We determined feeding preferences of invertebrate seed predators and the effect of seed predation on weed emergence. Feeding choice studies were completed with three species of common ground beetles: (Amara aenea DeGeer, Anisodactylus sanctaecrucis F., and Harpalus pensylvanicus DeGeer) (Coleoptera: Carabidae) and the northern field cricket (Gryllus pennsylvanicus DeGeer) (Orthoptera: Gryllidae). Anisodactylus sanctaecrucis, H. pensylvanicus, and the female and male G. pennsylvanicus consumed more redroot pigweed seeds compared with giant foxtail seeds; A. aenea seed consumption did not differ between these two weed species. All invertebrates consumed fewer velvetleaf seeds compared with redroot pigweed and giant foxtail seeds; however, when seed biomass was compared, A. aenea consumed similar biomass of velvetleaf, giant foxtail, and redroot pigweed, whereas A. sanctaecrucis and H. pensylvanicus consumed greater biomass of velvetleaf compared with giant foxtail seed. Seed burial depths of 0.5 or 1.0 cm reduced redroot pigweed and giant foxtail seed consumption by A. aenea and A. sanctaecrucis but not by the larger carabid beetle, H. pensylvanicus. In a greenhouse study, A. sanctaecrucis decreased total weed emergence by 15%, and G. pennsylvanicus females and males decreased weed emergence by 16 and 5%, respectively. Emergence of redroot pigweed, but not velvetleaf or giant foxtail, decreased when A. sanctaecrucis and the male G. pennsylvanicus were present, whereas the emergence of all three weed species decreased in the presence of the female G. pennsylvanicus. In field experiments, vertebrate access to velvetleaf seeds reduced emergence from 4 to 9% across field sites; invertebrate access reduced emergence 4 to 6%. Vertebrate access to giant foxtail seeds reduced emergence 3 to 7%, and invertebrate access reduced emergence 4 to 13%. These results suggest that predation of weed seeds by both vertebrates and invertebrates may reduce weed emergence and influence the weed community.

A standard method for evaluating weed seed predation is needed to facilitate generalizations across studies. Identification of general trends could allow practical recommendations for enhancing weed seed predation in agricultural systems. The objective of this study was to compare the commonly used sandpaper and soil substrate methods for offering weed seeds when assessing seed predation rates. Invertebrate seed predators and associated weed seed predation levels were measured in June to July, August, and September of 2005 and 2006 within a conventionally managed corn system. Seed predation levels of three common weed species, velvetleaf, giant foxtail, and common lambsquarters, were estimated using feeding trials in which 40 seeds of each species were offered over a 48 h period using the two substrates. Exclosures were used to distinguish total predation from predation by invertebrates alone. In addition, we investigated the use of geospatial analysis to estimate spatial autocorrelation of invertebrate populations and seed removal rates. Results suggest caution in using synthetic substrates, such as sandpaper, when assessing seed predation, especially when investigating small-seeded species (< 1 mg seed−1) or when seed predators are predominantly invertebrates. By contrast, predation of the larger-seeded species, velvetleaf, was less affected by substrate, perhaps because of removal predominately by vertebrates. One way to overcome problems with the sandpaper substrate method is for studies to include some soil substrate samples for on-site calibration of the sandpaper substrate. If necessary, data could then be corrected by multiplying by the ratio of soil substrate measured-predation rate to sandpaper measured-predation rate. Spatial autocorrelation explained between 6 and 9% of the variation in giant foxtail and common lambsquarters removal rates attributed to invertebrates alone. Researchers should, therefore, be careful not to neglect the impact of clustered invertebrate populations and associated seed removal rates.

Contrasting cover-cropping systems were compared to determine whether fundamental differences in cover-cropping strategies affect weed seed predators and resulting seed predation. We conducted typical “feeding” trials in which 25 seeds of each of six weed species, including velvetleaf, wild mustard, yellow foxtail, common lambsquarters, redroot pigweed, and hairy galinsoga, were placed in the field. Exclosures showed that the majority of seed predation could be attributed to invertebrates: 43% out of a total of 56% seed predation for 11 d in 2002 and 40% out of a total of 58% seed predation for 4 d in 2003. The predominant invertebrate seed predator across all entry points of four cropping systems was a ground-dwelling carabid beetle, Harpalus rufipes, which was more abundant in vegetated treatments, particularly red clover, compared with treatments recently tilled and planted to a fall cover crop. In the absence of vertebrates, H. rufipes activity–density was positively correlated with mean seed predation in 2002 (Spearman ρ = 0.489; P < 0.001) but not in 2003 (Spearman ρ = 0.090; P = 0.504), possibly because of a delay between pitfall trapping and predation assay. The activity–density of invertebrate seed predators measured in these systems and the high level of predation imposed on weed seeds at the soil surface indicate that cover-cropping strategies should consider late-season weed management, which maintains seeds on the soil surface and provides desirable habitat for invertebrate predators.

