Dry under water: Comparative morphology and functional aspects of air‐retaining insect surfaces

Superhydrophobic surfaces prevent certain body parts of semiaquatic and aquatic insects from getting wet while submerged in water. The air layer on these surfaces can serve the insects as a physical gill. Using scanning electron microscopy, we investigated the morphology of air‐retaining surfaces in five insect species with different levels of adaptation to aquatic habitats. We found surfaces with either large and sparse hairs (setae), small and dense hairs (microtrichia), or hierarchically structured surfaces with both types of hairs. The structural parameters and air‐film persistence of these surfaces were compared. Air‐film persistence varied between 2 days in the beetle Galerucella nymphaea possessing only sparse setae and more than 120 days in the bugs Notonecta glauca and Ilyocoris cimicoides possessing dense microtrichia (up to 6.6 × 10⁶ microtrichia per millimeter square). From our results, we conclude that the density of the surface structures is the most important factor that affects the persistence of air films. Combinations of setae and microtrichia are not decisive for the overall persistence of the air film but might provide a thick air store for a short time and a thin but mechanically more stable air film for a long time. Thus, we assume that a dense cover of microtrichia acts as a “backup system” preventing wetting of the body surface in case the air–water interface is pressed toward the surface. Our findings might be beneficial for the development of biomimetic surfaces for long‐term air retention and drag reduction under water. In addition, the biological functions of the different air retention capabilities are discussed. J. Morphol., 2011. © 2011 Wiley‐Liss, Inc.     

Origin and pathway of the epidermal secretion in the damselfly head-arresting system (Insecta: Odonata)

In damselflies, the arrester system is responsible for an additional attachment of the head to the neck. It consists of a pair of mobile postcervical sclerites (SPC) covered by microtrichia. In their lateral position, SPCs can fixate the head on fields of microtrichia on the back surface of the head. The intact surface of microtrichia of the SPC is usually covered by a lipid-containing secretion. The present study provides ultrastructural data on the secretory epidermis and pore channels adapted to transport the secretion to the cuticle surface. 1) Shock-frozen preparations of the contact area show that microtrichia of co-opted surfaces do not interlock with each other. When co-opted fields are pressed to each other, deformations of flexible microtrichia of the SPC result in an increase of contact area between corresponding structures and consequently in an increase of frictional forces. 2) In the area of the SPC, only electron-lucent vesicles have been found. Histochemical procedures revealed that the material stored in vesicles and liberated on the external surface of the SPC is presumably non-volatile lipid. 3) Only a small number of large pore channels reach the surface of a microtrichium. Most of them terminate with tiny terminal channels, whose diameter is approximately six to twenty times smaller than the diameter of structures of secretory blooms occurring in SEM in shock-frozen and air-dried preparations. The terminal channels do not penetrate the epicuticular layer. It seems that the secretion reaches the epicuticle through terminal channels and diffuses through the epicuticle without any channel structures.     

Ultrastructural studies on the sporulation of oocysts of Toxoplasma gondii. II. Formation of the sporocyst and structure of the sporocyst wall

The ultrastructural changes observed during sporocyst formation and the structure of the sporocyst wall was examined in oocysts which had been allowed to sporulate for between 12 and 48 hours at 27 degrees C. As the spherical sporoblast developed into the sporocyst the cytoplasmic mass became ellipsoidal in shape although no change was noted in the organelle compliment, which cosisted of two nuclei plus a number of polysaccharide granules, lipid globules, mitochondria, Golgi bodies, and some rough endoplasmic reticulum. The sporocyst wall consisted of a thin outer layer (15-20 nm) which was formed from two limiting membranes of the sporoblast and an inner layer (40-50 nm) which was comprised of four curved plates. This inner layer was formed under the outer layer and, although no specific cytoplasmic organelle disappeared with its formation, some unit membranes were observed close to the plasmalemma during its formation. Each curved plate has a marginal swelling and an interposing strip of material is present between the margins of adjacent plates. The plates are joined to the interposing strip by a thin band of osmiophilic material. In oblique and tangential sections through the plates two types of cross banding were observed which differed in periodicity.     

