Chromosome numbers in wild and semidomesticated Brazilian Capsicum L. (Solanaceae) species: do x = 12 and x = 13 represent two evolutionary lines?

Chromosome numbers were determined in 29 accessions of wild and semidomesticated Capsicum species from the EMBRAPA Hortaliças (Brazil) germplasm collection. 2 n  = 24 was found in C. baccatum var. praetermissum , C. chinense , C. flexuosum and C. parvifolium , while C. buforum , C. campylopodium , C. cornutum , C. schottianum , C. villosum var. villosum and five other native south-eastern Brazilian species not yet taxonomically named all had 2 n  = 26 chromosomes. These are the first chromosome number determinations for C. cornutum , C. schottianum , C. villosum var. villosum and the five other Brazilian taxa. Our data confirm published data for C. baccatum var. praetermissum , C. campylopodium , C. chinense , C. flexuosum and C. parvifolium , but not for C. buforum . The prevalence of 2 n  = 26 chromosomes among Brazilian species, along with the morphological and ecological characteristics presented by the wild and semidomesticated species occurring in Brazil, form a pattern different from that found in Andean wild and semidomesticated species. This supports the hypothesis that there are two different evolutionary lines in the genus and that the native south-eastern Brazilian species belong to the ancestral Capsicum gene pool. © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 151 , 259–269.     

Molecular Phylogeny and Biogeography of the Genus Ilex L. (Aquifoliaceae)

The chloroplast atpB-rbcL spacer was sequenced for 115 speciesof Ilex and forNemopanthus mucronatus (Aquifoliaceae). In addition,rbcL sequences were obtained for 47 selected species. Takentogether with fossil records in the literature, the data indicatethat: (1) the lineage Ilex was already cosmopolitan long beforethe end of the Cretaceous. A relative test of the rate of nucleotidesubstitution indicates that extant species do not representthe entire lineage because of the extinction of its basal branches.The common ancestor of the extant species probably appearedat the upper Tertiary. (2) Several Asian/North American disjunctionsare observed, as well as North American/South American relationships.The directions of these relationships are yet to be determined.The African species Ilex mitis is closely related to Asian species.Ilex anomala (Hawaii and Tahiti) is related to American species.Ilex perado and Ilex canariensis (both in Macaronesia) havetotally different relationships, the former being related toEurasian species, while relationships of the latter remain obscure.(3) Gene trees substantially contradict the systematics of Loesener.Nemopanthus,closely related to Ilex amelanchier, is nested in the genusIlex. The family Aquifoliaceae is organized in four groups,each of them having a geographic or ecological peculiarity.Copyright 2000 Annals of Botany Company Aquifoliaceae, chloroplast DNA, fossil record, historical biogeography, Ilex (holly tree), molecular phylogeny.     

Vestiges of an ancestral host plant: preference and performance in the butterfly Polygonia faunus and its sister species P. c‐album

1. In the study of the evolution of insect–host plant interactions, important information is provided by host ranking correspondences among female preference, offspring preference, and offspring performance. Here, we contrast such patterns in two polyphagous sister species in the butterfly family Nymphalidae, the Nearctic Polygonia faunus, and the Palearctic P. c‐album. 2. These two species have similar host ranges, but according to the literature P. faunus does not use the ancestral host plant clade – the ‘urticalean rosids’. Comparisons of the species can thus test the effects of a change in insect–plant associations over a long time scale. Cage experiments confirmed that P. faunus females avoid laying eggs on Urtica dioica (the preferred host of P. c‐album), instead preferring Salix, Betula, and Ribes. 3. However, newly hatched larvae of both species readily accept and grow well on U. dioica, supporting the general theory that evolutionary changes in host range are initiated through shifts in female host preferences, whereas larvae are more conservative and also can retain the capacity to perform well on ancestral hosts over long time spans. 4. Similar rankings of host plants among female preference, offspring preference, and offspring performance were observed in P. c‐album but not in P. faunus. This is probably a result of vestiges of larval adaptations to the lost ancestral host taxon in the latter species. 5. Female and larval preferences seem to be largely free to evolve independently, and consequently larval preferences warrant more attention.     

Diagnosing and assessing uncertainties of terrestrial ecosystem models in a multimodel ensemble experiment: 2. Carbon balance

