Seed micromorphology in the genus Neotinea Rchb.f. (Orchidaceae, Orchidinae)

The ultrastructure of testa seed in the genus Neotinea (Orchidaceae, Orchidinae) was examined for the first time. The morphology of the seed and of the anticlinal and periclinal walls was analysed by scanning electron microscopy. Quantitative data concerning the length and width of the seed and embryo, seed and embryo volume, free air space, and number of cells along the longitudinal axis are presented. In all species, the seeds are fusiform in shape with transverse ridges on the inner periclinal walls. This ornamentation pattern is characteristic for the genus Neotinea . It is a good diagnostic value supporting the monophyly of this genus, which has recently been proposed by several authors.  © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society , 2007, 153 , 133–140.     

A metabolomic study in oats (Avena sativa) highlights a drought tolerance mechanism based upon salicylate signalling pathways and the modulation of carbon,antioxidant and photo‐oxidative metabolism

Although a wealth of information is available on the induction of one or several drought‐related responses in different species, little is known of how their timing, modulation and crucially integration influence drought tolerance. Based upon metabolomic changes in oat (Avena sativa L.), we have defined key processes involved in drought tolerance. During a time course of increasing water deficit, metabolites from leaf samples were profiled using direct infusion–electrospray mass spectroscopy (DI‐ESI‐MS) and high‐performance liquid chromatography (HPLC) ESI‐MS/MS and analysed using principal component analysis (PCA) and discriminant function analysis (DFA). The involvement of metabolite pathways was confirmed through targeted assays of key metabolites and physiological experiments. We demonstrate an early accumulation of salicylic acid (SA) influencing stomatal opening, photorespiration and antioxidant defences before any change in the relative water content. These changes are likely to maintain plant water status, with any photoinhibitory effect being counteracted by an efficient antioxidant capacity, thereby representing an integrated mechanism of drought tolerance in oats. We also discuss these changes in relation to those engaged at later points, consequence of the different water status in susceptible and resistant genotypes.     

Geographic variation of body size and reproductive patterns in Continental versus Mediterranean asp vipers, Vipera aspis

The occurrence of variation in body size and reproductive traits of Vipera aspis was assessed by analysing 74 reproductive females of different populations, collected throughout a large part of the distribution range of the taxon, from central‐western France to central Italy. Six populations were analysed, two of plain habitats, in France and Italy, characterized by a Continental climate, whereas the other four derived from two coastal and two inland, hilly Italian habitats, respectively, showing a Mediterranean climate. Females of the French area showed the smallest mean body size, whereas the pre‐ and post‐partum body masses of females from the coolest, central Italic area were significantly higher. Litter size varied among habitats and was significantly correlated with maternal body size. If the snout–vent length feature varied largely among offspring of different habitats (with the longest size occurring in representatives of the coastal, central Italian area), the average of both body mass and total mass of offsprings did not exhibit any clear pattern among populations colonizing different habitats. Nevertheless, relative litter mass was higher in the French continental populations, and lower in the coolest, Mediterranean, Italian ones. It is worth emphasizing the positive correlation between the snout–vent length feature of females and the total litter mass to environmental factors, such as hottest month temperature and total rainfall. The available literature records that female body size affects offspring size and fecundity. If the present study bolsters this correlation, it also rules out any other effect of female body size on the offspring characteristics analysed. Finally, evidence is provided for the role of climatic factors on life‐history traits (e.g. pre‐partum body mass) of asp vipers, although confounding effects pursued, for example, by food availability may occur. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 96 , 383–391.     

Home-ranges and patterns of spatial use in territorial Bonelli's Eagles Aquila fasciata

