Developmental features of calcium oxalate crystal sand deposition inBeta vulgaris L. Leaves

Summary Sugar beet (Beta vulgaris L.) leaf has a layer of cells extended laterally between the palisade parenchyma and spongy mesophyll that develop numerous small crystals (crystal sand) within their vacuoles. Solubility studies and histochemical staining indicate the crystals are calcium oxalate. The crystals are deposited within the vacuoles early during leaf development, and at maturity the cells are roughly spherical in shape and 2 to 3 times larger than other mesophyll cells. Crystal deposition is preceeded by formation of membrane vesicles within the vacuole. The membranes are synthesizedde novo in the vacuole and have a typical trilaminate structure as viewed with the TEM. The membranes are formed within paracrystalline aggregates of tubular particles (6–8nm outer diameter) as membrane sheets, but are later organized into chambers or vesicles. Calcium oxalate is then precipitated within the membrane chambers. The tubular particles involved in membrane synthesis are usually present in the vacuoles of mature crystal cells, but in very small amounts.     

Functional morphology of the dorsal vessel in the adult fly Protophormia terraenovae (diptera,calliphoridae)

The morphology and ultrastructure of the contractile tubular vessel acting as the cardiac pump in Protophormia terraenovae flies were analyzed by means of light microscopy, SEM and TEM. The results provide a novel anatomical picture of the two vessel portions, the abdominal heart and the aorta, and lay the foundations for an interpretation of the cardiocirculatory function in the fly. In the thorax, the thin and unchambered aorta is without apertures, while the abdominal heart presents a very small caudal aperture and pairs of lateral ostia, one in each of the five chambers of which it is composed. The ostia of the four more distal chambers are of the incurrent type, which is to say that they act as valves ensuring that hemolymph flows only into the heart. Conversely, the ostia in the most proximal chamber allow hemolymph to flow both into and out of the heart. The entire vessel is composed of a single layer of myofibers that are oriented circularly around the lumen in the abdominal heart and longitudinally in the thoracic aorta. The abdominal heart has a thicker wall, a far more diffused and thick distribution of tracheoles, and a far greater number of mitochondria with respect to the aorta. This arrangement ensures a greater availability of oxygen and energy in the abdominal heart compared to the aorta and leads one to suppose that the high‐ and low‐frequency contractions of the cardiac cycle (Thon, [1982] J. Insect Physiol. 28:411–416) can be attributed to the abdominal heart and the aorta, respectively. J. Morphol. 240:15–31, 1999. © 1999 Wiley‐Liss, Inc.     

Fine Structure of Heart,Pericardium and Glomerular Vessel in Cephalodiscus gracilis M'Intosh, 1882 (Pterobranchia,Hemichordata)

Heart, pericardium and glomerular vessel of Cephalodiscus gracilis have been studied with the electron microscope. The lumen of the heart is lined by a basal lamina and an associated epithelium, composed of myoepithelial cells with well developed thin and thick myofilaments. The heart is located in the pericardial cavity, which is deliminated by the pericardium. The latter is composed of two flat layers of myoepithelia with fused basal laminae. The outer layer of the pericardium is the protocoelomic lining, and the inner layer is the ‘parietal’ pericardial epithelium. The myoepithelium forming the heart wall can be considered to represent the ‘visceral’ pericardial epithelium. The spacious glomerular vessel is lined by a basal lamina, on which typical podocytes rest. These cells indicate that ultrafiltration takes place through the wall of the glomerular vessel. The lumen of the vessel contains fine granular material (presumably precipitated blood proteins), fibrils with a faint cross striation, suggesting that they represent collagen, and stellate cells, which in part line the vessel. Since ultrafiltration requires hydrostatic pressure, it is inferred that the blood flow is from the dorsal region then through the heart and into the glomerular vessel.     

