Effect of lamellae autotomy on survival and foraging success of the damselfly Lestes sponsa (Odonata: Lestidae)

Damselfly larvae can autotomize their caudal lamellae to escape predation. Costs of caudal lamellae autotomy were investigated by directly manipulating lamellae condition of Lestes sponsa in laboratory experiments. Larvae without lamellae had higher predation mortality in the presence of Notonecta. Both lamellae loss and larval density increased the probability of being cannibalized. The results suggest that the increased vulnerability after lamellae loss resulted from a reduced escape performance. Larvae were less mobile after lamellae loss or in the presence of a predator, but the decrease was no longer significant when both factors were combined. This indicates that larvae compensate for the increased predation risk with a fixed response. Both lamellae loss and predator presence reduced hunting success, but the decrease after lamellae loss was only significant in the absence of a predator. The fitness consequences of these effects for both the larval and adult stages are discussed. In general, the data strongly suggest that lamellae autotomy plays a role in population regulation of damselflies. Received: 1 April 1998 / Accepted: 28 August 1998     

On the relationship between the microstructure of bone and its mechanical stiffness.

A recent study of bone structure shows that the plate-shaped carbonate apatite crystals in individual lamellae are arranged in layers across the lamellae, and that the orientation of these layers are different in alternate lamellae. Based on these findings, a new micromechanical model for the Young's modulus of bone is proposed, which accounts for the anisotropy and geometrical characteristics of the material. The model incorporates the platelet-like geometry of the basic reinforcing unit, the presence of alternating thin and thick lamellae, and the orientations of the crystal platelets in the lamellae. The thin and thick lamellae are modeled as orthotropic composite layers made up of thin rectangular apatite platelets within a collagen matrix, and classical orthotropic elasticity theory is used to calculate the Young's modulus of the lamellae. Bone is viewed as an assembly of such orthotropic lamellae bent into cylindrical structures, and having a constant, alternating angle between successive lamellae. The micromechanical model employs a modified rule-of-mixtures to account for the two types of lamellae. The model provides a curve similar to the published experimental data on the angular dependence of Young's modulus, including a local maximum at an angle between 0 and 90 degrees. A rigorous testing of the model awaits additional experimental data.     

Observations on the Fine Structure of Plant Cell Walls II. The Microfibrillar Framework of the Parenchymatous Cell Wall in Cucurbita

The microfibrillar framework of parenchymatous walls in Cucurbitawas observed in petioles treated so as to remove various non-cellulosiccell wall components. Such extraction typically results in separationof the microfibrillar components into concentric lamellae. Thenumber and thickness of these lamellae vary according to theage and type of cell wall. The microfibrils appear to be orientatedwithin the plane of their lamellae but the orientation may varyin successive lamellae, and in many walls the crossed polylamellatecondition was detected. The collenchyma—and the outerepidermal cell walls show an alternation of lamellae with almostvertical microfibrils with those with a practically transverseorientation. In ordinary parenchymatous walls the alternationis not so extreme and is revealed only by the occasional presenceof the ‘herring bone pattern’ in non-radial sections.As a rule the lamellae are continuous around the circumferenceof a cell though individual lamellae may vary in thickness andsometimes appear to ‘fade out’. The present observationssuggest that growth of the primary wall occurs by depositionof microfibrils in successive lamellae thus confirming the basicpremise of the multinet theory of growth.     

Differentiation of Acmaea digitalis oocytes with special reference to lipid-endoplasmic reticulum-annulate lamellae-polyribosome relationships