This paper examines carbon stocks and their relative balance in terrestrial ecosystems simulated by Biome‐BGC, LPJ, and CASA in an ensemble model experiment conducted using the Terrestrial Observation and Prediction System. We developed the Hierarchical Framework for Diagnosing Ecosystem Models to separate the simulated biogeochemistry into a cascade of functional tiers and examine their characteristics sequentially. The analyses indicate that the simulated biomass is usually two to three times higher in Biome‐BGC than LPJ or CASA. Such a discrepancy is mainly induced by differences in model parameters and algorithms that regulate the rates of biomass turnover. The mean residence time of biomass in Biome‐BGC is estimated to be 40–80 years in temperate/moist climate regions, while it mostly varies between 5 and 30 years in CASA and LPJ. A large range of values is also found in the simulated soil carbon. The mean residence time of soil carbon in Biome‐BGC and LPJ is ～200 years in cold regions, which decreases rapidly with increases of temperature at a rate of ～10 yr °C^?1. Because long‐term soil carbon pool is not simulated in CASA, its corresponding mean residence time is only about 10–20 years and less sensitive to temperature. Another key factor that influences the carbon balance of the simulated ecosystem is disturbance caused by wildfire, for which the algorithms vary among the models. Because fire emissions are balanced by net ecosystem production (NEP) at steady states, magnitudes, and spatial patterns of NEP vary significantly as well. Slight carbon imbalance may be left by the spin‐up algorithm of the models, which adds uncertainty to the estimated carbon sources or sinks. Although these results are only drawn on the tested model versions, the developed methodology has potential for other model exercises.     

Habitat invasion risk assessment based on Landsat 5 data,exemplified by the shrub Rosa rubiginosa in southern Argentina

Prediction of invasive species spread helps to plan management actions. We performed a risk assessment by quantifying habitat invasibility, predicted the potential distribution of an invasive species using the Maxent modelling program and confirmed patterns using detailed field studies. Our study was conducted in southern Argentina, Patagonia, where large areas are already invaded by the European shrub Rosa rubiginosa. A total of 163 R. rubiginosa locations served as ground truth data, and predictors were obtained from the spaceborne sensor Landsat 5. Based on the Maxent Method (area under the receiver operating characteristic curve 0.8), the habitat invasibility map covered about 5000 km². Our model revealed that R. rubiginosa has the potential to invade 36% of the area along a steep precipitation gradient (target region 600–1400 mm per year). The Tasseled Cap brightness index and the normalized vegetation index explained most of the variance in our model, followed by the Tasseled Cap greenness and wetness indices, which can be interpreted as indicators of disturbance. Highest levels of invasibility were predicted for urban areas, along roads and rivers, on pastures, in Austrocedrus chilensis forests and inside Nothofagus dombeyi forest gaps. Detailed field assessments of rose cover performed in seven habitat types supported these results: rose cover significantly decreased with increasing tree cover (P < 0.01). Our data revealed that the occurrence of R. rubiginosa is not connected to a certain habitat type, but that it thrives in open patches following habitat disturbance. Our approach is a widely applicable, cost‐free remote sensing method that can serve as a risk assessment tool for alien plant species invasion of habitats.     

Comparative response of δ13C, δ18O and δ15N in durum wheat exposed to salinity at the vegetative and reproductive stages

This study compared the performance of the stable isotope composition of carbon (δ¹³C), oxygen (δ¹⁸O) and nitrogen (δ¹⁵N) by tracking plant response and genotypic variability of durum wheat to different salinity conditions. To that end, δ¹³C, δ¹⁸O and δ¹⁵N were analysed in dry matter (dm) and the water‐soluble fraction (wsf) of leaves from plants exposed to salinity, either soon after plant emergence or at anthesis. The δ¹³C and δ¹⁸O of the wsf recorded the recent growing conditions, including changes in evaporative conditions. Regardless of the plant part (dm or wsf), δ¹³C and δ¹⁸O increased and δ¹⁵N decreased in response to stress. When the stress conditions were established just after emergence, δ¹⁵N and δ¹³C correlated positively with genotypic differences in biomass, whereas δ¹⁸O correlated negatively in the most severe treatment. When the stress conditions were imposed at anthesis, relationships between the three isotope signatures and biomass were only significant and positive within the most severe treatments. The results show that nitrogen metabolism, together with stomatal limitation, is involved in the genotypic response to salinity, with the relative importance of each factor depending on the severity and duration of the stress as well as the phenological stage that the stress occurs.     

Life history strategy of Leptinaria unilamellata (d'Orbigny, 1835) (Mollusca,Pulmonata, Subulinidae)

Abstract

Life history theory predicts that the patterns of resource allocation in animals are associated with different strategies, selected in the course of evolution. In the present study, the life history of Leptinaria unilamellata was characterized under laboratory conditions. We determined the growth, reproduction, and longevity patterns of this species and elucidated the strategy related to the development of embryos, through direct observations and examination of the morphology of the gravid uterus. Furthermore, we attempted to analyze the glycogen and galactogen contents of the albumen gland, digestive gland and cephalopedal mass in order to understand energy allocation to life history traits, for three life stages. Leptinaria unilamellata's life history is characterized by great longevity, a short juvenile phase, early sexual maturity, and repeated reproductive events, with little reproductive effort at each event and some mortality shortly after the first reproduction. In the terraria, we found juveniles but no eggs. However, the results of the anatomical study showed no morphological connection between the embryos and the parental organism. Thus, this species should be described as ovoviviparous rather than viviparous. Egg retention in the parent organism is the primary cause of the release of juveniles, instead of eggs, enabling the offspring to withstand environmental stress. The higher quantity of galactogen found in the adults' albumen gland, as compared to juveniles and senescent individuals, as well as the ratio of glycogen to galactogen, reveal the allocation of energy to reproduction rather than to growth. The remaining energy is directed to the maintenance of omeostasis. Such pattern was confirmed by the low levels of glycogen and galactogen observed in the senescent stage, compared to the juvenile and adult stages. In the life strategy of L. unilamellata, the distribution of the reproductive effort among many events associated with ovoviviparity indicates a long-term investment in reproductive success.     

