composed of three segments: an amino-terminal histidine and aspartic acid-rich sequence, a proline-rich sequence in the middle, and a histidine and threonine-rich sequence at the carboxyl terminus. Histidine always forms HX or HHX repeats, in which most of X positions are occupied by glycine, aspartic acid, or threonine. Recombinant glassin reproduces the silica precipitation activity observed in the native proteins. The highly modular composition of glassin, composed of imidazole, acidic, and hydroxyl residues, favors silica polycondensation and provides insights into the molecular mechanisms of skeletal formation in hexactinellid sponges.

Currey discusses the hierarchies in biomineral structures. Euplectella, a deepwater sponge whose glassy skeleton is a hollow cylinder, is an example of an organism that displays various levels of structural hierarchy of its biomineralization processes.

Some superior technological secrets have come to light from a deep-sea organism. Modern technology cannot yet compete with some of the sophisticated optical systems possessed by biological organisms 1 , 2 , 3 . Here we show that the spicules of the deep-sea 'glass' sponge Euplectella have remarkable fibre-optical properties, which are surprisingly similar to those of commercial telecommunication fibres — except that the spicules themselves are formed under normal ambient conditions and have some technological advantages over man-made versions.

This article describes or redescribes four hexactinellid sponges, namely Poliopogon amadou, Euplectella sanctipauli sp. nov., Bolosoma perezi sp. nov. and Advhena magnifica gen. et sp. nov. P. amadou, E. sanctipauli sp. nov. and B. perezi sp. nov. represent new findings for the South Atlantic deep-sea fauna, including the first record of Bolosoma for this ocean. Advhena magnifica gen. et sp. nov., on the other hand, was collected by NOAA oceanographic expeditions in the North Pacific (Pigafetta Guyot).

Biological systems have, through the course of time, evolved unique solutions for complex optical problems. These solutions are often achieved through a sophisticated control of fine structural features. Here we present a detailed study of the optical properties of basalia spicules from the glass sponge Euplectella aspergillum and reconcile them with structural characteristics. We show these biosilica fibers to have a distinctive layered design with specific compositional variations in the glass/organic composite and a corresponding nonuniform refractive index profile with a high-index core and a low-index cladding. The spicules can function as single-mode, few-mode, or multimode fibers, with spines serving as illumination points along the spicule shaft. The presence of a lens-like structure at the end of the fiber increases its light-collecting efficiency. Although free-space coupling experiments emphasize the similarity of these spicules to commercial optical fibers, the absence of any birefringence, the presence of technologically inaccessible dopants in the fibers, and their improved mechanical properties highlight the advantages of the low-temperature synthesis used by biology to construct these remarkable structures.

The depth of the ocean is plentifully populated with a highly diverse fauna and flora, from where the Challenger expedition (1873–1876) treasured up a rich collection of vitreous sponges [Hexactinellida]. They have been described by Schulze and represent the phylogenetically oldest class of siliceous sponges [phylum Porifera]; they are eye-catching because of their distinct body plan, which relies on a filigree skeleton. It is constructed by an array of morphologically determined elements, the spicules. Later, during the German Deep Sea Expedition “Valdivia” (1898-1899), Schulze could describe the largest siliceous hexactinellid sponge on Earth, the up to 3 m high Monorhaphis chuni, which develops the equally largest bio-silica structures, the giant basal spicules (3 m × 10 mm). With such spicules as a model, basic knowledge on the morphology, formation, and development of the skeletal elements could be elaborated. Spicules are formed by a proteinaceous scaffold which mediates the formation of siliceous lamellae in which the proteins are encased. Up to eight hundred 5 to 10 μm thick lamellae can be concentrically arranged around an axial canal. The silica matrix is composed of almost pure silicon and oxygen, providing it with unusual optophysical properties that are superior to those of man-made waveguides. Experiments indicated that the spicules function in vivo as a nonocular photoreception system. In addition, the spicules have exceptional mechanical properties, combining mechanical stability with strength and stiffness. Like demosponges the hexactinellids synthesize their silica enzymatically, via the enzyme silicatein. All these basic insights will surely contribute also to a further applied utilization and exploration of bio-silica in material/medical science.

Descriptions of hexactinellid sponges collected by the RV ‘Marion Dufresne’ MD55 expedition on the Vitória–Trindade seamounts chain (off Espírito Santo State, south-eastern Brazil) in 1987 and stored in the MNHN (Muséum National d'Histoire Naturelle in Paris) are presented. Hyalonema (Cyliconema) conqueror sp. nov. (the first finding of this subgenus in the Atlantic Ocean) and H. (Prionema) dufresnei sp. nov. (the second record of this subgenus for the Atlantic Ocean) are described as new species. The holotype of H. (C.) conqueror sp. nov. was collected with a ROV at Campos Basin (off Rio de Janeiro State, south-eastern Brazil), while the paratypes originated from Vitória–Trindade seamounts chain and off Bahía State (eastern Brazil). Other hexactinellids reported here, Farrea sp., Sarostegia aff. oculata, Aphrocallistes aff. beatrix, Dactylocalyx aff. subglobosus and Euplectella suberea were known before to be widely distributed in the Atlantic Ocean. The total number of hexactinellid sponges known from Brazil has risen to 15 and from the south-western Atlantic to 23.

The population structure of the deep-sea sponge-associated shrimp Spongicola japonica was investigated, and the mechanism of pair formation analysed from field samples. The composition pattern of shrimp in host sponges was divided into three patterns by sex and number as follows: solitary, a solitary inhabitant; sexually paired, a pair with a male and a female; grouped, multiple individuals excluding those designated as sexually paired. Juveniles usually remained grouped or solitary in a host cavity until the size at which gonadal maturity starts. Before forming sexual pairs, shrimp appear to have a free-living period outside the host, when the ovarian stages of females correspond to early to late vitellogenesis. Re-invasion is just before the first spawning, when females are in the ovarian stage of late vitellogenesis.