Postdispersal seed predation by ground beetles may be an important form of biological weed control. Field experiments conducted in 2002 and 2003 determined invertebrate seed predators' ability to detect and remove seeds from different experimental substrates. Predation of wild mustard and common lambsquarters was greater when seeds were presented on sand compared with the two types of synthetic finishing pads; however, predation of velvetleaf, redroot pigweed, and hairy galinsoga was unaffected by substrate. Predation rates were not consistent across all experimental substrates. Estimates of invertebrate predation of common lambsquarters, yellow foxtail, and velvetleaf were greater for seeds offered on sand or synthetic pads than for seeds offered on soil or double-sided tape covered with soil. Although each substrate would be useful to estimate treatment effects on relative predation rates, the weed species by substrate interaction should be considered when comparing predation rates across experiments or when the absolute rate predation is of critical importance.

Organic grain growers rely on cultural practices and biological control to regulate pests, and the implementation and timing of cultural practices can affect many characteristics of the cropping system as a habitat for natural enemies of arthropod pests. Ground beetles (Coleoptera: Carabidae) in particular are important insect and weed-seed predators, and are sensitive to crop rotations, tillage and environmental complexity. In a reduced tillage system in transition to organic management, we evaluated the effect of cover crop species and termination date, crop rotation and high residue cultivation on ground and tiger beetle (Coleoptera: Carabidae) activity-density, community composition and size and trophic groups. The 3-year experiment included a sequence of corn (Zea mays L.), soybean (Glycine max (L.) Merr.) and winter wheat (Triticum aestivum L.). A mixture of hairy vetch (Vicia villosa Roth) and triticale (x Triticosecale Wittmack) preceded corn, and cereal rye (Secale cereale L.) preceded soybean, and each crop sequence was present in each year (full-entry). We compared three cover crop termination (and cash crop planting) dates by terminating the overwintered cover crops with a roller-crimper, and immediately or soon after, we no-till planted corn and soybean through the mat created by the rolled cover crops. In the corn and soybean phases of the rotation, we also compared inter-row cultivation as a pest management strategy to a control treatment (no inter-row cultivation in corn, and an alternative row-spacing in soybean). Wheat was planted on a single date in each year into tilled soil. Carabids were sampled using pitfall traps 2 weeks after termination of the two cover crop treatments, and in mid-June in wheat. Carabid activity-density and species richness increased across the experimental site during the 3-year transition, and community evenness across the experimental site increased by the third year. Crop species influenced carabid community composition, and by the third year, the carabid community was comparable between wheat and hairy vetch-triticale cover crop. The late cover crop termination date was positively associated with higher activity-densities of large carabids in rolled hairy vetch-triticale and rolled cereal rye; carnivorous beetles in rolled hairy vetch-triticale; and granivorous beetles in rolled cereal rye. Inter-row cultivation occurring in corn and soybean resulted in a significantly higher proportion of small beetles in the wheat phase of the rotation, with a significantly higher proportion of large beetles in wheat treatments, which had not received inter-row cultivation in corn and soybean. Results have strong implications for management during the transition to organic, including the importance of plant residue, reduced tillage and timing of cover crop termination dates for augmenting carabid populations.

Granivory can play a pivotal role in influencing regeneration, colonization as well as abundance and distribution of plants. Due to their high abundance, nutrient content and longevity, seeds are an important food source for many animals. Among insects, carabid beetles consume substantial numbers of seeds and are thought to be responsible for a significant amount of seed loss. However, the processes that govern which seeds are eaten and are therefore prevented from entering the seedbank are poorly understood. Here, we assess if DNA-based diet analysis allows tracking the consumption of seeds by carabids. Adult individuals of Harpalus rufipes were fed with seeds of Taraxacum officinale and Lolium perenne allowing them to digest for up to 3 days. Regurgitates were tested for the DNA of ingested seeds at eight different time points post-feeding using general and species-specific plant primers. The detection of seed DNA decreased with digestion time for both seed species, albeit in a species-specific manner. Significant differences in overall DNA detection rates were found with the general plant primers but not with the species-specific primers. This can have implications for the interpretation of trophic data derived from next-generation sequencing, which is based on the application of general primers. Our findings demonstrate that seed predation by carabids can be tracked, molecularly, on a species-specific level, providing a new way to unravel the mechanisms underlying in-field diet choice in granivores.

