White-Tailed Deer Foraging Habitat in Intensively Established Loblolly Pine Plantations

ABSTRACT Stand establishment techniques involving multiple herbicide applications are commonly used on industrial pine (Pinus spp.) plantations, raising concern over potential effects on white-tailed deer (Odocoileus virginianus) forage production. We tested effects of stand establishment intensity on deer forage in 1–5-year-old loblolly pine (Pinus taeda) plantations (n = 4) in the East Gulf Coastal Plain of Mississippi using forage biomass and 4 measures of nutritional carrying capacity that reflected crude protein or digestible energy requirements for body maintenance and lactation. We also assessed whether forage biomass combined with a deer use rating effectively indexed nutritional carrying capacity. Treatments were combinations of mechanical site preparation, chemical site preparation (CSP), and herbaceous weed control (HWC). Total forage biomass and forage biomass of grasses and forbs were reduced by broadcast HWC. Forage biomass of vines was reduced both by CSP and by multiple broadcast HWC applications. Maintenance-level carrying capacity estimates were reduced by broadcast HWC; lactation-level estimates were higher in moderate-intensity treatments. We believe the inherently low fertility of this region makes high-quality forage production a more important management priority than increasing forage quantity. Chemical or chemical and mechanical site preparation combined with banded HWC provided the best option for providing both forage quality and quantity in open-canopied, intensively managed pine plantations. Biomass-based indices may be suitable for indexing protein-based maintenance-level carrying capacity in this region, but our results indicated they were not useful for indexing other carrying capacity estimates.     

Trophic level asynchrony in rates of phenological change for marine,freshwater and terrestrial environments

Recent changes in the seasonal timing (phenology) of familiar biological events have been one of the most conspicuous signs of climate change. However, the lack of a standardized approach to analysing change has hampered assessment of consistency in such changes among different taxa and trophic levels and across freshwater, terrestrial and marine environments. We present a standardized assessment of 25 532 rates of phenological change for 726 UK terrestrial, freshwater and marine taxa. The majority of spring and summer events have advanced, and more rapidly than previously documented. Such consistency is indicative of shared large scale drivers. Furthermore, average rates of change have accelerated in a way that is consistent with observed warming trends. Less coherent patterns in some groups of organisms point to the agency of more local scale processes and multiple drivers. For the first time we show a broad scale signal of differential phenological change among trophic levels; across environments advances in timing were slowest for secondary consumers, thus heightening the potential risk of temporal mismatch in key trophic interactions. If current patterns and rates of phenological change are indicative of future trends, future climate warming may exacerbate trophic mismatching, further disrupting the functioning, persistence and resilience of many ecosystems and having a major impact on ecosystem services.     

Cytokine profiles in the joint depend on pathology,but are different between synovial fluid,cartilage tissue and cultured chondrocytes

Introduction

This study aimed to evaluate whether profiles of several soluble mediators in synovial fluid and cartilage tissue are pathology-dependent and how their production is related to in vitro tissue formation by chondrocytes from diseased and healthy tissue.

Methods

Samples were obtained from donors without joint pathology (n = 39), with focal defects (n = 65) and osteoarthritis (n = 61). A multiplex bead assay (Luminex) was performed measuring up to 21 cytokines: Interleukin (IL)-1α, IL-1β, IL-1RA, IL-4, IL-6, IL-6Rα, IL-7, IL-8, IL-10, IL-13, tumor necrosis factor (TNF)α, Interferon (IFN)γ, oncostatin M (OSM), leukemia inhibitory factor (LIF), adiponectin, leptin, monocyte chemotactic factor (MCP)1, RANTES, basic fibroblast growth factor (bFGF), hepatocyte growth factor (HGF), vascular growth factor (VEGF).

