Light production by organisms, or bioluminescence, has fascinated not only scientists but also ordinary people all over the world, and it has been especially so in Japan. Here we review the biological information available to date for all luminous terrestrial animals known from Japan, particularly focusing on their diversity and systematics, their biology and ecology in Japan, and putative function and biochemistry of their luminescence. In total 58 luminous terrestrial animals have been described from Japan, which consist of 50 fireflies (Coleoptera: Lampyridae), one glowworm beetle (Coleoptera: Phengodidae), two fungus gnats (Diptera: Keroplatidae), one springtail (Collembola), one millipede (Diplopoda), one centipede (Chilopoda) and two earthworms (Oligochaeta). For all except some firefly species, the DNA “barcode” sequences of a cytochrome oxidase subunit I region are provided. We also introduce how intricately the seasonal appearance and glimmering of luminous insects, in particular those of fireflies, have been interwoven into the culture, art, literature and mentality of Japanese people.

In our laboratory, a single autosomal recessive mutation in a phenotype similar to ruby-eye (ru/Hps6^ru) or ruby-eye 2 (ru2/Hps5^ru2) spontaneously occurred in siblings of C57BL/10JHir ( / , black) mice in 2006. RT-PCR analysis revealed that this novel mutation, named ru2^d/Hps5^ru2-d, exhibited frameshift by 997G deletion in the Hps5 gene. To clarify the mechanism of the hypopigmentation, the characteristics of proliferation and differentiation of ru2^d/ru2^d epidermal melanoblasts and melanocytes cultured in a serum-free medium were investigated. The proliferation of ru2^d/ru2^d melanoblasts and melanocytes did not differ from that of / melanoblasts and melanocytes. However, the differentiation of ru2^d/ru2^d melanocytes was greatly inhibited. Tyrosinase (TYR) activity, expression of TYR, TYR-related protein 1 (TRP1) and TRP2 (dopachrome tautomerase, DCT), eumelanin synthesis, and the number of stage IV melanosomes markedly decreased in ru2^d/ru2^d melanocytes. However, excess L-tyrosine (Tyr) added to culture media from initiation of the primary culture rescued the reduced differentiation through increase in TYR activity, expression of TYR, TRP1, TRP2 and Kit, eumelanin synthesis, and stage IV melanosomes. L-Tyr injected into ru2^d/ru2^d mice also stimulated melanocyte differentiation. These results suggest that the ru2^d allele inhibits melanocyte differentiation, and that its impaired differentiation is rescued by excess Tyr.

The ovaries of Euborellia fulviceps are composed of five elongated ovarioles of meroistic-polytrophic type. The individual ovariole has three discernible regions: the terminal filament, germarium, and vitellarium. The terminal filament is a stalk of flattened, disc-shaped somatic cells. In the germarium, germline cells in subsequent stages of differentiation are located, and the vitellarium comprises numerous ovarian follicles arranged linearly. The individual ovarian follicles within the vitellarium are separated by prominent interfollicular stalks. The follicles are composed by two germline cells only: an oocyte and a single, polyploid nurse cell, which are surrounded by a monolayer of somatic follicular cells (FCs). During subsequent stages of oogenesis, initially uniform follicular epithelium begins to diversify into morphologically and physiologically distinct subpopulations. In E. fulviceps, the FC diversification mode is rather simple and leads to the formation of only three different FC subpopulations: (1) cuboidal FCs covering the oocyte, (2) stretched FCs surrounding the nurse cell and (3) FCs actively migrating between oocyte and a nurse cell. We found that FCs from the latter subpopulation send long and thin filopodium-like and microtubule-rich processes penetrating between the oocyte and nurse cell membranes. This suggests that, in E. fulviceps, cells from at least one FCs subpopulation show the ability to change position within an ovarian follicle by means of active migration.

