Nonparasitic Nematoda provide evidence for a linear response of functionally important soil biota to increasing livestock density

Soil acidity, nutrient availability and livestock density have a major influence on the belowground ecological community. As fast decomposition rates are due mostly to bacterial-based pathways and slower decomposition rates mostly to fungal-based pathways, it is helpful to condense empirical information in the so-called Nematode Channel Ratio (NCR). The NCR is shown to be a good indicator of efficiency in soil decomposition processes. We argue that in intensive agroecosystems, other fungivore members of the decomposer food web may outcompete the hyphal-feeding nematodes. We demonstrate how the NCR can be used to set ecological standards for sustainable use of the soil in agroecosystems. To summarize the interactions between the microbial resources and the decomposer nematofauna according to increasing land management, we propose the use of the fifth percentile as proxy for a sustainable environmental quality of grasslands on sandy soils, and the NCR mean as the upper threshold for low-stocked farms.     

Carbon dynamics in wood products

The carbon (C) reservoir of wood products in Finnishconstruction and civil engineering was estimated by three inventoriesincluding the years 1980, 1990 and 1995. The inventory method ismainly based on the statistics of Finnish building stock. The use of differentconstruction materials in different parts of buildings is estimated for eachbuilding type. Information collected through building permits includes thematerials of bearing frames and facades. More information about the useof wood products in construction is gathered by many enquiries. The mixof construction materials has changed during each decade. Furthermore, thetimber stocks in construction not subject to permission and in civilengineering (e.g. bridges) were estimated. The C reservoir is calculated onthe basis of dry matter content of wooden construction materials. The timeparameters of a simple exponential decay model and a more detailed Cbalance model of wood products were calibrated to the inventory resultsusing the estimated wood flows to construction as model inputs.According to the inventories the C pool in sawn wood and wood-basedpanels of the Finnish building stock was 8.7 Tg C in 1980, 10.7 Tg C in1990 and 11.5 Tg C in 1995. The mean annual increases, 0.20 Tg Cfrom 1980 to 1990 and 0.15 Tg C from 1990 to 1995, areapproximately 1.3% and 0.8% of the fossil fuel C emissions in Finlandduring the same periods. When also taking into account construction notsubject to permission and civil engineering works, the estimated C stock ofwood products in Finland was 16.5 Tg C in 1995, which is about 3.3 MgC per capita and approximately 2.4% of the C reservoir in Finnish forestbiomass. The total C reservoir of wood products (excluding wood wasteand paper products) coming from Finnish forests might be as much as 7%of the standing biomass if exported wood products are also included. Theaverage lifetime of sawn wood in Finnish construction is less than 40 years.     

First-trimester diagnosis of hypophosphatasia. Importance of gestational age and of purity of CV samples

Prenatal diagnosis of hypophosphatasia was made by alkaline phosphatase (ALP) assay on a chorionic villous sample taken in the first trimester. Very low activities of the LBK isoenzyrnes indicated an affected fetus. Diagnosis was confirmed at 12 weeks of gestation by measurement of LBK isoenzyme activities in fetal bone tissue. In control chorionic villous samples an inverse relation was observed between LBK and placental ALP percentage during gestational age. High LBK ALP activities are observed in decidual tissue. Chorionic villous tissue must not be sampled after 12 weeks of gestation and decidual tissue must be excluded from the sample.     

New insights into temperature-induced white muscle growth plasticity during Dicentrarchus labrax early life: a developmental and allometric study