We conducted a cropping systems experiment in central Pennsylvania, USA, to determine the effects of initial cover crop species and soil management on the abundance and composition of the ground-dwelling arthropod community. We hypothesized that we would detect legacy effects of the cover crops planted in year 1 of a 3-yr crop sequence on the arthropod community in the subsequent 2 yrs, and that these effects would be influenced by the intensity of tillage. We compared four systems in a factorial combination of perennial sod and legumes or annual cereal grain and legume as initial cover crops and moldboard or chisel plow tillage implemented in soybeans followed by maize in the subsequent 2 yrs. The entire experiment was initiated twice in adjacent locations, starting in 2003 (Start 1) and 2004 (Start 2). We quantified soil arthropod activity-density and community composition and identified all arthropods to order or family, and the ground and tiger beetles (Coleoptera: Carabidae) to species. In Start 1, but not Start 2, arthropod activity-density increased with each year following implementation of organic management. We observed few legacy effects of cover crop or tillage intensity on arthropod activity-density. The composition of the soil arthropod community was primarily defined by the initial cover crop in the first year, and by the interaction between cover crop and tillage intensity in the second and third year. A legacy effect associated with a yr-1 cover crop of cereal rye was observed for Scarabaeidae beetles and Formicidae (ants) in yr 2 and Carabidae beetles in yr 3 of Start 1, but not Start 2. Weed indicators contributed significantly to the variation in the soil arthropod community that was explained by the environment in yr 2 in Start 1, and in yr 3 in both Starts. Our observations support the concept that both immediate and legacy effects of management shape arthropod communities during the organic transition period, suggesting that transitioning systems could be managed in ways that conserve or enhance natural enemy populations.

In the present study, body length and dispersal ability were examined in carabid beetles (Coleoptera: Carabidae) sampled in the Peruvian Andes along two altitudinal gradients: old-growth forest and anthropogenically disturbed region. Dispersal ability was estimated by the flight-wing condition (i.e. macropterous or brachypterous) and the cuticular length of the flight muscle (medial length of the metasternum). The relationship between body length and altitude for combined gradients varied by tribe; all possible relationships were found: positive; negative; no relationship. At the family level, a negative relationship between altitude and insect body length was found; this was predicted because of a decrease in the diversity of resources, habitat area and primary productivity, and the increase in the unfavourable environment observed at high altitudes. Flight muscle length was also highly variable among tribes; however, for combined gradients, a negative correlation with altitude was found at the family level. Some tribes were either completely macropterous or brachypterous, but at the family level, the percentage of brachyptery increased with altitude. We suggest two hypotheses that may explain the increased incidence of flightlessness observed with increasing altitude: constraints of energy use and reduced need for dispersal potential. At the family level, carabid beetles tended to have a greater body length and decreased brachyptery in disturbed regions compared with old-growth forests. Increased dispersal ability was expected because of the need to find a suitable habitat in disturbed areas. Observed relationships may depend upon which tribes are examined and whether the forest on an altitudinal gradient has been disturbed.

When assessing the benefits and risks of transgenic crops, one consideration is their relative effects on non-target arthropod (NTA) abundance and functions within agroecosystems. Several laboratory and field trials have been conducted in Spain since the late 1990s to assess this issue. A consideration in the design of field trials is whether it is necessary to sample most NTAs living in the crop or only representative taxa that perform main ecological functions and have a good capacity to detect small changes in their abundance. Small changes in the field abundance of an effective representative taxon should be detectable using standard experimental protocols. The ability of a species to reveal differences across treatments may be analysed by examining the detectable treatment effects for surveyed non-target organisms. Analysis of data from several NTAs recorded in 14 field trials conducted over 10 years using complete block designs allowed us to select a number of representative taxa capable of detecting changes in the density or activity of arthropod herbivores, predators, parasitoids and decomposers in transgenic and non-transgenic maize varieties. The most suitable NTA as representative taxa (with detectable treatment effects below 50%) included leafhoppers among arthropod herbivores, Orius spp., Araneae, and Carabidae among predators, chalcidids, particularly the family Mymaridae, among parasitoids and Chloropidae as decomposer. Details of sampling techniques for each sampled taxa and their advantages and disadvantages are discussed. It is concluded that abundance of taxa is the most influential factor determining their capacity to detect changes caused by genetically modified varieties.

