Evolution of the population structure of Venturia inaequalis,the apple scab fungus,associated with the domestication of its host

Evaluating the impact of plant domestication on the population structure of the associated pathogens provides an opportunity to increase our understanding of how and why diseases emerge. Here, we investigated the evolution of the population structure of the apple scab fungus Venturia inaequalis in response to the domestication of its host. Inferences were drawn from multilocus microsatellite data obtained from samples collected on (i) the Central Asian Malus sieversii, the main progenitor of apple, (ii) the European crabapple, Malus sylvestris, a secondary progenitor of apple, and (iii) the cultivated apple, Malus×domestica, in orchards from Europe and Central Asia. Using clustering methods, we identified three distinct populations: (i) a large European population on domesticated and wild apples, (ii) a large Central Asian population on domesticated and wild apples in urban and agricultural areas, and (iii) a more geographically restricted population in M. sieversii forests growing in the eastern mountains of Kazakhstan. Unique allele richness and divergence time estimates supported a host‐tracking co‐evolutionary scenario in which this latter population represents a relict of the ancestral populations from which current populations found in human‐managed habitats were derived. Our analyses indicated that the domestication of apple induced a significant change in the genetic differentiation of populations of V. inaequalis in its centre of origin, but had little impact on its population dynamics and mating system. We discuss how the structure of the apple‐based agrosystem may have restricted changes in the population structure of the fungus in response to the domestication of its host.     

Bacterial degradability of an intrafeather unmelanized ornament: a role for feather‐degrading bacteria in sexual selection?

The impact of feather‐degrading bacilli on feathers depends on the presence or absence of melanin. In vitro studies have demonstrated that unmelanized (white) feathers are more degradable by bacteria than melanized (dark) ones. However, no previous study has looked at the possible effect of feather‐degrading bacilli on the occurrence of patterns of unmelanized patches on otherwise melanized feathers. The pied flycatcher Ficedula hypoleuca Pallas, 1764 is a sexually dimorphic passerine with white wing bands consisting of unmelanized patches on dark flight feathers. These patches are considered to be a sexually selected trait in Ficedula flycatchers, especially in males, where the patches are more conspicuous (larger and possibly whiter) than in females. Using in vitro tests of feather bacterial degradation, we compared the degradability of unmelanized and melanized areas of the same feather for 127 primaries collected from the same number of individuals in a population breeding in central Spain (58 males and 69 females). In addition, we also looked for sex differences in feather degradability. Based on honest signalling theory and on the fact that there is stronger sexual selection for males to signal feather quality than in females, we predicted that unmelanized areas should be more degradable by bacteria than melanized ones within the same feather, and that these unmelanized areas should also be more degradable in males than in females. We confirmed both predictions. Microstructural differences between cross‐section dimensions of unmelanized and melanized barbs, but not differences in the density of barbs within unmelanized and melanized areas of feathers in males and females, could partly explain differences in degradability. This is the first study to show differences in bacterial degradability among markings on the same feather and among unmelanized feather patches between males and females as predicted by sexual selection theory. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, 105 , 409–419.     

Ecotone delimitation: Epigean–hypogean transition in cave ecosystems

Abstract The ecotone zone between epigean and hypogean environments has been delimited for two limestone caves using a new method proposed herein. The richness and the diversity of the ecotone, epigean and hypogean environments and their similarities have also been determined. The ecotones were delimited using a similarity matrix between the inner and outer sectors of each cave. The ecotone of Dona Rita's cave was estimated to be 12 m long and the ecotone of Retiro's cave 16 m. The richness (S) of arthropods in Dona Rita's cave was higher in the ecotone (S = 131), intermediate in the epigean environment (S = 75) and lower in the hypogean system (S = 45). The invertebrate diversity (H′) was lower in the hypogean environment (H′ = 2.89) and not statistically different between the epigean environment and the ecotone (H′ = 3.56 and H′ = 3.76, respectively). The richness in Retiro's cave was higher in the ecotone (S = 86), intermediate in the epigean environment (S = 39) and lower in the hypogean system (S = 12). The invertebrate diversity was lower in the hypogean environment (H′ = 0.48), intermediate in the ecotone (H′ = 3.02) and higher in the epigean region (H′ = 3.29). Species migration patterns, differential environmental barriers and determination of accidental versus trogloxenes/troglophylous species are topics that are primarily approached by establishing ecotone zones in caves. The aim of the present paper is to establish the delimitation of theses zones.     

