The spiny,thorny and prickly plants in the flora of Israel

To examine whether spininess evolved at random or differently in various life forms and plant organs, we characterized spiny, thorny and prickly organs in the entire wild flora of Israel (294 such species). Of the species, 63.3% defended their reproductive organs (the most‐defended organ) and 67.0% defended various non‐reproductive organs. Ninety‐three species defended both their reproductive organs and at least one other part; 48.3% defended their leaves and 36.4% their stems and branches. Spiny wings defended stems and branches only in herbaceous (annual or perennial) species. There were clear differences between the life forms. Annuals and perennial herbs defended mostly their reproductive organs (95.7 and 83.0%, respectively), dwarf shrubs defended mostly their leaves (54.2%) and shrubs and trees mostly their branches (89.7 and 76.2%, respectively). Trees do not defend their reproductive organs by associated sharp appendages. The differences in defence on various organs among different life forms may influence the results of meta‐analysis studies of the optimal defence allocation if such differences are not taken into account. We noted spine, thorn and prickle colours for 167 species with yellow, red, orange and white being the dominant, supporting hypotheses about spines being visually aposematic. © 2012 The Linnean Society of London, Botanical Journal of the Linnean Society, 2012, 168 , 344–352.     

The cephalic and pharyngeal sense organs of Calliphora vicina 3rd instar larvae are mechanosensitive but have no profound effect on ongoing feeding related motor patterns

The anterior segments of cyclorraphous Diptera larvae bear various sense organs: the dorsal- and terminal organ located on the cephalic lobes, the ventral- and labial organs associated with the mouthplate and the internal labral organ which lies on the dorsal surface of the esophagus. The sense organs are connected to the brain via the antennal nerve (dorsal- and labral organ) or the maxillary nerve (terminal-, ventral-, labial organ). Although their ultrastructure suggests also a mechanosensory function only their response to olfactory and gustatory stimuli has been investigated electrophysiologically. Here we stimulated the individual organs with step-, ramp-, and sinusoidal stimuli of different amplitude while extracellulary recording their afferents from the respective nerves. The external organs show a threshold of approximately 2 μm. All organs responded phasically and did not habituate to repetitive stimuli. The low threshold of the external organs combined with their rhythmically exposure to the substrate suggested a putative role in the temporal coordination of feeding. We therefore repetitively stimulated individual organs while simultaneously monitoring the centrally generated motor pattern for food ingestion. Neither the dorsal-, terminal- or ventral organ afferents had an obvious effect on the ongoing motor rhythm. Various reasons explaining these results are discussed.     

Transformation of sensory organs by mutations of the cut locus of D. melanogaster

The identities of two types of sensory organs in the body wall of Drosophila, namely the external sensory organs and the chordotonal organs, are under genetic control. Embryonic lethal mutations in the cut gene complex transform the external sensory organs into chordotonal organs. The neurons, as well as the support cells forming the external sensory structures, change their morphological and antigenic characteristics to those of chordotonal organs, providing genetic evidence that these two types of sensory organs are homologous. Similar transformations of external sensory organs are observed in adult mosaic flies. Analysis of mosaic larvae and flies suggests that the cut gene function is required either in or near external sensory organs in order for them to acquire their correct identity.     

Embryonic development and evolutionary origin of the Orthopteran auditory organs

Two different types of ears characterize the order of Orthopteran insects. The auditory organs of grasshoppers and locusts (Caelifera) are located in the first abdominal segment, those of bushcrickets and crickets (Ensifera) are found in the tibiae of the prothoracic legs. Using neuron-specific antibody labelling, we describe the ontogenetic origin of these two types of auditory organs, use comparative developmental studies to identify their segmental homologs, and on the basis of homology postulate their evolutionary origin. In grasshoppers the auditory receptors develop by epithelial invagination of the body wall ectoderm in the first abdominal segment. Subsequently, at least a part of the receptor cells undergo active migration and project their out-growing axons onto the next anterior intersegmental nerve. During this time the receptor cells and their axons express the cell-cell adhesion molecule, Fasciclin I. Similar cellular and molecular differentiation processes in neighboring segments give rise to serially homologous sensory organs, the pleural chordotonal organs in the pregenital abdominal segments, and the wing-hinge chordotonal organs in the thoracic segments. In more primitive earless grasshoppers pleural chordotonal organs are found in place of auditory organs in the first abdominal segment. In bushcrickets the auditory receptors develop in association with the prothoracic subgenual organ from a common developmental precursor. The auditory receptor neurons in these insects are homologous to identified mechanoreceptors in the meso- and metathoracic legs. The established intra- and interspecies homologies provide insight into the evolution of the auditory organs of Orthopterans.     