Activity of 12 beneficial invertebrate groups was assessed in 2005 and 2006 on a farm in northern England split into conventional and organic management halves, using pitfall and pan traps set in both crops and field boundaries. Management, crop and boundary structure influences on invertebrate activity were assessed, as was the relationship between crop and boundary type. Classification of crop and boundary assemblages produced three and two groups, respectively, in both years. Organic arable crops had well-defined assemblages in both years; and, while grass and grass/clover fields were separated from conventional arable fields in 2005, there was mixing in 2006. One boundary group, in both years, was dominated by conventional arable fields with tall herbaceous boundary vegetation. The other group had more organic arable and grassy fields with shorter boundary vegetation. Redundancy analyses showed that a number of groups (Cantharidae, Coccinellidae, Syrphidae, Ichneumonidae, Braconidae, Proctotrupoidea, Lycosidae) were more active in organic arable fields with more Staphylinidae in conventional arable crops and no obvious trend with Carabidae, Hemiptera, Neuroptera and Linyphiidae. Activity of some groups, especially Coccinellidae, Syrphidae and parasitic wasps, was strongly related to weed cover. Staphylinidae were most active in tall herbaceous boundaries by conventional arable crops with more of a number of groups (Cantharidae, Coccinellidae, parasitic wasps) in short herbaceous boundaries by organic arable crops. Organic management produced most differences in aerially-dispersed invertebrates, and management had a profound effect on activity in field boundaries. Possible management prescriptions to increase invertebrate activity include changing sowing times, weed cover manipulation and field boundary and margin management.

Arion lusitanicus has become a major pest species in western Norway in the last few years. This species originates from southern Europe but has been spread by humans over large parts of central and northern Europe during recent decades. Slugs have traditionally been controlled by the use of molluscicides; but, as these may have serious ecological side effects, biological control of slugs is highly desirable. Potential biological control agents include nematodes, gastropods and arthropods. In laboratory experiments, we tested whether five common predator beetles would feed on eggs and juveniles of A. lusitanicus. The species Carabus nemoralis, Nebria brevicollis, Pterostichus melanarius and Pterostichus niger (Carabidae) as well as Staphylinus erythropterus (Staphylinidae) were tested, of which only P. melanarius has been tested on A. lusitanicus previously. Nebria brevicollis did not feed on slug eggs or newly hatched slugs, but the remaining four species all killed and ate a large proportion of the eggs and hatchlings offered. Both P. melanarius and P. niger also destroyed A. lusitanicus eggs and hatchlings under conditions emulating those in the field. Prey size choice experiments were conducted by feeding C. nemoralis, P. niger and S. erythropterus on different sizes of A. lusitanicus. Carabus nemoralis was also given a choice between two slug species, A. lusitanicus and Deroceras reticulatum. A significant preference for slugs smaller than one gram was evident for C. nemoralis, while the other beetles struggled much more to overcome the mucus of juvenile slugs. No significant preference was found between A. lusitanicus and D. reticulatum as prey for C. nemoralis. We also discuss the feasibility of biological control of A. lusitanicus using beetle predators.

The rates of water loss and humidity preference of carabids from dry tropical habitats have been studied and compared with corresponding data from temperate carabids and tropical tenebrionids. Within each group of beetles the rate of relative water loss decreases with increasing body size. Carabids from dry tropical areas have rates of water loss which are lower than those of temperate species, but considerably higher than the values for tenebrionids from dry tropical habitats. Small temperate carabids can stay in dry air for only a few hours, whereas large tropical tenebrionids may survive for weeks without becoming critically dehydrated. Given the choice between a dry and a humid atmosphere, well hydrated beetles of all groups will initially choose the dry atmosphere. Most temperate carabids will switch to humid atmosphere after a few hours and tropical carabids after 1–3 days, whereas tropical tenebrionids may remain in dry air for almost 3 weeks. The temperate carabids are very sensitive to dehydration and will shift to a humid atmosphere when dehydrated by only 2–5%. Tropical carabids and tenebrionids will shift first when they are dehydrated by 7–20% of their body weight in a hydrated state, implying that these beetles are considerably less sensitive to water loss than temperate carabids.