Morphological basis of cardiac glycoside sequestration by Oncopeltus fasciatus (Dallas) (Hemiptera: Lygaeidae)

Summary The integument of Oncopeltus fasciatus is made up of a vacuolated and a pigmented epidermal cell layer. This double layered integument is present from late embryo to adult in male and female animals reared on milkweed or sunflower seeds. Experiments with a labelled glycoside as well as retrograde ink injections suggest that O. fasciatus concentrates cardiac glycosides, normally derived from the host plants, within the vacuolated epidermal cell layer throughout its life cycle. In the adult, droplets of glycoside-rich fluid appear at precise points along the dorsolateral margins when external pressure is applied to the thorax and abdomen. This pressure causes separation of cuticular flanges in the metathoracic epimeral lobe and rupture of the cuticle in restricted areas in the mesothorax and abdomen. In addition the pigmented epidermal cell layer and the distal membranes of the vacuolated epidermal cell layer rupture with the result that the contents of the vacuolated cell layer are eliminated onto the surface of the animal where they are retained as discrete droplets by the cuticular morphology. Release of cardiac glycosides into the haemolymph is prevented by a thick basal lamina on the haemolymph side of the vacuolated epidermal cells. No specialized muscles involved with fluid release were observed. The vacuolated epidermal cells do not show ultrastructural features characteristic of actively transporting tissues, i.e., abundant mitochondria and elaborate membrane infoldings. This suggests that glycoside sequestration is essentially a passive process and should not be associated with any physiological cost. Large concentration gradients of cardiac glycosides are maintained across the basal lamina, basal plasma and vacuolar membranes of the vacuolated epidermal cell layer. Possible mechanisms by which O. fasciatus is able to concentrate cardiac glycosides as well as the possible function of this phenomenon are discussed.Abbreviations A abdominal trabeculum - Ap mesofurcal apodeme - C metathoracic supracoxal lobe - D metathoracic stink gland duct - E metathoracic epimeral lobe - Ep pigmented epidermal cell layer - Ev vacuolated epidermal cell layer - G last thoracic ganglion - H haemocoel - M midgut - N nerve cord - P second phragma - R reproductive organ - T trachea - V dorsal vessel - W wing - bl basal lamina - c cuticle - cf cytoplasmic fragments - cv coated vesicle - d hemidesmosome - ep epidermal cell - en endocuticle - ex exocuticle - f flange - fp foot processes - gc glycoside compartment - h hair - is intersegmental region - id ink deposits - l lumen of metathoracic stink gland - m mitochondria - mb mushroom bodies - mt microtrichia - n nucleus - p pigment granule - s slit - sp spine - tsm tergosternal muscle - v vacuole     

Adriamycin as a probe for the transversal distribution of cardiolipin in the inner mitochondrial membrane

The ability of adriamycin to complex cardiolipin was used to determine the distribution of cardiolipin across the inner membrane of rat liver and heart mitochondria. In both mitochondrial types, about 57 +/- 5% of the total cardiolipin was found to be located in the cytoplasmic face of the inner membrane. Mitochondria and mitoplasts were used to study the cytoplasmic face of the inner membrane, purified submitochondrial vesicles with inverted membrane orientation for the matrix face. The cardiolipin amount titrated by adriamycin in the latter was found to be complementary to the amount titrated in the cytoplasmic face. The adriamycin association constant determined for the first saturation level of mitochondria was in good agreement with the value published by Goormaghtigh et al. (Goormaghtigh, E., Chatelain, P., Caspers, J., and Ruysschaert, J. M. (1980) Biochim. Biophys. Acta 597, 1-14) for cardiolipin in artificial membranes. Two binding plateaus were observed when increasing amounts of adriamycin were added to mitochondria. The plateau at higher concentrations is conveniently explained by the penetration of adriamycin into mitochondria and the titration of cardiolipin in the matrix face. Scatchard plot analysis of the binding curves leading to the two plateaus produced almost identical association constants. The total amount of cardiolipin in mitochondria calculated from curves of this type corresponded to the total amount of cardiolipin determined by phosphate analysis of extracts, analyzed by thin layer chromatography.     

