How do plants make mitochondria?

Plant mitochondria can differ in size, shape, number and protein content across different tissue types and over development. These differences are a result of signaling and regulatory processes that ensure mitochondrial function is tuned in a cell-specific manner to support proper plant growth and development. In the last decade, the processes involved in mitochondrial biogenesis are becoming clearer, including; how dormant seeds transition from empty promitochondria to fully functional mitochondria with extensive cristae structures and various biochemical activities, the regulation of nuclear genes encoding mitochondrial proteins via regulators of the diurnal cycle in plants, the mitochondrial stress response, the targeting of proteins to mitochondria and other organelles and connections between the respiratory chain and protein import complexes. All these findings indicate that mitochondrial function is a part of an integrated cellular network, and communication between mitochondria and other cellular processes extends beyond the known exchange or transport of metabolites. Our current knowledge now needs to be used to gain more insight into the molecular components at various levels of this hierarchical and complex regulatory and communication network, so that mitochondrial function can be predicted and modified in a rational manner.     

Field metabolic rates of instrumented Adélie penguins using double-labelled water

Summary Adélie penguins (Pygoscelis adeliae) carrying dummy instruments were used to determine field metabolic rates using double-labelled water. All penguins injected with double-labelled water showed a marked loss of body mass (-4.5%) during the period of the experiments (20–131 h), irrespective of the time of the breeding season. Total body water averaged 57.3% and water flux estimates of field metabolic rates correlated with double-labelled water estimates of field metabolic rate (r ²=0.68), indicating that Adélie penguins do not ingest significant amounts of sea water. Brooding Adélie penguins had a mean field metabolic rate of 10.1 W·kg^-1 and at sea a field metabolic rate of 13.3 W·kg^-1, both of which compare well with previously published estimates based on time/activity budgets and respirometry. Mean field metabolic rate in penguins with crèching chicks was 14.1 W·kg^-1, and the birds spent 65 h absent from the nest as opposed to previous estimates of 7.1 W·kg^-1 and 21 h. The effects of weather, disturbance and manipulation on the behaviour and field metabolic rate of penguins late in the breeding season are discussed. Adélie penguins (crèching chicks) equipped with externally attached instruments spent more time absent from the nest than noninstrumented controls (76 vs 54 h), but had a lower field metabolic rate.Abbreviations ANOVA analysis of variance - DLW double-labelled water - FMR field metabolic rate - MR metabolic rate - RMR resting metabolic rate - TBW total body water - VSMOW Vienna standard mean ocean water - WF water flux     

Commodity specific rates of temporal discounting: Does metabolic function underlie differences in rates of discounting?

Discounting rates vary as a function of commodity type. Previous studies suggest five potential characteristics of the commodity that could explain these differences: type of reinforcer (primary or secondary), if the commodity is perishable, if the commodity is satiable, if the commodity can be directly consumed, and immediacy of consumption. This paper suggests that these characteristics may best be viewed as related to a more fundamental characteristic: metabolic processing. In order to explore the possibility that metabolic processing underlies changes in discount rates, the difference in discounting between food, money, music CDs, DVDs, and books are compared. Music CDs, DVDs, and books share many characteristics in common with food, including gaining value through a physiological process, but are not directly metabolized. Results are consistent with previous findings of commodity specific discount rates and show that metabolic function plays a role in determining discount rates with those commodities that are metabolized being discounted at a higher rate. These results are interpreted as evidence that the discount rate for different commodities lies along a continuum with those that serve an exchange function rather than a direct function (money) anchoring the low end and those that serve a direct metabolic function capping the high end (food, alcohol, drugs).     

Adaptive strategies of desmids in two tropical monomictic lakes in southeast Brazil: do morphometric differences promote life strategies selection?

Adaptive strategies of desmids in two tropical monomictic lakes were studied in relation to morphometric differences. The study aimed at evaluating desmids' strategies during inter-annual succession patterns in two tropical lakes (Dom Helvécio and Carioca) in southeast Brazil. From monthly samples of freshwater algae collected during five consecutive years (2002–2006) from the two lakes, the desmids were classified according to size, life form, and life strategies (competitive, stress tolerant, and ruderal). Our results indicated that Lake Carioca (19º45′20″S, 42º37′12″W), a small, shallow, turbid, and mesotrophic system showed dominance of invasive/opportunistic taxa (C) and R-strategists (Staurastrum species <20 μm), whereas Lake Dom Helvécio (19º45′–19º48′45″S, 42º33′45″W), a large, deep, and clear system was dominated by ruderal (R) species (Closterium aciculare and Pleurotaenium trabecula >50 μm) and tolerant to stress (S) species (Staurastrum and Staurodesmus species >20 μm). A significant number of desmids from the lakes had low MLD (≤20 μm), low volume (<10³), and high SV^?1 ratio (>1). Consequently, C-strategist species were abundant and formed a group having great adaptive value in the lakes, with higher resilience and capacity to change composition after the turnover period. Stratification stability and atelomixis were the main driving forces to sustain high desmid biomass in these two lakes, despite the greater macrophyte richness and great water column depth at Lake Dom Helvécio and the main factor influencing richness and contribution of complex forms.     