The effects of predators on prey populations can be modified by a number of abiotic factors. Here, we investigated the combined and separate effects of rain and ground-dwelling predators on aphid populations in a microcosm experiment lasting for 21 days, using PCR to analyse the gut content of the predators. Rain significantly dislodged aphids from shoots and ears by 57% and 25%, respectively. The gut content analysis showed that more predators consumed aphids in the rain treatment than without rain, indicating higher availability of aphids to ground-dwelling predators after rain. However, no synergistic effects of rain and ground-dwelling predators on aphid population development could be demonstrated. Rain alone significantly decreased aphid populations by 27%, suggesting that this is a significant mortality factor. Predators alone had no significant effect on aphid numbers, but the gut content analyses showed aphid consumption also in the no-rain treatments, indicating that aphids were available to the predators on the soil surface even without rain. Our results suggest that weather conditions such as rain can modify predator-prey interactions in the field. Employing PCR-based predator gut content analyses proved to be useful as trophic links could be directly verified.

PCR-based techniques to investigate predator-prey trophic interactions are starting to be used more widely, but factors affecting DNA decay in predator guts are still poorly understood. Here, we investigated the effects of time since feeding, temperature and amplicon size on the detectability of prey DNA in the gut content of two closely related predator species. Cereal aphids, Sitobion avenae, were fed to the carabid beetles Pterostichus melanarius and Nebria brevicollis. Beetles were allowed to digest their meal at 12°C, 16°C and 20°C, and batches of beetles were subsequently frozen at time periods from 0–72 h after feeding. Aphid DNA was detected within beetles' gut contents using primers amplifying fragments of 85, 231, 317 and 383 bp. Prey DNA detection rates were significantly higher in N. brevicollis than in P. melanarius, indicating fundamental dissimilarities in prey digestion capacities. High temperatures (20°C) and large amplicons (383 bp) significantly decreased detection rates. The shortest amplicon gave the highest prey DNA detection success, whereas no differences were observed between the 231 bp and the 317 bp fragment. Our results indicate that factors such as ambient temperature, predator taxon and amplicon size should all be considered when interpreting data derived from PCR-based prey detection. Correction for such factors should make calculation of predation rates in the field more accurate and could help us to estimate when predation events occur in the field.

Carabid inventories gained via pitfall trapping were compared to manual samples from light towers. A comparison of the two methods indicated that pitfall traps recorded a significantly higher diversity of carabids and were efficient in indicating changes of habitat conditions. Nevertheless, this method failed to give near-complete inventories of all carabid species present. Manual sampling at light towers resulted in far greater sample sizes, and this method was particularly efficient in monitoring potential pest species, but again failed to record all species present. Both methods hence showed different strengths, and only a combination, potentially also including further sampling techniques, will enable the generation of complete species inventories.

Environment-friendly farming techniques seek to increase invertebrate biodiversity in part with the intention of encouraging greater numbers of predators that will help to control crop pests. However, in theory, this effect may be negated if the availability of a greater abundance and diversity of alternative prey diverts predators away from feeding on pests. The hypothesis that access to alternative prey can lead to reduced pest suppression under semi-field conditions was tested. Alternative prey type and diversity were manipulated in 70 mesocosms over 7+ weeks in the presence of the carabid Pterostichus melanarius (Illiger), a known predator of slugs, and reproducing populations of the slug Deroceras reticulatum (Müller). Significantly fewer slugs survived where no alternative prey were provided. Maximum slug numbers and biomass were found in treatments containing either carabids plus a high diversity of alternative prey (many species of earthworm and three of Diptera larvae) or a single additional prey (blowfly larvae, Calliphora vomitoria Linnaeus). In these treatments slug numbers and biomass were as high as in plots lacking predators. The effects of alternative prey were taxon-specific. Alternative prey strongly affected carabid fitness in terms of biomass and egg load. The fittest predators (those with access to high alternative prey diversity or C. vomitoria larvae) reduced slug numbers the least. The mean individual slug weights were greater in treatments with alternative prey than where no alternative prey were provided to the carabids. These results suggest that pests may survive and reproduce more rapidly in patches where predators have access to alternative prey.