Armored cuticular membranes in Brachycera (Insecta,Diptera)

This study describes and quantifies the ultrastructural design of some cuticular protuberances in the Diptera-Brachycera that appear to have a specialized mechanical function. The microsculpture of membranes in the transitional areas of prothorax-neck, neck-head, head-mouthparts, and in the articulations thorax-coxa and coxa-trochanter was investigated in eight species from six families (Tabanidae, Stratiomyidae, Calliphoridae, Syrphidae, Muscidae and Drosophilidae) by means of scanning electron microscopy. The membrane armatures are single or grouped microtrichia, often located on microplates in the flexible membrane. The different membranes were compared using the following details: microtrichia length, microplate length and width, the shortest distance between microplates, and the number of microtrichia per microplate. Five different types of microstructure were observed: (1) single short papilla-like microtrichia directly arising from the flexible membrane, (2) single elongated microtrichia directly arising from the flexible membrane, (3) single microtrichia located on small areas of the inflexible cuticle, here called microplates, (4) microtrichia groups located on the microplates, and (5) microplates without microtrichia in the flexible membrane. The study reveals the differences in the surface ultrastructure of membranes between different parts of body and between different taxa of flies. The prothorax-neck transition is less specialized in membrane armature as compared with the head-neck articulation, and especially with that of the head-proboscis. The head-proboscis transition has the most complex membrane armature of those species studied. The membrane of the basal joints of the legs has larger plates and a higher number of microtrichia per plate than that of the more distal joints. The complexity of the membrane armature depends on the dimensions of the animal: the smallest species have short ungrouped microtrichia or micropapillae, whereas large species have the highest degree of grouping, the longest microtrichia, and the largest microplates. Three main mechanical functions served by the different armored membranes are suggested, based on the specific characteristics of the microsculptural design: (1) fixation of the folds, (2) prevention of folding, and (3) determination of direction of folding. J. Morphol. 234:213–222, 1997. © 1997 Wiley-Liss, Inc.     

Sensilla coeloconica ringed by microtrichia in host‐seeking biting midges

The distribution and morphology of antennal sensilla coeloconica in parasitic and predaceous biting midges were studied in females of Forcipomyia (feeding on the blood of frogs), Atrichopogon (feeding on haemolymph), Austroconops, Culicoides (feeding on the blood of birds and mammals) and Brachypogon (feeding on haemolymph and dissolved tissues of insects) (all: Diptera: Ceratopogonidae). A Lower Cretaceous female of Archiculicoides (Diptera: Ceratopogonidae) from Lebanese amber, which fed on the blood of unknown vertebrates, was also examined. In sensilla coeloconica ringed by microtrichia, the peg is grooved longitudinally and protrudes distinctly from the pit. We suggest that the microtrichia encircling the protruding peg form a structure resembling a picket fence in order to maintain a higher level of humidity, which facilitates the capture and transport of odour molecules through the channels in the peg wall. Sensilla coeloconica ringed by microtrichia function as very effective chemoreceptors in host‐ and prey‐seeking activity. During the evolution of Ceratopogonidae, sensilla coeloconica with a fence of microtrichia have evolved twice in groups feeding on the blood of vertebrates (i.e. in the basal lineage: Lower Cretaceous or earlier) and in the subgenus Lasiohelea of Forcipomyia (Palaeogene). Sensilla coeloconica ringed by microtrichia are described for the first time in the relict genus Austroconops.     

Targeting of tRNA into yeast and human mitochondria: the role of anticodon nucleotides

In vivo, yeast mitochondria import a single cytoplasmic tRNA, tRNA(CUU)Lys, while human mitochondria do not import any cytoplasmic tRNA. We have previously demonstrated that both yeast and human isolated mitochondria can specifically internalize tRNA(CUU)Lys, several of its mutant versions and some mutant versions of yeast cytosolic tRNA(UUU)Lys (not imported in vivo). Aminoacylation of tRNA(CUU)Lys by the cytoplasmic lysyl-tRNA synthetase was a prerequisite for its import. Here we are studying the influence of one-base replacements in the anticodon of tRNAs(Lys) on their aminoacylation, on binding to the precursor of the mitochondrial lysyl-tRNA synthetase (carrier protein directing the import), and on the efficiency of import into isolated yeast and human mitochondria. We show that the base U35 is the main identity element for the yeast cytoplasmic lysyl-tRNA synthetase. The single replacement that abolished import was C34G, while all the others only modulated the import efficiency. The need of aminoacylation for import and for interaction with the carrier protein was shown only for a subset of mutant versions, while the others could be recognized and internalized without aminoacylation or in misacylated forms.     