Bonelli's Eagle Aquila fasciata is one of the rarest birds of prey in Europe, where it has suffered a significant decline in recent decades. We present information on the home-ranges and spatial parameters of 18 Bonelli's Eagles radiotracked in 2002–2006 in Catalonia (northeast Spain) and describe the home-range probability kernel, distances moved, breeding area eccentricity, territorial overlap, nearest neighbour distance and breeding site fidelity, and assess the influence of sex, breeding status, season and geographical area on these parameters. Median home-range according to the minimum convex polygon (MCP) and 95% kernel were 50.3 and 36.1 km², respectively. The median breeding area eccentricity was 1477 m. There was considerable overlap in the home-range of both sexes within pairs (MCP: 71.4% and 95% kernel: 98.5%), indicating close pair bonding and similar foraging patterns. Overlap in home-ranges of up to 15% between neighbouring individuals also occurred and was positively related to breeding pair density. There was no difference in spatial parameters between sexes or with breeding status, but during the non-breeding season Eagles had larger home-ranges and stayed further from nests. The high consistency across birds suggests a pattern of spatial use that is characteristic of this species. The high level of use of breeding areas and their surroundings (50% kernel) throughout the year makes it important that these areas be protected from human disturbance. Additionally, it is necessary that heavily used areas away from nesting sites, which are used for foraging and roosting, are identified, protected and managed in a sustainable fashion.     

Rarity and decline in palaeoendemic Martino's vole Dinaromys bogdanovi

• 1 Martino's vole Dinaromys bogdanovi is the only living member of the Tertiary genus Dinaromys, and probably also the only surviving member of the Pliomys lineage. The range of the genus Dinaromys has historically been small and its rate of evolution has been low.
• 2 Martino's vole shows all three attributes of rarity in accordance with Rabinowitz's ‘seven forms of rarity’ model: (i) its range is estimated at 43 545 km² but the area of occupancy is <5200 km²; (ii) its habitat requirements are narrow and the species is strictly tied to exposed, karstified bedrock; and (iii) current populations are invariably small and frequently isolated.
• 3 The Pleistocene range of Martino's vole exceeded the recent one, at least in the north‐western part of the Balkans, and its shrinkage continued into the Holocene.
• 4 Martino's vole may be in competition with the European snow vole Chionomys nivalis, which has a very similar morphology and presumably identical habitat requirements, but is shifted towards an r‐selected life‐history strategy. Long‐term sympatry of these voles has probably resulted in competitive exclusion of the relatively K‐selected Martino's vole by the relatively r‐selected European snow vole.
• 5 Martino's vole consists of two deeply divergent (about one million years ago) phylogeographical lineages, which may represent distinct cryptic species. Rarity is particularly pronounced in the north‐western lineage to the west of the Neretva River, where rocky habitats are largely occupied by the European snow vole.
• 6 In the IUCN Red List of Threatened Animals, Martino's vole is classified as ‘near threatened’. However, the north‐western lineage, which is phylogeographically most divergent and has the greatest genetic diversity, is classed as a ‘vulnerable’ evolutionary significant unit on the basis of its small area of occupancy (<2000 km²). Long‐term population monitoring is an essential step in evaluating the conservation needs of Martino's vole.

     

GLOBE students, teachers, and scientists demonstrate variable differences between urban and rural leaf phenology

The urban heat island effect, classically associated with high impervious surface area (ISA), low vegetation fractional cover (Fr), and high land surface temperature (LST), has been linked to changing patterns of vegetation phenology, especially spring growth. In this study, a collaboration with the Global Learning and Observations to Benefit the Environment (GLOBE) program, we investigated the effect of the urban environment on the timing of leaf budburst of native deciduous trees in seven cities: Asia (Tokyo, Japan; Bangkok and Korat, Thailand), Europe (Jyväskylä, Finland; Bishkek, Kyrgyzstan), Africa (Dakar, Senegal), and North America (Fairbanks, Alaska). The cities differed not only in population size but also in climate and vegetation type. Using Landsat satellite imagery from each city, we calculated LST, Fr, and ISA, and classified sites within each study area as rural or urban. The timing of leaf flushing, measured by students using GLOBE budburst protocols, was statistically different within all cities, with absolute differences ranging from 1 to 23 days. We assessed the classic urban phenology paradigm, which proposes higher LST, lower Fr, and earlier budburst in urban areas of temperate cities. Of the four temperate cities, Tokyo followed the classic paradigm, but no other city demonstrated consistent support. Urban budburst was advanced in three of the four temperate cities, but in only one of the three tropical cities. Results suggest that while vegetation phenology is consistently different between urban and rural areas, a uniform paradigm based on the explanatory variables in this study did not emerge. Although not testable here, it is likely that alterations to chilling requirements in temperate climates and humidity in tropical climates may also influence observed budburst differences.