Does hardness make flower love less promiscuous? Effect of biomechanical floral traits on visitation rates and pollination assemblages

Visitation rates and assemblage composition of pollinators have often been related to environmental, ecological and phenotypic variables. However, the interaction between flowers and pollinators has not been evaluated in a biomechanical context. Floral rewards in keel flowers (Fabaceae, Faboideae) are concealed behind four joined petals, the keel-wing unit, and are accessible only if pollinators open this unit by exerting force on it. Force needed to open the flower is expected to affect the interaction with pollinators because pollinators must invest time and energy to open the keels. Consequently, plants with stiff flowers should be expected to experience diminished visitation frequency, particularly by weak visitors. To test this expectation of diminished visitation rates and of assemblage composition biased by pollinator strength, we measured the force needed to open the keel flowers of five co-occurring legume species and, using a canonical correspondence analysis (CCA), we tested their association with pollinator visitation rates and assemblage composition. We additionally included a size flag variable in CCA to test the effect of attractiveness on pollinator visits. There was no association between flower stiffness and visitation frequency. According to the CCA, pollinator assemblage compositions were associated with the force needed to open the keel and not flag size. As a general pattern, weak flowers are pollinated by an uneven assemblage of weak bees while the stiffest flowers are pollinated by an even assemblage of large and strong bees. These results supports the idea that force has an effect in controlling pollinator assemblage composition.     

Few immigrant phytophagous insects on woody plants in Europe: legacy of the European crucible?

Exotic phytophagous insects are invading forest ecosystems worldwide. So far, 109 invasive insects on woody plants, 57 from North American (NA), and 52 from Asia (A) have established populations in European forests. Four orders account for about 84% of the immigrants: Homoptera 39%, Lepidoptera 13%, Coleoptera 19%, and Hymenoptera 13%. The majority of these invasive species (63% of NA and 77% of A) live on deciduous trees, of which 36% have been introduced from NA and Asia. The remaining insect species (37% NA and 25% A) live on various conifers, of which 53% have also been introduced. Most (57%) of the NA insects feeding on coniferous plants live upon their introduced, native host plants. These data suggest that many NA immigrant phytophagous species in Europe have been successful in establishing permanent populations because their native hosts preceded or accompanied them into Europe and/or were asexually reproducing species. We propose that fewer invasive phytophagous insects have become established in European compared to North American woodlands because of the unique legacy of the European Pleistocene/Holocene crucible (i.e. endless cycles of populations contracting into highly disparate, dispersed metapopulation refugia and eventually expanding out of them) on European species and ecosystems that caused highly diminished heterogeneity. This translates to fewer and less penetrable tri-trophic niches in Europe due to fewer and less available host plants, but greater zootic resistance per niche derived from more competition-hardened competitors and possibly natural enemies. Moreover, many European species are probably superior invasion specialists because the crucible favored traits that are conducive to success in highly subdivided, and extinction-prone metapopulations: asexual reproduction, polyploidy, and other traits especially conducive to persistence under stress, and explosive growth/spread under amelioration.     

What do fish make of mirror images?

Fish act aggressively towards their mirror image suggesting that they consider it another individual, whereas in some mammals behavioural response to mirrors may be an evidence of self-recognition. Since fish cannot self-recognize, we asked whether they could distinguish between fighting a mirror image and fighting a real fish. We compared molecular, physiological and behavioural responses in each condition and found large differences in brain gene expression levels. Although neither levels of aggressive behaviour nor circulating androgens differed between these conditions, males fighting a mirror image had higher immediate early gene (IEG) expression in brain areas homologous to the amygdala and hippocampus than controls. Since amygdalar responses are associated with fear and fear conditioning in other species, higher levels of brain activation when fighting a mirror suggest fish experience fear in response to fights with a mirror image. Clearly, the fish recognize something unusual about the mirror image and the differential brain response may reflect a cognitive distinction.     

Allometry of sexual size dimorphism in dioecious plants: do plants obey Rensch's rule?

