Long-Term Storage of Infective Microsporidian Spores in Liquid Nitrogen

Thirty-one species of microsporidia, isolated from insects and stored in liquid nitrogen for up to 25 yr, were infectious when removed from liquid nitrogen. The natural hosts of all of these microsporidia were terrestrial insects, representing six different insect orders: Coleoptera, Diptera, Hemiptera, Hymenoptera, Lepidoptera, and Orthoptera. All microsporidia from terrestrial insects that were tested survived storage in liquid nitrogen, while Nosema algerae , a microsporidium from aquatic mosquito hosts did not survive freezing in liquid nitrogen. A Nosema species from the alfalfa weevil, Hypera postica , lost some infectivity in a water storage medium after 25 yr in liquid nitrogen. Liquid nitrogen storage of microsporidian spores in 50% and 100% glycerol media reduced loss of infectivity and is recommended for extended storage of microsporidia from terrestrial insect hosts.     

Osmotic and Metabolic-Induced Changes in Light Scattering of Leishmania donovani as Measured by Flow Cytometry

Leishmania donovani promastigotes were collected from cultures in log and stationary phases of growth and resuspended in Hank's Balanced Salt Solution containing 1 mM sodium acetate. Changes in the forward and side scattering of the cells were measured by flow cytometry in response to acute changes in osmolality and to the addition of several different substrates. Forward and side scattering of cells from log phase cultures decreased when the osmolality was decreased by the addition of H₂O and increased when the osmolality was increased by the addition of NaCl. Cells from stationary phase cultures had about the same forward scatter as cells from log phase cultures, but almost a four-fold lower side scatter, and their side scatter values did not change significantly in response to a reduction in osmolality. Microscopic observation showed that both log and stationary cells got longer and thinner, on average, in response to hyperosmolality. The light scattering properties of log (but not of stationary) cells changed in a reproducible manner when substrates were added to the buffer. The ratio of forward to side scatter increased in the following order: controls in balanced salt solution >aspartate >glutamate, glucose or 2-deoxyglucose >alanine >proline. Thus the light scattering properties of L. donovani promastigotes change with culture age, in response to changes in osmolality, and, in log phase cells, in response to the presence of several substrates.     

Identification of CO2 Chemoreceptors in Helix pomatia

SYNOPSIS. Gas exchange in pulmonate snails of the family Helicidaeoccurs through a highly vascularized diffusion lung known asthe mantle. The extent of ventilation of the mantle dependsupon the duration and size of opening of an occlusible poreknown as the pneumostome. In Helix aspersa and Helix pomatia,pneumostomal size and frequency of opening are exquisitely sensitiveto CO₂. Respiratory CO₂ chemosensitivity resides in a discreteregion of the subesophageal ganglia. The discharge pattern ofmany neurons in the chemoreceptor area changes during stimulationwith CO₂. However, the electrophysiological response to CO,stimulation alone does not discriminate between CO₂ chemoreceptorcells and CO₂-insensitive neurons active in the pneumostomalresponse to CO₂. We identified a subset of CO₂-sensitive neuronsfrom the larger population of neurons active during CO₂ stimulation.The action potential discharge frequency of CO₂ chemosensoryneurons increased in response to CO₂ stimulation. An increaseddischarge frequency of CO₂-sensitive neurons was associatedwith increased pneumostomal opening, and both the size and thefrequency of pneumostomal opening increased during CO₂ stimulation.Injecting depolarizing current into individual chemosensoryneurons elicited opening of the pneumostome in the absence ofCO₂. Action potential generation in response to CO₂ was independentof synaptic transmission. Removal of individual CO₂-sensitivecells or inhibition of action potential generation in CO₂-sensitivecells reduced or eliminated pneumostomal responses to CO₂. CO₂sensitivity in chemoreceptor cells required extracellular calcium,but not sodium. Substituting barium for calcium supported chemoreceptoractivity. In summary, we have identified respiratory related,chemosensory neurons that are CO₂ sensitive in the absence ofsynaptic input.     

Phylogenetic relationships among marsupial frog genera (Anura: Hylidae: Hemiphractinae) based on evidence from morphology and natural history

We reassess the phylogenetic relationships of genera of hemiphractine hylid frogs (Marsupial Treefrogs) and discuss the evolution of several distinctive characters within this group using parsimony analysis. Fifty-one morphological and life-history characters were sampled from two species of Cryptobatrachus , three species of Flectonotus , 17 species of Gastrotheca , all five species of Hemiphractus , and one species of Stefania as the ingroup and three hyline, one phyllomedusine, and one pelodryadine species as outgroups. Our results support the mon-ophyly of Flectonotus, Cryptobatrachus , and Hemiphractus. Gastrotheca is paraphyletic with respect to Hemiphractus , dorsal pouches were lost in the ancestor of Hemiphractus. Direct development is a synapomorphy for Hemiphractinae and tadpoles were regained independently several times. These results stand in stark contrast to the prevailing paradigm regarding marsupial frog relationships.     

