Global warming and positive fitness response in mountain populations of common lizards Lacerta vivipara

Recent global warming threatens many species and has already caused population‐ and species‐level extinctions. In particular, high risks of extinction are expected for isolated populations of species with low dispersal abilities. These predictions rely on widely used ‘climatic envelope’ models, while individual responses, the ultimate driver of a species response to climate change, have been most often neglected. Here, we report on some changes in life‐history traits of a dispersal‐limited reptile species (a poorly studied taxa) living in isolated populations. Using long‐term data on common lizards collected in southern France, we show that individual body size dramatically increased in all the four populations studied over the past 18 years. This increase in body size in all age classes appeared related to a concomitant increase in temperature experienced during the first month of life (August). Daily maximum temperature in August increased by 2.2°C and yearling snout‐vent‐length increased by about 28%. As a result, adult female body size increased markedly, and, as fecundity is strongly dependent on female body size, clutch size and total reproductive output also increased. For one population where capture–recapture data were available, adult survival was positively related to May temperature. All fitness components investigated therefore responded positively to the increase in temperature, such that it might be concluded that the common lizard has been advantaged by the shift in temperature. We contrast these short‐term results with the long‐term habitat‐based prediction that these populations located close to mountain tops on the southern margin of the species range should be unable to cope with the alteration of their habitat. To achieve a better prediction of a species persistence, one will probably need to combine both habitat and individual‐based approaches.     

Comparison of High Performance Liquid Chromatography and Stereological Image Analysis for the Quantitation of Eumelanins and Pheomelanins in Melanoma Cells*

The aim of the study was to compare two methods quantifying eumelanins and pheomelanins, pigments synthesized by melanocytes. One is based on the high performance liquid chromatography (HPLC) quantitation of specific degradation products of each melanin type. The other requires image analysis, transmission election microscopy (TEM), and stereology. This study was carried out in cultured human melanoma cells and for each line, melanins were measured by HPLC and cells were fixed and embedded as pellets for TEM. Ultrathin sections were treated or not by the alkali elution method allowing the elimination of pheomelanins. The obtained micrographs were analyzed with our image analysis program permitting the estimation of several primary parameters. Stereology was used for estimating melanosomal maturation, intracellular melanins content, and number of melanized melanosomes per cell, for total melanin, eumelanins, or pheomelanins. Our results show a good correlation between both methods for total melanin, particularly when using the cytoplasmic volume density of melanin (r=0.93). Moreover, we report that the number of melanized melanosomes per cell and not the melanosomal maturation is responsible for the differences in total melanin content observed between the different cell lines. However, none of the stereological melanization parameters was correlated in the case of eumelanins or pheomelanins. In order to demonstrate the utter relevancy of this stereological approach, utilization of more pigmented melanoma cells, comparative study of HPLC and stereology, in normal epidermal melanocytes and a new evaluation of the alkali elution method in appropriate animal models would help us to explain the present results.     

Interactive influences of fire intensity and vertical distribution of seed banks on post‐fire recolonization of a tall‐tussock grassland in Argentina

Abstract Recolonization patterns of a tall‐tussock grassland differ between low‐frequency and high‐intensity fires. A series of laboratory and field experiments were performed on the seed bank and on seeds of the main colonizing species (Carduus acanthoides, Cirsium vulgare, Lotus glaber) to determine and compare the effects of fire frequency and fire intensity on their recolonization potential. Seed‐bank size of colonizing species did not show a significant variation with contrasting fire frequencies, so overall interval‐dependent effects do not seem to affect their propagule pool at the time of fire. However, frequency of fire modified the proportion of viable seeds and their dormancy state according to species. Accumulated emergence from experimentally buried soft‐seeds of Lotus was lower after high‐intensity fires (following wind direction) than after back‐fires (against wind direction), but no significant effects of fire‐front direction on seedling emergence were observed for hard‐seeds of Lotus nor Carduus and Cirsium. Seedling emergence from buried seeds of Cirsium was increased with doubling fuel loads, particularly from deepen soil layers, where Cirsium had most of their viable seeds after a low frequency of fire. Emergence from hard‐seeds of Lotus was less promoted than Cirsium by doubling fuel loads, and according to analysis of excavated seedlings, it was completely inhibited from upper soil layers of the seed bank. Integration of species‐specific and burial depth‐specific responses of Cirsium and Lotus seeds according to fuel load, vertical distribution of the seed banks, seed dormant states and mean emergence depths, resulted in expected emergence values which agree with their previously observed patterns of recolonization. Thus, event‐dependent mechanisms had a better predictive value on recolonization success of the studied species than the observed cumulative effects of fire history on their seed‐bank size.     