Ultrastructural study of the mycelium-yeast transition in Histoplasma capsulatum. I. Changes at 37 degrees C

Ultrastructural changes observed during the first 24 hours of mycelium to yeast transition in the dimorphic fungus Histoplasma capsulatum are reported. During this period the plasma membrane becomes undulated and the cell wall loses its characteristic fibrous outer layer. At 8 h the ordered lamellar structure of the mitochondria is no longer apparent. 24 h after the temperature shift 70% of the cells are lysed. The remaining cells contain many cytoplasmic membrane structures; mitochondria are rarely observed. These morphological changes are probably correlated with the physiological events characteristic of mycelial to yeast transition.     

DISTRIBUTION OF MATURATION-PROMOTING FACTOR IN STARFISH OOCYTE STRATIFIED BY CENTRIFUGATION

In starfish, cytoplasm taken from maturing oocytes is capable of inducing breakdown of the germinal vesicle and subsequent maturation when injected into immature oocytes. The cytoplasmic factor has been designated as "maturation-promoting factor" (MPF). Ooplasm was stratified by centrifugation of maturing oocytes in density-graded Ficoll-seawater, without disrupting the cell. Three strata were distinguished beginning with the centripetal side: oil cap, hyaline layer and yellow layer. MPF activity was shown to be localized in the hyaline layer. Electron microscopic observation revealed that the hyaline layer contains Golgi complexes, many lucent vesicles and multi-vesicular bodies as distinct organelles, but seldom contains such inclusions as the lipid droplets forming the oil cap, mitochondria, yolk and pigment granules contained in the yellow layer. Based on these observations, a possible cytoplasmic component with MPF activity is discussed.     

In vitro evidence for the involvement of mitochondrial folate metabolism in the supply of cytoplasmic one-carbon units

We present in vitro evidence for a novel intercompartmental pathway in which folate-mediated reactions in mitochondria generate one-carbon units for utilization in cytoplasmic processes. Rat liver mitochondria are shown to contain the enzymatic activities for catabolism of serine or sarcosine to produce formate. Intact mitochondria rapidly convert the 3-carbon of serine or the N-methyl group of sarcosine to formate, which exits the mitochondria. Labeled formate is incorporated into purine by a cytoplasmic purine synthesizing system only after activation to 10-formyl-THF via the ATP-dependent 10-formyl-THF synthetase reaction. In a coupled system where one-carbon donors are catabolized by mitochondria before addition to the cytoplasmic purine synthesizing system, incorporation into purine shows a marked dependence on ATP. These observations demonstrate that mitochondria can metabolize one-carbon donors via THF-dependent reactions to the level of formate which then exits mitochondria for utilization in the cytoplasm. The proposed pathway is discussed in relation to genetic evidence for its operation in vivo as well as compartmentation of folate coenzymes and their one-carbon units.     

Morphological analysis of the cellular interactions between the eugregarine Gregarina garnhami (Apicomplexa) and the epithelium of its host, the desert locust Schistocerca gregaria

Morphological features of the eugregarine Gregarina garnhami (Canning, 1956) parasitic in the caeca and mid-gut of the desert locust, Schistocerca gregaria, have been studied by transmission and scanning electron microscopy, with particular attention to the epimerite and the relationship between the epimerite and the host epithelium. The cytoplasmic core of the globular epimerite is overlain by a distinct cortical zone, limited on its cytoplasmic face by a membrane-like structure, with an underlying layer of mitochondria. The periphery of the cortical zone is strengthened by a mass of fine filaments, especially at its base. Fine tubular structures, apparently arising from the membrane-like structure, pass through the cortical zone and attach to the epimerite-host cell interface. The base of the cortical zone is supported by a distinct osmiophilic ring. The epimerite is separated from the rest of the gregarine body by a discontinuous septum. Maturing and mature trophozoites possess conically arranged fibrils, which arise from the epimeritic septum and continue into the protomerite region. The epimerite and associated structures are here discussed with regard to the detachment of the trophozoite from the host epithelium. In individuals already detached from the host epithelium, a central depression remained at the top of their protomerite, in the area formerly bearing the epimerite.     

