Most multicellular organisms can only survive under atmospheric pressure. The reduced pressure of a high vacuum usually leads to rapid dehydration and death. Here we show that a simple surface modification can render multicellular organisms strongly tolerant to high vacuum. Animals that collapsed under high vacuum continued to move following exposure of their natural extracellular surface layer (or that of an artificial coat-like polysorbitan monolaurate) to an electron beam or plasma ionization (i.e., conditions known to enhance polymer formation). Transmission electron microscopic observations revealed the existence of a thin polymerized extra layer on the surface of the animal. The layer acts as a flexible "nano-suit" barrier to the passage of gases and liquids and thus protects the organism. Furthermore, the biocompatible molecule, the component of the nano-suit, was fabricated into a "biomimetic" free-standing membrane. This concept will allow biology-related fields especially to use these membranes for several applications.animal behavior | biophysics | microscopy | nanotechnology | plasma physics

Taxonomically restricted genes or lineage-specific genes contribute to morphological diversification in metazoans and provide unique functions for particular taxa in adapting to specific environments. To understand how such genes arise and participate in morphological evolution, we have investigated a gene called nematogalectin in Hydra, which has a structural role in the formation of nematocysts, stinging organelles that are unique to the phylum Cnidaria. Nematogalectin is a 28-kDa protein with an N-terminal GlyXY domain (glycine followed by two hydrophobic amino acids), which can form a collagen triple helix, followed by a galactose-binding lectin domain. Alternative splicing of the nematogalectin transcript allows the gene to encode two proteins, nematogalectin A and nematogalectin B. We demonstrate that expression of nematogalectin A and B is mutually exclusive in different nematocyst types: Desmonemes express nematogalectin B, whereas stenoteles and isorhizas express nematogalectin B early in differentiation, followed by nematogalectin A. Like Hydra, the marine hydrozoan Clytia also has two nematogalectin transcripts, which are expressed in different nematocyte types. By comparison, anthozoans have only one nematogalectin gene. Gene phylogeny indicates that tandem duplication of nematogalectin B exons gave rise to nematogalectin A before the divergence of Anthozoa and Medusozoa and that nematogalectin A was subsequently lost in Anthozoa. The emergence of nematogalectin A may have played a role in the morphological diversification of nematocysts in the medusozoan lineage.O rganisms within a phylum commonly share phenotypic traits that are unique to the phylum and strongly associated with specific adaptations. These phenotypic traits are often associated with taxonomically restricted genes. In Cnidaria, the nematocyst, an explosive organelle used to capture prey or repel predators, is such a phylum-specific trait. All nematocysts consist of two primary structures, a capsule and a tubule (1, 2) (Fig. S1A). Modifications of the nematocyst structure such as the capsule size and the armature of the tubule with spines generate different types of nematocysts. Anthozoans have simple nematocyst types (3), whereas medusozoans (Hydrozoa, Cubozoa, and Scyphozoa) have more complex nematocysts exhibiting various tubule and spine morphologies (4). Hydra, a freshwater hydrozoan, has four types of nematocysts: stenotele, desmoneme, holotrichous isorhiza, and atrichous isorhiza.Nematocysts are formed in large post-Golgi vacuoles during the differentiation of nematocytes. The capsule wall is formed on the inner surface of the vacuole, which grows in size with continuing input of precursor proteins from the Golgi complex (5). After completion of the capsule, tubule formation begins at the apical end, growing outward as a long extension that pushes the vacuole membrane into the cytoplasm (Fig. S1B). After completion of the external tubule, it invaginates through itself to form the internal tubule (1, 6); at that point, spines ar...

Nerve cells and spontaneous coordinated behavior first appeared near the base of animal evolution in the common ancestor of cnidarians and bilaterians. Experiments on the cnidarian Hydra have demonstrated that nerve cells are essential for this behavior, although nerve cells in Hydra are organized in a diffuse network and do not form ganglia. Here we show that the gap junction protein innexin-2 is expressed in a small group of nerve cells in the lower body column of Hydra and that an anti-innexin-2 antibody binds to gap junctions in the same region. Treatment of live animals with innexin-2 antibody eliminates gap junction staining and reduces spontaneous body column contractions. We conclude that a small subset of nerve cells, connected by gap junctions and capable of synchronous firing, act as a pacemaker to coordinate the contraction of the body column in the absence of ganglia.

Evidence is presented to demonstrate that colour polymorphism in a beetle arises from structural colours produced by a five-layered reflector in the elytron. The colour of leaf beetles, Plateumaris sericea, ranges across the visible spectrum from blackish-blue to red. The elytra have two distinct layers: epicuticle and exocuticle. Morphological observations reveal that the multilayer structure within the exocuticle differs little among the different colour morphs but the layers within the epicuticle have characteristic thicknesses corresponding to the observed colour. The reflectors, consisting of five layers within the epicuticle, are responsible for all the different colours observed in P. sericea, as shown by theoretical analyses for a multilayer stack, and by showing that removal of the elytral surface, including epicuticle, results in the disappearance of the iridescent colour.

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