Properties of an unusual isolate of raspberry ringspot virus from grapevine in Germany and evidence for its possible transmission by Paralongidorus maximus

An isolate of raspberry ringspot nepovirus (RRV-P) commonly found infecting grapevine in localised areas of the German Palatinate, was serologically closely related to, but distinguishable from, the English type strain of this virus (RRV-E) which is transmitted by Longidorus macrosoma. However, unlike RRV-E, RRV-P had a restricted herbaceous host range and produced symptoms reliably in only two hosts, Chenopodium quinoa and Nicotiana occidentalis-accession 37B: these symptoms were a faint systemic vein clearing which, on most occasions in C. quinoa, was transient. In in vitro studies with herbaceous plant sap, RRV-P infectivity was lost after diluting 1/100 -1/500, after storage at 20^oC for 1–3 days and at 4^oC for 45 days: for similar studies with RRV-E, the values were 1/125 000, and more than 15 days at 20^oC and 4^oC, respectively. RRV-P was difficult to purify in quantity and in most preparations seemed to sediment as a single component corresponding to ‘bottom’ component of RRV-E. Purified particles of RRV-P, like those of RRV-E, contained a major polypeptide and two RNA species of M_r 54 000, 2.6 times 10⁶and 1.6 times 10⁶respectively. There was no evidence from RNA preparations from purified virus particles or, from analysis of dsRNA from infected plants, that RRV-P contained a satellite RNA. The incidence of RRV-P in vineyards was not associated with the presence in soils of Longidorus nematodes, but was associated with the distribution in the Palatinate of Paralongidorus maximus. Furthermore, results from an experiment in Germany in a vineyard planted with healthy grapevines in soil fumigated to destroy nematodes, showed spread of RRV-P into these plants from an adjoining source of infected grapevines and soil infested with P. maximus. In laboratory studies, RRV-P was transmitted by P. maximus at a very low level between grapevines (used as the virus source and test plants) but not to, or between, herbaceous hosts.     

Chloroplast protection in plum pox virus‐infected peach plants by L‐2‐oxo‐4‐thiazolidine‐carboxylic acid treatments: effect in the proteome

Sharka, a disease caused by plum pox virus (PPV), has a significant economic impact on fruit tree production. In this work, we analysed the effect of (2,1,3)‐benzothiadiazole (BTH) and L‐2‐oxo‐4‐thiazolidine‐carboxylic acid (OTC) on plant growth and virus content. OTC reduced sharka symptom, stimulated plant growth and alleviated PPV‐induced oxidative stress, indicated by a lack of changes in some oxidative stress parameters. PPV infection reduced chloroplast electron transport efficiency. However, in the presence of BTH or OTC, no changes in the chlorophyll fluorescence parameters were observed. PPV produced an alteration in chloroplast ultrastructure, giving rise to a decrease in starch contents that was less dramatic in OTC‐treated plants. Furthermore, PPV reduced the abundance of proteins associated with photosynthesis, carbohydrate and amino acid metabolism and photorespiration. These changes did not take place in OTC‐treated plants, and increases in the expression of proteins related with the aforementioned processes, including ADP‐glucose pyrophosphorylase, were produced, which correlated with the lower decrease in starch contents observed in PPV‐infected plants treated with OTC. The results suggested that OTC treatment provides protection to the photosynthetic machinery and/or the chloroplast metabolism in PPV‐infected peaches. Thus, OTC could have practical implications in agriculture in improving the vigour of different plant species as well as in immunizing plants against pathogens.