Abstract:Environmental filtering, including the influence of environmental constraints and biological interactions on species' survival, is known to significantly affect patterns of community assembly in terrestrial ecosystems. However, its role in regulating patterns and processes of community assembly in deep-sea environments is poorly studied. Here we investigated the role of wood characteristics in the assembly of deep-sea wood fall communities. Ten different wood species (substrata) that varied in structural compl… Show more
“…The δ 13 C values of the 40 specimens of Xylophaga s.l. zierenbergi removed from different types of wood by Judge and Barry (2016) and likely preserved in the same batch of 95% ethanol exceeded the isotopic δ 13 C range of the other 32 specimens considered, regardless of different chemicals used to preserve the latter (Figure 1). The specimens analyzed that were preserved by different chemical treatments (Table 1) did not significantly differ in either δ 13 C or δ 15 N isotopic values from specimens reported in the literature that had been frozen (noted in Table 3) prior to isotopic analyses (for δ 13 C isotopic values W = 0.514; p > 0.05; for δ 15 N isotopic values W = 0.543; p > 0.05).…”
Section: Preservation Artifact?mentioning
confidence: 94%
“…Specimens of Xylophaga zierenbergi removed from bark-covered pine and oak logs have distinctly depleted δ 13 C values compared to conspecifics from the wood of spice bush, island ironwood, and Douglas fir. Those from logs of P. pinea, identified by Judge and Barry (2016), also have relatively enriched δ 15 N values. Why these seemingly anomalous values are present remains open to conjecture and may offer an attractive area for future research.…”
Section: The Effects Of Woodmentioning
confidence: 99%
“…zierenbergi from six deployments. wood bundles (WB) except aqua diamonds: from Douglas fir on Endeavour Segment, Juan de Fuca Ridge at 2211 m depth (Voight, 2007); all others are from deployments near Monterey Canyon at 3100 m depth (Judge and Barry, 2016): blue crosses bark-covered pine log (WB17); green circles bark-covered oak log (WB23); orange triangles gingko logs (WB26); pink stars spicebush sticks (WB19); purple squares island ironwood (WB32).…”
Section: Clade Membership and Preservation Effectsmentioning
confidence: 99%
“…Although filter feeding may be opportunistic and not necessarily occur in every habitat or in every taxon, assuming that wood is the sole source of energy available to wood-fall communities may be fallacious. The amount of unknown variation in the composition of wood-fall communities (McClain and Barry, 2014;Judge and Barry, 2016) argues that assumptions should be re-examined.…”
Section: Xylophagy: a Flawed Conclusion?mentioning
Deep-sea wood-boring xylophagaid bivalves are thought to ingest only wood and to use nitrogen fixed by their symbiotic microbes. Reconsidering this assumption, we tested whether δ 13 C and δ 15 N isotopic values of ten species in four xylophagaid genera collected between 18 m and 4626 m depth suggest that some may use different trophic strategies. Isotopic signatures of six species were entirely consistent with predicted xylophagy, but four species, three members of the Xylophaga dorsalis clade and Abditoconus heterosiphon, had δ 15 N signatures over 3.7 , significantly higher than the value predicted for nitrogen fixed by bacteria. These species may supplement freshly fixed nitrogen with an alternate source, such as particulate organic material. Although the animals' reduced palps and the lack of microbes in the gut of laboratorymaintained specimens were cited as arguing against filter feeding, the animals may filter feed opportunistically. A. heterosiphon was unique in having δ 13 C signatures more negative than the wood into which they bored, inconsistent with cellulose consumption, and δ 15 N values higher than predicted for nitrogen fixed by bacteria. We suggest that greater trophic diversity may exist among xylophagaids than has been expected. Ecological studies of wood-fall communities cannot assume that the entire community is sustained only by wood-bound energy. We attribute variation in δ 13 C signatures among 42 specimens of X. s.l. zierenbergi from six collections, five at the same depth, to variation in the type of wood bored. Investigators beginning food web studies should sample xylophagaids and wood itself; if the deployment is large, repeated samples of the wood, closely matched to xylophagaids, may be necessarily to fully define the substrate's stable isotopic signal.
