Elephants harbour intestinal nematode infections, particularly cyathostomine nematodes (Cyathostomini: Strongylidae). Monitoring helminths in rare and endemic species is crucial, as infections can contribute to population declines. The Sumatran elephant (Elephas maximus sumatranus), a subspecies of the Asian elephant, is native exclusively to the island of Sumatra, Indonesia. The studies on nematodes of Sumatran elephants remain limited. In this study, three cyathostomine nematodes not previously reported from Indonesia – Quilonia renniei, Murshidia (Murshidia) falcifera, and M. (M.) murshida – were redescribed using light microscopy and scanning electron microscopy. This approach enabled the observation of previously unreported morphological features of taxonomic significance and corrected existing errors. Our SEM observations showed for the first time the detailed morphology of the cephalic extremity and the bursa of Murshidia (M.) falcifera, and M. (M.) murshida. Additionally, we provide the first molecular data on the nuclear DNA region (ITS1, 5.8S, and ITS2) of Q. renniei, the first mitochondrial partial cytochrome c oxidase I (COI) sequences for M. (M.) murshida and M. (M.) falcifera, and newly generated COI data for Q. renniei. These sequences were used to construct a phylogenetic tree of the elephant nematodes belonging to the Tribe Cyathostomini. The ITS phylogeny supported the monophyly of Murshidia and Quilonia and placed Khalilia sameera as a basal lineage, whereas the COI dataset failed to resolve relationships at the generic level. The ITS tree also confirmed the identity of Q. renniei, which appeared as sister to Q. africana.

En este trabajo se presentan los resultados del análisis de una pieza ósea que brinda información pionera sobre aspectos tecnológicos prehispánicos en el sector ribereño Paraguay-Paraná del Chaco argentino. Se analizó un elemento óseo de Rhea americana con evidencias de formatización. Con el objetivo de caracterizar la etapa de producción representada, se registraron marcas de manufactura, una de las cuales fue analizada con microscopio electrónico de barrido a fin de identificar el material con que se produjo la formatización (piedra o valva). A partir del análisis, se define el elemento como un núcleo con “extracción bosquejada”, es decir, una pieza en la cual se evidencia una forma base que aún no ha sido extraída. Se propone que la técnica de manufactura consistió en el ranurado a partir de filos de valva (Diplodon sp.). Este trabajo constituye el primer aporte con evidencias sobre el uso de filos de valvas de molusco en el proceso de confección de artefactos óseos en sitios arqueológicos de Argentina.

This study aimed to examine in vivo starch digestion kinetics and to unravel the mechanisms of starch hydrolysing enzymes. Ninety pigs (23 (sd 2·1) kg body weight) were assigned to one of nine treatments in a 3×3 factorial arrangement, with starch source (barley, maize, high-amylose (HA) maize) and form (isolated, within cereal matrix, extruded) as factors. We determined starch digestion coefficients (DC), starch breakdown products and digesta retention times in four small-intestinal segments (SI1–4). Starch digestion in SI2 of pigs fed barley and maize, exceeded starch digestion of pigs fed HA maize by 0·20–0·33 DC units (P<0·01). In SI3–4, barley starch were completely digested, whereas the cereal matrix of maize hampered digestion and generated 16 % resistant starch in the small intestine (P<0·001). Extrusion increased the DC of maize and HA maize starch throughout the small intestine but not that of barley (P<0·05). Up to 25 % of starch residuals in the proximal small intestine of pigs was present as glucose and soluble α(1–4) maltodextrins. The high abundance of glucose, maltose and maltotriose in the proximal small intestine indicates activity of brush-border enzymes in the intestinal lumen, which is exceeded by α-amylase activity. Furthermore, we found that in vivo starch digestion exceeded our in vitro predictions for rapidly digested starch, which indicates that the role of the stomach on starch digestion is currently underestimated. Consequently, in vivo glucose release of slowly digestible starch is less gradual than expected, which challenges the prediction quality of the in vitro assay.

Scanning electron micrographs that depict the surface and internal structure of several starch-encapsulated granular formulations of EPTC (S-ethyl dipropylthiocarbamate) and butylate (S-ethyl diisobutylthiocarbamate) relate well with herbicidal release rates previously reported. Fast-release formulations appear to have a porous surface with little distinctive internal structure. Diffusion would be expected to be more rapid as fewer diffusion barriers are present. Slow-release formulations have a smooth, hard surface with irregular surface pores and a honeycombed internal structure. The slower release characteristics are associated with stronger oxidants used for crosslinking xanthate in the entrapment of herbicides. The scanning electron microscope would be an excellent quality control technique in the preparation of starch-encapsulated herbicides.

In the present investigation, AA6351 aluminum alloy matrix composites reinforced with various percentages of AlN particles were fabricated by stir casting technique. The percentage of AlN was varied from 0 to 20% in a step of 4%. The prepared AA6351-AlN composites were characterized using scanning electron microscope (SEM) and x-ray diffraction (XRD). The mechanical properties such as micro-hardness, compression strength, flexural strength, and tensile strength of the proposed composite have been studied. X-ray diffraction patterns confirm the presence of AlN particles in the composites. SEM analysis reveals the homogeneous distribution of AlN particles in the AA6351 matrix. The mechanical properties of the composite were found to be noticeably higher than that of the plain matrix alloy due to augmented particle content. The produced composites exhibit superior mechanical properties when compared with unreinforced matrix alloy. Fracture surface analysis of tensile specimens show the ductile–brittle nature of failure in the composites.