Role of the vomeronasal organ in neonatal offspring recognition in sheep

Twenty-five pregnant Dorsett ewes were randomly divided into three groups to test if ewes use their vomeronasal organs for offspring recognition during nursing. One group of eight ewes (procaine) were made anosmic by irrigation of the nasal olfactory apparatus with a zinc sulphate procaine solution. The second group of nine ewes (cauterized) had their vomeronasal organs rendered nonfunctional by cauterization of the nasoincisive duct. The third group of eight ewes were the controls. Parturition was synchronized in all ewes with betamethasone on Day 145 of gestation. Maternal responsiveness was tested two separate times with 1- to 2-day-old alien lambs. Each alien lamb trial was conducted 24 h apart. Cauterized ewes allowed alien lambs to suckle and they were unable to distinguish alien lambs from their own lambs, whereas the ewes in both groups with functional vomeronasal organs (procaine and control) violently rejected any alien lamb's attempt to suckle. Thus, female sheep use their vomeronasal organs for neonatal offspring recognition.     

Immunohistochemical verification of kisspeptins and their receptor in human fetal organs during prenatal development

Kisspeptins (KPs) and their receptor (KISS1R) play an important role in many physiological processes in the body, such as sexual maturation, reproductive system functioning, placentation, insulin secretion, and vasoconstriction. The highest level of kisspeptins and their receptor is observed in the organs of hypothalamic-pituitary-gonadal and hypothalamic-pituitary-adrenal axes, both in the form of mRNA and peptide. Kisspeptins are found in various body tissues: spinal cord (Dun et al., 2003), pancreas (Song et al., 2014), esophagus (Kostakis et al., 2013), adrenal glands and secretory system organs (Wahab et al., 2015), and in malignancies (Lee and Welch, 1997). However, the localization and the role of kisspeptins and their receptor in organs during fetal development have not yet been studied. At the same time, ample published data regarding the localization of kisspeptins and their receptors in human organs and tissues are discrepant, which requires the development of a standard staining technique. The modified technique presented in this paper made it possible to identify and evaluate the expression of kisspeptins and their receptor in human fetal organs at different stages of development. Kisspeptins and their receptors were found in all organs and tissues examined by us, but the degree of reaction was different. The highest level was observed in the hypothalamus material in the 28–32-week period, and the lowest amount of the protein was detected in the uterine material at all stages. Maximum level of KISS1R was detected in the pituitary material in the 36–40-week period. A correlation between gestational age and the level of kisspeptins in the ovaries, uterus, and adrenal glands was found: a significant increase in the amount of protein was detected. A significant increase in the amount of the kisspeptin receptor in pituitary, ovary, and uterus material was shown.     

Entrails,heart, brain,limbs, and lymphatics- a recipe for success?

A recent Juan March Foundation workshop entitled Developmental Mechanisms in Vertebrate Organogenesis brought 50 developmental biologists together in Madrid to share some of their latest findings. Discussion topics included ectodermal organs such as the central nervous system (CNS) and skin, mesodermal organs such as the heart, limb, vasculature, and kidney, and endodermal organs such as the pancreas and liver. Discussions extended into the late hours of the night as the meeting participants indulged in tasting some of their favorite organs, in the form of Spanish delicacies.     