The epidermis serves as a barrier protecting organs and tissues from the environment, and comprises many types of cells. A cell renewal system is established in epidermis: old epithelial cells are replaced by newly differentiated cells, which are derived from epidermal stem cells located near basement membrane. In order to examine the mechanism of epidermal development, we isolated a novel gene expressed in Xenopus epidermis and named the gene Xenopus polka dots (Xpod) from its polka dot-like expression pattern throughout larval periods. Several immunohistochemical examinations showed that the Xpod-expressing cell type is neither p63-positive epidermal stem cells, nor the α-tubulin-positive ciliated cells, but a subset of the foxi1e-positive ionocytes. The forced gene expression of foxi1e caused the suppression of Xpod expression, while Xpod showed no effect on foxi1e expression. In a comparison of several osmotic conditions, we found that hypertonic culture caused the increase in number of the Xpod-expressing cell, whereas number of the foxi1e-expressing cells was reduced under the hypertonic condition. These results show the possibility that Xpod is involved in the establishment of a certain subpopulation of ionocytes under hypertonic conditions.

The determination of color patterns of butterfly wing eyespots has been explained by the morphogen concentration gradient model. The induction model has been proposed recently as a more realistic alternative, in which the eyespot-specifying signal does not depend entirely on focal activity. However, this model requires further elaboration and supporting evidence to be validated. Here, I examined various color patterns of nymphalid butterflies to propose the mechanics of the induction model. Based on cases in which an eyespot light ring is identical to the background in color, I propose that eyespots are fundamentally composed of dark rings and non-dark “background” spaces between them. In the induction model, the dark-ring-inducing signal that is released from a prospective eyespot focus (the primary organizing center) as a slow-moving wave effects both selfenhancement and peripheral induction of the dark-ring-inhibitory signal at the secondary organizing centers, resulting in an eyespot that has alternate dark and light rings. Moreover, there are cases in which an unseen “imaginary light ring” surrounds an eyespot proper and in which PFEs are integrated into the eyespot. It appears that PFEs constitute a periodic continuum of eyespot dark rings; thus, a background space between the eyespot and a PFE is mechanistically equivalent to eyespot light rings. The eyespot dark-ring-inducing signals and PFE-inducing signal are likely to be identical in quality, but released at different times from the same organizing center. Computer simulations based on the reaction-diffusion system support the feasibility of the induction model.

The p450 aromatase gene has a tissue-specific promoter that is regulated by specific transcriptional factors. In rats and humans, a cAMP response element-like sequence (CLS) and an NR5A1/NR5A2 binding sequence have been identified as cis elements in the aromatase promoter; these cis elements mediate cAMP-induced expression in the ovaries and testes. CLS is recognized by a cAMP-responsive element binding protein (CREB) as the principal component. In this study, we performed a gel shift assay to analyze the proteins that interact with the cis-element in Xenopus aromatase. An electrophpretic mobility gel shift assay (EMSA) and matrix-associated laser desorption ionization time of flight (MALDI-TOF) mass spectrometry (MS) analysis of the proteins responsible for retarding the mobility of CLS revealed that ATF4 interacted in vitro with CLS in gonadal specific aromatase promoter sequence of Xenopus embryos. Although a significant difference was observed in aromatase mRNA expression between male and female gonads, no difference in the expression of ATF4 was observed between them at stage 50. With regard to aromatase expression in the gonad of Xenopus embryos, ATF4 might act in combination with multiple transcription factors as a trans-element of CLS in place of CREB.

Odorrana ishikawae is listed as a class IB endangered species in the IUCN Red List and is protected by law in both Okinawa and Kagoshima Prefectures, Japan. Here, in an effort to help effectively preserve the genetic diversity of this endangered species in the laboratory, we tested a farming technique involving the artificial breeding of frogs, and also promoted natural breeding in the laboratory. Field-caught male/female pairs of the Amami and Okinawa Island populations were artificially bred using an artificial insemination method in the 2004, 2006, and 2008 breeding seasons (March to April). Although fewer than 50% of the inseminated eggs achieved metamorphosis, approximately 500, 300, and 250 offspring from the three respective trials are currently being raised in the laboratory. During the 2009 and 2010 breeding seasons, second-generation offspring were produced by the natural mating activities of the first offspring derived from the two artificial matings in 2004. The findings and the methods presented here appear to be applicable to the temporary protection of genetic diversity of local populations in which the number of individuals has decreased or the environmental conditions have worsened to levels that frogs are unable to survive by themselves.

