Preflight PEMBSIS cell cultures were prepared about a week before launch. Twelve chambers were filled with a semi-solid medium. Six were transported to KSC and kept in an unlit incubator at 22±2 °C until they were loaded into the Shuttle. The other six were used as ground controls. Approximately 36 hours before launch, 148 prefertilized newt eggs were loaded into the three cassettes of the AAEU. Four adult newts were also loaded into the cassettes; two cassettes each contained one newt apiece, while a third contained two. Fresh, aerated water at 24 °C circulated continuously through the unit. A similar unit was maintained at KSC as a ground-control. to maintain a cooled or heated internal environment. Twenty-four hours before launch, four groups of six jellyfish polyps each were given iodine in artificial sea water (ASW) to induce
strobilization of polyps into the ephyrae form. Shortly before flight, the jellyfish samples were loaded into a total of 10 Nizemi cuvettes containing ASW and placed in Type I containers. For the behavior study, a group of normal
ephyrae and a group of ephyrae without
statoliths were placed in the Biorack 22 °C incubator. The third group of ephyrae was placed in the Biorack 1-G centrifuge. Two groups of polyps were used for the development study. One group was placed in the incubator and the other was placed in the 1-G centrifuge. A similar set of equipment was maintained at the KSC ground-control facility.
Inflight The Ambient Temperature Recorder (ATR-4) is a self-contained, battery-powered instrument, approximately the size of a deck of cards. It may be placed in almost any environment (not submersible in liquid) to provide recording of up to four channels of temperature data. On flight days 6, 8, and 11, the crew carried out video observations of newt eggs to document the rate of development. The crew also made observations of the adult newts at specified times. On both the fifth and ninth days of flight, an adult newt was found dead, causing the loss of some eggs because of contamination. The remaining two adult newts survived the flight and were recovered live upon landing. One cuvette from each group of jellyfish ephyrae and polyps were videotaped on the rotating microscope/centrifuge at intervals throughout the mission to determine the G-threshold for the swimming behavior of the ephyrae. On flight day five, both the flight and ground-control groups of ephyrae with statoliths that had been hatched on Earth were fixed. On flight day 13, two of the four groups of polyps that had been strobilation-induced were fixed. The remaining ephyrae and polyps were returned to Earth for postflight analysis. To provide a comparison between flight-fixed and ground-fixed groups in the PEMBSIS experiment, the crew fixed some cultures shortly before landing. The fixative was a three-percent glutaraldehyde (balance water) solution. Each chamber was fixed with a 20-ml injection of fixative.
Postflight The flight cassettes containing the newts were retrieved approximately six hours after landing. Some of the larvae were fixed and preserved for later analysis, while some were tested to estimate how space flight affected the gain of the otolith-ocular reflex and measure the otolith volumes and areas of associated sensory epithelia. Living jellyfish were counted, coded, and photographed beginning at five hours postflight. The pulse rate, numbers of arms, rhopalia, and statoliths were counted in each of the ephyrae. Those with abnormal pulsing were videotaped after landing and again approximately 24 hours later. Some of both the flight and control jellyfish were allowed to form clones, which were then examined for arm number and other structural differences. After the PEMBSIS cell culture chambers were recovered from the Shuttle, specimens of living cells and somatic embryos were photographed, counted, and chemically fixed within nine hours of landing, before their first division cycle on Earth was complete. Chromosomes were measured and compared within and among cultures. ==Results==