Systematic revision of Hoggicosa Roewer, 1960, the Australian ‘bicolor’ group of wolf spiders (Araneae: Lycosidae)

The Australian wolf spider genus Hoggicosa Roewer, 1960 with the type species Hoggicosa errans (Hogg, 1905) is revised to include ten species: Hoggicosa alfi sp. nov. ; Hoggicosa castanea (Hogg, 1905) comb. nov. (= Lycosa errans Hogg, 1905 syn. nov. ; = Lycosa perinflata Pulleine, 1922 syn. nov. ; = Lycosa skeeti Pulleine, 1922 syn. nov. ); Hoggicosa bicolor (McKay, 1973) comb. nov. ; Hoggicosa brennani sp. nov. ; Hoggicosa duracki (McKay, 1975) comb. nov. ; Hoggicosa forresti (McKay, 1973) comb. nov. ; Hoggicosa natashae sp. nov. ; Hoggicosa snelli (McKay, 1975) comb. nov. ; Hoggicosa storri (McKay, 1973) comb. nov. ; and Hoggicosa wolodymyri sp. nov. The Namibian Hoggicosa exigua Roewer, 1960 is transferred to Hogna, Hogna exigua (Roewer, 1960) comb. nov. A phylogenetic analysis including nine Hoggicosa species, 11 lycosine species from Australia and four from overseas, with Arctosa cinerea Fabricius, 1777 as outgroup, supported the monophyly of Hoggicosa, with a larger distance between the epigynum anterior pockets compared to the width of the posterior transverse part. The analysis found that an unusual sexual dimorphism for wolf spiders (females more colourful than males), evident in four species of Hoggicosa, has evolved multiple times. Hoggicosa are burrowing lycosids, several constructing doors from sand or debris, and are predominantly found in semi‐arid to arid regions of Australia. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 158 , 83–123.     

Chamber growth in ammonites inferred from colour markings and naturally etched surfaces of Cretaceous vascoceratids from Nigeria

Cretaceous Vascoceras and Jurassic Lytoceras show colour markings and etched surfaces representing original organic membranes between the septa. The main difference between the formation of ammonite and Nautilus chambers involved the continuous secretion of a gelatinous cameral liquid to support the ammonite mantle when it moved forward. The gel containing cyclically secreted membranes. here named pseudosepta, resembled the intra-cameral structures of the cuttlebone in Sepia. Pseudoscpta are attached to the shell wall in pseudosutures (Pseudoloben) which are particularly visible in the saddles of the septal suture and tend to mimic them. Their shape suggests reconstruction of posterior mantle shape during translocation. Drag-bands (Schleppstreifen) are spiral markings formed by the overlapping pseudosepta along the axial traces of the foliole folds. The chamber of ammonites was formed by a locally muscular mantle in a tripartite cycle: (1) the mantle initially remained attached to the saddles of the completed septal suture while muscular tissue within the umbilical lobes was contracted and rapidly reattached to the side of the lateral saddles; (2) the whole mantle subsequently crept forward by secreting a gelatinous matrix which contained telescoped membranes, with an adhesive function on pseudolobc flanks; (3) the mantle almost ceased to move within the sites of future lobules, but expanded and crept on before forming the mural and 'gutter' ridges of the septum. □ Ammonites, chamber growth, vascoceratids, LYTOCERAS, Nigeria.     

The diversity of hemi-epiphytic figs (Ficus ; Moraceae) in a Bornean lowland rain forest

The diversity and niche specificity of hemi-epiphytic figs in a lowland dipterocarp forest in Sarawak were investigated in 1998. Twenty-seven fig species (264 individuals, c. 120 ha) colonized a diversity of host taxa (35 families), but densities were very low and only 1.77% of trees> 30 cm d.b.h. were occupied. There were no significant associations with host taxa or host-bark roughness but among 11 common species (≥9 individuals) the distributions of all other parameters (host-d.b.h., height and position of colonization, crown illumination, soil-texture and slope-angle) were significantly different, and we identified five fig guilds. The guilds corresponded to canopy strata, and appeared to reflect the establishment microsite requirements of different species. A fundamental trade-off within the hemi-epiphytic habit was revealed: Species colonizing larger hosts were rarer, because of lower host densities and more specific microsite requirements, but had better light environments and attained a larger maximum size. The single strangler species appeared to escape many of these constraints, and an important source of mortality caused by host-toppling, indicating the advantages of this strategy. Thus, the hemi-epiphytic figs in this community have come to fill a remarkable diversity of niches, despite low levels of competition, through the exigencies of a complex environment.  © 2003 The Linnean Society of London, Biological Journal of the Linnean Society , 2003, 78 , 439–455     

