Burrowing dynamics and energy cost of transport in the soft-bodied marine invertebrates Polyphysia crassa and Priapulus caudatus

The dynamics and mechanical forces generated during burrowing in Polyphysia crassa (Annelida: Polychaeta) and Priapulus caudatus (Priapulida) were investigated. Both animals live in soft marine muds and burrow by utilizing a direct peristaltic wave alternating with a high internal pressure event which thrusts the anterior part of the body into the substratum. Forces generated during the various phases of a typical burrowing cycle were measured in animals moving beneath the natural substratum at 5±3 °C using electronic transducers and recorder. During 'head' advance Polyphysia generated 0.027 N, and during 'tail' advance 0.020 N, with peak internal pressures averaging 0.95 kPa (= 0.095 N/cm²). Force by Priapulus during head advance and tail advance was 0.081 N and 0.121 N, respectively, with peak internal pressures averaging 2.47 kPa (= 0.247 N/cm²). Polyphysia moves more slowly (0.24 cm/min) than does Priapulus (0.76 cm/min) and expends more energy on mass moved per unit distance. These force measurements during a burrowing cycle were used in place of respirometry as a basis for computation of net cost of transport (NCT) for each animal. NCT for Polyphysia was 635 J kg^-1 m^-1 and for Priapulus was 314Jkg^-1m^-l. Cost of transport for all burrowing animals thus far investigated is high compared to swimming, running and flying. For soft-bodied invertebrates that live an entirely buried existence this high cost must be interpreted in the broader context of the adaptive value of infaunal life, especially protection against predation, and not as simply a means of moving about.     

Major outer membrane protein in Salmonella typhimurium induced by maltose.

A maltose-induced major outer membrane protein (the 44K protein) is demonstrated in Salmonella typhimurium. This protein resembles the lambda receptor of Escherichia coli in its location, induction properties, apparent molecular weight, and association with the peptidoglycan layer of the cell wall. The 44K protein is missing in certain Salmonella Mal- mutants, which are also missing a protein analogous to the maltose-binding protein of E. coli. Thus, these mutants may be defective in the control of maltose genese in Salmonella. The proteins appear to be closely related, as indicated by cross-reaction of the Salmonella protein with the antiserum raised against the lambda receptor; however, they are not identical, since the peptide patterns obtained after limited proteolysis are completely different. Bacteriophage lambda does not use the 44K protein as a receptor.     

Near-infrared spectroscopy for bioprocess monitoring and control.

This article describes the calibration of a spectroscopic scanning instrument for the measurement of selected contaminants in a complex biological process stream. Its use is for the monitoring of a process in which contaminants are to be removed selectively by flocculation from yeast cell homogenate. The main contaminants are cell debris, protein, and RNA. A low-cost instrument has been developed for sensitivity in the region of the NIR spectrum (from 1900 to 2500 nm) where preliminary work found NIR signatures from cell debris, protein, and RNA. Calibration models have been derived using a multivariate method for concentrations of these contaminants, such as would be found after the flocculation process. Two strategies were compared for calibrating the NIR instrument. In one case, samples were prepared by adding materials representative of the contaminants to clarified yeast homogenate so the contaminant levels were well known but outside the range of interest. In the other case, where samples were like those from the process stream after flocculation and floc removal, there was uncertainty of analysis of contaminant level, but the calibration was in the range of interest. Calibration using process stream samples gave results close to those derived from traditional assays. When the calibration models were used to predict the contaminant concentrations in previously unseen samples, the correlation coefficients between measurements and predictions were above 90% in all cases but one. The prediction errors were similar to the errors in the traditional assays.     

The production of different morphs by alate viviparae of the aphid Myzus persicae temporarily exposed to long scotophases

The development of alatae of the green peach aphid, Myzus persicae, as gynoparae rather than as virginoparae was investigated with regard to the number of exposures to a long-night (LN) regime of 15 h darkness per diem which the aphids experienced before and/or after their birth. The minimum number of exposures to LN that resulted in all of the alatae developing into gynoparae was two prenatal plus one postnatal or one prenatal plus two postnatal, provided the scotophases in these treatments were at least 12 h long. A cumulative effect of several successive exposures to LN was also evident when the presumptive alatae were exposed to LN either from birth or not until several days after birth. Fewer exposures to LN were needed in the former case.

---

Zusammenfassung Die Entwicklung von Alatae der grünen Pfirsichblattlaus, Myzus persicae, hauptsächlich zu Gynoparae, eher als zu Virginoparae, wurde im Hinblick auf den Einfluss der Anzahl an Langnächten (LN: 15 Studen Dunkelheit pro Tag), denen die Aphiden vor und/oder nach der Geburt ausgesetzt waren, untersucht. Zur ausschliesslichen Entwicklung aller Alatae zu Gynoparae waren mindestens 2 prenatale und eine postnatale LN-Exposition oder eine prenatale und 2 postnatale LN-Expositionen notwendig, vorausgesetzt die Dunkelphasen betrugen mindestens 12 Stunden. Ausserdem zeigte sich ein kumulativer Effect durch mehrere, aufeinanderfolgende LN-Expositionen, wenn die Alatae diesen von Geburt an, oder einige Tage nach der Geburt, ausgesetzt waren. Im ersten Fall waren weniger LN-Expositionen notwendig.