Rensch's rule refers to a pattern in sexual size dimorphism (SSD) in which SSD decreases with body size when females are the larger sex and increases with body size when males are the larger sex. Many animal taxa conform to Rensch's rule, but it has yet to be investigated in plants. Using herbarium collections from New Zealand, we characterized the size of leaves and stems of 297 individuals from 38 dioecious plant species belonging to three distantly related phylogenetic lineages. Statistical comparisons of leaf sizes between males and females showed evidence for Rensch's rule in two of the three lineages, indicating SSD decreases with leaf size when females produce larger leaves and increases with leaf size when males produce larger leaves. A similar pattern in SSD was observed for stem sizes. However, in this instance, females of small-stemmed species produced much larger stems than did males, but as stem sizes increased, SSD often disappeared. We hypothesize that sexual dimorphism in stem sizes results from selection for larger stems in females, which must provide mechanical support for seeds, fruits, and dispersal vectors, and that scaling relationships in leaf sizes result from correlated evolution with stem sizes. The overall results suggest that selection for larger female stem sizes to support the weight of offspring can give rise to Rensch's rule in dioecious plants.     

A quantitative review of pollination syndromes: do floral traits predict effective pollinators?

The idea of pollination syndromes has been largely discussed but no formal quantitative evaluation has yet been conducted across angiosperms. We present the first systematic review of pollination syndromes that quantitatively tests whether the most effective pollinators for a species can be inferred from suites of floral traits for 417 plant species. Our results support the syndrome concept, indicating that convergent floral evolution is driven by adaptation to the most effective pollinator group. The predictability of pollination syndromes is greater in pollinator‐dependent species and in plants from tropical regions. Many plant species also have secondary pollinators that generally correspond to the ancestral pollinators documented in evolutionary studies. We discuss the utility and limitations of pollination syndromes and the role of secondary pollinators to understand floral ecology and evolution.     

The energy cost of flight: do small bats fly more cheaply than birds?

Flapping flight is one of the most expensive activities in terms of metabolic cost and this cost has previously been considered equal for the two extant vertebrate groups which evolved flapping flight. Owing to the difficulty of obtaining accurate measurements without disturbing flight performance, current estimates of flight cost within the group of small birds and bats differ by more than a factor of five for given body masses. To minimize the potential problem that flight behaviour may be affected by the measurements, we developed an indirect method of measuring flight energy expenditure based on time budget analysis in which small nectar-feeding bats (Glossophaginae) could continue their natural rhythm of flying and resting entirely undisturbed. Estimates of metabolic flight power based on 172 24-h time and energy budget measurements were obtained for nine individual bats from six species (mass 7–28 g). Metabolic flight power (P_F) of small bats was found to increase with body mass following the relation P_F = 50.2 M^0.771 (r² = 0.96, n = 13, P_F in W, M in kg). This is about 20–25% below the majority of current predictions of metabolic flight cost for small birds. Thus, either the flight cost of small birds is significantly lower than has previously been thought or, contrary to current opinion, small bats require less energy to fly than birds. Accepted: 29 September 1997     

Water channels in plants: do basic concepts of water transport change?

A review and re-examination of literature data shows that highlyselective water channels (aquaporins) have marked effects onthe overall transport properties of the plasma membrane of plantcells. The application of the channel blocker HgCl₂ (50 µM)or of high external concentrations of permeating solutes reducedthe water permeability (hydraulic conductivity, Lp) of Charainternodes down to 25% of the control. In treated cells, reflectioncoefficients (     

Prophylaxis and treatment of bacterial infections: do we need new strategies?

Bacterial infections in patients with hematologic malignancies still represent a severe and life-treating problem. Several observational studies during the last decade have revealed that neutropenic patients with fever are a heterogeneous population with various differences regarding response to initial therapy, development of serious complications and mortality. The role of neutropenia as main risk factor for infections in hematologic patients and the definition of different level of risk related to neutrophils count and duration of neutropenia have been extensively studied and different categories of patients based on the risk of infection, mostly the condition of neutropenia, have been clearly defined. The strategies on antimicrobial therapy and supportive care in hematologic patients need to be continuously assessed, in fact new conditions favouring the occurrence of infectious complications in patients with hematologic malignancies have progressively emerged. The use of oral prophylactic antibiotics in neutropenic cancer patients is still a matter of debate. Before 2005, several trials showed how the prevention of infection can be extremely important in this setting of patients but none was conclusive. In 2005 two meta-analysis and two large randomized clinical trials gave new evidence that antibacterial prophylaxis can reduce in neutropenic patients several important outcomes including mortality. The use of the empiric antibacterial therapy represents the cornerstone of the antimicrobial strategies in the febrile neutropenic patients leading, over the span of 20 years, to a dramatic decrease of deaths: Actually beta-lactam monotherapy is commonly used for the empiric treatment of febrile neutropenia. Recently, large randomized clinical trials and meta-analysis showed that the addition of an aminoglycoside and/or a glycopeptides results in a more favourable outcome only in selected severe infections. The use of antibiotics should be prudent and safe also in neutropenic hematologic patients to prevent emergence of microbial resistance, to save costs, to reduce toxicity. For this reasons, according to the evidence, antibacterial prophylaxis should be restricted to high risk hematologic patients and empiric parenteral antibiotic monotherapy should be recommended in case of febrile neutropenia limiting the use of amynoglicosides and glycopeptides. In the next future, a major effort should be made to state in hematologic patients new risk factors which could more accurately define subgroups for targeted anti-infective strategies.     