During initial stages of oogenesis, many nucleoli are adpressed to the inner membrane of the nuclear envelope. Small nucleolar fragments appear to traverse the pores of the nuclear envelope and accumulate in the perinuclear ooplasm as fibrogranular bodies. Mitochondria become closely associated with some of the fibrogranular bodies. In addition to ribosomes and polyribosomes that are present in small oocytes, lamellae of rough-surfaced endoplasmic reticulum (rER) increase greatly in number during early stages of differentiation. Some individual lamellae are attached at their ends to the outer membrane of the nuclear envelope. Many parallel lamellae of rER are then encountered as well as numerous circular profiles consisting of concentric loops of rER. Soon after the differentiation of the extensive system of rER, lipid droplets or spheres appear in the ooplasm and they are initially surrounded by many circular, concentric lamellae of rER. Initially, the number of concentric lamellae of rER surrounding a lipid droplet may vary from less than a dozen to more than two dozen. During middle and late phases of vitellogenesis, most of the lipid spheres that comprise the most numerous and significant component of the yolk are surrounded by only one or two concentric lamellae of rER (in some cases the lamellae are part rough-surfaced and part smooth-surfaced). In addition, annulate lamellae are then observed to be associated with a portion of the lipid droplet surface. The number of annulate lamellae that extend focally from the lipid sphere distally into the cytoplasm is variable; often two or three to more than a dozen lamellae. Small granules, many of which range from 6 to 12 nm and thin fibrils (approximately 2–3 nm in width) may be associated with the annulate lamellae. In addition, polyribosomes frequently appear to be continuous with the pore-associated material of the annulate lamellae. The ends of some annulate lamellae may extend as lamellae of the rER. The morphologic relationships and relationships and variations observed between the lipid droplets, rER, annulate lamellae, and polyribosomes during lipidogenesis in this oocyte are interpreted to support a recent hypothesis (Kessel, 1981a,b) that the pores of annulate lamellae may be involved in some manner with the processing of ribosomal subunits or precursors into functioning polyribosomes, and that their appearance in specific association with the surface of many lipid spheres and rER in the oocyte late in vitellogenesis may be related to the formation of additional functional polyribosomes necessary to complete the final synthesis of many lipid droplets that are present in the ooplasm of the full-grown oocyte.     

Photosporogenesis of Coprinus congregatus: Correlations between the physiological age of lamellae and the development of their potential for renewed fruiting

When the hymenial lamellae of Coprinus congregatus Bull ex Fr. are used as implants, their potential for renewed fruiting varies according to the photocontrolled meiosis and the consecutive sporogenesis. In the case of young lamellae, whose basidia are still at the dikaryon stage, one can observe immediate start of mycelial growth all around the lamellae and production of the first mature sporophores directly on the lamellae (direct fruiting). Simultaneously, meiosis does not occur in hymenial cells. Conversely, in the case of implantation of the oldest lamellae, whose basidia are characterized by meiotic nuclei beyond prophase 1 and rather near telophase 2 (tetranucleate stage), vegetative growth starts slowly and the first mature sporophores are not produced on the lamellae but on the surrounding vegetative mycelium (indirect fruiting). When the lamellae are isolated from photoindifferent primordia – for instance, 12 h before maturity – sporogenesis in hymenial cells proceeds normally until autolysis of the isolated lamellae. Such isolated lamellae no longer show direct fruiting where the first flush is concerned.     

The ecological role of caudal lamellae loss in the larval damselfly,Ischnura posita (Hagen) (Odonata: Zygoptera)

Summary Damselfly larvae may autotomize and regenerate any of their 3 caudal lamellae. At least one missing or regenerating lamella was evident in 50.1% of field collected Ischnura posita larvae. Lamellae loss during molting is very infrequent (1 out of 117 recorded molts). Laboratory trials indicate that conspecifics remove lamellae and that this process is density dependent. The percentage of larvae losing lamellae during 24 h trials ranged from 73.5 at the highest density tested to 17.3 at the lowest density. I. posita larvae are cannibalistic. The presence of lamellae reduces an individual's chance of being cannibalized. More than twice as many final instar lamellae-less larvae were cannibalized during 24 h trials than analogous individuals having 3 lamellae at experimental initiation. Costs are also associated with lamellae autotomy. 1) Although individuals without lamellae can swim they are more reluctant to release from a wooden stalk and swim when threatened (9% release) than are larvae with lamellae (29% release). Since swimming is part of their repertoire of anti-predator behaviors this behavioral shift should be detrimental. 2) Caudal lamellae function in O₂ uptake. Trials were conducted with larvae having and not having lamellae in an experimental horizontal oxygen gradient system. Relative to larvae without lamellae, those with lamellae preferred deeper depths at PO₂ values greater than 70 torr. Many lamellae-less larvae distributed themselves at the water surface throughout the range of PO₂ values tested. Differential depth distribution between larvae with and without lamellae is highly significant (P < 0.01).     

Olfactory organ of acipenseriformes and comparison with other actinopterygians: Patterns of diversity