The influence of farm management practices on ground-dwelling natural enemy communities and predation of insects and weed seeds was investigated over the first 2 years of the transition from conventional to organic production. Three transition strategies were selected that differed in their management and input intensities, and were characteristic of pasture/ley systems (low intensity), cash grain systems (intermediate intensity), and vegetable production (high intensity). Beneficial arthropods (insectivores and granivores) were monitored using pitfall (arthropod activity) and quadrat (arthropod density) samples. The frequency of predation on restrained larvae of Galleria mellonella and the species observed feeding were recorded. Weekly removal rates of weed seeds representative of abundant species at our site were monitored over a 3-week period during fall. Management intensity affected the activity and abundance of biological control agents. In year two of the transition, biological control agent densities were higher in the low-intensity treatment than in the other two treatments, but activity of insectivores and granivores was reduced in this treatment relative to the higher intensity systems. The patterns in the abundances of biological control agents may be explained by habitat stability within the different cropping systems. Quadrat samples were strongly correlated with the insectivory index, although pitfall samples were not. Insectivory rates were highest (>80% of G. mellonella larvae) in the low-intensity treatment. Predation patterns over a 17-h period differed substantially among the management treatments, indicating behaviorally distinct insectivore communities. Seed removal was also highest in the low-intensity treatment. We conclude that low-intensity cropping systems are most favorable to the abundance and function of beneficial ground-dwelling arthropod communities (insectivores and granivores) during the transition process.

Predatory beetles contribute to the control of crop pests and are an important food resource for farmland birds. Many of these beetle species overwinter as larvae within agricultural soils, however, their spatio-temporal emergence patterns are poorly understood, even though such knowledge can assist with their management for biocontrol. Soil moisture is considered to be a key factor influencing oviposition site selection and larval survival. The time, density and spatial pattern of Carabidae and Staphylidae emergence was therefore measured across two fields and compared to soil moisture levels in the previous winter and adult distribution in the previous July. The mean density of Carabidae and Staphylidae that emerged between April and harvest within each field was 157 and 86 m−2, indicating that soils are an important over-wintering habitat for beneficial invertebrates and should be managed sympathetically if numbers are to be increased. Of the species that were sufficiently numerous to allow their spatial pattern to be analysed, all showed a heterogeneous emergence pattern, although patches with high emergence were stable over the sampling period. The distribution of eight species was influenced by soil moisture levels in the previous winter and eight species, although not the same, were spatially associated with the distribution of adults in the previous summer suggesting that the females selected oviposition areas with the appropriate soil wetness.

Non-target organisms associated with the soil might be adversely affected by exposure to the Cry1Ab protein from Bacillus thuringiensis (Bt) in transgenic corn (Zea mays L.). To check for such exposure, we used ELISA to test for Cry1Ab in ground beetles collected live from fields with Bt corn residues and Bt corn (Bt/Bt), Bt corn residues and non-Bt crops (Bt/non-Bt), or non-Bt corn residues and non-Bt crops (non-Bt/non-Bt). In fields with Bt corn residues (Bt/Bt and Bt/non-Bt), Cry1Ab was present in all seven species of ground beetles examined (Agonum placidum, Bembidion rupicola, Clivina impressefrons, Cyclotrachelus iowensis, Harpalus pensylvanicus, Poecilus chalcites, and Poecilus lucublandus). For the two most abundant species, P. chalcites and P. lucublandus, the proportion of beetles with Cry1Ab was significantly higher in Bt/Bt fields (0.50–1.0) and Bt/non-Bt fields (0.41–0.50) than in non-Bt/non-Bt fields (0.0). This is the first field evidence that some ground beetle species are exposed to Cry1Ab. The implications of exposure on the performance of these non-target organisms are unclear.

The carabid beetle assemblage found feeding on fig fruit falls at night was studied in a terra firme rain forest near Manaus (Amazonia) from July 1991 to August 1996. A total of 8926 carabid beetles were collected on 64 fruit falls from 10 fig species. The most abundant genus was Notiobia with eight species, N. pseudolimbipennis being the most abundant. The Notiobia species comprised 92% of all specimens collected and all feed on small fig seeds. Their species abundance patterns varied considerably between individual fruit falls and during the course of a single fruit fall. However, the species abundance patterns for all Notiobia at all observed fruit falls for each of the two commonest fig species (Ficus subapiculata, F. guianensis), as well as for fruit falls of the remaining fig species, were very similar. Through feeding and breeding experiments and observations of reproductive success by dissection of females, only two of the eight Notiobia species were found to be specialized fig seed feeders, being able to reproduce only on fig fruit falls. The remaining six species of this genus use fig fruit falls as alternate hosts or ‘stepping stones’ between fruit falls of their host trees, which are widely separated both in time and space.