Research in Mammalian Mastication

Ongoing research efforts in mammalian mastication have definedseveral broad areas of mutual interest to workers in the discipline.They are (1) interrelationships between masticatory movements,(2) actions of the masticatory muscles, (3) comparisons betweenmasticatory structures and functions, (4) developmental aspects,(5) comparisons between limbs and jaws, and (6) neurophysiologicconsiderations. The roles (potential and actual) of masticatorycentral pattern generators, cerebral "mastication areas," differentneural mechanisms between mammalian taxa, neurophysiologic/morphologicinteractions, and biochemical factors within the total milieuof mammalian mastication are discussed.     

Microsporidian Spore Discharge and the Transfer of Polaroplast Organelle Membrane into Plasma Membrane

Electron microscopic examinations of Glugea hertwigi and Spraguea lophii spores indicated the presence of a single plasma membrane; however, this membrane remained in the spore during the discharge of the sporoplasm from the spore. Although discharged spores retained the old plasma membrane, the extruded sporoplasms acquired a new plasma membrane. In order to determine where the new plasma membrane came from, we used two fluorescent probes with membrane affinities. The markers were tested on unfired and discharged spores. The probe, N-phenyl-1-naphthylamine (NPN), labeled the polaroplast membrane in addition to the apolar groups in the posterior vacuoles of unfired spores. After spore discharge, NPN label disappeared from the spore ghosts except for a slight fluorescence on residual plasma membranes. Much of the NPN-labeled membrane reappeared after spore discharge on the outer envelope of discharged sporoplasms. The probe chlorotetracycline (CTC) labeled calcium-associated membranes of spore polaroplasts. During spore discharge, the CTC fluorescence shifted from the polaroplast organelle of unfired spores to the outer envelope of discharged sporoplasms. These results indicate that the polaroplast organelle may provide the new plasma membrane for discharged microsporidian sporoplasms.     

Registered Pesticides and Citrus Terpenes as Blackbird Repellents for Rice

Abstract: Nonlethal management alternatives are needed to minimize bird depredation of agricultural crops. We conducted 8 caged feeding tests and 2 field studies to evaluate 2 registered fungicides (GWN-4770, Gowan Company, Yuma, AZ; Quadris®, Syngenta Crop Protection, Greensboro, NC), a neem oil insecticide (Aza-Direct®, Gowan Company), and a novel terpene formulation (Gander Gone, Natural Earth Products, Winter Springs, FL) as avian repellents. For all candidate repellents, red-winged blackbirds (Agelaius phoeniceus) discriminated between untreated and treated rice during preference-testing in captivity. We observed a positive concentration-response relationship among birds offered rice treated with 2,500 ppm, 5,000 ppm, 7,500 ppm, 11,000 ppm, or 22,000 ppm GWN-4770. Relative to pretreatment, blackbirds consumed 34% and 77% less rice treated with 11,000 ppm and 22,000 ppm GWN-4770, respectively, during the concentration-response test. Maximum repellency among other tested compounds was <40% during the concentration-response test. Blackbirds consumed 28% of rice seeds treated with 20,000 ppm GWN-4770 and 68% of untreated seeds broadcast within rice fields in southwestern Louisiana, USA. We observed 50% fewer unprotected seedlings than those treated with 10,000 ppm GWN-4770 within a drill-seeded rice field in southeastern Missouri, USA. The manufacturer subsequently applied for a United States patent for the active ingredient of GWN-4770 as an avian repellent. Although additional registration criteria and formulation optimization must be satisfied to enable the commercial availability of GWN-4770 as an avian repellent, additional efficacy studies of GWN-4770 and other promising repellents under extended field conditions are warranted for protection of newly planted and ripening rice.     

Recovery of the Chesapeake Bay Bald Eagle Nesting Population

Abstract We conducted annual aerial surveys throughout the tidal reach of the Chesapeake Bay, USA, between 1977 and 2001 to estimate population size and reproductive performance for bald eagles (Haliaeetus leucocephalus). The population increased exponentially from 73 to 601 pairs with an average doubling time of 8.2 years. Annual population increase was highly variable and exhibited no indication of any systematic decline. A total of 7,590 chicks were produced from 5,685 breeding attempts during this period. The population has exhibited tremendous forward momentum such that >50% of young produced over the 25-year period were produced in the last 6 years. Rapid population growth may reflect the combined benefits of eliminating persistent biocides and active territory management. Reproductive rate along with associated success rate and average brood size increased throughout the study period. Average reproductive rate (chicks/breeding attempt) increased from 0.82 during the first 5 years of the survey to 1.50 during the last 5 years. Average success rate increased from 54.4% to >80.0% during the same time periods. The overall population will likely reach saturation within the next decade. The availability of undeveloped waterfront property has become the dominant limiting factor for bald eagles in the Chesapeake Bay. Maintaining the eagle population in the face of a rapidly expanding human population will continue to be the greatest challenge faced by wildlife biologists.     

Responsiveness of Thymus Cells to Syngeneic and Allogeneic Lymphoid Cells

THE thymus is necessary for the normal development of cell-mediated immunity in mice as shown by the immunological defects after neonatal thymectomy¹. Thymus cells themselves can be stimulated by allogeneic lymphoid cells in mixed leucocyte reaction (MLR)² and become killer cells or cytotoxic lymphocytes after stimulation with allogeneic spleen cells in vitro (H. Wagner and M. Feldmann, unpublished work) and in vivo^3,4. This suggests that the thymus as well as peripheral lymphoid tissues contain T cells which can be stimulated by foreign histocompatibility antigen to divide and differentiate into the cytotoxic lymphocytes which mediate cellular immunity. There have been suggestions that thymus cells might be stimulated to divide by “self” antigen, as well as foreign cells: incorporation of ³H-thymidine above background levels has been found in cultures with syngeneic spleen and thymus cells of adult rats⁵, although the experiments do not determine whether thymus or spleen cells have been stimulated. In contrast to these experiments, Howe et al. reported that only thymus cells of neonatal CBA mice reacted to allogeneic and syngeneic spleen cells of adult animals in “one way” MLR cultures^6,7. Whether the reaction of neonatal thymus cells to syngeneic adult spleen cells is recognition of “self” antigens is uncertain, since spleens of adult mice could carry antigens which do not occur in neonatal animals and are therefore “unknown” for neonatal thymus cells. We demonstrate here that neonatal thymus cells do not react to 4-day-old CBA spleen cells, but adult thymus cells do react against both allogeneic and syngeneic adult spleen cells.     

Restoration of the Immune Response to Sheep Erythrocytes by a Serum Factor

THE immune response of CBA mice to sheep erythrocytes (SRBC) is known to be thymus-dependent because strain members thymectomized during the first few hours of life exhibit a marked inability to respond to this antigen^1,2. Experiments with isoantisera suggested that a cell to cell interaction is involved in this response. Thymus cells per se do not develop into haemolytic plaque-forming cells, but in some, so far obscure, way they cause cells of bone marrow origin to become producers of haemolytic plaques^2,3. A study of spleen cells from neonatally thymectomized (NNT) mice in a tissue culture system indicated that the decreased responsiveness to SRBC is also expressed in vitro. In that case 15×10⁶ NNT spleen cells produced only 500 haemolytic plaques when assayed on day 4 of culture. But when 15×10⁶ thymus cells were added to identical cultures of NNT spleen cells at inception, the number of haemolytic plaque forming cells increased to 2,300 (ref. 4). When an equivalent number of thymus cells alone were incubated with SRBC there was no response.