The position and structure of the olfactory organ and its openings vary among actinopterygians. The anterior nasal opening is a simple perforation in the skin in many extant actinopterygians (e.g., acipenseriforms, lepisosteids, and primitive Recent teleosts) and represents the primitive condition. Polypterids and Amia each exhibit a derived condition, in which the anterior nasal opening extends into a tube. The olfactory organ is relatively far away from the anterior end of the elongate rostrum in acipenseriforms, whereas the olfactory organs are closer to the anterior end of the snout in extant actinopterygians (e.g., polypterids, lepisosteids, and amiids). In adults, olfactory organs are cuplike structures in most actinopterygians, but these organs are tubelike in polypterids. Among extant actinopterygians, a nasal diverticulum is present only in polypterids. Teleosts have accessory nasal sacs, but chondrosteans, polypterids, lepisosteids, and amiids lack them. The olfactory rosette is formed by primary folds or lamellae that may be placed anterior, lateral, posterior, and/or medial to the axis of the organ. Large acipenserids have 20–32 lamellae, polyodontids have 13–18 lamellae, lepisosteids have 8–10 lamellae, and Amia may have over 100. In teleosts, the number of lamellae varies from none or a few to over 200. Secondary lamellae are present in acipenseriforms, lepisosteids, and some advanced teleosts; secondary lamellae are interpreted as independently acquired in these lineages. Secondary lamellae are absent in Amia and primitive teleosts such as Elops and Hiodon. Tertiary lamellae are present in Acipenser oxyrhynchus. The arrangement of the primary lamellae in relation to the axis of the organ results in at least 11 patterns of the olfactory rosette in actinopterygians. Lamellae that are enclosed in a tubelike sac and that have an anteromedial diverticulum are specializations of polypterids. Primary lamellae anterior, lateral, and posterior to an elongate axis are characteristic of lepisosteids. The presence of primary lamellae lateral, medial, and posterior to an elongate olfactory axis is a synapomorphy of Halecomorpha (Amia plus teleosts). The absence of secondary lamellae is a synapomorphy of Halecomorpha. © 1994 Wiley-Liss, Inc.     

Accumulation of Annulate Lamellae in the Subcortical Layer during Progesterone-induced Oocyte Maturation in Xenopus Laevis

Changes in the fine structure, the location and the number of stacks of annulate lamellae during progesterone-induced maturation of oocytes of Xenopus were determined by electron microscopy. longitudinal sections of full-grown oocytes, about 260 stacks of annulate lamellae were observed with marked concentration in the subcortical layer, particularly in the vegetal hemisphere. After exposure to. progesterone, annulate lamellae increased and accumulated further in the subcortical layer. A significant increase of annulate lamellae around the vegetal side of the germinal vesicle seen 3 h after progesterone application. In oocytes 6 h after progesterone application, an average of 320 stacks of annulate lamellae were seen in longitudinal sections and more than two-thirds of the pore complexes of annulate lamellae were localized in the subcortical layer less than 50 from the oocyte surface, the rest being distributed in the deeper ooplasm. At the time of ger- minal vesicle breakdown, all the annulate lamellae underwent complete decomposition. The results were discussed from the view point of comparative developmental biology.     

Comparative Studies of the Thylakoid Proteins of Mesophyll and Bundle Sheath Plastids of Zea mays

The proteins from both grana and stroma lamellae of maize (Zea mays) mesophyll plastids and from maize bundle sheath plastid membranes have been compared by electrophoresis in sodium dodecyl sulfate-polyacrylamide gels using a discontinuous buffer system. Peptide differences between grana and stroma lamellae were essentially quantitative and not qualitative. Bundle sheath plastid membrane peptides more closely resembled those of the ultrastructurally similar stroma lamellae. However, bundle sheath membranes contained several peptides not apparent in the stroma lamellae.     

Structure of the gills of Barbus sophor (Ham), a cyprinid with tertiary lamellae

A study of the structure of the gills using light and transmission electron microscopy showed that though the basic organisation of the filaments and secondary lamellae is very similar to that of other bony fishes, there was also a number of unusual features. Most of the blood channels of the secondary lamellae remain embedded in the tissue of the primary lamellae. The secondary lamellar surface is increased by the presence of irregular expansions which may be referred to as tertiary lamellae. The presence of an unusual structure on one side of many secondary lamellae was observed; this structure might possibly be due to the presence of a parasite. The possible functional significance of these observations is discussed and indicates the need for morphometric and experimental investigation of the respiration of this species.     

Stacking Capacity and Chlorophyll Forms of Thylakoids in Normal and Mutant Maize Chloroplasts of Different Granum Content

Stacking of chloroplast lamellae, isolated from normal and carotenoid mutant chloroplasts of maize (Zea mays L.), was determined after a high-salt treatment. Stacking of isolated lamellae under favourable ionic conditions was almost identical with that occurring in intact chloroplasts; thus, differences in granum content could be attributed to the architectural properties of lamellae. Gaussian analyses, performed on the red band of room temperature absorption spectra, have shown that chloroplasts with lamellae of high stacking capacity contain relatively more Chl a₆₆₂ than chloroplasts containing lamellae of low stacking capacity. The presence of Chl a_705–708 was characteristic of preparations containing considerable amounts of stroma lamellae.     