Dicentrarchus labrax is a major finfish of interest in Mediterranean aquaculture. As the development of its hatchery production had gone with an increase of its larval rearing temperature, we studied the effect of a constant high (20°C) and two lower (13 and 15°C) temperatures on its early white muscle growth, with developmental and allometric approaches. D. labrax, sampled at hatching and at three developmental stages corresponding to main events in fish early life (first exogenous feeding, notochord flexion and completion of fin ray counts), were histologically processed in order to follow changes in the white myotomal muscle size, cellularity and localisation of proliferative nuclei. Morphometric analyses showed that, for 13, 15 and 20°C incubated/reared D. labrax, the total cross-sectional area of white muscle increased slowly in eleutheroembryos shorter than 5.2 mm, and four times faster in longer fish (free-swimming larvae). White muscle growth occurred both by hypertrophy (increase in muscle fibre size) and hyperplasia (increase in total number of muscle fibres) in all sampled fish, but both processes were higher in free-swimming larvae than in eleutheroembryos. The morphometric establishment of a higher hyperplastic growth of white muscle in free-swimming larvae was confirmed at immunological level by a high occurrence of proliferative nuclei. Early thermal environment was demonstrated to affect the growth process of white muscle on a different way in eleutheroembryos and free-swimming larvae: in the former, white muscle hypertrophy was stimulated at 20°C and hyperplasia at lower temperature, whereas in the latter, both white muscle hypertrophy and hyperplasia were more stimulated at 20°C than at lower temperatures. This was verified at once when the fish length and the white muscle total cross-sectional area were used as explicative variables.     

Experimental support for the cost–benefit model of lizard thermoregulation

According to Huey and Slatkin’s [Q Rev Biol 51:363–384, 1976] cost–benefit model of behavioural thermoregulation, lizards should adjust their thermoregulatory strategy between active thermoregulation and thermoconformity (no thermoregulation) according to the costs (time and energy spent thermoregulating, exposure to predators), benefits (optimised physiological performance) and thermal quality of environment associated with a given situation. However, Gilchrist’s [Am Nat 146:252–270, 1995] model of thermal specialisation suggests that apparently costly mechanisms of behavioural thermoregulation can greatly increase fitness if the optimal body temperature is achieved. Field studies of ectotherm thermoregulatory strategies under extreme cold conditions and experiments testing the effects of cool environments on thermoregulatory behaviour are surprisingly scarce. We conducted laboratory experiments to test if common lizards Zootoca vivipara (an active thermoregulator in the field) are able to switch between active thermoregulation and thermoconformity in response to different thermal environments. We found that lizards in treatments with an opportunity to reach their preferred body temperature thermoregulated accurately, maintained their level of daily activity and improved their body condition considerably. In contrast, lizards in the treatment where the preferred body temperature could not be reached became thermoconformers, decreased their daily activity (except for gravid females) and did not increase their body condition. Our results show that lizards can indeed change their thermoregulatory strategy but stress that maintaining the preferred body temperature and, thus, optimising the physiological performance have high priority in lizard behaviour.     

Differences in photosynthetic pigment signatures between phytoneuston and phytoplankton communities in a coastal lagoon of Baja California

In order to understand the relationships between the dynamics of phytoplankton populations in the surface microlayer (MIL) and in the water column below (SSW), this study used high-performance liquid chromatography-derived pigment markers in samples from a coastal lagoon of Baja California (Estero de Punta Banda, EPB) under summer (October 2003) and winter (December 2003) conditions. Photosynthetic pigment signatures of phytoplankton at the air–sea interface (phytoneuston) and subsurface measurements were related to bottom-up (temperature, salinity, nutrient concentrations) and top-down factors (zooplankton abundance). Slicks and scum layers were observed in the inner part of the lagoon and coincided with greater stratification of layers just below the sea surface and lower wind intensities. In general, spatial variability in pigment markers and ancillary data was very high and resulted in non-significant differences between MIL and subsurface samples when different regions of EPB or sampling dates were compared. However, different patterns were found between pigments and environmental factors of MIL and SSW samples when the relative numbers of stations with positive and negative differences (ΔX = X _MIL−X _SSW) were computed. For each survey, pigment markers of phytoneuston and phytoplankton samples were not necessarily correlated. Further analysis revealed that those markers (19′-butanoyloxyfucoxanthin, prasinoxanthin, divinil-chlorophyll a) corresponded to picophytoplankton groups (haptophyte, prasinophyte, and prochlorophyte). On both dates, the MIL was enriched in 19′-hexanoyloxyfucoxanthin (a marker for a type 4 haptophyte) and fucoxanthin (marker for bacillariophytes, haptophytes, and crysophytes) and depleted in peridinin (marker for dinophytes). Different zooplankton grazers accumulated in the MIL (loricate tintinnids) and in SSW (copepod nauplii).