Regulation of Organ Growth by Morphogen Gradients

Morphogen gradients play a fundamental role in organ patterning and organ growth. Unlike their role in patterning, their function in regulating the growth and the size of organs is poorly understood. How and why do morphogen gradients exert their mitogenic effects to generate uniform proliferation in developing organs, and by what means can morphogens impinge on the final size of organs? The decapentaplegic (Dpp) gradient in the Drosophila wing imaginal disc has emerged as a suitable and established system to study organ growth. Here, we review models and recent findings that attempt to address how the Dpp morphogen contributes to uniform proliferation of cells, and how it may regulate the final size of wing discs.     

Effects of 17β-estradiol and bisphenol A on the formation of reproductive organs in planarians

Planarians have a remarkable capacity for regeneration after ablation, and they reproduce asexually by fission. However, some planarians can also reproduce and maintain their sexual organs. During the regenerative process, their existing sexual organs degenerate and new ones develop. However, little is known about hormonal regulation during the development of reproductive organs in planarians. In this study, we investigated the effects of 17β-estradiol (a steroid) and bisphenol A (an endocrine disrupter) on the formation of sexual organs in the hermaphroditic planarian Dugesia ryukyuensis. Under control conditions, all worm tissues regenerated into sexual planarians with sexual organs within 4 weeks after ablation. However, in the presence of bisphenol A or 17β-estradiol, although they apparently regenerated into sexual planarians, the yolk glands, which are one of the female sexual organs, failed to regenerate even 7 weeks after ablation. These data suggest that planarians have a steroid hormone system, which plays a key role in the formation and maturation of sexual organs.     

The morphology of the accessory air-breathing organs of the catfish, Clarias batrachus: A SEM Study

The scanning electron microscope (SEM) has been used to study the morphology of the accessory air-breathing organs of the catfish Clarias batrachus . Although the gross morphology of the dendritic organs, the fan organs and the membrane lining the supra-branchial chambers differ, the nature of the respiratory surfaces are similar. The gaseous exchange surfaces of all three organs consist of double rows of paired lamellae, a feature strongly indicative of their common origin from the gills. The surfaces of the epithelial cells from the respiratory organs were seen to have numerous small projections consisting of microvilli and short microridges. This is in contrast to the concentric whorls of micro-ridges on the surface of cells from the interlamella regions of these organs.     

Distribution, Histochemical and Enzyme Histochemical Characterization of Mast Cells in Dogs

This study describes the distribution, proteoglycan properties and protease activity of mast cells from 15 different dog organs. In beagles and mixed breed dogs, staining with Alcian Blue-Safranin O revealed mast cells in all the organs examined. However, their numbers varied and they demonstrated unique localization patterns within some of these organs. Berberine sulphate fluorescence-positive mast cells were observed in the submucosa, muscularis and serosa of the intestines, as well as the tongue and liver (within the connective tissue). Mast cells within the intestinal mucosa were negative for, or demonstrated weak, berberine sulphate staining. Heterogeneity of mast cells in terms of the proteoglycans contained within their granules was further confirmed by determination of critical electrolyte concentrations (CECs). The CECs of mast cells within the connective tissue of several organs, including the intestines (submucosal and muscularis-serosal layers) were all greater than 1.0 M. The results from CEC experiments together with berberine staining indicate that heparin was contained within their granules. Relative to the CECs of mast cells in other organs, mast cells in the intestinal mucosa exhibited lower CECs, suggesting that the proteoglycans within their granules were of lower charge density and/or molecular weight. Although mast cells were classified into two groups by proteoglycans within the granules, enzyme histochemical analysis in beagles revealed three subtypes of mast cells: chymase (MC(C)), tryptase (MC(T)) and dual positive (MC(TC)) cells. There was no correlation between the proteoglycan content and enzyme properties of the mast cell granules.     

The pit organs of elasmobranchs: a review

Elasmobranchs have hundreds of tiny sensory organs, called pit organs, scattered over the skin surface. The pit organs were noted in many early studies of the lateral line, but their exact nature has long remained a mystery. Although pit organs were known to be innervated by the lateral line nerves, and light micrographs suggested that they were free neuromasts, speculation that they may be external taste buds or chemoreceptors has persisted until recently. Electron micrographs have now revealed that the pit organs are indeed free neuromasts. Their functional and behavioural role(s), however, are yet to be investigated.     