“…The δ 13 C values of the 40 specimens of Xylophaga s.l. zierenbergi removed from different types of wood by Judge and Barry (2016) and likely preserved in the same batch of 95% ethanol exceeded the isotopic δ 13 C range of the other 32 specimens considered, regardless of different chemicals used to preserve the latter (Figure 1). The specimens analyzed that were preserved by different chemical treatments (Table 1) did not significantly differ in either δ 13 C or δ 15 N isotopic values from specimens reported in the literature that had been frozen (noted in Table 3) prior to isotopic analyses (for δ 13 C isotopic values W = 0.514; p > 0.05; for δ 15 N isotopic values W = 0.543; p > 0.05).…”
Section: Preservation Artifact?mentioning
confidence: 94%
“…Specimens of Xylophaga zierenbergi removed from bark-covered pine and oak logs have distinctly depleted δ 13 C values compared to conspecifics from the wood of spice bush, island ironwood, and Douglas fir. Those from logs of P. pinea, identified by Judge and Barry (2016), also have relatively enriched δ 15 N values. Why these seemingly anomalous values are present remains open to conjecture and may offer an attractive area for future research.…”
Section: The Effects Of Woodmentioning
confidence: 99%
“…zierenbergi from six deployments. wood bundles (WB) except aqua diamonds: from Douglas fir on Endeavour Segment, Juan de Fuca Ridge at 2211 m depth (Voight, 2007); all others are from deployments near Monterey Canyon at 3100 m depth (Judge and Barry, 2016): blue crosses bark-covered pine log (WB17); green circles bark-covered oak log (WB23); orange triangles gingko logs (WB26); pink stars spicebush sticks (WB19); purple squares island ironwood (WB32).…”
Section: Clade Membership and Preservation Effectsmentioning
confidence: 99%
“…Although filter feeding may be opportunistic and not necessarily occur in every habitat or in every taxon, assuming that wood is the sole source of energy available to wood-fall communities may be fallacious. The amount of unknown variation in the composition of wood-fall communities (McClain and Barry, 2014;Judge and Barry, 2016) argues that assumptions should be re-examined.…”
Section: Xylophagy: a Flawed Conclusion?mentioning
Deep-sea wood-boring xylophagaid bivalves are thought to ingest only wood and to use nitrogen fixed by their symbiotic microbes. Reconsidering this assumption, we tested whether δ 13 C and δ 15 N isotopic values of ten species in four xylophagaid genera collected between 18 m and 4626 m depth suggest that some may use different trophic strategies. Isotopic signatures of six species were entirely consistent with predicted xylophagy, but four species, three members of the Xylophaga dorsalis clade and Abditoconus heterosiphon, had δ 15 N signatures over 3.7 , significantly higher than the value predicted for nitrogen fixed by bacteria. These species may supplement freshly fixed nitrogen with an alternate source, such as particulate organic material. Although the animals' reduced palps and the lack of microbes in the gut of laboratorymaintained specimens were cited as arguing against filter feeding, the animals may filter feed opportunistically. A. heterosiphon was unique in having δ 13 C signatures more negative than the wood into which they bored, inconsistent with cellulose consumption, and δ 15 N values higher than predicted for nitrogen fixed by bacteria. We suggest that greater trophic diversity may exist among xylophagaids than has been expected. Ecological studies of wood-fall communities cannot assume that the entire community is sustained only by wood-bound energy. We attribute variation in δ 13 C signatures among 42 specimens of X. s.l. zierenbergi from six collections, five at the same depth, to variation in the type of wood bored. Investigators beginning food web studies should sample xylophagaids and wood itself; if the deployment is large, repeated samples of the wood, closely matched to xylophagaids, may be necessarily to fully define the substrate's stable isotopic signal.
“…It is possible that this heterogeneity modifies the relationship. The importance of heterogeneity also plays a role in wood falls; for example, when there is heterogeneity in species of wood and what part of the tree is present, different communities are assembled on the food resource (Judge and Barry ). While the isolation of wood falls makes for excellent study systems, most other systems are not so isolated, and understanding the interplay between this lack of isolation and body‐size relationships will be important in explaining patterns across systems.…”
Patterns in body size are important to study as the size of an organism correlates with many biological traits of the organism. Changes in the size distribution of a community can be indicative of environmental change and/or anthropogenic impacts. What structures body size is, however, still poorly understood, with many factors proposed and shown to influence body size, including energy, which is likely a major driver. The deep sea is a good test bed to explore the relationship between body size and the availability of energy as it is an energy‐poor system, and strong responses to energy changes are expected. Here, we test the increased packing hypothesis that states that the modal size class should increase with energy, while other size classes reduce in abundance, resulting in less variance in the distribution. This has been demonstrated to be the case in a system with discrete food resources, but here we test what happens when energy is not discretely distributed. Furthermore, we test for alternative explanations using habitat structure to explain patterns in body size. We find no support for the increased packing hypothesis for the two energy variables used, but we did find strong patterns with habitat structure. Only when habitat structure was included did we find a small effect of particulate organic carbon on the mean body size. It is likely that how energy is partitioned in an ecosystem influences its structuring effect; when energy is not distributed in a discrete way, this can obfuscate the relationship. Habitat structure influences how energy is distributed in a system, and studying body size in relation to both habitat structure and energy may further our understanding in what structures this aspect of benthic communities.
Wood in the deep‐sea serves as substantial food source in an otherwise barren environment, forming specialized, endemic, and diverse community assemblages. This biodiversity reliance on a terrestrial source creates a linkage by which anthropogenic impacts on land can alter the deep oceans. Knowledge of alpha‐ or beta‐diversity of entire wood‐fall communities, and wooden drivers of each would elucidate the terrestrial and deep‐sea linkage. We report on a multifactorial experiment in the deep ocean in which alpha‐ and beta‐diversity of 43 wood‐falls and 11 tree species are quantified over time, wood density, and wood size. We tested multiple hypotheses seeking to link how biodiversity on land may impact the biodiversity in the deep oceans. A tremendous biodiversity occurred among these wood‐falls in the deep Gulf of Mexico; 114 invertebrate species from 10 phyla. Time, wood hardness, and wood size all impacted various components of community structure. In many cases, these effects were additive. Species occurring on soft versus hard woods and small versus large wood falls were compositionally different. Although a variety of processes can control community structure, this experiment suggests a strong influence of environmental filtering and host specificity of wood‐fall invertebrates suggesting and intimate coupling to tree biodiversity and biomass on land.This article is protected by copyright. All rights reserved.
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