Relationship between potassium fertilisation and nitrate assimilation in leaves and fruits of cucumber (Cucumis sativus) plants

The effect of application of different potassium rates on some parameters of nitrate metabolism and yield in cucumber plants (Cucumis sativus) was studied. All plants were grown under controlled conditions in an experimental greenhouse. The treatments consisted of applications of K⁺ at three rates in the form of K₂SO₄ (Kl: 0.075 mg ml^?1, K2: 0.15 mg ml^?1, and K3: 0.30 mg ml^?1). The results showed a positive effect of higher K⁺ fertilisation (0.30 mg ml^?1) on uptake, translocation and reduction of NO₃^? in leaves compared with the lowest K⁺ rate. In addition, the higher K⁺ rates strengthened the translocation of organic nitrogenous compounds (amino acids) towards the fruit, thereby perhaps also enhancing the maximal commercial yield. In conclusion, for improved cucumber cultivation under greenhouse conditions, 0.15 mg ml^?1 of K⁺ gave maximal yield, while the application of 0.30 mg ml^?1 increased the metabolism and efficient utilisation of NO₃^?.     

Do reproductive activities compromise immunological competence as measured by phenoloxidase activity? Field and experimental manipulation in females of two damselfly species

Recent studies of female insects indicate that reproductive activities, such as mating and oviposition, can impair immune ability. Using the two tropical damselfly species Argia anceps Garrison and Hetaerina americana (Fabricius), egg production and phenoloxidase (PO) activity, a key enzyme in insect immunity, are measured in mating, ovipositing and perching females in December and March. Perching females of both species have fewer eggs compared with mating and ovipositing females, which suggests that perching females are not engaged in reproduction. There is seasonal variation in egg number for the three categories in H. americana but not in A. anceps, which can be interpreted in terms of adaptive changes in egg production depending on female–male interactions in the former species but not in the latter species. There is no difference in PO activity among mating, ovipositing or perching females within either species, although measurements in December and March indicate distinct seasonal changes. Juvenile Hormone (JH) is known to reduce the effectiveness of the immune system by favouring the use of resources for reproduction. A possible role for JH is examined in H. americana, using the JH analogue methoprene to manipulate hormone activity, revealing that PO activity is reduced in methoprene‐treated H. americana females. Thus, although the results of the present study are indicative of possible hormone‐driven changes in PO, there is not necessarily a down‐regulation of immune function (as determined by PO activity) during mating or oviposition. The results complement some recent studies countering the idea that reproductive activities reduce the immune ability in insects.     

Ultrastructure de la spermiogenèse et du spermatozoïde de Loimosina wikoni et affinités phylétiques des Loimoidae (Plathelminthes, Monogenea, Monopisthocotylea)

In Loimosina, during spermiogenesis, the zone of differentiation of the spermatid contains two centrioles continued as two 9 +‘1’axonemes. One of the axonemes lengthens and will become the principal axoneme of the spermatozoon. The other axoneme is as long as the first one at the beginning of spermiogenesis, but is shorter in the mature sperm cell. The spermatozoon consists of several regions: (a) at the anterior end, the centriolar derivative of the principal axoneme; (b) a short region which shows cortical microtubules coinciding with external ornamentations; (c) a long uniflagellate region, with mitochondrion; (d) a biflagellate region containing the anterior slender part of the nucleus; (e) the posterior part of the nucleus, with no accompanying cytoplasmic organelles. Spermiogenesis and sperm structure in Loimosina differ from what is known in all other described monogeneans, excepting the monocotylid Heterocofyle to which they show close resemblances. However, the alteration of the second axoneme is more complete in Heterocofyle than in Loimosina. Comparative study of spermiogenesis and sperm ultrastructure thus shows an interesting coincidence with classical phylogenies of the monogeneans, in which the families Loimoidae and Monocotylidae are closely related. Chez Loimosina, pendant la spermiogenèse, la zone de différenciation de la spermatide contient deux centrioles prolongés par deux axonemes de type 9 +‘1′. L'un des axonemes s'allonge et deviendra l'axonème principal du spermatozoïde mûr. Le deuxième axontme est aussi long que le premier au début de la spermiogenèse, mais il est plus court dans le spermatozoïde mûr. Le spermatozoïde comprend: (a) à l'avant, le dérivé centriolaire de l'axonème principal; (b) une courte région contenant quelques microtubules corticaw longitudinaux coincidant avec des omementations extramembranaires; (c) une longue région miflagellée avec mitochondrie; (d) une région biflagellée contenant La partie antérieure effilée du noyau; (e) la région postérieure du noyau, sans organites cytoplasmiques accompagnateurs. La spermiogenèse et la structure du spermatozoïde de Loimosina sont différentes de ce qui est connu chez tous les autres Monogènes décrits, excepté le Monocotylidae Heterocofyle auquel elles ressemblent beaucoup. Toutefois, l'altération du deuxième axonème est moins complète chez Loimosina que chez Heterocotyle. L'étude comparée des spermatozoïdes et des spermiogenèses montre une bonne coincidence avec les phylogenèses classiques, dans lesquelles les familles Loimoidae et Monocotylidae sont proches.