Results

In synovial fluid of patients with cartilage pathology, IL-6, IL-13, IFNγ and OSM levels were higher than in donors without joint pathology (P ≤0.001). IL-13, IFNγ and OSM were also different between donors with cartilage defects and OA (P <0.05). In cartilage tissue from debrided defects, VEGF was higher than in non-pathological or osteoarthritic joints (P ≤0.001). IL-1α, IL-6, TNFα and OSM concentrations (in ng/ml) were markedly higher in cartilage tissue than in synovial fluid (P <0.01). Culture of chondrocytes generally led to a massive induction of most cytokines (P <0.001). Although the release of inflammatory cytokines was also here dependent on the pathological condition (P <0.001) the actual profiles were different from tissue or synovial fluid and between non-expanded and expanded chondrocytes. Cartilage formation was lower by healthy unexpanded chondrocytes than by osteoarthritic or defect chondrocytes.

Conclusions

Several pro-inflammatory, pro-angiogenic and pro-repair cytokines were elevated in joints with symptomatic cartilage defects and/or osteoarthritis, although different cytokines were elevated in synovial fluid compared to tissue or cells. Hence a clear molecular profile was evident dependent on disease status of the joint, which however changed in composition depending on the biological sample analysed. These alterations did not affect in vitro tissue formation with these chondrocytes, as this was at least as effective or even better compared to healthy chondrocytes.     

Detection of methanogens and methanotrophs in natural environments

The role of methane as a greenhouse gas and the contribution of bacteria to the production (methanogenesis) and destruction (methane oxidation) of methane is described. Using experimental approaches based on DNA sequences identifying either methanogen-specific or methanotroph-specific gene sequences methods were developed to broaden the detection and identification of methane metabolizing bacteria in natural environments. These methods were focused on blanket bog peat but are suitable for other environments. In addition to group specific 16S rRNA DNA sequences, specific functional gene probes based on methane coenzyme reductase sequences for methanogens and methane monooxygenase sequences for methanotrophs, were developed. These sequences were used in PCR-based protocols to detect and amplify specific gene sequences from the total DNA isolated from transverse sections of blanket bog peat. This permitted the analysis of the vertical distribution of methanogen and methanotroph populations, discrimination between different sub-sets of these populations, and the identification of novel organisms not previously detected by culture-based methods.     

Ultrasound production by genital stridulation in Syntonarcha iriastis (Lepidoptera: Pyralidae): long-distance signalling by male moths?

Males of the pyralid moth, Syntonarcha iriastis Meyrick, perch on vegetation at the tops of trees and bushes and produce ultrasound while their wings are spread and while sclerites at the end of the abdomen are spread to expose the genitalia. Exposing the genitalia appears to engage the sound-producing mechanism; the male genitalia and eighth abdominal sternite of this species are greatly modified and include a file and scraper and possible resonating areas. Sounds produced are consistent between individuals and comprise pulses which are narrow in frequency range, the first pulse being at about 42 kHz and two following pulses at about 57 kHz. The signal is detectable with an ultrasound 'bat' detector from 20 m. Two tettigoniid species (Orthoptera) at the same site produced ultrasonic calls of similar frequencies at the same times as the moth; differences in time-amplitude patterns could be used by orienting moths to recognize conspecifics. Signalling by male S. iriastis is compared with that of other pyralid species in which females are attracted to signalling males. The behaviour of S. iriastis males differs from that of other pyralids in that they do not signal in groups or from a resource attractive to females, and do not possess glands known to produce a 'calling' pheromone. It is suggested, because of these differences, that sound production in this species does not function at close range, as argued for the wax moth Achroia grisella (Fabricius), but instead as a long-distance calling signal.     

