Estimating Abundance From One-Dimensional Passive Acoustic Surveys

ABSTRACT Conventional distance sampling, the most-used method of estimating animal density and abundance, requires ranges to detected individuals, which are not easily measured for vocalizations. However, in some circumstances the sequential pattern of detection of vocalizations along a transect line gives information about the range of detection. Thus, from a one-dimensional acoustic point-transect survey (i.e., records of vocalizations detected or not detected at regularly spaced listening stations) it is possible to obtain a useful estimate of density or abundance. I developed equations for estimation of density for one-dimensional surveys. Using simulations I found that for the method to have little bias when both range of detection and rate of vocalization need to be estimated, stations needed to be spaced at 30–80% of the range of detection and the rate of vocalization should be >0.7. If either the range of detection or rate of vocalization is known, conditions are relaxed, and when both parameters are known the method works well almost universally. In favorable conditions for one-dimensional methods, estimated abundances have overall errors not much larger than those from conventional line-transect distance sampling. The methods appeared useful when applied to real acoustic data from whale surveys. The techniques may also be useful in surveys with nonacoustic detection of animals.     

Prevention of potato top-roll by aphicide and its effect on leaf area and photosynthesis

In a field of potatoes, top-roll, which is induced by the aphid Macrosiphum euphorbiae feeding on the leaves, was restricted to two rows of plants which accidentally received no phorate aphicide granules at planting. The photo-synthetic rate per unit leaf area and the ground cover of top-rolled leaves were respectively 50% and 20% less than those of normal plants which may account for the smaller yields of affected plants observed in previous experiments.     

Photosynthesis and wood structure in Pinus radiata D. Don during dehydration and immediately after rewatering

Abstract. Experiments were carried out on Pinus radiata (D. Don) trees grown as cuttings from clonal parent stock. Some of these trees were about 0.4 m high while others were about 5 m high; all were grown in containers. The stem diameters at the tops and at the bottoms of the large trees, rates of photosynthesis, and needle water potentials were measured both when the trees were well watered and as they dehydrated after water was withheld. The water potentials of well-watered plants was highest in the small trees and lowest at the top of the large trees. When water was withheld, photosynthesis was in most cases unaffected by a small reduction in water potential, but the rate of photosynthesis fell as water potentials declined further. The stems of the large trees expanded at a constant rate when the trees were well watered and for part of the dehydration period, while subsequent stem shrinkage and the fall in photosynthesis both occurred at approximately the same time.
Water potentials increased little in the 24 h after rewatering, and significant rates of photosynthesis were not measured until 2 or 3 d later while renewed stem expansion was not measured until 2 d after rewatering.
Water deficits reduced the lumen diameter of newly matured stem tracheids, but increased the thickness of their walls. After 1 month of water potentials of about −2.4 MPa, tracheid lumen diameter and wall thickness were both much reduced, and this reduction continued in tracheids maturing shortly after rewatering.     

Effects of biological invasions on forest carbon sequestration

There has been a rapidly developing literature on the effects of some of the major drivers of global change on carbon (C) sequestration, particularly carbon dioxide (CO₂) enrichment, land use change, nitrogen (N) deposition and climate change. However, remarkably little attention has been given to one major global change driver, namely biological invasions. This is despite growing evidence that invasive species can dramatically alter a range of aboveground and belowground ecosystem processes, including those that affect C sequestration. In this review, we assess the evidence for the impacts of biological invaders on forest C stocks and C sequestration by biological invaders. We first present case studies that highlight a range of invader impacts on C sequestration in forest ecosystems, and draw on examples that involve invasive primary producers, decomposers, herbivores, plant pathogens, mutualists and predators. We then develop a conceptual framework for assessing the effects of invasive species on C sequestration impacts more generally, by identifying the features of biological invaders and invaded ecosystems that are thought to most strongly regulate C in forests. Finally we assess the implications of managing invasive species on C sequestration. An important principle that emerges from this review is that the direct effects of invaders on forest C are often smaller and shorter‐term than their indirect effects caused by altered nutrient availability, primary productivity or species composition, all of which regulate long‐term C pools and fluxes. This review provides a conceptual basis for improving our general understanding of biological invaders on ecosystem C, but also points to a paucity of primary data that are needed to determine the quantitative effects of invaders on ecosystem processes that drive C sequestration.     

Control of pea cyst-nematode, Heterodera goettingiana, by small amounts of aldicarb, Du Pont 1410, Ciba-Geigy 10576 or Dowco 275 applied to the soil at planting time

Aldicarb, or Du Pont 1410 (S-methyl-I-(dimethylcarbamoyl)-N-[(methyl-carbamoyl)oxy]thioformimidate), at 2.8–22.4 kg a.i./ha incorporated in the seed-bed before sowing greatly increased the yield of peas in a clay loam and two sandy clay soils infested with pea cyst-nematode, Heterodera goettingiana, and lessened or prevented increase in the number of nematodes. CibaGeigy 10576 (an organophosphorus compound) at 5.6–22.4 kg a.i./ha was similarly effective in a sandy clay soil. Dowco 275 (O, O-diethylO-(6-fluoro-2 pyridyl) phosphorothioate) at 5.6 or 11.2 kg a.i./ha also controlled the nematode well in the clay loam and in a sandy clay soil but although it greatly increased the yield of peas in the clay loam, it did not increase yield in the sandy clay.     