TELOCYTES IN ENDOCARDIUM: Electron Microscope Evidence

The term TELOCYTES was very recently introduced, for replacing the name Interstitial Cajal‐Like Cells (ICLC). In fact, telocytes are not really Cajal‐like cells, they being different from all other interstitial cells by the presence of telopodes, which are cell‐body prolongations, very thin (under the resolving power of light microscopy), extremely long (tens up to hundreds of micrometers), with a moniliform aspect (many dilations along), and having caveolae. The presence of telocytes in epicardium and myocardium was previously documented. We present here electron microscope images showing the existence of telocytes, with telopodes, at the level of mouse endocardium. Telocytes are located in the subendothelial layer of endocardium, and their telopodes are interposed in between the endocardial endothelium and the cardiomyocytes bundles. Some telopodes penetrate from the endocardium among the cardiomyocytes and surround them, eventually. Telopodes frequently establish close spatial relationships with myocardial blood capillaries and nerve endings. Because we may consider endocardium as a ‘blood–heart barrier’, or more exactly as a ‘blood–myocardium barrier’, telocytes might have an important role in such a barrier being the dominant cell population in subendothelial layer of endocardium.     

MORPHOLOGY AND ULTRASTRUCTURE OF EMBRYOGENIC CELL SUSPENSION CULTURES OF PANICUM MAXIMUM (GUINEA GRASS) AND PENNISETUM PURPUREUM (NAPIER GRASS)

Morphological and ultrastructural changes during the growth of embryogenic cell suspension cultures of Panicum maximum and Pennisetum purpureum have been studied. The suspensions consist almost entirely of cell aggregates of 50–75 embryogenic cells. The cell aggregates vary in size from 90–400 μm in P. maximum and from 70–340 μm in P. purpureum. Following the period of exponential growth starch grains gradually disappear and vacuolation increases. Ten to 16 days after subculture, P. maximum cells enlarge and separate from each other, and organized embryo-like structures appear. Ultrastructural studies show that the cell aggregates are made up of discrete, individual groups of 2–6 cells each. Each cell group appears to arise from a single cell and breaks away from the ‘mother group’ as cell divisions continue. The embryogenic cells are small (20 μm), isodiametric with many starch grains and contain a large nucleus with a prominent nucleolus. Extensive profiles of endoplasmic reticulum, many small peripheral vacuoles, and several amyloplasts are present. Plasmodesmatal connections exist only between cells within a cell group but not between cells of different cell groups in the large cell aggregates.     

DYNAMIC RESPONSE OF ROOT BORDER CELLS AND THEIR ASSOCIATED MUCILAGE EXUDATION IN SOYBEAN TO AI STRESS AND RECOVERY

 以耐铝性明显差异的两个大豆(Glycine max)基因型‘浙秋2号’(耐性)和‘浙春3号’(敏感)为材料, 研究根尖边缘细胞比活度、粘液分泌和根长对铝胁迫和解除胁迫的反应, 明确边缘细胞的粘液分泌对策在铝毒环境中的生态学意义。结果表明, ‘浙秋2号’在100~400 µmol&;#8226;L^–1 Al³⁺处理的3~12 h, 边缘细胞比活率呈递减趋势, 12 h后比活率又略有上升。‘浙春3号’在300和400 µmol&;#8226;L^–1 Al³⁺处理的变化与前者一致。两个大豆基因型的粘液层随着Al³⁺浓度增加和时间延长而增厚, 并于400 µmol&;#8226;L^–1 Al³⁺处理24 h时达到最大(>17 µm)。‘浙秋2号’在低浓度Al3+ (100和200 µmol&;#8226;L^–1)处理3~6 h后就会分泌大量粘液, ‘浙春3号’则在300 µmol&;#8226;L^–1 Al³⁺处理12 h后才有类似的变化。‘浙秋2号’在400 µmol&;#8226;L^–1 Al³⁺处理下的根相对伸长率均高于100~300 µmol&;#8226;L^–1 Al³⁺处理, ‘浙春3号’则表现为Al³⁺浓度越高, 根伸长受抑越明显。Al³⁺胁迫解除后, ‘浙秋2号’的粘液分泌速度和分泌量急剧下降, ‘浙春3号’在胁迫解除后的24 h, 仍会持续、大量地分泌粘液(>19 µm)。可见, 耐性大豆通过在铝胁迫初期快速、大量地分泌粘液以维持较高的边缘细胞活性和解除胁迫后迅速降低粘液的分泌速度及分泌量来适应铝毒害环境。     

