Systematic revision of the Late Miocene sabre‐toothed felid Paramachaerodus in Spain

Abstract: A systematic revision of the sabre‐toothed cat genus Paramachaerodus  Pilgrim, 1913 is presented. Two species are recognized within Paramachaerodus, Pa. orientalis, and Pa. maximiliani, and the genus Promegantereon  Kretzoi, 1938 is retrieved to include Promegantereon ogygia. Material from the Turolian Spanish localities of Crevillente‐2 (MN 11, Alicante) and Las Casiones (MN 13, Teruel), which was previously assigned to Paramachaerodus, is now included in the tribe Metailurini. The exceptional discoveries at the Spanish Vallesian (MN 10, Madrid) fossil site of Batallones‐1 have made it possible to characterize the dentition and cranial anatomy of a previously very poorly known machairodontine cat, formerly included in Paramachaerodus as Pa. ogygia, which now can be distinguished from Pa. orientalis and Pa. maximiliani by the following features: canines without crenulations, P3 with a marked disto‐lingual expansion, P4 without ectostyle and with a well‐developed protocone, M1 bucco‐lingually elongated and double‐rooted, m1 with a larger talonid, and primitive mandible morphology. Thus, the population from Batallones‐1 constitutes a clearly different form from the genus Paramachaerodus, and we propose its inclusion in the genus Promegantereon  Kretzoi, 1938 , together with an upper canine from Crevillente‐2 (MN 11), very similar to those from Batallones‐1. In contrast, Pa. orientalis shows the following apomorphies: crenulated canines, P3 reduced in size and without disto‐lingual expansion, P4 with a clear ectostyle as well as a reduced, backwardly displaced protocone and with a rounded and single‐rooted M1. The species Pa. maximiliani is characterized by its slightly larger size, crenulated canines, very elongated P3 with a moderate disto‐lingual expansion and P4 and M1 similar to those of Pa. orientalis. Paramachaerodus orientalis is recorded at Puente Minero (MN 11, Teruel), Concud (MN 12, Teruel), Crevillente‐15, and Crevillente‐16 (both MN 12, Alicante), and Paramachaerodus maximiliani in Venta del Moro (MN 13, Valencia). The available data suggest that Pr. ogygia was present in the Iberian Late Vallesian and Early Turolian faunas (MN 10 and MN 11) but disappeared after that age. Paramachaerodus was present in the faunas throughout the Turolian, with the species Pa. orientalis and Pa. maximiliani, this latter being probably part of the same immigration event that occurred in the Late Turolian and involved other mammal taxa such as camelids and ursids.     

Fire research for conservation management in tropical savannas: Introducing the Kapalga fire experiment

Abstract Fire is a dominant feature of tropical savannas throughout the world, and provides a unique opportunity for habitat management at the landscape scale. We provide the background and methodology for a landscape-scale savanna fire experiment at Kapalga, located in Kakadu National Park in the seasonal tropics of northern Australia. The experiment addresses the limitations of previous savanna fire experiments, including inappropriately small sizes of experimental units, lack of replication, consideration of a narrow range of ecological responses and an absence of detailed measurement of fire behaviour. In contrast to those elsewhere in the world, Australia's savannas are sparsely populated and largely uncleared, with fires lit primarily in a conservation, rather than pastoral, context. Fire management has played an integral role in the traditional lifestyles of Aboriginal people, who have occupied the land for perhaps 50 000 years or more. Currently the dominant fire management paradigm is one of extensive prescribed burning early in the dry season (May-June), in order to limit the extent and severity of fires occurring later in the year. The ecological effects of different fire regimes are hotly debated, but we identify geo-chemical cycling, tree demography, faunal diversity and composition, phenology, and the relative importance of fire intensity, timing and frequency, as critical issues. Experimental units (‘compartments’) at Kapalga are 15–20km² catchments, centred on seasonal creeks that drain into major rivers. Each compartment has been burnt according to one of four treatments, each replicated at least three times: ‘Early’- fires lit early in the dry season, which is the predominant management regime in the region; ‘Late’- fires lit late in the dry season, as occurs extensively in the region as unmanaged ‘wildfires’; ‘Progressive’- fires lit progressively throughout the dry season, such that different parts of the landscape are burnt as they progressively dry out (believed to approximate traditional Aboriginal burning practices); and ‘Unburnt’- no fires lit, and wildfires excluded. All burning treatments have been applied annually for 5 years, from 1990 to 1994. Six core projects have been conducted within the experimental framework, focusing on nutrients and atmospheric chemistry, temporary streams, vegetation, insects, small mammals, and vertebrate predators. Detailed measurements of fire intensity have been taken to help interpret ecological responses. The Kapalga fire experiment is multidisciplinary, treatments have been applied at a landscape scale with replication, and ecological responses can be related directly to measurements of fire intensity. We are confident that this experiment will yield important insights into the fire ecology of tropical savannas, and will make a valuable contribution to their conservation management.     