Brood division and transition to independence in Blackbirds Turdus merula

Blackbirds Turdus merula rearing young in the Botanic Garden, Oxford, were observed over three summers (1979–81). Between 0 and 10 days after fledging the young were divided between the parents so that each fed only certain fledglings and refused to feed others. This division was temporally stable. In broods where another nesting attempt followed, the male usually took responsibility for all the young, but in final broods they were divided fairly evenly. The probability of a fledgling surviving to independence declined as the number of young a parent fed increased; thus division should be favoured. However, if the female fed some young the inter-nest interval increased and the potential number of young that could be raised in that season was curtailed. This trade-off is examined by means of a model. After fledging the young improved in their ability to capture prey successfully and increased the size of the prey taken. At 15–24 days after fledging, self-feeding became more profitable than parental feeding and the young became fully independent. The timing of this transition is influenced by the parents, and it is suggested that by dividing the brood, parental feeding can be more carefully regulated so that finer control over the timing of independence is achieved.     

Chimpanzee fetal G gamma and A gamma globin gene nucleotide sequences provide further evidence of gene conversions in hominine evolution

The fetal globin genes G gamma and A gamma from one chromosome of a chimpanzee (Pan troglodytes) were sequenced and found to be closely similar to the corresponding genes of man and the gorilla. These genes contain identical promoter and termination signals and have exons 1 and 2 separated by the conserved short intron 1 (122 bp) and exons 2 and 3 separated by the more rapidly evolving, larger intron 2 (893 bp and 887 bp in chimpanzee G gamma and A gamma, respectively). Each intron 2 has a stretch of simple sequence DNA (TG)n serving possibly as a "hot spot" for recombination. The two chimpanzee genes encode polypeptide chains that differ only at position 136 (glycine in G gamma and alanine in A gamma) and that are identical to the corresponding human chains, which have aspartic acid at position 73 and lysine at 104 in contrast to glycine and arginine at these respective positions of the gorilla A gamma chain. Phylogenetic analysis by the parsimony method revealed four silent (synonymous) base substitutions in evolutionary descent of the chimpanzee G gamma and A gamma codons and none in the human and gorilla codons. These Homininae (Pan, Homo, Gorilla) coding sequences evolved at one-tenth the average mammalian rate for nonsynonymous and one-fourth that for synonymous substitutions. Three sequence regions that were affected by gene conversions between chimpanzee G gamma and A gamma loci were identified: one extended 3' of the hot spot with G gamma replaced by the A gamma sequence, another extended 5' of the hot spot with A gamma replaced by G gamma, and the third conversion extended from the 5' flanking to the 5' end of intron 2, with G gamma replaced here by the A gamma sequence. A conversion similar to this third one has occurred independently in the descent of the gorilla genes. The four previously identified conversions, labeled C1-C4 (Scott et al. 1984), were substantiated with the addition of the chimpanzee genes to our analysis (C1 being shared by all three hominines and C2, C3, and C4 being found only in humans). Thus, the fetal genes from all three of these hominine species have been active in gene conversions during the descent of each species.      

The herbaceous lycophyte Haskinsia Grierson and Banks from the Devonian of western Venezuela, with observations on leaf morphology and fertile specimens

The Devonian herbaceous lycophyte genus Haskinsia Grierson and Banks is characterized by narrow dichotomizing stems and helically arranged petiolate leaves with a broad, approximately deltoid, lamina. New specimens are reported from four horizons in the Lower Member of the Campo Chico Formation, Sierra de Perijá, western Venezuela. H. sagittaka Edwards and Benedetto has sagittate leaves, and fertile specimens are reported for the first time; the ellipsoidal/obovoid adaxially-flattened sporangium is attached to unmodified leaves towards the top of the petiole in the adaxial position. H. sp. has sagittate leaves which are larger than any yet attributed to the genus but is represented by only three specimens. H. hastata sp. nov. has hastate leaves; the sporangia are more globose but positioned similarly to those of H. sagittata. The occurrence of the sporangia on unmodified microphylls indicates that Haskinsia is a member of Protolepidodendrales. The status of Haskinsiaceae is discussed. The Venezuelan specimens are compared with other records of Haskimi and Haskinsia -like plants from North America, Kazakhstan, North China, North Africa and Antarctica.