How do bryophytes govern generative recruitment of vascular plants?

Interactions between vascular plants and bryophytes determine plant community composition in many ecosystems. Yet, little is known about the importance of interspecific differences between bryophytes with respect to their effects on vascular plants. We compared the extent to which species-specific bryophyte effects on vascular plant generative recruitment depend on the following underlying mechanisms: allelopathy, mechanical obstruction, soil moisture and temperature control. We sowed 10 vascular plant species into monospecific mats of six chemically and structurally diverse bryophytes, and examined 1-yr seedling recruitment. Allelopathic effects were also assessed in a laboratory phyto-assay. Although all bryophytes suppressed vascular plant regeneration, there were significant differences between the bryophyte species. The lack of interactions indicated the absence of species-specific adaptations of vascular plants for recruitment in bryophyte mats. Differences between bryophyte species were best explained by alterations in temperature regime under bryophyte mats, mostly by reduced temperature amplitudes during germination. The temperature regime under bryophyte mats was well predicted by species-specific bryophyte cushion thickness. The fitness of established seedlings was not affected by the presence of bryophytes. Our results suggest that climatically or anthropogenically driven changes in the species' composition of bryophyte communities have knock-on effects on vascular plant populations via generative reproduction.     

A comparison of bats and rodents as reservoirs of zoonotic viruses: are bats special?

Bats are the natural reservoirs of a number of high-impact viral zoonoses. We present a quantitative analysis to address the hypothesis that bats are unique in their propensity to host zoonotic viruses based on a comparison with rodents, another important host order. We found that bats indeed host more zoonotic viruses per species than rodents, and we identified life-history and ecological factors that promote zoonotic viral richness. More zoonotic viruses are hosted by species whose distributions overlap with a greater number of other species in the same taxonomic order (sympatry). Specifically in bats, there was evidence for increased zoonotic viral richness in species with smaller litters (one young), greater longevity and more litters per year. Furthermore, our results point to a new hypothesis to explain in part why bats host more zoonotic viruses per species: the stronger effect of sympatry in bats and more viruses shared between bat species suggests that interspecific transmission is more prevalent among bats than among rodents. Although bats host more zoonotic viruses per species, the total number of zoonotic viruses identified in bats (61) was lower than in rodents (68), a result of there being approximately twice the number of rodent species as bat species. Therefore, rodents should still be a serious concern as reservoirs of emerging viruses. These findings shed light on disease emergence and perpetuation mechanisms and may help lead to a predictive framework for identifying future emerging infectious virus reservoirs.     

Stickleback fights: why do winners win? Influence of metabolic and morphometric parameters

Pairs of reproductively mature male three-spined stickleback (Gasterosteus aculeatus) were introduced into unfamiliar aquaria and observed until one male became dominant. Skin carotenoid content, morphometric indexes, and metabolic capacities of the axial and pectoral muscles were examined to establish whether morphological or physiological parameters differentiated winners and losers. Stickleback that initiated fights typically won. Quick initiation led to quick victory. Overall, winners and losers differed in few morphological or metabolic characteristics, but these properties and the differences between these attributes for losers and winners of specific fights were linked with initiation time and fight duration. Morphometric indexes of losers were the primary determinants of initiation time and fight duration, whereas for winners muscle metabolic capacities were linked to these fight characteristics. The greater the hepatosomatic index (HSI) of losers, the longer the fight initiation times. Similarly, losers with high HSI and carotenoid levels resisted defeat longer. In winners, initiation time decreased as axial muscle phosphofructokinase levels increased and citrate synthase levels decreased, whereas the metabolic capacities of the pectoral muscle were linked with time to achieve victory. When losers had greater HSI values than the winners of a specific fight, fight initiation was delayed and fights lasted longer. When losers had higher carotenoid levels than winners, fights also lasted longer. On the other hand, when losers had more visceral fat (fat body mass over somatic mass) than winners, both initiation time and combat duration were reduced. These results suggest that male stickleback assess their physiological status and that of their opponents, in particular the HSI, and adjust their combat strategies accordingly.