Controlled replication of ‘Candidatus Liberibacter asiaticus‘ DNA in citrus leaf discs

‘Candidatus Liberibacter asiaticus’ is a fastidious bacterium and a putative agent of citrus greening disease (a.k.a., huanglongbing, HLB), a significant agricultural disease that affects citrus fruit quality and tree health. In citrus, ‘Ca. L. asiaticus’ is phloem limited. Lack of culture tools to study ‘Ca. L. asiaticus’ complicates analysis of this important organism. To improve understanding of ‘Ca. L. asiaticus’–host interactions including parameters that affect ‘Ca. L. asiaticus’ replication, methods suitable for screening pathogen responses to physicochemical and nutritional variables are needed. We describe a leaf disc-based culture assay that allows highly selective measurement of changes in ‘Ca. L. asiaticus’ DNA within plant tissue incubated under specific physicochemical and nutritional conditions. qPCR analysis targeting the hypothetical gene CD16-00155 (strain A4) allowed selective quantification of ‘Ca. L. asiaticus’ DNA content within infected tissue. ‘Ca. L. asiaticus’ DNA replication was observed in response to glucose exclusively under microaerobic conditions, and the antibiotic amikacin further enhanced ‘Ca. L. asiaticus’ DNA replication. Metabolite profiling revealed a moderate impact of ‘Ca. L. asiaticus’ on the ability of leaf tissue to metabolize and respond to glucose.     

RELATION OF PLASTOCHRON TO ANATOMY AND GROWTH IN THE SHOOT APEX OF CHRYSANTHEMUM

The relation between plastochron stage, apical anatomy, and thymidine-C¹⁴ incorporation was studied in the shoot apex of Chrysanthemum morifolium ‘Albatross.’ Apices were sorted into early, middle, and late plastochron stage under a dissecting microscope, fixed, and sectioned longitudinally so that median sections included known sectors of the apical flank. Study of these sections revealed no discernible difference between apices in early, middle, or late plastochron with respect to regularity of cell pattern, presence of a cambium-like zone, appearance of the second tunica layer or staining pattern with pyronin or with toluidine blue. Likewise, apices that had been treated with thymidine-C¹⁴ for 2-4 hr showed no differences between the three stages in number or distribution of labeled cells.     

COMPARISON OF SPONTANEOUS LOSS OF CATECHOLAMINES AND ATP IN VITRO FROM ISOLATED BOVINE ADRENOMEDULLARY, VESICULAR GLAND, VAS DEFERENS AND SPLENIC NERVE GRANULES

The molar ratio catecholamines/ATP in the high speed sediment from homogenates of bovine adrenal medulla, vesicular gland, vas deferens and splenic nerve was relatively close to the‘equivalence ratio’of 4/1. On incubation in vitro the loss of amines and ATP from the medullary granules was slow and largely parallel. Thus the original amine/ATP ratio was maintained. The amine loss from the nerve granules occurred at a very high, and from the vesicular gland and vas deferens granules at an intermediate, rate. On the other hand, the decrease in ATP in these preparations was quite slow, leading to a marked change in the original amine/ATP ratio. These findings are regarded as further evidence of functional differences between granules derived from chromaffin cells and from sympathetic nerve tissue, and even between nerve granules from‘long’and 'short’noradrenergic neurons. The possible implications of these in vitro differences in amine and ATP release are discussed in relation to the mechanisms of amine release in vivo.     