Plasticity in photosynthetic response to nutrient supply of seedlings from a mixed conifer‐angiosperm forest

Abstract We measured the plasticity of the response of photosynthesis to nutrient supply in seedlings of the dominant four conifer and broadleaved angiosperm tree species from an indigenous forest in South‐westland, New Zealand. We hypothesized that the response of conifers to differing nutrient supply would be less than the response for the angiosperms because of greater adaptation to low fertility conditions. In Prumnopitys ferruginea (D. Don) de Laub. the maximum velocity of electron transport, J_max, doubled with a 10‐fold increase in concentration of nitrogen supply. In Dacrydium cupressinum Lamb. the maximum velocity of carboxylation, V_cmax, doubled with a 10‐fold increase in phosphorus supply. In contrast, photosynthetic capacity for the angiosperm species Weinmannia racemosa L.f. was affected only by the interaction of nitrogen and phosphorus and photosynthetic capacity of Metrosideros umbellata Cav. was not affected by nutrient supply. The response of the conifers to increasing availability of nutrient suggests greater plasticity in photosynthetic capacity, a characteristic not generally associated with adaptation to soil infertility, thus invalidating our hypothesis. Our data suggest that photosynthetic response to nutrient supply cannot be broadly generalized between the two functional groups.     

Swimbladder form in clupeoid fishes

The general form of the swimbladder is described and illustrated for representatives of 50 out of the 82 genera of clupeoid fishes (families Chirocentridae, Clupeidae, Pristigasteridae and Engraulididae of the suborder Clupeoidei), based mainly on preserved specimens. There is a remarkable diversity of shape, volume and silvering, as well as many curious specializations. The point of origin of the pneumatic duct from the gut, the presence or absence of an anal duct, and the length and diameter of the pre-coelomic ducts are noted, with attempts to explain their functional significance in terms of feeding and vertical migration. Specializations such as dorsal or lateral pockets, post-coelomic diverticula and internal muscular processes may be connected with sound production. The taxonomic implications of this diversity of swimbladder form are explored but, while some intra-and intergeneric relationships arc either confirmed or challenged, the swimbladder gives little help at suprageneric levels.     

Control of potato cyst-nematode, Heterodera rostochiensis, in three soils by small amounts of aldicarb, Du Pont 1410 or Nemacur applied to the soil at planting time

Aldicarb or Du Pont 1410 (S-methyl 1-(dimethylcarbamoyl)-N-[(methylcarbamoyl) oxy] thioformimidate) at 2.6–11.2 kg a.i./ha applied to the soil at planting time controlled potato cyst-nematode, Heterodera rostochiensis, in sandy loam, peaty loam and silt loam and greatly increased tuber yields of susceptible potatoes. Nemacur (O-ethyl-O-(3-methyl-4-methylthiophenyl) isopropylamido-phosphate) controlled potato cyst-nematode in sandy loam at 2.9–10.3 kg a.i./ha and in silt loam at 11.2 kg a.i./ha but did not control the nematode well in peaty loam even at 22.4 kg a.i./ha. In peaty loam aldicarb and Nemacur were more effectively incorporated by rotavation than by a modified power harrow.     

Control of potato cyst-nematodes, Heterodera rostochiensis and H. pallida, in sandy, peaty and silt loam soils by oximecarbamate and organophosphate nematicides

Small amounts (5.6 or n-2 kg a.i./ha) of aldicarb or oxamyl, incorporated in the soil before potatoes were planted in spring, controlled potato cyst-nematodes (Heterodera rostochiensis and H. pallida) on susceptible cultivars equally well in sandy, peaty and silt loam soils. In soils treated with either nematicide, nematode numbers increased little or decreased; in untreated soils nematode numbers increased greatly. In contrast organophosphate nematicides, similarly applied, fenamiphos (proposed BSI common name for O-ethyl-O-(3-methyl-4-methylthiophenyI)-isopropylamido-phosphate), ethoprophos (proposed BSI common name for (O-ethyl S, 5-dipropyl phos-phorodithioate), CGA 12223 (O, O-diethyl O-[i-isopropyl-5-chloro-i,2,4-triazoIyl-(3)] phosphorothioate) and Dowco 275 (O, O-diethyl O-(6-fluoro-2 pyridyl) phosphorothioate), were ineffective at one or more of the experimental sites. Potato yields were greatly increased by oximecarbamate or organophosphate nematicides only in soils heavily infested with the nematodes.