Evolution of Dendrocolaptes platyrostris (Aves: Furnariidae) between the South American open vegetation corridor and the Atlantic forest

The open vegetation corridor of South America is a region dominated by savanna biomes. It contains forests (i.e. riverine forests) that may act as corridors for rainforest specialists between the open vegetation corridor and its neighbouring biomes (i.e. the Amazonian and Atlantic forests). A prediction for this scenario is that populations of rainforest specialists in the open vegetation corridor and in the forested biomes show no significant genetic divergence. We addressed this hypothesis by studying plumage and genetic variation of the Planalto woodcreeper Dendrocolaptes platyrostris Spix (1824) (Aves: Furnariidae), a forest specialist that occurs in both open habitat and in the Atlantic forest. The study questions were: (1) is there any evidence of genetic continuity between populations of the open habitat and the Atlantic forest and (2) is plumage variation congruent with patterns of neutral genetic structure or with ecological factors related to habitat type? We used cytochrome b and mitochondrial DNA control region sequences to show that D. platyrostris is monophyletic and presents substantial intraspecific differentiation. We found two areas of plumage stability: one associated with Cerrado and the other associated with southern Atlantic Forest. Multiple Mantel tests showed that most of the plumage variation followed the transition of habitats but not phylogeographical gaps, suggesting that selection may be related to the evolution of the plumage of the species. The results were not compatible with the idea that forest specialists in the open vegetation corridor and in the Atlantic forest are linked at the population level because birds from each region were not part of the same genetic unit. Divergence in the presence of gene flow across the ecotone between both regions might explain our results. Also, our findings indicate that the southern Atlantic forest may have been significantly affected by Pleistocene climatic alteration, although such events did not cause local extinction of most taxa, as occurred in other regions of the globe where forests were significantly affected by global glaciations. Finally, our results neither support plumage stability areas, nor subspecies as full species. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 103 , 801–820.     

Phylogeny of Mesocyclops (Copepoda: Cyclopidae) inferred from morphological characters

Evolutionary relationships were investigated in the genus Mesocyclops, a pantropical freshwater cyclopid group. In the phylogenetic analyses that involved all 71 known species, and used 81 morphological characters (265 character states) mainly of the adult females, two different approaches were applied: global parsimony, and a new distance method based upon the recognition of sister‐groups on the basis of minimal distances iteratively corrected for unique character states (MICSEQ). In coding of the characters, half of which showed intraspecific variation, the ‘scaled’ method was employed, which assumes that any trait between its absence and fixed presence passes through a polymorphic stage. Impact of the reference points on topology of the trees generated by the parsimony method was tested in three ways where the outgroups comprised: (1) nine species representing six genera of two subfamilies; (2) three species from two genera supposedly not distant from Mesocyclops; and (3) one presumably close and one distant relative of Mesocyclops. The trees generated by the parsimony‐based and corrected distance methods agreed as to the monophyly of the following groups: reidae‐clade (M. reidae, M. chaci, M. yutsil); rarus‐clade (Mesocyclops annae, M. pseudoannae, M. splendidus, M. rarus, M. paludosus, M. darwini, M. dayakorum); annulatus‐clade (Mesocyclops intermedius, M. ellipticus, M. paranaensis, M. annulatus, M. tenuisaccus); meridianus‐clade (Mesocyclops meridionalis, M. varius, M. venezolanus, M. brasilianus, M. pseudomeridianus, M. meridianus); major‐clade (Mesocyclops major, M. pilosus, M. insulensis); dussarti‐clade (M. dussarti, M. dadayi, M. isabellae, M. thermocyclopoides); pubiventris‐clade (M. pubiventris, M. medialis, M. brooksi, M. notius). A majority of the analyses support a clade of the ‘true’Mesocyclops including all ingroup species except the reidae‐group, and point to monophyly of the Old World species lacking medial spine on P1 basipodite. There were, however, some components for which the two procedures, regardless of the outgroup choice and/or character set, suggested different relationships. Basal relationships of Mesocyclops[between M. edax (North and Central America), the Neotropical species (M. longisetus, M. araucanus, M. evadomingoi, meridianus‐ and annulatus‐clade), Old World group (P1 basipodite without medial spine) and the rarus‐clade (Old World; P1 basipodite with medial spine)] remained unresolved. © 2006 The Linnean Society of London, Zoological Journal of the Linnean Society, 2006, 147 , 1–70.