DEVELOPMENT OF CHAMBERED PITH IN STEMS OF PHYTOLACCA AMERICANA L. (PHYTOLACCACEAE)

An integrated microscopic (light and electron microscopy) and macroscopic investigation of chambered pith development was made of Phytolacca americana L. Terminal internodes have a solid pith cylinder in contrast to the alternating diaphragms and chambers occurring in subjacent pith. Macroscopically, chambers and diaphragms of any one internode are of equal size. Microscopically, diaphragms vary in height within an internode (from 1–6 cells high). Nevertheless, all diaphragms become thicker circumferentially (5–12 cells high) and connect with long files of intact peripheral pith cells. Diaphragm cells have a large centrally positioned vacuole with a thin, parietal layer of cytoplasm; nuclei, mitochondria, endoplasmic reticulum, and unidentified organelles differentiate in the cytoplasm of diaphragm cells. Although schizogenous activity has most often been implicated as the mechanism by which chambered pith develops in vegetative organs of angiosperms, the results of this study show that cavities in pokeweed result from both schizogenous and lysigenous mechanisms. Schizogeny is suggested by the fact that central pith cells of terminal internodes are longer and thinner walled than peripheral pith cells arranged in vertical files, thus indicating elongation of cells as a possible result of internode elongation. The precise developmental pattern and arrangement of chambers and diaphragms also suggest schizogenous processes. Lysigenous or enzymatic activity is indicated by the fact that cavities are bounded by broken cells, and wall fragments and organelles are often found within enlarging cavities. Chamber formation occurs continuously acropetally and centrifugally in the central pith. A comparison of diaphragms is made with Liriodendron tulipifera and Juglans nigra in an attempt to resolve differences in structure and terminology regarding the differentiation of chambered and diaphragmed pith.     

Variability in the Presence of Elastic Fibre-like Structures in the Ventral Aorta of Agnathans (Hagfishes and Lampreys)

This paper investigates whether elastic fibre-like structures are present in the ventral aorta of hagfishes and lampreys. Fibres, which are morphologically similar to the elastic fibres of gnathostomatous (jawed) vertebrates, are shown to be present in the ventral aorta of the hagfish Paramyxine atami, and also, but to a lesser extent, the dorsal aorta of this species and the ventral aorta of another hagfish, Eptatretus stouti.The ‘elastic’ tissue formed irregular sheet-like aggregates, comprising well-defined amorphous material surrounded by tubular microfibrils, whose diameters ranged from 10 to 15 nm. While this tissue was most abundant in the same region of the aortae as that occupied by the elastica interna in the blood vessels of gnathostomes, it was also found deeper in the wall of these blood vessels. Although tubular microfibrils were found in the ventral aorta of the hagfish Myxine glutinosaand the lamprey Geotria australis, these were never associated with well–defined, amorphous material. This parallels the results of previous studies on Myxine glutinosaand another species of lamprey, Petromyzon marinus.Thus, the elastic fibre–like tissues found in the ventral aortae of P. atamiand E. stoutiprovide the first examples of such structures in this region in agnathan vertebrates.     

COLONY-FORMING UNITS IN DIFFUSION CHAMBERS (CFU-d) AND COLONY-FORMING UNITS IN AGAR CULTURE (CFU-c) OBTAINED FROM NORMAL HUMAN BONE MARROW: A POSSIBLE PARENT–PROGENY RELATIONSHIP