Competition for space by predators in streams: field experiments on a net-spinning caddisfly

SUMMARY. 1. Field experiments in a fishless stream were carried out on an abundant caddisfly with a predatory, net-spinning larva, Plectrocnemia conspersa (Curtis), to assess whether net site availability affects their microdistribution.
2. Net sites were supplemented by adding nought, one or four artificial structures to replicated patches on the stream bed. In each of three experiments at different seasons (summer, autumn and late winter), caddis densities increased significantly in patches with extra net sites.
3. The response of caddis to supplemented net sites could be affected by the subsidiary effects of food and offish. These potential interactions were assessed in each experiment by varying net site density in two additional treatment stretches in which (1) prey abundance was increased by releasing Daphnia , and (2) brown trout ( Salmo trutta L.) were enclosed. The responses of caddis in these two treatments were compared to that in the reference stretch, where only net site density varied.
4. Increased food abundance enhanced the response of caddis to net site supplementation in winter, when natural prey was least abundant, but not in summer or autumn. We suggest that extra food affects the mechanism determining net building only when prey availability is below some threshold.
5. The presence of fish precluded any effect of extra net sites in summer, but had no effect in autumn (the winter fish treatment was lost). We suggest fish predation reduced the densities of caddis in summer, so that net sites no longer limited local densities. In autumn, fallen leaves provided refugia from fish, which consequently were less effective predators of P. conspersa.     

The action of cyclic-AMP on GA3 controlled responses I. Induction of barley endosperm protease and acid phosphatase activity by cyclic-3',5'-adenosine monophosphate

The effect of cyclic-AMP on the induction of protease and acidphosphatase activity in embryoless barley half-seeds was examined.Promotion of protease synthesis was observed with 5 mu cyclic-AMPand ADP. The protease induced by these compounds was similarto protease obtained with GA₃, in that the enzyme was dependenton ß-mercaptoethanol for enhanced activity and increasedprotease activity observed in the media after a 48 hr incubationwith cyclic-AMP and ADP was due to an increase in both the synthesisand release of this enzyme. Of a variety of adenine compoundsand nucleoside diphosphates tested only cyclic-AMP and ADP inducedprotease activity. When these same compounds were tested fortheir ability to induce acid phosphatase activity only cyclic-AMPwas consistently found to be active. The total amount of enzymeproduced as well as the rate of enzyme release was similar forhalf-seeds incubated with 5 mu cyclic-AMP or a saturating GA3concentration. Inhibition of the hormone or nucleotide inducedpromotion of acid phosphatase was observed when abscisic acidwas added to the incubation medium with one of these compounds.Some of the implications of these results are discussed. (Received May 11, 1971; )     

Phylogeny of the Aphnaeinae: myrmecophilous African butterflies with carnivorous and herbivorous life histories

The Aphnaeinae (Lepidoptera: Lycaenidae) are a largely African subfamily of 278 described species that exhibit extraordinary life‐history variation. The larvae of these butterflies typically form mutualistic associations with ants, and feed on a wide variety of plants, including 23 families in 19 orders. However, at least one species in each of 9 of the 17 genera is aphytophagous, parasitically feeding on the eggs, brood or regurgitations of ants. This diversity in diet and type of symbiotic association makes the phylogenetic relations of the Aphnaeinae of particular interest. A phylogenetic hypothesis for the Aphnaeinae was inferred from 4.4 kb covering the mitochondrial marker COI and five nuclear markers (wg, H3, CAD, GAPDH and EF1α) for each of 79 ingroup taxa representing 15 of the 17 currently recognized genera, as well as three outgroup taxa. Maximum Parsimony, Maximum Likelihood and Bayesian Inference analyses all support Heath's systematic revision of the clade based on morphological characters. Ancestral range inference suggests an African origin for the subfamily with a single dispersal into Asia. The common ancestor of the aphnaeines likely associated with myrmicine ants in the genus Crematogaster and plants of the order Fabales.     

DIAGNOSTIC SELF‐TESTING: AUTONOMOUS CHOICES AND RELATIONAL RESPONSIBILITIES

Diagnostic self‐testing devices are being developed for many illnesses, chronic diseases and infections. These will be used in hospitals, at point‐of‐care facilities and at home. Designed to allow earlier detection of diseases, self‐testing diagnostic devices may improve disease prevention, slow the progression of disease and facilitate better treatment outcomes. These devices have the potential to benefit both the individual and society by enabling individuals to take a more proactive role in the maintenance of their health and by helping society improve health and reduce health costs. However, the full implications of future home‐based diagnostic technology for individuals and society remain unclear due to their novelty. We argue that the development of diagnostic tools, especially for home use, will heighten a number of ethical challenges. This paper will explore some of the ethical implications of home‐based self‐testing diagnostic devices for the autonomous and relational dimensions of the person. This will be facilitated by examining the impact of diagnostic devices for individual autonomy, for the delivery of accurate diagnosis and for the personal significance of the information for the user. The latter will be examined using Charles Taylor's view of personhood and his emphasis on human agency and interpretation. While the ethical issues are not necessarily new, the development of home‐based self‐testing diagnostic devices will make issues regarding autonomy, accuracy of information and personal significance more and more demanding. This will be the case particularly when an individual's autonomous choices come into conflict with the person's relational responsibilities.     

The phenology of leaf life spans in woodland populations of the ferns Dryopteris filix-mas (L.) Schott and D. dilatata (Hoffm.) A. Gray in Derbyshire

WILLMOT, A., 1989. The phenology of leaf life spans in woodland populations of the ferns Dryopteris filix-mas (L.) Schott and D. dilatata (Hoffm.) A. Gray in Derbyshire. The results of a survey on the number of upright fronds per plant in a population of Dryopteris filix-mas and in a population of D. dilatata over a 14 month period are presented. These coupled with similar information on the number of developing fronds per plant demonstrate that large plants in the population of each species were summergreen, while small ones were wintergreen. This size-specific difference in leaf phenology does not seem to have been recorded before in Dryopteris filix-mas. It is suggested that this difference, in both species, may have been due to either the different environments in which the plants grew or to a risk-sensitive strategy in the small plants. It is considered that such a strategy might be concerned with the obtaining or retention of resources at a critical period in the life history of the species.