Effects of Purified Helminthosporium maydis Race T Toxin on the Structure and Function of Corn Mitochondria and Protoplasts

A toxin preparation from Helminthosporium maydis Race T containing several closely related molecules with apparently identical biological activities was highly active against mitochondria and protoplasts from Texas male-sterile (T) cytoplasm corn (T mitochondria and T protoplasts, respectively) but had no effect on their male-fertile (N) cytoplasm counterparts. The toxin preparation caused multiple changes in isolated T mitochondria, including uncoupling of oxidative phosphorylation, stimulation of succinate and NADH respiration, inhibition of malate respiration, increased swelling, loss of matrix density, and unfolding of the inner membrane. Only 6 to 7 nanograms toxin per milligram mitochondrial protein (1.8 nanogram per milliliter) were required to fully uncouple oxidative phosphorylation and to completely inhibit malate respiration in isolated T mitochondria. Similar low concentrations of toxin caused collapse of T protoplasts after several days of culture. Severe ultrastructural damage to mitochondria in T protoplasts was observed within 20 minutes; no changes in other cellular components were observed at this time. These observations on the cytoplasmic specificity, multiple effects, and high activity of the toxin at the mitochondrial and cellular levels highlight its biological significance and potential usefulness in determining the molecular basis of southern corn leaf blight disease.     

Friction and adhesion in the tarsal and metatarsal scopulae of spiders

Friction and adhesion forces of the ventral surface of tarsi and metatarsi were measured in the bird spider Aphonopelma seemanni (Theraphosidae) and the hunting spider Cupiennius salei (Ctenidae). Adhesion measurements revealed no detectable attractive forces when the ventral surfaces of the leg segments were loaded and unloaded against the flat smooth glass surface. Strong friction anisotropy was observed: friction was considerably higher during sliding in the distal direction. Such anisotropy is explained by an anisotropic arrangement of microtrichia on setae: only the setal surface facing in the distal direction of the leg is covered by the microtrichia with spatula-like tips. When the leg is pushed, the spatula-shaped tips of microtrichia contact the substrate, whereas, when the leg is pulled over a surface, setae bend in the opposite direction and contact the substrate with their spatulae-lacking sides. In an additional series of experiments, it was shown that desiccation has an effect on the friction force. Presumably, drying of the legs results in reduction of the flexibility of the setae, microtrichia, spatulae, and underlying cuticle; this diminishes the ability to establish proper contact with the substrate and thus reduces the contact forces.     

A Mathematical Model to Capture Complex Microstructure Orientation on Insect Wings

Microstructures on insect wings can promote directional drop shedding, and the local orientation of these structures is expected to facilitate drop removal. However, microstructures may exhibit very different orientations at different locations on the wing. Using the march fly Penthetria heteroptera, we propose that local orientation of small hairs (microtrichia) reflects a balance of three nonexclusive strategies: (1) preventing water from becoming stuck in intervenous grooves (microtrichia point upslope), (2) shedding water off the wing as readily as possible (microtrichia point towards the nearest edge), and, (3) shedding water away from the body (microtrichia point distally). We present evidence for all three and show that local microtrichial orientation is seldom determined by any one factor. We develop a mathematical model that employs factor-specific weighting values determined via optimization. Our predictions are tested against the orientation of microtrichia randomly sampled from a P. heteroptera specimen. Using the best-fit weighting parameters, the model displays a median residual of 20°; no residual is greater than 46°. The model also reproduces qualitative aspects of microtrichial orientation, such as bifurcation midway between veins and convergence toward peaks. This strong correspondence between modelled and observed orientation supports the role of microtrichia as directional antiwetting devices and highlights the importance of considering both function and wing geometry to explain the organization of natural microstructure arrays.     

Olfactory sensilla on the antenna and maxillary palp of the sheep head fly,Hydrotaea irritans (Fallen) (Diptera : Muscidae)

Antennae and maxillary palps of both sexes of the Sheep Head fly Hydrotaea irritans (Diptera : Muscidae) were investigated using scanning electron microscopy to describe the types, morphology, and distribution of olfactory sensory structures. Only socketed bristles and microtrichia were found on the scape of the antennae. These structures were also observed on the pedicel together with a group of 7–8 as yet undescribed sensilla, whose function is unknown. Olfactory sensilla were not found on these 2 segments or on the arista. Large numbers of olfactory sensilla and microtrichia were present on the funiculus. The former included sensilla trichodea (thick-walled, multiporous sensilla), sensilla styloconica and 6 types of sensilla basiconica (thin-walled, multiporous sensilla), 4 of which occurred individually and 2 of which were found in groups. An olfactory pit containing groups of thin-walled multiporous sensilla was located on the dorsomedian side of the funiculus. All sensilla basiconica were classified on morphological characteristics. The maxillary palps were covered with microtrichia and socketed bristles, but only 1 type of olfactory sensillum was found. This was a type of sensillum basiconicum that differed from any of those found on the antennae. No differences were found in sensilla diversity and distribution between males and females.     