Indirect effects of metal contamination on energetics of yellow perch (Perca flavescens) resulting from food web simplification

1. Benthic invertebrate community composition and yellow perch (Perca flavescens) diet, growth and activity levels from lakes along a metal‐contamination gradient were used to assess the importance of a naturally diverse prey base for maintaining energy transfer to growing fish, and how this transfer is disrupted by metal contamination. 2. Zoobenthic communities had lower diversity in metal‐contaminated lakes, with a notable absence of large bodied invertebrate taxa. 3. The average mass of non‐zooplankton prey items was significantly greater for 2+ and 3+ perch from the reference lake, and increased significantly with age in all except the most contaminated lakes where prey choice was limited. 4. Benthivorous perch from all contaminated lakes exhibited slowed growth. Perch from one of the contaminated lakes exhibited faster growth during piscivory, indicating slowed growth only while benthivorous. 5. Estimates of fish activity, using the activity of the glycolytic enzyme Lactate dehydrogenase in perch white muscle tissue as a proxy, suggested that shifts in diet to larger prey (in reference and intermediately contaminated lakes) lowered activity costs, which may explain how diet shifts maintain growth efficiency as perch grow larger.     

Ultrastructural Observations on the Infection of Rat Liver by Plasmodium berghei Sporozoites In Vivo1

The invasion of liver parenchymal cells by sporozoites of Plasmodium berghei Vincke & Lips, 1948, was studied in vivo using transmission electron microscopy. Livers of Brown Norway rats were examined 30 and 60 min after intraportal injection of 15 million sporozoites each. Sporozoites found after incorporation into vacuoles in hepatocytes were often located near a bile canaliculus at the lateral cell surface, surrounded by hepatocyte lysosomal structures; however, degradation of sporozoites caused by lysosomal digestion inside hepatocytes was never observed. Due to the crescent shape of sporozoites, serial sections were necessary to demonstrate the actual process of invasion of the hepatocyte. The hepatocyte's plasmalemma appeared to invaginate due to the sporozoite's action, thereby creating a parasitophorous vacuole. It was suggested that the sporozoite actively penetrated the hepatocyte; however, no visible depletion of rhoptries and micronemes was observed.     

Endocrinology of the Amphibian Pineal

McCord and Allen (1917) found that extracts of mammalian pinealglands contain a potent contracting agent of larval amphibianmelanophores. Lerner and his co-workers determined the chemicalstructure of this principle and named it melatonin. This agentcontracts dermal melanophores at a concentration as low as 10^–10g/ml. Both intact and eyeless larval amphibians blanch whenplaced in the dark, and the melanophore contraction which causesthis lightening response is abolished by pinealectomy. The amphibianpineal contains photoreceptive elements similar to those foundin the vertebrate lateral eyes, and these elements are inhibitedby light but are stimulated in its absence. There is evidencefor the presence of both HIOMT and melatonin the amphibian pineal.It has been proposed that the body-blanching response resultsfrom a direct stimulation of the pineal under conditions ofdarkness leading to a release of melatonin into the generalcirculation which is then responsible for a direct contractingeffect on dermal melanophores. The cytophysiological effectsof melatonin mimic those that take place in the body-blanchingresponse. Since no other hormone or pharmacological agent duplicatesthis response, this is strong evidence that melatonin is a hormonethat normally regulates body blanching. Other evidence for thesupport of this hypothesis is presented. Cytological features of both normal and melatonin-induced lighteningindicate that the effects of melatonin are at the effector celllevel rather than at either the hypothalamus or the pituitary.An inhibition of MSH-release by melatonin is not involved. Melatoninplays a normal role in young larvae to regulate the lighteningresponse that takes place in darkness (the primary chromaticresponse). Neither melatonin nor the pineal play a role in thelater (secondary stage) adaptive background responses of amphibians.As McCord and Allen first noted, the pineal may contain othersubstances which may have other physiological roles in amphibiansas well as other vertebrates. These have been little studied.     

The Structure and Development of the Dorsal Bristle Complex of Oxytricha fallax and Stylonychia pustulata*

SYNOPSIS. Oxytricha fallax and Stylonychia pustulata possess 6 rows of dorsal bristle units. Each dorsal bristle unit consists of a pair of kinetosomes; the anterior kinetosome has a cilium and the posterior kinetosome a ciliary stub. The kinetosome pair, located at the bottom of a cortical pit surrounding the cilium and ciliary stub, is surrounded by an asymmetrical fibrillar mass. Future rows 1-4 are formed from 2 sets of primordia originating within mature dorsal rows 1-3. Rows 5 and 6 originate from the anterior regions of both right marginal cirral primordia. Old dorsal bristle units utilized in formation of primordia are presumably maintained in the new rows of the proter and opisthe; those outside the primordia are resorbed. The morphogenetic pattern of the Oxytrichidae is similar to those of the Urostylidae and Holostichidae, but quite different from that of the Euplotidae.     

DISTANCE METHODS: A REPLY TO FARRIS

Abstract— Farris (1985) claimed that my assertions about unbiasedness and consistency of estimates of a phylogeny obtained by least squares fitting are in error. The counterexample he constructed violates the assumptions of additivity and independence of distances which were clearly stated in my earlier paper. As such it is not a valid counterexample. It is argued, contrary to Farris's claims, that one need not avoid nonmetric distances, and that one should avoid negative branch lengths in estimates of phylogenies from distance data. Statistical tests of clockness, and, to a limited extent, of alternative phylogenies can be constructed, and these are demonstrated by example. A computer program to infer phylogenies from distance matrices has been in free distribution by me for several years; it seems as effective as the program recently announced by Farris. Information on phylogenies is present in distance data, as in other kinds of data, and statistical methods can be developed to extract it.