A total of twenty-seven species of marine-living coccolithophores were recorded from seawater samples that were collected during two spring cruises along the shelf regions of the Yellow Sea (YS) and the East China Sea (ECS). They were classified into ten families and four orders, with some additional species incertae sedis. Most of these species were heterococcolithophores, and no holococcolithophores were examined from the YS waters. Six species were recorded for the first time from the coastal waters of the China Seas and their morphological characteristics are described and photographically illustrated in this paper. They were Cyrtosphaera lecaliae, Syracosphaera histrica, Syracosphaera marginaporata, Pappomonas cf. sp. type 3, Calyptrolithophora papillifera and Corisphaera strigilis. Three types of Emiliania huxleyi, type A, type B/C and type C, were examined. Species of the genus Syracosphaera, in addition to E. huxleyi and Gephyrocapsa oceanica, frequently occurred at the surveyed sites. The coccolithophore assemblages in the offshore waters of the ECS were characterized by high species diversity—fourteen species in one sample. This finding indicated that the shelf waters adjacent to the Kuroshio path were ideal habitats for living coccolithophores. The variation in taxonomic composition of these algae could be associated with differences in their preferred habitats.

The amino acid, fatty acid and mineral composition of Aspongubus viduatus F. (melon bug) and Agonoscelis pubescens (Thunberg) (sorghum bug) were investigated. The approximate analyses of A. viduatus and A. pubescens adults showed 8.3 and 7.6% moisture, 27.0 and 28.2% crude protein, 54.2 and 57.3% fat and 3.5 and 2.5% ash on a dry-matter basis, respectively. The bug protein contained 16 amino acids, including all of the essential ones. Compared with the amino acid profile recommended by FAO/WHO, the protein was of medium quality. The most predominant fatty acids in melon bug oil were oleic, palmitic, linoleic and linolenic acids, viz. 45.5, 31.3, 4.9 and 0.48%, respectively, and in sorghum bug 41.15, 11.41, 35.28 and 1.28%, respectively. The mineral analysis indicated high P and K content. Scanning electron microscopy was used to study ground insect structure before and after oil extraction. Micrographs of full-fat ground insects were different from defatted ones.

Over the past decades, pollution, overfishing, and habitat degradation have driven the population size of Taiwan shoveljaw carp down markedly in Taiwan. Cryopreservation is a useful tool which could be used to maintain genetic resources to protect and preserve this endemic species. Four cryoprotectants [dimethyl sulphoxide (DMSO), dimethylacetamide (DMA), glycerol and methanol] and six freezing rates (0.5, 1, 2, 4, 8, 16 °C min-1) were tested in order to develop an optimal controlled slow-freezing protocol for Taiwan shoveljaw carp spermatozoa. Samples were subsequently examined under the scanning electron microscope to reveal whether cryopreservation had affected their ultrastructural morphology. The highest survival rate (50.1 ± 2.0%) was observed with a freezing rate of 8 °C min-1 in 1M DMSO, using SYBR-14 + PI staining. Fertility and hatching rate results using frozen-thawed spermatozoa (90.2 ± 2.2% and 22.3 ± 2.5%, respectively) were not significantly different from results with fresh spermatozoa. After cryopreservation, 21.0 ± 1.6% of frozen-thawed spermatozoa had mid-piece swelling and rupture of the head. Cryopreservation might, therefore, slightly affect Taiwan shoveljaw carp spermatozoa in terms of morphological change. However, these alterations could be compensated by using large enough numbers of normally functioning frozen-thawed spermatozoa to achieve a standard equal to fresh spermatozoa. This is the first report of successful cryopreservation of Taiwan shoveljaw carp spermatozoa using a controlled slow-cooling method.

It appears that squid statoliths cannot yet be regarded as accurate an ageing tool as fish otoliths. Statoliths from the same pair, prepared differently for viewing and counting increments, were compared. Increment counts do not imply age in days, because this was not validated. One statolith from each pair was examined by light microscopy (LM) after preparation following a new method. The other was viewed by Scanning Electron microscopy (SEM) with a modified etching solution. Shape of each statolith was similar when compared by multiple regression analysis (11 variables, n=53). There was a weak but significant difference between sexes (statoliths of females were slightly larger). All other differences were insignificant. Microscopic observation and increment counts of increments were successfully carried out for 37 pairs of statoliths. Significant differences between two independent counts were found for the LM method, but no significant differences were found between two independent SEM counts. Counts were significantly different when interpreted by both LM and SEM, probably because of poor resolution in the LM readings and over-resolution (growth layers prominent and numerous) in those read by SEM. Recommendations are made on how ageing studies, based on statoliths, should be structured and the results evaluated.