A series of experiments was performed to elucidate the relationship between cells that form granulocytic colonies in fibrin clot diffusion chambers implanted into the peritoneum (i.p.) of irradiated mice (CFU-d) and day 7 and day 14 CFU-c which give rise to colonies after 7 and 14 days in agar cultures in vitro, respectively. Normal human bone marrow cells were cultured in suspension in vitro or in diffusion chambers implanted into irradiated or non-irradiated mice. During these culture conditions there was an initial decrease in the number of CFU-c per culture. This was followed by an increase between day 2 and day 7 of culture. No similar increase of neutrophilic CFU-d was observed. When CFU-d, day 14 and day 7 CFU-c in normal marrow were separated by velocity sedimentation and cultured in suspension culture or in diffusion chambers for 7 days, the maximum increase of day 7 and day 14 CFU-c was observed in slowly sedimenting cell fractions which contained the majority of CFU-d. After 3 days in suspension culture, the maximum increase of day 14 CFU-c was found in fractions which also gave rise to maximum numbers of CFU-c after 7 days. However, day 7 CFU-c were found in fractions which initially contained the majority of day 14 CFU-c. No increase in CFU-d was found in fractions initially containing peak numbers of CFU-c. Between 53 and 71% of CFU-c harvested from diffusion chambers in irradiated mice or from suspension cultures were sensitive to pulse incubation with tritiated thymidine, suggesting that the cells were proliferating during these culture conditions. In diffusion chambers implanted into non-irradiated mice, however, CFU-c were found to be relatively resistant to this treatment (3–11% sensitive to tritiated thymidine). Thus marked increases in CFU-c were also observed during experimental conditions, where no significant DNA synthesis was detected. A reproducible time sequence of increase in CFU-c populations in culture was observed. Day 14 CFU-c and cells that gave rise to clusters on day 7 in agar increased between day 2 and day 4, whereas day 7 CFU-c increased between day 4 and day 7. The results suggested that CFU-d gave rise to CFU-c in culture and that day 14 CFU-c were precursors of day 7 CFU-c.     

Electrophysiological studies on embryonic heart cells in culture. Scorpion toxin as a tool to reveal latent fast sodium channel

Trypsin-dispersed heart cells were obtained from 11-day-old chick embryos. After culture as unstirred suspensions in dimethylsulfoxide-containing medium, spherical aggregates of cells beating spontaneously and apparently synchronously for months were obtained. Two kinds of cell were characterized by electrophysiological recordings: (1) cells with a slow rate of depolarizing phase showing tetrodotoxin-resistant action potential and blocked by D 600 (‘slow’ cells); (2) cells with high value of rising phase which was strongly decreased by tetrodotoxin and in which D 600 provoked uncoupling of excitation-contraction (‘fast’ cells).Toxin II from Androctonus australis scorpion venom increased the duration of action potential, which was ascribed to a slowing down of Na⁺ current inactivation and enhance the maximum rate of depolarization, especially in slow cells. Effects were antagonized by tetrodotoxin in both fast and slow cells. Washing experiments confirmed the results of previous studies, namely that tetrodotoxin and scorpion toxin bind to different receptors. It is concluded that slow cells with tetrodotoxin-resistant action potential contain latent fast Na⁺ channels that are revealed (activated) by toxin binding to the membrane.     

TTN/OBSCN ‘Double-Hit’ predicts favourable prognosis, ‘immune-hot’ subtype and potentially better immunotherapeutic efficacy in colorectal cancer

Colorectal cancer (CRC) remains a leading cause of cancer-related deaths worldwide. Although treatment strategies for solid tumours have been revolutionized by immunotherapy, only a small subset of CRC patients benefit. Using two-independent cohorts, we found the common frequently mutated genes TTN and OBSCN had the significant correlation with higher tumour mutation burden (TMB) and favourable overall survival. TTN and OBSCN also displayed significant commutation phenomenon. Therefore, based on the status of TTN and OBSCN, we stratified patients into ‘Double-WT’ phenotype, ‘Single-Hit’ phenotype and ‘Double-Hit’ phenotype. Importantly, the ‘Double-Hit’ phenotype had favourable prognosis, low malignant events propensity, and highest TMB, immune cells infiltration abundance, POLE mutation rate, microsatellite instability ratio, as well as immune checkpoints expression compared with the other two phenotypes. These results indicated that the ‘Double-Hit’ phenotype suggested ‘immune-hot’ tumours and potentially better immunotherapeutic efficacy. Bioinformatic algorithm assessment of immunotherapy responses also confirmed this conclusion, and the ‘Double-Hit’ phenotype was found to be a better predictor of immunotherapy than PD-L1, PD-1, CTLA-4, TMB and microsatellite status. This study revealed CRC patients with TTN/OBSCN ‘Double-Hit’ was significantly associated favourable prognosis, ‘immune-hot’ subtype and potentially better immunotherapeutic efficacy.     

