Phylum Nematoda: feeding habits for all valid genera using a new, universal scheme encompassing the entire phylum, with descriptions of morphological characteristics of the stoma, a key, and discussion of the evidence for trophic relationships.

This paper details a system for classifying the trophic relationships of the entire Phylum Nematoda, together with a table specifying the categories of every valid genus. This system encompasses both the diets of nematodes and how the food is obtained. The types of evidence used to evaluate trophic relationships and the inferences that can be drawn from each are evaluated. The general morphological and ecological characteristics of each trophic type are detailed, and a morphological key is presented. This information will enable the trophic relationships of any valid genus of nematodes to be assessed, along with currently undescribed genera, provided their affinities to existing genera can be ascertained. The system and list can add value to ecological, environmental and biodiversity studies where there is no morphological information, for example in environmental sequencing or metabarcoding studies.

Phylum Nematoda: trends in species descriptions, the documentation of diversity, systematics, and the species concept.

This paper summarizes the trends in nematode species description and systematics emerging from a comparison of the latest comprehensive classification and census of Phylum Nematoda (Hodda 2022a, b) with earlier classifications (listed in Hodda 2007). It also offers some general observations on trends in nematode systematics emerging from the review of the voluminous literature used to produce the classification. The trends in nematodes can be compared with developments in the systematics of other organisms to shed light on many of the general issues confronting systematists now and into the future.

Phylum Nematoda: a classification, catalogue and index of valid genera, with a census of valid species.

A classification of the entire Phylum Nematoda is presented, based on current molecular, developmental and morphological evidence. The classification reflects the evolutionary relationships within the phylum, as well as significant areas of uncertainty, particularly related to the early evolution of nematodes. It includes 3 classes, 8 subclasses, 12 superorders, 32 orders, 53 suborders, 101 superfamilies, 276 families, 511 subfamilies, 3030 genera, and 28537 species. All valid species named from the time of publication of the previous classification and census (2010) to the end of 2019 are listed, along with the number of valid species in each genus. Taxonomic authorities are provided for taxon names of all ranks. The habitats where the species in each genus are found are listed, and an alphabetic index of genus names is provided. The systematics of nematodes is reviewed, along with a history of nematode classification; evolutionary affinities and origins of nematodes; and the current diagnosis of the group. Short overviews of the general biology, ecology, scientific and economic importance of the group are presented.

Consistency of effects of tropical-forest disturbance on species composition and richness relative to use of indicator taxa.

Lawton et al. (1998) found, in a highly cited study, that the species richness of 8 taxa each responds differently to anthropogenic disturbance in Cameroon forests. Recent developments in conservation science suggest that net number of species is an insensitive measure of change and that understanding which species are affected by disturbance is more important. It is also recognized that all disturbance types are not equal in their effect on species and that grouping species according to function rather than taxonomy is more informative of responses of biodiversity to change. In a reanalysis of most of the original Cameroon data set (canopy and ground ants, termites, canopy beetles, nematodes, and butterflies), we focused on changes in species and functional composition rather than richness and used a more inclusive measure of forest disturbance based on 4 component drivers of change: years since disturbance, tree cover, soil compaction, and degree of tree removal. Effects of disturbance on compositional change were largely concordant between taxa. Contrary to Lawton et al.'s findings, species richness for most groups did not decline with disturbance level, providing support for the view that trends in species richness at local scales do not reflect the resilience of ecosystems to disturbance. Disturbance affected species composition more strongly than species richness for butterflies, canopy beetles, and litter ants. For these groups, disturbance caused species replacements rather than just species loss. Only termites showed effects of disturbance on species richness but not composition, indicating species loss without replacement. Although disturbance generally caused changes in composition, the strength of this relationship depended on the disturbance driver. Butterflies, litter ants, and nematodes were correlated with amount of tree cover, canopy beetles were most strongly correlated with time since disturbance, and termites were most strongly correlated with degree of soil disturbance. There were moderately divergent responses to disturbance between functional feeding groups. Disturbance was most strongly correlated with compositional differences of herbivores within beetles and nematodes and humus feeders within termites. Our results suggest that consideration of the impact of different forms of disturbance on species and functional composition, rather than on net numbers of species, is important when assessing the impacts of disturbance on biodiversity.

Dispersal of potato cyst nematodes measured using historical and spatial statistical analyses.

Rates and modes of dispersal of potato cyst nematodes (PCNs) were investigated. Analysis of records from eight countries suggested that PCNs spread a mean distance of 5.3 km/year radially from the site of first detection, and spread 212 km over ≈40 years before detection. Data from four countries with more detailed histories of invasion were analyzed further, using distance from first detection, distance from previous detection, distance from nearest detection, straight line distance, and road distance. Linear distance from first detection was significantly related to the time since the first detection. Estimated rate of spread was 5.7 km/year, and did not differ statistically between countries. Time between the first detection and estimated introduction date varied between 0 and 20 years, and differed among countries. Road distances from nearest and first detection were statistically significantly related to time, and gave slightly higher estimates for rate of spread of 6.0 and 7.9 km/year, respectively. These results indicate that the original site of introduction of PCNs may act as a source for subsequent spread and that this may occur at a relatively constant rate over time regardless of whether this distance is measured by road or by a straight line. The implications of this constant radial rate of dispersal for biosecurity and pest management are discussed, along with the effects of control strategies.

Economic impact from unrestricted spread of potato cyst nematodes in australia.

ABSTRACT Potato cyst nematodes (PCN) (Globodera spp.) are quarantine pests with serious potential economic consequences. Recent new detections in Australia, Canada, and the United States have focussed attention on the consequences of spread and economic justifications for alternative responses. Here, a full assessment of the economic impact of PCN spread from a small initial incursion is presented. Models linking spread, population growth, and economic impact are combined to estimate costs of spread without restriction in Australia. Because the characteristics of the Australian PCN populations are currently unknown, the known ranges of parameters were used to obtain cost scenarios, an approach which makes the model predictions applicable generally. Our analysis indicates that mean annual costs associated with spread of PCN would increase rapidly initially, associated with increased testing. Costs would then increase more slowly to peak at over AUD$20 million per year approximately 10 years into the future. Afterward, this annual cost would decrease slightly due to discounting factors. Mean annual costs over 20 years were $18.7 million, with a 90% confidence interval between AUD$11.9 million and AUD$27.0 million. Thus, cumulative losses to Australian agriculture over 20 years may exceed $370 million without action to prevent spread of PCN and entry to new areas.

The effects of forest disturbance on diversity of tropical soil nematodes.

We provide the first account of the effects of forest disturbance on species richness of nematodes in tropical forest soils, from 24 sites along gradients of disturbance and regeneration in the Mbalmayo Forest Reserve, Cameroon. Species richness was very high. Samples of 200 nematodes from individual soil cores contained a maximum of 89 and an average of 61 species; in total we recorded 431 species and approximately 194 genera. The model of Siemann et al. (1996), predicting that species richness scales as the number of individuals I 0.5, underestimates nematode diversity 4-6 fold in these samples. Over 90% of specimens cannot be assigned to known species. Although nematode species richness declined with forest disturbance, statistically significant effects were detectable only under the most extreme conditions (active slash-and-burn agriculture and complete mechanical forest clearance) and even here remained at 40% of the richness of near primary sites. Impacts on trophic structure were also small, and there were no significant changes in the maturity index (MI) (Bongers 1990) with disturbance (mean MI across all treatments was very high, at 3.58). In the light of this study, the problems of completing reliable all-taxon inventories in tropical forests are briefly discussed.