The coordination of growth among Drosophila organs in response to localized growth-perturbation

The developmental mechanisms by which growth is coordinated among developing organs are largely unknown and yet are essential to generate a correctly proportioned adult. In particular, such coordinating mechanisms must be able to accommodate perturbations in the growth of individual organs caused by environmental or developmental stress. By autonomously slowing the growth of the developing wing discs within Drosophila larvae, we show that growing organs are able to signal localized growth perturbation to the other organs in the body and slow their growth also. Growth rate is so tightly coordinated among organs that they all show approximately the same reduction in growth rate as the developing wings, thereby maintaining their correct size relationship relative to one another throughout development. Further, we show that the systemic growth effects of localized growth-perturbation are mediated by ecdysone. Application of ecdysone to larvae with growth-perturbed wing discs rescues the growth rate of other organs in the body, indicating that ecdysone is limiting for their growth, and disrupts the coordination of their growth with growth of the wing discs. Collectively our data demonstrate the existence of a novel growth-coordinating mechanism in Drosophila that synchronizes growth among organs in response to localized growth perturbation.     

Sink-limitation and the size-number trade-off of organs: production of organs using a fixed amount of reserves

To analyze the nature of size-number trade-off of organs, we develop models in which the effects of sink-limitation in the growth of organs and the loss of resources by maintenance respiration are taken into consideration. In these models, the resource absorption rate of an organ is proportional to either its absolute size or its surface area and either the initial size of an organ or the total initial size of the organs produced is fixed. In all models, organs are produced using a fixed amount of reserved resources and no additional resources become newly available for their growth. We theoretically show that size-number trade-offs are nonlinear if the resource absorption rate of an organ is proportional to the absolute size of the organ and the initial size of the individual organs is fixed or if the resource absorption rate of an organ is proportional to the surface area of the organ. In these nonlinear size-number trade-offs, the size of individual organs increases less rapidly than in linear trade-offs with a decrease in the number of organs and the total size of organs is an increasing function of the number of organs produced. This implies that increasing the number of organs produced is advantageous in terms of resource-use efficiency. In contrast, size-number trade-off is linear if the resource absorption rate of an organ is proportional to the absolute size of the organ and there is a linear trade-off between the initial size of organs and their number. To exemplify the effects of those size-number trade-offs on the life-history evolution, we calculate the optimal offspring sizes that maximize the number of offspring successfully being established. In the case of nonlinear size-number trade-offs, the optimal offspring sizes are smaller than the optimal offspring size in the case of linear size-number trade-offs, namely, that in the model of Smith and Fretwell (1974). Our optimal offspring size depends on the metabolism of organ development; the optimal offspring size decreases with an increase in maintenance respiration rate relative to the growth coefficient of organs.     

External sense organs in freshwater oligochaetes (Annelida, Clitellata) revealed by scanning electron microscopy

Freshwater oligochaetes have at least two kinds of external sense organs: multiciliate organs of short cilia (also present in earthworms) and sense organs with one to three long cilia (unknown in earthworms and possibly acting as rheoreceptors). Ciliate sense organs of freshwater oligochaetes are distributed over their entire body surface, including the clitellum. They are scattered on the prostomium and pigidium and are arranged into a transversal chaetal row and dispersed or forming a few other discrete transversal rows on chaetal segments. Three species display very prominent sense organs (sensory buds in Protuberodrilus tourenqui and papillae in Ophidonais serpentina and Spirosperma velutinus). The number of cilia per organ at the prostomium of freshwater families appears to be fewer than that of terrestrial ones. It is suggested that the total number of cilia at the prostomium of the freshwater species could be related to their habitat, evolving from an epibenthic to an endobenthic way of life.     

