Gyrodactylus anarhichatis n. sp. and G. microanchoratus n. sp. (Monogenea: Gyrodactylidae) from the Atlantic wolf-fish Anarhichas lupus (Anarhichadidae) off the coast of Norway - T.A. Mo; Nora K. Lile (Systematic Parasitology, 1998)

Longitudinal changes in Ca, Mg, Fe, Cu, and Zn in breast milk of women in Taiwan over a lactation period of one year - Te-Hsien Lin; Yuh-Jyh Jong; Chi-Hsiun chiang; Mo-Hsiung Yang (Biological Trace Element Research, 1998)

Bioconcentration Effects of Heavy Metal Pollution in Soil on the Mucosa Epithelia Cell Ultrastructure Injuring of the Earthworm's Gastrointestinal Tract - Guo Yongcan; Wang Zhenzhong; Zhang Youmei; Mo Xiaoyang (Bulletin of Environmental Contamination and Toxicology, 1998)

Osmotic Regulation of Na + Transport Across A6 Epithelium: Interactions with Prostaglandin E 2 and Cyclic AMP - P.S. Matsumoto; L. Mo; N.K. Wills (The Journal of Membrane Biology, 1997)

Two Groups of Endogenous MMTV Related Retroviral env Transcripts Expressed in Human Tissues - Andreas Willer; Susanne Saußele; Wolfgang Gimbel; Wolfgang Zeifarth; Peter Kister; Christine Leib-Mo¨sch; Ru¨diger Hehlmann (Virus Genes, 1997)

Biomass Estimation for Temperate Broadleaf Forests of the United States Using Inventory Data - Paul Schroeder; Sandra Brown; Jiangming Mo; Richard Birdsey; Chris Cieszewski (Forest Science, 1997)
A potentially valuable data source for estimating forest biomass is forest volume inventory data that are widely collected and available throughout the world. In this paper we present a general methodology for using such data to reliably estimate aboveground biomass density (AGBD) and to develop expansion factors for converting volume directly to AGBD from USDA Forest Service Forest Inventory and Analysis (FIA) data. Growing stock volume inventory data and stand tables were combined with independently developed biomass regression equations to estimate AGBD and to calculate biomass expansion factors (BEF: factors that convert volume to mass, accounting for noncommercial components) for the extensive oak-hickory and maple-beech-birch forest types of the eastern United States. Estimated aboveground biomass for both forest types ranged between 28 and 200 Mg ha-1. Expansion factors decreased from more than 4.0 at low growing stock volume to nearly 1.0 when growing stock volume was as high as 190 m³ ha-1, consistent with theoretical expectations. In stands with low AGBD (< 50 Mg ha-1), small diameter trees (< 10 cm diameter) contained up to 75% of the AGBD in trees ≥ 10 cm diameter; this proportion dropped to < 10% for stands with AGBD > 175 Mg ha-1. The similarity of our results for two major forest types suggests that they may be generally applicable for estimating AGBD from inventory data for other temperate broadleaf forests. Further, the pattern between BEF and stand volume was similar to that obtained for tropical broadleaf forests, except that tropical forests generally had larger BEFs than temperate forests at a given volume. The implications of these results suggest that a recent assessment of forest biomass in developed countries is too low. For. Sci.: 43(32):424-434.

Seed bank strategies in Patagonian semi-arid grasslands in relation to their management and conservation - Mo´nica B. Bertiller; Diana A. Aloia (Biodiversity and Conservation, 1997)

The equation and properties of a ray path in a linearly varying velocity field - Woohan Kim; Jung Mo Lee (Geosciences Journal, 1997)

Comparison of three rodent neuropathic pain models - Kwang Jin Kim; Jin Mo Chung (Experimental Brain Research, 1997)

Detection of cardamine chlorotic fleck carmovirus in soil by the polymerase chain reaction - M.L. Skotnicki; J.-Q. Mo (Australasian Plant Pathology, 1996)

RNA hybrid mismatch polymorphisms in Australian populations of turnip yellow mosaic tymovirus - M. L. Skotnicki; A. M. Mackenzie; S. W. Ding; J. Q. Mo; A. J. Gibbs (Archives of Virology, 1993)