Electron-cytochemical study of the localization of ATPase activity in the brain tissue of white rats]

A localization of ATPase activity in a rat's brain was studied by the lead method at the presence of Mg2+. The highest activity was noticed in the capillar basal layer, in nucleoli and nuclear chromatin. Less intensive sedimentation of precipitate was observed on the external nuclear membrane, granular cytoplasmic reticulum, ribosomes and in lipofuscin granules. Besides, the reaction product was observed on the cytomembrane of neurons, in synaptic slits and on the vesicles of some terminals. No ATPase activity was seen in mitochondria in the experimental conditions. Equal distribution of reaction product was seen in the cortex and hypothalamus.     

RNA biosynthesis in mitochondria under conditions of prolonged inhibition of protein biosynthesis in rat liver cytoplasm]

When cytoplasmic protein synthesis is inhibited by cycloheximide (CHI) in vivo synthesis of water-soluble mitochondrial proteins and of mitochondrial RNA is decreased. These changes measured in isolated rat liver mitochondria are similar to those observed in vivo and correlate with the changes the synthesis of water-soluble proteins in mitochondria. When the cytoplasmic fraction (30,000 g-supernatant) had been added to the mitochondria showing decreased RNA synthesis, the RNA synthesis increased to the control level (the incubation conditions were favourable for the protein transport from microsomes to mitochondria). RNA synthesis in mitochondria was not stimulated by cytoplasmic fractions from the CHI-pretreated rats. After prolonged dialysis these fraction stimulated RNA synthesis even to a greater extent than cytoplasmic fractions from the untreated animals. Mitochondrial RNA polymerase activity (measured in mitochondrial extracts supplemented with exogenous DNA) was higher in extracts of mitochondria from livers of normal rats than in extracts of mitochondria from livers of animals injected with CHI.     

Mammalian HSP60 is quickly sorted into the mitochondria under conditions of dehydration.

There are few reports concerning the sorting mechanisms of mammalian HSP60 into the mitochondria from the cytoplasm. In the present study we investigated the protein import system. Based on immunoblotting and immuno-histochemistry, HSP60 was detected in both the cytoplasm and mitochondria. The purified cytoplasmic HSP60 showed chaperone activity, and the protein was imported into the mitochondria in vitro by a mitochondrial import assay. HSP60 mRNA was increased in the kidney papilla of rats that had been water restricted for three and five days, but no changes in HSP60 mRNA were detected in the cortex or the medulla of the rat kidneys. Upon immunoblotting, HSP60 was detected in both the cytoplasm and the mitochondria of normal rat kidney cortex, medulla, and papilla in almost the same quantity. HSP60 was remarkably decreased in the kidney papilla of rats that were water restricted but the protein was increased in the mitochondria of the rat kidney papilla. We also analysed binding of the protein to the signal sequence of HSP60 using signal sequence-affinity column chromatography. We identified only one protein band with a molecular mass of 70 kDa on SDS/PAGE. The protein was eluted from the affinity column by an excess of signal peptide or by 5 mm ATP. Upon immunoblotting, the 70-kDa protein cross-reacted with an antibody against HSP70. These results suggested that mammalian HSP60 is located both in the cytoplasm as a stable cytoplasmic HSP60 and also in the mitochondria under normal conditions. The cytoplasmic HSP60 is quickly imported into the mitochondria under severe conditions by cytoplasmic HSP70.     

Ribosomal Ribonucleic Acids of Chloroplastic and Mitochondrial Preparations

RNA prepared from fractions of chloroplasts and mitochondria sedimented at rates characteristic of ribosomal RNA. A predominance of the 18S species was frequently observed in preparations from chloroplasts from romaine lettuce and endive. The usual distribution, a preponderance of the 28S species, was observed in studies on tomato and spinach chloroplasts and mitochondria from mushroom and cauliflower. Comparisons of the base composition of RNA from organelles with their cytoplasmic ribosomal counterparts revealed that the 18S component from romaine lettuce chloroplast was different. A marginally significant difference was observed in the 28S particle from mushroom mitochondria preparations whereas distinct differences, reflected in all the bases, were seen when the 18S component of cauliflower mitochondria preparations was compared with cytoplasmic RNA.