洞庭湖区社鼠脏器重量的比较

对洞庭湖区社鼠(Niviventer confucianus)野外自然种群脏器的重量指标进行了测定,并比较了其在年龄组、性别、季节及生境间的差异。结果表明,社鼠内脏(心、肺、肝、脾、肾脏)随着年龄组的增加,重量有明显的增加,其重量与体重有极其显著的相关性。两性间的脏器重量指标没有显著性差异。脏器季节变化的共同特征是夏季脏器重量较低,四季间比较,仅有心脏重量有显著的季节变化。生境间心脏和肾脏重量的变化相对较大,达显著水平。参与繁殖与未参与繁殖的雌鼠相比,心、肺、肝、肾脏的各项指标均较高,脾脏则相反,但均未有显著性差异。总的来看,洞庭湖社鼠种群的脏器指标相对稳定,尽管重量指标随着年龄组而增加,受性别、季节、生境及繁殖行为的影响相对较小。     

黑线姬鼠与大林姬鼠组织中超氧化物酶和过氧化物酶的分布与活性比较

以黑线姬鼠(Apodemus agrarius)和大林姬鼠(A. peninsulae)为研究对象,采用聚丙烯酰胺凝胶电泳(PAGE)不连续体系的方法,比较分析了心、肝、肾、肌肉、脑、肺6种器官和组织中超氧化物酶(SOD)和过氧化物酶(POD)活性,并建立了2种酶的电泳图谱。结果显示,上述2种酶在黑线姬鼠和大林姬鼠的6种器官和组织中均有表达并表现出明显的特异性,其中,2种鼠中超氧化物酶共分离出迁移率由0.15～0.66的9条电泳谱带,过氧化物酶共分离出迁移率由0.09～0.83的20条电泳谱带。在肝和肺中酶的活性最强,黑线姬鼠6种器官和组织中超氧化物酶活性均强于大林姬鼠,2种鼠组织中过氧化物酶的活性和分布相似,但在同一物种不同器官和组织间过氧化物酶的活性及分布存在明显差异。     

A fundamental symmetry between morphogenesis and function of branched organs]

It is generally difficult to find any relationship between the morphogenesis of an organ and its final function. A priori, such a relationship has no reason to exist, since organs do not actually function during their formation. I will show in this article that, for a very large class of organs--the branched organs--there exists a hidden relationship between their morphogenesis and their function. This class of organs comprises: the lungs, the salivary mammary and lacrymal glands, the kidneys, the pancreas, and possibly other organs, such as testes. For all these organs, a fundamental fact that comes from recent developments in physics explains at the same time how they form, and why they work. This suggests, first, that complex organs are not the result of gradual and long selection processes, and, second, that this specific structure for the organs is imposed by the laws of physics. The growth process, as described here, is possibly the only one that allows both to build a fluid-secreting organ, and make it work.     

Plant reaction to drilling wastes of petroleum complex in the zone of Middle Taiga of Ob region

Data on the change in plant condition under the impact of drilling wastes (DWs) of petroleum clefts and on the transport of toxic elements from the stratum (soil) to vegetative organs are obtained. Stimulation of plant growth and productivity is revealed at a DW concentration in oligotrophic strata of up to 20% without translocations of their separate elements in vegetative organs.     

The emerging role of cranial nerves in shaping craniofacial development

Organs and structures of the vertebrate head perform a plethora of tasks including visualization, digestion, vocalization/communication, auditory functions, and respiration in response to neuronal input. This input is primarily derived from afferent and efferent fibers of the cranial nerves (sensory and motor respectively) and efferent fibers of the cervical sympathetic trunk. Despite their essential contribution to the function and integration of processes necessary for survival, how organ innervation is established remains poorly understood. Furthermore, while it has been appreciated for some time that innervation of organs by cranial nerves is regulated in part by secreted factors and cell surface ligands expressed by those organs, whether nerves also regulate the development of facial organs is only beginning to be elucidated. This review will provide an overview of cranial nerve development in relation to the organs they innervate, and outline their known contributions to craniofacial development, thereby providing insight into how nerves may shape the organs they innervate during development. Throughout, the interaction between different cell and tissue types will be highlighted.