Solute Uptake of Acer pseudoplatanus Cell Suspensions during Recovery from Gas Shock

When the ambient atmosphere of Acer pseudoplatanus cells in suspension culture is rapidly changed by opening the culture flasks and gently stirring (‘mild gas-shock’) or by filtering and suspending in new medium (‘strong gas-shock’), drastic modifications of the rates of leucine, methionine, glucose, adenine, sulphate and phosphate uptake are observed. Following the gas-shock, rates of uptake rapidly decrease within a few minutes. Subsequently the rates increase again to the intial level within several hours. The uptake of potassium, which is known to be passively distributed between the medium and the interior of many plant cells, at least at high external concentrations, is apparently independent of gas-shock. The shock and recovery kinetics are similar for all solutes investigated (except K⁺), in particular for different solutes studied in double labelling experiments with the same batch of cells. At the maximum of the after-effect of shock, i.e. at minimum rates of uptake, uptake shows a highly reduced dependence on temperatures. Gas-shock probably inactivates, denatures, structurally alters or releases membrane macromolecules engaged in transport. These molecules are then re-synthesized and re-incorporated into the membrane during recovery.     

Importance of Sox2 in maintenance of cell proliferation and multipotency of mesenchymal stem cells in low-density culture

Objectives: This study has aimed to repopulate ‘primitive’ cells from late‐passage mesenchymal stem cells (MSCs) of poor multipotentiality and low cell proliferation rate, by simply altering plating density. Materials and methods: Effects of low density culture compared t high density culture on late‐passage bone marrow (BM)‐derived MSCs and pluripotency markers of multipotentiality were investigated. Cell proliferation, gene expression, RNA interference and differentiation potential were assayed. Results and conclusions: We repopulated ‘primitive’ cells by replating late‐passage MSCs at low density (17 cells/cm²) regardless of donor age. Repopulated MSCs from low‐density culture were smaller cells with spindle shaped morphology compared to MSCs from high‐density culture. The latter had enhanced colony‐forming ability, proliferation rate, and adipogenic and chondrogenic potential. Strong expression of osteogenic‐related genes (Cbfa1, Dlx5, alkaline phosphatase and type Ι collagen) in late‐passage MSCs was reduced by replating at low density, whereas expression of three pluripotency markers (Sox2, Nanog and Oct‐4), Osterix and Msx2 reverted to levels of early‐passage MSCs. Knockdown of Sox2 and Msx2 but not Nanog, using RNA interference, showed significant decrease in colony‐forming ability. Specifically, knockdown of Sox2 significantly inhibited multipotentiality and cell proliferation. Our data suggest that plating density should be considered to be a critical factor for enrichment of ‘primitive’ cells from heterogeneous BM and that replicative senescence and multipotentiality of MSCs during in vitro expansion may be predominantly regulated through Sox2.     