On the Ultrastructure of Pollen Exine in Metasequoia Hu and Cheng

Metasequoia is endemic to China. Present study deals with ultrastructure of pollen exine of M. glyptostroboides Hu et Cheng, and in comparision with other genera of the family. Pollen grains of Metasequoia are spheroidal or subsphoroidal and 27.8(24.3–32.3) μm in diameter. There is a papilla in the distal face. The papilla is wide at the base, 3.5–5.2 μm high, with pointed and circular end and the base crooked toward one side. Exine is about L5 μm thick, layers distinct, Nexine is as thick as sexine. Surface weakly granulate. According to observation by SEM, exine is covered with fine granules and rather coarse tuberculae. The former can be easily separated from the latter. The loose and uneven tuberculae are provided with minute spinules on the surface and generally fall off after acetolysis. The fine and dense granulae, however, remain intact after acetolysis. The study by TEM shows that ektexine is made of granules densely arranged and connected with each other. In addition, sparse Ubisch bodies are unevenly distributed on granular layer with geminate surface. The thick endexine, is composed of 10–15 lamellae. It is worthy to note that all lamellae possess tripartite structure. But lamellae of endexine in other genera of Taxodiaceae have no tripartite structure except the lamella near ektexine. Number of lamella and thickness of endexine in Metasequoia differ from those of other genera in Taxodiaceae; for example endexine with 8–10 lamellae in Taxodium, 8–9 lamellae in Sequoia, 6–7 lamellae in Glyptostrobus, 6–8 lamellae in Cunninghamia, about 16 lamellae in Cryptomeria etc.     

Relationships between annulate lamellae and filament bundles in oocytes of the zebrafish,Brachydanio rerio

Summary Bundles of filaments have been observed in the vitellogenic oocyte of the zebrafish, Brachydanio rerio; and these filaments illustrate a close spatial and structural relationship to annulate lamellae. The filaments range from 6–8 nm in diameter, and the annulate lamellae may cap both rounded ends of the bundle as well as extend parallel to the surface of the filament bundles. The ends of the filaments can be observed to exhibit an apparent termination in close relation to pore margins of the annulate lamellae, the membrane of the interpore regions of the annulate lamellae, as well as many nearby polyribosomes. The possible functional significance of this unique relationship is discussed in reference to a recent hypothesis regarding the function of annulate lamellae.     

A multilamellate body in the granulated hypophysial cells of the teleost,Hemihaplochromis philander

Summary A multilamellate body (MLB), bearing close resemblance to an array of annulate lamellae, has been observed in several adenohypophysial cell types of the teleost, Hemihaplochromis philander. In longitudinal section, each MLB comprises a ladder-like row of 12–50 sausage-shaped profiles, termed lamellae. A few lamellae in each section show connections with the endoplasmic reticulum. Apposition of paired lamellar membranes at regularly spaced intervals results in a beaded appearance, whereby sites of membrane apposition are probable pore sites. The MLB differs from annulate lamellae in having poorly developed pores and closer packing of lamellae. It is suggested that the MLBs described here, may represent annulate lamellae at a stage of development or break-down when pores are incomplete.Acknowledgement is made to the South African Council for Scientific and Industrial Research for financial aid towards this work. The authors also wish to thank the Natal Parks, Game and Fish Preservation Board for providing specimens     

Epithelial and pillar cell replacement in gills of juvenile trout, Salmo gairdneri Richardson

Young rainbow trout, Salmo gairdneri (Richardson) were injected intraperitoneally with tritiated thymidine, and killed at intervals between 2 hr and 16 days after inoculation. Labelled epithelial cells were first detected autoradiographically along the base of gill lamellae. Epithelial cells proliferated here and then migrated toward the tips of the lamellae. Uniform labelling along the length of the filaments at the base of lamellae indicated that cells were dividing at a constant rate. Transverse sections of filaments showed that epithelial proliferation was also uniform across the base of the lamellae. The interior of the lamellae often had labelled pillar cells, indicating that these cells also divide. The high intensity of the label in animals killed 16 days after inoculation with tritiated thymidine suggests that division probably occurs slowly, less than once every 16 days.     