Salamander Dispersal Across a Forested Landscape Fragmented by a Golf Course

Abstract: We assessed dispersal behavior of 78 radiotagged adult spotted salamanders (Ambystoma maculatum) at a 36-hole golf course in southeastern Connecticut, USA. Lake of Isles Golf Course is atypical of most golf courses in North America because it is much larger (461 ha) than average 18-hole golf courses (54 ha) and deciduous forests accounted for 70% landscape composition on the course. We tracked individuals an average of 164 days as they emigrated from 3 seasonal pools surrounded by golf course fairways and one pool located in contiguous forest (control pool) from March through December 2004. Males and females dispersed similar distances at the control pool, averaging 71 ± 10 m. However, females migrating across the golf course dispersed twice as far (214 ± 25 m) as males on the golf course (102 ± 15 m) and both genders at the control pool. Over 40% the salamanders at the golf course crossed fairways; thus, fairways were not a dispersal barrier to adult spotted salamanders. Previous researchers have suggested establishing a 164-m life zone around breeding ponds to protect pond-breeding amphibian populations. Our results suggest that strategies that protect core upland habitat within 164 m of wetland boundaries would include 82% of adult males and only 50% of adult females. Empirical estimates based on our telemetry study suggest that core terrestrial habitat would have to extend 370 m to protect 95% of adult females, which is much farther than previous estimates.     

Responses of cetaceans to anthropogenic noise

• 1 Since the last thorough review of the effects of anthropogenic noise on cetaceans in 1995, a substantial number of research reports has been published and our ability to document response(s), or the lack thereof, has improved. While rigorous measurement of responses remains important, there is an increased need to interpret observed actions in the context of population‐level consequences and acceptable exposure levels. There has been little change in the sources of noise, with the notable addition of noise from wind farms and novel acoustic deterrent and harassment devices (ADDs/AHDs). Overall, the noise sources of primary concern are ships, seismic exploration, sonars of all types and some AHDs.
• 2 Responses to noise fall into three main categories: behavioural, acoustic and physiological. We reviewed reports of the first two exhaustively, reviewing all peer‐reviewed literature since 1995 with exceptions only for emerging subjects. Furthermore, we fully review only those studies for which received sound characteristics (amplitude and frequency) are reported, because interpreting what elicits responses or lack of responses is impossible without this exposure information. Behavioural responses include changes in surfacing, diving and heading patterns. Acoustic responses include changes in type or timing of vocalizations relative to the noise source. For physiological responses we address the issues of auditory threshold shifts and ‘stress’, albeit in a more limited capacity; a thorough review of physiological consequences is beyond the scope of this paper.
• 3 Overall, we found significant progress in the documentation of responses of cetaceans to various noise sources. However, we are concerned about the lack of investigation into the potential effects of prevalent noise sources such as commercial sonars, depth finders and fisheries acoustics gear. Furthermore, we were surprised at the number of experiments that failed to report any information about the sound exposure experienced by their experimental subjects. Conducting experiments with cetaceans is challenging and opportunities are limited, so use of the latter should be maximized and include rigorous measurements and or modelling of exposure.

     

Vertical stratification of feeding guilds and body size in beetle assemblages from an Australian tropical rainforest

Abstract The vertical stratification of insect species assemblages inhabiting tropical rainforests is well established but few have examined whether these patterns are reflected in vertical stratification of body size or feeding guilds. We used Malaise and Flight Interception Traps to sample beetle assemblages from five locations, at both canopy and ground zones of a tropical lowland rainforest site near Cape Tribulation, Australia. Beetles from 4 years of sampling were sorted to Family and morphospecies, and allocated to one of five feeding guilds. Within feeding guilds the number of species and individuals, from canopy‐ and ground‐caught traps were compared. The body lengths of species were measure and compared within feeding guilds and families. Herbivores was the dominant guild but was not the majority of all species or individuals. Most beetle species (69%) were less than 5 mm in length and the mean size of canopy‐caught species was greater than that for ground‐caught species. This was probably due to slightly more species of plant feeders (herbivores and xylophages) present in the canopy, which were significantly larger than saprophages, fungivores and predators. Among feeding guilds, there were few overall canopy–ground differences. These results contrast with species composition results presented elsewhere where strong differences between the canopy and the ground were evident. We suggest that our guild groupings may have been too coarse to detect fine‐scale differences and that resource partitioning may have also masked faunal stratification. We propose that fine‐scale differences in resources between the canopy and the ground, together with strong microclimate gradients, are likely to be important in structuring the vertical stratification of insect assemblages at the level of species, but not with respect to functional groups.