On the Origin of Thymic Lymphocytes

In the leopard frog (Rana pipiens), thymic lymphocytes do notoriginate from blood-borne stem cells that migrate into thethymus anlage; rather they arise in situ from elements in thethymic rudiment itself. After thymic differentiation, the lymphocytes(or their descendants) leave the thymus and extensively seedthe peripheral lymphoid organs. Indeed, virtually all the lymphocytesin the spleen, kidney, and bone marrow are ontogenically derivedfrom thymic cells. In postmetamorphic life, the thymus representsan organ in which lymphopoiesis is genuinely self-sustaining.Throughout the juvenile life of the frog, there is no indicationof an inward afferent stream of cells entering the intact thymus.     

The Distribution of Na+, K+ and Glycinebetaine in Salicornia bigelovii

Stems of young actively growing Salicornia bigelovii were dissectedinto the three major tissue layers: vascular, spongy mesophylland palisade. Each layer was analysed for chlorophyll, ash (salt),protein and glycinebetaine content. When glycinebetaine contentwas based on protein content, the vascular and spongy mesophylllayers had nearly identical values. Correction for probableRuBP carboxylase content in the palisade layer gave a glycinebetaine/proteinratio similar to that of the other tissues. All three tissuelayers were found to contain significant amounts of salt. Key words: Salicornia bigelovii, Salt distribution     

Parthenogenesis in Mites and Ticks (Arachnida: Acari)

SYNOPSIS. Parthenogenesis is discussed according to type (arrhenotoky,thelytoky, deuteroLoky, artificial parthenogenesis, gynogenesis)and presence in various acarine taxa. Evidence for parthenogenesisis based on rearing and/or cytological studies. Arrhenotokyoccurs in Mesostigmata, Prostigmata and Astigmata and usuallydoes not occur sporadically throughout these taxa; when presentit operates in many closely related species as the major typeof reproduction in certain genera, subfamilies or families.Thelytoky is present in Mesostigmata, Metastigmata, Prostigmata,Astigmata and Cryptostigmata, but in no case is the major modeof reproduction in higher taxa, i.e. subfamilies, families.Its sporadic occurrence may or may not be accompanied by polyploidy.Deuterotoky occurs in one acarine group (Listrophoridae) andartificial parthenogenesis is possible in ticks (Metastigmata).Gynogenesis is present in several species of haplo-diploid Mesostigmata(some Dermanyssidae, Phytoseiidae), although it is usually consideredin connection with thelytoky. Current studies of the effectsof ploidy level on morphological variation indicate greatercharacter variability in diploid females than in haploid males.In some species of ticks thelytoky is expressed differentiallyeven on an intraspecific level. One geographic strain of a speciesmay have the ability to reproduce thelytokously, but if matedproduces males and females.     

The Genetic Structure and Evolutionary Fate of Parthenogenetic Amphibian Populations as Determined by Markovian Analysis

SYNOPSIS. One-locus, two-allele models are presented which describethe genetic consequences of naturally occurring andexperimentallyinduced parthenogesis in triploid and diploid amphibians. Themodels may in general be used to investigate genetic changeresulting from apomictic (ameiotic) and automictic (meiotic)parthenogenetic reproduction. These models quantify the influence of mutation, segregation,and selection upon genetic variability in parthenogeneticpopulations.They also allow an estimate of the relative importance of stochasticforces in altering this variability. They thus provide a basisfor understanding evolution in these populations. Some of the conclusions derived from this study contradict previouspredictions regarding genetic variability in parthenogeneticpopulations. First, if mutation is the sole source of geneticchange (i.e., strict apomixis), parthenogenetic populationsshould not become completely heterozygous. Second, small amountsof segregation occurring in apomictic populations have enormouseffects upon the genetic variability of these populations, i.e.,they should lose much of their heterozygosity. In addition to these conclusions, the results of this studysuggest that studies of protein variability in parthenogeneticspecies should contribute toward answering the question: Howmuch of the genetic variability observed in nature is evolutionarilyrelevant?     

The Recent Terebratulina Community in the rocky subtidal zone of the Bay of Fundy, Canada

A distinctive rocky subtidal benthic community (the Terebratulina Community) is described from the Bay of Fundy, Canada. It is shown to consist of three closely intcrspersed sub-communities: a cavity sub-community, characterised by chitons, coelenterates, brachiopods, bryozoans, chordates and annelids; a rock-face subcommunity, similar in composition but enriched in brachiopods and sponges; and an upper-surface subcommunity, dominated by algae, chitons, bivalves and echinoids.
Comparison with recently described Jurassic, Cretaceous and Recent (Mediterranean) hard-ground communities suggests a relative constancy in composition, in terms of higher taxa, since the Mesozoic. Development of these (sub-)communities occurs wherever crevice or cavity systems on hard substrates lead to microenvironments differentiated mainly on the basis of water energy and light.
The composition and trophic structure of the community and the life habits of Terebratulina septentrionalis (Couthouy) are related to aspects of the environment. Marked differences in composition between the living cavity sub-community and the death assemblage in the sediments are shown to be due to differential preservation, fragmentation, population dynamics and limited local transportation.     

Dating of graptolite zones by sedimentation rates: implications for rates of evolution

Preliminary determinations of ancient pelagic sedimentation rates agree with modern rates at about 4 meters per million years. By combining data on the thickness of graptolite zones from the North American Cordillera with data from other parts of the world, we have refined the Early Silurian time scale and obtained much better resolution than is possible for radiometric dates. The new Early Silurian time scale allows estimation of true rates of change in graptolite diversity. The Llandoverian diversity explosion is twice as rapid as was previously thought. The brevity of diversity lows and rapidity of speciation support modern theories of quantum evolution.     

Biology of a new species of socially parasitic thrips (Thysanoptera: Phlaeothripidae) inside Dunatothrips nests,with evolutionary implications for inquilinism in thrips

Akainothrips francisi sp. nov. is shown to be an inquiline (i.e. it invades, and breeds within, domiciles of another species). Currently, its only known host is Dunatothrips aneurae, a subsocial thrips that creates silken domiciles by securing together phyllodes of mulga (Acacia aneura) in the arid zone of Australia. We found Ak. francisi prolifically breeding inside live D. aneurae host domiciles, both immature and mature. Akainothrips francisi did not kill its host and we saw no evidence of antagonistic host‐inquiline interactions. This is thus the second demonstrably inquiline species of Acacia thrips, although other possible inquilines have been suggested including two Akainothrips. We found that Ak. francisi occurred with positive density dependence, and was associated with moderately reduced host reproduction. This latter association was especially evident in larger host domiciles, suggesting that Ak. francisi either inhibits further host reproduction after invasion or exploits poor quality hosts more successfully. Sex ratios were slightly female biased. Akainothrips francisi males were exceptionally variable in size, colour, and foreleg size compared to females, with morphs co‐occurring within domiciles, suggesting sexual selection and the possibility of different male reproductive strategies. The discovery of Ak. francisi highlights particular morphological affinities among known or suspected inquiline Acacia thrips within Akainothrips and other genera, allowing us to hypothesize a common origin of this lifestyle from within Akainothrips. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ?? , ??–??.