Thirty male specimens of Dendropsophus minutus Peters, 1972, were collected from April 2004 to March 2005 in the region de Sao José do Rio Preto/SP, to conduct a histological study during the seasonal and annual cycles. Testicular activity was inferred based on the volume occupied by each type of cellular cyst present in the seminiferous tubules, as well as the quantity of germ cells in the final development stage, the spermatozoids. All data analyzed were correlated with climatic variables (temperature, rainfall and photoperiod) registered in the region where specimens were collected. A significant variation was verified in the quantity of spermatozoids as well as in the volume occupied by spermatids and spermatozoids throughout the year and between the cold/dry and hot/ humid seasons. It has also been reported that environmental conditions are important factors closely related to species reproduction and that production of germ cells and volume occupied by germ cysts is independent of anatomical aspect of the gonads. Thus, it was possible to verify that although the species reproduces throughout the year, individuals exhibit a preferential reproduction season, resulting in a reproductive (October to the end of February) and a post-reproductive period.

Differentiation and development of steroid-producing cells (SPCs) and folliculogenesis during ovarian differentiation in the Nile tilapia Oreochromis niloticus were immunohistochemically and ultrastructurally examined. Clusters of immunopositive cells (IPCs) against antibodies (ABs) of cholesterol side-chain cleavage cytochrome P450 (P450scc), 3β-hydroxysteroid dehydrogenase (3βHSD), and cytochrome P450aromatase (P450arom) only appeared in the area near blood vessels in the fish ovaries at 50–60 days after hatching (dah). Ultrastructural results showed that differentiation and development of SPCs from undifferentiated to maturation occurred in the area near blood vessels, indicating that it would be the original site of SPCs. At 70–80 dah, IPC clusters invaded the interstices among oocytes at the perinucleolar stage from the area near the blood vessels. IPCs increased in number in the interstices among the previtellogenic oocytes, and some clusters began to enclose the outer thecal layer of the previtellogenic oocytes at 90 dah. The process of folliculogenesis was ultrastructurally observed. SPCs enclosed by fibroblastic cells invaded the interstitial areas among oocytes and some reached the surfaces of oocytes. The upper portions of these elongations opened and began to enclose the outer surfaces of developed oocytes to become thecal layer. Later, newly migrated SPCs reach the thecal layer to become thecal cells. These results indicate that steroid-producing thecal cells originate from the SPCs in the area near blood vessels. After thecal layer formation, an immunopositive reaction against P450arom AB, but not against P450scc or 3β-HSD ABs, appeared first in the granulosa cells enclosing the vitellogenic oocytes at 100 dah. At this time, estrogen production in serum levels rapidly increased. Thus, folliculogenesis could be essential for active production of estrogen in the ovary.

A new genus and two new species of Peltogastridae, Peltogaster postica sp. nov. and Ommatogaster nana gen. et sp. nov., are described from Okinawa Island, Ryukyu Islands, southwestern Japan. The two new rhizocephalans were found to be parasitic on the estuarine hermit crabs, Pagurus minutus Hess, 1865 and Diogenes leptocerus Forest, 1956, respectively. Peltogaster postica sp. nov. is allied to P. curvata Kossmann, 1874, P. paguri Rathke, 1842, and P. reticulata Shiino, 1943, but is distinguished by its relative length and internal and external structures of the mature externa. Ommatogaster gen. nov. is established for the present new species O. nana based on the morphologies of the visceral mass of the externa and the presence of a nauplius eye in the larvae. Partial COI sequences were obtained from the two new species and one known species, Dipterosaccus indicus Van Kampen and Boschma, 1925, to test the possible usefulness of the sequences as tags for species identification.