Late migration and seawater entry is physiologically disadvantageous for American shad juveniles

Juvenile American shad Alosa sapidissima were subjected to isothermal transfers into sea water (salinity 24)‘early’(1 September; 24° C) and ‘late’(10 November; 10° C) in the autumn migratory season. Early acclimation resulted in a modest osmotic perturbation that recovered rapidly. Haematocrit declined by 14% at 24 h, recovering within 48 h. Plasma osmolality increased by 6% at 4 h, recovering within 8 h. Early acclimation caused a two‐fold increase in gill Na⁺, K⁺‐ATPase activity by 24 h and a four‐fold increase by 4 days. The number of chloride cells on the primary gill filament increased two‐fold by 4 days. Chloride cells on the secondary lamellae rapidly decreased from 22 cells mm^?1 to <2 cells mm^?1 within 4 days. Late acclimation resulted in a severe and protracted osmotic perturbation. Haematocrit levels declined by 23% at 4 days, recovering by 14 days. Plasma osmolality increased by 36% by 48 h, recovering by 4 days. Initial gill Na⁺, K⁺‐ATPase activity was two‐fold greater than in ‘early’ fish and did not change during acclimation. Initial numbers of chloride cells on the primary filament were two‐fold greater than ‘early’ fish and did not increase during acclimation. Initial number of chloride cells on the secondary lamellae was five‐fold greater than ‘early’ fish (116 v. 22 cells mm^?1) and declined to negligible numbers over 14 days. Differences between initial measures for ‘early’ and ‘late’ fish reflect previously described physiological changes associated with migration. These data indicate that late migrants face a greater physiological challenge during seawater acclimation than early migrants. Physiological performance apparently limits the observed duration of autumnal migration.     

Population dynamics of the shrub Acacia suaveolens (Sm.) Willd.: Dispersal and the dynamics of the soil seed-bank

Genet survival in seeds of Acacia suaveolens was examined through both dispersal and dormancy in the soil in populations near Sydney. Following initial passive seed-fall, the majority of seeds lie within a 1 m radius of the stem of the parent. Further dispersal is predominately mediated by ants. A. suaveolens seeds possess an elaiosome which attracts ants. When elaiosomes are removed, the potential for further dispersal of seeds is greatly reduced. Three species of ant disperse seeds of A. suaveolens and the fate of seeds following ant dispersal was observed to depend on the particular species of ant involved. Ants of both Iridomyrmex sp. and Pheidole sp. B are too small to drag seeds and, instead, ants of these species usually remove the elaiosome in situ, with little dispersal of the-seed resulting. Ants of Pheidole sp. A are larger and disperse seeds further, frequently taking them into their nests where the elaisosome is removed. Seeds are retained inside the nests and incorporated into the floors and walls of passageways and chambers. Several supposed ‘advantages’ of myrmecochory were examined but none were verified. Instead, two distinct ‘disadvantages’ were identified. These were: burial of seeds by ants of Pheidole sp. A into ‘unsafe sites’; and too deep a burial of seeds in nests for seeds to receive a stimulus to germinate during fires, and for seedlings to emerge successfully. Outside nests of Pheidole sp. A. seeds are concentrated in the top 5 cm of the soil, whilst within nests of these ants, seeds are found up to 15 cm deep. The dynamics of various components of the soil seed-bank were examined using seeds buried in nylon mesh containers. The seed-bank is persistent without annual recruitment to seedlings, enabling a population to persist as seeds after all above-ground plants have perished.     

Bacteriocinogenesis in cells of Xenorhabdus nematophilus and Photorhabdus luminescens: Enterobacteriaceae associated with entomopathogenic nematodes

Summary— Xenorhabdus nematophilus FI strain and Photorhabdus luminescens NC19 strain produced bacteriocins after mitomycin C treatment and under natural conditions respectively. The ultrastructure of these two strains was described and compared to the ultrastructure of untreated or normal cells. After image processing of purified bacteriocins we found morphological homology in infected cells with protoplasmic rods in longitudinal section and hexagonal aggregates in transversal section. We concluded that these particular structures, so-called ‘lattice structures’ and previously interpreted as ‘photosomes’, are in fact the early stages of in situ production of bacteriocins in these two bacterial genera. Natural occurrence of Photorhabdus spp bacteriocinogenesis was observed in other strains, while other lysogenic strains of Xenorhabdus spp are lysed after a mitomycin C treatment.