Annulate lamellae and crystalline inclusions in granular endoplasmic reticulum of the islet organ and associated tissues of a cyclostome,Myxine glutinosa

Cytoplasmic annylate lamellae were found in the islet organ of a cyclostome, the hagfish (Myxine glutinosa), predominantly in cells interpreted as young proliferating beta-cells, and also in endocrine cells and enterocytes of the bile duct and gut and in the endothelial cells of small blood vessels. A close association was observed annulate lamellae and granular endoplasmic reticulum. Both in cells with and in those without annulate lamellae, crystalline inclusions of proteinaceous nature were seen in granular endoplasmic reticulum. These inclusions were occasionally closely associated to annulate lamellae, and a direct continuity could be seen between granular endoplasmic reticulum and the outer nuclear membrane surrounding an inclusion partially situated in the perinuclear cisterna. Rod-shaped structures and rounded electron dense bodies were seen in the nuclei of some islet parenchymal cells. The presence of annulate lamellae in the islet organ and associated tissues of Myxine glutinosa is believed to be related to the very high phylogenetic age of this species. The close association observed between annulate lamellae, granular endoplasmic reticulum, crystalline inclusions, and sometimes also nuclear membranes, may be of functional significance.     

Two new species of Paraprionospio (Polychaeta: Spionidae) from the Grand Caribbean region and comments of the genus status

Material earlier recorded from the Grand Caribbean region as Paraprionospio pinnata (Ehlers, 1901) was reexamined and referred to two new species: Paraprionospio tamaii sp. nov. and P. yokoyamai sp. nov. Paraprionospio tamaii sp. nov. has dorsal crests on segments 20–29, notopodial lamellae oval on chaetigers 1–2, reniform on chaetiger four, neuropodial lamellae abovate on chaetiger three, and branchiae with two kinds of lamellae: (1) bifoliate, rounded lamellae positioned basally, and (2) flabellate lamellae positioned from the middle to distal region of branchiae. Paraprionospio yokoyamai sp. nov. has no dorsal crests, notopodial lamellae triangular and elongate on chaetiger 1–2, subtriangular on chaetiger four, neuropodial lamellae cordate on chaetiger three, and branchiae with three kinds of lamellae: (1) small subtriangular (unipinnate) in the basal region, (2) bifoliate in the middle region and (3) flabellate from the middle to distal region. None specimen revised from the Grand Caribbean region was identified as Paraprionospio pinnata. The geographic distribution of this ‘cosmopolitan’ species should be carefully verified. An identification key to currently recognized species of Paraprionospio is provided.     

Intranuclear and cytoplasmic annulate lamellae in grasshopper spermatocytes (Genus Melanoplus)

Intranuclear and cytoplasmic annulate lamellae were studied in grasshopper spermatocytes (Melanoplus) with the electron microscope. Although cytoplasmic annulate lamellae were observed in all three species examined, intranuclear annulate lamellae were found in only one species. The intranuclear annulate lamellae encompass certain nuclear material adjacent to the nuclear envelope forming a vesicle that is extruded into the spermatocyte cytoplasm. In this same species, cytoplasmic annulate lamellae are seen contiguous with granular masses of varying size. These structures were noted as being morphologically indistinguishable from the "yolk nuclei" of dragonfly oocytes (Kessel and Beams, 1969; Kessel, 1973).     

The apoprotein precursor of the major light-harvesting complex of photosystem II (LHCIIb) is inserted primarily into stromal lamellae and subsequently migrates to the grana

The formation of the lateral distribution of the major antenna complex of photosystem II (LHCIIb) between the granal and stromal lamellae was studied. Specifically, the localization of the insertion and the assembly of the precursor of the apoprotein of LHCIIb (pLHCP) were studied with isolated thylakoids. After insertion of pLHCP into isolated thylakoids, fractionation of the latter into granal and stromal lamellar was performed. At 25 °C most of the precursor was located in the granal lamellae, although both highly purified granal and stromal lamellar fractions demonstrated a similar capability to insert pLHCP. When the insertion reaction to the thylakoids was performed at 10 °C, followed by their separation into stromal and granal lamellae, the labelled pLHCP was localized in the stromal ones. To examine whether pLHCP inserts into both granal and stromal lamellae, or preferentially into stromal lamellae and subsequently migrating to granal lamellae, a chase experiment was performed. Insertion of pLHCP at 10 °C was followed by chase of the radioactive precursor with excess of non-radioactive pLHCP at 25 °C. From the results presented it is evident that the level of pLHCP in stromal lamellae was gradually reduced, while it gradually accumulated in the granal lamellae. Furthermore, the pLHCP in the stromal lamellae was found to be in a free form, while after migrating to the granal lamellae it assembled into the pigmented LHCIIb.     

Annulate lamellae in rete ovarii of juvenile rabbits

Annulate lamellae, though few, were observed in the epithelial cells of rete ovarii of 1-month-old rabbits, but not of other-aged juvenile rabbits examined. There were little differences in the fine structural details between the rete ovarii with annulate lamellae and those without annulate lamellae. Most rete ovarii cells were undergoing atrophy. This finding suggests that annulate lamellae may be quite ordinal, transitory organelles common to virtually all cell types.